This is a Validated Antibody Database (VAD) review about human MYH2, based on 226 published articles (read how Labome selects the articles), using MYH2 antibody in all methods. It is aimed to help Labome visitors find the most suited MYH2 antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
MYH2 synonym: IBM3; MYH2A; MYHSA2; MYHas8; MYPOP; MyHC-2A; MyHC-IIa

Santa Cruz Biotechnology
mouse monoclonal (N2.261)
  • immunohistochemistry - frozen section; mouse; 1:200; loading ...; fig s8a
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, sc-53096) was used in immunohistochemistry - frozen section on mouse samples at 1:200 (fig s8a). Nat Commun (2021) ncbi
mouse monoclonal (B-5)
  • western blot; mouse; loading ...; fig 9
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, sc-376157) was used in western blot on mouse samples (fig 9). Physiol Rep (2021) ncbi
mouse monoclonal (F59)
  • immunocytochemistry; human; loading ...; fig 2c
  • western blot; human; 1:300; loading ...; fig 2c
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz Biotechnology, Sc-32732) was used in immunocytochemistry on human samples (fig 2c) and in western blot on human samples at 1:300 (fig 2c). elife (2020) ncbi
mouse monoclonal (B-5)
  • western blot; mouse; 1:2000; loading ...; fig 1c
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, sc-376157) was used in western blot on mouse samples at 1:2000 (fig 1c). Aging (Albany NY) (2020) ncbi
mouse monoclonal (F59)
  • immunohistochemistry; giant danio ; 2 ug/ml; loading ...; fig 4i
Santa Cruz Biotechnology MYH2 antibody (Santa, sc?\32732) was used in immunohistochemistry on giant danio samples at 2 ug/ml (fig 4i). Dev Dyn (2019) ncbi
mouse monoclonal (B-5)
  • immunocytochemistry; human; 1:100; loading ...
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz Biotechnology, sc-376157) was used in immunocytochemistry on human samples at 1:100. elife (2019) ncbi
mouse monoclonal (N2.261)
  • immunohistochemistry - paraffin section; human; loading ...; fig 3a
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, sc-53096) was used in immunohistochemistry - paraffin section on human samples (fig 3a). Circ Cardiovasc Genet (2017) ncbi
mouse monoclonal (B-5)
  • immunocytochemistry; mouse; 1:2000; loading ...; fig 2c
  • western blot; mouse; 1:2000; loading ...; fig 2b
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, sc-376157) was used in immunocytochemistry on mouse samples at 1:2000 (fig 2c) and in western blot on mouse samples at 1:2000 (fig 2b). Gene (2017) ncbi
mouse monoclonal (B-5)
  • western blot; mouse; 1:1000; fig 4d
Santa Cruz Biotechnology MYH2 antibody (SantaCruz, sc-376157) was used in western blot on mouse samples at 1:1000 (fig 4d). Sci Rep (2017) ncbi
mouse monoclonal (B-5)
  • immunocytochemistry; mouse; 1:100; loading ...; fig 5b ii
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, sc-376157) was used in immunocytochemistry on mouse samples at 1:100 (fig 5b ii). Biomater Res (2017) ncbi
mouse monoclonal (B-5)
  • western blot; mouse; loading ...; fig 1c
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, sc-376157) was used in western blot on mouse samples (fig 1c). Oncotarget (2016) ncbi
mouse monoclonal (6D595)
  • immunohistochemistry - paraffin section; rat; fig 2
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, sc-71632) was used in immunohistochemistry - paraffin section on rat samples (fig 2). Springerplus (2016) ncbi
mouse monoclonal (A4.1025)
  • immunocytochemistry; human; 1:250; loading ...; fig 1c
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, sc-53088) was used in immunocytochemistry on human samples at 1:250 (fig 1c). Invest Ophthalmol Vis Sci (2016) ncbi
mouse monoclonal (F59)
  • western blot; mouse; fig 5
In order to analyze promotion of development of distinct sarcoma subtypes in hepatocyte growth factor-mediated satellite cells niche disruption, Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, sc-32732) was used in western blot on mouse samples (fig 5). elife (2016) ncbi
mouse monoclonal (A4.74)
  • immunocytochemistry; mouse; 1:50; loading ...; fig 1d
  • western blot; mouse; 1:1000; loading ...; fig 1b
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, sc-53095) was used in immunocytochemistry on mouse samples at 1:50 (fig 1d) and in western blot on mouse samples at 1:1000 (fig 1b). Cell Signal (2016) ncbi
mouse monoclonal (A4.1025)
  • western blot; pigs
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, SC-53088) was used in western blot on pigs samples . Eur J Nutr (2016) ncbi
mouse monoclonal (F59)
  • western blot; human
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, SC-32732) was used in western blot on human samples . PLoS ONE (2015) ncbi
mouse monoclonal (A4.1519)
Santa Cruz Biotechnology MYH2 antibody (Santa Cruz, sc-53094) was used . PLoS Pathog (2013) ncbi
Invitrogen
mouse monoclonal (MYSN02 (MY-32))
  • immunohistochemistry - frozen section; mouse; 1:100; loading ...; fig 6c
  • immunocytochemistry; mouse; 1:100; loading ...; fig 4b
In order to study the role of myomerger in skeletal muscle development, Invitrogen MYH2 antibody (ThermoFisher, MA5-11748) was used in immunohistochemistry - frozen section on mouse samples at 1:100 (fig 6c) and in immunocytochemistry on mouse samples at 1:100 (fig 4b). Nat Commun (2017) ncbi
mouse monoclonal (MY32)
  • immunohistochemistry - frozen section; mouse; fig 1
In order to test if the "dying back" axonopathy in a pure fast-fatigable alpha-motor axon nerve is a length-dependent process, Invitrogen MYH2 antibody (Thermo Fisher, My32) was used in immunohistochemistry - frozen section on mouse samples (fig 1). Neuroscience (2016) ncbi
Abcam
domestic rabbit monoclonal (EPR5280)
  • immunohistochemistry - frozen section; Daurian ground squirrel; 1:400; loading ...; fig 5
Abcam MYH2 antibody (Abcam, ab124937) was used in immunohistochemistry - frozen section on Daurian ground squirrel samples at 1:400 (fig 5). J Appl Physiol (1985) (2019) ncbi
Developmental Studies Hybridoma Bank
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; loading ...; fig 4f
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF-20) was used in immunocytochemistry on mouse samples (fig 4f). elife (2022) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; human; 1:500; loading ...; fig 1k
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on human samples at 1:500 (fig 1k). Mol Ther Methods Clin Dev (2022) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; axolotl; 1:100; loading ...; fig s3c
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry on axolotl samples at 1:100 (fig s3c). Development (2022) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; human; loading ...; fig 4e
  • immunohistochemistry - paraffin section; zebrafish ; loading ...; fig s5b
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF-20) was used in immunocytochemistry on human samples (fig 4e) and in immunohistochemistry - paraffin section on zebrafish samples (fig s5b). Cell Rep (2022) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - paraffin section; mouse; 1:50; loading ...; fig 3g
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - paraffin section on mouse samples at 1:50 (fig 3g). J Cachexia Sarcopenia Muscle (2022) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; 0.5 ug/ml; loading ...; fig 2a
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples at 0.5 ug/ml (fig 2a). J Clin Invest (2022) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:10; loading ...; fig 1a
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on mouse samples at 1:10 (fig 1a). Dev Cell (2021) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; mouse; loading ...; fig 2f
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry on mouse samples (fig 2f). Nat Commun (2021) ncbi
mouse monoclonal (MF 20)
  • western blot; human; loading ...; fig 1b
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in western blot on human samples (fig 1b). PLoS Genet (2021) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 2b
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples (fig 2b). Cell Metab (2021) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:500; loading ...; fig 5g
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on mouse samples at 1:500 (fig 5g). J Cell Mol Med (2021) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; 1:50; loading ...; fig 2a
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples at 1:50 (fig 2a). Front Cell Dev Biol (2021) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; fig 5c
  • western blot; mouse; fig 5a
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on mouse samples (fig 5c) and in western blot on mouse samples (fig 5a). BMC Biol (2021) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:300; loading ...; fig 1d
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF 20) was used in immunocytochemistry on mouse samples at 1:300 (fig 1d). Nat Commun (2021) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:50; loading ...; fig 2d
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF-20) was used in immunocytochemistry on mouse samples at 1:50 (fig 2d). Skelet Muscle (2021) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; mouse; 1:50; loading ...; fig 2e
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF 20) was used in immunohistochemistry on mouse samples at 1:50 (fig 2e). J Exp Med (2021) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; mouse; 1:20; loading ...; fig 2d
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry on mouse samples at 1:20 (fig 2d). Nat Commun (2021) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; 1:250; loading ...; fig 2b
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples at 1:250 (fig 2b). Aging Cell (2021) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; mouse; 5 ug/ml; loading ...; fig 3b
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry on mouse samples at 5 ug/ml (fig 3b). Int J Mol Sci (2021) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; mouse; loading ...
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry on mouse samples . Cell Rep (2021) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; 1:100; fig 2a
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples at 1:100 (fig 2a). Nat Commun (2021) ncbi
mouse monoclonal (A4.74)
  • western blot; human; 1:200
Developmental Studies Hybridoma Bank MYH2 antibody (DHSB, A4.74) was used in western blot on human samples at 1:200. Am J Hum Genet (2021) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 5d
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples (fig 5d). J Biol Chem (2021) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 2e
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples (fig 2e). Nutrients (2021) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; human; 1:50; fig 1a
  • western blot; human; 1:200; fig 2c
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry on human samples at 1:50 (fig 1a) and in western blot on human samples at 1:200 (fig 2c). elife (2021) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; loading ...; fig 7a, 7c
  • immunocytochemistry; human; loading ...; fig 7b
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF-20) was used in immunocytochemistry on mouse samples (fig 7a, 7c) and in immunocytochemistry on human samples (fig 7b). J Clin Invest (2021) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; 1:200; loading ...; fig 3b
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples at 1:200 (fig 3b). J Clin Invest (2021) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:10; loading ...; fig 3c
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, AB_2147781) was used in immunocytochemistry on mouse samples at 1:10 (fig 3c). Cell Death Dis (2020) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; zebrafish ; 1:300; loading ...; fig 4i
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry on zebrafish samples at 1:300 (fig 4i). elife (2020) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; loading ...; fig s2a
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC71) was used in immunohistochemistry - frozen section on mouse samples (fig s2a). Acta Neuropathol Commun (2020) ncbi
mouse monoclonal (SC-71)
  • western blot; mouse; loading ...; fig 6c
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in western blot on mouse samples (fig 6c). elife (2020) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; mouse; 1:500; loading ...; fig s4-2a, 2b
Developmental Studies Hybridoma Bank MYH2 antibody (DHSB, MF 20) was used in immunohistochemistry on mouse samples at 1:500 (fig s4-2a, 2b). elife (2020) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 1a
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry - frozen section on mouse samples (fig 1a). elife (2020) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; 2 ug/ml; loading ...; fig s6a
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples at 2 ug/ml (fig s6a). Hum Mol Genet (2020) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; human; 1:10; loading ...; fig 4b
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on human samples at 1:10 (fig 4b). Front Physiol (2020) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; mouse; 1:5; loading ...
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry on mouse samples at 1:5. Acta Neuropathol Commun (2020) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; human; 1:1000; loading ...; fig 1b
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on human samples at 1:1000 (fig 1b). elife (2020) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; mouse; loading ...; fig 2c
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF 20) was used in immunohistochemistry on mouse samples (fig 2c). Cell Rep (2020) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; mouse; loading ...; fig 4b
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry on mouse samples (fig 4b). Physiol Rep (2020) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; 1:100; loading ...; fig 3f
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry - frozen section on mouse samples at 1:100 (fig 3f). elife (2019) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - frozen section; human; 1:100; loading ...; fig 7s1c
  • immunocytochemistry; human; 1:100; loading ...; fig 1d
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry - frozen section on human samples at 1:100 (fig 7s1c) and in immunocytochemistry on human samples at 1:100 (fig 1d). elife (2019) ncbi
mouse monoclonal (SC-71)
  • western blot; human; 1:200; loading ...; fig 2c
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in western blot on human samples at 1:200 (fig 2c). elife (2019) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - frozen section; mouse; 1:100; loading ...; fig s2a
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry - frozen section on mouse samples at 1:100 (fig s2a). Cell Rep (2019) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - frozen section; jerboas; 1:20; loading ...; fig 2s1
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry - frozen section on jerboas samples at 1:20 (fig 2s1). elife (2019) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:50; loading ...; fig 6s2a
  • western blot; mouse; 1:200; loading ...; fig 6s2e
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF 20) was used in immunocytochemistry on mouse samples at 1:50 (fig 6s2a) and in western blot on mouse samples at 1:200 (fig 6s2e). elife (2019) ncbi
mouse monoclonal (MF 20)
  • western blot; mouse; loading ...; fig 2d
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF-20) was used in western blot on mouse samples (fig 2d). Sci Rep (2019) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - paraffin section; mouse; 1:50; loading ...; fig 2f
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry - paraffin section on mouse samples at 1:50 (fig 2f). Cell Res (2019) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - paraffin section; dogs; 1:10; loading ...; fig 14
  • western blot; human; 1:400; loading ...; fig 2c
  • immunohistochemistry - paraffin section; rat; 1:10; loading ...; fig 9
  • western blot; rat; 1:100; loading ...; fig 11, 12c
Developmental Studies Hybridoma Bank MYH2 antibody (DHSB, MF-20) was used in immunohistochemistry - paraffin section on dogs samples at 1:10 (fig 14), in western blot on human samples at 1:400 (fig 2c), in immunohistochemistry - paraffin section on rat samples at 1:10 (fig 9) and in western blot on rat samples at 1:100 (fig 11, 12c). Heliyon (2019) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 4g
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, P3U-1) was used in immunohistochemistry - frozen section on mouse samples (fig 4g). Dev Biol (2019) ncbi
mouse monoclonal (MF 20)
  • flow cytometry; human; 1:20; loading ...; fig s3f, s3h
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in flow cytometry on human samples at 1:20 (fig s3f, s3h). Cell Rep (2019) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - frozen section; human; 1:20; loading ...; fig s2b
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, P13538) was used in immunohistochemistry - frozen section on human samples at 1:20 (fig s2b). Dev Cell (2019) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; rat; 1:600; loading ...; fig 4b
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on rat samples at 1:600 (fig 4b). Sci Adv (2019) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:40; loading ...; fig 2g
Developmental Studies Hybridoma Bank MYH2 antibody (DHSB, MF20) was used in immunocytochemistry on mouse samples at 1:40 (fig 2g). Cell Stem Cell (2018) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 4a
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71-c) was used in immunohistochemistry - frozen section on mouse samples (fig 4a). FASEB J (2019) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:40; fig 4a
Developmental Studies Hybridoma Bank MYH2 antibody (DHSB, MF20) was used in immunocytochemistry on mouse samples at 1:40 (fig 4a). Nature (2018) ncbi
mouse monoclonal (MF 20)
  • flow cytometry; mouse; 1:10; loading ...; fig 1a
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF 20) was used in flow cytometry on mouse samples at 1:10 (fig 1a). Sci Rep (2018) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:50; loading ...; fig 6e
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF-20) was used in immunocytochemistry on mouse samples at 1:50 (fig 6e). Dev Cell (2017) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; fig 4e
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on mouse samples (fig 4e). Dev Cell (2017) ncbi
mouse monoclonal (F59)
  • immunohistochemistry; zebrafish ; fig 1c
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, F59) was used in immunohistochemistry on zebrafish samples (fig 1c). Dev Cell (2017) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 3b
  • western blot; mouse; loading ...; fig 3c
In order to study the role of PPAR beta in PGC-1 alpha metabolism and mitochondria integrity, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples (fig 3b) and in western blot on mouse samples (fig 3c). Cell Metab (2017) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; mouse; 1:1000; loading ...; fig 4a
In order to report the effects of short- and long-term high-fat diets on fast-twitch skeletal muscles, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry on mouse samples at 1:1000 (fig 4a). Physiol Rep (2017) ncbi
mouse monoclonal (BF-35)
  • immunohistochemistry; mouse; 1:100; loading ...; fig 4a
In order to report the effects of short- and long-term high-fat diets on fast-twitch skeletal muscles, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, BF-35) was used in immunohistochemistry on mouse samples at 1:100 (fig 4a). Physiol Rep (2017) ncbi
mouse monoclonal (A4.74)
  • western blot; human; 1:200; loading ...; fig 3c
In order to determine the effects of longitudinal training in older adults, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, A4.74) was used in western blot on human samples at 1:200 (fig 3c). Physiol Rep (2017) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; 1:50; loading ...; fig 1g
In order to elucidate the mechanism by which the I4895T mutation in the type 1 ryanodine receptor/Ca(2+) release channel results in disease, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, sc-71) was used in immunohistochemistry - frozen section on mouse samples at 1:50 (fig 1g). Nat Commun (2017) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; fig 6h
  • western blot; mouse; 1:1000; fig 6d
In order to examine the impact of the unfolded protein response in satellite cell homeostasis during regenerative myogenesis, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on mouse samples (fig 6h) and in western blot on mouse samples at 1:1000 (fig 6d). elife (2017) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 3b
In order to report the physiological role of sarcolipin upregulation in muscle myopathy, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry - frozen section on mouse samples (fig 3b). PLoS ONE (2017) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; 1:200; loading ...; fig 3c
In order to find that the rate of mitochondrial oxidation of calories is important in metabolic disease, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples at 1:200 (fig 3c). Proc Natl Acad Sci U S A (2017) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:100; loading ...; fig 7e
In order to examine the role of laminin on type I and type II pericyte proliferation and differentiation, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF-20) was used in immunocytochemistry on mouse samples at 1:100 (fig 7e). Stem Cell Res Ther (2017) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 1f
In order to characterize the importance of glycolysis transcriptional regulator Nur77 during muscle growth, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples (fig 1f). PLoS ONE (2017) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; 1:100; loading ...; fig 3
In order to implicate 25-hydroxycholesterol as an inducer of muscle wasting, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry - frozen section on mouse samples at 1:100 (fig 3). EBioMedicine (2017) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; mouse; loading ...; fig 5a
In order to discover that a common null polymorphism (R577X) in ACTN3 results in significantly reduced muscle strength in patients with Duchenne muscular dystrophy, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC71) was used in immunohistochemistry on mouse samples (fig 5a). Nat Commun (2017) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; zebrafish ; 1:10; loading ...; fig 3c
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry on zebrafish samples at 1:10 (fig 3c). Sci Rep (2017) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; fig 5e
In order to describe a cardiovascular progenitor population derived during embryonic stem cell differentiation, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunocytochemistry on mouse samples (fig 5e). Stem Cells Int (2016) ncbi
mouse monoclonal (MF 20)
  • western blot; mouse; 1:100; fig 1c
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in western blot on mouse samples at 1:100 (fig 1c). Nat Commun (2017) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; human; fig 2g
In order to describe the transdifferentiation of human dermal fibroblasts towards the cardiac cell lineage, Developmental Studies Hybridoma Bank MYH2 antibody (DHSB, MF20) was used in immunocytochemistry on human samples (fig 2g). Sci Rep (2017) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:100; fig 6e
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on mouse samples at 1:100 (fig 6e). J Neurosci (2017) ncbi
mouse monoclonal (MF 20)
  • flow cytometry; human; 1:20; fig 1d
In order to report that cell density deterministically alters anteroposterior patterning of primitive streak-like priming, Developmental Studies Hybridoma Bank MYH2 antibody (Hybridoma Bank, MF20) was used in flow cytometry on human samples at 1:20 (fig 1d). Nat Commun (2016) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; human; 1:30; loading ...; fig 3b
In order to discuss factors to optimize the repair volumetric tissue defects, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry on human samples at 1:30 (fig 3b). Sci Rep (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; human; 1:200; loading ...
In order to study the effects of ageing, physical activity, pre-frailty on skeletal muscle phenotype and examine the mitochondrial and intramyocellular lipid content of men, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry on human samples at 1:200. J Cachexia Sarcopenia Muscle (2017) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; human; 1:300; fig 2a
In order to identify Ret as a downstream mediator of DUX4 signaling, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF-20) was used in immunocytochemistry on human samples at 1:300 (fig 2a). elife (2016) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; loading ...; fig 2c
  • western blot; mouse; loading ...; fig 2d
In order to explore the expression and function of 4.1R during myogenesis, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF-20) was used in immunocytochemistry on mouse samples (fig 2c) and in western blot on mouse samples (fig 2d). J Biol Chem (2016) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:400; loading ...; fig 4d
In order to investigate the contribution of DUX4 constructs to cell proliferation and differentiation, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on mouse samples at 1:400 (fig 4d). J Cell Sci (2016) ncbi
mouse monoclonal (BF-35)
  • immunohistochemistry; mouse; 1:2
In order to investigate the contribution of TEAD1 to muscle regeneration and pathology, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, BF-35) was used in immunohistochemistry on mouse samples at 1:2. elife (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; mouse; 1:2
In order to investigate the contribution of TEAD1 to muscle regeneration and pathology, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry on mouse samples at 1:2. elife (2016) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; mouse; 1:20; fig 9
In order to investigate the contribution of TEAD1 to muscle regeneration and pathology, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry on mouse samples at 1:20 (fig 9). elife (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; human; 1:500; loading ...; fig 9a
In order to compare the effects of cold water immersion and active recovery on inflammatory and cellular stress responses in skeletal muscle from exercise-trained men, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry on human samples at 1:500 (fig 9a). J Physiol (2017) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; human; loading ...; fig 1a
In order to discuss factors that contribute to the decrease mobility of patients with lower extremity peripheral artery disease, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC.71) was used in immunohistochemistry on human samples (fig 1a). J Transl Med (2016) ncbi
mouse monoclonal (MF 20)
  • western blot; mouse; fig 3
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in western blot on mouse samples (fig 3). Sci Rep (2016) ncbi
mouse monoclonal (A4.74)
  • western blot; human; 1:200; loading ...; fig 7
In order to investigate the effects of unilateral lower limb suspension and subsequent resistance training on muscle function and NKA, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, A4.74) was used in western blot on human samples at 1:200 (fig 7). J Appl Physiol (1985) (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; human; 1:200; loading ...; fig 4a
In order to clarify the role of denervation in modulating mitochondrial function in ageing muscle, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, Sc71) was used in immunohistochemistry - frozen section on human samples at 1:200 (fig 4a). J Physiol (2016) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; mouse; 1:50; loading ...; fig 3g
In order to find a role for chicken ovalbumin upstream promoter-transcription factor II in a murine model of duchenne muscular dystrophy, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry on mouse samples at 1:50 (fig 3g). J Clin Invest (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; rat; 1:200; fig 1
In order to discuss the age-related presence of denervated myofibers and accelerated muscle atrophy, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on rat samples at 1:200 (fig 1). Skelet Muscle (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 4a
In order to explore the role of GRK2 in skeletal muscle physiology, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry - frozen section on mouse samples (fig 4a). J Biol Chem (2016) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; loading ...; tbl 1
In order to evaluate a myotonic dystrophy 1 cellular model, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Hybridoma Bank, MF 20) was used in immunocytochemistry on mouse samples (tbl 1). J Vis Exp (2016) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:5
In order to use transgenic mice to study how endogenous c-Kit receptor activation affects cardiac cell homeostasis and repair, Developmental Studies Hybridoma Bank MYH2 antibody (Hybridoma Bank, MF20) was used in immunocytochemistry on mouse samples at 1:5. Cell Death Dis (2016) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:20; loading ...; fig s3e
In order to explore how the interaction between beta1-integrin and Fgf2 contributes to the satellite cell niche, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunocytochemistry on mouse samples at 1:20 (fig s3e). Nat Med (2016) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; fig 3
  • western blot; mouse; fig 2
In order to analyze the attenuation of the cardiomyogenesis of mouse embryonic stem cells by HIF-1alpha deficiency, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on mouse samples (fig 3) and in western blot on mouse samples (fig 2). PLoS ONE (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; rat; 1:100; loading ...; fig 1d
In order to identify muscle fiber types in rotator cuff muscles in rats, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry on rat samples at 1:100 (fig 1d). Anat Rec (Hoboken) (2016) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; mouse; 1:500; fig s2
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF-20) was used in immunohistochemistry on mouse samples at 1:500 (fig s2). Sci Rep (2016) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - paraffin section; rat; 1:50; fig 2
In order to determine the involvement of the CXCL12 system in adapting skeletal muscles to physical exercise, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry - paraffin section on rat samples at 1:50 (fig 2). Cell Signal (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; fig 5
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples (fig 5). PLoS Genet (2016) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; mouse; 1:100; fig 5
  • western blot; mouse; fig 5
In order to study regulation of muscle development and PDGRFbeta(+)cell stemness by laminin, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry on mouse samples at 1:100 (fig 5) and in western blot on mouse samples (fig 5). Nat Commun (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; mouse; fig 2
In order to study slow-twitch type 1 muscle fibers and diaphragm assessment in mice overexpressing phospholamban, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry on mouse samples (fig 2). Brain Behav (2016) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; human; 1:20
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunocytochemistry on human samples at 1:20. BMC Biol (2016) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - frozen section; Japanese common newt; 1:200; fig 4f
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20-c) was used in immunohistochemistry - frozen section on Japanese common newt samples at 1:200 (fig 4f). Nat Commun (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; rat; loading ...
In order to identify contributing factors of sarcopenia and investigate their mechanism, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC71) was used in immunohistochemistry - frozen section on rat samples . Aging (Albany NY) (2016) ncbi
mouse monoclonal (MF 20)
  • western blot; mouse; loading ...; fig 4b
In order to identify ASC-1 as a regulator of late myogenic differentiation and propose that myotube growth defects are a novel myopathic mechanism, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in western blot on mouse samples (fig 4b). Hum Mol Genet (2016) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:10,000; fig 5
  • western blot; mouse; 1:100; fig 3
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunocytochemistry on mouse samples at 1:10,000 (fig 5) and in western blot on mouse samples at 1:100 (fig 3). Nat Commun (2016) ncbi
mouse monoclonal (MF 20)
  • western blot; mouse; fig 5
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF-20) was used in western blot on mouse samples (fig 5). Dis Model Mech (2016) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; mouse; 1:50; loading ...; tbl 4
In order to describe methods to culture mid-gestation explanted mouse embryos, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunohistochemistry on mouse samples at 1:50 (tbl 4). Differentiation (2016) ncbi
mouse monoclonal (BF-35)
  • immunohistochemistry - frozen section; human; 1:50; fig 2
In order to study a randomized controlled trial of 65 year old healthy males and the effect of 52 weeks of soccer or resistance training on body composition and muscle function, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, BF-35) was used in immunohistochemistry - frozen section on human samples at 1:50 (fig 2). PLoS ONE (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; human; 1:200; loading ...; tbl 2
In order to test if a period of additional speed endurance training improves intense intermittent exercise performance in highly trained soccer players, Developmental Studies Hybridoma Bank MYH2 antibody (Hybridoma Bank, SC-71) was used in immunohistochemistry on human samples at 1:200 (tbl 2). Med Sci Sports Exerc (2016) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; fig 1b
  • western blot; mouse; fig 4a
In order to analyze TBP/TFIID-dependent activation of MyoD target genes in skeletal muscle cells, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on mouse samples (fig 1b) and in western blot on mouse samples (fig 4a). elife (2016) ncbi
mouse monoclonal (A4.74)
  • immunohistochemistry - paraffin section; mouse; 1:50; fig 2
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, A474) was used in immunohistochemistry - paraffin section on mouse samples at 1:50 (fig 2). Sci Rep (2016) ncbi
mouse monoclonal (BF-35)
  • immunohistochemistry - frozen section; bovine; 1:10
In order to study myofibrillar protein degradation and Warner-Bratzler shear force of beef M. semitendinosus steaks and the effect of extended postmortem aging and steak location, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, BF-35) was used in immunohistochemistry - frozen section on bovine samples at 1:10. J Anim Sci (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; 1:1000; fig 1
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples at 1:1000 (fig 1). Oxid Med Cell Longev (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; human; loading ...; fig 7a
In order to report the effects of bed rest on skeletal muscle satellite cell content and fiber type atrophy in middle-aged adults, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC.71) was used in immunohistochemistry - frozen section on human samples (fig 7a). J Appl Physiol (1985) (2016) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; domestic horse; 1:8; fig 1
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry on domestic horse samples at 1:8 (fig 1). Stem Cell Reports (2016) ncbi
mouse monoclonal (BF-35)
  • immunohistochemistry; mouse; fig 4
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, BF-35) was used in immunohistochemistry on mouse samples (fig 4). PLoS ONE (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; mouse; fig 4
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71 (type 2a)) was used in immunohistochemistry on mouse samples (fig 4). PLoS ONE (2016) ncbi
mouse monoclonal (A4.74)
  • western blot; human; 1:200; fig 1
In order to determine cell differences in skeletal muscle from aged individuals regardidng protein abundances of GAPDH and NA,K-ATPase, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, A4.74) was used in western blot on human samples at 1:200 (fig 1). Exp Gerontol (2016) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; dogs; fig S1f
  • western blot; human; fig 4c
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunocytochemistry on dogs samples (fig S1f) and in western blot on human samples (fig 4c). Nucleic Acids Res (2016) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; dogs; fig 2
Developmental Studies Hybridoma Bank MYH2 antibody (Hybridoma, MF20) was used in immunocytochemistry on dogs samples (fig 2). Stem Cells Int (2016) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; human; 1:200; fig 1b
In order to investigate the effects of age on the resilience of slow type fibers, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on human samples at 1:200 (fig 1b). Am J Physiol Cell Physiol (2016) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:50; fig 2h
In order to study embryonic cell self-renewal via Wnt beta-catenin and LIF-Stat3 signalling pathways funneling into Sp5, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF-20) was used in immunocytochemistry on mouse samples at 1:50 (fig 2h). J Cell Sci (2016) ncbi
mouse monoclonal (F59)
  • immunohistochemistry; zebrafish ; fig 2
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, F59) was used in immunohistochemistry on zebrafish samples (fig 2). PLoS ONE (2015) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - frozen section; mouse; 1:50; fig 1
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunohistochemistry - frozen section on mouse samples at 1:50 (fig 1). Skelet Muscle (2015) ncbi
mouse monoclonal (A4.74)
  • western blot; human; fig 1
In order to assess how match performance parameters in trained footballers relate to skeletal muscle parameters, sprint ability, and intermittent exercise performance, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, A4.74) was used in western blot on human samples (fig 1). Eur J Appl Physiol (2016) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - frozen section; mouse; fig 3
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF-20) was used in immunohistochemistry - frozen section on mouse samples (fig 3). PLoS ONE (2015) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; fig 2
  • western blot; mouse; fig 1
In order to analyze myogenic differentiation promotion by syntaxin 4 regulation on the surface localization of Cdo, a promyogenic receptor, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on mouse samples (fig 2) and in western blot on mouse samples (fig 1). Skelet Muscle (2015) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; mouse; fig 1
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry on mouse samples (fig 1). J Biol Chem (2015) ncbi
mouse monoclonal (F59)
  • immunohistochemistry; mouse; loading ...
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, F59) was used in immunohistochemistry on mouse samples . J Cell Biol (2015) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; human; fig s5
In order to investigate how the interaction between protein kinase G and Orai1 contributes to cardiac hypertrophy, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on human samples (fig s5). Stem Cells (2015) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; fig 9
In order to study attenuation of regeneration by blunting the response to pro-inflammatory macrophages due to upregulation of IL-1beta in dysferlin-deficient muscle, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunocytochemistry on mouse samples (fig 9). Skelet Muscle (2015) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - frozen section; mouse; 1:1000; fig s8
  • immunocytochemistry; mouse; 1:1000; fig s1
In order to study how regenerative progenitors can be turned into terminally differentiated skeletal muscle cells, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry - frozen section on mouse samples at 1:1000 (fig s8) and in immunocytochemistry on mouse samples at 1:1000 (fig s1). Nat Commun (2015) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; mouse; fig s5
In order to study the therapeutic use of the inhibitory core of the prodomain of myostatin, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry on mouse samples (fig s5). PLoS ONE (2015) ncbi
mouse monoclonal (A4.74)
  • western blot; human; fig 2
In order to study mechanisms by which chronic beta2-adrenergic stimulation enhances muscle force and power output during maximal cycle ergometer exercise in young men, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, A4.74) was used in western blot on human samples (fig 2). J Appl Physiol (1985) (2015) ncbi
mouse monoclonal (MF 20)
  • western blot; mouse; fig 1
In order to elucidate the molecular mechanism by which histone KMTs and KDMs regulate MyoD transcriptional activity, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in western blot on mouse samples (fig 1). Biochim Biophys Acta (2015) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; fig 3
In order to investigate the role of nebulin in muscle cells using transgenic mice, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples (fig 3). Hum Mol Genet (2015) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; mouse; 1:200; fig 2
Developmental Studies Hybridoma Bank MYH2 antibody (Hybridoma, MF-20) was used in immunohistochemistry on mouse samples at 1:200 (fig 2). Nat Biotechnol (2015) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; fig 2
  • western blot; mouse; fig 2
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on mouse samples (fig 2) and in western blot on mouse samples (fig 2). Nat Commun (2015) ncbi
mouse monoclonal (MF 20)
  • western blot; mouse; 1:1000; fig S2
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in western blot on mouse samples at 1:1000 (fig S2). Nat Commun (2015) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; human
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC.71) was used in immunohistochemistry on human samples . Physiol Rep (2015) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; fig 5
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples (fig 5). Dis Model Mech (2015) ncbi
mouse monoclonal (SC-71)
  • immunocytochemistry; mouse
In order to study SERCA dysfunction in mice overexpressing phospholamban, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunocytochemistry on mouse samples . Dis Model Mech (2015) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; pigs ; 1:200
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Hybridoma Bank, SC-71) was used in immunohistochemistry - frozen section on pigs samples at 1:200. J Anim Sci (2015) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; fig 2
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF-20) was used in immunocytochemistry on mouse samples (fig 2). Skelet Muscle (2015) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; mouse; 1:100; fig 6
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry on mouse samples at 1:100 (fig 6). Nat Commun (2015) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry; newts; 1:2000; fig 1
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry on newts samples at 1:2000 (fig 1). Methods Mol Biol (2015) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; human
In order to examine the effects of CHIR inductionin in stem cells to determine if it enhances development of the cardiomyogenic lineage, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunocytochemistry on human samples . PLoS ONE (2015) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:500
In order to assess how FRG1 expression contributes to myoblast differentiation defects, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunocytochemistry on mouse samples at 1:500. PLoS ONE (2015) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; human; 1:200; tbl 4
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on human samples at 1:200 (tbl 4). J Vis Exp (2015) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - paraffin section; mouse; 1:50
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunohistochemistry - paraffin section on mouse samples at 1:50. Am J Physiol Cell Physiol (2015) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - paraffin section; mouse; 1:100
In order to study heart valve development and cardiac function in Galnt1 KO mice, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunohistochemistry - paraffin section on mouse samples at 1:100. PLoS ONE (2015) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; human; fig 1
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry on human samples (fig 1). Appl Physiol Nutr Metab (2015) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; fig 9
In order to study mice lacking ERK1/2 selectively in skeletal myofibers, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry - frozen section on mouse samples (fig 9). Mol Cell Biol (2015) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; fig 6
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on mouse samples (fig 6). Mol Cell Biol (2015) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; fig 2
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC-71) was used in immunohistochemistry - frozen section on mouse samples (fig 2). Mol Cell Biol (2015) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - frozen section; mouse; 1:100
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunohistochemistry - frozen section on mouse samples at 1:100. J Dent Res (2015) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; fig 1
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunocytochemistry on mouse samples (fig 1). Mol Ther Methods Clin Dev (2014) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse; 1:100
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC.71) was used in immunohistochemistry - frozen section on mouse samples at 1:100. Nat Med (2015) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; 1:2
Developmental Studies Hybridoma Bank MYH2 antibody (DHSB, MF20) was used in immunocytochemistry on mouse samples at 1:2. PLoS ONE (2014) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; rat; 1:40
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry on rat samples at 1:40. Physiol Rep (2014) ncbi
mouse monoclonal (MF 20)
  • chromatin immunoprecipitation; human
  • western blot; human
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF-20) was used in chromatin immunoprecipitation on human samples and in western blot on human samples . Mol Biol Cell (2015) ncbi
mouse monoclonal (MF 20)
  • western blot; human; fig s7
In order to analyze down-regulation in alveolar rhabdomyosarcomas by Caveolin-1 and negative regulation of tumor growth, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF 20) was used in western blot on human samples (fig s7). Oncotarget (2014) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - paraffin section; mouse; 1:50
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunohistochemistry - paraffin section on mouse samples at 1:50. Dev Biol (2014) ncbi
mouse monoclonal (F59)
  • immunohistochemistry; zebrafish ; 1:10
In order to study the role of BAG3 in myofibrillar myopathy, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, F59) was used in immunohistochemistry on zebrafish samples at 1:10. Acta Neuropathol (2014) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; human; 1:500
In order to study the effects of speed endurance training and heavy resistance training on running performance improvement, Developmental Studies Hybridoma Bank MYH2 antibody (Hybridoma Bank, SC-71) was used in immunohistochemistry on human samples at 1:500. J Appl Physiol (1985) (2014) ncbi
mouse monoclonal (F59)
  • immunocytochemistry; mouse; fig 9
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, F59) was used in immunocytochemistry on mouse samples (fig 9). Anat Rec (Hoboken) (2014) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse; fig 6
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF20) was used in immunocytochemistry on mouse samples (fig 6). Anat Rec (Hoboken) (2014) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; mouse; 1:200
  • immunohistochemistry; human; 1:200
  • immunohistochemistry; rat; 1:200
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry on mouse samples at 1:200, in immunohistochemistry on human samples at 1:200 and in immunohistochemistry on rat samples at 1:200. PLoS ONE (2014) ncbi
mouse monoclonal (MF 20)
  • western blot; human; 1:1000
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF 20) was used in western blot on human samples at 1:1000. Pflugers Arch (2015) ncbi
mouse monoclonal (A4.74)
  • immunohistochemistry; human
Developmental Studies Hybridoma Bank MYH2 antibody (Development Studies Hybridoma Bank, A4.74) was used in immunohistochemistry on human samples . Invest Ophthalmol Vis Sci (2014) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; human; 1:500
In order to investigate the effects of regular football training in men with type 2 diabetes mellitus, Developmental Studies Hybridoma Bank MYH2 antibody (Hybridoma Bank, SC-71) was used in immunohistochemistry on human samples at 1:500. Scand J Med Sci Sports (2014) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; human
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC.71) was used in immunohistochemistry on human samples . J Physiol (2014) ncbi
mouse monoclonal (MF 20)
  • western blot; human; 1:1000
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF 20) was used in western blot on human samples at 1:1000. Front Physiol (2014) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse
In order to show that geriatric satellite cells do not maintain their normal quiescent state in muscle homeostatic conditions and that this irreversibly affects their intrinsic regenerative and self-renewal capacities, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry - frozen section on mouse samples . Nature (2014) ncbi
mouse monoclonal (BF-35)
  • immunohistochemistry; bovine
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, BF-35) was used in immunohistochemistry on bovine samples . J Anim Sci (2014) ncbi
mouse monoclonal (A4.74)
  • western blot; human; 1:200; fig 1a
In order to compare calcium uptake of the sarcoplasmic reticulum between type I and type II fibers of vastus lateralis muscle of young healthy adults, Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, A4.74) was used in western blot on human samples at 1:200 (fig 1a). J Physiol (2014) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF-20) was used in immunocytochemistry on mouse samples . PLoS ONE (2014) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; human; 1:200
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry - frozen section on human samples at 1:200. FASEB J (2014) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry; mouse; fig 3
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, SC71) was used in immunohistochemistry on mouse samples (fig 3). Hum Mol Genet (2014) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse
  • western blot; mouse
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF20) was used in immunocytochemistry on mouse samples and in western blot on mouse samples . Muscle Nerve (2014) ncbi
mouse monoclonal (A4.74)
  • immunohistochemistry; human; 1:100
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, A4.74) was used in immunohistochemistry on human samples at 1:100. PLoS ONE (2013) ncbi
mouse monoclonal (MF 20)
  • immunocytochemistry; mouse
  • western blot; mouse
Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, MF-20) was used in immunocytochemistry on mouse samples and in western blot on mouse samples . Nucleic Acids Res (2013) ncbi
mouse monoclonal (MF 20)
  • immunohistochemistry - paraffin section; chicken; 1:200
Developmental Studies Hybridoma Bank MYH2 antibody (DSHB, MF 20) was used in immunohistochemistry - paraffin section on chicken samples at 1:200. J Comp Neurol (2013) ncbi
mouse monoclonal (SC-71)
  • immunohistochemistry - frozen section; mouse
In order to study the role of local IGF production in skeletal muscle and body growth using GRP94 knockout mice, Developmental Studies Hybridoma Bank MYH2 antibody (Developmental Studies Hybridoma Bank, SC-71) was used in immunohistochemistry - frozen section on mouse samples . FASEB J (2012) ncbi
MilliporeSigma
mouse monoclonal (MY-32)
  • immunohistochemistry; mouse; 10 ug/ml; loading ...; fig 1h
MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunohistochemistry on mouse samples at 10 ug/ml (fig 1h). elife (2022) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry - paraffin section; mouse; 1:400; loading ...; fig 2a
MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunohistochemistry - paraffin section on mouse samples at 1:400 (fig 2a). Cell Rep (2022) ncbi
mouse monoclonal (MY-32)
  • immunocytochemistry; mouse; 1:200; loading ...; fig s8h
MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunocytochemistry on mouse samples at 1:200 (fig s8h). Nat Commun (2021) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry; human; 1:200; loading ...; fig 2c
MilliporeSigma MYH2 antibody (Sigma Aldrich, M4276) was used in immunohistochemistry on human samples at 1:200 (fig 2c). elife (2020) ncbi
mouse monoclonal (MY-32)
  • western blot; rat; 1:4500; loading ...; fig 2o
MilliporeSigma MYH2 antibody (Sigma, M4276) was used in western blot on rat samples at 1:4500 (fig 2o). Ann Clin Transl Neurol (2020) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry - frozen section; human; 1:200; loading ...; fig 4c
MilliporeSigma MYH2 antibody (Sigma-Aldrich, M4276) was used in immunohistochemistry - frozen section on human samples at 1:200 (fig 4c). Front Physiol (2020) ncbi
mouse monoclonal (MY-32)
  • western blot; mouse; 1:5000; loading ...; fig s18f
MilliporeSigma MYH2 antibody (Sigma Aldrich, MY32) was used in western blot on mouse samples at 1:5000 (fig s18f). Science (2019) ncbi
mouse monoclonal (MY-32)
  • western blot; mouse; 1:1000; loading ...; fig s2b
MilliporeSigma MYH2 antibody (Sigma, MY-32) was used in western blot on mouse samples at 1:1000 (fig s2b). Redox Biol (2019) ncbi
mouse monoclonal (MY-32)
  • immunocytochemistry; mouse; 1:200; loading ...; fig s3d
MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunocytochemistry on mouse samples at 1:200 (fig s3d). Sci Adv (2018) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry - paraffin section; mouse; loading ...; fig 1m
MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunohistochemistry - paraffin section on mouse samples (fig 1m). J Biol Chem (2017) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 3a
In order to characterize the importance of glycolysis transcriptional regulator Nur77 during muscle growth, MilliporeSigma MYH2 antibody (Sigma, MY32) was used in immunohistochemistry - frozen section on mouse samples (fig 3a). PLoS ONE (2017) ncbi
mouse monoclonal (MY-32)
  • western blot; mouse; 1:1000; fig 1g
MilliporeSigma MYH2 antibody (Sigma-Aldrich, M4276) was used in western blot on mouse samples at 1:1000 (fig 1g). Cell Discov (2016) ncbi
mouse monoclonal (MY-32)
  • immunocytochemistry; human; 1:1000; fig 3
In order to discuss different cell sources from which to generate muscle cells, MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunocytochemistry on human samples at 1:1000 (fig 3). Skelet Muscle (2016) ncbi
mouse monoclonal (MY-32)
  • western blot; mouse; fig 2
In order to investigate the modulator of skeletal muscle sarcomeric morphometry associated to modulation of protein-protein interactions by O-GlcNAcylation, MilliporeSigma MYH2 antibody (Sigma, my32) was used in western blot on mouse samples (fig 2). Biochim Biophys Acta (2016) ncbi
mouse monoclonal (MY-32)
  • immunocytochemistry; mouse; fig 7
MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunocytochemistry on mouse samples (fig 7). Nucleic Acids Res (2016) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry - frozen section; human; 1:2000; loading ...; fig 3a, b
MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunohistochemistry - frozen section on human samples at 1:2000 (fig 3a, b). Biomed Res Int (2016) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry - frozen section; mouse; 1:300; fig 4
MilliporeSigma MYH2 antibody (Sigma-Aldrich, M4276) was used in immunohistochemistry - frozen section on mouse samples at 1:300 (fig 4). PLoS ONE (2016) ncbi
mouse monoclonal (MY-32)
  • immunocytochemistry; mouse; 1:400; fig 1
  • western blot; mouse; 1:3000; fig 2
  • immunocytochemistry; human; 1:400; fig 1
  • western blot; human; 1:3000; fig 2
MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunocytochemistry on mouse samples at 1:400 (fig 1), in western blot on mouse samples at 1:3000 (fig 2), in immunocytochemistry on human samples at 1:400 (fig 1) and in western blot on human samples at 1:3000 (fig 2). Sci Rep (2015) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry - paraffin section; human; 1:1000; fig 5
MilliporeSigma MYH2 antibody (Sigma, M1570) was used in immunohistochemistry - paraffin section on human samples at 1:1000 (fig 5). Physiol Rep (2015) ncbi
mouse monoclonal (MY-32)
  • immunocytochemistry; mouse; fig 5
In order to study the therapeutic use of the inhibitory core of the prodomain of myostatin, MilliporeSigma MYH2 antibody (Sigma-Aldrich, MY-32) was used in immunocytochemistry on mouse samples (fig 5). PLoS ONE (2015) ncbi
mouse monoclonal (MY-32)
  • western blot; chicken; 1:500
MilliporeSigma MYH2 antibody (Sigma-Aldrich, M4276) was used in western blot on chicken samples at 1:500. Biosci Biotechnol Biochem (2015) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry; mouse; 1:250; fig 3
In order to determine tissue specific functions of DLL1 or DLL4 using transgenic mice, MilliporeSigma MYH2 antibody (Sigma-Aldrich, My32) was used in immunohistochemistry on mouse samples at 1:250 (fig 3). PLoS Genet (2015) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry - paraffin section; human; fig 5a
MilliporeSigma MYH2 antibody (SIGMA, M4276) was used in immunohistochemistry - paraffin section on human samples (fig 5a). BMC Genomics (2015) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry - paraffin section; mouse; 1:800; fig 3
MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunohistochemistry - paraffin section on mouse samples at 1:800 (fig 3). Am J Physiol Endocrinol Metab (2015) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry; rat; 1:100
MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunohistochemistry on rat samples at 1:100. Muscle Nerve (2015) ncbi
mouse monoclonal (MY-32)
  • immunocytochemistry; mouse; 1:250; fig 6e
MilliporeSigma MYH2 antibody (Sigma-Aldrich, M4276) was used in immunocytochemistry on mouse samples at 1:250 (fig 6e). Hum Mol Genet (2015) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry - frozen section; human; 1:2000; fig 1
MilliporeSigma MYH2 antibody (sigma, M4276) was used in immunohistochemistry - frozen section on human samples at 1:2000 (fig 1). Biomed Res Int (2015) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry - paraffin section; human
MilliporeSigma MYH2 antibody (Sigma-Aldrich, M4276) was used in immunohistochemistry - paraffin section on human samples . J Surg Res (2015) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry - frozen section; mouse
MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunohistochemistry - frozen section on mouse samples . Skelet Muscle (2015) ncbi
mouse monoclonal (MY-32)
  • immunocytochemistry; mouse; 1:2000; fig 3
MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunocytochemistry on mouse samples at 1:2000 (fig 3). J Cell Biol (2014) ncbi
mouse monoclonal (MY-32)
  • immunocytochemistry; mouse
  • western blot; mouse; 1:4000
MilliporeSigma MYH2 antibody (Sigma-Aldrich, M4276) was used in immunocytochemistry on mouse samples and in western blot on mouse samples at 1:4000. Cell Physiol Biochem (2014) ncbi
mouse monoclonal (MY-32)
  • immunohistochemistry - paraffin section; mouse
In order to study the contribution of chemokine-like receptor-1 in skeletal muscles, MilliporeSigma MYH2 antibody (Sigma, M4276) was used in immunohistochemistry - paraffin section on mouse samples . Am J Physiol Cell Physiol (2012) ncbi
Articles Reviewed
  1. Sefton E, Gallardo M, Tobin C, Collins B, Colasanto M, Merrell A, et al. Fibroblast-derived Hgf controls recruitment and expansion of muscle during morphogenesis of the mammalian diaphragm. elife. 2022;11: pubmed publisher
  2. Wheeler J, Whitney O, Vogler T, Nguyen E, Pawlikowski B, Lester E, et al. RNA-binding proteins direct myogenic cell fate decisions. elife. 2022;11: pubmed publisher
  3. Meng J, Moore M, Counsell J, Muntoni F, Popplewell L, Morgan J. Optimized lentiviral vector to restore full-length dystrophin via a cell-mediated approach in a mouse model of Duchenne muscular dystrophy. Mol Ther Methods Clin Dev. 2022;25:491-507 pubmed publisher
  4. Schr xf6 tter S, Yuskaitis C, MacArthur M, Mitchell S, Hosios A, Osipovich M, et al. The non-essential TSC complex component TBC1D7 restricts tissue mTORC1 signaling and brain and neuron growth. Cell Rep. 2022;39:110824 pubmed publisher
  5. Walker S, Sabin K, Gearhart M, Yamamoto K, Echeverri K. Regulation of stem cell identity by miR-200a during spinal cord regeneration. Development. 2022;149: pubmed publisher
  6. Hsu J, Danis E, Nance S, O Brien J, Gustafson A, Wessells V, et al. SIX1 reprograms myogenic transcription factors to maintain the rhabdomyosarcoma undifferentiated state. Cell Rep. 2022;38:110323 pubmed publisher
  7. Luan Y, Zhang Y, Yu S, You M, Xu P, Chung S, et al. Development of ovarian tumour causes significant loss of muscle and adipose tissue: a novel mouse model for cancer cachexia study. J Cachexia Sarcopenia Muscle. 2022;13:1289-1301 pubmed publisher
  8. Bartoli F, Debant M, Chuntharpursat Bon E, Evans E, Musialowski K, Parsonage G, et al. Endothelial Piezo1 sustains muscle capillary density and contributes to physical activity. J Clin Invest. 2022;132: pubmed publisher
  9. Eigler T, Zarfati G, Amzallag E, Sinha S, Segev N, Zabary Y, et al. ERK1/2 inhibition promotes robust myotube growth via CaMKII activation resulting in myoblast-to-myotube fusion. Dev Cell. 2021;56:3349-3363.e6 pubmed publisher
  10. Langdon C, Gadek K, Garcia M, Evans M, Reed K, Bush M, et al. Synthetic essentiality between PTEN and core dependency factor PAX7 dictates rhabdomyosarcoma identity. Nat Commun. 2021;12:5520 pubmed publisher
  11. Zhang H, Shang R, Bi P. Feedback regulation of Notch signaling and myogenesis connected by MyoD-Dll1 axis. PLoS Genet. 2021;17:e1009729 pubmed publisher
  12. Fan Z, Turiel G, Ardicoglu R, Ghobrial M, Masschelein E, Kocijan T, et al. Exercise-induced angiogenesis is dependent on metabolically primed ATF3/4+ endothelial cells. Cell Metab. 2021;: pubmed publisher
  13. Song R, Zhao S, Xu Y, Hu J, Ke S, Li F, et al. MRTF-A regulates myoblast commitment to differentiation by targeting PAX7 during muscle regeneration. J Cell Mol Med. 2021;25:8645-8661 pubmed publisher
  14. Joanne P, Hovhannisyan Y, Bencze M, Daher M, Parlakian A, Toutirais G, et al. Absence of Desmin Results in Impaired Adaptive Response to Mechanical Overloading of Skeletal Muscle. Front Cell Dev Biol. 2021;9:662133 pubmed publisher
  15. Coudert L, Osseni A, Gangloff Y, Schaeffer L, Leblanc P. The ESCRT-0 subcomplex component Hrs/Hgs is a master regulator of myogenesis via modulation of signaling and degradation pathways. BMC Biol. 2021;19:153 pubmed publisher
  16. Esteves de Lima J, Bou Akar R, Machado L, Li Y, Drayton Libotte B, Dilworth F, et al. HIRA stabilizes skeletal muscle lineage identity. Nat Commun. 2021;12:3450 pubmed publisher
  17. Kurosaka M, Ogura Y, Sato S, Kohda K, Funabashi T. Transcription factor signal transducer and activator of transcription 6 (STAT6) is an inhibitory factor for adult myogenesis. Skelet Muscle. 2021;11:14 pubmed publisher
  18. Rupert J, Narasimhan A, Jengelley D, Jiang Y, Liu J, Au E, et al. Tumor-derived IL-6 and trans-signaling among tumor, fat, and muscle mediate pancreatic cancer cachexia. J Exp Med. 2021;218: pubmed publisher
  19. Park Y, Lee J, Yan Z, McKernan K, O Haren T, Wang W, et al. Interplay of BAF and MLL4 promotes cell type-specific enhancer activation. Nat Commun. 2021;12:1630 pubmed publisher
  20. Wallace M, Aguirre N, Marcotte G, Marshall A, Baehr L, Hughes D, et al. The ketogenic diet preserves skeletal muscle with aging in mice. Aging Cell. 2021;20:e13322 pubmed publisher
  21. Nichenko A, Sorensen J, Southern W, Qualls A, Schifino A, McFaline Figueroa J, et al. Lifelong Ulk1-Mediated Autophagy Deficiency in Muscle Induces Mitochondrial Dysfunction and Contractile Weakness. Int J Mol Sci. 2021;22: pubmed publisher
  22. Steinert N, Potts G, Wilson G, Klamen A, Lin K, Hermanson J, et al. Mapping of the contraction-induced phosphoproteome identifies TRIM28 as a significant regulator of skeletal muscle size and function. Cell Rep. 2021;34:108796 pubmed publisher
  23. Seo J, Kang J, Kim Y, Jo Y, Kim J, Hann S, et al. Maintenance of type 2 glycolytic myofibers with age by Mib1-Actn3 axis. Nat Commun. 2021;12:1294 pubmed publisher
  24. Wyckelsma V, Venckunas T, Houweling P, Schlittler M, Lauschke V, Tiong C, et al. Loss of α-actinin-3 during human evolution provides superior cold resilience and muscle heat generation. Am J Hum Genet. 2021;108:446-457 pubmed publisher
  25. Chen T, Kuo T, Dandan M, Lee R, Chang M, Villivalam S, et al. The role of striated muscle Pik3r1 in glucose and protein metabolism following chronic glucocorticoid exposure. J Biol Chem. 2021;296:100395 pubmed publisher
  26. Akashi S, Morita A, Mochizuki Y, Shibuya F, Kamei Y, Miura S. Citrus hassaku Extract Powder Increases Mitochondrial Content and Oxidative Muscle Fibers by Upregulation of PGC-1α in Skeletal Muscle. Nutrients. 2021;13: pubmed publisher
  27. Ramirez Martinez A, Zhang Y, Chen K, Kim J, Cenik B, McAnally J, et al. The nuclear envelope protein Net39 is essential for muscle nuclear integrity and chromatin organization. Nat Commun. 2021;12:690 pubmed publisher
  28. Ortiz Cordero C, Magli A, Dhoke N, Kuebler T, Selvaraj S, Oliveira N, et al. NAD+ enhances ribitol and ribose rescue of α-dystroglycan functional glycosylation in human FKRP-mutant myotubes. elife. 2021;10: pubmed publisher
  29. Azar C, Valentine M, Trausch Azar J, Rois L, Mahjoub M, Nelson D, et al. RNA-Seq identifies genes whose proteins are upregulated during syncytia development in murine C2C12 myoblasts and human BeWo trophoblasts. Physiol Rep. 2021;9:e14671 pubmed publisher
  30. Pal A, Leung J, Ang G, Rao V, Pignata L, Lim H, et al. EHMT2 epigenetically suppresses Wnt signaling and is a potential target in embryonal rhabdomyosarcoma. elife. 2020;9: pubmed publisher
  31. Uezumi A, Ikemoto Uezumi M, Zhou H, Kurosawa T, Yoshimoto Y, Nakatani M, et al. Mesenchymal Bmp3b expression maintains skeletal muscle integrity and decreases in age-related sarcopenia. J Clin Invest. 2021;131: pubmed publisher
  32. Chung L, Liu S, Huang S, Salter D, Lee H, Hsu Y. High phosphate induces skeletal muscle atrophy and suppresses myogenic differentiation by increasing oxidative stress and activating Nrf2 signaling. Aging (Albany NY). 2020;12:21446-21468 pubmed publisher
  33. Shen X, Xu F, Li M, Wu S, Zhang J, Wang A, et al. miR-322/-503 rescues myoblast defects in myotonic dystrophy type 1 cell model by targeting CUG repeats. Cell Death Dis. 2020;11:891 pubmed publisher
  34. Ganassi M, Badodi S, Wanders K, Zammit P, Hughes S. Myogenin is an essential regulator of adult myofibre growth and muscle stem cell homeostasis. elife. 2020;9: pubmed publisher
  35. Schuld J, Orfanos Z, Chevessier F, Eggers B, Heil L, Uszkoreit J, et al. Homozygous expression of the myofibrillar myopathy-associated p.W2710X filamin C variant reveals major pathomechanisms of sarcomeric lesion formation. Acta Neuropathol Commun. 2020;8:154 pubmed publisher
  36. Nowinski S, Solmonson A, Rusin S, Maschek J, Bensard C, Fogarty S, et al. Mitochondrial fatty acid synthesis coordinates oxidative metabolism in mammalian mitochondria. elife. 2020;9: pubmed publisher
  37. Stefanovic S, Laforest B, Desvignes J, Lescroart F, Argiro L, Maurel Zaffran C, et al. Hox-dependent coordination of mouse cardiac progenitor cell patterning and differentiation. elife. 2020;9: pubmed publisher
  38. Arnold L, Cecchini A, Stark D, Ihnat J, Craigg R, Carter A, et al. EphA7 promotes myogenic differentiation via cell-cell contact. elife. 2020;9: pubmed publisher
  39. Perrin A, Metay C, Villanova M, Carlier R, Pegoraro E, Juntas Morales R, et al. A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency. Ann Clin Transl Neurol. 2020;7:846-854 pubmed publisher
  40. Pereira J, Gerber J, Ghidinelli M, Gerber D, Tortola L, Ommer A, et al. Mice carrying an analogous heterozygous dynamin 2 K562E mutation that causes neuropathy in humans develop predominant characteristics of a primary myopathy. Hum Mol Genet. 2020;29:1253-1273 pubmed publisher
  41. Arc Chagnaud C, Py G, Fovet T, Roumanille R, Demangel R, Pagano A, et al. Evaluation of an Antioxidant and Anti-inflammatory Cocktail Against Human Hypoactivity-Induced Skeletal Muscle Deconditioning. Front Physiol. 2020;11:71 pubmed publisher
  42. Laitila J, McNamara E, Wingate C, Goullee H, Ross J, Taylor R, et al. Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb. Acta Neuropathol Commun. 2020;8:18 pubmed publisher
  43. Choi I, Lim H, Cho H, Oh Y, Chou B, Bai H, et al. Transcriptional landscape of myogenesis from human pluripotent stem cells reveals a key role of TWIST1 in maintenance of skeletal muscle progenitors. elife. 2020;9: pubmed publisher
  44. Li Q, Mao F, Zhou B, Huang Y, Zou Z, Dendekker A, et al. p53 Integrates Temporal WDR5 Inputs during Neuroectoderm and Mesoderm Differentiation of Mouse Embryonic Stem Cells. Cell Rep. 2020;30:465-480.e6 pubmed publisher
  45. Vang P, Vasdev A, Zhan W, Gransee H, Sieck G, Mantilla C. Diaphragm muscle sarcopenia into very old age in mice. Physiol Rep. 2020;8:e14305 pubmed publisher
  46. Owen A, Patel S, Smith J, Balasuriya B, Mori S, Hawk G, et al. Chronic muscle weakness and mitochondrial dysfunction in the absence of sustained atrophy in a preclinical sepsis model. elife. 2019;8: pubmed publisher
  47. Selvaraj S, Mondragón González R, Xu B, Magli A, Kim H, Laine J, et al. Screening identifies small molecules that enhance the maturation of human pluripotent stem cell-derived myotubes. elife. 2019;8: pubmed publisher
  48. Arai H, Sato F, Yamamoto T, Woltjen K, Kiyonari H, Yoshimoto Y, et al. Metalloprotease-Dependent Attenuation of BMP Signaling Restricts Cardiac Neural Crest Cell Fate. Cell Rep. 2019;29:603-616.e5 pubmed publisher
  49. Tran M, Tsutsumi R, Erberich J, Chen K, Flores M, Cooper K. Evolutionary loss of foot muscle during development with characteristics of atrophy and no evidence of cell death. elife. 2019;8: pubmed publisher
  50. Jia Z, Nie Y, Yue F, Kong Y, Gu L, Gavin T, et al. A requirement of Polo-like kinase 1 in murine embryonic myogenesis and adult muscle regeneration. elife. 2019;8: pubmed publisher
  51. Kim K, Rana A, Park C. Orai1 inhibitor STIM2β regulates myogenesis by controlling SOCE dependent transcriptional factors. Sci Rep. 2019;9:10794 pubmed publisher
  52. Nelson H, Coffing G, Chilson S, Hester K, Carrillo C, Ostreicher S, et al. Structure, development, and functional morphology of the cement gland of the giant danio, Devario malabaricus. Dev Dyn. 2019;248:1155-1174 pubmed publisher
  53. Ma X, Chang H, Wang Z, Xu S, Peng X, Zhang J, et al. Differential activation of the calpain system involved in individualized adaptation of different fast-twitch muscles in hibernating Daurian ground squirrels. J Appl Physiol (1985). 2019;127:328-341 pubmed publisher
  54. Herdy J, Schäfer S, Kim Y, Ansari Z, Zangwill D, Ku M, et al. Chemical modulation of transcriptionally enriched signaling pathways to optimize the conversion of fibroblasts into neurons. elife. 2019;8: pubmed publisher
  55. Gao R, Liang X, Cheedipudi S, Cordero J, Jiang X, Zhang Q, et al. Pioneering function of Isl1 in the epigenetic control of cardiomyocyte cell fate. Cell Res. 2019;29:486-501 pubmed publisher
  56. Powell P, Wei C, Fu L, Pat B, Bradley W, Collawn J, et al. Chymase uptake by cardiomyocytes results in myosin degradation in cardiac volume overload. Heliyon. 2019;5:e01397 pubmed publisher
  57. Rajderkar S, Mann J, Panaretos C, Yumoto K, Li H, Mishina Y, et al. Trim33 is required for appropriate development of pre-cardiogenic mesoderm. Dev Biol. 2019;450:101-114 pubmed publisher
  58. Yap L, Wang J, Moreno Moral A, Chong L, Sun Y, Harmston N, et al. In Vivo Generation of Post-infarct Human Cardiac Muscle by Laminin-Promoted Cardiovascular Progenitors. Cell Rep. 2019;26:3231-3245.e9 pubmed publisher
  59. Chakraborty A, Laukka T, Myllykoski M, Ringel A, Booker M, Tolstorukov M, et al. Histone demethylase KDM6A directly senses oxygen to control chromatin and cell fate. Science. 2019;363:1217-1222 pubmed publisher
  60. Sahara M, Santoro F, Sohlmér J, Zhou C, Witman N, Leung C, et al. Population and Single-Cell Analysis of Human Cardiogenesis Reveals Unique LGR5 Ventricular Progenitors in Embryonic Outflow Tract. Dev Cell. 2019;48:475-490.e7 pubmed publisher
  61. Bergmeister K, Aman M, Muceli S, Vujaklija I, Manzano Szalai K, Unger E, et al. Peripheral nerve transfers change target muscle structure and function. Sci Adv. 2019;5:eaau2956 pubmed publisher
  62. Baghdadi M, Firmino J, Soni K, Evano B, Di Girolamo D, Mourikis P, et al. Notch-Induced miR-708 Antagonizes Satellite Cell Migration and Maintains Quiescence. Cell Stem Cell. 2018;23:859-868.e5 pubmed publisher
  63. Chang H, Kao C, Chung S, Chen W, Aninda L, Chen Y, et al. Bhlhe40 differentially regulates the function and number of peroxisomes and mitochondria in myogenic cells. Redox Biol. 2019;20:321-333 pubmed publisher
  64. Gallot Y, Bohnert K, Straughn A, Xiong G, Hindi S, Kumar A. PERK regulates skeletal muscle mass and contractile function in adult mice. FASEB J. 2019;33:1946-1962 pubmed publisher
  65. Han W, Anderson S, Mohiuddin M, Barros D, Nakhai S, Shin E, et al. Synthetic matrix enhances transplanted satellite cell engraftment in dystrophic and aged skeletal muscle with comorbid trauma. Sci Adv. 2018;4:eaar4008 pubmed publisher
  66. Baghdadi M, Castel D, Machado L, Fukada S, Birk D, Relaix F, et al. Reciprocal signalling by Notch-Collagen V-CALCR retains muscle stem cells in their niche. Nature. 2018;557:714-718 pubmed publisher
  67. Marroncelli N, Bianchi M, Bertin M, Consalvi S, Saccone V, De Bardi M, et al. HDAC4 regulates satellite cell proliferation and differentiation by targeting P21 and Sharp1 genes. Sci Rep. 2018;8:3448 pubmed publisher
  68. Tucker N, McLellan M, Hu D, Ye J, Parsons V, Mills R, et al. Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy. Circ Cardiovasc Genet. 2017;10: pubmed publisher
  69. Chen X, Wang R, Liu X, Wu Y, Zhou T, Yang Y, et al. A Chemical-Genetic Approach Reveals the Distinct Roles of GSK3? and GSK3? in Regulating Embryonic Stem Cell Fate. Dev Cell. 2017;43:563-576.e4 pubmed publisher
  70. Wang X, Zeng R, Xu H, Xu Z, Zuo B. The nuclear protein-coding gene ANKRD23 negatively regulates myoblast differentiation. Gene. 2017;629:68-75 pubmed publisher
  71. Guo Y, Wang J, Zhu M, Zeng R, Xu Z, Li G, et al. Identification of MyoD-Responsive Transcripts Reveals a Novel Long Non-coding RNA (lncRNA-AK143003) that Negatively Regulates Myoblast Differentiation. Sci Rep. 2017;7:2828 pubmed publisher
  72. Raices M, Bukata L, Sakuma S, Borlido J, Hernandez L, Hart D, et al. Nuclear Pores Regulate Muscle Development and Maintenance by Assembling a Localized Mef2C Complex. Dev Cell. 2017;41:540-554.e7 pubmed publisher
  73. Quinn M, Goh Q, Kurosaka M, Gamage D, Petrany M, Prasad V, et al. Myomerger induces fusion of non-fusogenic cells and is required for skeletal muscle development. Nat Commun. 2017;8:15665 pubmed publisher
  74. Koh J, Hancock C, Terada S, Higashida K, Holloszy J, Han D. PPARβ Is Essential for Maintaining Normal Levels of PGC-1α and Mitochondria and for the Increase in Muscle Mitochondria Induced by Exercise. Cell Metab. 2017;25:1176-1185.e5 pubmed publisher
  75. Zhu X, Yuan X, Wang M, Fang Y, Liu Y, Zhang X, et al. A Wnt/Notch/Pax7 signaling network supports tissue integrity in tongue development. J Biol Chem. 2017;292:9409-9419 pubmed publisher
  76. Eshima H, Tamura Y, Kakehi S, Kurebayashi N, Murayama T, Nakamura K, et al. Long-term, but not short-term high-fat diet induces fiber composition changes and impaired contractile force in mouse fast-twitch skeletal muscle. Physiol Rep. 2017;5: pubmed publisher
  77. Wyckelsma V, Levinger I, Murphy R, Petersen A, Perry B, Hedges C, et al. Intense interval training in healthy older adults increases skeletal muscle [3H]ouabain-binding site content and elevates Na+,K+-ATPase ?2 isoform abundance in Type II fibers. Physiol Rep. 2017;5: pubmed publisher
  78. Lee C, Hanna A, Wang H, Dagnino Acosta A, Joshi A, Knoblauch M, et al. A chemical chaperone improves muscle function in mice with a RyR1 mutation. Nat Commun. 2017;8:14659 pubmed publisher
  79. Xiong G, Hindi S, Mann A, Gallot Y, Bohnert K, Cavener D, et al. The PERK arm of the unfolded protein response regulates satellite cell-mediated skeletal muscle regeneration. elife. 2017;6: pubmed publisher
  80. Fajardo V, Gamu D, Mitchell A, Bloemberg D, Bombardier E, Chambers P, et al. Sarcolipin deletion exacerbates soleus muscle atrophy and weakness in phospholamban overexpressing mice. PLoS ONE. 2017;12:e0173708 pubmed publisher
  81. Morrow R, Picard M, Derbeneva O, Leipzig J, McManus M, Gouspillou G, et al. Mitochondrial energy deficiency leads to hyperproliferation of skeletal muscle mitochondria and enhanced insulin sensitivity. Proc Natl Acad Sci U S A. 2017;114:2705-2710 pubmed publisher
  82. Gautam J, Nirwane A, Yao Y. Laminin differentially regulates the stemness of type I and type II pericytes. Stem Cell Res Ther. 2017;8:28 pubmed publisher
  83. Cortez Toledo O, Schnair C, Sangngern P, Metzger D, Chao L. Nur77 deletion impairs muscle growth during developmental myogenesis and muscle regeneration in mice. PLoS ONE. 2017;12:e0171268 pubmed publisher
  84. Shen C, Zhou J, Wang X, Yu X, Liang C, Liu B, et al. Angiotensin-II-induced Muscle Wasting is Mediated by 25-Hydroxycholesterol via GSK3? Signaling Pathway. EBioMedicine. 2017;16:238-250 pubmed publisher
  85. Hogarth M, Houweling P, Thomas K, Gordish Dressman H, Bello L, Pegoraro E, et al. Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy. Nat Commun. 2017;8:14143 pubmed publisher
  86. Witzel H, Cheedipudi S, Gao R, Stainier D, Dobreva G. Isl2b regulates anterior second heart field development in zebrafish. Sci Rep. 2017;7:41043 pubmed publisher
  87. Maltabe V, Barka E, Kontonika M, Florou D, Kouvara Pritsouli M, Roumpi M, et al. Isolation of an ES-Derived Cardiovascular Multipotent Cell Population Based on VE-Cadherin Promoter Activity. Stem Cells Int. 2016;2016:8305624 pubmed publisher
  88. Cha S, Lee H, Koh W. Study of myoblast differentiation using multi-dimensional scaffolds consisting of nano and micropatterns. Biomater Res. 2017;21:1 pubmed publisher
  89. Yue F, Bi P, Wang C, Shan T, Nie Y, Ratliff T, et al. Pten is necessary for the quiescence and maintenance of adult muscle stem cells. Nat Commun. 2017;8:14328 pubmed publisher
  90. Christoforou N, Chakraborty S, Kirkton R, Adler A, Addis R, Leong K. Core Transcription Factors, MicroRNAs, and Small Molecules Drive Transdifferentiation of Human Fibroblasts Towards The Cardiac Cell Lineage. Sci Rep. 2017;7:40285 pubmed publisher
  91. Taetzsch T, Tenga M, Valdez G. Muscle Fibers Secrete FGFBP1 to Slow Degeneration of Neuromuscular Synapses during Aging and Progression of ALS. J Neurosci. 2017;37:70-82 pubmed publisher
  92. Kempf H, Olmer R, Haase A, Franke A, Bolesani E, Schwanke K, et al. Bulk cell density and Wnt/TGFbeta signalling regulate mesendodermal patterning of human pluripotent stem cells. Nat Commun. 2016;7:13602 pubmed publisher
  93. Kim J, Ko I, Atala A, Yoo J. Progressive Muscle Cell Delivery as a Solution for Volumetric Muscle Defect Repair. Sci Rep. 2016;6:38754 pubmed publisher
  94. St Jean Pelletier F, Pion C, Leduc Gaudet J, Sgarioto N, Zovilé I, Barbat Artigas S, et al. The impact of ageing, physical activity, and pre-frailty on skeletal muscle phenotype, mitochondrial content, and intramyocellular lipids in men. J Cachexia Sarcopenia Muscle. 2017;8:213-228 pubmed publisher
  95. Moyle L, Blanc E, Jaka O, Prueller J, Banerji C, Tedesco F, et al. Ret function in muscle stem cells points to tyrosine kinase inhibitor therapy for facioscapulohumeral muscular dystrophy. elife. 2016;5: pubmed publisher
  96. Beyer S, Pontis J, Schirwis E, Battisti V, Rudolf A, Le Grand F, et al. Canonical Wnt signalling regulates nuclear export of Setdb1 during skeletal muscle terminal differentiation. Cell Discov. 2016;2:16037 pubmed
  97. Huang S, Zhou A, Nguyen D, Zhang H, Benz E. Protein 4.1R Influences Myogenin Protein Stability and Skeletal Muscle Differentiation. J Biol Chem. 2016;291:25591-25607 pubmed
  98. Knopp P, Krom Y, Banerji C, Panamarova M, Moyle L, den Hamer B, et al. DUX4 induces a transcriptome more characteristic of a less-differentiated cell state and inhibits myogenesis. J Cell Sci. 2016;129:3816-3831 pubmed
  99. Southard S, Kim J, Low S, Tsika R, Lepper C. Myofiber-specific TEAD1 overexpression drives satellite cell hyperplasia and counters pathological effects of dystrophin deficiency. elife. 2016;5: pubmed publisher
  100. Peake J, Roberts L, Figueiredo V, Egner I, Krog S, Aas S, et al. The effects of cold water immersion and active recovery on inflammation and cell stress responses in human skeletal muscle after resistance exercise. J Physiol. 2017;595:695-711 pubmed publisher
  101. White S, McDermott M, Sufit R, Kosmac K, Bugg A, Gonzalez Freire M, et al. Walking performance is positively correlated to calf muscle fiber size in peripheral artery disease subjects, but fibers show aberrant mitophagy: an observational study. J Transl Med. 2016;14:284 pubmed publisher
  102. Kotoku T, Kosaka K, Nishio M, Ishida Y, Kawaichi M, Matsuda E. CIBZ Regulates Mesodermal and Cardiac Differentiation of by Suppressing T and Mesp1 Expression in Mouse Embryonic Stem Cells. Sci Rep. 2016;6:34188 pubmed publisher
  103. Kim E, Page P, Dellefave Castillo L, McNally E, Wyatt E. Direct reprogramming of urine-derived cells with inducible MyoD for modeling human muscle disease. Skelet Muscle. 2016;6:32 pubmed publisher
  104. Perry B, Wyckelsma V, Murphy R, Steward C, Anderson M, Levinger I, et al. Dissociation between short-term unloading and resistance training effects on skeletal muscle Na+,K+-ATPase, muscle function, and fatigue in humans. J Appl Physiol (1985). 2016;121:1074-1086 pubmed publisher
  105. Spendiff S, Vuda M, Gouspillou G, Aare S, Pérez A, Morais J, et al. Denervation drives mitochondrial dysfunction in skeletal muscle of octogenarians. J Physiol. 2016;594:7361-7379 pubmed publisher
  106. Xie X, Tsai S, Tsai M. COUP-TFII regulates satellite cell function and muscular dystrophy. J Clin Invest. 2016;126:3929-3941 pubmed publisher
  107. Aare S, Spendiff S, Vuda M, Elkrief D, Pérez A, Wu Q, et al. Failed reinnervation in aging skeletal muscle. Skelet Muscle. 2016;6:29 pubmed publisher
  108. Woodall B, Woodall M, Luongo T, Grisanti L, Tilley D, Elrod J, et al. Skeletal Muscle-specific G Protein-coupled Receptor Kinase 2 Ablation Alters Isolated Skeletal Muscle Mechanics and Enhances Clenbuterol-stimulated Hypertrophy. J Biol Chem. 2016;291:21913-21924 pubmed
  109. Ramazzotti G, Billi A, Manzoli L, Mazzetti C, Ruggeri A, Erneux C, et al. IPMK and β-catenin mediate PLC-β1-dependent signaling in myogenic differentiation. Oncotarget. 2016;7:84118-84127 pubmed publisher
  110. Liang R, Dong W, Shen X, Peng X, Aceves A, Liu Y. Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells. J Vis Exp. 2016;: pubmed publisher
  111. Di Siena S, Gimmelli R, Nori S, Barbagallo F, Campolo F, Dolci S, et al. Activated c-Kit receptor in the heart promotes cardiac repair and regeneration after injury. Cell Death Dis. 2016;7:e2317 pubmed publisher
  112. Moon Y, Kim M, Kim S, Kim T. Apoptotic action of botulinum toxin on masseter muscle in rats: early and late changes in the expression of molecular markers. Springerplus. 2016;5:991 pubmed publisher
  113. Rozo M, Li L, Fan C. Targeting ?1-integrin signaling enhances regeneration in aged and dystrophic muscle in mice. Nat Med. 2016;22:889-96 pubmed publisher
  114. Kudová J, Prochazkova J, Vašíček O, Perecko T, Sedláčková M, Pesl M, et al. HIF-1alpha Deficiency Attenuates the Cardiomyogenesis of Mouse Embryonic Stem Cells. PLoS ONE. 2016;11:e0158358 pubmed publisher
  115. Rui Y, Pan F, Mi J. Composition of Muscle Fiber Types in Rat Rotator Cuff Muscles. Anat Rec (Hoboken). 2016;299:1397-401 pubmed publisher
  116. Lambert M, Richard E, Duban Deweer S, Krzewinski F, Deracinois B, Dupont E, et al. O-GlcNAcylation is a key modulator of skeletal muscle sarcomeric morphometry associated to modulation of protein-protein interactions. Biochim Biophys Acta. 2016;1860:2017-30 pubmed publisher
  117. Vilmont V, Cadot B, Vezin E, Le Grand F, Gomes E. Dynein disruption perturbs post-synaptic components and contributes to impaired MuSK clustering at the NMJ: implication in ALS. Sci Rep. 2016;6:27804 pubmed publisher
  118. Puchert M, Adams V, Linke A, Engele J. Evidence for the involvement of the CXCL12 system in the adaptation of skeletal muscles to physical exercise. Cell Signal. 2016;28:1205-15 pubmed publisher
  119. Rao V, Ow J, Shankar S, Bharathy N, Manikandan J, Wang Y, et al. G9a promotes proliferation and inhibits cell cycle exit during myogenic differentiation. Nucleic Acids Res. 2016;44:8129-43 pubmed publisher
  120. Jensen L, Jørgensen L, Bech R, Frandsen U, Schrøder H. Skeletal Muscle Remodelling as a Function of Disease Progression in Amyotrophic Lateral Sclerosis. Biomed Res Int. 2016;2016:5930621 pubmed publisher
  121. Riaz M, Raz Y, van Putten M, Paniagua Soriano G, Krom Y, Florea B, et al. PABPN1-Dependent mRNA Processing Induces Muscle Wasting. PLoS Genet. 2016;12:e1006031 pubmed publisher
  122. Yao Y, Norris E, Mason C, Strickland S. Laminin regulates PDGFR?(+) cell stemness and muscle development. Nat Commun. 2016;7:11415 pubmed publisher
  123. Fajardo V, Smith I, Bombardier E, Chambers P, Quadrilatero J, Tupling A. Diaphragm assessment in mice overexpressing phospholamban in slow-twitch type I muscle fibers. Brain Behav. 2016;6:e00470 pubmed publisher
  124. Cheng A, Yin H, Chen A, Liu Y, Chuang M, He H, et al. Celecoxib and Pioglitazone as Potential Therapeutics for Regulating TGF-?-Induced Hyaluronan in Dysthyroid Myopathy. Invest Ophthalmol Vis Sci. 2016;57:1951-9 pubmed publisher
  125. Carrió E, Magli A, Muñoz M, Peinado M, Perlingeiro R, Suelves M. Muscle cell identity requires Pax7-mediated lineage-specific DNA demethylation. BMC Biol. 2016;14:30 pubmed publisher
  126. Tanaka H, Ng N, Yang Yu Z, Casco Robles M, Maruo F, Tsonis P, et al. A developmentally regulated switch from stem cells to dedifferentiation for limb muscle regeneration in newts. Nat Commun. 2016;7:11069 pubmed publisher
  127. Pannérec A, Springer M, Migliavacca E, Ireland A, Piasecki M, Karaz S, et al. A robust neuromuscular system protects rat and human skeletal muscle from sarcopenia. Aging (Albany NY). 2016;8:712-29 pubmed publisher
  128. Davignon L, Chauveau C, Julien C, Dill C, Duband Goulet I, Cabet E, et al. The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease. Hum Mol Genet. 2016;25:1559-73 pubmed publisher
  129. Morena D, Maestro N, Bersani F, Forni P, Lingua M, Foglizzo V, et al. Hepatocyte Growth Factor-mediated satellite cells niche perturbation promotes development of distinct sarcoma subtypes. elife. 2016;5: pubmed publisher
  130. Park S, Yun Y, Lim J, Kim M, Kim S, Kim J, et al. Stabilin-2 modulates the efficiency of myoblast fusion during myogenic differentiation and muscle regeneration. Nat Commun. 2016;7:10871 pubmed publisher
  131. Stewart M, Lopez S, Nagandla H, Soibam B, Benham A, Nguyen J, et al. Mouse myofibers lacking the SMYD1 methyltransferase are susceptible to atrophy, internalization of nuclei and myofibrillar disarray. Dis Model Mech. 2016;9:347-59 pubmed publisher
  132. Gonçalves A, Thorsteinsdóttir S, Deries M. Rapid and simple method for in vivo ex utero development of mouse embryo explants. Differentiation. 2016;91:57-67 pubmed publisher
  133. Andersen T, Schmidt J, Pedersen M, Krustrup P, Bangsbo J. The Effects of 52 Weeks of Soccer or Resistance Training on Body Composition and Muscle Function in +65-Year-Old Healthy Males--A Randomized Controlled Trial. PLoS ONE. 2016;11:e0148236 pubmed publisher
  134. Nyberg M, Fiorenza M, Lund A, Christensen M, Rømer T, Piil P, et al. Adaptations to Speed Endurance Training in Highly Trained Soccer Players. Med Sci Sports Exerc. 2016;48:1355-64 pubmed publisher
  135. Malecova B, Dall Agnese A, Madaro L, Gatto S, Coutinho Toto P, Albini S, et al. TBP/TFIID-dependent activation of MyoD target genes in skeletal muscle cells. elife. 2016;5: pubmed publisher
  136. Barone R, Macaluso F, Sangiorgi C, Campanella C, Marino Gammazza A, Moresi V, et al. Skeletal muscle Heat shock protein 60 increases after endurance training and induces peroxisome proliferator-activated receptor gamma coactivator 1 α1 expression. Sci Rep. 2016;6:19781 pubmed publisher
  137. Phelps K, Drouillard J, Silva M, Miranda L, Ebarb S, Van Bibber Krueger C, et al. Effect of extended postmortem aging and steak location on myofibrillar protein degradation and Warner-Bratzler shear force of beef M. semitendinosus steaks. J Anim Sci. 2016;94:412-23 pubmed publisher
  138. Nagahisa H, Okabe K, Iuchi Y, Fujii J, Miyata H. Characteristics of Skeletal Muscle Fibers of SOD1 Knockout Mice. Oxid Med Cell Longev. 2016;2016:9345970 pubmed publisher
  139. Arentson Lantz E, English K, Paddon Jones D, Fry C. Fourteen days of bed rest induces a decline in satellite cell content and robust atrophy of skeletal muscle fibers in middle-aged adults. J Appl Physiol (1985). 2016;120:965-75 pubmed publisher
  140. Quattrocelli M, Giacomazzi G, Broeckx S, Ceelen L, Bolca S, Spaas J, et al. Equine-Induced Pluripotent Stem Cells Retain Lineage Commitment Toward Myogenic and Chondrogenic Fates. Stem Cell Reports. 2016;6:55-63 pubmed publisher
  141. Watanabe H, Nakano T, Saito R, Akasaka D, Saito K, Ogasawara H, et al. Serotonin Improves High Fat Diet Induced Obesity in Mice. PLoS ONE. 2016;11:e0147143 pubmed publisher
  142. Foltz S, Modi J, Melick G, Abousaud M, Luan J, Fortunato M, et al. Abnormal Skeletal Muscle Regeneration plus Mild Alterations in Mature Fiber Type Specification in Fktn-Deficient Dystroglycanopathy Muscular Dystrophy Mice. PLoS ONE. 2016;11:e0147049 pubmed publisher
  143. Wyckelsma V, McKenna M, Levinger I, Petersen A, Lamboley C, Murphy R. Cell specific differences in the protein abundances of GAPDH and Na(+),K(+)-ATPase in skeletal muscle from aged individuals. Exp Gerontol. 2016;75:8-15 pubmed publisher
  144. Loperfido M, Jarmin S, Dastidar S, Di Matteo M, Perini I, Moore M, et al. piggyBac transposons expressing full-length human dystrophin enable genetic correction of dystrophic mesoangioblasts. Nucleic Acids Res. 2016;44:744-60 pubmed publisher
  145. Palazzolo G, Quattrocelli M, Toelen J, Dominici R, Anastasia L, Tettamenti G, et al. Cardiac Niche Influences the Direct Reprogramming of Canine Fibroblasts into Cardiomyocyte-Like Cells. Stem Cells Int. 2016;2016:4969430 pubmed publisher
  146. Power G, Minozzo F, Spendiff S, Filion M, Konokhova Y, Purves Smith M, et al. Reduction in single muscle fiber rate of force development with aging is not attenuated in world class older masters athletes. Am J Physiol Cell Physiol. 2016;310:C318-27 pubmed publisher
  147. Ye S, Zhang D, Cheng F, Wilson D, Mackay J, He K, et al. Wnt/β-catenin and LIF-Stat3 signaling pathways converge on Sp5 to promote mouse embryonic stem cell self-renewal. J Cell Sci. 2016;129:269-76 pubmed publisher
  148. Tallon C, Russell K, Sakhalkar S, Andrapallayal N, Farah M. Length-dependent axo-terminal degeneration at the neuromuscular synapses of type II muscle in SOD1 mice. Neuroscience. 2016;312:179-89 pubmed publisher
  149. Lee S, Won J, Yang J, Lee J, Kim S, Lee E, et al. AKAP6 inhibition impairs myoblast differentiation and muscle regeneration: Positive loop between AKAP6 and myogenin. Sci Rep. 2015;5:16523 pubmed publisher
  150. He Q, Liu K, Tian Z, Du S. The Effects of Hsp90α1 Mutations on Myosin Thick Filament Organization. PLoS ONE. 2015;10:e0142573 pubmed publisher
  151. Filareto A, Rinaldi F, Arpke R, Darabi R, Belanto J, Toso E, et al. Pax3-induced expansion enables the genetic correction of dystrophic satellite cells. Skelet Muscle. 2015;5:36 pubmed publisher
  152. Zhang Y, Li W, Zhu M, Li Y, Xu Z, Zuo B. FHL3 differentially regulates the expression of MyHC isoforms through interactions with MyoD and pCREB. Cell Signal. 2016;28:60-73 pubmed publisher
  153. Mohr M, Thomassen M, Girard O, Racinais S, Nybo L. Muscle variables of importance for physiological performance in competitive football. Eur J Appl Physiol. 2016;116:251-62 pubmed publisher
  154. Dyer L, Lockyer P, Wu Y, Saha A, Cyr C, Moser M, et al. BMPER Promotes Epithelial-Mesenchymal Transition in the Developing Cardiac Cushions. PLoS ONE. 2015;10:e0139209 pubmed publisher
  155. Yoo M, Kim B, Lee S, Jeong H, Park J, Seo D, et al. Syntaxin 4 regulates the surface localization of a promyogenic receptor Cdo thereby promoting myogenic differentiation. Skelet Muscle. 2015;5:28 pubmed publisher
  156. Ebert S, Dyle M, Bullard S, Dierdorff J, Murry D, Fox D, et al. Identification and Small Molecule Inhibition of an Activating Transcription Factor 4 (ATF4)-dependent Pathway to Age-related Skeletal Muscle Weakness and Atrophy. J Biol Chem. 2015;290:25497-511 pubmed publisher
  157. Lo H, Nixon S, Hall T, Cowling B, Ferguson C, Morgan G, et al. The caveolin-cavin system plays a conserved and critical role in mechanoprotection of skeletal muscle. J Cell Biol. 2015;210:833-49 pubmed publisher
  158. Wang Y, Li Z, Zhang P, Poon E, Kong C, Boheler K, et al. Nitric Oxide-cGMP-PKG Pathway Acts on Orai1 to Inhibit the Hypertrophy of Human Embryonic Stem Cell-Derived Cardiomyocytes. Stem Cells. 2015;33:2973-84 pubmed publisher
  159. Pourteymour S, Lee S, Langleite T, Eckardt K, Hjorth M, Bindesbøll C, et al. Perilipin 4 in human skeletal muscle: localization and effect of physical activity. Physiol Rep. 2015;3: pubmed publisher
  160. Cohen T, Many G, Fleming B, Gnocchi V, Ghimbovschi S, Mosser D, et al. Upregulated IL-1β in dysferlin-deficient muscle attenuates regeneration by blunting the response to pro-inflammatory macrophages. Skelet Muscle. 2015;5:24 pubmed publisher
  161. Wang H, Lööf S, Borg P, Nader G, Blau H, Simon A. Turning terminally differentiated skeletal muscle cells into regenerative progenitors. Nat Commun. 2015;6:7916 pubmed publisher
  162. Ohsawa Y, Takayama K, Nishimatsu S, Okada T, Fujino M, Fukai Y, et al. The Inhibitory Core of the Myostatin Prodomain: Its Interaction with Both Type I and II Membrane Receptors, and Potential to Treat Muscle Atrophy. PLoS ONE. 2015;10:e0133713 pubmed publisher
  163. Zou T, He D, Yu B, Yu J, Mao X, Zheng P, et al. Moderately increased maternal dietary energy intake delays foetal skeletal muscle differentiation and maturity in pigs. Eur J Nutr. 2016;55:1777-87 pubmed publisher
  164. Hostrup M, Kalsen A, Onslev J, Jessen S, Haase C, Habib S, et al. Mechanisms underlying enhancements in muscle force and power output during maximal cycle ergometer exercise induced by chronic β2-adrenergic stimulation in men. J Appl Physiol (1985). 2015;119:475-86 pubmed publisher
  165. Jung E, Sim Y, Jeong H, Kim S, Yun Y, Song J, et al. Jmjd2C increases MyoD transcriptional activity through inhibiting G9a-dependent MyoD degradation. Biochim Biophys Acta. 2015;1849:1081-94 pubmed publisher
  166. Ueda S, Kokaji Y, Simizu S, Honda K, Yoshino K, Kamisoyama H, et al. Chicken heat shock protein HSPB1 increases and interacts with αB-crystallin in aged skeletal muscle. Biosci Biotechnol Biochem. 2015;79:1867-75 pubmed publisher
  167. Li F, Buck D, De Winter J, Kolb J, Meng H, Birch C, et al. Nebulin deficiency in adult muscle causes sarcomere defects and muscle-type-dependent changes in trophicity: novel insights in nemaline myopathy. Hum Mol Genet. 2015;24:5219-33 pubmed publisher
  168. Preuße K, Tveriakhina L, Schuster Gossler K, Gaspar C, Rosa A, Henrique D, et al. Context-Dependent Functional Divergence of the Notch Ligands DLL1 and DLL4 In Vivo. PLoS Genet. 2015;11:e1005328 pubmed publisher
  169. Lindskog C, Linné J, Fagerberg L, Hallström B, Sundberg C, Lindholm M, et al. The human cardiac and skeletal muscle proteomes defined by transcriptomics and antibody-based profiling. BMC Genomics. 2015;16:475 pubmed publisher
  170. Maza I, Caspi I, Zviran A, Chomsky E, Rais Y, Viukov S, et al. Transient acquisition of pluripotency during somatic cell transdifferentiation with iPSC reprogramming factors. Nat Biotechnol. 2015;33:769-74 pubmed publisher
  171. Faggi F, Codenotti S, Poliani P, Cominelli M, Chiarelli N, Colombi M, et al. MURC/cavin-4 Is Co-Expressed with Caveolin-3 in Rhabdomyosarcoma Tumors and Its Silencing Prevents Myogenic Differentiation in the Human Embryonal RD Cell Line. PLoS ONE. 2015;10:e0130287 pubmed publisher
  172. Nasipak B, Padilla Benavides T, Green K, Leszyk J, Mao W, Konda S, et al. Opposing calcium-dependent signalling pathways control skeletal muscle differentiation by regulating a chromatin remodelling enzyme. Nat Commun. 2015;6:7441 pubmed publisher
  173. Shi S, Lu S, Sivasubramaniyam T, Revelo X, Cai E, Luk C, et al. DJ-1 links muscle ROS production with metabolic reprogramming and systemic energy homeostasis in mice. Nat Commun. 2015;6:7415 pubmed publisher
  174. Walton R, Finlin B, Mula J, Long D, Zhu B, Fry C, et al. Insulin-resistant subjects have normal angiogenic response to aerobic exercise training in skeletal muscle, but not in adipose tissue. Physiol Rep. 2015;3: pubmed publisher
  175. Tian L, Ding S, You Y, Li T, Liu Y, Wu X, et al. Leiomodin-3-deficient mice display nemaline myopathy with fast-myofiber atrophy. Dis Model Mech. 2015;8:635-41 pubmed publisher
  176. Fajardo V, Bombardier E, McMillan E, TRAN K, Wadsworth B, Gamu D, et al. Phospholamban overexpression in mice causes a centronuclear myopathy-like phenotype. Dis Model Mech. 2015;8:999-1009 pubmed publisher
  177. Clark D, Clark D, Beever J, Dilger A. Increased prenatal IGF2 expression due to the porcine intron3-G3072A mutation may be responsible for increased muscle mass. J Anim Sci. 2015;93:2546-58 pubmed publisher
  178. Yamaleyeva L, Pulgar V, Lindsey S, Yamane L, Varagic J, McGee C, et al. Uterine artery dysfunction in pregnant ACE2 knockout mice is associated with placental hypoxia and reduced umbilical blood flow velocity. Am J Physiol Endocrinol Metab. 2015;309:E84-94 pubmed publisher
  179. Oishi Y, Roy R, Ogata T, Ohira Y. Heat-Stress effects on the myosin heavy chain phenotype of rat soleus fibers during the early stages of regeneration. Muscle Nerve. 2015;52:1047-56 pubmed publisher
  180. Lamarche Ã, Lala Tabbert N, Gunanayagam A, St Louis C, Wiper Bergeron N. Retinoic acid promotes myogenesis in myoblasts by antagonizing transforming growth factor-beta signaling via C/EBPβ. Skelet Muscle. 2015;5:8 pubmed publisher
  181. Adams K, Rousso D, Umbach J, Novitch B. Foxp1-mediated programming of limb-innervating motor neurons from mouse and human embryonic stem cells. Nat Commun. 2015;6:6778 pubmed publisher
  182. Sohn J, Lu A, Tang Y, Wang B, Huard J. Activation of non-myogenic mesenchymal stem cells during the disease progression in dystrophic dystrophin/utrophin knockout mice. Hum Mol Genet. 2015;24:3814-29 pubmed publisher
  183. Jensen L, Andersen L, Schrøder H, Frandsen U, Sjøgaard G. Neuronal nitric oxide synthase is dislocated in type I fibers of myalgic muscle but can recover with physical exercise training. Biomed Res Int. 2015;2015:265278 pubmed publisher
  184. Koutakis P, Myers S, Cluff K, Ha D, Haynatzki G, McComb R, et al. Abnormal myofiber morphology and limb dysfunction in claudication. J Surg Res. 2015;196:172-9 pubmed publisher
  185. Anderson C, Hu J, Barnes R, Heidt A, Cornelissen I, Black B. Myocyte enhancer factor 2C function in skeletal muscle is required for normal growth and glucose metabolism in mice. Skelet Muscle. 2015;5:7 pubmed publisher
  186. Simon H, ODELBERG S. Assessing cardiomyocyte proliferative capacity in the newt heart and primary culture. Methods Mol Biol. 2015;1290:227-40 pubmed publisher
  187. Kim M, Horst A, Blinka S, Stamm K, Mahnke D, Schuman J, et al. Activin-A and Bmp4 levels modulate cell type specification during CHIR-induced cardiomyogenesis. PLoS ONE. 2015;10:e0118670 pubmed publisher
  188. Feeney S, McGrath M, Sriratana A, Gehrig S, Lynch G, D Arcy C, et al. FHL1 reduces dystrophy in transgenic mice overexpressing FSHD muscular dystrophy region gene 1 (FRG1). PLoS ONE. 2015;10:e0117665 pubmed publisher
  189. Agley C, Rowlerson A, Velloso C, Lazarus N, Harridge S. Isolation and quantitative immunocytochemical characterization of primary myogenic cells and fibroblasts from human skeletal muscle. J Vis Exp. 2015;:52049 pubmed publisher
  190. Hotchkiss A, Feridooni T, Baguma Nibasheka M, McNeil K, Chinni S, Pasumarthi K. Atrial natriuretic peptide inhibits cell cycle activity of embryonic cardiac progenitor cells via its NPRA receptor signaling axis. Am J Physiol Cell Physiol. 2015;308:C557-69 pubmed publisher
  191. Tian E, Stevens S, Guan Y, Springer D, Anderson S, Starost M, et al. Galnt1 is required for normal heart valve development and cardiac function. PLoS ONE. 2015;10:e0115861 pubmed publisher
  192. Mitchell C, Oikawa S, Ogborn D, Nates N, MacNeil L, Tarnopolsky M, et al. Daily chocolate milk consumption does not enhance the effect of resistance training in young and old men: a randomized controlled trial. Appl Physiol Nutr Metab. 2015;40:199-202 pubmed publisher
  193. Seaberg B, Henslee G, Wang S, Paez Colasante X, Landreth G, Rimer M. Muscle-derived extracellular signal-regulated kinases 1 and 2 are required for the maintenance of adult myofibers and their neuromuscular junctions. Mol Cell Biol. 2015;35:1238-53 pubmed publisher
  194. Tontonoz P, Cortez Toledo O, Wroblewski K, Hong C, Lim L, Carranza R, et al. The orphan nuclear receptor Nur77 is a determinant of myofiber size and muscle mass in mice. Mol Cell Biol. 2015;35:1125-38 pubmed publisher
  195. Zhong Z, Zhao H, Mayo J, Chai Y. Different requirements for Wnt signaling in tongue myogenic subpopulations. J Dent Res. 2015;94:421-9 pubmed publisher
  196. Muir L, Nguyen Q, Hauschka S, Chamberlain J. Engraftment potential of dermal fibroblasts following in vivo myogenic conversion in immunocompetent dystrophic skeletal muscle. Mol Ther Methods Clin Dev. 2014;1:14025 pubmed
  197. Zhang D, Wang X, Li Y, Zhao L, Lu M, Yao X, et al. Thyroid hormone regulates muscle fiber type conversion via miR-133a1. J Cell Biol. 2014;207:753-66 pubmed publisher
  198. Fry C, Lee J, Mula J, Kirby T, Jackson J, Liu F, et al. Inducible depletion of satellite cells in adult, sedentary mice impairs muscle regenerative capacity without affecting sarcopenia. Nat Med. 2015;21:76-80 pubmed publisher
  199. Langone F, Cannata S, Fuoco C, Lettieri Barbato D, Testa S, Nardozza A, et al. Metformin protects skeletal muscle from cardiotoxin induced degeneration. PLoS ONE. 2014;9:e114018 pubmed publisher
  200. Mori T, Agata N, Itoh Y, Miyazu Inoue M, Sokabe M, Taguchi T, et al. Stretch speed-dependent myofiber damage and functional deficits in rat skeletal muscle induced by lengthening contraction. Physiol Rep. 2014;2: pubmed publisher
  201. Yi P, Chew L, Zhang Z, Ren H, Wang F, Cong X, et al. KIF5B transports BNIP-2 to regulate p38 mitogen-activated protein kinase activation and myoblast differentiation. Mol Biol Cell. 2015;26:29-42 pubmed publisher
  202. Huertas Martínez J, Rello Varona S, Herrero Martín D, Barrau I, García Monclús S, Sáinz Jaspeado M, et al. Caveolin-1 is down-regulated in alveolar rhabdomyosarcomas and negatively regulates tumor growth. Oncotarget. 2014;5:9744-55 pubmed
  203. Lockhart M, Boukens B, Phelps A, Brown C, Toomer K, Burns T, et al. Alk3 mediated Bmp signaling controls the contribution of epicardially derived cells to the tissues of the atrioventricular junction. Dev Biol. 2014;396:8-18 pubmed publisher
  204. Brun C, Périé L, Baraige F, Vernus B, Bonnieu A, Blanquet V. Absence of hyperplasia in Gasp-1 overexpressing mice is dependent on myostatin up-regulation. Cell Physiol Biochem. 2014;34:1241-59 pubmed publisher
  205. Ruparelia A, Oorschot V, Vaz R, Ramm G, Bryson Richardson R. Zebrafish models of BAG3 myofibrillar myopathy suggest a toxic gain of function leading to BAG3 insufficiency. Acta Neuropathol. 2014;128:821-33 pubmed publisher
  206. Skovgaard C, Christensen P, Larsen S, Andersen T, Thomassen M, Bangsbo J. Concurrent speed endurance and resistance training improves performance, running economy, and muscle NHE1 in moderately trained runners. J Appl Physiol (1985). 2014;117:1097-109 pubmed publisher
  207. White J, Barro M, Makarenkova H, Sanger J, Sanger J. Localization of sarcomeric proteins during myofibril assembly in cultured mouse primary skeletal myotubes. Anat Rec (Hoboken). 2014;297:1571-84 pubmed publisher
  208. Gouspillou G, Sgarioto N, Norris B, Barbat Artigas S, Aubertin Leheudre M, Morais J, et al. The relationship between muscle fiber type-specific PGC-1α content and mitochondrial content varies between rodent models and humans. PLoS ONE. 2014;9:e103044 pubmed publisher
  209. Stefanetti R, Lamon S, Wallace M, Vendelbo M, Russell A, Vissing K. Regulation of ubiquitin proteasome pathway molecular markers in response to endurance and resistance exercise and training. Pflugers Arch. 2015;467:1523-1537 pubmed publisher
  210. Janbaz A, Lindström M, Liu J, Pedrosa Domellöf F. Intermediate filaments in the human extraocular muscles. Invest Ophthalmol Vis Sci. 2014;55:5151-9 pubmed publisher
  211. Andersen T, Schmidt J, Thomassen M, Hornstrup T, Frandsen U, Randers M, et al. A preliminary study: effects of football training on glucose control, body composition, and performance in men with type 2 diabetes. Scand J Med Sci Sports. 2014;24 Suppl 1:43-56 pubmed publisher
  212. Fry C, Noehren B, Mula J, Ubele M, Westgate P, Kern P, et al. Fibre type-specific satellite cell response to aerobic training in sedentary adults. J Physiol. 2014;592:2625-35 pubmed publisher
  213. Stefanetti R, Zacharewicz E, Della Gatta P, Garnham A, Russell A, Lamon S. Ageing has no effect on the regulation of the ubiquitin proteasome-related genes and proteins following resistance exercise. Front Physiol. 2014;5:30 pubmed publisher
  214. Sousa Victor P, Gutarra S, García Prat L, Rodriguez Ubreva J, Ortet L, Ruiz Bonilla V, et al. Geriatric muscle stem cells switch reversible quiescence into senescence. Nature. 2014;506:316-21 pubmed publisher
  215. Phelps K, Drouillard J, Jennings J, Depenbusch B, Van Bibber Krueger C, Miller K, et al. Effects of the Programmed Nutrition Beef Program on meat quality characteristics. J Anim Sci. 2014;92:1780-91 pubmed publisher
  216. Lamboley C, Murphy R, McKenna M, Lamb G. Sarcoplasmic reticulum Ca2+ uptake and leak properties, and SERCA isoform expression, in type I and type II fibres of human skeletal muscle. J Physiol. 2014;592:1381-95 pubmed publisher
  217. Galicia Vázquez G, Di Marco S, Lian X, Ma J, Gallouzi I, Pelletier J. Regulation of eukaryotic initiation factor 4AII by MyoD during murine myogenic cell differentiation. PLoS ONE. 2014;9:e87237 pubmed publisher
  218. Gouspillou G, Sgarioto N, Kapchinsky S, Purves Smith F, Norris B, Pion C, et al. Increased sensitivity to mitochondrial permeability transition and myonuclear translocation of endonuclease G in atrophied muscle of physically active older humans. FASEB J. 2014;28:1621-33 pubmed publisher
  219. Garton F, Seto J, Quinlan K, Yang N, Houweling P, North K. ?-Actinin-3 deficiency alters muscle adaptation in response to denervation and immobilization. Hum Mol Genet. 2014;23:1879-93 pubmed publisher
  220. Gastaldello S, Chen X, Callegari S, Masucci M. Caspase-1 promotes Epstein-Barr virus replication by targeting the large tegument protein deneddylase to the nucleus of productively infected cells. PLoS Pathog. 2013;9:e1003664 pubmed publisher
  221. Tanaka M, Kishimoto K, Okuno H, Saito H, Itoi E. Vitamin D receptor gene silencing effects on differentiation of myogenic cell lines. Muscle Nerve. 2014;49:700-8 pubmed publisher
  222. Hauerslev S, Sveen M, Vissing J, Krag T. Protein turnover and cellular stress in mildly and severely affected muscles from patients with limb girdle muscular dystrophy type 2I. PLoS ONE. 2013;8:e66929 pubmed publisher
  223. Hernández Hernández J, Mallappa C, Nasipak B, Oesterreich S, Imbalzano A. The Scaffold attachment factor b1 (Safb1) regulates myogenic differentiation by facilitating the transition of myogenic gene chromatin from a repressed to an activated state. Nucleic Acids Res. 2013;41:5704-16 pubmed publisher
  224. Kobayashi N, Homma S, Okada T, Masuda T, Sato N, Nishiyama K, et al. Elucidation of target muscle and detailed development of dorsal motor neurons in chick embryo spinal cord. J Comp Neurol. 2013;521:2987-3002 pubmed publisher
  225. Barton E, Park S, James J, Makarewich C, Philippou A, Eletto D, et al. Deletion of muscle GRP94 impairs both muscle and body growth by inhibiting local IGF production. FASEB J. 2012;26:3691-702 pubmed publisher
  226. Issa M, Muruganandan S, Ernst M, Parlee S, Zabel B, Butcher E, et al. Chemokine-like receptor 1 regulates skeletal muscle cell myogenesis. Am J Physiol Cell Physiol. 2012;302:C1621-31 pubmed publisher