This is a Validated Antibody Database (VAD) review about rat Myh4, based on 45 published articles (read how Labome selects the articles), using Myh4 antibody in all methods. It is aimed to help Labome visitors find the most suited Myh4 antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
Santa Cruz Biotechnology
mouse monoclonal (B-5)
  • immunocytochemistry; human; 1:100; loading ...
Santa Cruz Biotechnology Myh4 antibody (Santa Cruz Biotechnology, sc-376157) was used in immunocytochemistry on human samples at 1:100. elife (2019) ncbi
mouse monoclonal (B-5)
  • immunocytochemistry; mouse; 1:2000; loading ...; fig 2c
  • western blot; mouse; 1:2000; loading ...; fig 2b
Santa Cruz Biotechnology Myh4 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 Myh4 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 Myh4 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 Myh4 antibody (Santa Cruz, sc-376157) was used in western blot on mouse samples (fig 1c). Oncotarget (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 Myh4 antibody (Santa Cruz, sc-32732) was used in western blot on mouse samples (fig 5). elife (2016) ncbi
mouse monoclonal (F59)
  • western blot; human
Santa Cruz Biotechnology Myh4 antibody (Santa Cruz, SC-32732) was used in western blot on human samples . PLoS ONE (2015) ncbi
Invitrogen
mouse monoclonal (MF20)
  • flow cytometry; mouse; 1:100; loading ...; fig 3b
Invitrogen Myh4 antibody (eBioscience, 53-6503-82) was used in flow cytometry on mouse samples at 1:100 (fig 3b). Mol Med Rep (2018) ncbi
mouse monoclonal (MF20)
  • immunohistochemistry - frozen section; zebrafish ; 1:75; loading ...; fig s2c
In order to examine cardiac revascularization in zebrafish, Invitrogen Myh4 antibody (eBiosciences, MF20) was used in immunohistochemistry - frozen section on zebrafish samples at 1:75 (fig s2c). Proc Natl Acad Sci U S A (2016) ncbi
mouse monoclonal (MF20)
  • flow cytometry; mouse
Invitrogen Myh4 antibody (Affymetrix eBioscience, 53-6503-82) was used in flow cytometry on mouse samples . Circ Cardiovasc Genet (2014) ncbi
mouse monoclonal (MF20)
  • immunocytochemistry; mouse; 1:200
In order to analyze the conversion increase of fibroblasts to induced cardiomyocytes through inhibition of TGFbeta signaling, Invitrogen Myh4 antibody (eBioscience, 53-6503-82) was used in immunocytochemistry on mouse samples at 1:200. PLoS ONE (2014) ncbi
mouse monoclonal (MF20)
  • immunocytochemistry; mouse; 1:200
In order to evaluate the method for measuring fibroblast reprogramming to cardiomyocytes, Invitrogen Myh4 antibody (eBioscience, 53-6503-82) was used in immunocytochemistry on mouse samples at 1:200. J Mol Cell Cardiol (2013) ncbi
Developmental Studies Hybridoma Bank
mouse monoclonal (BF-F3)
  • immunohistochemistry - frozen section; mouse; 1:100; loading ...; fig 3f
Developmental Studies Hybridoma Bank Myh4 antibody (Developmental Studies Hybridoma Bank, BF-F3) was used in immunohistochemistry - frozen section on mouse samples at 1:100 (fig 3f). elife (2019) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry - frozen section; rat; 1:100; loading ...; fig 4b
Developmental Studies Hybridoma Bank Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry - frozen section on rat samples at 1:100 (fig 4b). Sci Adv (2019) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry - frozen section; mouse; 1:50; loading ...; fig s3a
Developmental Studies Hybridoma Bank Myh4 antibody (Developmental Studies Hybridoma Bank, BF-F3) was used in immunohistochemistry - frozen section on mouse samples at 1:50 (fig s3a). Nat Commun (2018) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 4a
Developmental Studies Hybridoma Bank Myh4 antibody (DSHB, BF-F3-c) was used in immunohistochemistry - frozen section on mouse samples (fig 4a). FASEB J (2019) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry; mouse; loading ...; fig 3c
In order to research the regulatory role of vestigial-like 2 in muscle fiber type distribution, Developmental Studies Hybridoma Bank Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry on mouse samples (fig 3c). Sci Rep (2017) ncbi
mouse monoclonal (BF-F3)
  • 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 Myh4 antibody (DSHB, BF-F3) 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 (BF-F3)
  • 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 Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry - frozen section on mouse samples at 1:50 (fig 1g). Nat Commun (2017) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 3b
In order to report the physiological role of sarcolipin upregulation in muscle myopathy, Developmental Studies Hybridoma Bank Myh4 antibody (Developmental Studies Hybridoma Bank, BF-F3) was used in immunohistochemistry - frozen section on mouse samples (fig 3b). PLoS ONE (2017) ncbi
mouse monoclonal (BF-F3)
  • 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 Myh4 antibody (DSHB, BF-F3) 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 (BF-F3)
  • 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 Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry - frozen section on mouse samples (fig 1f). PLoS ONE (2017) ncbi
mouse monoclonal (BF-F3)
  • 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 Myh4 antibody (Developmental Studies Hybridoma Bank, BF-F3) was used in immunohistochemistry - frozen section on mouse samples at 1:100 (fig 3). EBioMedicine (2017) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry; mouse; 1:10; 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 Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry on mouse samples at 1:10 (fig 5a). Nat Commun (2017) ncbi
mouse monoclonal (BF-F3)
  • 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 Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry - frozen section on rat samples at 1:200 (fig 1). Skelet Muscle (2016) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry; mouse; loading ...; fig 2g
In order to test if decreased skeletal muscle expression of myostatin mRNA prevents the loss of muscle mass in diabetic mice, Developmental Studies Hybridoma Bank Myh4 antibody (Developmental Studies Hybridoma Bank, BF-F3) was used in immunohistochemistry on mouse samples (fig 2g). Sci Rep (2016) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry - frozen section; mouse; loading ...; fig 4a
In order to explore the role of GRK2 in skeletal muscle physiology, Developmental Studies Hybridoma Bank Myh4 antibody (Developmental Studies Hybridoma Bank, BF-F3) was used in immunohistochemistry - frozen section on mouse samples (fig 4a). J Biol Chem (2016) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry; mouse; 1:100; fig s6
In order to determine the function of MRF4 in adult skeletal muscle, Developmental Studies Hybridoma Bank Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry on mouse samples at 1:100 (fig s6). Nat Commun (2016) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry; rat; 1:100; loading ...; fig 1d
In order to identify muscle fiber types in rotator cuff muscles in rats, Developmental Studies Hybridoma Bank Myh4 antibody (Developmental Studies Hybridoma Bank, BF-F3) was used in immunohistochemistry on rat samples at 1:100 (fig 1d). Anat Rec (Hoboken) (2016) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry - frozen section; human; fig 5
  • immunohistochemistry - frozen section; mouse; fig 5
Developmental Studies Hybridoma Bank Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry - frozen section on human samples (fig 5) and in immunohistochemistry - frozen section on mouse samples (fig 5). PLoS Genet (2016) ncbi
mouse monoclonal (BF-F3)
  • 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 Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry on mouse samples (fig 2). Brain Behav (2016) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry - frozen section; rat; loading ...
In order to identify contributing factors of sarcopenia and investigate their mechanism, Developmental Studies Hybridoma Bank Myh4 antibody (DSHB, BFF3) was used in immunohistochemistry - frozen section on rat samples . Aging (Albany NY) (2016) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry; mouse; fig 1
Developmental Studies Hybridoma Bank Myh4 antibody (Developmental Studies Hybridoma Bank, BF-F3) was used in immunohistochemistry on mouse samples (fig 1). J Biol Chem (2015) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry; mouse; fig s5
In order to study the therapeutic use of the inhibitory core of the prodomain of myostatin, Developmental Studies Hybridoma Bank Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry on mouse samples (fig s5). PLoS ONE (2015) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry - frozen section; mouse; fig 3
In order to investigate the role of nebulin in muscle cells using transgenic mice, Developmental Studies Hybridoma Bank Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry - frozen section on mouse samples (fig 3). Hum Mol Genet (2015) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry - frozen section; mouse; fig 5
Developmental Studies Hybridoma Bank Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry - frozen section on mouse samples (fig 5). Dis Model Mech (2015) ncbi
mouse monoclonal (BF-F3)
  • immunocytochemistry; mouse
In order to study SERCA dysfunction in mice overexpressing phospholamban, Developmental Studies Hybridoma Bank Myh4 antibody (Developmental Studies Hybridoma Bank, BF-F3) was used in immunocytochemistry on mouse samples . Dis Model Mech (2015) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry - frozen section; swine; 1:10
Developmental Studies Hybridoma Bank Myh4 antibody (Developmental Hybridoma Bank, BF-F3) was used in immunohistochemistry - frozen section on swine samples at 1:10. J Anim Sci (2015) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry - frozen section; mouse; fig 2
Developmental Studies Hybridoma Bank Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry - frozen section on mouse samples (fig 2). Mol Cell Biol (2015) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry - frozen section; mouse; 1:100
Developmental Studies Hybridoma Bank Myh4 antibody (Developmental Studies Hybridoma Bank, BF.F3) was used in immunohistochemistry - frozen section on mouse samples at 1:100. Nat Med (2015) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry; rat; 1:40
Developmental Studies Hybridoma Bank Myh4 antibody (Developmental Studies Hybridoma Bank, BF-F3) was used in immunohistochemistry on rat samples at 1:40. Physiol Rep (2014) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry; mouse; 1:200
  • immunohistochemistry; rat; 1:200
Developmental Studies Hybridoma Bank Myh4 antibody (Developmental Studies Hybridoma Bank, BF-F3) was used in immunohistochemistry on mouse samples at 1:200 and in immunohistochemistry on rat samples at 1:200. PLoS ONE (2014) ncbi
mouse monoclonal (BF-F3)
  • 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 Myh4 antibody (Developmental Studies Hybridoma Bank, BF-F3) was used in immunohistochemistry - frozen section on mouse samples . Nature (2014) ncbi
mouse monoclonal (BF-F3)
  • immunohistochemistry; mouse; fig 3
Developmental Studies Hybridoma Bank Myh4 antibody (DSHB, BF-F3) was used in immunohistochemistry on mouse samples (fig 3). Hum Mol Genet (2014) ncbi
mouse monoclonal (BF-F3)
  • 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 Myh4 antibody (Developmental Studies Hybridoma Bank, BF-F3) was used in immunohistochemistry - frozen section on mouse samples . FASEB J (2012) ncbi
Articles Reviewed
  1. 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
  2. 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
  3. 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
  4. Maani N, Sabha N, Rezai K, Ramani A, Groom L, Eltayeb N, et al. Tamoxifen therapy in a murine model of myotubular myopathy. Nat Commun. 2018;9:4849 pubmed publisher
  5. 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
  6. Tian J, Wang R, Hou Q, Li M, Chen L, Deng X, et al. Optimization and enrichment of induced cardiomyocytes derived from mouse fibroblasts by reprogramming with cardiac transcription factors. Mol Med Rep. 2018;17:3912-3920 pubmed publisher
  7. Honda M, Hidaka K, Fukada S, Sugawa R, Shirai M, Ikawa M, et al. Vestigial-like 2 contributes to normal muscle fiber type distribution in mice. Sci Rep. 2017;7:7168 pubmed publisher
  8. 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
  9. 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
  10. 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
  11. 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
  12. 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
  13. 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
  14. 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
  15. 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
  16. 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
  17. 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
  18. Marín Juez R, Marass M, Gauvrit S, Rossi A, Lai S, Materna S, et al. Fast revascularization of the injured area is essential to support zebrafish heart regeneration. Proc Natl Acad Sci U S A. 2016;113:11237-11242 pubmed
  19. 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
  20. Coleman S, Rebalka I, D Souza D, Deodhare N, Desjardins E, Hawke T. Myostatin inhibition therapy for insulin-deficient type 1 diabetes. Sci Rep. 2016;6:32495 pubmed publisher
  21. 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
  22. 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
  23. Moretti I, Ciciliot S, Dyar K, Abraham R, Murgia M, Agatea L, et al. MRF4 negatively regulates adult skeletal muscle growth by repressing MEF2 activity. Nat Commun. 2016;7:12397 pubmed publisher
  24. 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
  25. 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
  26. 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
  27. 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
  28. 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
  29. 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
  30. 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
  31. 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
  32. 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
  33. 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
  34. 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
  35. 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
  36. 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
  37. 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
  38. 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
  39. 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
  40. Martinez Fernandez A, Nelson T, Reyes S, Alekseev A, Secreto F, Perez Terzic C, et al. iPS cell-derived cardiogenicity is hindered by sustained integration of reprogramming transgenes. Circ Cardiovasc Genet. 2014;7:667-76 pubmed publisher
  41. Ifkovits J, Addis R, Epstein J, Gearhart J. Inhibition of TGF? signaling increases direct conversion of fibroblasts to induced cardiomyocytes. PLoS ONE. 2014;9:e89678 pubmed publisher
  42. 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
  43. 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
  44. Addis R, Ifkovits J, Pinto F, Kellam L, Esteso P, Rentschler S, et al. Optimization of direct fibroblast reprogramming to cardiomyocytes using calcium activity as a functional measure of success. J Mol Cell Cardiol. 2013;60:97-106 pubmed publisher
  45. 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