| Published Application/Species/Sample/Dilution | Reference |
|---|
- immunohistochemistry; mouse; 1:500; loading ...; fig 4c
| Wang H, Marrosu E, Brayson D, Wasala N, Johnson E, Scott C, et al. Proteomic analysis identifies key differences in the cardiac interactomes of dystrophin and micro-dystrophin. Hum Mol Genet. 2021;30:1321-1336 pubmed publisher |
- immunohistochemistry; human; 1:400; loading ...; fig s1a
| Reinhard J, Lin S, McKee K, Meinen S, Crosson S, Sury M, et al. Linker proteins restore basement membrane and correct LAMA2-related muscular dystrophy in mice. Sci Transl Med. 2017;9: pubmed publisher |
- immunohistochemistry - frozen section; mouse; fig 1d
| McKee K, Crosson S, Meinen S, Reinhard J, Ruegg M, Yurchenco P. Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype. J Clin Invest. 2017;127:1075-1089 pubmed publisher |
- immunohistochemistry - frozen section; mouse; 1:1000; loading ...; fig 2
| Dumont N, Rudnicki M. Characterizing Satellite Cells and Myogenic Progenitors During Skeletal Muscle Regeneration. Methods Mol Biol. 2017;1560:179-188 pubmed publisher |
- immunohistochemistry; mouse; 1:200; loading ...; fig s1b
| Wang C, Wang M, Arrington J, Shan T, Yue F, Nie Y, et al. Ascl2 inhibits myogenesis by antagonizing the transcriptional activity of myogenic regulatory factors. Development. 2017;144:235-247 pubmed publisher |
- immunohistochemistry - frozen section; mouse; 1:1000; loading ...; fig 6a
| Paris N, Soroka A, Klose A, Liu W, Chakkalakal J. Smad4 restricts differentiation to promote expansion of satellite cell derived progenitors during skeletal muscle regeneration. elife. 2016;5: pubmed publisher |
- immunocytochemistry; mouse; 1:200; loading ...; fig s2b
| Gautam J, Zhang X, Yao Y. The role of pericytic laminin in blood brain barrier integrity maintenance. Sci Rep. 2016;6:36450 pubmed publisher |
- immunohistochemistry - frozen section; mouse; 1:500; loading ...; fig 1a
| Meehan D, Delimont D, Dufek B, Zallocchi M, Phillips G, Gratton M, et al. Endothelin-1 mediated induction of extracellular matrix genes in strial marginal cells underlies strial pathology in Alport mice. Hear Res. 2016;341:100-108 pubmed publisher |
- immunohistochemistry; mouse; fig 4
| Dumont N, Wang Y, von Maltzahn J, Pasut A, Bentzinger C, Brun C, et al. Dystrophin expression in muscle stem cells regulates their polarity and asymmetric division. Nat Med. 2015;21:1455-63 pubmed publisher |
- immunocytochemistry; mouse; 1:200; loading ...; fig s5
| Van Ry P, Wuebbles R, Key M, Burkin D. Galectin-1 Protein Therapy Prevents Pathology and Improves Muscle Function in the mdx Mouse Model of Duchenne Muscular Dystrophy. Mol Ther. 2015;23:1285-1297 pubmed publisher |
- immunohistochemistry - frozen section; mouse; 1:300; fig 3
| Hausburg M, Doles J, Clement S, Cadwallader A, Hall M, Blackshear P, et al. Post-transcriptional regulation of satellite cell quiescence by TTP-mediated mRNA decay. elife. 2015;4:e03390 pubmed publisher |
- immunocytochemistry; mouse; 1:200
| Bernet J, Doles J, Hall J, Kelly Tanaka K, Carter T, Olwin B. p38 MAPK signaling underlies a cell-autonomous loss of stem cell self-renewal in skeletal muscle of aged mice. Nat Med. 2014;20:265-71 pubmed publisher |
- immunocytochemistry; mouse; 1:100; fig 6d
| Kim Y, Remacle A, Chernov A, Liu H, Shubayev I, Lai C, et al. The MMP-9/TIMP-1 axis controls the status of differentiation and function of myelin-forming Schwann cells in nerve regeneration. PLoS ONE. 2012;7:e33664 pubmed publisher |
- immunohistochemistry; mouse
| Prins K, Lowe D, Ervasti J. Skeletal muscle-specific ablation of gamma(cyto)-actin does not exacerbate the mdx phenotype. PLoS ONE. 2008;3:e2419 pubmed publisher |
| Gras S, Blasco A, Mòdol Caballero G, Tarabal O, Casanovas A, Piedrafita L, et al. Beneficial effects of dietary supplementation with green tea catechins and cocoa flavanols on aging-related regressive changes in the mouse neuromuscular system. Aging (Albany NY). 2021;13:18051-18093 pubmed publisher |
| Sansa A, Hidalgo I, Miralles M, de la Fuente S, Perez Garcia M, Munell F, et al. Spinal Muscular Atrophy autophagy profile is tissue-dependent: differential regulation between muscle and motoneurons. Acta Neuropathol Commun. 2021;9:122 pubmed publisher |
| Futaki S, Nakano I, Kawasaki M, Sanzen N, Sekiguchi K. Molecular profiling of the basement membrane of pluripotent epiblast cells in post-implantation stage mouse embryos. Regen Ther. 2019;12:55-65 pubmed publisher |
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| Harish P, Malerba A, Lu Nguyen N, Forrest L, Cappellari O, Roth F, et al. Inhibition of myostatin improves muscle atrophy in oculopharyngeal muscular dystrophy (OPMD). J Cachexia Sarcopenia Muscle. 2019;10:1016-1026 pubmed publisher |
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| Wang Y, Feige P, Brun C, Hekmatnejad B, Dumont N, Renaud J, et al. EGFR-Aurka Signaling Rescues Polarity and Regeneration Defects in Dystrophin-Deficient Muscle Stem Cells by Increasing Asymmetric Divisions. Cell Stem Cell. 2019;24:419-432.e6 pubmed publisher |
| Betts C, McClorey G, Healicon R, Hammond S, Manzano R, Muses S, et al. Cmah-dystrophin deficient mdx mice display an accelerated cardiac phenotype that is improved following peptide-PMO exon skipping treatment. Hum Mol Genet. 2019;28:396-406 pubmed publisher |
| Olthoff J, Lindsay A, Abo Zahrah R, Baltgalvis K, Patrinostro X, Belanto J, et al. Loss of peroxiredoxin-2 exacerbates eccentric contraction-induced force loss in dystrophin-deficient muscle. Nat Commun. 2018;9:5104 pubmed publisher |
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| Bulaklak K, Xiao B, Qiao C, Li J, Patel T, Jin Q, et al. MicroRNA-206 Downregulation Improves Therapeutic Gene Expression and Motor Function in mdx Mice. Mol Ther Nucleic Acids. 2018;12:283-293 pubmed publisher |
| Filareto A, Maguire Nguyen K, Gan Q, Aldanondo G, Machado L, Chamberlain J, et al. Monitoring disease activity noninvasively in the mdx model of Duchenne muscular dystrophy. Proc Natl Acad Sci U S A. 2018;115:7741-7746 pubmed publisher |
| Blain A, Greally E, McClorey G, Manzano R, Betts C, Godfrey C, et al. Peptide-conjugated phosphodiamidate oligomer-mediated exon skipping has benefits for cardiac function in mdx and Cmah-/-mdx mouse models of Duchenne muscular dystrophy. PLoS ONE. 2018;13:e0198897 pubmed publisher |
| You J, Dooley M, Kim C, Kim E, Xu W, Goodman C, et al. A DGKζ-FoxO-ubiquitin proteolytic axis controls fiber size during skeletal muscle remodeling. Sci Signal. 2018;11: pubmed publisher |
| Koo T, Lu Nguyen N, Malerba A, Kim E, Kim D, Cappellari O, et al. Functional Rescue of Dystrophin Deficiency in Mice Caused by Frameshift Mutations Using Campylobacter jejuni Cas9. Mol Ther. 2018;26:1529-1538 pubmed publisher |
| Harada A, Maehara K, Ono Y, Taguchi H, Yoshioka K, Kitajima Y, et al. Histone H3.3 sub-variant H3mm7 is required for normal skeletal muscle regeneration. Nat Commun. 2018;9:1400 pubmed publisher |
| Nelson D, Lindsay A, Judge L, Duan D, Chamberlain J, Lowe D, et al. Variable rescue of microtubule and physiological phenotypes in mdx muscle expressing different miniaturized dystrophins. Hum Mol Genet. 2018;27:2090-2100 pubmed publisher |
| Jin Q, Qiao C, Li J, Li J, Xiao X. Neonatal Systemic AAV-Mediated Gene Delivery of GDF11 Inhibits Skeletal Muscle Growth. Mol Ther. 2018;26:1109-1117 pubmed publisher |
| Sciandra F, Scicchitano B, Signorino G, Bigotti M, Tavazzi B, Lombardi F, et al. Evaluation of the effect of a floxed Neo cassette within the dystroglycan (Dag1) gene. BMC Res Notes. 2017;10:601 pubmed publisher |
| Figlia G, Norrmen C, Pereira J, Gerber D, Suter U. Dual function of the PI3K-Akt-mTORC1 axis in myelination of the peripheral nervous system. elife. 2017;6: pubmed publisher |
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| Nakajima T, Wang B, Ono T, Uehara Y, Nakamura S, Ichinohe K, et al. Differences in sustained alterations in protein expression between livers of mice exposed to high-dose-rate and low-dose-rate radiation. J Radiat Res. 2017;58:421-429 pubmed publisher |
| Chenette D, Cadwallader A, Antwine T, Larkin L, Wang J, Olwin B, et al. Targeted mRNA Decay by RNA Binding Protein AUF1 Regulates Adult Muscle Stem Cell Fate, Promoting Skeletal Muscle Integrity. Cell Rep. 2016;16:1379-1390 pubmed publisher |
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| Tjondrokoesoemo A, Schips T, Sargent M, Vanhoutte D, Kanisicak O, Prasad V, et al. Cathepsin S Contributes to the Pathogenesis of Muscular Dystrophy in Mice. J Biol Chem. 2016;291:9920-8 pubmed publisher |
| Xu R, Singhal N, Serinagaoglu Y, Chandrasekharan K, Joshi M, Bauer J, et al. Deletion of Galgt2 (B4Galnt2) reduces muscle growth in response to acute injury and increases muscle inflammation and pathology in dystrophin-deficient mice. Am J Pathol. 2015;185:2668-84 pubmed publisher |
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| Godfrey C, Muses S, McClorey G, Wells K, Coursindel T, Terry R, et al. How much dystrophin is enough: the physiological consequences of different levels of dystrophin in the mdx mouse. Hum Mol Genet. 2015;24:4225-37 pubmed publisher |
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