Homer Bouthiette C, Xiao L, Hurley M. Gait disturbances and muscle dysfunction in fibroblast growth factor 2 knockout mice. Sci Rep. 2021;11:11005 pubmed 出版商

Tsutsui K, Machida H, Nakagawa A, Ahn K, Morita R, Sekiguchi K, et al. Mapping the molecular and structural specialization of the skin basement membrane for inter-tissue interactions. Nat Commun. 2021;12:2577 pubmed 出版商

. Increased dystrophin production with golodirsen in patients with Duchenne muscular dystrophy. Neurology. 2020;94:e2270-e2282 pubmed 出版商

You H, Shang W, Min X, Weinreb J, Li Q, Leapman M, et al. Sight and switch off: Nerve density visualization for interventions targeting nerves in prostate cancer. Sci Adv. 2020;6:eaax6040 pubmed 出版商

de Morrée A, Klein J, Gan Q, Farup J, Urtasun A, Kanugovi A, et al. Alternative polyadenylation of Pax3 controls muscle stem cell fate and muscle function. Science. 2019;366:734-738 pubmed 出版商

Benz F, Wichitnaowarat V, Lehmann M, Germano R, Mihova D, Macas J, et al. Low wnt/β-catenin signaling determines leaky vessels in the subfornical organ and affects water homeostasis in mice. elife. 2019;8: pubmed 出版商

Segarra M, Aburto M, Cop F, Llaó Cid C, Härtl R, Damm M, et al. Endothelial Dab1 signaling orchestrates neuro-glia-vessel communication in the central nervous system. Science. 2018;361: pubmed 出版商

Nie Y, Chen H, Guo C, Yuan Z, Zhou X, Zhang Y, et al. Palmdelphin promotes myoblast differentiation and muscle regeneration. Sci Rep. 2017;7:41608 pubmed 出版商

Naito M, Mori M, Inagawa M, Miyata K, Hashimoto N, Tanaka S, et al. Dnmt3a Regulates Proliferation of Muscle Satellite Cells via p57Kip2. PLoS Genet. 2016;12:e1006167 pubmed 出版商

Zhao Y, Ogawa H, Yonekura S, Mitsuhashi H, Mitsuhashi S, Nishino I, et al. Functional analysis of SERCA1b, a highly expressed SERCA1 variant in myotonic dystrophy type 1 muscle. Biochim Biophys Acta. 2015;1852:2042-7 pubmed 出版商

Brett J, Arjona M, Ikeda M, Quarta M, de Morrée A, Egner I, et al. Exercise rejuvenates quiescent skeletal muscle stem cells in old mice through restoration of Cyclin D1. Nat Metab. 2020;2:307-317 pubmed 出版商

Elmore S, Aeffner F, Bangari D, Crabbs T, FOSSEY S, Gad S, et al. Proceedings of the 2017 National Toxicology Program Satellite Symposium. Toxicol Pathol. 2017;45:799-833 pubmed 出版商

Luo D, de Morrée A, Boutet S, Quach N, Natu V, Rustagi A, et al. Deltex2 represses MyoD expression and inhibits myogenic differentiation by acting as a negative regulator of Jmjd1c. Proc Natl Acad Sci U S A. 2017;114:E3071-E3080 pubmed 出版商

Brolin C, Shiraishi T, Hojman P, Krag T, Nielsen P, Gehl J. Electroporation Enhanced Effect of Dystrophin Splice Switching PNA Oligomers in Normal and Dystrophic Muscle. Mol Ther Nucleic Acids. 2015;4:e267 pubmed 出版商

Raphael A, Couthouis J, Sakamuri S, Siskind C, Vogel H, Day J, et al. Congenital muscular dystrophy and generalized epilepsy caused by GMPPB mutations. Brain Res. 2014;1575:66-71 pubmed 出版商

Serra C, Tangherlini F, Rudy S, Lee D, Toraldo G, Sandor N, et al. Testosterone improves the regeneration of old and young mouse skeletal muscle. J Gerontol A Biol Sci Med Sci. 2013;68:17-26 pubmed 出版商

Ackroyd M, Whitmore C, Prior S, Kaluarachchi M, Nikolic M, Mayer U, et al. Fukutin-related protein alters the deposition of laminin in the eye and brain. J Neurosci. 2011;31:12927-35 pubmed 出版商

Cui C, Miyoshi S, Tsuji H, Makino H, Kanzaki S, Kami D, et al. Dystrophin conferral using human endothelium expressing HLA-E in the non-immunosuppressive murine model of Duchenne muscular dystrophy. Hum Mol Genet. 2011;20:235-44 pubmed 出版商

Weihl C, Miller S, Hanson P, Pestronk A. Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice. Hum Mol Genet. 2007;16:919-28 pubmed