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Systemic investigation of bone and muscle abnormalities in dystrophin/utrophin double knockout mice during postnatal development and the mechanisms

The dystrophin(−/−/)utrophin(−/−/) double knockout (dKO-Hom) mouse is a murine model of human Duchenne muscular dystrophy. This study investigated the bone and muscle abnormalities of dKO-Hom mouse and mechanisms. We collected bone and skeletal muscle samples from control mice and three muscular dys...

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Detalhes bibliográficos
Publicado no:Hum Mol Genet
Main Authors: Gao, Xueqin, Tang, Ying, Amra, Sarah, Sun, Xuying, Cui, Yan, Cheng, Haizi, Wang, Bing, Huard, Johnny
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2019
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7275811/
https://ncbi.nlm.nih.gov/pubmed/30689868
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddz012
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