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Inhibition of myostatin does not ameliorate disease features of severe spinal muscular atrophy mice

There is currently no treatment for the inherited motor neuron disease, spinal muscular atrophy (SMA). Severe SMA causes lower motor neuron loss, impaired myofiber development, profound muscle weakness and early mortality. Myostatin is a transforming growth factor-β family member that inhibits muscl...

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Detalhes bibliográficos
Main Authors: Sumner, Charlotte J., Wee, Claribel D., Warsing, Leigh C., Choe, Dong W., Ng, Andrew S., Lutz, Cathleen, Wagner, Kathryn R.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2733819/
https://ncbi.nlm.nih.gov/pubmed/19477958
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp253
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