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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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Hlavní autoři: Sumner, Charlotte J., Wee, Claribel D., Warsing, Leigh C., Choe, Dong W., Ng, Andrew S., Lutz, Cathleen, Wagner, Kathryn R.
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2009
Témata:
On-line přístup: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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