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Expression profiling reveals altered satellite cell numbers and glycolytic enzyme transcription in nemaline myopathy muscle

The nemaline myopathies (NMs) are a clinically and genetically heterogeneous group of disorders characterized by nemaline rods and skeletal muscle weakness. Mutations in five sarcomeric thin filament genes have been identified. However, the molecular consequences of these mutations are unknown. Usin...

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Autores principales: Sanoudou, Despina, Haslett, Judith N., Kho, Alvin T., Guo, Shaoqiang, Gazda, Hanna T., Greenberg, Steven A., Lidov, Hart G. W., Kohane, Isaac S., Kunkel, Louis M., Beggs, Alan H.
Formato: Artigo
Lenguaje:Inglês
Publicado: The National Academy of Sciences 2003
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC153613/
https://ncbi.nlm.nih.gov/pubmed/12677001
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0330960100
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