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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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Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: The National Academy of Sciences 2003
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Accés en línia: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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