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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Bibliografiske detaljer
Main Authors: 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
Sprog:Inglês
Udgivet: The National Academy of Sciences 2003
Fag:
Biological Sciences
Online adgang: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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