Muscular atrophy of caveolin-3–deficient mice is rescued by myostatin inhibition

Caveolin-3, the muscle-specific isoform of caveolins, plays important roles in signal transduction. Dominant-negative mutations of the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy 1C (LGMD1C) with loss of caveolin-3. However, identification of the precise molecular mechani...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Ohsawa, Yutaka, Hagiwara, Hiroki, Nakatani, Masashi, Yasue, Akihiro, Moriyama, Keiji, Murakami, Tatsufumi, Tsuchida, Kunihiro, Noji, Sumihare, Sunada, Yoshihide
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Society for Clinical Investigation 2006
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1592547/
https://ncbi.nlm.nih.gov/pubmed/17039257
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI28520
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