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Dasatinib as a treatment for Duchenne muscular dystrophy

Identification of a systemically acting and universal small molecule therapy for Duchenne muscular dystrophy would be an enormous advance for this condition. Based on evidence gained from studies on mouse genetic models, we have identified tyrosine phosphorylation and degradation of β-dystroglycan a...

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Detalles Bibliográficos
Publicado en:Hum Mol Genet
Main Authors: Lipscomb, Leanne, Piggott, Robert W., Emmerson, Tracy, Winder, Steve J.
Formato: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2016
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4706114/
https://ncbi.nlm.nih.gov/pubmed/26604135
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv469
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