A carregar...

Restoration of normal BMP signaling levels and osteogenic differentiation in FOP mesenchymal progenitor cells by mutant allele-specific targeting

Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disorder of progressive heterotopic ossification for which there is presently no cure. FOP is caused by a recurrent heterozygous activating mutation (c.617G>A; R206H) of Activin receptor type IA/Activin-like kinase-2 (ACVR1/...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Kaplan, Josef, Kaplan, Frederick S., Shore, Eileen M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3390458/
https://ncbi.nlm.nih.gov/pubmed/22011642
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gt.2011.152
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!