Flt-1 haploinsufficiency ameliorates muscular dystrophy phenotype by developmentally increased vasculature in mdx mice

Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disease caused by mutations in the gene coding for the protein dystrophin. Recent work demonstrates that dystrophin is also found in the vasculature and its absence results in vascular deficiency and abnormal blood flow. This induces...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Verma, Mayank, Asakura, Yoko, Hirai, Hiroyuki, Watanabe, Shuichi, Tastad, Christopher, Fong, Guo-Hua, Ema, Masatsugu, Call, Jarrod A., Lowe, Dawn A., Asakura, Atsushi
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2010
Konular:
Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2951865/
https://ncbi.nlm.nih.gov/pubmed/20705734
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq334
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller