ロード中...

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...

詳細記述

保存先:
書誌詳細
主要な著者: Verma, Mayank, Asakura, Yoko, Hirai, Hiroyuki, Watanabe, Shuichi, Tastad, Christopher, Fong, Guo-Hua, Ema, Masatsugu, Call, Jarrod A., Lowe, Dawn A., Asakura, Atsushi
フォーマット: Artigo
言語:Inglês
出版事項: Oxford University Press 2010
主題:
オンライン・アクセス: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
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!