Inhibition of FLT1 ameliorates muscular dystrophy phenotype by increased vasculature in a mouse model of Duchenne muscular dystrophy

Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disease in which the dystrophin coding for a membrane stabilizing protein is mutated. Recently, the vasculature has also shown to be perturbed in DMD and DMD model mdx mice. Recent DMD transcriptomics revealed the defects were correl...

Полное описание

Сохранить в:
Библиографические подробности
Опубликовано в: :PLoS Genet
Главные авторы: Verma, Mayank, Shimizu-Motohashi, Yuko, Asakura, Yoko, Ennen, James P., Bosco, Jennifer, Zhou, Zhiwei, Fong, Guo-Hua, Josiah, Serene, Keefe, Dennis, Asakura, Atsushi
Формат: Artigo
Язык:Inglês
Опубликовано: Public Library of Science 2019
Предметы:
Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC6932757/
https://ncbi.nlm.nih.gov/pubmed/31877123
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1008468
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы