Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome

Rett syndrome (RTT) is a neurodevelopmental disorder mainly caused by mutations in the gene encoding the transcriptional regulator Methyl-CpG-binding protein 2 (MeCP2), located on the X chromosome. Many RTT patients have breathing abnormalities, such as apnea and breathing irregularity, and respirat...

Полное описание

Сохранить в:
Библиографические подробности
Опубликовано в: :Sci Rep
Главные авторы: Kida, Hiroshi, Takahashi, Tomoyuki, Nakamura, Yuki, Kinoshita, Takashi, Hara, Munetsugu, Okamoto, Masaki, Okayama, Satoko, Nakamura, Keiichiro, Kosai, Ken-ichiro, Taniwaki, Takayuki, Yamashita, Yushiro, Matsuishi, Toyojiro
Формат: Artigo
Язык:Inglês
Опубликовано: Nature Publishing Group UK 2017
Предметы:
Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC5607245/
https://ncbi.nlm.nih.gov/pubmed/28931890
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-12293-8
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы