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Male-biased aganglionic megacolon in the TashT mouse model of Hirschsprung disease involves upregulation of p53 protein activity and Ddx3y gene expression

Hirschsprung disease (HSCR) is a complex genetic disorder of neural crest development resulting in incomplete formation of the enteric nervous system (ENS). This life-threatening neurocristopathy affects 1/5000 live births, with a currently unexplained male-biased ratio. To address this lack of know...

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Detalhes bibliográficos
Publicado no:PLoS Genet
Main Authors: Cardinal, Tatiana, Bergeron, Karl-Frédérik, Soret, Rodolphe, Souchkova, Ouliana, Faure, Christophe, Guillon, Amélina, Pilon, Nicolas
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7500598/
https://ncbi.nlm.nih.gov/pubmed/32898154
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1009008
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