Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy

Noonan syndrome (NS) is characterized by reduced growth, craniofacial abnormalities, congenital heart defects, and variable cognitive deficits. NS belongs to the RASopathies, genetic conditions linked to mutations in components and regulators of the Ras signaling pathway. Approximately 50% of NS cas...

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Detalhes bibliográficos
Publicado no:PLoS Genet
Main Authors: Altmüller, Franziska, Pothula, Santosh, Annamneedi, Anil, Nakhaei-Rad, Saeideh, Montenegro-Venegas, Carolina, Pina-Fernández, Eneko, Marini, Claudia, Santos, Monica, Schanze, Denny, Montag, Dirk, Ahmadian, Mohammad R., Stork, Oliver, Zenker, Martin, Fejtova, Anna
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2017
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5386306/
https://ncbi.nlm.nih.gov/pubmed/28346493
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1006684
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