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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Publicat a:PLoS Genet
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2017
Matèries:
Research Article
Accés en línia: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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