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Role of ERK1/2 signaling in congenital valve malformations in Noonan syndrome

Noonan syndrome (NS) is the most common nonchromosomal genetic disorder associated with cardiovascular malformations. The most prominent cardiac defects in NS are pulmonary valve stenosis and hypertrophic cardiomyopathy. Gain-of-function mutations in the protein tyrosine phosphatase Shp2 have been i...

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Bibliografiske detaljer
Main Authors: Krenz, Maike, Gulick, James, Osinska, Hanna E., Colbert, Melissa C., Molkentin, Jeffery D., Robbins, Jeffrey
Format: Artigo
Sprog:Inglês
Udgivet: National Academy of Sciences 2008
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2596231/
https://ncbi.nlm.nih.gov/pubmed/19017799
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0806556105
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