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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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Hlavní autoři: Krenz, Maike, Gulick, James, Osinska, Hanna E., Colbert, Melissa C., Molkentin, Jeffery D., Robbins, Jeffrey
Médium: Artigo
Jazyk:Inglês
Vydáno: National Academy of Sciences 2008
Témata:
On-line přístup: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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