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The Q510E mutation in Shp2 perturbs heart valve development by increasing cell migration

Tightly regulated cellular signaling is critical for correct heart valve development, but how and why signaling is dysregulated in congenital heart disease is not very well known. We focused on protein tyrosine phosphatase Shp2, because mutations in this signaling modulator frequently cause valve ma...

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Detalhes bibliográficos
Publicado no:J Appl Physiol (1985)
Main Authors: Edwards, Michelle A., Crombie, Kathryn, Schramm, Christine, Krenz, Maike
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2014
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4281644/
https://ncbi.nlm.nih.gov/pubmed/25359717
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/japplphysiol.00008.2014
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