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Mutations in NOTCH1 cause aortic valve disease.
Serum response factor regulates a muscle-specific microRNA that targets Hand2 during cardiogenesis.
Thymosin beta4 activates integrin-linked kinase and promotes cardiac cell migration, survival and cardiac repair.
Heart disease: an ongoing genetic battle?
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency.
Rapid regulation of steroidogenesis by mitochondrial protein import.
A genetic blueprint for cardiac development.
Essential role for oncogenic Ras in tumour maintenance.
The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM.