Map2k6 is a potent genetic modifier of arterial rupture in vascular Ehlers-Danlos syndrome mice
Caitlin J. Bowen(Howard Hughes Medical Institute), Harry C. Dietz(Howard Hughes Medical Institute)
Cited by 1
Related Papers
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
|Nature Genetics|2005|1.8k
Angiotensin II Blockade and Aortic-Root Dilation in Marfan's Syndrome
|New England Journal of Medicine|2008|839
TGF-β–dependent pathogenesis of mitral valve prolapse in a mouse model of Marfan syndrome
|Journal of Clinical Investigation|2004|519
TGF-β–dependent pathogenesis of mitral valve prolapse in a mouse model of Marfan syndrome
|Journal of Clinical Investigation|2004|478
Lineage-specific events underlie aortic root aneurysm pathogenesis in Loeys-Dietz syndrome
|Journal of Clinical Investigation|2019|117