Chapter 4b – Loeys-Dietz Syndrome
暂无分享，去创建一个
[1] M. Goumans,et al. Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections , 2015, Journal of the American College of Cardiology.
[2] H. Dietz,et al. Loeys–Dietz syndrome: a primer for diagnosis and management , 2014, Genetics in Medicine.
[3] Sarah J. Parker,et al. Angiotensin II-dependent TGF-β signaling contributes to Loeys-Dietz syndrome vascular pathogenesis. , 2014, The Journal of clinical investigation.
[4] E. Fishman,et al. Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm , 2012, Nature Genetics.
[5] H. Dietz,et al. Lessons on the pathogenesis of aneurysm from heritable conditions , 2011, Nature.
[6] Barry Merriman,et al. Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1 , 2011, Nature Genetics.
[7] G. Vriend,et al. Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis , 2011, Nature Genetics.
[8] George H. Thomas,et al. Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor , 2006 .
[9] Wolfram Kress,et al. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2 , 2005, Nature Genetics.