Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Death and SMAD3[original query] |
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Low yield of genetic testing for known vascular connective tissue disorders in patients with fibromuscular dysplasia. Vascular medicine (London, England) 2012 Dec 17 (6): 371-8. Poloskey Stacey L, Kim Esther Sh, Sanghani Ruchi, Al-Quthami Adeeb H, Arscott Patricia, Moran Rocio, Rigelsky Christina M, Gornik Heather |
Higher risk of aggressive pancreatic neuroendocrine tumors in MEN1 patients with MEN1 mutations affecting the CHES1 interacting MENIN domain. The Journal of clinical endocrinology and metabolism 2014 Nov 99 (11): E2387-91. Bartsch Detlef K, Slater Emily P, Albers Max, Knoop Richard, Chaloupka Brunhilde, Lopez Caroline L, Fendrich Volker, Kann Peter H, Waldmann Je |
Association between SRC-1 gene polymorphisms and coronary artery aneurysms formation in Taiwanese children with Kawasaki disease. Journal of clinical laboratory analysis 2014 Nov 28 (6): 435-9. Chen Yng-Tay, Liao Wen-Lin, Lin Ying-Ju, Chen Shih-Yin, Tsai Fuu-J |
Genetic variants underlying vitamin D metabolism and VDR-TGFß-1-SMAD3 interaction may impact on HCV progression: a study based on dbGaP data from the HALT-C study. Journal of human genetics 2017 Nov 62 (11): 969-977. de Azevedo Laura A, Matte Ursula, da Silveira Themis R, Álvares-da-Silva Mário |
Clinical and genetic data of 22 new patients with SMAD3 pathogenic variants and review of the literature. Molecular genetics & genomic medicine 2020 3 8 (5): e1132. Chesneau Bertrand, Edouard Thomas, Dulac Yves, Colineaux Hélène, Langeois Maud, Hanna Nadine, Boileau Catherine, Arnaud Pauline, Chassaing Nicolas, Julia Sophie, Jondeau Guillaume, Plancke Aurélie, Khau Van Kien Philippe, Plaisancié Jul |
Genetic profiling and cardiovascular phenotypic spectrum in a Chinese cohort of Loeys-Dietz syndrome patients. Orphanet journal of rare diseases 2020 1 15 (1): 6. Yang Hang, Ma Yanyun, Luo Mingyao, Zhu Guoyan, Zhang Yinhui, Li Binbin, Shu Chang, Zhou Zh |
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