Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and SMAD6[original query] |
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| Association of polymorphisms of IGF1R and genes in the transforming growth factor- beta /bone morphogenetic protein pathway with bacteremia in sickle cell anemia. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2006 Sep 43 (5): 593-8. Adewoye Adeboye H, Nolan Vikki G, Ma Qianli, Baldwin Clinton, Wyszynski Diego F, Farrell John J, Farrer Lindsay A, Steinberg Martin |
| Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease. Heart rhythm : the official journal of the Heart Rhythm Society 2009 Dec 6 (12): 1745-50. Tseng Zian H, Vittinghoff Eric, Musone Stacy L, Lin Feng, Whiteman Dean, Pawlikowska Ludmila, Kwok Pui-Yan, Olgin Jeffrey E, Aouizerat Bradley |
| SNPs in the TGF-ß signaling pathway are associated with increased risk of brain metastasis in patients with non-small-cell lung cancer. PloS one 2012 7 (12): 12. Li Q, Wu H, Chen B, Hu G, Huang L, Qin K, Chen Y, Yuan X, Liao Z |
| De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis. Proceedings of the National Academy of Sciences of the United States of America 2017 8 114 (35): E7341-E7347. Timberlake Andrew T, Furey Charuta G, Choi Jungmin, Nelson-Williams Carol, , Loring Erin, Galm Amy, Kahle Kristopher T, Steinbacher Derek M, Larysz Dawid, Persing John A, Lifton Richard |
| Targeted next-generation sequencing identified ADAMTS5 as novel genetic substrate in patients with bicuspid aortic valve. International journal of cardiology 2017 Nov . Lin Xiaoping, Liu Xianbao, Wang Lihan, Jiang Jubo, Sun Yinghao, Zhu Qifeng, Chen Zexin, He Yuxin, Hu Po, Xu Qiyuan, Gao Feng, Lin Yan, Jaiswal Sanjay, Xiang Meixiang, Wang Jian' |
| ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm. Nature genetics 2018 11 51 (1): 42-50. Gould Russell A, Aziz Hamza, Woods Courtney E, Seman-Senderos Manuel Alejandro, Sparks Elizabeth, Preuss Christoph, Wünnemann Florian, Bedja Djahida, Moats Cassandra R, McClymont Sarah A, Rose Rebecca, Sobreira Nara, Ling Hua, MacCarrick Gretchen, Kumar Ajay Anand, Luyckx Ilse, Cannaerts Elyssa, Verstraeten Aline, Björk Hanna M, Lehsau Ann-Cathrin, Jaskula-Ranga Vinod, Lauridsen Henrik, Shah Asad A, Bennett Christopher L, Ellinor Patrick T, Lin Honghuang, Isselbacher Eric M, Lino Cardenas Christian Lacks, Butcher Jonathan T, Hughes G Chad, Lindsay Mark E, , , Mertens Luc, Franco-Cereceda Anders, Verhagen Judith M A, Wessels Marja, Mohamed Salah A, Eriksson Per, Mital Seema, Van Laer Lut, Loeys Bart L, Andelfinger Gregor, McCallion Andrew S, Dietz Harry |
| Genetics of renovascular hypertension in children. Journal of hypertension 2020 Oct 38 (10): 1964-1970. Viering Daan H H M, Chan Melanie M Y, Hoogenboom Lieke, Iancu Daniela, de Baaij Jeroen H F, Tullus Kjell, Kleta Robert, Bockenhauer Detl |
| Rare deleterious variants of NOTCH1, GATA4, SMAD6, and ROBO4 are enriched in BAV with early onset complications but not in BAV with heritable thoracic aortic disease. Molecular genetics & genomic medicine 2020 Aug e1406. Musfee Fadi I, Guo Dongchuan, Pinard Amélie C, Hostetler Ellen M, Blue Elizabeth E, Nickerson Deborah A, , Bamshad Michael J, Milewicz Dianna M, Prakash Siddharth |
| Analysis of the contribution of 129 candidate genes to thoracic aortic aneurysm or dissection of a mixed cohort of sporadic and familial cases in South China. American journal of translational research 2021 6 13 (5): 4281-4295. Li Ying, Fang Miaoxian, Yang Jue, Yu Changjiang, Kuang Juntao, Sun Tucheng, Fan Ruix |
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