Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and SMAD1[original query] |
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| Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT patients. Human mutation 2006 Jun 27 (6): 598. Lesca Gaëtan, Burnichon Nelly, Raux Grégory, Tosi Mario, Pinson Stéphane, Marion Marie-Jeanne, Babin Emmanuel, Gilbert-Dussardier Brigitte, Rivière Sophie, Goizet Cyril, Faivre Laurence, Plauchu Henri, Frébourg Thierry, Calender Alain, Giraud Sophie, |
| Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance. American journal of human genetics 2007 Oct 81 (4): 799-807. Milet Jacqueline, Dehais Valerie, Bourgain Catherine, Jouanolle Anne Marie, Mosser Annick, Perrin Michele, Morcet Jeff, Brissot Pierre, David Veronique, Deugnier Yves, Mosser Je |
| 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 |
| Molecular genetic characterization of SMAD signaling molecules in pulmonary arterial hypertension. Human mutation 2011 Dec 32 (12): 1385-9. Nasim Md Talat, Ogo Takeshi, Ahmed Mohammad, Randall Rebecca, Chowdhury Hasnin M, Snape Katie M, Bradshaw Teisha Y, Southgate Laura, Lee Grace J, Jackson Ian, Lord Graham M, Gibbs J Simon R, Wilkins Martin R, Ohta-Ogo Keiko, Nakamura Kazufumi, Girerd Barbara, Coulet Florence, Soubrier Florent, Humbert Marc, Morrell Nicholas W, Trembath Richard C, Machado Rajiv |
| Genetic variation in the transforming growth factor-ß signaling pathway and survival after diagnosis with colon and rectal cancer. Cancer 2011 Sep 117 (18): 4175-83. Slattery Martha L, Lundgreen Abbie, Herrick Jennifer S, Wolff Roger K, Caan Bette |
| HJV and HFE Play Distinct Roles in Regulating Hepcidin. Antioxidants & redox signaling 2015 May 22 (15): 1325-36. Wu Qian, Wang Hao, An Peng, Tao Yunlong, Deng Jiali, Zhang Zhuzhen, Shen Yuanyuan, Chen Caiyong, Min Junxia, Wang Fu |
| Genome-wide network-based pathway analysis of CSF t-tau/Aß1-42 ratio in the ADNI cohort. BMC genomics 2017 May 18 (1): 421. Cong Wang, Meng Xianglian, Li Jin, Zhang Qiushi, Chen Feng, Liu Wenjie, Wang Ying, Cheng Sipu, Yao Xiaohui, Yan Jingwen, Kim Sungeun, Saykin Andrew J, Liang Hong, Shen Li, |
| Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns. Genome medicine 2017 Oct 9 (1): 95. Li Alexander H, Hanchard Neil A, Furthner Dieter, Fernbach Susan, Azamian Mahshid, Nicosia Annarita, Rosenfeld Jill, Muzny Donna, D'Alessandro Lisa C A, Morris Shaine, Jhangiani Shalini, Parekh Dhaval R, Franklin Wayne J, Lewin Mark, Towbin Jeffrey A, Penny Daniel J, Fraser Charles D, Martin James F, Eng Christine, Lupski James R, Gibbs Richard A, Boerwinkle Eric, Belmont John |
| Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia. Orphanet journal of rare diseases 2020 9 15 (1): 254. Giraud Sophie, Bardel Claire, Dupuis-Girod Sophie, Carette Marie-France, Gilbert-Dussardier Brigitte, Riviere Sophie, Saurin Jean-Christophe, Eyries Mélanie, Patri Sylvie, Decullier Evelyne, Calender Alain, Lesca Gaët |
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