Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: 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 |
Investigation of DNA polymorphisms in SMAD genes for genetic predisposition to diabetic nephropathy in patients with type 1 diabetes mellitus. Diabetologia 2009 May 52 (5): 844-9. McKnight A J, Woodman A M, Parkkonen M, Patterson C C, Savage D A, Forsblom C, Pettigrew K A, Sadlier D, Groop P H, Maxwell A P, |
A new nonsense mutation of SMAD8 associated with pulmonary arterial hypertension. Journal of medical genetics 2009 May 46 (5): 331-7. Shintani M, Yagi H, Nakayama T, Saji T, Matsuoka |
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 |
Genetic variant in the promoter of connective tissue growth factor gene confers susceptibility to nephropathy in type 1 diabetes. Journal of medical genetics 2010 Jun 47 (6): 391-7. Wang Bing, Carter Rickey E, Jaffa Miran A, Nakerakanti Sashidhar, Lackland Daniel, Lopes-Virella Maria, Trojanowska Maria, Luttrell Louis M, Jaffa Ayad A, |
Genetic variation in the TGF-? signaling pathway and colon and rectal cancer risk. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2011 Jan 20 (1): 57-69. Slattery Martha L, Herrick Jennifer S, Lundgreen Abbie, Wolff Roger |
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 |
TGF-ß signaling pathway and breast cancer susceptibility. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2011 Jun 20 (6): 1112-9. Scollen Serena, Luccarini Craig, Baynes Caroline, Driver Kristy, Humphreys Manjeet K, Garcia-Closas Montserrat, Figueroa Jonine, Lissowska Jolanta, Pharoah Paul D, Easton Douglas F, Hesketh Robin, Metcalfe James C, Dunning Alison |
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 |
Different subtypes of intraductal papillary mucinous neoplasm in the pancreas have distinct pathways to pancreatic cancer progression. Journal of gastroenterology 2012 Feb 47 (2): 203-13. Mohri Dai, Asaoka Yoshinari, Ijichi Hideaki, Miyabayashi Koji, Kudo Yotaro, Seto Motoko, Ohta Miki, Tada Motohisa, Tanaka Yasuo, Ikenoue Tsuneo, Tateishi Keisuke, Isayama Hiroyuki, Kanai Fumihiko, Fukushima Noriyoshi, Tada Minoru, Kawabe Takao, Omata Masao, Koike Kazuhi |
A single nucleotide polymorphism in the human bone morphogenetic protein-2 gene (109T > G) affects the Smad signaling pathway and the predisposition to ossification of the posterior longitudinal ligament of the spine. Chinese medical journal 2013 Mar 126 (6): 1112-8. Yan Liang, Chang Zhen, Liu Yang, Li Yi-Bing, He Bao-Rong, Hao Ding-J |
The influence of genetic ancestry and ethnicity on breast cancer survival associated with genetic variation in the TGF-ß-signaling pathway: The Breast Cancer Health Disparities Study. Cancer causes & control : CCC 2014 Mar 25 (3): 293-307. Slattery Martha L, Lundgreen Abbie, Stern Marianna C, Hines Lisa, Wolff Roger K, Giuliano Anna R, Baumgartner Kathy B, John Esther |
Mutations of NOTCH3 in childhood pulmonary arterial hypertension. Molecular genetics & genomic medicine 2014 May 2 (3): 229-39. Chida Ayako, Shintani Masaki, Matsushita Yoshihisa, Sato Hiroki, Eitoku Takahiro, Nakayama Tomotaka, Furutani Yoshiyuki, Hayama Emiko, Kawamura Yoichi, Inai Kei, Ohtsuki Shinichi, Saji Tsutomu, Nonoyama Shigeaki, Nakanishi Tosh |
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 |
Non-HFE mutations in haemochromatosis in China: combination of heterozygous mutations involving HJV signal peptide variants. Journal of medical genetics 2018 9 55 (10): 650-660. Lv Tingxia, Zhang Wei, Xu Anjian, Li Yanmeng, Zhou Donghu, Zhang Bei, Li Xiaojin, Zhao Xinyan, Wang Yu, Wang Xiaoming, Duan Weijia, Wang Qianyi, Xu Hexiang, Zheng JiShun, Zhao Rongrong, Zhu Longdong, Dong Yuwei, Lu Lungen, Chen Yongpeng, Long Jiang, Zheng Sujun, Wang Wei, You Hong, Jia Jidong, Ou Xiaojuan, Huang Ji |
Genetic polymorphisms in bone morphogenetic protein receptor type IA gene predisposes individuals to ossification of the posterior longitudinal ligament of the cervical spine via the smad signaling pathway. BMC musculoskeletal disorders 2018 Feb 19 (1): 61. Wang Hao, Jin Weitao, Li Haib |
Bone morphogenetic protein 2 is a depot-specific regulator of human adipogenesis. International journal of obesity (2005) 2019 7 43 (12): 2458-2468. Denton Nathan F, Eghleilib Mohamed, Al-Sharifi Sama, Todor?evi? Marijana, Neville Matt J, Loh Nellie, Drakesmith Alexander, Karpe Fredrik, Pinnick Katherine |
Osteoporosis genome-wide association study variant c.3781 C>A is regulated by a novel anti-osteogenic factor miR-345-5p. Human mutation 2019 12 41 (3): 709-718. Wang Ya, Ye Weiyuan, Liu Yuyong, Mei Bing, Liu Xinhong, Huang Qingya |
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 |
Variants of SMAD1 gene increase the risk of colorectal cancer in the Bangladeshi population. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2020 Sep 42 (9): 1010428320958955. Karmokar Priyanka Florina, Shabnaz Samia, Aziz Md Abdul, Asaduzzaman Md, Shahriar Mohammad, Bhuiyan Mohiuddin Ahmed, Mosaddek Abu Syed Md, Islam Mohammad Safiq |
Differential expression of BMP/SMAD signaling and ovarian-associated genes in the granulosa cells of FecB introgressed GMM sheep. Systems biology in reproductive medicine 2020 1 66 (3): 185-201. Kumar Satish, Rajput Pradeep Kumar, Bahire Sangharatna V, Jyotsana Basanti, Kumar Vijay, Kumar Davend |
Goat SMAD family member 1 (SMAD1): mRNA expression, genetic variants, and their associations with litter size. Theriogenology 2022 Sep 193 11-19. Wijayanti Dwi, Zhang Sihuan, Yang Yuta, Bai Yangyang, Akhatayeva Zhanerke, Pan Chuanying, Zhu Haijing, Qu Lei, Lan Xianyo |
Whole Exome Sequencing of Patients With Heritable and Idiopathic Pulmonary Arterial Hypertension in Central Taiwan. Frontiers in cardiovascular medicine 2022 9 911649. Liang Kae-Woei, Chang Sheng-Kai, Chen Yu-Wei, Lin Wei-Wen, Tsai Wan-Jane, Wang Kuo-Ya |
Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis. Orphanet journal of rare diseases 2022 6 17 (1): 216. Zhang Wei, Li Yanmeng, Xu Anjian, Ouyang Qin, Wu Liyan, Zhou Donghu, Wu Lina, Zhang Bei, Zhao Xinyan, Wang Yu, Wang Xiaoming, Duan Weijia, Wang Qianyi, You Hong, Huang Jian, Ou Xiaojuan, Jia Jidong, |
Correlation between SMADs and Colorectal Cancer Expression, Prognosis, and Immune Infiltrates. International journal of analytical chemistry 2023 3 2023 8414040. Ding Ning, Luo Hongbiao, Zhang Tao, Peng Tianshu, Yao Yanru, He Yonghe |
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- Page last updated:Apr 22, 2024
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