Human Genome Epidemiology Literature Finder
|
Records 1 - 22 (of 22 Records) |
| Query Trace: Disease and SMAD2[original query] |
|---|
| A catalog of 106 single-nucleotide polymorphisms (SNPs) and 11 other types of variations in genes for transforming growth factor-beta1 (TGF-beta1) and its signaling pathway. Journal of human genetics 2002 47 (9): 478-83. Watanabe Yukio, Kinoshita Akira, Yamada Takahiro, Ohta Tohru, Kishino Tatsuya, Matsumoto Naomichi, Ishikawa Mutsuo, Niikawa Norio, Yoshiura Koh-ichi |
| SMAD2 and the relationship of colorectal cancer to inflammatory bowel disease. The International journal of biological markers 0 23 (3): 169-75. Mahid S S, Minor K S, Brangers B C, Cobbs G A, Galandiuk |
| 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 |
| FBXO11, a regulator of the TGFß pathway, is associated with severe otitis media in Western Australian children. Genes and immunity 2011 Jul 12 (5): 352-9. Rye M S, Wiertsema S P, Scaman E S H, Oommen J, Sun W, Francis R W, Ang W, Pennell C E, Burgner D, Richmond P, Vijayasekaran S, Coates H L, Brown S D, Blackwell J M, Jamieson S |
| Wound healing genes and susceptibility to cutaneous leishmaniasis in Brazil. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2012 Jul 12 (5): 1102-10. Castellucci Léa, Jamieson Sarra E, Almeida Lucas, Oliveira Joyce, Guimarães Luiz Henrique, Lessa Marcus, Fakiola Michaela, Jesus Amélia Ribeiro de, Nancy Miller E, Carvalho Edgar M, Blackwell Jenefer |
| De novo mutations in histone-modifying genes in congenital heart disease. Nature 2013 Jun 498 (7453): 220-3. Zaidi Samir, Choi Murim, Wakimoto Hiroko, Ma Lijiang, Jiang Jianming, Overton John D, Romano-Adesman Angela, Bjornson Robert D, Breitbart Roger E, Brown Kerry K, Carriero Nicholas J, Cheung Yee Him, Deanfield John, DePalma Steve, Fakhro Khalid A, Glessner Joseph, Hakonarson Hakon, Italia Michael J, Kaltman Jonathan R, Kaski Juan, Kim Richard, Kline Jennie K, Lee Teresa, Leipzig Jeremy, Lopez Alexander, Mane Shrikant M, Mitchell Laura E, Newburger Jane W, Parfenov Michael, Pe'er Itsik, Porter George, Roberts Amy E, Sachidanandam Ravi, Sanders Stephan J, Seiden Howard S, State Mathew W, Subramanian Sailakshmi, Tikhonova Irina R, Wang Wei, Warburton Dorothy, White Peter S, Williams Ismee A, Zhao Hongyu, Seidman Jonathan G, Brueckner Martina, Chung Wendy K, Gelb Bruce D, Goldmuntz Elizabeth, Seidman Christine E, 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' |
| An admixture mapping meta-analysis implicates genetic variation at 18q21 with asthma susceptibility in Latinos. The Journal of allergy and clinical immunology 2018 9 143 (3): 957-969. Gignoux Christopher R, Torgerson Dara G, Pino-Yanes Maria, Uricchio Lawrence H, Galanter Joshua, Roth Lindsey A, Eng Celeste, Hu Donglei, Nguyen Elizabeth A, Huntsman Scott, Mathias Rasika A, Kumar Rajesh, Rodriguez-Santana Jose, Thakur Neeta, Oh Sam S, McGarry Meghan, Moreno-Estrada Andres, Sandoval Karla, Winkler Cheryl A, Seibold Max A, Padhukasahasram Badri, Conti David V, Farber Harold J, Avila Pedro, Brigino-Buenaventura Emerita, Lenoir Michael, Meade Kelley, Serebrisky Denise, Borrell Luisa N, Rodriguez-Cintron William, Thyne Shannon, Joubert Bonnie R, Romieu Isabelle, Levin Albert M, Sienra-Monge Juan-Jose, Del Rio-Navarro Blanca Estela, Gan Weiniu, Raby Benjamin A, Weiss Scott T, Bleecker Eugene, Meyers Deborah A, Martinez Fernando J, Gauderman W James, Gilliland Frank, London Stephanie J, Bustamante Carlos D, Nicolae Dan L, Ober Carole, Sen Saunak, Barnes Kathleen, Williams L Keoki, Hernandez Ryan D, Burchard Esteban |
| Variable cardiovascular phenotypes associated with SMAD2 pathogenic variants. Human mutation 2018 8 39 (12): 1875-1884. Granadillo Jorge L, Chung Wendy K, Hecht Leah, Corsten-Janssen Nicole, Wegner Daniel, Nij Bijvank Sebastiaan W A, Toler Tomi L, Pineda-Alvarez Daniel E, Douglas Ganka, Murphy Joshua J, Shimony Joshua, Shinawi Marw |
| Dynamics of Genome Alterations in Crohn's Disease-Associated Colorectal Carcinogenesis. Clinical cancer research : an official journal of the American Association for Cancer Research 2018 Jul . Hirsch Daniela, Wangsa Darawalee, Zhu Yuelin J, Hu Yue, Edelman Daniel C, Meltzer Paul S, Heselmeyer-Haddad Kerstin, Ott Claudia, Kienle Peter, Galata Christian, Horisberger Karoline, Ried Thomas, Gaiser Ti |
| Reduced SMAD2/3 activation independently predicts increased depth of human cutaneous squamous cell carcinoma. Oncotarget 2018 3 9 (18): 14552-14566. Rose Aidan M, Spender Lindsay C, Stephen Christopher, Mitchell Alastair, Rickaby William, Bray Susan, Evans Alan T, Dayal Jasbani, Purdie Karin J, Harwood Catherine A, Proby Charlotte M, Leigh Irene M, Coates Philip J, Inman Gareth |
| Targeted sequencing of cancer-related genes in nasopharyngeal carcinoma identifies mutations in the TGF-? pathway. Cancer medicine 2019 Jul . Chung An-Ko, OuYang Chun-Nan, Liu Hsuan, Chao Mei, Luo Ji-Dung, Lee Cheng-Yang, Lu Yen-Jung, Chung I-Che, Chen Lih-Chyang, Wu Shao-Min, Tsang Ngan-Ming, Chang Kai-Ping, Hsu Cheng-Lung, Li Hsin-Pai, Chang Yu-S |
| Genetic variants of SMAD2/3/4/7 are associated with susceptibility to ulcerative colitis in a Japanese genetic background. Immunology letters 2019 Jan . Yamashita Arisa, Inamine Tatsuo, Suzuki Shota, Fukuda Sayaka, Unoike Miki, Kawafuchi Yuka, Machida Haruhisa, Isomoto Hajime, Nakao Kazuhiko, Tsukamoto Kazuhi |
| A scan for genes associated with cancer mortality and longevity in pedigree dog breeds. Mammalian genome : official journal of the International Mammalian Genome Society 2020 7 31 (7-8): 215-227. Doherty Aoife, Lopes Inês, Ford Christopher T, Monaco Gianni, Guest Patrick, de Magalhães João Ped |
| Identification of new candidate genes and signalling pathways associated with the development of neuroendocrine pancreatic tumours based on next generation sequencing data. Molecular biology reports 2020 5 47 (6): 4233-4243. Kit Oleg I, Trifanov Vladimir S, Petrusenko Nataliya A, Gvaldin Dmitry Y, Kutilin Denis S, Timoshkina Nataliya |
| De novo damaging variants associated with congenital heart diseases contribute to the connectome. Scientific reports 2020 Apr 10 (1): 7046. Ji Weizhen, Ferdman Dina, Copel Joshua, Scheinost Dustin, Shabanova Veronika, Brueckner Martina, Khokha Mustafa K, Ment Laura |
| Statistical methods with exhaustive search in the identification of gene-gene interactions for colorectal cancer. Genetic epidemiology 2020 11 45 (2): 222-234. Kafaie Somayeh, Xu Ling, Hu Ti |
| Implication of rare genetic variants of NODAL and ACVR1B in congenital heart disease patients from Indian population. Experimental cell research 2021 10 409 (1): 112869. Yadav Manohar Lal, Ranjan Prashant, Das Parimal, Jain Dharmendra, Kumar Ashok, Mohapatra Bhagyalax |
| Signaling pathways of genetic variants and miRNAs in the pathogenesis of myasthenia gravis. Gland surgery 2021 1 9 (6): 1933-1944. Qian Kai, Xu Jia-Xin, Deng Yi, Peng Hao, Peng Jun, Ou Chun-Mei, Liu Zu, Jiang Li-Hong, Tai Yong-Ha |
| Comprehensive characterization of clonality of driver genes revealing their clinical relevance in colorectal cancer. Journal of translational medicine 2022 8 20 (1): 362. Shi Jian, Wang Li, Yin Xiangzhe, Wang Lixia, Bo Lin, Liu Kailai, Feng Ke, Lin Shihua, Xu Yanjun, Ning Shangwei, Zhao Hongyi |
| Are SMAD2/4/7 genetic variants associated with rheumatoid arthritis susceptibility and severity? Clinical and experimental rheumatology 2022 11 . Wajda Anna, Stypi?ska Barbara, Czarnecka Magdalena, Hasan Diana, Jaro?czyk Ma?gorzata, Ha?adyj Ewa, Romanowska-Próchnicka Katarzyna, Olesi?ska Marzena, Pawlik Andrzej, Paradowska-Gorycka Agniesz |
| [Clinical and genetic characteristics of 12 cases of Loeys-Dietz syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 8 40 (9): 1093-1099. Jiaqi Fan, Hairui Sun, Xin Wang, Yuduo Wu, Siyao Zhang, Xiaoyan Hao, Jiancheng Han, Xiaoyan Gu, Ye Zhang, Lin Sun, Yihua |
- Page last reviewed:Feb 1, 2024
- Content source: