Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: MGST1[original query] |
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Genetic analysis of the glutathione s-transferase genes MGST1, GSTM3, GSTT1, and GSTM1 in patients with hereditary pancreatitis. Journal of gastroenterology 2004 Aug 39 (8): 783-7. Schneider Alexander, Tögel Sandra, Barmada M Michael, Whitcomb David |
Functional candidate genes in age-related macular degeneration: significant association with VEGF, VLDLR, and LRP6. Investigative ophthalmology & visual science 2006 Jan 47 (1): 329-35. Haines Jonathan L, Schnetz-Boutaud Nathalie, Schmidt Silke, Scott William K, Agarwal Anita, Postel Eric A, Olson Lana, Kenealy Shannon J, Hauser Michael, Gilbert John R, Pericak-Vance Margaret |
Microsomal glutathione S-transferase gene polymorphisms and colorectal cancer risk in a Han Chinese population. International journal of colorectal disease 2007 Oct 22 (10): 1185-94. Zhang Hao, Liao Ling-Hong, Liu Shuk-Ming, Lau Kwok-Wai, Lai Albert Kai-Cheong, Zhang Jin-Hui, Wang Qi, Chen Xiao-Qian, Wei Wei, Liu Hua, Cai Jian-Hua, Lung Maria Li, Tai Susan S W, Wu Madeli |
The role of xenobotic metabolism MGST1 gene polymorphism in colorectal cancer patients. Acta medica Indonesiana 2012 Oct 44 (4): 4. Akil F, Akil HA, Lutfie AM, Wibowo WS, Miskad U, Yusuf I |
Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants.
JAMA 2015 Mar 313 (11): 1133-42. Nan Hongmei, Hutter Carolyn M, Lin Yi, Jacobs Eric J, Ulrich Cornelia M, White Emily, Baron John A, Berndt Sonja I, Brenner Hermann, Butterbach Katja, Caan Bette J, Campbell Peter T, Carlson Christopher S, Casey Graham, Chang-Claude Jenny, Chanock Stephen J, Cotterchio Michelle, Duggan David, Figueiredo Jane C, Fuchs Charles S, Giovannucci Edward L, Gong Jian, Haile Robert W, Harrison Tabitha A, Hayes Richard B, Hoffmeister Michael, Hopper John L, Hudson Thomas J, Jenkins Mark A, Jiao Shuo, Lindor Noralane M, Lemire Mathieu, Le Marchand Loic, Newcomb Polly A, Ogino Shuji, Pflugeisen Bethann M, Potter John D, Qu Conghui, Rosse Stephanie A, Rudolph Anja, Schoen Robert E, Schumacher Fredrick R, Seminara Daniela, Slattery Martha L, Thibodeau Stephen N, Thomas Fridtjof, Thornquist Mark, Warnick Greg S, Zanke Brent W, Gauderman W James, Peters Ulrike, Hsu Li, Chan Andrew T, , |
Germline variation in inflammation-related pathways and risk of Barrett's oesophagus and oesophageal adenocarcinoma. Gut 2016 Aug . Buas Matthew F, He Qianchuan, Johnson Lisa G, Onstad Lynn, Levine David M, Thrift Aaron P, Gharahkhani Puya, Palles Claire, Lagergren Jesper, Fitzgerald Rebecca C, Ye Weimin, Caldas Carlos, Bird Nigel C, Shaheen Nicholas J, Bernstein Leslie, Gammon Marilie D, Wu Anna H, Hardie Laura J, Pharoah Paul D, Liu Geoffrey, Iyer Prassad, Corley Douglas A, Risch Harvey A, Chow Wong-Ho, Prenen Hans, Chegwidden Laura, Love Sharon, Attwood Stephen, Moayyedi Paul, MacDonald David, Harrison Rebecca, Watson Peter, Barr Hugh, deCaestecker John, Tomlinson Ian, Jankowski Janusz, Whiteman David C, MacGregor Stuart, Vaughan Thomas L, Madeleine Margaret |
Genome-wide comparative analyses of correlated and uncorrelated phenotypes identify major pleiotropic variants in dairy cattle. Scientific reports 2017 8 7 (1): 9248. Xiang Ruidong, MacLeod Iona M, Bolormaa Sunduimijid, Goddard Michael |
Maternal and infant genetic variants, maternal periconceptional use of selective serotonin reuptake inhibitors, and risk of congenital heart defects in offspring: population based study. BMJ (Clinical research ed.) 2017 Mar 356 j832. Nembhard Wendy N, Tang Xinyu, Hu Zhuopei, MacLeod Stewart, Stowe Zachary, Webber Daniel, |
Gene-by-gene interactions associated with the risk of conotruncal heart defects. Molecular genetics & genomic medicine 2019 Dec e1010. Lyu Chen, Webber Daniel M, MacLeod Stewart L, Hobbs Charlotte A, Li Ming, |
Genomic Analysis of Germline Variation Associated with Survival of Patients with Colorectal Cancer Treated with Chemotherapy Plus Biologics in CALGB/SWOG 80405 (Alliance).
Clinical cancer research : an official journal of the American Association for Cancer Research 2020 (1): 267-275. Innocenti Federico, Sibley Alexander B, Patil Sushant A, Etheridge Amy S, Jiang Chen, Ou Fang-Shu, Howell Stefanie D, Plummer Sarah J, Casey Graham, Bertagnolli Monica M, McLeod Howard L, Auman James T, Blanke Charles D, Furukawa Yoichi, Venook Alan P, Kubo Michiaki, Lenz Heinz-Josef, Parker Joel S, Ratain Mark J, Owzar Kour |
Genome-Wide Association Study for Chronic Hepatitis B Infection in the Thai Population. Frontiers in genetics 2022 13 887121. Ashouri Saeideh, Khor Seik-Soon, Hitomi Yuki, Sawai Hiromi, Nishida Nao, Sugiyama Masaya, Kawai Yosuke, Posuwan Nawarat, Tangkijvanich Pisit, Komolmit Piyawat, Tsuiji Makoto, Shotelersuk Vorasuk, Poovorawan Yong, Mizokami Masashi, Tokunaga Katsus |
Identification of ferroptosis-related molecular subtypes and a methylation-related ferroptosis gene prognostic signature in cervical squamous cell carcinoma. Journal of cancer research and clinical oncology 2023 8 . Lijun Yu, Zhenwei Gao, Zeyu Li, Ping Liu, Ya Gao, Gang Lia |
SNPs Sets in Codifying Genes for Xenobiotics-Processing Enzymes Are Associated with COPD Secondary to Biomass-Burning Smoke. Current issues in molecular biology 2023 2 45 (2): 799-819. Ambrocio-Ortiz Enrique, Pérez-Rubio Gloria, Ramírez-Venegas Alejandra, Hernández-Zenteno Rafael de Jesús, Fernández-López Juan Carlos, Ramírez-Díaz María Elena, Cruz-Vicente Filiberto, Martínez-Gómez María de Lourdes, Sansores Raúl, Pérez-Ramos Julia, Falfán-Valencia Ramc |
Gene-Folic Acid Interactions and Risk of Conotruncal Heart Defects: Results from the National Birth Defects Prevention Study. Genes 2023 1 14 (1): . Webber Daniel M, Li Ming, MacLeod Stewart L, Tang Xinyu, Levy Joseph W, Karim Mohammad A, Erickson Stephen W, Hobbs Charlotte A, The National Birth Defects Prevention Stud |
A combined immune and exosome-related risk signature as prognostic biomakers in acute myeloid leukemia. Hematology (Amsterdam, Netherlands) 2024 1 29 (1): 2300855. Zenghui Fang, Jiali Fu, Xin Ch |
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- Page last updated:Mar 25, 2024
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