Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and TNRC6B[original query] |
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Sequence variants at 22q13 are associated with prostate cancer risk.
Cancer research 2009 Jan 69 (1): 10-5. Sun Jielin, Zheng Siqun Lilly, Wiklund Fredrik, Isaacs Sarah D, Li Ge, Wiley Kathleen E, Kim Seong-Tae, Zhu Yi, Zhang Zheng, Hsu Fang-Chi, Turner Aubrey R, Stattin Pär, Liu Wennuan, Kim Jin Woo, Duggan David, Carpten John, Isaacs William, Grönberg Henrik, Xu Jianfeng, Chang Bao- |
| Genetic variants in miRNA processing genes and pre-miRNAs are associated with the risk of chronic lymphocytic leukemia. PloS one 2015 10 (3): e0118905. Martin-Guerrero Idoia, Gutierrez-Camino Angela, Lopez-Lopez Elixabet, Bilbao-Aldaiturriaga Nerea, Pombar-Gomez Maria, Ardanaz Maite, Garcia-Orad Afri |
| Association of BET1L and TNRC6B with uterine leiomyoma risk and its relevant clinical features in Han Chinese population. Scientific reports 2018 May 8 (1): 7401. Liu Bailing, Wang Tao, Jiang Jue, Li Miao, Ma Wenqi, Wu Haibin, Zhou |
| The rs12532734 Polymorphism Near the Solute Carrier 26A3 Gene Locus Is Associated With Gallstone Disease in Children. Journal of pediatric gastroenterology and nutrition 2022 Sep . Krawczyk Marcin, Niewiadomska Olga, Jankowska Irena, Jankowski Krzysztof, ?widerska Jolanta, Lebensztejn Dariusz, Wi?cek Sabina, Gozdowska Jolanta, Ku?aga Zbigniew, Weber Susanne N, Lammert Frank, Socha Pio |
| A minority of somatically mutated genes in pre-existing fatty liver disease have prognostic importance in the development of NAFLD. Liver international : official journal of the International Association for the Study of the Liver 2022 4 42 (8): 1823-1835. Mann Jake P, Hoare Matth |
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