Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Disease and XRCC4[original query] |
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| Identification of single nucleotide polymorphisms in human DNA repair genes. Carcinogenesis 2000 Nov 21 (11): 1977-81. Ford B N, Ruttan C C, Kyle V L, Brackley M E, Glickman B |
| Variants in the GH-IGF axis confer susceptibility to lung cancer. Genome research 2006 Jun 16 (6): 693-701. Rudd Matthew F, Webb Emily L, Matakidou Athena, Sellick Gabrielle S, Williams Richard D, Bridle Helen, Eisen Tim, Houlston Richard S, |
| Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma. Human molecular genetics 2007 Dec 16 (24): 3117-27. Hayden Patrick J, Tewari Prerna, Morris Derek W, Staines Anthony, Crowley Dominique, Nieters Alexandra, Becker Nikolaus, de Sanjosé Silvia, Foretova Lenka, Maynadié Marc, Cocco Pier Luigi, Boffetta Paolo, Brennan Paul, Chanock Stephen J, Browne Paul V, Lawler Ma |
| Significant association of XRCC4 single nucleotide polymorphisms with prostate cancer susceptibility in Taiwanese males. Molecular medicine reports 0 1 (4): 525-30. Chang Chao-Hsiang, Chiu Chang-Fang, Wu Hsi-Chin, Tseng Hsien-Chang, Wang Chung-Hsing, Lin Cheng-Chieh, Tsai Chia-Wen, Liang Shiu-Yun, Wang Cheng-Li, Bau Da-Ti |
| RAD52 polymorphisms contribute to the development of papillary thyroid cancer susceptibility in Middle Eastern population. Journal of endocrinological investigation 2008 Oct 31 (10): 893-9. Siraj A K, Al-Rasheed M, Ibrahim M, Siddiqui K, Al-Dayel F, Al-Sanea O, Uddin S, Al-Kuraya |
| Lung cancer susceptibility and prognosis associated with polymorphisms in the nonhomologous end-joining pathway genes: a multiple genotype-phenotype study. Cancer 2009 Jul 115 (13): 2939-48. Tseng Ruo-Chia, Hsieh Feng-Jen, Shih Chuen-Ming, Hsu Han-Shui, Chen Chih-Yi, Wang Yi-Chi |
| The role of common variants of non-homologous end-joining repair genes XRCC4, LIG4 and Ku80 in thyroid cancer risk. Oncology reports 2010 Oct 24 (4): 1079-85. Gomes Bruno Costa, Silva Susana Nunes, Azevedo Ana Paula, Manita Isabel, Gil Octávia Monteiro, Ferreira Teresa Cruz, Limbert Edward, Rueff José, Gaspar Jorge Francis |
Two-marker association tests yield new disease associations for coronary artery disease and hypertension.
Human genetics 2011 Dec 130 (6): 725-33. Slavin Thomas P, Feng Tao, Schnell Audrey, Zhu Xiaofeng, Elston Robert |
| DNA repair genes polymorphisms in multiple myeloma: no association with XRCC1 (Arg399Gln) polymorphism, but the XRCC4 (VNTR in intron 3 and G-1394T) and XPD (Lys751Gln) polymorphisms is associated with the disease in Turkish patients. Hematology (Amsterdam, Netherlands) 2011 Nov 16 (6): 361-7. Cifci S, Yilmaz M, Pehlivan M, Sever T, Okan V, Pehlivan |
| Genetic polymorphisms in DNA repair genes XRCC4 and XRCC5 and aflatoxin B1-related hepatocellular carcinoma. Epidemiology (Cambridge, Mass.) 2013 Sep 24 (5): 671-81. Long Xi-Dai, Zhao Dong, Wang Chao, Huang Xiao-Ying, Yao Jin-Guang, Ma Yun, Wei Zhong-Hua, Liu Min, Zeng Li-Xiao, Mo Xiao-Qiang, Zhang Jian-Jun, Xue Feng, Zhai Bo, Xia Qia |
| Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer. Genetics in medicine : official journal of the American College of Medical Genetics 2015 Feb 17 (2): 131-42. Esteban-Jurado Clara, Vila-Casadesús Maria, Garre Pilar, Lozano Juan José, Pristoupilova Anna, Beltran Sergi, Muñoz Jenifer, Ocaña Teresa, Balaguer Francesc, López-Cerón Maria, Cuatrecasas Miriam, Franch-Expósito Sebastià, Piqué Josep M, Castells Antoni, Carracedo Angel, Ruiz-Ponte Clara, Abulí Anna, Bessa Xavier, Andreu Montserrat, Bujanda Luis, Caldés Trinidad, Castellví-Bel Ser |
| DNA repair gene XRCC1 and XRCC4 variations and risk of endometriosis: an association study. Gynecologic and obstetric investigation 2015 80 (2): 85-8. Saliminejad Kioomars, Saket Mitra, Kamali Koorosh, Memariani Toktam, Khorram Khorshid Hamid Re |
| Susceptibility to Colorectal Cancer and Two Genetic Polymorphisms of XRCC4. Pathology oncology research : POR 2015 Sep 21 (4): 881-5. Emami Naghmeh, Saadat Iraj, Omidvari Shahpo |
| Brief Report: Whole-Exome Sequencing for Identification of Potential Causal Variants for Diffuse Cutaneous Systemic Sclerosis. Arthritis & rheumatology (Hoboken, N.J.) 2016 Apr . Mak Angel Cy, Tang Paul Lf, Cleveland Clare, Smith Melanie H, Connolly M Kari, Katsumoto Tamiko R, Wolters Paul J, Kwok Pui-Yan, Criswell Lindsey |
| Polymorphisms in double strand break repair related genes influence radiosensitivity phenotype in lymphocytes from healthy individuals. DNA repair 2016 Mar 40 27-34. Mumbrekar Kamalesh Dattaram, Goutham Hassan Venkatesh, Vadhiraja Bejadi Manjunath, Bola Sadashiva Satish R |
| Somatic Variants in DNA Damage Response Genes in Ovarian Cancer Patients Using Whole-exome Sequencing. Anticancer research 2023 4 43 (5): 1891-1900. Joanna Lopacinska-Joergensen, Douglas V N P Oliveira, Tim Svenstrup Poulsen, Claus K Hoegdall, Estrid V Hoegda |
| The effect of DNA repair gene variants on COVID-19 disease: susceptibility, severity, and clinical course. Nucleosides, nucleotides & nucleic acids 2023 1 1-15. Senkal Naci, Serin Istemi, Pehlivan Sacide, Pehlivan Mustafa, Medetalibeyoglu Alpay, Cebeci Timurhan, Konyaoglu Hilal, Oyac? Yasemin, Say?n Gozde Yesil, Isoglu-Alkac Ummuhan, Tukek Tufan, Kose Mur |
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