HuGE Literature Finder
Records 1-27
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Effects of polymorphic DNA genes involved in BER and caspase pathways on the clinical outcome of myeloproliferative neoplasms under treatment with hydroxyurea.
Molecular medicine reports 2018 Oct . Azevedo Ana P, Silva Susana N, Reichert Alice, Lima Fernando, Júnior Esmeraldina, Rueff Jo |
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The polymorphism of XRCC1 and coronary artery disease risk: a meta-analysis.
European review for medical and pharmacological sciences 2017 Apr 21 (7): 1559-1567. Guo S-J, Zhou Y-T, Liu W-Y, Zuo Q-N, Li X |
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Polymorphism of the XRCC1 Gene Is Associated with Susceptibility and Short-Term Recovery of Ischemic Stroke.
International journal of environmental research and public health 2016 Oct 13 (10): . He Wei, Huang Peng, Liu Dinghua, Zhong Lingling, Yu Rongbin, Li Jian |
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Study of association between pre-senile cataracts and rs11615 of ERCC1, rs13181 of ERCC2, and rs25487 of XRCC1 polymorphisms in a Spanish population.
Ophthalmic genetics 2016 Sep 1-6. López-Valverde Gloria, Garcia-Martin Elena, Fernández-Mateos Javier, Cruz-González Fernando, Larrosa-Povés José M, Polo-Llorens Vicente, Pablo-Júlvez Luis |
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Arsenic and subclinical vascular damage in a sample of Italian young adults: a cross-sectional analysis.
Environmental science and pollution research international 2016 Jul . Stea Francesco, Faita Francesco, Borghini Andrea, Faita Francesca, Bianchi Fabrizio, Bustaffa Elisa, Minichilli Fabrizio, Andreassi Maria Grazia, Sicari Ro |
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Association of Polymorphisms (rs 1799782, rs25489 and rs25487) in XRCC1 and (rs 13181) XPD genes with Acute Coronary Artery Syndrome in Subjects from Multan, Pakistan.
Pakistan journal of pharmaceutical sciences 2016 May 29 (3): 869-76. Hameed Hafsa, Faryal Maemona, Aslam Muhammad Assad, Akbar Atif, Saad Abu Bakar Ali, Pasha Muhammad Burhan, Latif Muhammad, Rehan Sadiq Shaikh Rehan Rehan Sadiq Shaikh, Ali Muhammad, Iqbal Furh |
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Leukocyte telomere shortening in grown-up patients with congenital heart disease.
International journal of cardiology 2015 Nov 204 17-22. Vecoli Cecilia, Borghini Andrea, Foffa Ilenia, Ait-Ali Lamia, Picano Eugenio, Andreassi Maria Graz |
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Up-regulation of MSH2, XRCC1 and ATM genes in patients with type 2 diabetes and coronary artery disease.
Diabetes research and clinical practice 2015 Sep 109 (3): 500-6. Ahmadi Amirhossein, Behmanesh Mehrdad, Boroumand Mohammad Ali, Tavallaei Mahmo |
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Association Analysis of Polymorphisms in Genes Related to Oxidative Stress in South Indian Type 2 Diabetic Patients with Retinopathy.
Ophthalmic genetics 2015 Aug 1-8. Narne Parimala, Ponnaluri Kamakshi Chaithri, Siraj Mohammed, Ishaq Mohamm |
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Do genetic defects of DNA repair relevant proteins alter susceptibility to hypertension? A case-control study in northeastern Han Chinese.
Clinica chimica acta; international journal of clinical chemistry 2015 Feb 441 171-5. Jia Nan, Xu Junxia, Zhao Hongye, Wang Yanli, Wang Bin, Niu Wenqu |
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Synergistic association of DNA repair relevant gene polymorphisms with the risk of coronary artery disease in northeastern Han Chinese.
Thrombosis research 2013 Nov . Yu X, Liu J, Zhu H, Xia Y, Gao L, Dong Y, Jia N, Shen W, Yang Y, Niu W |
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Association of the 399Arg/Gln XRCC1, the 194 Arg/Trp XRCC1, the 326Ser/Cys OGG1, and the 324Gln/His MUTYH gene polymorphisms with clinical parameters and the risk for development of primary open-angle glaucoma.
Mutation research 2013 Mar . Szaflik JP, Cuchra M, Przybylowska-Sygut K, Dziki L, Kurowska AK, Gacek M, Drzewoski J, Szaflik J, Majsterek I |
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Arg399Gln Polymorphism of X-Ray Repair Cross-Complementing Group 1 Gene Is Associated with Angiographically Documented Coronary Artery Disease in South Indian Type 2 Diabetic Patients.
Genetic testing and molecular biomarkers 2013 Jan . Narne P, Ponnaluri KC, Singh S, Siraj M, Ishaq M |
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Association Between Genetic Variants of DNA Repair Genes and Coronary Artery Disease.
Genetic testing and molecular biomarkers 2013 Jan . Gokkusu C, Cakmakoglu B, Dasdemir S, Tulubas F, Elitok A, Tamer S, Seckin S, Umman B |
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Polymorphisms of DNA repair pathway genes and cigarette smoking in relation to susceptibility to large artery atherosclerotic stroke among ethnic Chinese in Taiwan.
Journal of atherosclerosis and thrombosis 2012 19 (4): 316-25. Shyu Hann-Yeh, Shieh Jia-Ching, Ji-Ho Lin, Wang Hsiao-Wei, Cheng Chun-W |
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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 |
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Impact on response and survival of DNA repair single nucleotide polymorphisms in relapsed or refractory multiple myeloma patients treated with thalidomide.
Leukemia research 2011 Sep 35 (9): 1178-83. Cibeira María Teresa, de Larrea Carlos Fernández, Navarro Alfons, Díaz Tania, Fuster Dolors, Tovar Natalia, Rosiñol Laura, Monzó Mariano, Bladé Jo |
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Large-scale candidate gene analysis of HDL particle features.
PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
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Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
American journal of human genetics 2009 Nov 85 (5): 628-42. Talmud Philippa J, Drenos Fotios, Shah Sonia, Shah Tina, Palmen Jutta, Verzilli Claudio, Gaunt Tom R, Pallas Jacky, Lovering Ruth, Li Kawah, Casas Juan Pablo, Sofat Reecha, Kumari Meena, Rodriguez Santiago, Johnson Toby, Newhouse Stephen J, Dominiczak Anna, Samani Nilesh J, Caulfield Mark, Sever Peter, Stanton Alice, Shields Denis C, Padmanabhan Sandosh, Melander Olle, Hastie Claire, Delles Christian, Ebrahim Shah, Marmot Michael G, Smith George Davey, Lawlor Debbie A, Munroe Patricia B, Day Ian N, Kivimaki Mika, Whittaker John, Humphries Steve E, Hingorani Aroon D, , , |
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Multi-ethnic genetic association study of carotid intima-media thickness using a targeted cardiovascular SNP microarray.
Stroke; a journal of cerebral circulation 2009 Oct 40 (10): 3173-9. Lanktree Matthew B, Hegele Robert A, Yusuf Salim, Anand Sonia |
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Common genetic variants in candidate genes and risk of familial lymphoid malignancies.
British journal of haematology 2009 Aug 146 (4): 418-23. Liang Xueying Sharon, Caporaso Neil, McMaster Mary Lou, Ng David, Landgren Ola, Yeager Meredith, Chanock Stephen, Goldin Lynn |
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DNA repair gene XRCC1 and XPD polymorphisms and their association with coronary artery disease risks and micronucleus frequency.
Heart and vessels 2007 Nov 22 (6): 355-60. Guven Mehmet, Guven Gulgun S, Oz Erdinc, Ozaydin Ahmet, Batar Bahadir, Ulutin Turgut, Hacihanefioglu Seniba, Domanic Nerg |
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A prospective study of polymorphisms of DNA repair genes XRCC1, XPD23 and APE/ref-1 and risk of stroke in Linxian, China.
Journal of epidemiology and community health 2007 Aug 61 (8): 737-41. Mahabir Somdat, Abnet Christian C, Qiao You-Lin, Ratnasinghe Luke D, Dawsey Sanford M, Dong Zhi-Wei, Taylor Philip R, Mark Steven |
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PAH-DNA adducts in environmentally exposed population in relation to metabolic and DNA repair gene polymorphisms.
Mutation research 2007 Jul 620 (1-2): 49-61. Binkova Blanka, Chvatalova Irena, Lnenickova Zdena, Milcova Alena, Tulupova Elena, Farmer Peter B, Sram Radim |
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Analysis of the XRCC1 gene as a modifier of the cerebral response in ischemic stroke.
BMC medical genetics 2006 7 (): 78. Dutra Ana V C, Lin Hsiu-Fen, Juo Suh-Hang H, Mohrenweiser Harvey, Sen Souvik, Grewal Raji |
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[The peculiarities of polymorphism of XPD and XRCC1 repair genes in cells of Down and Ehlers-Danlo syndrome patients characterized by increased radiosensitivity].
Radiatsionnaia biologiia, radioecologiia / Rossi?skaia akademiia nauk 0 51 (4): 405-10. Shagirova Zh M, Kurbatova L A, Shulenina L V, Semiachkina A N, Mikha?lov V F, Zasukhina G |
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DNA repair gene polymorphism is associated with the genetic basis of atherosclerotic coronary artery disease.
Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology 0 20 (1): e9-15. Bazo Ana Paula, Salvadori Décio, Salvadori Ricardo A F, Sodré Luciandro P, da Silva Glenda N, de Camargo Elaine A, Ribeiro Lúcia R, Salvadori Daisy Maria Fáve |
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- Page last updated:Sep 23, 2020
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