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Renal Failure Volume 37, 2015 - Issue 1
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Laboratory Study

DNA repair genes XPD and XRCC1 polymorphisms and risk of end-stage renal disease in Egyptian population

Wafaa M. RadwanDepartment of Clinical Pathology, Faculty of Medicine, Menoufia University, Menoufia, Egypt, Correspondence[email protected]
,
Hany S. ElbarbaryDepartment of Internal Medicine, Faculty of Medicine, Menoufia University, Menoufia, Egypt, and
&
Nevein M. AlsheikhDepartment of Biochemistry, Faculty of Medicine, Menoufia University, Menoufia, Egypt
Pages 122-128 | Published online: 13 Oct 2014

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Sacide Pehlivan, Ahmet Bulent Yazici, Nazan Aydin, Ayse Feyda Nursal, Selin Kurnaz, Ayca Ongel Atar, Ulgen Sever, Zeliha Kincir, Mustafa Pehlivan & Pınar Cetinay Aydin. (2018) Possible association between DNA repair gene variants and cannabis dependence in a Turkish cohort: a pilot study. Psychiatry and Clinical Psychopharmacology 28:4, pages 402-407.
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Elif Citak, Serkan Feyyaz Yalin, Mehmet Riza Altiparmak & Mehmet Guven. (2023) Investigation of XPD, miR-145 and miR-770 expression in patients with end-stage renal disease. Molecular Biology Reports 50:8, pages 6843-6850.
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Dalia M. Abd EL-Hassib, Magda A. Zidan, Medhat M. El Amawy, Hind A. Hegazy & Seham Gouda Ameen. (2021) Polymorphism of XRCC1 Arg399Gln may predict for development of end-stage renal disease. A PCR confirmed case-control study. Meta Gene 29, pages 100915.
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Rosa Roy Barcelona. (2020) Impact of polymorphism in DNA repair genes OGG1 and XRCC1 on seminal parameters and human male infertility: Response to rebuttal. Andrologia 53:1.
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Mohamed A. Mortada, Haidy E. Zidan, Noha A. Abdelsalam & Mirvat A. Eltoukhy. (2020) Gene XRCC1Arg399Gln polymorphism and its genotype variations: clinical associations in Egyptian systemic lupus erythematosus patients. Egyptian Rheumatology and Rehabilitation 47:1.
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Zuray Corredor, Miguel Inácio da Silva Filho, Lara Rodríguez-Ribera, Antonia Velázquez, Alba Hernández, Calogerina Catalano, Kari Hemminki, Elisabeth Coll, Irene Silva, Juan Manuel Diaz, José Ballarin, Martí Vallés Prats, Jordi Calabia Martínez, Asta Försti, Ricard Marcos & Susana Pastor. (2020) Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population. Scientific Reports 10:1.
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Xiaokai Fang & Yonghu Sun. (2019) Whole-Exome Sequencing Enables the Diagnosis of Variant-Type Xeroderma Pigmentosum. Frontiers in Genetics 10.
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Tugce Yesil-Devecioglu, Akın Dayan, Refik Demirtunc & Semra Sardas. (2019) Role of DNA repair genes XRCC3 and XRCC1 in predisposition to type 2 diabetes mellitus and diabetic nephropathy. Endocrinología, Diabetes y Nutrición 66:2, pages 90-98.
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Tugce Yesil-Devecioglu, Akın Dayan, Refik Demirtunc & Semra Sardas. (2019) Role of DNA repair genes XRCC3 and XRCC1 in predisposition to type 2 diabetes mellitus and diabetic nephropathy. Endocrinología, Diabetes y Nutrición (English ed.) 66:2, pages 90-98.
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Cindy George, Yandiswa Y Yako, Ikechi G Okpechi, Tandi E Matsha, Francois J. Kaze Folefack & Andre P Kengne. (2018) An African perspective on the genetic risk of chronic kidney disease: a systematic review. BMC Medical Genetics 19:1.
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