نتایج جستجو برای: ercc5

تعداد نتایج: 216  

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009
Shehnaz K Hussain Li-Na Mu Lin Cai Shen-Chih Chang Sungshim Lani Park Sam S Oh Yiren Wang Binh Y Goldstein Bao-Guo Ding Qingwu Jiang Jianyu Rao Nai-Chieh Y You Shun-Zhang Yu Jeanette C Papp Jin-Kou Zhao Hua Wang Zuo-Feng Zhang

The incidence of stomach cancer is high in certain parts of the world, particularly in China. Chronic Helicobacter pylori infection is the main risk factor, yet the vast majority of infected individuals remain unaffected with cancer, suggesting an important role of other risk factors. We conducted a population-based case-control study including 196 incident stomach cancer cases and 397 matched ...

Journal: :Cell 2011
Jillian Orans Elizabeth A. McSweeney Ravi R. Iyer Michael A. Hast Homme W. Hellinga Paul Modrich Lorena S. Beese

Human exonuclease 1 (hExo1) plays important roles in DNA repair and recombination processes that maintain genomic integrity. It is a member of the 5' structure-specific nuclease family of exonucleases and endonucleases that includes FEN-1, XPG, and GEN1. We present structures of hExo1 in complex with a DNA substrate, followed by mutagenesis studies, and propose a common mechanism by which this ...

Journal: :Journal of B.U.ON. : official journal of the Balkan Union of Oncology 2013
J Ruiz-Cosano D Torres-Moreno P Conesa-Zamora

PURPOSE Functions pertaining to DNA repair and synthesis are believed to play a critical role in cancer development and seem to be affected by genetic polymorphisms. Herein we performed a case-control study evaluating the influence of three single nucleotide polymorphisms (SNPs) in XPA, ERCC5 and MTR [rs1800975 (G-4A), rs17655 (Asp1104His) and rs1805087 (A2756G), respectively] in lymphoma risk....

2015
María Moriel-Carretero Emilia Herrera-Moyano Andrés Aguilera

Nucleotide Excision Repair (NER) is a pathway that removes lesions distorting the DNA helix. The molecular basis of the rare diseases Xeroderma pigmentosum (XP) and Cockayne Syndrome (CS) are explained based on the defects happening in 2 NER branches: Global-Genome Repair and Transcription-Coupled Repair, respectively. Nevertheless, both afflictions sporadically occur together, giving rise to X...

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