نتایج جستجو برای: ercc5

تعداد نتایج: 216  

Journal: :Genetics and molecular research : GMR 2016
L Q Yang Y Zhang H F Sun

Our study aimed to investigate the role of 2 ERCC5 promoter SNPs (rs2094258 and rs751402) in the development of gastric cancer in the Chinese population. The present hospital-based case-control study consisted of 155 patients with gastric cancer and 246 healthy controls recruited between March 2012 and December 2014. Genotyping for the rs2094258 and rs751402 polymorphic sites was carried out us...

Journal: :International journal of clinical and experimental pathology 2015
Fuli Zhao Yuhong Shang Chen Zeng Dongdong Gao Ke Li

In our study, we conducted a case-control study to investigate the association of ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, XPA, XPC and DDB2 gene polymorphisms in the risk of pancreatic cancer. Between May 2012 and May 2014, a total of 246 patients with who were newly diagnosed with histopathologically confirmed primary pancreatic cancer and 246 controls were selected into our study. Genotyping of ER...

2016
Bengang Wang Qian Xu Huai-wei Yang Li-ping Sun Yuan Yuan

BACKGROUND Hundreds of single nucleotide polymorphisms (SNPs) of the genes encoding nucleotide excision repair (NER) proteins are involved in every step of the DNA recognition-unwinding-incision process, which may affect cancer risk. However, only a limited number of studies have examined the association of NER SNPs with hepatocellular cancer (HCC) risk. RESULTS In screening stage, single-loc...

Journal: :International journal of clinical and experimental pathology 2013
Miguel Aracil Lisa M Dauffenbach Marta Martínez Diez Rana Richeh Victoria Moneo Juan Fernando Martínez Leal Luis Francisco García Fernández Christopher A Kerfoot Carlos M Galmarini

XPG (Xeroderma pigmentosum group G complementing factor) is a protein associated with DNA repair and transcription. Point mutations in ERCC5, the gene coding for XPG, cause the cancer-prone disorder xeroderma pigmentosum (XP) while truncation mutations give rise to individuals with the combined clinical features of XP and Cockayne syndrome. Polymorphisms of ERCC5 or alterations in XPG mRNA expr...

Journal: :Journal of B.U.ON. : official journal of the Balkan Union of Oncology 2017
Caiming Zhang Zhengwen Liao Guodong Yu Wenhua Huang Xiaoning Song

PURPOSE DNA repair genes play important roles in the genesis of esophageal cancer, and their functional single nucleotide polymorphism (SNP) loci may affect the susceptibility to esophageal cancer through changing the capability of DNA damage repair. METHODS A total of 557 patients with esophageal squamous cell carcinoma and 1503 age- and gender-matched healthy people were selected in this st...

2016
Jungnam Joo Kyong-Ah Yoon Tomonori Hayashi Sun-Young Kong Hye-Jin Shin Boram Park Young Min Kim Sang-Hyun Hwang Jeongseon Kim Aesun Shin Joo-Young Kim

PURPOSE Defects in the DNA damage repair process can cause genomic instability and play an important role in cervical carcinogenesis. The purpose of this study was to analyze the association of 29 candidate single nucleotide polymorphisms (SNPs) in genes in the DNA repair pathway, TP53, and TP53BP1 with the risk of cervical cancer. MATERIALS AND METHODS Twenty-nine SNPs in four genes in the D...

Journal: :Oncology reports 2011
Preeyaporn Koedrith Young Rok Seo

XPG, a structure-specific DNA endonuclease responsible for the 3' incision of DNA lesions during nucleotide excision repair (NER), is associated with high risk of skin cancer as well as skeletal, neurological and developmental abnormalities when functionally defective. These observations have led to the model wherein the endonuclease activity of XPG is important for NER. Herein, we first demons...

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