نتایج جستجو برای: 1q22

تعداد نتایج: 68  

2010
Lynda Li Song Larissa Ponomareva Hui Shen Xin Duan Fatouma Alimirah Divaker Choubey

BACKGROUND Increased levels of interferon (IFN)-inducible IFI16 protein (encoded by the IFI16 gene located at 1q22) in human normal prostate epithelial cells and diploid fibroblasts (HDFs) are associated with the onset of cellular senescence. However, the molecular mechanisms by which the IFI16 protein contributes to cellular senescence-associated cell growth arrest remain to be elucidated. Her...

Journal: :Journal of applied genetics 2005
Kamilla Schlade-Bartusiak Agnieszka Stembalska David Ramsey

Head and neck squamous cell carcinoma (HNSCC) is a heterogeneous group of tumours with various clinical characteristics. These tumours generally exhibit complex karyotypes. Few studies of genomic imbalances have been performed exclusively in subgroups of larynx cancer samples at different stages of the disease. In the present study, chromosomal gains and losses were investigated in 52 larynx tu...

2013
Miao Li Liu Huang Hong Qiu Qiang Fu Wen Li Qianqian Yu Li Sun Lihong Zhang Guangyuan Hu Junbo Hu Xianglin Yuan

BACKGROUND Three recent genome-wide association studies (GWASs) have reported that three SNPs (rs4072037, rs13361707 and rs2274223) located on genes related to host inflammatory response are significantly associated with susceptibility to gastric cancer (GC) in Chinese populations. Helicobacter pylori infection is also an important risk factor for GC through causing inflammatory response in the...

2014
Jian-Wei Liang Zhi-Zhou Shi Tian-Yun Shen Xu Che Zheng Wang Su-Sheng Shi Xin Xu Yan Cai Ping Zhao Cheng-Feng Wang Zhi-Xiang Zhou Ming-Rong Wang

BACKGROUND Genomic aberration is a common feature of human cancers and also is one of the basic mechanisms that lead to overexpression of oncogenes and underexpression of tumor suppressor genes. Our study aims to identify frequent genomic changes in pancreatic cancer. MATERIALS AND METHODS We used array comparative genomic hybridization (array CGH) to identify recurrent genomic alterations an...

2017
Zhaoming Wang Juncheng Dai Nan Hu Xiaoping Miao Christian C Abnet Ming Yang Neal D Freedman Jinfei Chen Laurie Burdette Xun Zhu Charles C Chung Chuanli Ren Sanford M Dawsey Meilin Wang Ti Ding Jiangbo Du Yu-Tang Gao Rong Zhong Carol Giffen Wenting Pan Woon-Puay Koh Ningbing Dai Linda M Liao Caiwang Yan You-Lin Qiao Yue Jiang Xiao-Ou Shu Jiaping Chen Chaoyu Wang Hongxia Ma Hua Su Zhendong Zhang Lemin Wang Chen Wu Yong-Bing Xiang Zhibin Hu Jian-Min Yuan Lu Xie Wei Zheng Dongxin Lin Stephen J Chanock Yongyong Shi Alisa M Goldstein Guangfu Jin Philip R Taylor Hongbing Shen

OBJECTIVE Although several genome-wide association studies (GWAS) of non-cardia gastric cancer have been published, more novel association signals could be exploited by combining individual studies together, which will further elucidate the genetic susceptibility of non-cardia gastric cancer. DESIGN We conducted a meta-analysis of two published Chinese GWAS studies (2031 non-cardia gastric ca...

2012
Voichiţa Mogoş Simona Mogoş

FAMILIAL NONMEDULLARY THYROID CANCER (Abstract): Follicular cell-derived thyroid cancer which represents 90-95% of all thyroid malignancies may occur in at least 5% of cases as familial disease. Familial nonmedullary thyroid cancer (FNMTC) is defined as the existence of two or more first degree relatives affected within a family. FNMTC may occur in two situations: pure FNMTC in which FNMTC is t...

Journal: :Cancer research 1992
J W Bare R V Lebo E H Epstein

Basal cell carcinomas, the most common human tumors, generally appear sporadically and in small numbers. Rarely, they may appear in great numbers and at an earlier age as a manifestation of the basal cell nevus syndrome, an autosomal dominant inherited disorder. Drawing on the retinoblastoma paradigm, we have begun a search for tumor suppressor genes important in the development of basal cell c...

Journal: :European Heart Journal Supplements 2022

Abstract The proband was patient A2, suffering by severe left ventricular dysfunction (EF 20%) and II degree Mobitz type 1 atrioventricular block, requiring dual chamber ICD implantation, retinitis pigmentosa. He had three brothers A1, A4, A5 also dilated cardiomyopathy ICD/CRTD recipients. His sister A3, his daughter B1 the firstborn brother A1 were affected Genetic analysis performed in A2 NG...

Journal: :British medical journal 1962
S C TRUELOVE G WATKINSON G DRAPER

Anderson, R. McD., and Blackwood, W. (1959). J. Path. Bact., 77. 101. Biumi, F. (1765). Observationes Anatomicae. Milan. Brnnton, W. (1851). Trans. path. Soc. Lond., 3, 47. Brolin, S. E., and Hassler, 0. (1958). Acta path. microbiol. scand., 44, 59. Bull, J. W. D. (1962). Lond. Clin. med. J., 3, 47. Collier, J. (1Q22). In X Textbook of the Practice of Medicine, edited by F. W. Price. Frowde and...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید