Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 14 (of 14 Records) |
Query Trace: Cockayne Syndrome[original query] |
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Associations between ERCC2 polymorphisms and gliomas. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2001 Apr 10 (4): 355-60. Caggana M, Kilgallen J, Conroy J M, Wiencke J K, Kelsey K T, Miike R, Chen P, Wrensch M |
Influence of genetic markers on survival in non-small cell lung cancer. Drugs of today (Barcelona, Spain : 1998) 2003 Oct 39 (10): 775-86. Rosell Rafael, Taron Miquel, Camps Carlos, López-Vivanco Guiller |
Assessment of nucleotide excision repair XPD polymorphisms in the peripheral blood of gemcitabine/cisplatin-treated advanced non-small-cell lung cancer patients. Clinical lung cancer 2003 Jan 4 (4): 237-41. Camps Carlos, Sarries Carmen, Roig Bárbara, Sanchez José Javier, Queralt Cristina, Sancho Eva, Martinez Natividad, Tarón Miguel, Rosell Rafa |
Genetic polymorphisms of the XPG and XPD nucleotide excision repair genes in sarcoma patients. International journal of cancer. Journal international du cancer 2006 Oct 119 (7): 1732-5. Le Morvan Valérie, Longy Michel, Bonaïti-Pellié Catherine, Bui Binh, Houédé Nadine, Coindre Jean-Michel, Robert Jacques, Pourquier Philip |
A variant of the Cockayne syndrome B gene ERCC6 confers risk of lung cancer. Human mutation 2008 Jan 29 (1): 113-22. Lin Zhongning, Zhang Xuemei, Tuo Jingsheng, Guo Yongli, Green Bridgett, Chan Chi-Chao, Tan Wen, Huang Ying, Ling Wenhua, Kadlubar Fred F, Lin Dongxin, Ning Baita |
ERCC6/CSB gene polymorphisms and lung cancer risk. Cancer letters 2009 Jan 273 (1): 172-6. Ma Hongxia, Hu Zhibin, Wang Haifeng, Jin Guangfu, Wang Ying, Sun Weiwei, Chen Dan, Tian Tian, Jin Li, Wei Qingyi, Lu Daru, Huang Wei, Shen Hongbi |
Association between common genetic variation in Cockayne syndrome A and B genes and nucleotide excision repair capacity among smokers. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008 Aug 17 (8): 2062-9. Leng Shuguang, Bernauer Amanda, Stidley Christine A, Picchi Maria A, Sheng Xin, Frasco Melissa A, Van Den Berg David, Gilliland Frank D, Crowell Richard E, Belinsky Steven |
High carriers frequency of an apparently ancient founder mutation p.Tyr322X in the ERCC8 gene responsible for Cockayne syndrome among Christian Arabs in Northern Israel. American journal of medical genetics. Part A 2010 Dec 152A (12): 3091-4. Khayat Morad, Hardouf Hagar, Zlotogora Joel, Shalev Stavit All |
The ERCC6 gene and age-related macular degeneration. PloS one 2010 5 (11): e13786. Baas Dominique C, Despriet Dominiek D, Gorgels Theo G M F, Bergeron-Sawitzke Julie, Uitterlinden André G, Hofman Albert, van Duijn Cornelia M, Merriam Joanna E, Smith R Theodore, Barile Gaetano R, ten Brink Jacoline B, Vingerling Johannes R, Klaver Caroline C W, Allikmets Rando, Dean Michael, Bergen Arthur A |
Xeroderma pigmentosum complementation group C single-nucleotide polymorphisms in the nucleotide excision repair pathway correlate with prolonged progression-free survival in advanced ovarian cancer. Cancer 2012 Feb 118 (3): 689-97. Fleming Nicole D, Agadjanian Hasmik, Nassanian Hoorig, Miller Carl W, Orsulic Sandra, Karlan Beth Y, Walsh Christine |
XAB2 tagSNPs contribute to non-small cell lung cancer susceptibility in Chinese population. BMC cancer 2015 15 (1): 560. Pei Na, Cao Lei, Liu Yingwen, Wu Jing, Song Qinqin, Zhang Zhi, Yuan Juxiang, Zhang Xuem |
Why Cockayne syndrome patients do not get cancer despite their DNA repair deficiency. Proceedings of the National Academy of Sciences of the United States of America 2016 Aug . Reid-Bayliss Kate S, Arron Sarah T, Loeb Lawrence A, Bezrookove Vladimir, Cleaver James |
Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A. Scientific reports 2017 Oct 7 (1): 13686. Wang Xiaozhu, Huang Yu, Yan Ming, Li Jiuwei, Ding Changhong, Jin Hong, Fang Fang, Yang Yanling, Wu Baiyan, Chen Dafa |
Biallelic structural variants in three patients with ERCC8-related Cockayne syndrome and a potential pitfall of copy number variation analysis. Scientific reports 2024 8 14 (1): 19741. Daisuke Watanabe, Nobuhiko Okamoto, Yuichi Kobayashi, Hisato Suzuki, Mitsuhiro Kato, Shinji Saitoh, Yonehiro Kanemura, Toshiki Takenouchi, Mamiko Yamada, Daisuke Nakato, Masayuki Sato, Tatsuhiko Tsunoda, Kenjiro Kosaki, Fuyuki Mi |
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