HuGE Literature Finder
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Records 1-5
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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 |
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Predicting therapy response to Mycophenolic acid using UGT1A9 genotyping: Towards personalized medicine in atopic dermatitis.
The Journal of dermatological treatment 2016 Aug 1-15. Thijs J L, van der Geest B A M, van der Schaft J, van den Broek M P, van Seggelen W O, Bruijnzeel-Koomen C A F, Hijnen D J, van Schaik R H, de Bruin-Weller M |
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Body Composition in Children and Adolescents with Osteogenesis Imperfecta.
The Journal of pediatrics 2015 Nov . Palomo Telma, Glorieux Francis H, Schoenau Eckhard, Rauch Fra |
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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 |
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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 |
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- Page last updated:Dec 12, 2019
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