HuGE Literature Finder
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| Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, or Family Cancer History by NGS Analysis of 217 Genes. Biomedicines 2020 Oct 8 (10): . Stolarova Lenka, Jelinkova Sandra, Storchova Radka, Machackova Eva, Zemankova Petra, Vocka Michal, Kodet Ondrej, Kral Jan, Cerna Marta, Volkova Zuzana, Janatova Marketa, Soukupova Jana, Stranecky Viktor, Dundr Pavel, Foretova Lenka, Macurek Libor, Kleiblova Petra, Kleibl Zden |
| Genetic variation in WRN and ischemic stroke: General population studies and meta-analyses. Experimental gerontology 2017 03 89 69-77. Christoffersen Mette, Frikke-Schmidt Ruth, Nordestgaard Børge G, Tybjærg-Hansen An |
| Genetic Variants That Predispose to DNA Double-Strand Breaks in Lymphocytes From a Subset of Patients With Familial Colorectal Carcinomas. Gastroenterology 2015 Sep . Arora Sanjeevani, Yan Hong, Cho Iltaeg, Fan Hua-Ying, Luo Biao, Gai Xiaowu, Bodian Dale L, Vockley Joseph G, Zhou Yan, Handorf Elizabeth, Egleston Brian L, Andrake Mark, Nicolas Emmanuelle, Serebriiskii Ilya, Yen Timothy J, Hall Michael J, Golemis Erica A, Enders Greg |
| A missense single nucleotide polymorphism, V114I of the Werner syndrome gene, is associated with risk of osteoporosis and femoral fracture in the Japanese population. Journal of bone and mineral metabolism 2015 Jan . Zhou Heying, Mori Seijiro, Tanaka Masashi, Sawabe Motoji, Arai Tomio, Muramatsu Masaaki, Mieno Makiko Naka, Shinkai Shoji, Yamada Yoshiji, Miyachi Motohiko, Murakami Haruka, Sanada Kiyoshi, Ito Hide |
| Association of the rs1346044 Polymorphism of the Werner Syndrome Gene RECQL2 with Increased Risk and Premature Onset of Breast Cancer. International journal of molecular sciences 2015 16 (12): 29643-53. Zins Karin, Frech Barbara, Taubenschuss Eva, Schneeberger Christian, Abraham Dietmar, Schreiber Mart |
| WRN Cys1367Arg polymorphism is not associated with skull base chordoma. Biomedical reports 2014 Jul 2 (4): 521-524. Wang Ke, Wang Liang, Feng Jie, Hao Shuyu, Tian Kaibing, Wu Zhen, Zhang Liwei, Jia Guijun, Wan Hong, Zhang Junti |
| Polymorphisms of the WRN gene and DNA damage of peripheral lymphocytes in age-related cataract in a Han Chinese population. Age (Dordrecht, Netherlands) 2013 Dec 35 (6): 2435-44. Jiang Shengqun, Hu Nan, Zhou Jing, Zhang Junfang, Gao Ruifang, Hu Jianyan, Guan Huaij |
| The non-synonymous polymorphism at position 114 of the WRN protein affects cholesterol efflux in vitro and correlates with cholesterol levels in vivo. Experimental gerontology 2013 Jun 48 (6): 533-8. Bérubé Julien, Garand Chantal, Lettre Guillaume, Lebel Mich |
| Applying and testing the conveniently optimized enzyme mismatch cleavage method to clinical DNA diagnosis. Molecular genetics and metabolism 2012 Nov 107 (3): 580-5. Niida Yo, Kuroda Mondo, Mitani Yusuke, Okumura Akiko, Yokoi Aya |
| Single nucleotide polymorphism WRN Leu1074Phe is associated with prostate cancer susceptibility in Chinese subjects. Acta medica Okayama 2011 Oct 65 (5): 315-23. Wang Lei, Kaku Haruki, Huang Peng, Xu Kexin, Yang Kai, Zhang Jiheng, Li Ming, Xie Liping, Wang Xiaofeng, Sakai Akiko, Watanabe Masami, Nasu Yasutomo, Shimizu Kenji, Kumon Hiromi, Na Yanq |
| Lack of association of the WRN C1367T polymorphism with senile cataract in the Israeli population. Molecular vision 2010 16 1771-5. Ehrenberg M, Dratviman-Storobinsky O, Avraham-Lubin B R, Goldenberg-Cohen |
| The Werner's syndrome 4330T>C (Cys1367Arg) gene variant does not affect the in vitro cytotoxicity of topoisomerase inhibitors and platinum compounds. Cancer chemotherapy and pharmacology 2009 Apr 63 (5): 881-7. Innocenti Federico, Mirkov Snezana, Nagasubramanian Ramamoorthy, Ramírez Jacqueline, Liu Wanqing, Bleibel Wasim K, Shukla Sunita J, Hennessy Kathleen, Rosner Gary L, Cook Edwin, Eileen Dolan M, Ratain Mark |
| WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brazil. Journal of neuro-oncology 2008 Dec 90 (3): 253-8. Pinto Giovanny R, Yoshioka France K N, Clara Carlos A, Santos Marcelo J, Almeida José R W, Burbano Rommel R, Rey Juan A, Casartelli Cacil |
| WRN polymorphisms affect expression levels of plasminogen activator inhibitor type 1 in cultured fibroblasts. BMC cardiovascular disorders 2008 8 (1): 5. Castro Elena, Oviedo-Rodríguez Vladimir, Angel-Chávez Luis |
| Genetic variation in the premature aging gene WRN: a case-control study on breast cancer susceptibility. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007 Feb 16 (2): 263-9. Ding Shian-ling, Yu Jyh-Cherng, Chen Shou-Tung, Hsu Giu-Cheng, Shen Chen-Ya |
| Impact of genetic variations in the WRN gene on age related pathologies and mortality. Mechanisms of ageing and development 2006 Mar 127 (3): 307-13. Kuningas Maris, Slagboom P Eline, Westendorp Rudi G J, van Heemst Dia |
| Polymorphisms of the TP53 codon 72 and WRN codon 1367 in individuals from Northern Brazil with gastric adenocarcinoma. Clinical and experimental medicine 2005 Dec 5 (4): 161-8. Khayat A S, Lobo Gatti L, Moura Lima E, de Assumpção P P, Nascimento Motta F J, Harada M L, Casartelli C, Marques Payão S L, Cardoso Smith M A, Burbano R |
| WRN gene 1367 Arg allele protects against development of type 2 diabetes mellitus. Diabetes research and clinical practice 2005 Sep 69 (3): 287-92. Hirai Masashi, Suzuki Susumu, Hinokio Yoshinori, Yamada Takahiro, Yoshizumi Shinsuke, Suzuki Chitose, Satoh Jo, Oka Yoshito |
| The mitochondrial DNA A3243G mutation in Werner's syndrome. Experimental gerontology 2003 Mar 38 (3): 339-42. Takeuchi Fujio, Harihara Shinji, Nakamura Kenichi, Takubo Kaiyo, Kanamori Masao, Goto Mako |
| A polymorphic variant at the Werner helicase (WRN) gene is associated with bone density, but not spondylosis, in postmenopausal women. Journal of bone and mineral metabolism 2001 19 (5): 296-301. Ogata N, Shiraki M, Hosoi T, Koshizuka Y, Nakamura K, Kawaguchi |
| Polymorphisms at the Werner locus: II. 1074Leu/Phe, 1367Cys/Arg, longevity, and atherosclerosis. American journal of medical genetics 2000 Dec 95 (4): 374-80. Castro E, Edland S D, Lee L, Ogburn C E, Deeb S S, Brown G, Panduro A, Riestra R, Tilvis R, Louhija J, Penttinen R, Erkkola R, Wang L, Martin G M, Oshima |
| [The role of Werner's syndrome gene in the genetic susceptibility to the type 2 diabetes in Chinese population]. Zhonghua yi xue za zhi 2000 May 80 (5): 360-1. Luo Y, Ji L, Han |
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- Page last updated:Jun 22, 2022
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