Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Werner Syndrome and WRN[original query] |
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| 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 |
| Werner helicase polymorphism is not associated with Alzheimer's disease. Journal of Alzheimer's disease : JAD 2005 1 6 (6): 591-4; discussion 673-81. Payão Spencer Luiz Marques, de Labio Roger Willian, Gatti Luciano Lobo, Rigolin Valdeci O S, Bertolucci Paulo H F, Smith Marília de A |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Werner Syndrome Protein Expression in Breast Cancer. Clinical breast cancer 2020 9 21 (1): 57-73.e7. Savva Constantinos, Sadiq Maaz, Sheikh Omar, Karim Syed, Trivedi Sachin, Green Andrew R, Rakha Emad A, Madhusudan Srinivasan, Arora Arvi |
| WRN-Mutated Colorectal Cancer Is Characterized by a Distinct Genetic Phenotype. Cancers 2020 5 12 (5): . Zimmer Kai, Puccini Alberto, Xiu Joanne, Baca Yasmine, Spizzo Gilbert, Lenz Heinz-Josef, Battaglin Francesca, Goldberg Richard M, Grothey Axel, Shields Anthony F, Salem Mohamed E, Marshall John L, Korn W Michael, Wolf Dominik, Kocher Florian, Seeber Andre |
| A high prevalence of myeloid malignancies in progeria with Werner syndrome is associated with p53 insufficiency. Experimental hematology 2022 3 109 11-17. Kato Hisaya, Maezawa Yoshiro, Nishijima Dai, Iwamoto Eisuke, Takeda June, Kanamori Takashi, Yamaga Masaya, Mishina Tatsuzo, Takeda Yusuke, Izumi Shintaro, Hino Yutaro, Nishi Hiroyuki, Ishiko Jun, Takeuchi Masahiro, Kaneko Hiyori, Koshizaka Masaya, Mimura Naoya, Kuzuya Masafumi, Sakaida Emiko, Takemoto Minoru, Shiraishi Yuichi, Miyano Satoru, Ogawa Seishi, Iwama Atsushi, Sanada Masashi, Yokote Kouta |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 29, 2023
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