Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Osteopetrosis and CLCN7[original query] |
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| Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2003 Oct 18 (10): 1740-7. Frattini Annalisa, Pangrazio Alessandra, Susani Lucia, Sobacchi Cristina, Mirolo Massimiliano, Abinun Mario, Andolina Marino, Flanagan Adrienne, Horwitz Edwin M, Mihci Ercan, Notarangelo Luigi D, Ramenghi Ugo, Teti Anna, Van Hove Johan, Vujic Dragana, Young Terri, Albertini Alberto, Orchard Paul J, Vezzoni Paolo, Villa An |
| Polymorphisms in the CLCN7 gene modulate bone density in postmenopausal women and in patients with autosomal dominant osteopetrosis type II. The Journal of clinical endocrinology and metabolism 2006 Mar 91 (3): 995-1000. Kornak U, Ostertag A, Branger S, Benichou O, de Vernejoul M |
| Polymorphisms of the CLCN7 gene are associated with BMD in women. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2005 Nov 20 (11): 1960-7. Pettersson Ulrika, Albagha Omar M E, Mirolo Max, Taranta Anna, Frattini Annalisa, McGuigan Fiona E A, Vezzoni Paolo, Teti Anna, van Hul Wim, Reid David M, Villa Anna, Ralston Stuart |
| CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men. Bone 2008 Dec 43 (6): 995-8. Chu Kang, Koller Daniel L, Ichikawa Shoji, Snyder Richard, Curry Leah, Lai Dongbing, Austin Anthony, Xuei Xiaoling, Edenberg Howard J, Hui Siu L, Foroud Tatiana M, Peacock Munro, Econs Michael |
| Novel mutations of CLCN7 cause autosomal dominant osteopetrosis type II (ADO-II) and intermediate autosomal recessive osteopetrosis (IARO) in Chinese patients. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2015 Sep . Pang Q, Chi Y, Zhao Z, Xing X, Li M, Wang O, Jiang Y, Liao R, Sun Y, Dong J, Xia |
| Extending the Spectrum of Radiological Findings in Patients With Severe Osteopetrosis and Different Genetic Backgrounds. Pediatric blood & cancer 2016 Mar . Simanovsky Natalia, Rozovsky Katya, Hiller Nurith, Weintraub Michael, Stepensky Poli |
| Novel mutations of TCIRG1 cause a malignant and mild phenotype of autosomal recessive osteopetrosis (ARO) in four Chinese families. Acta pharmacologica Sinica 2017 8 38 (11): 1456-1465. Zhang Xiao-Ya, He Jin-Wei, Fu Wen-Zhen, Wang Chun, Zhang Zhen-L |
| [Analysis of clinical presentation and genetic characteristics of malignant infantile osteopetrosis]. Zhonghua er ke za zhi = Chinese journal of pediatrics 2023 10 61 (11): 1038-1042. A Wei, G H Zhu, M Q Qin, C G Jia, B Wang, J Yang, Y H Luo, Y F Jing, Y Yan, X Zhou, T Y Wa |
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