Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Osteoporosis and WNT1[original query] |
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Variation in the Kozak sequence of WNT16 results in an increased translation and is associated with osteoporosis related parameters. Bone 2014 Feb 59 57-65. Hendrickx Gretl, Boudin Eveline, Fija?kowski Igor, Nielsen Torben Leo, Andersen Marianne, Brixen Kim, Van Hul W |
Defective WNT signaling associates with bone marrow fibrosis-a cross-sectional cohort study in a family with WNT1 osteoporosis. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2017 11 29 (2): 479-487. Mäkitie R E, Niinimäki R, Kakko S, Honkanen T, Kovanen P E, Mäkitie |
Evaluation of WISP1 as a candidate gene for bone mineral density in the Old Order Amish. Scientific reports 2018 May 8 (1): 7141. Wang Xing, Salimi Shabnam, Deng Zhongliang, Perry James, Ryan Kathleen A, Li Zhizhen, Liu Dongfang, Streeten Elizabeth, Shuldiner Alan R, Fu M |
Primary Osteoporosis in Young Adults: Genetic Basis and Identification of Novel Variants in Causal Genes. JBMR plus 2018 Jan 2 (1): 12-21. Collet Corinne, Ostertag Agnès, Ricquebourg Manon, Delecourt Marine, Tueur Giulia, Isidor Bertrand, Guillot Pascale, Schaefer Elise, Javier Rose-Marie, Funck-Brentano Thomas, Orcel Philippe, Laplanche Jean-Louis, Cohen-Solal Marti |
Lipocalin-2 is associated with FGF23 in WNT1 and PLS3 osteoporosis. Frontiers in endocrinology 2022 9 13 954730. Loid Petra, Hauta-Alus Helena, Mäkitie Outi, Magnusson Per, Mäkitie Riikka |
Case report: Early-onset osteoporosis in a patient carrying a novel heterozygous variant of the WNT1 gene. Frontiers in endocrinology 2022 8 13 918682. Campopiano Maria Cristina, Fogli Antonella, Michelucci Angela, Mazoni Laura, Longo Antonella, Borsari Simona, Pardi Elena, Benelli Elena, Sardella Chiara, Pierotti Laura, Dinoi Elisa, Marcocci Claudio, Cetani Filome |
Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders. The Journal of clinical endocrinology and metabolism 2022 3 107 (7): e3048-e3057. Oheim Ralf, Tsourdi Elena, Seefried Lothar, Beller Gisela, Schubach Max, Vettorazzi Eik, Stürznickel Julian, Rolvien Tim, Ehmke Nadja, Delsmann Alena, Genest Franca, Krüger Ulrike, Zemojtel Tomasz, Barvencik Florian, Schinke Thorsten, Jakob Franz, Hofbauer Lorenz C, Mundlos Stefan, Kornak U |
Osteoporosis related to WNT1 variants: a not infrequent cause of osteoporosis. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2022 11 34 (2): 405-411. Peris Pilar, Monegal Ana, Mäkitie Riikka E, Guañabens Nuria, González-Roca E |
Genotypic and phenotypic spectrum and pathogenesis of WNT1 variants in a large cohort of patients with OI/osteoporosis. The Journal of clinical endocrinology and metabolism 2023 1 . Hu Jing, Lin Xiaoyun, Gao Peng, Zhang Qian, Zhou Bingna, Wang Ou, Jiang Yan, Xia Weibo, Xing Xiaoping, Li M |
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- Page last updated:Apr 16, 2024
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