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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 4, 2024. (Total: 232145Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Syndrome and LRP5[original query]
Association between bone mineral density and LDL receptor-related protein 5 gene polymorphisms in young Korean men.
Journal of Korean medical science 2004 Jun 19 (3): 407-12.
Koh Jung Min, Jung Min Hui, Hong Jeong Soo, Park Hyung Joo, Chang Jae Suk, Shin Hyoung Doo, Kim Shin Yoon, Kim Ghi
Low density lipoprotein receptor-related protein 5 (LRP5) mutations and osteoporosis, impaired glucose metabolism and hypercholesterolaemia.
Clinical endocrinology 2010 Apr 72 (4): 481-8.
Saarinen Anne, Saukkonen Tero, Kivelä Tero, Lahtinen Ulla, Laine Christine, Somer Mirja, Toiviainen-Salo Sanna, Cole William G, Lehesjoki Anna-Elina, Mäkitie Ou
The joint effect of cigarette smoking and polymorphisms on LRP5, LEPR, near MC4R and SH2B1 genes on metabolic syndrome susceptibility in Taiwan.
Molecular biology reports 2013 Jan 40 (1): 525-33.
Yang Chuan-Wei, Li Chia-Ing, Liu Chiu-Shong, Bau Da-Tian, Lin Chih-Hsueh, Lin Wen-Yuan, Li Tsai-Chung, Lin Cheng-Chi
No mutations in the serotonin related TPH1 and HTR1B genes in patients with monogenic sclerosing bone disorders.
Bone 2013 Jul 55 (1): 52-6.
Boudin Eveline, Jennes Karen, de Freitas Fenna, Tegay David, Mortier Geert, Van Hul W
Novel Homozygous LRP5 Mutations in Mexican Patients with Osteoporosis-Pseudoglioma Syndrome.
Genetic testing and molecular biomarkers 2017 11 21 (12): 742-746.
Astiazarán Mirena C, Cervantes-Sodi María, Rebolledo-Enríquez Erick, Chacón-Camacho Oscar, Villegas Vanessa, Zenteno Juan Carl
Mutations in the fourth ?-propeller domain of LRP4 are associated with isolated syndactyly with fusion of the third and fourth fingers.
Human mutation 2018 3 39 (6): 811-815.
Sukenik Halevy Rivka, Chien Huan-Chieh, Heinz Bo, Bamshad Michael J, Nickerson Deborah A, , Kircher Martin, Ahituv Nad
Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia.
Journal of translational medicine 2024 1 22 (1): 75.
Yi Jiang, Xueshan Xiao, Wenmin Sun, Yingwei Wang, Shiqiang Li, Xiaoyun Jia, Panfeng Wang, J Fielding Hejtmancik, Qingjiong Zha
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