Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Osteoporosis and AXIN1[original query] |
---|
Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures.
Nature communications 2016 Jan 7 10129. Styrkarsdottir Unnur, Thorleifsson Gudmar, Gudjonsson Sigurjon A, Sigurdsson Asgeir, Center Jacqueline R, Lee Seung Hun, Nguyen Tuan V, Kwok Timothy C Y, Lee Jenny S W, Ho Suzanne C, Woo Jean, Leung Ping-C, Kim Beom-Jun, Rafnar Thorunn, Kiemeney Lambertus A, Ingvarsson Thorvaldur, Koh Jung-Min, Tang Nelson L S, Eisman John A, Christiansen Claus, Sigurdsson Gunnar, Thorsteinsdottir Unnur, Stefansson Ka |
The genetic polymorphisms of key genes in WNT pathway (LRP5 and AXIN1) was associated with osteoporosis susceptibility in Chinese Han population. Endocrine 2021 Sep . Cui Yongsheng, Hu Xinglv, Zhang Chen, Wang Kunzhe |
GATA4 and estrogen receptor alpha bind at SNPs rs9921222 and rs10794639 to regulate AXIN1 expression in osteoblasts. Human genetics 2022 6 141 (12): 1849-1861. Suthon Sarocha, Perkins Rachel S, Lin Jianjian, Crockarell John R, Miranda-Carboni Gustavo A, Krum Susan |
Association between AXIN1 gene polymorphism (rs9921222) of WNT signaling pathway and susceptibility to osteoporosis in Egyptian patients: a case-control study. BMC musculoskeletal disorders 2023 6 24 (1): 527. Eman Saad Nassar, Rehab Elnemr, Ahmed Shaaban, Asmaa Abd Elhameed, Raghda Saad Zaghloul Tal |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: