Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Osteoporosis and WNT5B[original query] |
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A specific haplotype in potential miRNAs binding sites of secreted frizzled-related protein 1 (SFRP1) is associated with BMD variation in osteoporosis. Gene 2018 Jul . Amjadi-Moheb Fatemeh, Hosseini Seyed Reza, Kosari-Monfared Mohadeseh, Ghadami Elham, Nooreddini Hajighorban, Akhavan-Niaki Hal |
Estrogen receptor alpha and NFATc1 bind to a bone mineral density-associated SNP to repress WNT5B in osteoblasts. American journal of human genetics 2021 12 109 (1): 97-115. Suthon Sarocha, Lin Jianjian, Perkins Rachel S, Crockarell John R, Miranda-Carboni Gustavo A, Krum Susan |
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- Page last updated:Apr 16, 2024
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