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Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease.
Song HD, Liang J, Shi JY, Zhao SX, Liu Z, Zhao JJ, Peng YD, Gao GQ, Tao J, Pan CM, Shao L, Cheng F, Wang Y, Yuan GY, Xu C, Han B, Huang W, Chu X, Chen Y, Sheng Y, Li RY, Su Q, Gao L, Jia WP, Jin L, Chen MD, Chen SJ, Chen Z, Chen JL. Song HD, et al. Among authors: cheng f. Hum Mol Genet. 2009 Mar 15;18(6):1156-70. doi: 10.1093/hmg/ddn442. Epub 2009 Jan 6. Hum Mol Genet. 2009. PMID: 19126779
Upregulation of GBP1 in thyroid primordium is required for developmental thyroid morphogenesis.
Yang RM, Zhan M, Zhou QY, Ye XP, Wu FY, Dong M, Sun F, Fang Y, Zhang RJ, Zhang CR, Yang L, Guo MM, Zhang JX, Liang J, Cheng F, Liu W, Han B, Zhou Y, Zhao SX, Song HD. Yang RM, et al. Among authors: cheng f. Genet Med. 2021 Oct;23(10):1944-1951. doi: 10.1038/s41436-021-01237-3. Epub 2021 Jun 30. Genet Med. 2021. PMID: 34194003 Free PMC article.
Pathogenic variations in MAML2 and MAMLD1 contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway.
Wu FY, Yang RM, Zhang HY, Zhan M, Tu PH, Fang Y, Zhang CX, Song SY, Dong M, Cui RJ, Liu XY, Yang L, Yan CY, Sun F, Zhang RJ, Wang Z, Liang J, Song HD, Cheng F, Zhao SX. Wu FY, et al. Among authors: cheng f. J Med Genet. 2023 Sep;60(9):874-884. doi: 10.1136/jmg-2022-108866. Epub 2023 Mar 10. J Med Genet. 2023. PMID: 36898841
4,675 results