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Sex-specific phenotypic effects and evolutionary history of an ancient polymorphic deletion of the human growth hormone receptor.
Sci Adv. 2021 Sep 24;7(39):eabi4476. doi: 10.1126/sciadv.abi4476. Epub 2021 Sep 24.
Sci Adv. 2021.
PMID: 34559564
Free PMC article.
Edematous severe acute malnutrition is characterized by hypomethylation of DNA.
Schulze KV, Swaminathan S, Howell S, Jajoo A, Lie NC, Brown O, Sadat R, Hall N, Zhao L, Marshall K, May T, Reid ME, Taylor-Bryan C, Wang X, Belmont JW, Guan Y, Manary MJ, Trehan I, McKenzie CA, Hanchard NA.
Schulze KV, et al. Among authors: lie nc.
Nat Commun. 2019 Dec 19;10(1):5791. doi: 10.1038/s41467-019-13433-6.
Nat Commun. 2019.
PMID: 31857576
Free PMC article.
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Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension.
Copeland I, Wonkam-Tingang E, Gupta-Malhotra M, Hashmi SS, Han Y, Jajoo A, Hall NJ, Hernandez PP, Lie N, Liu D, Xu J, Rosenfeld J, Haldipur A, Desire Z, Coban-Akdemir ZH, Scott DA, Li Q, Chao HT, Zaske AM, Lupski JR, Milewicz DM, Shete S, Posey JE, Hanchard NA.
Copeland I, et al.
JCI Insight. 2024 May 8;9(9):e172152. doi: 10.1172/jci.insight.172152.
JCI Insight. 2024.
PMID: 38716726
Free article.
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Integrated omics approaches to characterize a nuclear receptor corepressor-associated histone deacetylase in mouse skeletal muscle.
Gong Y, Cao R, Ding G, Hong S, Zhou W, Lu W, Damle M, Fang B, Wang CC, Qian J, Lie N, Lanzillotta C, Rabinowitz JD, Sun Z.
Gong Y, et al.
Mol Cell Endocrinol. 2018 Aug 15;471:22-32. doi: 10.1016/j.mce.2017.05.024. Epub 2017 May 26.
Mol Cell Endocrinol. 2018.
PMID: 28554803
Free PMC article.
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