Zhang H - Search Results

1

Obesity-induced excess of 17-hydroxyprogesterone promotes hyperglycemia through activation of glucocorticoid receptor.

Lu Y, Wang E, Chen Y, Zhou B, Zhao J, Xiang L, Qian Y, Jiang J, Zhao L, Xiong X, Lu Z, Wu D, Liu B, Yan J, Zhang R, Zhang H, Hu C, Li X. Lu Y, et al. Among authors: zhang r, zhang h. J Clin Invest. 2020 Jul 1;130(7):3791-3804. doi: 10.1172/JCI134485. J Clin Invest. 2020. PMID: 32510471 Free PMC article.

2

Variations in the promoter of CYP21A2 gene identified in a Chinese patient with simple virilizing form of 21-hydroxylase deficiency.

Zhang HJ, Yang J, Zhang MN, Zhang W, Liu JM, Wang WQ, Ning G, Li XY. Zhang HJ, et al. Clin Endocrinol (Oxf). 2009 Feb;70(2):201-7. doi: 10.1111/j.1365-2265.2008.03356.x. Epub 2008 Aug 13. Clin Endocrinol (Oxf). 2009. PMID: 18702679

3

G protein-coupled receptor 48 upregulates estrogen receptor alpha expression via cAMP/PKA signaling in the male reproductive tract.

Li XY, Lu Y, Sun HY, Wang JQ, Yang J, Zhang HJ, Fan NG, Xu J, Jiang JJ, Liu RY, Li DL, Liu MY, Ning G. Li XY, et al. Development. 2010 Jan;137(1):151-7. doi: 10.1242/dev.040659. Development. 2010. PMID: 20023170

4

A novel missense mutation, GGC(Arg454) --> TGC(Cys), of CYP11B1 gene identified in a Chinese family with steroid 11beta-hydroxylase deficiency.

Ye ZQ, Zhang MN, Zhang HJ, Jiang JJ, Li XY, Zhang KQ. Ye ZQ, et al. Chin Med J (Engl). 2010 May 20;123(10):1264-8. Chin Med J (Engl). 2010. PMID: 20529578

5

Seven novel DAX1 mutations with loss of function identified in Chinese patients with congenital adrenal hypoplasia.

Li N, Liu R, Zhang H, Yang J, Sun S, Zhang M, Liu Y, Lu Y, Wang W, Mu Y, Ning G, Li X. Li N, et al. Among authors: zhang m, zhang h. J Clin Endocrinol Metab. 2010 Sep;95(9):E104-11. doi: 10.1210/jc.2009-2408. Epub 2010 Jun 23. J Clin Endocrinol Metab. 2010. PMID: 20573681

6

Metabolic disorders in newly diagnosed young adult female patients with simple virilizing 21-hydroxylase deficiency.

Zhang HJ, Yang J, Zhang MN, Liu CQ, Xu M, Li XJ, Yang SY, Li XY. Zhang HJ, et al. Endocrine. 2010 Oct;38(2):260-5. doi: 10.1007/s12020-010-9382-9. Epub 2010 Oct 27. Endocrine. 2010. PMID: 20978868

7

A novel SRD5A2 mutation with loss of function identified in Chinese patients with hypospadias.

Zhang M, Yang J, Zhang H, Ning G, Li X, Sun S. Zhang M, et al. Among authors: zhang h. Horm Res Paediatr. 2011;76(1):44-9. doi: 10.1159/000324692. Epub 2011 May 3. Horm Res Paediatr. 2011. PMID: 21540559

8

GPR48 increases mineralocorticoid receptor gene expression.

Wang J, Li X, Ke Y, Lu Y, Wang F, Fan N, Sun H, Zhang H, Liu R, Yang J, Ye L, Liu M, Ning G. Wang J, et al. Among authors: zhang h. J Am Soc Nephrol. 2012 Feb;23(2):281-93. doi: 10.1681/ASN.2011040351. Epub 2011 Dec 1. J Am Soc Nephrol. 2012. PMID: 22135314 Free PMC article.

9

Activation of nuclear factor-κB pathway is responsible for tumor necrosis factor-α-induced up-regulation of endothelin B2 receptor expression in vascular smooth muscle cells in vitro.

Zhang W, Li XJ, Zeng X, Shen DY, Liu CQ, Zhang HJ, Xu CB, Li XY. Zhang W, et al. Toxicol Lett. 2012 Mar 7;209(2):107-12. doi: 10.1016/j.toxlet.2011.12.005. Epub 2011 Dec 20. Toxicol Lett. 2012. PMID: 22207076

10

[Clinical and genetic analysis of 11β-hydroxylase deficiency].

Sun SY, Zhang MN, Yang J, Zhang HJ, Liu JM, Hong J, Ning G, Li XY. Sun SY, et al. Zhonghua Yi Xue Za Zhi. 2011 Nov 15;91(42):2999-3002. Zhonghua Yi Xue Za Zhi. 2011. PMID: 22333028 Chinese.

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