Zhao S - Search Results

1

Effects of Osteoglycin (OGN) on treating senile osteoporosis by regulating MSCs.

Chen X, Chen J, Xu D, Zhao S, Song H, Peng Y. Chen X, et al. Among authors: zhao s. BMC Musculoskelet Disord. 2017 Oct 26;18(1):423. doi: 10.1186/s12891-017-1779-7. BMC Musculoskelet Disord. 2017. PMID: 29073887 Free PMC article.

2

Stevioside ameliorates high-fat diet-induced insulin resistance and adipose tissue inflammation by downregulating the NF-κB pathway.

Wang Z, Xue L, Guo C, Han B, Pan C, Zhao S, Song H, Ma Q. Wang Z, et al. Among authors: zhao s. Biochem Biophys Res Commun. 2012 Jan 27;417(4):1280-5. doi: 10.1016/j.bbrc.2011.12.130. Epub 2012 Jan 3. Biochem Biophys Res Commun. 2012. PMID: 22240021

3

Polymorphism in the Alternative Donor Site of the Cryptic Exon of LHCGR: Functional Consequences and Associations with Testosterone Level.

Liu W, Han B, Zhu W, Cheng T, Fan M, Wu J, Yang Y, Zhu H, Si J, Lyu Q, Chai W, Zhao S, Song H, Kuang Y, Qiao J. Liu W, et al. Among authors: zhao s. Sci Rep. 2017 Apr 3;7:45699. doi: 10.1038/srep45699. Sci Rep. 2017. PMID: 28367994 Free PMC article.

4

Oxidative stress increases the 17,20-lyase-catalyzing activity of adrenal P450c17 through p38α in the development of hyperandrogenism.

Zhu W, Han B, Fan M, Wang N, Wang H, Zhu H, Cheng T, Zhao S, Song H, Qiao J. Zhu W, et al. Among authors: zhao s. Mol Cell Endocrinol. 2019 Mar 15;484:25-33. doi: 10.1016/j.mce.2019.01.020. Epub 2019 Jan 23. Mol Cell Endocrinol. 2019. PMID: 30682387

5

A refined study of FCRL genes from a genome-wide association study for Graves' disease.

Zhao SX, Liu W, Zhan M, Song ZY, Yang SY, Xue LQ, Pan CM, Gu ZH, Liu BL, Wang HN, Liang L, Liang J, Zhang XM, Yuan GY, Li CG, Chen MD, Chen JL, Gao GQ, Song HD; China Consortium for the Genetics of Autoimmune Thyroid Disease. Zhao SX, et al. PLoS One. 2013;8(3):e57758. doi: 10.1371/journal.pone.0057758. Epub 2013 Mar 7. PLoS One. 2013. PMID: 23505439 Free PMC article.

6

Phenotypic and molecular characteristics in eleven Chinese patients with 5α-reductase Type 2 deficiency.

Zhu H, Liu W, Han B, Fan M, Zhao S, Wang H, Lu Y, Pan C, Chen F, Chen M, Song H, Cheng K, Qiao J. Zhu H, et al. Among authors: zhao s. Clin Endocrinol (Oxf). 2014 Nov;81(5):711-20. doi: 10.1111/cen.12456. Epub 2014 Apr 21. Clin Endocrinol (Oxf). 2014. PMID: 24665940

7

Somatic mosaicism of androgen receptor gene in an androgen insensitivity syndrome patient conceived through assisted reproduction technique.

Wang H, Zhu H, Wang N, Cheng T, Han B, Zhao S, Song H, Cheng K, Liu Y, Qiao J. Wang H, et al. Among authors: zhao s. Mol Genet Genomic Med. 2019 Oct;7(10):e00906. doi: 10.1002/mgg3.906. Epub 2019 Aug 20. Mol Genet Genomic Med. 2019. PMID: 31429517 Free PMC article.

8

Phenotypic and biochemical characteristics and molecular basis in 36 Chinese patients with androgen receptor variants.

Zhu H, Yao H, Xu Y, Chen Y, Han B, Wang N, Wang H, Zhang Q, Zhu W, Shi Y, Sun H, Zhao S, Song H, Liu Y, Qiao J. Zhu H, et al. Among authors: zhao s. Orphanet J Rare Dis. 2021 Mar 9;16(1):122. doi: 10.1186/s13023-021-01765-w. Orphanet J Rare Dis. 2021. PMID: 33750429 Free PMC article.

9

Phenotypic Heterogeneity and Fertility Potential of Patients With 17-Hydroxylase/17,20-lyase Deficiency.

Xu Y, Jiang S, Yan Z, Niu Y, Du W, Liu B, Han B, Liu X, Zhao S, Song H, Kuang Y, Qiao J. Xu Y, et al. Among authors: zhao s. J Clin Endocrinol Metab. 2022 May 17;107(6):e2610-e2618. doi: 10.1210/clinem/dgac029. J Clin Endocrinol Metab. 2022. PMID: 35043964

10

Clinical and molecular manifestation of fifteen 17OHD patients: a novel mutation and a founder effect.

Han B, Xue L, Fan M, Zhao S, Liu W, Zhu H, Cheng T, Lu Y, Cheng K, Song H, Liu Y, Qiao J. Han B, et al. Among authors: zhao s. Endocrine. 2016 Sep;53(3):784-90. doi: 10.1007/s12020-016-0957-y. Epub 2016 May 5. Endocrine. 2016. PMID: 27150612

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