Zhou S - Search Results

1

Risk factors and methylenetetrahydrofolate reductase gene in congenital heart disease.

Wang L, Yang B, Zhou S, Gao H, Wang F, Zhou J, Wang H, Wang Y. Wang L, et al. Among authors: zhou j, zhou s. J Thorac Dis. 2018 Jan;10(1):441-447. doi: 10.21037/jtd.2017.12.08. J Thorac Dis. 2018. PMID: 29600076 Free PMC article.

2

Association of DNMT1 Gene Polymorphisms with Congenital Heart Disease in Child Patients.

Wang F, Zhou S, Wang Y, Wang L, Zhou J, Wang H, Li C, Chang M. Wang F, et al. Among authors: zhou j, zhou s. Pediatr Cardiol. 2015 Jun;36(5):906-11. doi: 10.1007/s00246-015-1093-9. Epub 2015 Jan 18. Pediatr Cardiol. 2015. PMID: 25596970

3

BRCA1 germline mutations dominate familial breast cancer patients in Henan China.

Wang L, Zhou S, Xie J, Gao H, Wang F, Zhou J, Wang Y, Wang H. Wang L, et al. Among authors: zhou j, zhou s. J Thorac Dis. 2017 Dec;9(12):5295-5299. doi: 10.21037/jtd.2017.11.71. J Thorac Dis. 2017. PMID: 29312738 Free PMC article.

4

Association Between Single Nucleotide Polymorphisms in NFATC1 Signaling Pathway Genes and Susceptibility to Congenital Heart Disease in the Chinese Population.

Wang F, Wang H, Wang L, Zhou S, Chang M, Zhou J, Dou Y, Wang Y, Shi X. Wang F, et al. Among authors: zhou j, zhou s. Pediatr Cardiol. 2016 Dec;37(8):1548-1561. doi: 10.1007/s00246-016-1469-5. Epub 2016 Aug 27. Pediatr Cardiol. 2016. PMID: 27567908

5

A novel FBN2 mutation cosegregates with congenital contractural arachnodactyly in a five-generation Chinese family.

Zhou S, Wang F, Dou Y, Zhou J, Hao G, Xu C, Wang QK, Wang H, Wang P. Zhou S, et al. Among authors: zhou j. Clin Case Rep. 2018 Jul 3;6(8):1612-1617. doi: 10.1002/ccr3.1693. eCollection 2018 Aug. Clin Case Rep. 2018. PMID: 30147916 Free PMC article.

6

Research on the influence of bilateral oophorectomy on the BMD, body components and sex hormone of women during the perimenopause.

Wang H, Wang C, Sun L, Zhou S, Wang F. Wang H, et al. Among authors: zhou s. Pak J Pharm Sci. 2017 Jul;30(4(Suppl.)):1497-1500. Pak J Pharm Sci. 2017. PMID: 29044004

7

Loss of heterozygosity detected at three short tandem repeat locus commonly used for human DNA identification in a case of paternity testing.

Zhou S, Wang H, Wang QK, Wang P, Wang F, Xu C. Zhou S, et al. Leg Med (Tokyo). 2017 Jan;24:7-11. doi: 10.1016/j.legalmed.2016.11.001. Epub 2016 Nov 5. Leg Med (Tokyo). 2017. PMID: 28081793

8

[Identification of a missense mutation in SEDL gene from a Chinese family with X-linked spondyloepiphyseal dysplasia tarda].

Zhou WJ, Zhou SY, Huang SW, Zhou JP, Xu XM. Zhou WJ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Feb;25(1):15-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18247296 Chinese.

9

Characterization of a novel disease-causing mutation in exon 1 of SH2D1A gene through amplicon sequencing: a case report on HLH.

Zhou S, Ma H, Gao B, Fang G, Zeng Y, Zhang Q, Qi G. Zhou S, et al. BMC Med Genet. 2017 Feb 14;18(1):15. doi: 10.1186/s12881-017-0376-9. BMC Med Genet. 2017. PMID: 28196537 Free PMC article.

10

Regulation of SCN3B/scn3b by Interleukin 2 (IL-2): IL-2 modulates SCN3B/scn3b transcript expression and increases sodium current in myocardial cells.

Zhao Y, Sun Q, Zeng Z, Li Q, Zhou S, Zhou M, Xue Y, Cheng X, Xia Y, Wang Q, Tu X. Zhao Y, et al. Among authors: zhou s, zhou m. BMC Cardiovasc Disord. 2016 Jan 4;16:1. doi: 10.1186/s12872-015-0179-x. BMC Cardiovasc Disord. 2016. PMID: 26728597 Free PMC article.

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