Liu S - Search Results

1

A Novel CD40L Mutation Associated with X-Linked Hyper IgM Syndrome in a Chinese Family.

Li L, Ji J, Han M, Xu Y, Zhang X, Liu W, Liu S. Li L, et al. Among authors: liu s, liu w. Immunol Invest. 2020 Apr;49(3):307-316. doi: 10.1080/08820139.2019.1638397. Epub 2019 Aug 12. Immunol Invest. 2020. PMID: 31401902

2

Role of IL-17 Variants in Preeclampsia in Chinese Han Women.

Wang H, Guo M, Liu F, Wang J, Zhou Z, Ji J, Ye Y, Song W, Liu S, Sun B. Wang H, et al. Among authors: liu s, liu f. PLoS One. 2015 Oct 9;10(10):e0140118. doi: 10.1371/journal.pone.0140118. eCollection 2015. PLoS One. 2015. PMID: 26451724 Free PMC article.

3

A De novo PAX8 mutation in a Chinese child with congenital thyroid dysgenesis.

Zou H, Chai J, Liu S, Zang H, Yu X, Tian L, Li H, Han B. Zou H, et al. Among authors: liu s. Int J Clin Exp Pathol. 2015 Sep 1;8(9):11434-9. eCollection 2015. Int J Clin Exp Pathol. 2015. PMID: 26617871 Free PMC article.

4

A missense mutation in the androgen receptor gene causing androgen insensitivity syndrome in a Chinese family.

Li L, Liu WM, Liu MX, Zheng SQ, Zhang JX, Che FY, Liu SG. Li L, et al. Asian J Androl. 2017 Mar-Apr;19(2):260-261. doi: 10.4103/1008-682X.172647. Asian J Androl. 2017. PMID: 26806084 Free PMC article. No abstract available.

5

A Novel COL4A4 Mutation Identified in a Chinese Family with Thin Basement Membrane Nephropathy.

Xu Y, Guo M, Dong H, Jiang W, Ma R, Liu S, Li S. Xu Y, et al. Among authors: liu s. Sci Rep. 2016 Feb 2;6:20244. doi: 10.1038/srep20244. Sci Rep. 2016. PMID: 26833262 Free PMC article.

6

Investigation of a Possible Role for the Histidine Decarboxylase Gene in Tourette Syndrome in the Chinese Han Population: A Family-Based Study.

Dong H, Liu W, Liu M, Xu L, Li Q, Zhang R, Zhang X, Liu S. Dong H, et al. Among authors: liu m, liu s, liu w. PLoS One. 2016 Aug 16;11(8):e0160265. doi: 10.1371/journal.pone.0160265. eCollection 2016. PLoS One. 2016. PMID: 27529419 Free PMC article.

7

The rs9932581 and rs1049255 Polymorphisms in CYBA is not Associated with Preeclampsia in Chinese Han Women.

Liu S, Li X, Wang J, Ji J, Liu J, Lin Y, Jia X, Song W, Wu C, Li L. Liu S, et al. Among authors: liu j. Cell Physiol Biochem. 2016;39(4):1471-8. doi: 10.1159/000447850. Epub 2016 Sep 9. Cell Physiol Biochem. 2016. PMID: 27607450 Free article.

8

Association between COMT Val158Met polymorphism and preeclampsia in the Chinese Han population.

Zhao X, Liu J, Zhao C, Ye P, Ji J, Wang J, Song W, Xu J, Liu S. Zhao X, et al. Among authors: liu j, liu s. Hypertens Pregnancy. 2016 Nov;35(4):565-572. doi: 10.1080/10641955.2016.1211677. Epub 2016 Sep 19. Hypertens Pregnancy. 2016. PMID: 27646972 Free article.

9

Choline acetyltransferase may contribute to the risk of Tourette syndrome: Combination of family-based analysis and case-control study.

Yang X, Liu W, Yi M, Zhang R, Xu Y, Huang Z, Liu S, Li T. Yang X, et al. Among authors: liu s, liu w. World J Biol Psychiatry. 2018 Oct;19(7):521-526. doi: 10.1080/15622975.2017.1282176. Epub 2017 Feb 14. World J Biol Psychiatry. 2018. PMID: 28090804

10

Next-generation sequencing of NKX2.1, FOXE1, PAX8, NKX2.5, and TSHR in 100 Chinese patients with congenital hypothyroidism and athyreosis.

Wang F, Liu C, Jia X, Liu X, Xu Y, Yan S, Jia X, Huang Z, Liu S, Gu M. Wang F, et al. Among authors: liu x, liu c, liu s. Clin Chim Acta. 2017 Jul;470:36-41. doi: 10.1016/j.cca.2017.04.020. Epub 2017 Apr 25. Clin Chim Acta. 2017. PMID: 28455095

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