Hou J - Search Results

1

Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population.

An Y, Duan W, Huang G, Chen X, Li L, Nie C, Hou J, Gui Y, Wu Y, Zhang F, Shen Y, Wu B, Wang H. An Y, et al. Among authors: hou j. BMC Med Genomics. 2016 Jan 8;9:2. doi: 10.1186/s12920-015-0163-4. BMC Med Genomics. 2016. PMID: 26742958 Free PMC article.

2

Functional variant in methionine synthase reductase intron-1 significantly increases the risk of congenital heart disease in the Han Chinese population.

Zhao JY, Yang XY, Gong XH, Gu ZY, Duan WY, Wang J, Ye ZZ, Shen HB, Shi KH, Hou J, Huang GY, Jin L, Qiao B, Wang HY. Zhao JY, et al. Among authors: hou j. Circulation. 2012 Jan 24;125(3):482-90. doi: 10.1161/CIRCULATIONAHA.111.050245. Epub 2011 Dec 16. Circulation. 2012. PMID: 22179537

3

A functional variant in the cystathionine β-synthase gene promoter significantly reduces congenital heart disease susceptibility in a Han Chinese population.

Zhao JY, Yang XY, Shi KH, Sun SN, Hou J, Ye ZZ, Wang J, Duan WY, Qiao B, Chen YJ, Shen HB, Huang GY, Jin L, Wang HY. Zhao JY, et al. Among authors: hou j. Cell Res. 2013 Feb;23(2):242-253. doi: 10.1038/cr.2012.135. Epub 2012 Sep 18. Cell Res. 2013. PMID: 22986502 Free PMC article.

4

A genetic variant in vitamin B12 metabolic genes that reduces the risk of congenital heart disease in Han Chinese populations.

Wang J, Zhao JY, Wang F, Peng QQ, Hou J, Sun SN, Gui YH, Duan WY, Qiao B, Wang HY. Wang J, et al. Among authors: hou j. PLoS One. 2014 Feb 12;9(2):e88332. doi: 10.1371/journal.pone.0088332. eCollection 2014. PLoS One. 2014. PMID: 24533076 Free PMC article.

5

Melatonin alleviates vascular endothelial cell damage by regulating an autophagy-apoptosis axis in Kawasaki disease.

Zheng Y, Huang S, Zhang J, Hou J, Wu F, Wang W, Han X, Gui Y. Zheng Y, et al. Among authors: hou j. Cell Prolif. 2022 Jun;55(6):e13251. doi: 10.1111/cpr.13251. Epub 2022 May 17. Cell Prolif. 2022. PMID: 35582751 Free PMC article.

6

Promoter analysis of ventricular myosin heavy chain (vmhc) in zebrafish embryos.

Jin D, Ni TT, Hou J, Rellinger E, Zhong TP. Jin D, et al. Among authors: hou j. Dev Dyn. 2009 Jul;238(7):1760-7. doi: 10.1002/dvdy.22000. Dev Dyn. 2009. PMID: 19517572 Free PMC article.

7

Efficacy of tocilizumab therapy in a patient with severe pancytopenia associated with a STAT3 gain-of-function mutation.

Wang W, Liu L, Hui X, Wang Y, Ying W, Zhou Q, Hou J, Yang M, Sun B, Sun J, Wang X. Wang W, et al. Among authors: hou j. BMC Immunol. 2021 Mar 17;22(1):19. doi: 10.1186/s12865-021-00411-1. BMC Immunol. 2021. PMID: 33731004 Free PMC article.

8

Report of a Chinese Cohort with Activated Phosphoinositide 3-Kinase δ Syndrome.

Wang Y, Wang W, Liu L, Hou J, Ying W, Hui X, Zhou Q, Liu D, Yao H, Sun J, Wang X. Wang Y, et al. Among authors: hou j. J Clin Immunol. 2018 Nov;38(8):854-863. doi: 10.1007/s10875-018-0568-x. Epub 2018 Nov 29. J Clin Immunol. 2018. PMID: 30499059

9

Novel Heterogeneous Mutation of TNFAIP3 in a Chinese Patient with Behçet-Like Phenotype and Persistent EBV Viremia.

Dong X, Liu L, Wang Y, Yang X, Wang W, Lin L, Sun B, Hou J, Ying W, Hui X, Zhou Q, Liu D, Yao H, Sun J, Wang X. Dong X, et al. Among authors: hou j. J Clin Immunol. 2019 Feb;39(2):188-194. doi: 10.1007/s10875-019-00604-9. Epub 2019 Feb 27. J Clin Immunol. 2019. PMID: 30810840

10

Chromosomal abnormalities related to fever of unknown origin in a Chinese pediatric cohort and literature review.

Sun B, Yang M, Hou J, Wang W, Ying W, Hui X, Zhou Q, Yao H, Sun J, Wang X. Sun B, et al. Among authors: hou j. Orphanet J Rare Dis. 2022 Jul 27;17(1):292. doi: 10.1186/s13023-022-02444-0. Orphanet J Rare Dis. 2022. PMID: 35897075 Free PMC article. Review.

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