Ou Q - Search Results

1

[Studies on the association of single nucleotide polymorphisms of HLA-DP and DQ genes with the outcome of chronic hepatitis B virus infection].

Su M, Zeng Y, Chen J, Jiang L, Chen T, Liu C, Yang B, Ou Q. Su M, et al. Among authors: ou q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):765-9. doi: 10.3760/cma.j.issn.1003-9406.2014.06.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449085 Chinese.

2

[Study on a new point mutation of nt7444 G-->A in the mitochondrial DNA in a type 2 diabetes mellitus family].

Cheng ZJ, Yang B, Liu QC, Jiang L, Xie HH, Ou QS. Cheng ZJ, et al. Yi Chuan. 2007 Apr;29(4):433-7. doi: 10.1360/yc-007-0433. Yi Chuan. 2007. PMID: 17548305 Chinese.

3

Novel mutation and polymorphism of PRSS1 gene in the Chinese patients with hereditary pancreatitis and chronic pancreatitis.

Liu QC, Gao F, Ou QS, Zhuang ZH, Lin SR, Yang B, Cheng ZJ. Liu QC, et al. Chin Med J (Engl). 2008 Jan 20;121(2):108-11. Chin Med J (Engl). 2008. PMID: 18272034

4

[Mitochondrial DNA A1555G mutation of seven families with nonsyndromic hearing loss].

Ou QS, Cheng ZJ, Yang B, Jiang L, Chen J. Ou QS, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):550-4. doi: 10.3760/cma.j.issn.1003-9406.2009.05.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19806580 Chinese.

5

[Correlation between degree of mitochondrial DNA 1555 mutation and clinical phenotype of nonsyndromic hearing loss].

Cheng ZJ, Zhang R, Yang B, Liu QC, Jiang L, Chen J, Chen Y, Ou QS. Cheng ZJ, et al. Zhonghua Yi Xue Za Zhi. 2009 Sep 29;89(36):2536-9. Zhonghua Yi Xue Za Zhi. 2009. PMID: 20137613 Chinese.

6

The effect of the expression of virulence-associated DEAD-box RNA helicase mRNA on the imbalance of Th1-Th2 cytokines in the CSF of patients with Cryptococcus neoformans meningitis.

Jiang L, Lin N, Cheng Z, Yang B, Ou Q. Jiang L, et al. Among authors: ou q. Eur J Clin Microbiol Infect Dis. 2011 Dec;30(12):1483-7. doi: 10.1007/s10096-011-1245-7. Epub 2011 Apr 13. Eur J Clin Microbiol Infect Dis. 2011. PMID: 21487762

7

Construction of a capsule associated protein 10 gene eukaryotic expression vector for RNA interference and confirmation of biologic relevance.

Ou QS, Su XJ, Lin N, Jiang L, Yang B. Ou QS, et al. Chin Med J (Engl). 2011 Sep;124(17):2741-5. Chin Med J (Engl). 2011. PMID: 22040434

8

Novel mutations of PRSS1 gene in patients with pancreatic cancer among Han population.

Zeng K, Liu QC, Lin JH, Lin XH, Zhuang ZH, Gao F, Ou QS. Zeng K, et al. Chin Med J (Engl). 2011 Jul 5;124(13):2065-7. Chin Med J (Engl). 2011. PMID: 22088471

9

Analysis of the ratio of mitchondrial DNA with A1555G mutant to wild type in deaf patients of Fujian province in China by a new method and its relationship with the severity of hearing loss.

Ou QS, Cheng ZJ, Yang B, Jiang L, Chen J. Ou QS, et al. Chin Med J (Engl). 2011 Oct;124(20):3347-52. Chin Med J (Engl). 2011. PMID: 22088533

10

Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree.

Chen T, Liu Q, Jiang L, Liu C, Ou Q. Chen T, et al. Among authors: ou q. Genet Test Mol Biomarkers. 2013 Feb;17(2):122-30. doi: 10.1089/gtmb.2012.0251. Epub 2012 Dec 20. Genet Test Mol Biomarkers. 2013. PMID: 23256547 Free PMC article.

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