Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 114

1.

Cardiac myosin binding protein C and MAP-kinase activating death domain-containing gene polymorphisms and diastolic heart failure.

Wu CK, Huang YT, Lee JK, Chiang LT, Chiang FT, Huang SW, Lin JL, Tseng CD, Chen YH, Tsai CT.

PLoS One. 2012;7(4):e35242. doi: 10.1371/journal.pone.0035242. Epub 2012 Apr 17.

2.

Genetic polymorphisms of the angiotensin II type 1 receptor gene and diastolic heart failure.

Wu CK, Tsai CT, Chang YC, Luo JL, Wang YC, Hwang JJ, Lin JL, Tseng CD, Chiang FT.

J Hypertens. 2009 Mar;27(3):502-7.

PMID:
19330904
3.

Genetic polymorphisms of the HCR gene and a genomic segment in close proximity to HLA-C are associated with patients with psoriasis in Taiwan.

Chang YT, Shiao YM, Chin PJ, Liu YL, Chou FC, Wu S, Lin YF, Li LH, Lin MW, Liu HN, Tsai SF.

Br J Dermatol. 2004 Jun;150(6):1104-11.

PMID:
15214895
4.

Association analysis of ERBB2 amplicon genetic polymorphisms and STARD3 expression with risk of gastric cancer in the Chinese population.

Qiu Y, Zhang ZY, Du WD, Ye L, Xu S, Zuo XB, Zhou FS, Chen G, Ma XL, Schneider ME, Xia HZ, Zhou Y, Wu JF, Yuan-Hong X, Zhang XJ.

Gene. 2014 Feb 10;535(2):225-32. doi: 10.1016/j.gene.2013.11.030. Epub 2013 Nov 28.

PMID:
24291029
5.

The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population.

Fei Q, Wu Z, Wang H, Zhou X, Wang N, Ding Y, Wang Y, Qiu G.

Spine (Phila Pa 1976). 2010 Apr 20;35(9):983-8. doi: 10.1097/BRS.0b013e3181bc963c.

PMID:
20228709
6.

Association between single-nucleotide polymorphisms in the SEC8L1 gene, which encodes a subunit of the exocyst complex, and rheumatoid arthritis in a Japanese population.

Hamada D, Takata Y, Osabe D, Nomura K, Shinohara S, Egawa H, Nakano S, Shinomiya F, Scafe CR, Reeve VM, Miyamoto T, Moritani M, Kunika K, Inoue H, Yasui N, Itakura M.

Arthritis Rheum. 2005 May;52(5):1371-80.

7.

A propensity score-based case-control study of renin-angiotensin system gene polymorphisms and diastolic heart failure.

Wu CK, Luo JL, Wu XM, Tsai CT, Lin JW, Hwang JJ, Lin JL, Tseng CD, Chiang FT.

Atherosclerosis. 2009 Aug;205(2):497-502. doi: 10.1016/j.atherosclerosis.2008.12.033. Epub 2008 Dec 30.

PMID:
19185300
8.

[Variations within OLF1/EBF-associated zinc finger protein gene confer susceptibility to lupus nephritis in Chinese population].

Liang D, Huang XQ, Shen N, Mao HQ, Feng XB, Huang XF, Tang JP, Chen XX, Chen SL, Gu YY, Bao CD, Wang Y, Qian J.

Zhonghua Yi Xue Za Zhi. 2005 Apr 13;85(14):949-54. Chinese.

PMID:
16061000
9.

Association study of the genetic polymorphisms of the transcription factor 7-like 2 (TCF7L2) gene and type 2 diabetes in the Chinese population.

Chang YC, Chang TJ, Jiang YD, Kuo SS, Lee KC, Chiu KC, Chuang LM.

Diabetes. 2007 Oct;56(10):2631-7. Epub 2007 Jun 19.

10.

[An association study between transforming growth factor-β1 receptor 2 gene polymorphisms and essential hypertension].

Chen JF, Wang HR, Yang S, Zhao YP, Zhao XH, Chen YC, DU QL, Liu SJ, Shen C, Xu YC.

Zhonghua Yu Fang Yi Xue Za Zhi. 2012 Sep;46(9):825-30. Chinese.

PMID:
23157888
11.
13.

Single-nucleotide polymorphisms in the TSPYL-4 and NT5DC1 genes are associated with susceptibility to chronic obstructive pulmonary disease.

Guo Y, Gong Y, Shi G, Yang K, Pan C, Li M, Li Q, Cheng Q, Dai R, Fan L, Wan H.

Mol Med Rep. 2012 Sep;6(3):631-8. doi: 10.3892/mmr.2012.964. Epub 2012 Jun 25.

PMID:
22736055
14.

Renalase gene is a novel susceptibility gene for essential hypertension: a two-stage association study in northern Han Chinese population.

Zhao Q, Fan Z, He J, Chen S, Li H, Zhang P, Wang L, Hu D, Huang J, Qiang B, Gu D.

J Mol Med (Berl). 2007 Aug;85(8):877-85. Epub 2007 Jan 10.

PMID:
17216203
15.

Single nucleotide polymorphisms in human Paneth cell defensin A5 may confer susceptibility to inflammatory bowel disease in a New Zealand Caucasian population.

Ferguson LR, Browning BL, Huebner C, Petermann I, Shelling AN, Demmers P, McCulloch A, Gearry RB, Barclay ML, Philpott M.

Dig Liver Dis. 2008 Sep;40(9):723-30. doi: 10.1016/j.dld.2008.02.011. Epub 2008 Apr 3.

PMID:
18394979
16.

[Association of the tagging single nucleotide polymorphisms in transforming growth factor beta-1 gene with hypertension in the Han nationality population in Xinjiang].

Yang JF, Shi XP, Zhao D, Deng FM, Zhong H, Wang G, Wang ZH, Chen XY, He F.

Zhonghua Xin Xue Guan Bing Za Zhi. 2010 Jun;38(6):503-9. Chinese.

PMID:
21033130
17.

Angiotensin II type I receptor gene and myocardial infarction: tagging SNPs and haplotype based association study. The Beijing atherosclerosis study.

Su S, Chen J, Zhao J, Huang J, Wang X, Chen R, Gu D; Beijing Atherosclerosis Study..

Pharmacogenetics. 2004 Oct;14(10):673-81.

PMID:
15454732
18.

Common variation in KLKB1 and essential hypertension risk: tagging-SNP haplotype analysis in a case-control study.

Lu X, Zhao W, Huang J, Li H, Yang W, Wang L, Huang W, Chen S, Gu D.

Hum Genet. 2007 May;121(3-4):327-35. Epub 2007 Feb 23.

PMID:
17318641
19.
20.

Analyses of single nucleotide polymorphisms and haplotype linkage of LOC387715 and the HTRA1 gene in exudative age-related macular degeneration in a Chinese cohort.

Jiang H, Qu Y, Dang G, Zhang X, Yin N, Zhang Y, Bi H, Pan X, Xu X, Zhou F, Dai H.

Retina. 2009 Jul-Aug;29(7):974-9. doi: 10.1097/IAE.0b013e3181a3b90e.

PMID:
19491722

Supplemental Content

Support Center