Shi YR - Search Results

1

Angiotensin II type 1 receptor gene adenine/cytosine1166 polymorphism is not associated with mitral valve prolapse syndrome in Taiwan Chinese.

Chou HT, Shi YR, Wu JY, Tsai FJ. Chou HT, et al. Among authors: shi yr. Circ J. 2002 Feb;66(2):163-6. doi: 10.1253/circj.66.163. Circ J. 2002. PMID: 11999641 Free article.

2

Lack of association between transforming growth factor-beta1 gene polymorphisms and mitral valve prolapse in Taiwan Chinese.

Chou HT, Shi YR, Hsu Y, Tsai FJ. Chou HT, et al. Among authors: shi yr. J Heart Valve Dis. 2002 Jul;11(4):478-84. J Heart Valve Dis. 2002. PMID: 12150293

3

Association between angiotensinogen gene M235T polymorphism and mitral valve prolapse syndrome in Taiwan Chinese.

Chou HT, Hung JS, Chen YT, Shi YR, Tsai FJ. Chou HT, et al. Among authors: shi yr. J Heart Valve Dis. 2002 Nov;11(6):830-6. J Heart Valve Dis. 2002. PMID: 12479284

4

Association between angiotensin I-converting enzyme gene insertion/deletion polymorphism and mitral valve prolapse syndrome.

Chou HT, Chen YT, Shi YR, Tsai FJ. Chou HT, et al. Among authors: shi yr. Am Heart J. 2003 Jan;145(1):169-73. doi: 10.1067/mhj.2003.26. Am Heart J. 2003. PMID: 12514670

5

The polymorphisms of codon 727 and 52 of thyroid-stimulating hormone receptor gene are not associated with mitral valve prolapse syndrome in Taiwan Chinese.

Chou HT, Shi YR, Chang CT, Tsai FJ. Chou HT, et al. Among authors: shi yr. Jpn Heart J. 2002 Nov;43(6):655-66. doi: 10.1536/jhj.43.655. Jpn Heart J. 2002. PMID: 12558129 Free article.

6

Lack of association of genetic polymorphisms in the interleukin-1beta, interleukin-1 receptor antagonist, interleukin-4 and interleukin-10 genes with mitral valve prolapse in Taiwan Chinese.

Chou HT, Shi YR, Hsu Y, Tsai FJ. Chou HT, et al. Among authors: shi yr. J Heart Valve Dis. 2003 Jan;12(1):38-44. J Heart Valve Dis. 2003. PMID: 12578333

7

Association between fibrillin-1 gene exon 15 and 27 polymorphisms and risk of mitral valve prolapse.

Chou HT, Shi YR, Hsu Y, Tsai FJ. Chou HT, et al. Among authors: shi yr. J Heart Valve Dis. 2003 Jul;12(4):475-81. J Heart Valve Dis. 2003. PMID: 12918850

8

Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method.

Shi YR, Hsieh KS, Wu JY, Lee CC, Tsai CH, Tsai FJ. Shi YR, et al. Pediatr Int. 2002 Jun;44(3):264-8. doi: 10.1046/j.1442-200x.2002.01553.x. Pediatr Int. 2002. PMID: 11982893

9

Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan.

Shi YR, Wu JY, Hsu YA, Lee CC, Tsai CH, Tsai FJ. Shi YR, et al. Genet Test. 2002 Fall;6(3):237-43. doi: 10.1089/109065702761403441. Genet Test. 2002. PMID: 12490068

10

Genetic analysis of chromosome 22q11.2 markers in congenital heart disease.

Shi YR, Hsieh KS, Wu JY, Lee CC, Tsai CH, Yu MT, Chang JS, Tsai FJ. Shi YR, et al. J Clin Lab Anal. 2003;17(1):28-35. doi: 10.1002/jcla.10062. J Clin Lab Anal. 2003. PMID: 12526020 Free PMC article.

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