Shen Y - Search Results

1

CACNA1I is not associated with childhood absence epilepsy in the Chinese Han population.

Wang J, Zhang Y, Liang J, Pan H, Wu H, Xu K, Liu X, Jiang Y, Shen Y, Wu X. Wang J, et al. Among authors: shen y. Pediatr Neurol. 2006 Sep;35(3):187-90. doi: 10.1016/j.pediatrneurol.2006.03.006. Pediatr Neurol. 2006. PMID: 16939858

2

Single nucleotide polymorphisms in CAPN10 gene of Chinese people and its correlation with type 2 diabetes mellitus in Han people of northern China.

Sun HX, Zhang KX, Du WN, Shi JX, Jiang ZW, Sun H, Zuo J, Huang W, Chen Z, Shen Y, Yao ZJ, Qiang BQ, Fang FD. Sun HX, et al. Among authors: shen y. Biomed Environ Sci. 2002 Mar;15(1):75-82. Biomed Environ Sci. 2002. PMID: 12046551

3

[Case-control study and transmission/disequilibrium test of childhood absence epilepsy].

Lu J, Chen Y, Zhang Y, Pan H, Liu X, Jiang Y, Du W, Shen Y, Xu K, Wu H, Wu X. Lu J, et al. Among authors: shen y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Jun;19(3):183-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 12048673 Chinese.

4

MECP2 gene mutation analysis in Chinese patients with Rett syndrome.

Pan H, Wang YP, Bao XH, Meng HD, Zhang Y, Wu XR, Shen Y. Pan H, et al. Among authors: shen y. Eur J Hum Genet. 2002 Aug;10(8):484-6. doi: 10.1038/sj.ejhg.5200827. Eur J Hum Genet. 2002. PMID: 12111643

5

[Mutational analysis of MECP2 gene in Rett syndrome].

Pan H, Wang Y, Meng H, Bao X, Zhang Y, Shen Y, Wu X. Pan H, et al. Among authors: shen y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Aug;19(4):276-80. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 12170461 Chinese.

6

[Association analysis of childhood absence epilepsy by microsatellite DNA].

Lu J, Chen Y, Pan H, Zhang Y, Jiang Y, Di W, Shen Y, Xu K, Wu H, Wu X. Lu J, et al. Among authors: shen y. Zhonghua Yi Xue Za Zhi. 2002 Aug 10;82(15):1029-32. Zhonghua Yi Xue Za Zhi. 2002. PMID: 12194792 Chinese.

7

Mutation screen of the GABA(A) receptor gamma 2 subunit gene in Chinese patients with childhood absence epilepsy.

Lu J, Chen Y, Zhang Y, Pan H, Wu H, Xu K, Liu X, Jiang Y, Bao X, Ding K, Shen Y, Wu X. Lu J, et al. Among authors: shen y. Neurosci Lett. 2002 Oct 31;332(2):75-8. doi: 10.1016/s0304-3940(02)00805-4. Neurosci Lett. 2002. PMID: 12384214 Clinical Trial.

8

Extensive association analysis between polymorphisms of PON gene cluster with coronary heart disease in Chinese Han population.

Wang X, Fan Z, Huang J, Su S, Yu Q, Zhao J, Hui R, Yao Z, Shen Y, Qiang B, Gu D. Wang X, et al. Among authors: shen y. Arterioscler Thromb Vasc Biol. 2003 Feb 1;23(2):328-34. doi: 10.1161/01.atv.0000051702.38086.c1. Arterioscler Thromb Vasc Biol. 2003. PMID: 12588779

9

T-type calcium channel gene alpha (1G) is not associated with childhood absence epilepsy in the Chinese Han population.

Chen Y, Lu J, Zhang Y, Pan H, Wu H, Xu K, Liu X, Jiang Y, Bao X, Zhou J, Liu W, Shi G, Shen Y, Wu X. Chen Y, et al. Among authors: shen y. Neurosci Lett. 2003 Apr 24;341(1):29-32. doi: 10.1016/s0304-3940(03)00124-1. Neurosci Lett. 2003. PMID: 12676336

10

The gene encoding GABBR1 is not associated with childhood absence epilepsy in the Chinese Han population.

Lu J, Chen Y, Pan H, Zhang Y, Wu H, Xu K, Liu X, Jiang Y, Bao X, Shen Y, Wu X. Lu J, et al. Among authors: shen y. Neurosci Lett. 2003 Jun 12;343(3):151-4. doi: 10.1016/s0304-3940(03)00316-1. Neurosci Lett. 2003. PMID: 12770685

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