Wang GX - Search Results

1

Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat.

Igarashi S, Takiyama Y, Cancel G, Rogaeva EA, Sasaki H, Wakisaka A, Zhou YX, Takano H, Endo K, Sanpei K, Oyake M, Tanaka H, Stevanin G, Abbas N, Dürr A, Rogaev EI, Sherrington R, Tsuda T, Ikeda M, Cassa E, Nishizawa M, Benomar A, Julien J, Weissenbach J, Wang GX, Agid Y, St George-Hyslop PH, Brice A, Tsuji S. Igarashi S, et al. Among authors: wang gx. Hum Mol Genet. 1996 Jul;5(7):923-32. doi: 10.1093/hmg/5.7.923. Hum Mol Genet. 1996. PMID: 8817326

2

Machado-Joseph disease in four Chinese pedigrees: molecular analysis of 15 patients including two juvenile cases and clinical correlations.

Zhou YX, Takiyama Y, Igarashi S, Li YF, Zhou BY, Gui DC, Endo K, Tanaka H, Chen ZH, Zhou LS, Fan MZ, Yang BX, Weissenbach J, Wang GX, Tsuji S. Zhou YX, et al. Among authors: wang gx. Neurology. 1997 Feb;48(2):482-5. doi: 10.1212/wnl.48.2.482. Neurology. 1997. PMID: 9040742

3

Spinocerebellar ataxia type 2 in China: molecular analysis and genotype-phenotype correlation in nine families.

Zhou YX, Wang GX, Tang BS, Li WD, Wang DA, Lee HS, Sambuughin N, Zhou LS, Tsuji S, Yang BX, Goldfarb LG. Zhou YX, et al. Among authors: wang da, wang gx. Neurology. 1998 Aug;51(2):595-8. doi: 10.1212/wnl.51.2.595. Neurology. 1998. PMID: 9710044

4

Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 families.

Zhou YX, Qiao WH, Gu WH, Xie H, Tang BS, Zhou LS, Yang BX, Takiyama Y, Tsuji S, He HY, Deng CX, Goldfarb LG, Wang GX. Zhou YX, et al. Among authors: wang gx. Arch Neurol. 2001 May;58(5):789-94. doi: 10.1001/archneur.58.5.789. Arch Neurol. 2001. PMID: 11346374

5

The shortest expanded allele of the MJD1 gene in a Chinese MJD kindred with autonomic dysfunction.

Gu W, Ma H, Wang K, Jin M, Zhou Y, Liu X, Wang G, Shen Y. Gu W, et al. Eur Neurol. 2004;52(2):107-11. doi: 10.1159/000080221. Epub 2004 Aug 13. Eur Neurol. 2004. PMID: 15316156

6

[A study on PARKIN gene in three pedigrees with autosomal recessive early-onset Parkinson's disease].

Jin M, Jiao JS, Gu WH, Wang K, Zou HQ, Chen B, Wang GX. Jin M, et al. Among authors: wang k, wang gx. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Oct;22(5):514-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16215938 Chinese.

7

Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystonia.

Wang K, Takahashi Y, Gao ZL, Wang GX, Chen XW, Goto J, Lou JN, Tsuji S. Wang K, et al. Among authors: wang gx. Neurogenetics. 2009 Oct;10(4):337-45. doi: 10.1007/s10048-009-0194-0. Epub 2009 May 21. Neurogenetics. 2009. PMID: 19458970

8

[Mitochondrial ND5 as the causative gene of Leight syndrome].

Wang K, Yan CZ, Wang GX, Jiao JS, Jin M. Wang K, et al. Among authors: wang gx. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Dec;27(6):616-9. doi: 10.3760/cma.j.issn.1003-9406.2010.06.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 21154318 Chinese.

9

[Analysis of fragile X mental retardation 1 gene premutation in multiple system atrophy patients].

Zhang LW, Gu WH, Wang GX, Chen YY, Hao Y, Zhang J, Wang K, Jin M. Zhang LW, et al. Among authors: wang k, wang gx. Zhonghua Yi Xue Za Zhi. 2013 Dec 17;93(47):3744-7. Zhonghua Yi Xue Za Zhi. 2013. PMID: 24548388 Chinese.

10

[Genetics and clinical study of Chinese kindreds with dentatorubral pallidoluysian atrophy].

Zhang X, Hao Y, Gu WH, Chen YY, Zhang J, Wang GX, Wang K, Jin M, Duan XH. Zhang X, et al. Among authors: wang k, wang gx. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Feb;30(1):31-5. doi: 10.3760/cma.j.issn.1003-9406.2013.01.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23450475 Chinese.

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