Zhao GX - Search Results

1

Novel mutation in the ABCA1 gene identified in a chinese patient with dementia and atherothrombotic cerebral infarction.

Xue XH, Wang N, Lin Y, Zhao GX, Fang L, Murong S, Wu ZY. Xue XH, et al. Among authors: zhao gx. Dement Geriatr Cogn Disord. 2008;26(3):234-8. doi: 10.1159/000160954. Epub 2008 Oct 8. Dement Geriatr Cogn Disord. 2008. PMID: 18841006

2

Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease.

Wu ZY, Zhao GX, Chen WJ, Wang N, Wan B, Lin MT, Murong SX, Yu L. Wu ZY, et al. Among authors: zhao gx. J Mol Med (Berl). 2006 May;84(5):438-42. doi: 10.1007/s00109-005-0036-y. Epub 2006 Jan 28. J Mol Med (Berl). 2006. PMID: 16649058

3

A novel mutation in the senataxin gene identified in a Chinese patient with sporadic amyotrophic lateral sclerosis.

Zhao ZH, Chen WZ, Wu ZY, Wang N, Zhao GX, Chen WJ, Murong SX. Zhao ZH, et al. Among authors: zhao gx. Amyotroph Lateral Scler. 2009 Apr;10(2):118-22. doi: 10.1080/17482960802572673. Amyotroph Lateral Scler. 2009. PMID: 19058054

4

Association between novel TARDBP mutations and Chinese patients with amyotrophic lateral sclerosis.

Xiong HL, Wang JY, Sun YM, Wu JJ, Chen Y, Qiao K, Zheng QJ, Zhao GX, Wu ZY. Xiong HL, et al. Among authors: zhao gx. BMC Med Genet. 2010 Jan 19;11:8. doi: 10.1186/1471-2350-11-8. BMC Med Genet. 2010. PMID: 20082726 Free PMC article.

5

High frequency of Machado-Joseph disease identified in southeastern Chinese kindreds with spinocerebellar ataxia.

Gan SR, Shi SS, Wu JJ, Wang N, Zhao GX, Weng ST, Murong SX, Lu CZ, Wu ZY. Gan SR, et al. Among authors: zhao gx. BMC Med Genet. 2010 Mar 25;11:47. doi: 10.1186/1471-2350-11-47. BMC Med Genet. 2010. PMID: 20334689 Free PMC article.

6

A Chinese pedigree with an individual homozygous for CAG repeats of Huntington's disease.

Shi SS, Lin Y, Zhao GX, Gan SR, Wu ZY. Shi SS, et al. Among authors: zhao gx. Psychiatr Genet. 2012 Feb;22(1):53-4. doi: 10.1097/YPG.0b013e328347c203. Psychiatr Genet. 2012. PMID: 21610555 No abstract available.

7

Impaired regulatory function and enhanced intrathecal activation of B cells in neuromyelitis optica: distinct from multiple sclerosis.

Quan C, Yu H, Qiao J, Xiao B, Zhao G, Wu Z, Li Z, Lu C. Quan C, et al. Mult Scler. 2013 Mar;19(3):289-98. doi: 10.1177/1352458512454771. Epub 2012 Aug 3. Mult Scler. 2013. PMID: 22864301

8

Variants in the promoter region of CYP7A1 are associated with neuromyelitis optica but not with multiple sclerosis in the Han Chinese population.

Zhao GX, Liu Y, Li ZX, Lv CZ, Traboulsee A, Sadovnick AD, Wu ZY. Zhao GX, et al. Neurosci Bull. 2013 Oct;29(5):525-30. doi: 10.1007/s12264-013-1347-6. Epub 2013 Jun 5. Neurosci Bull. 2013. PMID: 23740208 Free PMC article.

9

Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification.

Chen WJ, Yao XP, Zhang QJ, Ni W, He J, Li HF, Liu XY, Zhao GX, Murong SX, Wang N, Wu ZY. Chen WJ, et al. Among authors: zhao gx. Gene. 2013 Oct 15;529(1):159-62. doi: 10.1016/j.gene.2013.07.071. Epub 2013 Aug 11. Gene. 2013. PMID: 23939468

10

No association between identified multiple sclerosis non-MHC risk loci and neuromyelitis optica.

Liu QB, Li ZX, Zhao GX, Yu H, Wu ZY. Liu QB, et al. Among authors: zhao gx. Neurosci Bull. 2014 Dec;30(6):1036-1044. doi: 10.1007/s12264-013-1457-1. Epub 2014 Jun 13. Neurosci Bull. 2014. PMID: 24927785 Free PMC article.

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