Yao YG - Search Results

1

Common promoter variants of the NDUFV2 gene do not confer susceptibility to schizophrenia in Han Chinese.

Zhang W, Chen X, Gong W, Tang J, Tan L, Guo H, Yao YG. Zhang W, et al. Among authors: yao yg. Behav Brain Funct. 2010 Dec 29;6:75. doi: 10.1186/1744-9081-6-75. Behav Brain Funct. 2010. PMID: 21190551 Free PMC article. Clinical Trial.

2

Analysis of the 18S rRNA genes of Sarcocystis species suggests that the morphologically similar organisms from cattle and water buffalo should be considered the same species.

Yang ZQ, Zuo YX, Yao YG, Chen XW, Yang GC, Zhang YP. Yang ZQ, et al. Among authors: yao yg. Mol Biochem Parasitol. 2001 Jul;115(2):283-8. doi: 10.1016/s0166-6851(01)00283-3. Mol Biochem Parasitol. 2001. PMID: 11420115 No abstract available.

3

Phylogeographic differentiation of mitochondrial DNA in Han Chinese.

Yao YG, Kong QP, Bandelt HJ, Kivisild T, Zhang YP. Yao YG, et al. Am J Hum Genet. 2002 Mar;70(3):635-51. doi: 10.1086/338999. Epub 2002 Feb 8. Am J Hum Genet. 2002. PMID: 11836649 Free PMC article.

4

mtDNA mutation C1494T, haplogroup A, and hearing loss in Chinese.

Wang CY, Kong QP, Yao YG, Zhang YP. Wang CY, et al. Among authors: yao yg. Biochem Biophys Res Commun. 2006 Sep 22;348(2):712-5. doi: 10.1016/j.bbrc.2006.07.119. Epub 2006 Jul 31. Biochem Biophys Res Commun. 2006. PMID: 16890911

5

Strikingly different penetrance of LHON in two Chinese families with primary mutation G11778A is independent of mtDNA haplogroup background and secondary mutation G13708A.

Wang HW, Jia X, Ji Y, Kong QP, Zhang Q, Yao YG, Zhang YP. Wang HW, et al. Among authors: yao yg. Mutat Res. 2008 Aug 25;643(1-2):48-53. doi: 10.1016/j.mrfmmm.2008.06.004. Epub 2008 Jun 21. Mutat Res. 2008. PMID: 18619472

6

The acquisition of an inheritable 50-bp deletion in the human mtDNA control region does not affect the mtDNA copy number in peripheral blood cells.

Bi R, Zhang AM, Zhang W, Kong QP, Wu BL, Yang XH, Wang D, Zou Y, Zhang YP, Yao YG. Bi R, et al. Among authors: yao yg. Hum Mutat. 2010 May;31(5):538-43. doi: 10.1002/humu.21220. Hum Mutat. 2010. PMID: 20151402

7

Molecular characterization of six Chinese families with m.3460G>A and Leber hereditary optic neuropathy.

Yu D, Jia X, Zhang AM, Guo X, Zhang YP, Zhang Q, Yao YG. Yu D, et al. Among authors: yao yg. Neurogenetics. 2010 Jul;11(3):349-56. doi: 10.1007/s10048-010-0236-7. Epub 2010 Mar 16. Neurogenetics. 2010. PMID: 20232220

8

The MT-ND1 and MT-ND5 genes are mutational hotspots for Chinese families with clinical features of LHON but lacking the three primary mutations.

Zou Y, Jia X, Zhang AM, Wang WZ, Li S, Guo X, Kong QP, Zhang Q, Yao YG. Zou Y, et al. Among authors: yao yg. Biochem Biophys Res Commun. 2010 Aug 20;399(2):179-85. doi: 10.1016/j.bbrc.2010.07.051. Epub 2010 Jul 17. Biochem Biophys Res Commun. 2010. PMID: 20643099

9

No association between the SNPs (rs3749446 and rs1402000) in the PARL gene and LHON in Chinese patients with m.11778G>A.

Zhang AM, Jia X, Zhang Q, Yao YG. Zhang AM, et al. Among authors: yao yg. Hum Genet. 2010 Oct;128(4):465-8. doi: 10.1007/s00439-010-0875-7. Epub 2010 Aug 14. Hum Genet. 2010. PMID: 20711738

10

Inland post-glacial dispersal in East Asia revealed by mitochondrial haplogroup M9a'b.

Peng MS, Palanichamy MG, Yao YG, Mitra B, Cheng YT, Zhao M, Liu J, Wang HW, Pan H, Wang WZ, Zhang AM, Zhang W, Wang D, Zou Y, Yang Y, Chaudhuri TK, Kong QP, Zhang YP. Peng MS, et al. Among authors: yao yg. BMC Biol. 2011 Jan 10;9:2. doi: 10.1186/1741-7007-9-2. BMC Biol. 2011. PMID: 21219640 Free PMC article.

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