Yao YG - Search Results

1

Screening the three LHON primary mutations in the general Chinese population by using an optimized multiplex allele-specific PCR.

Bi R, Zhang AM, Yu D, Chen D, Yao YG. Bi R, et al. Among authors: yao yg. Clin Chim Acta. 2010 Nov 11;411(21-22):1671-4. doi: 10.1016/j.cca.2010.06.026. Epub 2010 Jul 1. Clin Chim Acta. 2010. PMID: 20599858

2

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.

3

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

4

Somatic mutations of mitochondrial genome in early stage breast cancer.

Wang CY, Wang HW, Yao YG, Kong QP, Zhang YP. Wang CY, et al. Among authors: yao yg. Int J Cancer. 2007 Sep 15;121(6):1253-6. doi: 10.1002/ijc.22822. Int J Cancer. 2007. PMID: 17514652

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

Co-occurrence of A1555G and G11778A in a Chinese family with high penetrance of Leber's hereditary optic neuropathy.

Zhang AM, Jia X, Yao YG, Zhang Q. Zhang AM, et al. Among authors: yao yg. Biochem Biophys Res Commun. 2008 Nov 7;376(1):221-4. doi: 10.1016/j.bbrc.2008.08.128. Epub 2008 Sep 4. Biochem Biophys Res Commun. 2008. PMID: 18775412

7

Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation.

Ji Y, Zhang AM, Jia X, Zhang YP, Xiao X, Li S, Guo X, Bandelt HJ, Zhang Q, Yao YG. Ji Y, et al. Among authors: yao yg. Am J Hum Genet. 2008 Dec;83(6):760-8. doi: 10.1016/j.ajhg.2008.11.002. Epub 2008 Nov 20. Am J Hum Genet. 2008. PMID: 19026397 Free PMC article.

8

Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese.

Zhang AM, Zou Y, Guo X, Jia X, Zhang Q, Yao YG. Zhang AM, et al. Among authors: yao yg. Biochem Biophys Res Commun. 2009 Aug 21;386(2):392-5. doi: 10.1016/j.bbrc.2009.06.051. Epub 2009 Jun 13. Biochem Biophys Res Commun. 2009. PMID: 19527690

9

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

10

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

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