Zhang AM - Search Results

1

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: zhang yp, zhang w, zhang am. Hum Mutat. 2010 May;31(5):538-43. doi: 10.1002/humu.21220. Hum Mutat. 2010. PMID: 20151402

2

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: zhang q. 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

3

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: zhang yp, zhang q, zhang am. 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.

4

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: zhang q. 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

5

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: zhang yp, zhang q, zhang am. Neurogenetics. 2010 Jul;11(3):349-56. doi: 10.1007/s10048-010-0236-7. Epub 2010 Mar 16. Neurogenetics. 2010. PMID: 20232220

6

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: zhang am. 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

7

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: zhang q, zhang am. 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

8

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: zhang q. Hum Genet. 2010 Oct;128(4):465-8. doi: 10.1007/s00439-010-0875-7. Epub 2010 Aug 14. Hum Genet. 2010. PMID: 20711738

9

Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C.

Yu D, Jia X, Zhang AM, Li S, Zou Y, Zhang Q, Yao YG. Yu D, et al. Among authors: zhang q, zhang am. PLoS One. 2010 Oct 18;5(10):e13426. doi: 10.1371/journal.pone.0013426. PLoS One. 2010. PMID: 20976138 Free PMC article.

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: zhang yp, zhang w, zhang am. 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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