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Results: 1 to 20 of 87

Similar articles for PubMed (Select 21918550)

1.

Mitochondrial gene replacement in human pluripotent stem cell-derived neural progenitors.

Iyer S, Xiao E, Alsayegh K, Eroshenko N, Riggs MJ, Bennett JP Jr, Rao RR.

Gene Ther. 2012 May;19(5):469-75. doi: 10.1038/gt.2011.134. Epub 2011 Sep 15.

PMID:
21918550
2.

Mitochondrial gene therapy improves respiration, biogenesis, and transcription in G11778A Leber's hereditary optic neuropathy and T8993G Leigh's syndrome cells.

Iyer S, Bergquist K, Young K, Gnaiger E, Rao RR, Bennett JP Jr.

Hum Gene Ther. 2012 Jun;23(6):647-57. doi: 10.1089/hum.2011.177. Epub 2012 Apr 17.

3.

A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy.

Mimaki M, Ikota A, Sato A, Komaki H, Akanuma J, Nonaka I, Goto Y.

J Hum Genet. 2003;48(1):47-50.

PMID:
12560876
4.

Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy.

Kumar M, Tanwar M, Saxena R, Sharma P, Dada R.

Mol Vis. 2010 Apr 30;16:782-92.

5.

The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutation.

Qian Y, Zhou X, Liang M, Qu J, Guan MX.

Mitochondrion. 2011 Nov;11(6):871-7. doi: 10.1016/j.mito.2011.06.006. Epub 2011 Jul 1.

PMID:
21742061
6.

Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation.

Cai W, Fu Q, Zhou X, Qu J, Tong Y, Guan MX.

J Genet Genomics. 2008 Nov;35(11):649-55. doi: 10.1016/S1673-8527(08)60086-7.

PMID:
19022198
7.

The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation.

Qu J, Li R, Zhou X, Tong Y, Lu F, Qian Y, Hu Y, Mo JQ, West CE, Guan MX.

Invest Ophthalmol Vis Sci. 2006 Feb;47(2):475-83.

PMID:
16431939
8.

Novel therapeutic approaches for Leber's hereditary optic neuropathy.

Iyer S.

Discov Med. 2013 Mar;15(82):141-9. Review.

9.

The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity.

Ghelli A, Porcelli AM, Zanna C, Vidoni S, Mattioli S, Barbieri A, Iommarini L, Pala M, Achilli A, Torroni A, Rugolo M, Carelli V.

PLoS One. 2009 Nov 19;4(11):e7922. doi: 10.1371/journal.pone.0007922.

10.

Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells.

Wong A, Cavelier L, Collins-Schramm HE, Seldin MF, McGrogan M, Savontaus ML, Cortopassi GA.

Hum Mol Genet. 2002 Feb 15;11(4):431-8.

11.

Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy.

Qian Y, Zhou X, Hu Y, Tong Y, Li R, Lu F, Yang H, Mo JQ, Qu J, Guan MX.

Biochem Biophys Res Commun. 2005 Jul 1;332(2):614-21.

PMID:
15896721
12.

[The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].

Mao YJ, Qu J, Guan MX.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Feb;25(1):45-9. Review. Chinese.

PMID:
18247303
13.

Leber's hereditary optic neuropathy: clinical and molecular genetic results in a patient with a point mutation at np T11253C (isoleucine to threonine) in the ND4 gene and spontaneous recovery.

Leo-Kottler B, Luberichs J, Besch D, Christ-Adler M, Fauser S.

Graefes Arch Clin Exp Ophthalmol. 2002 Sep;240(9):758-64. Epub 2002 Aug 2.

PMID:
12271374
14.

The role of the ND5 gene in LHON: characterization of a new, heteroplasmic LHON mutation.

Mayorov V, Biousse V, Newman NJ, Brown MD.

Ann Neurol. 2005 Nov;58(5):807-11.

PMID:
16240359
15.

[Leber's hereditary optic neuropathy is associated with the mitochondrial G11696A mutation in two Chinese families].

Zhao FX, Zhou XT, Qu J, Wei QP, Tong Y, Yang L, Lv JX, Guan MX.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Oct;24(5):556-9. Chinese.

PMID:
17922426
17.

Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families.

Zhou X, Wei Q, Yang L, Tong Y, Zhao F, Lu C, Qian Y, Sun Y, Lu F, Qu J, Guan MX.

Biochem Biophys Res Commun. 2006 Feb 3;340(1):69-75. Epub 2005 Dec 6.

PMID:
16364244
18.

Leber's hereditary optic neuropathy with 3460 mitochondrial DNA mutation.

Hwang JM, Chang BL, Koh HJ, Kim JY, Park SS.

J Korean Med Sci. 2002 Apr;17(2):283-6.

19.

Leber's hereditary optic neuropathy with molecular characterization in two Indian families.

Verma IC, Bijarnia S, Saxena R, Kohli S, Puri RD, Thomas E, Chowdhary D, Jha SN, Grover AK.

Indian J Ophthalmol. 2005 Sep;53(3):167-71.

20.

Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families.

Zhang J, Zhou X, Zhou J, Li C, Zhao F, Wang Y, Meng Y, Wang J, Yuan M, Cai W, Tong Y, Sun YH, Yang L, Qu J, Guan MX.

Biochem Biophys Res Commun. 2010 Sep 3;399(4):647-53. doi: 10.1016/j.bbrc.2010.07.135. Epub 2010 Aug 4.

PMID:
20691156
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