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Items: 1 to 20 of 90

1.

Human complex I defects in neurodegenerative diseases.

Schapira AH.

Biochim Biophys Acta. 1998 May 6;1364(2):261-70. Review.

2.

Complex I function in familial and sporadic dystonia.

Schapira AH, Warner T, Gash MT, Cleeter MW, Marinho CF, Cooper JM.

Ann Neurol. 1997 Apr;41(4):556-9.

PMID:
9124815
3.

The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy.

Cock HR, Tabrizi SJ, Cooper JM, Schapira AH.

Ann Neurol. 1998 Aug;44(2):187-93.

PMID:
9708540
4.

Mitochondria in the etiology and pathogenesis of Parkinson's disease.

Schapira AH, Gu M, Taanman JW, Tabrizi SJ, Seaton T, Cleeter M, Cooper JM.

Ann Neurol. 1998 Sep;44(3 Suppl 1):S89-98. Review.

PMID:
9749579
5.

Mitochondrial dysfunction in neurodegenerative disorders.

Schapira AH.

Biochim Biophys Acta. 1998 Aug 10;1366(1-2):225-33.

PMID:
9714816
6.

Leber's hereditary optic neuropathy and complex I deficiency in muscle.

Larsson NG, Andersen O, Holme E, Oldfors A, Wahlström J.

Ann Neurol. 1991 Nov;30(5):701-8.

PMID:
1763894
7.

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.

8.
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10.

Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.

De Vries DD, Went LN, Bruyn GW, Scholte HR, Hofstra RM, Bolhuis PA, van Oost BA.

Am J Hum Genet. 1996 Apr;58(4):703-11.

11.

Mitochondrial biogenesis: pharmacological approaches.

Valero T.

Curr Pharm Des. 2014;20(35):5507-9.

PMID:
24606795
12.

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.

13.

Mitochondrial encephalomyopathies.

DiMauro S, Moraes CT.

Arch Neurol. 1993 Nov;50(11):1197-208. Review.

PMID:
8215979
14.

The mitochondrial DNA mutation ND6*14,484C associated with leber hereditary optic neuropathy, leads to deficiency of complex I of the respiratory chain.

Oostra RJ, Van Galen MJ, Bolhuis PA, Bleeker-Wagemakers EM, Van den Bogert C.

Biochem Biophys Res Commun. 1995 Oct 24;215(3):1001-5.

PMID:
7488023
15.
16.

Changes in mitochondrial complex I activity and coenzyme Q binding site in Leber's hereditary optic neuropathy (LHON).

Ghelli A, Degli Esposti M, Carelli V, Lenaz G.

Mol Aspects Med. 1997;18 Suppl:S263-7.

PMID:
9266534
17.

Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation.

Shoffner JM, Brown MD, Stugard C, Jun AS, Pollock S, Haas RH, Kaufman A, Koontz D, Kim Y, Graham JR, et al.

Ann Neurol. 1995 Aug;38(2):163-9.

PMID:
7654063
18.

Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G>A mutation in nine Han Chinese families.

Zhang J, Jiang P, Jin X, Liu X, Zhang M, Xie S, Gao M, Zhang S, Sun YH, Zhu J, Ji Y, Wei QP, Tong Y, Guan MX.

Mitochondrion. 2014 Sep;18:18-26. doi: 10.1016/j.mito.2014.08.008. Epub 2014 Sep 4.

PMID:
25194554
19.

Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegeneration.

Carelli V, Rugolo M, Sgarbi G, Ghelli A, Zanna C, Baracca A, Lenaz G, Napoli E, Martinuzzi A, Solaini G.

Biochim Biophys Acta. 2004 Jul 23;1658(1-2):172-9. Review.

20.

Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy.

Floreani M, Napoli E, Martinuzzi A, Pantano G, De Riva V, Trevisan R, Bisetto E, Valente L, Carelli V, Dabbeni-Sala F.

FEBS J. 2005 Mar;272(5):1124-35.

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