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Results: 1 to 20 of 23

1.

Disruption of Interleukin-1β Autocrine Signaling Rescues Complex I Activity and Improves ROS Levels in Immortalized Epithelial Cells with Impaired Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Function.

Clauzure M, Valdivieso AG, Massip Copiz MM, Schulman G, Teiber ML, Santa-Coloma TA.

PLoS One. 2014 Jun 5;9(6):e99257. doi: 10.1371/journal.pone.0099257. eCollection 2014.

PMID:
24901709
[PubMed - in process]
Free PMC Article
2.

CFTR activity and mitochondrial function.

Valdivieso AG, Santa-Coloma TA.

Redox Biol. 2013 Feb 5;1(1):190-202. doi: 10.1016/j.redox.2012.11.007. Review.

PMID:
24024153
[PubMed]
Free PMC Article
3.

Next-generation sequencing of mitochondrial targeted AAV transfer of human ND4 in mice.

Yu H, Mehta A, Wang G, Hauswirth WW, Chiodo V, Boye SL, Guy J.

Mol Vis. 2013 Jul 14;19:1482-91. Print 2013.

PMID:
23869167
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.

Valdivieso AG, Clauzure M, Marín MC, Taminelli GL, Massip Copiz MM, Sánchez F, Schulman G, Teiber ML, Santa-Coloma TA.

PLoS One. 2012;7(11):e48059. doi: 10.1371/journal.pone.0048059. Epub 2012 Nov 21.

PMID:
23185247
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

LHON: Mitochondrial Mutations and More.

Kirches E.

Curr Genomics. 2011 Mar;12(1):44-54. doi: 10.2174/138920211794520150.

PMID:
21886454
[PubMed]
Free PMC Article
6.

Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.

Yu-Wai-Man P, Griffiths PG, Chinnery PF.

Prog Retin Eye Res. 2011 Mar;30(2):81-114. doi: 10.1016/j.preteyeres.2010.11.002. Epub 2010 Nov 26. Review.

PMID:
21112411
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Inherited mitochondrial optic neuropathies.

Yu-Wai-Man P, Griffiths PG, Hudson G, Chinnery PF.

J Med Genet. 2009 Mar;46(3):145-58. doi: 10.1136/jmg.2007.054270. Epub 2008 Nov 10. Review. Erratum in: J Med Genet. 2011 Apr;48(4):284.

PMID:
19001017
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Data mining of NCI's anticancer screening database reveals mitochondrial complex I inhibitors cytotoxic to leukemia cell lines.

Glover CJ, Rabow AA, Isgor YG, Shoemaker RH, Covell DG.

Biochem Pharmacol. 2007 Feb 1;73(3):331-40. Epub 2006 Oct 13.

PMID:
17109823
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Increase of mitochondrial DNA in blood cells of patients with Leber's hereditary optic neuropathy with 11778 mutation.

Yen MY, Chen CS, Wang AG, Wei YH.

Br J Ophthalmol. 2002 Sep;86(9):1027-30.

PMID:
12185132
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Leber hereditary optic neuropathy.

Man PY, Turnbull DM, Chinnery PF.

J Med Genet. 2002 Mar;39(3):162-9. Review.

PMID:
11897814
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Mutants of Chlamydomonas reinhardtii deficient in mitochondrial complex I: characterization of two mutations affecting the nd1 coding sequence.

Remacle C, Baurain D, Cardol P, Matagne RF.

Genetics. 2001 Jul;158(3):1051-60.

PMID:
11454754
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

alpha-Tocopherol/lipid ratio in blood is decreased in patients with Leber's hereditary optic neuropathy and asymptomatic carriers of the 11778 mtDNA mutation.

Klivenyi P, Karg E, Rozsa C, Horvath R, Komoly S, Nemeth I, Turi S, Vecsei L.

J Neurol Neurosurg Psychiatry. 2001 Mar;70(3):359-62.

PMID:
11181859
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Complex I impairment, respiratory compensations, and photosynthetic decrease in nuclear and mitochondrial male sterile mutants of Nicotiana sylvestris.

Sabar M, De Paepe R, de Kouchkovsky Y.

Plant Physiol. 2000 Nov;124(3):1239-50.

PMID:
11080300
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Compensatory elevation of complex II activity in Leber's hereditary optic neuropathy.

Yen MY, Lee HC, Liu JH, Wei YH.

Br J Ophthalmol. 1996 Jan;80(1):78-81.

PMID:
8664239
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

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.

PMID:
8644732
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

The 14484 ND6 mtDNA mutation in Leber hereditary optic neuropathy does not affect fibroblast complex I activity.

Cock HR, Cooper JM, Schapira AH.

Am J Hum Genet. 1995 Dec;57(6):1501-2. No abstract available.

PMID:
8533781
[PubMed - indexed for MEDLINE]
Free PMC Article
18.
19.

Mitochondrial gene mutations and human diseases: a prolegomenon.

Howell N.

Am J Hum Genet. 1994 Aug;55(2):219-24. No abstract available.

PMID:
8037201
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Deletion of the structural gene for the NADH-dehydrogenase subunit 4 of Synechocystis 6803 alters respiratory properties.

Dzelzkalns VA, Obinger C, Regelsberger G, Niederhauser H, Kamensek M, Peschek GA, Bogorad L.

Plant Physiol. 1994 Dec;106(4):1435-42.

PMID:
7846157
[PubMed - indexed for MEDLINE]
Free PMC Article

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