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Results: 1 to 20 of 237

Related Citations for PubMed (Select 11925565)

1.

Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus.

Manfredi G, Fu J, Ojaimi J, Sadlock JE, Kwong JQ, Guy J, Schon EA.

Nat Genet. 2002 Apr;30(4):394-9. Epub 2002 Feb 25.

PMID:
11925565
2.

Allotopic mRNA localization to the mitochondrial surface rescues respiratory chain defects in fibroblasts harboring mitochondrial DNA mutations affecting complex I or v subunits.

Bonnet C, Kaltimbacher V, Ellouze S, Augustin S, Bénit P, Forster V, Rustin P, Sahel JA, Corral-Debrinski M.

Rejuvenation Res. 2007 Jun;10(2):127-44.

PMID:
17518546
3.

Oligomycin induces a decrease in the cellular content of a pathogenic mutation in the human mitochondrial ATPase 6 gene.

Manfredi G, Gupta N, Vazquez-Memije ME, Sadlock JE, Spinazzola A, De Vivo DC, Schon EA.

J Biol Chem. 1999 Apr 2;274(14):9386-91.

4.

Positive contribution of pathogenic mutations in the mitochondrial genome to the promotion of cancer by prevention from apoptosis.

Shidara Y, Yamagata K, Kanamori T, Nakano K, Kwong JQ, Manfredi G, Oda H, Ohta S.

Cancer Res. 2005 Mar 1;65(5):1655-63.

5.
6.

Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy.

Guy J, Qi X, Pallotti F, Schon EA, Manfredi G, Carelli V, Martinuzzi A, Hauswirth WW, Lewin AS.

Ann Neurol. 2002 Nov;52(5):534-42.

PMID:
12402249
7.

Recombinant adeno-associated virus vector-based gene transfer for defects in oxidative metabolism.

Owen R IV, Lewin AP, Peel A, Wang J, Guy J, Hauswirth WW, Stacpoole PW, Flotte TR.

Hum Gene Ther. 2000 Oct 10;11(15):2067-78.

PMID:
11044909
8.

In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I.

D'Aurelio M, Pallotti F, Barrientos A, Gajewski CD, Kwong JQ, Bruno C, Beal MF, Manfredi G.

J Biol Chem. 2001 Dec 14;276(50):46925-32. Epub 2001 Oct 10.

9.

GUG is an efficient initiation codon to translate the human mitochondrial ATP6 gene.

Dubot A, Godinot C, Dumur V, Sablonnière B, Stojkovic T, Cuisset JM, Vojtiskova A, Pecina P, Jesina P, Houstek J.

Biochem Biophys Res Commun. 2004 Jan 16;313(3):687-93.

PMID:
14697245
10.

Biochemical consequences in yeast of the human mitochondrial DNA 8993T>C mutation in the ATPase6 gene found in NARP/MILS patients.

Kucharczyk R, Rak M, di Rago JP.

Biochim Biophys Acta. 2009 May;1793(5):817-24. doi: 10.1016/j.bbamcr.2009.02.011. Epub 2009 Mar 6.

11.

The typically mitochondrial DNA-encoded ATP6 subunit of the F1F0-ATPase is encoded by a nuclear gene in Chlamydomonas reinhardtii.

Funes S, Davidson E, Claros MG, van Lis R, Pérez-Martínez X, Vázquez-Acevedo M, King MP, González-Halphen D.

J Biol Chem. 2002 Feb 22;277(8):6051-8. Epub 2001 Dec 14.

12.

Functional polypeptides can be synthesized from human mitochondrial transcripts lacking termination codons.

Chrzanowska-Lightowlers ZM, Temperley RJ, Smith PM, Seneca SH, Lightowlers RN.

Biochem J. 2004 Feb 1;377(Pt 3):725-31.

13.

A yeast model of the neurogenic ataxia retinitis pigmentosa (NARP) T8993G mutation in the mitochondrial ATP synthase-6 gene.

Rak M, Tetaud E, Duvezin-Caubet S, Ezkurdia N, Bietenhader M, Rytka J, di Rago JP.

J Biol Chem. 2007 Nov 23;282(47):34039-47. Epub 2007 Sep 12.

14.

Enhanced expression of the human vacuolar H+-ATPase c subunit gene (ATP6L) in response to anticancer agents.

Torigoe T, Izumi H, Ishiguchi H, Uramoto H, Murakami T, Ise T, Yoshida Y, Tanabe M, Nomoto M, Itoh H, Kohno K.

J Biol Chem. 2002 Sep 27;277(39):36534-43. Epub 2002 Jul 19.

15.
16.

Limitations of allotopic expression of mitochondrial genes in mammalian cells.

Oca-Cossio J, Kenyon L, Hao H, Moraes CT.

Genetics. 2003 Oct;165(2):707-20.

17.

Pathogenesis of primary defects in mitochondrial ATP synthesis.

Schon EA, Santra S, Pallotti F, Girvin ME.

Semin Cell Dev Biol. 2001 Dec;12(6):441-8. Review.

PMID:
11735378
18.

Human NARP mitochondrial mutation metabolism corrected with alpha-ketoglutarate/aspartate: a potential new therapy.

Sgarbi G, Casalena GA, Baracca A, Lenaz G, DiMauro S, Solaini G.

Arch Neurol. 2009 Aug;66(8):951-7. doi: 10.1001/archneurol.2009.134.

PMID:
19667215
20.
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