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Results: 1 to 20 of 115

1.

Correcting human mitochondrial mutations with targeted RNA import.

Wang G, Shimada E, Zhang J, Hong JS, Smith GM, Teitell MA, Koehler CM.

Proc Natl Acad Sci U S A. 2012 Mar 27;109(13):4840-5. doi: 10.1073/pnas.1116792109. Epub 2012 Mar 12.

PMID:
22411789
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells.

Kolesnikova OA, Entelis NS, Jacquin-Becker C, Goltzene F, Chrzanowska-Lightowlers ZM, Lightowlers RN, Martin RP, Tarassov I.

Hum Mol Genet. 2004 Oct 15;13(20):2519-34. Epub 2004 Aug 18.

PMID:
15317755
[PubMed - indexed for MEDLINE]
Free Article
3.

Mutation in PNPT1, which encodes a polyribonucleotide nucleotidyltransferase, impairs RNA import into mitochondria and causes respiratory-chain deficiency.

Vedrenne V, Gowher A, De Lonlay P, Nitschke P, Serre V, Boddaert N, Altuzarra C, Mager-Heckel AM, Chretien F, Entelis N, Munnich A, Tarassov I, Rötig A.

Am J Hum Genet. 2012 Nov 2;91(5):912-8. doi: 10.1016/j.ajhg.2012.09.001. Epub 2012 Oct 18.

PMID:
23084291
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Correction of the consequences of mitochondrial 3243A>G mutation in the MT-TL1 gene causing the MELAS syndrome by tRNA import into mitochondria.

Karicheva OZ, Kolesnikova OA, Schirtz T, Vysokikh MY, Mager-Heckel AM, Lombès A, Boucheham A, Krasheninnikov IA, Martin RP, Entelis N, Tarassov I.

Nucleic Acids Res. 2011 Oct;39(18):8173-86. doi: 10.1093/nar/gkr546. Epub 2011 Jun 30.

PMID:
21724600
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

PNPASE and RNA trafficking into mitochondria.

Wang G, Shimada E, Koehler CM, Teitell MA.

Biochim Biophys Acta. 2012 Sep-Oct;1819(9-10):998-1007. doi: 10.1016/j.bbagrm.2011.10.001. Epub 2011 Oct 13. Review.

PMID:
22023881
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Identification and structural characterization of nucleus-encoded transfer RNAs imported into wheat mitochondria.

Glover KE, Spencer DF, Gray MW.

J Biol Chem. 2001 Jan 5;276(1):639-48.

PMID:
11027690
[PubMed - indexed for MEDLINE]
Free Article
7.

A novel mutation in the mitochondrial tRNA(Ser(AGY)) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency.

Wong LJ, Yim D, Bai RK, Kwon H, Vacek MM, Zane J, Hoppel CL, Kerr DS.

J Med Genet. 2006 Sep;43(9):e46.

PMID:
16950817
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Human mitochondrial tRNAs in health and disease.

Florentz C, Sohm B, Tryoen-Tóth P, Pütz J, Sissler M.

Cell Mol Life Sci. 2003 Jul;60(7):1356-75. Review.

PMID:
12943225
[PubMed - indexed for MEDLINE]
9.

A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.

von Ameln S, Wang G, Boulouiz R, Rutherford MA, Smith GM, Li Y, Pogoda HM, Nürnberg G, Stiller B, Volk AE, Borck G, Hong JS, Goodyear RJ, Abidi O, Nürnberg P, Hofmann K, Richardson GP, Hammerschmidt M, Moser T, Wollnik B, Koehler CM, Teitell MA, Barakat A, Kubisch C.

Am J Hum Genet. 2012 Nov 2;91(5):919-27. doi: 10.1016/j.ajhg.2012.09.002. Epub 2012 Oct 18.

PMID:
23084290
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Human mitochondrial diseases caused by lack of taurine modification in mitochondrial tRNAs.

Suzuki T, Nagao A, Suzuki T.

Wiley Interdiscip Rev RNA. 2011 May-Jun;2(3):376-86. doi: 10.1002/wrna.65. Epub 2011 Feb 25. Review.

PMID:
21957023
[PubMed - indexed for MEDLINE]
11.

[Wobble modification defect suppresses translational activity of tRNAs with MERRF and MELAS mutations].

Yasukawa T, Suzuki T, Watanabe K, Yasukawa T, Ohta S.

Nihon Rinsho. 2002 Apr;60 Suppl 4:197-201. Review. Japanese. No abstract available.

PMID:
12013848
[PubMed - indexed for MEDLINE]
12.

Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial disease.

Yasukawa T, Suzuki T, Ishii N, Ohta S, Watanabe K.

EMBO J. 2001 Sep 3;20(17):4794-802.

PMID:
11532943
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Mammalian mitochondria have the innate ability to import tRNAs by a mechanism distinct from protein import.

Rubio MA, Rinehart JJ, Krett B, Duvezin-Caubet S, Reichert AS, Söll D, Alfonzo JD.

Proc Natl Acad Sci U S A. 2008 Jul 8;105(27):9186-91. doi: 10.1073/pnas.0804283105. Epub 2008 Jun 27.

PMID:
18587046
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Identification of nuclear encoded precursor tRNAs within the mitochondrion of Trypanosoma brucei.

Hancock K, LeBlanc AJ, Donze D, Hajduk SL.

J Biol Chem. 1992 Nov 25;267(33):23963-71.

PMID:
1385429
[PubMed - indexed for MEDLINE]
Free Article
15.

The analysis of tRNA import into mammalian mitochondria.

Mager-Heckel AM, Entelis N, Brandina I, Kamenski P, Krasheninnikov IA, Martin RP, Tarassov I.

Methods Mol Biol. 2007;372:235-53. doi: 10.1007/978-1-59745-365-3_17.

PMID:
18314730
[PubMed - indexed for MEDLINE]
16.

High prevalence of the COII/tRNA(Lys) intergenic 9-bp deletion in mitochondrial DNA of Taiwanese patients with MELAS or MERRF syndrome.

Liu CS, Cheng WL, Chen YY, Ma YS, Pang CY, Wei YH.

Ann N Y Acad Sci. 2005 May;1042:82-7.

PMID:
15965049
[PubMed - indexed for MEDLINE]
17.

PNPASE regulates RNA import into mitochondria.

Wang G, Chen HW, Oktay Y, Zhang J, Allen EL, Smith GM, Fan KC, Hong JS, French SW, McCaffery JM, Lightowlers RN, Morse HC 3rd, Koehler CM, Teitell MA.

Cell. 2010 Aug 6;142(3):456-67. doi: 10.1016/j.cell.2010.06.035.

PMID:
20691904
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases.

Suzuki T, Nagao A, Suzuki T.

Annu Rev Genet. 2011;45:299-329. doi: 10.1146/annurev-genet-110410-132531. Epub 2011 Sep 6. Review.

PMID:
21910628
[PubMed - indexed for MEDLINE]
19.

Localization of mRNAs coding for mitochondrial proteins in the yeast Saccharomyces cerevisiae.

Gadir N, Haim-Vilmovsky L, Kraut-Cohen J, Gerst JE.

RNA. 2011 Aug;17(8):1551-65. doi: 10.1261/rna.2621111. Epub 2011 Jun 24.

PMID:
21705432
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

A novel point mutation in the mitochondrial tRNA(Ser(UCN)) gene detected in a family with MERRF/MELAS overlap syndrome.

Nakamura M, Nakano S, Goto Y, Ozawa M, Nagahama Y, Fukuyama H, Akiguchi I, Kaji R, Kimura J.

Biochem Biophys Res Commun. 1995 Sep 5;214(1):86-93.

PMID:
7669057
[PubMed - indexed for MEDLINE]

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