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Items: 1 to 20 of 116

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.

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
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.

4.

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.

5.
6.

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.

7.

[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
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
9.

Import of Fluorescent RNA into Mitochondria of Living Cells.

Zelenka J, Ježek P.

Methods Mol Biol. 2016;1351:175-81. doi: 10.1007/978-1-4939-3040-1_13.

PMID:
26530682
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
11.

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.

12.

Mitochondrially-imported RNA in drug discovery.

Cannon MV, Irwin MH, Pinkert CA.

Drug Dev Res. 2015 Mar;76(2):61-71. doi: 10.1002/ddr.21241. Epub 2015 Apr 3.

PMID:
25847616
13.

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.

14.

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.

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
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
17.

An Essential Role for COPI in mRNA Localization to Mitochondria and Mitochondrial Function.

Zabezhinsky D, Slobodin B, Rapaport D, Gerst JE.

Cell Rep. 2016 Apr 19;15(3):540-9. doi: 10.1016/j.celrep.2016.03.053. Epub 2016 Apr 7.

18.

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.

19.

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
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

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