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Items: 1 to 20 of 86

1.

Manipulating the metazoan mitochondrial genome with targeted restriction enzymes.

Xu H, DeLuca SZ, O'Farrell PH.

Science. 2008 Jul 25;321(5888):575-7. doi: 10.1126/science.1160226.

2.

False positive results of mitochondrial DNA depletion/deletion due to single nucleotide substitutions causing appearance of additional PvuII restriction sites.

Weglewska-Jurkiewicz A, Jakóbkiewicz-Banecka J, Pronicka E, Wegrzyn G.

Diagn Mol Pathol. 2007 Jun;16(2):116-20.

PMID:
17525683
3.

Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria.

Tanaka M, Borgeld HJ, Zhang J, Muramatsu S, Gong JS, Yoneda M, Maruyama W, Naoi M, Ibi T, Sahashi K, Shamoto M, Fuku N, Kurata M, Yamada Y, Nishizawa K, Akao Y, Ohishi N, Miyabayashi S, Umemoto H, Muramatsu T, Furukawa K, Kikuchi A, Nakano I, Ozawa K, Yagi K.

J Biomed Sci. 2002;9(6 Pt 1):534-41.

PMID:
12372991
4.

Altering the balance between healthy and mutated mitochondrial DNA.

Smith PM, Lightowlers RN.

J Inherit Metab Dis. 2011 Apr;34(2):309-13. doi: 10.1007/s10545-010-9122-6. Epub 2010 May 27. Review.

PMID:
20506041
5.

Modulating mtDNA heteroplasmy by mitochondria-targeted restriction endonucleases in a 'differential multiple cleavage-site' model.

Bacman SR, Williams SL, Hernandez D, Moraes CT.

Gene Ther. 2007 Sep;14(18):1309-18. Epub 2007 Jun 28.

6.

Genetic mosaic analysis of a deleterious mitochondrial DNA mutation in Drosophila reveals novel aspects of mitochondrial regulation and function.

Chen Z, Qi Y, French S, Zhang G, Covian Garcia R, Balaban R, Xu H.

Mol Biol Cell. 2015 Feb 15;26(4):674-84. doi: 10.1091/mbc.E14-11-1513. Epub 2014 Dec 10.

7.
8.

Experimental evidence supports a sex-specific selective sieve in mitochondrial genome evolution.

Innocenti P, Morrow EH, Dowling DK.

Science. 2011 May 13;332(6031):845-8. doi: 10.1126/science.1201157.

9.

Selective elimination of mutant mitochondrial genomes as therapeutic strategy for the treatment of NARP and MILS syndromes.

Alexeyev MF, Venediktova N, Pastukh V, Shokolenko I, Bonilla G, Wilson GL.

Gene Ther. 2008 Apr;15(7):516-23. doi: 10.1038/sj.gt.2008.11. Epub 2008 Feb 7.

PMID:
18256697
10.

Manipulation of mtDNA heteroplasmy in all striated muscles of newborn mice by AAV9-mediated delivery of a mitochondria-targeted restriction endonuclease.

Bacman SR, Williams SL, Duan D, Moraes CT.

Gene Ther. 2012 Nov;19(11):1101-6. doi: 10.1038/gt.2011.196. Epub 2011 Dec 1.

11.

Mitochondrial DNA remains intact during Drosophila aging, but the levels of mitochondrial transcripts are significantly reduced.

Calleja M, Peña P, Ugalde C, Ferreiro C, Marco R, Garesse R.

J Biol Chem. 1993 Sep 5;268(25):18891-7.

12.

Restriction fragment analysis as a source of error in detection of heteroplasmic mtDNA mutations.

Finnilä S, Hassinen IE, Majamaa K.

Mutat Res. 1999 Aug;406(2-4):109-14.

PMID:
10479727
13.

Specific elimination of mutant mitochondrial genomes in patient-derived cells by mitoTALENs.

Bacman SR, Williams SL, Pinto M, Peralta S, Moraes CT.

Nat Med. 2013 Sep;19(9):1111-3. doi: 10.1038/nm.3261. Epub 2013 Aug 4.

14.

Depletion of the other genome-mitochondrial DNA depletion syndromes in humans.

Elpeleg O, Mandel H, Saada A.

J Mol Med (Berl). 2002 Jul;80(7):389-96. Epub 2002 May 24.

PMID:
12110944
15.

Animal models for mitochondrial disease.

Wallace DC.

Methods Mol Biol. 2002;197:3-54. Review.

PMID:
12013805
16.

Utility of array CGH in molecular diagnosis of mitochondrial disorders.

Wang J, Rakhade M.

Methods Mol Biol. 2012;837:301-12. doi: 10.1007/978-1-61779-504-6_20.

PMID:
22215556
17.

Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography.

van Den Bosch BJ, de Coo RF, Scholte HR, Nijland JG, van Den Bogaard R, de Visser M, de Die-Smulders CE, Smeets HJ.

Nucleic Acids Res. 2000 Oct 15;28(20):E89.

18.
19.

Animal models of mitochondrial DNA transactions in disease and ageing.

Oliveira MT, Garesse R, Kaguni LS.

Exp Gerontol. 2010 Aug;45(7-8):489-502. doi: 10.1016/j.exger.2010.01.019. Epub 2010 Feb 1. Review.

20.

[Mitochondrial genome and human mitochondrial diseases].

Mazunin IO, Volod'ko NV, Starikovskaia EB, Sukernik RI.

Mol Biol (Mosk). 2010 Sep-Oct;44(5):755-72. Review. Russian.

PMID:
21090233
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