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Items: 1 to 20 of 74

1.
3.

Mitochondrial DNA mutations provoke dominant inhibition of mitochondrial inner membrane fusion.

Sauvanet C, Duvezin-Caubet S, Salin B, David C, Massoni-Laporte A, di Rago JP, Rojo M.

PLoS One. 2012;7(11):e49639. doi: 10.1371/journal.pone.0049639. Epub 2012 Nov 16.

4.

Mitochondrial medicine--molecular pathology of defective oxidative phosphorylation.

Fosslien E.

Ann Clin Lab Sci. 2001 Jan;31(1):25-67. Review.

PMID:
11314862
5.

Mitochondrial DNA mutations in disease and aging.

Wallace DC.

Environ Mol Mutagen. 2010 Jun;51(5):440-50. doi: 10.1002/em.20586. Review.

PMID:
20544884
6.

Fast adaptive coevolution of nuclear and mitochondrial subunits of ATP synthetase in orangutan.

Bayona-Bafaluy MP, Müller S, Moraes CT.

Mol Biol Evol. 2005 Mar;22(3):716-24. Epub 2004 Dec 1. Erratum in: Mol Biol Evol. 2005 Apr;22(4):1159.

PMID:
15574809
7.

Genetic control of oxidative phosphorylation and experimental models of defects.

Trounce I.

Hum Reprod. 2000 Jul;15 Suppl 2:18-27. Review.

PMID:
11041510
8.

Drosophila simulans as a novel model for studying mitochondrial metabolism and aging.

Ballard JW.

Exp Gerontol. 2005 Oct;40(10):763-73. Review.

PMID:
16169180
9.

Mitochondrial mutations in cancer.

Brandon M, Baldi P, Wallace DC.

Oncogene. 2006 Aug 7;25(34):4647-62. Review.

PMID:
16892079
10.

Probable presence of an ubiquitous cryptic mitochondrial gene on the antisense strand of the cytochrome oxidase I gene.

Faure E, Delaye L, Tribolo S, Levasseur A, Seligmann H, Barthélémy RM.

Biol Direct. 2011 Oct 24;6:56. doi: 10.1186/1745-6150-6-56.

12.

Clinical characterization and mitochondrial DNA sequence variations in Leber hereditary optic neuropathy.

Kumar M, Kaur P, Kumar M, Saxena R, Sharma P, Dada R.

Mol Vis. 2012;18:2687-99. Epub 2012 Nov 12.

13.

New insights into the bioenergetics of mitochondrial disorders using intracellular ATP reporters.

Gajewski CD, Yang L, Schon EA, Manfredi G.

Mol Biol Cell. 2003 Sep;14(9):3628-35. Epub 2003 Jun 27.

14.

Adaptation of the Mitochondrial Genome in Cephalopods: Enhancing Proton Translocation Channels and the Subunit Interactions.

Almeida D, Maldonado E, Vasconcelos V, Antunes A.

PLoS One. 2015 Aug 18;10(8):e0135405. doi: 10.1371/journal.pone.0135405. eCollection 2015.

15.

Mitogroup: continent-specific clusters of mitochondrial OXPHOS complexes based on nuclear non-synonymous polymorphisms.

Pierron D, Letellier T, Grossman LI.

Mitochondrion. 2012 Mar;12(2):237-41. doi: 10.1016/j.mito.2011.09.005. Epub 2011 Sep 24.

PMID:
21968253
16.

Adaptive selection of mitochondrial complex I subunits during primate radiation.

Mishmar D, Ruiz-Pesini E, Mondragon-Palomino M, Procaccio V, Gaut B, Wallace DC.

Gene. 2006 Aug 15;378:11-8. Epub 2006 Jul 7.

PMID:
16828987
17.

Coevolution predicts direct interactions between mtDNA-encoded and nDNA-encoded subunits of oxidative phosphorylation complex i.

Gershoni M, Fuchs A, Shani N, Fridman Y, Corral-Debrinski M, Aharoni A, Frishman D, Mishmar D.

J Mol Biol. 2010 Nov 19;404(1):158-71. doi: 10.1016/j.jmb.2010.09.029. Epub 2010 Sep 22.

PMID:
20868692
18.

Parallel Structural Evolution of Mitochondrial Ribosomes and OXPHOS Complexes.

van der Sluis EO, Bauerschmitt H, Becker T, Mielke T, Frauenfeld J, Berninghausen O, Neupert W, Herrmann JM, Beckmann R.

Genome Biol Evol. 2015 Apr 9;7(5):1235-51. doi: 10.1093/gbe/evv061.

19.

Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.

Blok MJ, Spruijt L, de Coo IF, Schoonderwoerd K, Hendrickx A, Smeets HJ.

J Med Genet. 2007 Apr;44(4):e74.

20.

[Mitochondrial DNA: properties and applications].

Atig RK, Hsouna S, Beraud-Colomb E, Abdelhak S.

Arch Inst Pasteur Tunis. 2009;86(1-4):3-14. French.

PMID:
20707216

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