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Items: 11

1.

Migration of mitochondrial DNA in the nuclear genome of colorectal adenocarcinoma.

Srinivasainagendra V, Sandel MW, Singh B, Sundaresan A, Mooga VP, Bajpai P, Tiwari HK, Singh KK.

Genome Med. 2017 Mar 29;9(1):31. doi: 10.1186/s13073-017-0420-6.

2.

Engineered AAA+ proteases reveal principles of proteolysis at the mitochondrial inner membrane.

Shi H, Rampello AJ, Glynn SE.

Nat Commun. 2016 Oct 27;7:13301. doi: 10.1038/ncomms13301.

3.

Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation.

Hartmann B, Wai T, Hu H, MacVicar T, Musante L, Fischer-Zirnsak B, Stenzel W, Gräf R, van den Heuvel L, Ropers HH, Wienker TF, Hübner C, Langer T, Kaindl AM.

Elife. 2016 Aug 6;5. pii: e16078. doi: 10.7554/eLife.16078.

4.

StAR enhances transcription of genes encoding the mitochondrial proteases involved in its own degradation.

Bahat A, Perlberg S, Melamed-Book N, Lauria I, Langer T, Orly J.

Mol Endocrinol. 2014 Feb;28(2):208-24. doi: 10.1210/me.2013-1275. Epub 2013 Jan 1.

5.

Loss of Yme1L perturbates mitochondrial dynamics.

Ruan Y, Li H, Zhang K, Jian F, Tang J, Song Z.

Cell Death Dis. 2013 Oct 31;4:e896. doi: 10.1038/cddis.2013.414.

6.

Regulation of mitochondrial dynamics: convergences and divergences between yeast and vertebrates.

Zhao J, Lendahl U, Nistér M.

Cell Mol Life Sci. 2013 Mar;70(6):951-76. doi: 10.1007/s00018-012-1066-6. Epub 2012 Jul 18. Review.

7.

YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation.

Stiburek L, Cesnekova J, Kostkova O, Fornuskova D, Vinsova K, Wenchich L, Houstek J, Zeman J.

Mol Biol Cell. 2012 Mar;23(6):1010-23. doi: 10.1091/mbc.E11-08-0674. Epub 2012 Jan 19.

8.

Unmasking a temperature-dependent effect of the P. anserina i-AAA protease on aging and development.

Weil A, Luce K, Dröse S, Wittig I, Brandt U, Osiewacz HD.

Cell Cycle. 2011 Dec 15;10(24):4280-90. doi: 10.4161/cc.10.24.18560. Epub 2011 Dec 15.

9.

Translocation and assembly of mitochondrially coded Saccharomyces cerevisiae cytochrome c oxidase subunit Cox2 by Oxa1 and Yme1 in the absence of Cox18.

Fiumera HL, Dunham MJ, Saracco SA, Butler CA, Kelly JA, Fox TD.

Genetics. 2009 Jun;182(2):519-28. doi: 10.1534/genetics.109.101196. Epub 2009 Mar 23.

10.

OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L.

Song Z, Chen H, Fiket M, Alexander C, Chan DC.

J Cell Biol. 2007 Aug 27;178(5):749-55. Epub 2007 Aug 20.

11.

Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia.

Atorino L, Silvestri L, Koppen M, Cassina L, Ballabio A, Marconi R, Langer T, Casari G.

J Cell Biol. 2003 Nov 24;163(4):777-87. Epub 2003 Nov 17.

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