536 related articles for article (PubMed ID: 20396601)
1. Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficiencies.
Smits P; Smeitink J; van den Heuvel L
J Biomed Biotechnol; 2010; 2010():737385. PubMed ID: 20396601
[TBL] [Abstract][Full Text] [Related]
2. Bi-allelic Mutations in the Mitochondrial Ribosomal Protein MRPS2 Cause Sensorineural Hearing Loss, Hypoglycemia, and Multiple OXPHOS Complex Deficiencies.
Gardeitchik T; Mohamed M; Ruzzenente B; Karall D; Guerrero-Castillo S; Dalloyaux D; van den Brand M; van Kraaij S; van Asbeck E; Assouline Z; Rio M; de Lonlay P; Scholl-Buergi S; Wolthuis DFGJ; Hoischen A; Rodenburg RJ; Sperl W; Urban Z; Brandt U; Mayr JA; Wong S; de Brouwer APM; Nijtmans L; Munnich A; Rötig A; Wevers RA; Metodiev MD; Morava E
Am J Hum Genet; 2018 Apr; 102(4):685-695. PubMed ID: 29576219
[TBL] [Abstract][Full Text] [Related]
3. Blackout in the powerhouse: clinical phenotypes associated with defects in the assembly of OXPHOS complexes and the mitoribosome.
Hock DH; Robinson DRL; Stroud DA
Biochem J; 2020 Nov; 477(21):4085-4132. PubMed ID: 33151299
[TBL] [Abstract][Full Text] [Related]
4. The effect of small molecules on nuclear-encoded translation diseases.
Soiferman D; Ayalon O; Weissman S; Saada A
Biochimie; 2014 May; 100():184-91. PubMed ID: 24012549
[TBL] [Abstract][Full Text] [Related]
5. Loss of COX4I1 Leads to Combined Respiratory Chain Deficiency and Impaired Mitochondrial Protein Synthesis.
Čunátová K; Reguera DP; Vrbacký M; Fernández-Vizarra E; Ding S; Fearnley IM; Zeviani M; Houštěk J; Mráček T; Pecina P
Cells; 2021 Feb; 10(2):. PubMed ID: 33578848
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways.
Tang JX; Thompson K; Taylor RW; Oláhová M
Int J Mol Sci; 2020 May; 21(11):. PubMed ID: 32481479
[TBL] [Abstract][Full Text] [Related]
7. Mitochondrial Diseases Part I: mouse models of OXPHOS deficiencies caused by defects in respiratory complex subunits or assembly factors.
Torraco A; Peralta S; Iommarini L; Diaz F
Mitochondrion; 2015 Mar; 21():76-91. PubMed ID: 25660179
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial medicine: a metabolic perspective on the pathology of oxidative phosphorylation disorders.
Smeitink JA; Zeviani M; Turnbull DM; Jacobs HT
Cell Metab; 2006 Jan; 3(1):9-13. PubMed ID: 16399500
[TBL] [Abstract][Full Text] [Related]
9. Mutation in subdomain G' of mitochondrial elongation factor G1 is associated with combined OXPHOS deficiency in fibroblasts but not in muscle.
Smits P; Antonicka H; van Hasselt PM; Weraarpachai W; Haller W; Schreurs M; Venselaar H; Rodenburg RJ; Smeitink JA; van den Heuvel LP
Eur J Hum Genet; 2011 Mar; 19(3):275-9. PubMed ID: 21119709
[TBL] [Abstract][Full Text] [Related]
10. Synchronized mitochondrial and cytosolic translation programs.
Couvillion MT; Soto IC; Shipkovenska G; Churchman LS
Nature; 2016 May; 533(7604):499-503. PubMed ID: 27225121
[TBL] [Abstract][Full Text] [Related]
11. Plasticity of Mitochondrial Translation.
Dennerlein S; Wang C; Rehling P
Trends Cell Biol; 2017 Oct; 27(10):712-721. PubMed ID: 28606446
[TBL] [Abstract][Full Text] [Related]
12. Fyn kinase regulates translation in mammalian mitochondria.
Koc EC; Miller-Lee JL; Koc H
Biochim Biophys Acta Gen Subj; 2017 Mar; 1861(3):533-540. PubMed ID: 27940153
[TBL] [Abstract][Full Text] [Related]
13. An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defect.
Janer A; Antonicka H; Lalonde E; Nishimura T; Sasarman F; Brown GK; Brown RM; Majewski J; Shoubridge EA
Am J Hum Genet; 2012 Oct; 91(4):737-43. PubMed ID: 23022098
[TBL] [Abstract][Full Text] [Related]
14. Sequence variants in four candidate genes (NIPSNAP1, GBAS, CHCHD1 and METT11D1) in patients with combined oxidative phosphorylation system deficiencies.
Smits P; Rodenburg RJ; Smeitink JA; van den Heuvel LP
J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S13-9. PubMed ID: 24137763
[TBL] [Abstract][Full Text] [Related]
15. Mitochondrial disorders due to nuclear OXPHOS gene defects.
Ugalde C; Morán M; Blázquez A; Arenas J; Martín MA
Adv Exp Med Biol; 2009; 652():85-116. PubMed ID: 20225021
[TBL] [Abstract][Full Text] [Related]
16. Mitochondria: mitochondrial OXPHOS (dys) function ex vivo--the use of primary fibroblasts.
Saada A
Int J Biochem Cell Biol; 2014 Mar; 48():60-5. PubMed ID: 24412346
[TBL] [Abstract][Full Text] [Related]
17. MTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary intervention.
Tischner C; Hofer A; Wulff V; Stepek J; Dumitru I; Becker L; Haack T; Kremer L; Datta AN; Sperl W; Floss T; Wurst W; Chrzanowska-Lightowlers Z; De Angelis MH; Klopstock T; Prokisch H; Wenz T
Hum Mol Genet; 2015 Apr; 24(8):2247-66. PubMed ID: 25552653
[TBL] [Abstract][Full Text] [Related]
18. Combined defects in oxidative phosphorylation and fatty acid β-oxidation in mitochondrial disease.
Nsiah-Sefaa A; McKenzie M
Biosci Rep; 2016 Feb; 36(2):. PubMed ID: 26839416
[TBL] [Abstract][Full Text] [Related]
19. Balanced mitochondrial and cytosolic translatomes underlie the biogenesis of human respiratory complexes.
Soto I; Couvillion M; Hansen KG; McShane E; Moran JC; Barrientos A; Churchman LS
Genome Biol; 2022 Aug; 23(1):170. PubMed ID: 35945592
[TBL] [Abstract][Full Text] [Related]
20. Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency.
Ugalde C; Janssen RJ; van den Heuvel LP; Smeitink JA; Nijtmans LG
Hum Mol Genet; 2004 Mar; 13(6):659-67. PubMed ID: 14749350
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]