306 related articles for article (PubMed ID: 32818253)
1. Posttranscriptional modifications in mitochondrial tRNA and its implication in mitochondrial translation and disease.
Kazuhito T; Wei FY
J Biochem; 2020 Nov; 168(5):435-444. PubMed ID: 32818253
[TBL] [Abstract][Full Text] [Related]
2. Human mitochondrial diseases caused by lack of taurine modification in mitochondrial tRNAs.
Suzuki T; Nagao A; Suzuki T
Wiley Interdiscip Rev RNA; 2011; 2(3):376-86. PubMed ID: 21957023
[TBL] [Abstract][Full Text] [Related]
3. Defective Mitochondrial tRNA Taurine Modification Activates Global Proteostress and Leads to Mitochondrial Disease.
Fakruddin M; Wei FY; Suzuki T; Asano K; Kaieda T; Omori A; Izumi R; Fujimura A; Kaitsuka T; Miyata K; Araki K; Oike Y; Scorrano L; Suzuki T; Tomizawa K
Cell Rep; 2018 Jan; 22(2):482-496. PubMed ID: 29320742
[TBL] [Abstract][Full Text] [Related]
4. Human mitochondrial diseases associated with tRNA wobble modification deficiency.
Kirino Y; Suzuki T
RNA Biol; 2005 Apr; 2(2):41-4. PubMed ID: 17132941
[TBL] [Abstract][Full Text] [Related]
5. Taurine as a constituent of mitochondrial tRNAs: new insights into the functions of taurine and human mitochondrial diseases.
Suzuki T; Suzuki T; Wada T; Saigo K; Watanabe K
EMBO J; 2002 Dec; 21(23):6581-9. PubMed ID: 12456664
[TBL] [Abstract][Full Text] [Related]
6. The mitochondrial epitranscriptome: the roles of RNA modifications in mitochondrial translation and human disease.
Bohnsack MT; Sloan KE
Cell Mol Life Sci; 2018 Jan; 75(2):241-260. PubMed ID: 28752201
[TBL] [Abstract][Full Text] [Related]
7. Human transfer RNA modopathies: diseases caused by aberrations in transfer RNA modifications.
Chujo T; Tomizawa K
FEBS J; 2021 Dec; 288(24):7096-7122. PubMed ID: 33513290
[TBL] [Abstract][Full Text] [Related]
8. Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases.
Suzuki T; Nagao A; Suzuki T
Annu Rev Genet; 2011; 45():299-329. PubMed ID: 21910628
[TBL] [Abstract][Full Text] [Related]
9. Complete chemical structures of human mitochondrial tRNAs.
Suzuki T; Yashiro Y; Kikuchi I; Ishigami Y; Saito H; Matsuzawa I; Okada S; Mito M; Iwasaki S; Ma D; Zhao X; Asano K; Lin H; Kirino Y; Sakaguchi Y; Suzuki T
Nat Commun; 2020 Aug; 11(1):4269. PubMed ID: 32859890
[TBL] [Abstract][Full Text] [Related]
10. Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease.
Asano K; Suzuki T; Saito A; Wei FY; Ikeuchi Y; Numata T; Tanaka R; Yamane Y; Yamamoto T; Goto T; Kishita Y; Murayama K; Ohtake A; Okazaki Y; Tomizawa K; Sakaguchi Y; Suzuki T
Nucleic Acids Res; 2018 Feb; 46(4):1565-1583. PubMed ID: 29390138
[TBL] [Abstract][Full Text] [Related]
11. Cdk5rap1-mediated 2-methylthio modification of mitochondrial tRNAs governs protein translation and contributes to myopathy in mice and humans.
Wei FY; Zhou B; Suzuki T; Miyata K; Ujihara Y; Horiguchi H; Takahashi N; Xie P; Michiue H; Fujimura A; Kaitsuka T; Matsui H; Koga Y; Mohri S; Suzuki T; Oike Y; Tomizawa K
Cell Metab; 2015 Mar; 21(3):428-42. PubMed ID: 25738458
[TBL] [Abstract][Full Text] [Related]
12. Wobble modification deficiency in mutant tRNAs in patients with mitochondrial diseases.
Yasukawa T; Kirino Y; Ishii N; Holt IJ; Jacobs HT; Makifuchi T; Fukuhara N; Ohta S; Suzuki T; Watanabe K
FEBS Lett; 2005 May; 579(13):2948-52. PubMed ID: 15893315
[TBL] [Abstract][Full Text] [Related]
13. Disease-associated mutations in mitochondrial precursor tRNAs affect binding, m1R9 methylation, and tRNA processing by mtRNase P.
Karasik A; Wilhelm CA; Fierke CA; Koutmos M
RNA; 2021 Apr; 27(4):420-432. PubMed ID: 33380464
[TBL] [Abstract][Full Text] [Related]
14. A complete landscape of post-transcriptional modifications in mammalian mitochondrial tRNAs.
Suzuki T; Suzuki T
Nucleic Acids Res; 2014 Jun; 42(11):7346-57. PubMed ID: 24831542
[TBL] [Abstract][Full Text] [Related]
15. Cooperativity between different tRNA modifications and their modification pathways.
Sokołowski M; Klassen R; Bruch A; Schaffrath R; Glatt S
Biochim Biophys Acta Gene Regul Mech; 2018 Apr; 1861(4):409-418. PubMed ID: 29222069
[TBL] [Abstract][Full Text] [Related]
16. Mitochondria-specific RNA-modifying enzymes responsible for the biosynthesis of the wobble base in mitochondrial tRNAs. Implications for the molecular pathogenesis of human mitochondrial diseases.
Umeda N; Suzuki T; Yukawa M; Ohya Y; Shindo H; Watanabe K; Suzuki T
J Biol Chem; 2005 Jan; 280(2):1613-24. PubMed ID: 15509579
[TBL] [Abstract][Full Text] [Related]
17. TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated with Multiple Respiratory-Chain Deficiencies.
Powell CA; Kopajtich R; D'Souza AR; Rorbach J; Kremer LS; Husain RA; Dallabona C; Donnini C; Alston CL; Griffin H; Pyle A; Chinnery PF; Strom TM; Meitinger T; Rodenburg RJ; Schottmann G; Schuelke M; Romain N; Haller RG; Ferrero I; Haack TB; Taylor RW; Prokisch H; Minczuk M
Am J Hum Genet; 2015 Aug; 97(2):319-28. PubMed ID: 26189817
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial Aminoacyl-tRNA Synthetase and Disease: The Yeast Contribution for Functional Analysis of Novel Variants.
Figuccia S; Degiorgi A; Ceccatelli Berti C; Baruffini E; Dallabona C; Goffrini P
Int J Mol Sci; 2021 Apr; 22(9):. PubMed ID: 33926074
[TBL] [Abstract][Full Text] [Related]
19. Mitochondrial tRNA import and its consequences for mitochondrial translation.
Schneider A
Annu Rev Biochem; 2011; 80():1033-53. PubMed ID: 21417719
[TBL] [Abstract][Full Text] [Related]
20. The ROS-sensitive microRNA-9/9* controls the expression of mitochondrial tRNA-modifying enzymes and is involved in the molecular mechanism of MELAS syndrome.
Meseguer S; Martínez-Zamora A; García-Arumí E; Andreu AL; Armengod ME
Hum Mol Genet; 2015 Jan; 24(1):167-84. PubMed ID: 25149473
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
