225 related articles for article (PubMed ID: 30262995)
1. Overexpression of human mitochondrial alanyl-tRNA synthetase suppresses biochemical defects of the mt-tRNA
Zhao X; Han J; Zhu L; Xiao Y; Wang C; Hong F; Jiang P; Guan MX
Int J Biol Sci; 2018; 14(11):1437-1444. PubMed ID: 30262995
[TBL] [Abstract][Full Text] [Related]
2. Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNA
Gong S; Wang X; Meng F; Cui L; Yi Q; Zhao Q; Cang X; Cai Z; Mo JQ; Liang Y; Guan MX
J Biol Chem; 2020 Jan; 295(4):940-954. PubMed ID: 31819004
[TBL] [Abstract][Full Text] [Related]
3. Novel alanyl-tRNA synthetase 2 (AARS2) homozygous mutation in a consanguineous Chinese family with premature ovarian insufficiency.
Zhou Y; Chen B; Li L; Pan H; Liu B; Li T; Wang R; Ma X; Wang B; Cao Y
Fertil Steril; 2019 Sep; 112(3):569-576.e2. PubMed ID: 31280959
[TBL] [Abstract][Full Text] [Related]
4. Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy.
Sommerville EW; Zhou XL; Oláhová M; Jenkins J; Euro L; Konovalova S; Hilander T; Pyle A; He L; Habeebu S; Saunders C; Kelsey A; Morris AAM; McFarland R; Suomalainen A; Gorman GS; Wang ED; Thiffault I; Tyynismaa H; Taylor RW
Hum Mol Genet; 2019 Jan; 28(2):258-268. PubMed ID: 30285085
[TBL] [Abstract][Full Text] [Related]
5. Human mitochondrial leucyl tRNA synthetase can suppress non cognate pathogenic mt-tRNA mutations.
Hornig-Do HT; Montanari A; Rozanska A; Tuppen HA; Almalki AA; Abg-Kamaludin DP; Frontali L; Francisci S; Lightowlers RN; Chrzanowska-Lightowlers ZM
EMBO Mol Med; 2014 Feb; 6(2):183-93. PubMed ID: 24413189
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial aminoacyl-tRNA synthetase disorders: an emerging group of developmental disorders of myelination.
Fine AS; Nemeth CL; Kaufman ML; Fatemi A
J Neurodev Disord; 2019 Dec; 11(1):29. PubMed ID: 31839000
[TBL] [Abstract][Full Text] [Related]
7. Expression of Arabidopsis thaliana mitochondrial alanyl-tRNA synthetase is not sufficient to trigger mitochondrial import of tRNAAla in yeast.
Mireau H; Cosset A; Marechal-Drouard L; Fox TD; Small ID; Dietrich A
J Biol Chem; 2000 May; 275(18):13291-6. PubMed ID: 10788435
[TBL] [Abstract][Full Text] [Related]
8. A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function.
Wang M; Peng Y; Zheng J; Zheng B; Jin X; Liu H; Wang Y; Tang X; Huang T; Jiang P; Guan MX
Nucleic Acids Res; 2016 Dec; 44(22):10974-10985. PubMed ID: 27536005
[TBL] [Abstract][Full Text] [Related]
9. A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function.
Jiang P; Wang M; Xue L; Xiao Y; Yu J; Wang H; Yao J; Liu H; Peng Y; Liu H; Li H; Chen Y; Guan MX
Mol Cell Biol; 2016 Jul; 36(14):1920-30. PubMed ID: 27161322
[TBL] [Abstract][Full Text] [Related]
10. Allosteric interaction of nucleotides and tRNA(ala) with E. coli alanyl-tRNA synthetase.
Dignam JD; Guo J; Griffith WP; Garbett NC; Holloway A; Mueser T
Biochemistry; 2011 Nov; 50(45):9886-900. PubMed ID: 21985608
[TBL] [Abstract][Full Text] [Related]
11. Mechanistic insights into mitochondrial tRNA
Ji Y; Nie Z; Meng F; Hu C; Chen H; Jin L; Chen M; Zhang M; Zhang J; Liang M; Wang M; Guan MX
J Biol Chem; 2021 Jul; 297(1):100816. PubMed ID: 34023389
[TBL] [Abstract][Full Text] [Related]
12. Translocation within the acceptor helix of a major tRNA identity determinant.
Lovato MA; Chihade JW; Schimmel P
EMBO J; 2001 Sep; 20(17):4846-53. PubMed ID: 11532948
[TBL] [Abstract][Full Text] [Related]
13. Editing activity for eliminating mischarged tRNAs is essential in mammalian mitochondria.
Hilander T; Zhou XL; Konovalova S; Zhang FP; Euro L; Chilov D; Poutanen M; Chihade J; Wang ED; Tyynismaa H
Nucleic Acids Res; 2018 Jan; 46(2):849-860. PubMed ID: 29228266
[TBL] [Abstract][Full Text] [Related]
14. Suppression of temperature-sensitive aminoacyl-tRNA synthetase mutations by ribosomal mutations: a possible mechanism.
Buckel P; Piepersberg W; Böck A
Mol Gen Genet; 1976 Nov; 149(1):51-61. PubMed ID: 796671
[TBL] [Abstract][Full Text] [Related]
15. Structural modeling of tissue-specific mitochondrial alanyl-tRNA synthetase (AARS2) defects predicts differential effects on aminoacylation.
Euro L; Konovalova S; Asin-Cayuela J; Tulinius M; Griffin H; Horvath R; Taylor RW; Chinnery PF; Schara U; Thorburn DR; Suomalainen A; Chihade J; Tyynismaa H
Front Genet; 2015; 6():21. PubMed ID: 25705216
[TBL] [Abstract][Full Text] [Related]
16. Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy.
Götz A; Tyynismaa H; Euro L; Ellonen P; Hyötyläinen T; Ojala T; Hämäläinen RH; Tommiska J; Raivio T; Oresic M; Karikoski R; Tammela O; Simola KO; Paetau A; Tyni T; Suomalainen A
Am J Hum Genet; 2011 May; 88(5):635-42. PubMed ID: 21549344
[TBL] [Abstract][Full Text] [Related]
17. Fine-Tuning of Alanyl-tRNA Synthetase Quality Control Alleviates Global Dysregulation of the Proteome.
Kelly P; Kavoor A; Ibba M
Genes (Basel); 2020 Oct; 11(10):. PubMed ID: 33081015
[TBL] [Abstract][Full Text] [Related]
18. Isoleucyl-tRNA synthetase levels modulate the penetrance of a homoplasmic m.4277T>C mitochondrial tRNA(Ile) mutation causing hypertrophic cardiomyopathy.
Perli E; Giordano C; Tuppen HA; Montopoli M; Montanari A; Orlandi M; Pisano A; Catanzaro D; Caparrotta L; Musumeci B; Autore C; Morea V; Di Micco P; Campese AF; Leopizzi M; Gallo P; Francisci S; Frontali L; Taylor RW; d'Amati G
Hum Mol Genet; 2012 Jan; 21(1):85-100. PubMed ID: 21945886
[TBL] [Abstract][Full Text] [Related]
19. Role of Mutations of Mitochondrial Aminoacyl-tRNA Synthetases Genes on Epileptogenesis.
Kong LY; Wu YZ; Cheng RQ; Wang PH; Peng BW
Mol Neurobiol; 2023 Sep; 60(9):5482-5492. PubMed ID: 37316759
[TBL] [Abstract][Full Text] [Related]
20. Phenotypic diversity of brain MRI patterns in mitochondrial aminoacyl-tRNA synthetase mutations.
Roux CJ; Barcia G; Schiff M; Sissler M; Levy R; Dangouloff-Ros V; Desguerre I; Edvardson S; Elpeleg O; Rötig A; Munnich A; Boddaert N
Mol Genet Metab; 2021 Jun; 133(2):222-229. PubMed ID: 33972171
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
