258 related articles for article (PubMed ID: 30737337)
81. Vanishing white matter: a leukodystrophy due to astrocytic dysfunction.
Bugiani M; Vuong C; Breur M; van der Knaap MS
Brain Pathol; 2018 May; 28(3):408-421. PubMed ID: 29740943
[TBL] [Abstract][Full Text] [Related]
82. Human mitochondrial tRNA quality control in health and disease: a channelling mechanism?
Belostotsky R; Frishberg Y; Entelis N
RNA Biol; 2012 Jan; 9(1):33-9. PubMed ID: 22258151
[TBL] [Abstract][Full Text] [Related]
83. A deafness-associated tRNA mutation caused pleiotropic effects on the m1G37 modification, processing, stability and aminoacylation of tRNAIle and mitochondrial translation.
Meng F; Zhou M; Xiao Y; Mao X; Zheng J; Lin J; Lin T; Ye Z; Cang X; Fu Y; Wang M; Guan MX
Nucleic Acids Res; 2021 Jan; 49(2):1075-1093. PubMed ID: 33398350
[TBL] [Abstract][Full Text] [Related]
84. 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]
85. Kinetic Origin of Substrate Specificity in Post-Transfer Editing by Leucyl-tRNA Synthetase.
Dulic M; Cvetesic N; Zivkovic I; Palencia A; Cusack S; Bertosa B; Gruic-Sovulj I
J Mol Biol; 2018 Jan; 430(1):1-16. PubMed ID: 29111343
[TBL] [Abstract][Full Text] [Related]
86. A Quantitative Spectrophotometric Assay to Monitor the tRNA-Dependent Pathway for Lipid Aminoacylation In Vitro.
Grube CD; Roy H
J Biomol Screen; 2016 Aug; 21(7):722-8. PubMed ID: 27073192
[TBL] [Abstract][Full Text] [Related]
87. Archaeal evidence for the role of 2' aminoacylation of RNA in the origin of amino acid homochirality.
Bailey JM
Biochem Soc Trans; 1998 Aug; 26(3):S262. PubMed ID: 9765981
[No Abstract] [Full Text] [Related]
88. Anticodon recognition and discrimination by the alpha-helix cage domain of class I lysyl-tRNA synthetase.
Levengood JD; Roy H; Ishitani R; Söll D; Nureki O; Ibba M
Biochemistry; 2007 Oct; 46(39):11033-8. PubMed ID: 17760422
[TBL] [Abstract][Full Text] [Related]
89. A Label-Free Assay for Aminoacylation of tRNA.
Gamper H; Hou YM
Genes (Basel); 2020 Oct; 11(10):. PubMed ID: 33036365
[TBL] [Abstract][Full Text] [Related]
90. Biallelic pathogenic variants in
Macintosh J; Perrier S; Pinard M; Tran LT; Guerrero K; Prasad C; Prasad AN; Pastinen T; Thiffault I; Coulombe B; Bernard G
Front Neurol; 2023; 14():1254140. PubMed ID: 37915380
[TBL] [Abstract][Full Text] [Related]
91. LARS2 Regulates Apoptosis via ROS-Mediated Mitochondrial Dysfunction and Endoplasmic Reticulum Stress in Ovarian Granulosa Cells.
Feng S; Wan S; Liu S; Wang W; Tang M; Bai L; Zhu Y
Oxid Med Cell Longev; 2022; 2022():5501346. PubMed ID: 35585880
[TBL] [Abstract][Full Text] [Related]
92. Neuronal ablation of mt-AspRS in mice induces immune pathway activation prior to severe and progressive cortical and behavioral disruption.
Nemeth CL; Tomlinson SN; Rosen M; O'Brien BM; Larraza O; Jain M; Murray CF; Marx JS; Delannoy M; Fine AS; Wu D; Trifunovic A; Fatemi A
Exp Neurol; 2020 Apr; 326():113164. PubMed ID: 31887305
[TBL] [Abstract][Full Text] [Related]
93. Genomic sequencing highlights the diverse molecular causes of Perrault syndrome: a peroxisomal disorder (PEX6), metabolic disorders (CLPP, GGPS1), and mtDNA maintenance/translation disorders (LARS2, TFAM).
Tucker EJ; Rius R; Jaillard S; Bell K; Lamont PJ; Travessa A; Dupont J; Sampaio L; Dulon J; Vuillaumier-Barrot S; Whalen S; Isapof A; Stojkovic T; Quijano-Roy S; Robevska G; van den Bergen J; Hanna C; Simpson A; Ayers K; Thorburn DR; Christodoulou J; Touraine P; Sinclair AH
Hum Genet; 2020 Oct; 139(10):1325-1343. PubMed ID: 32399598
[TBL] [Abstract][Full Text] [Related]
94. Escherichia coli K-12 lysyl-tRNA synthetase mutant with a novel reversion pattern.
Hirshfield IN; Tenreiro R; Vanbogelen RA; Neidhardt FC
J Bacteriol; 1984 May; 158(2):615-20. PubMed ID: 6373723
[TBL] [Abstract][Full Text] [Related]
95. An Application of NGS for Molecular Investigations in Perrault Syndrome: Study of 14 Families and Review of the Literature.
Lerat J; Jonard L; Loundon N; Christin-Maitre S; Lacombe D; Goizet C; Rouzier C; Van Maldergem L; Gherbi S; Garabedian EN; Bonnefont JP; Touraine P; Mosnier I; Munnich A; Denoyelle F; Marlin S
Hum Mutat; 2016 Dec; 37(12):1354-1362. PubMed ID: 27650058
[TBL] [Abstract][Full Text] [Related]
96. SURF-1 gene mutation associated with leukoencephalopathy in a 2-year-old.
Timothy J; Geller T
J Child Neurol; 2009 Oct; 24(10):1296-301. PubMed ID: 19805825
[TBL] [Abstract][Full Text] [Related]
97. Leukoencephalopathy with brain stem and spinal cord involvement and high lactate: a genetically proven case without elevated white matter lactate.
Sharma S; Sankhyan N; Kumar A; Scheper GC; van der Knaap MS; Gulati S
J Child Neurol; 2011 Jun; 26(6):773-6. PubMed ID: 21493805
[TBL] [Abstract][Full Text] [Related]
98. Mitochondrial aminoacyl-tRNA synthetase single-nucleotide polymorphisms that lead to defects in refolding but not aminoacylation.
Banerjee R; Reynolds NM; Yadavalli SS; Rice C; Roy H; Banerjee P; Alexander RW; Ibba M
J Mol Biol; 2011 Jul; 410(2):280-93. PubMed ID: 21601574
[TBL] [Abstract][Full Text] [Related]
99. New insights into the phenotype of FARS2 deficiency.
Vantroys E; Larson A; Friederich M; Knight K; Swanson MA; Powell CA; Smet J; Vergult S; De Paepe B; Seneca S; Roeyers H; Menten B; Minczuk M; Vanlander A; Van Hove J; Van Coster R
Mol Genet Metab; 2017 Dec; 122(4):172-181. PubMed ID: 29126765
[TBL] [Abstract][Full Text] [Related]
100. Functional significance of aminoacyl-tRNA synthetase complex in the aminoacylation of tRNA(Leu) isoacceptors.
Lindqvist L; Mäenpää PH; Pösö AR
Biochem Biophys Res Commun; 1989 Aug; 163(1):513-9. PubMed ID: 2775284
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
