Structural modeling of tissue-specific mitochondrial alanyl-tRNA synthetase (AARS2) defects predicts differential effects on aminoacylation-Reference-Cited by-同舟云学术

Structural modeling of tissue-specific mitochondrial alanyl-tRNA synthetase (AARS2) defects predicts differential effects on aminoacylation

Published:2015-02-06 Issue: Volume:6 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Euro Liliya,Konovalova Svetlana,Asin-Cayuela Jorge,Tulinius MÃ¡r,Griffin Helen,Horvath Rita,Taylor Robert W.,Chinnery Patrick F.,Schara Ulrike,Thorburn David R.,Suomalainen Anu,Chihade Joseph,Tyynismaa Henna

Publisher

Frontiers Media SA

Subject

Genetics(clinical),Genetics,Molecular Medicine

Reference36 articles.

1. Mitochondrial EFTs defects in juvenile-onset Leigh disease, ataxia, neuropathy, and optic atrophy.;Ahola;Neurology,2014

2. Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans.;Bayat;PLoS Biol.,2012

3. Elucidation of tRNA-dependent editing by a class II tRNA synthetase and significance for cell viability.;Beebe;EMBO J.,2003

4. Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndrome.;Belostotsky;Am. J. Hum. Genet.,2011

5. Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing.;Calvo;Sci. Transl. Med.,2012

Cited by 50 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. AARS2 ameliorates myocardial ischemia via fine-tuning PKM2-mediated metabolism;2024-08-15

2. AARS2 ameliorates myocardial ischemia via fine-tuning PKM2-mediated metabolism;2024-08-15

3. AARS2 ameliorates myocardial ischemiaviafine-tuning PKM2-mediated metabolism;2024-06-05

4. Hypoxia induces mitochondrial protein lactylation to limit oxidative phosphorylation;Cell Research;2024-01-02

5. Mitochondrial aminoacyl-tRNA synthetases trigger unique compensatory mechanisms in neurons;Human Molecular Genetics;2023-11-17