Correspondence on “Treatment of ARS deficiencies with specific amino acids” by Kok et al
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical)
Reference9 articles.
1. Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V;Antonellis;Am J Hum Genet,2003
2. Kok G, Tseng L, Schene IF, et al. Treatment of ARS deficiencies with specific amino acids. Genet Med. Published online June 30, 2021 June. https://doi.org/10.1038/s41436-021-01249-z.
3. Newly acquired N-terminal extension targets threonyl-tRNA synthetase-like protein into the multiple tRNA synthetase complex;Zhou;Nucleic Acids Res,2019
4. Reinvestigation of aminoacyl-tRNA synthetase core complex by affinity purification-mass spectrometry reveals TARSL2 as a potential member of the complex;Kim;PLoS One,2013
5. Expression of the aminoacyl-tRNA synthetase complex in cultured Chinese hamster ovary cells. Specific depression of the methionyl-tRNA synthetase component upon methionine restriction;Lazard;J Biol Chem,1987
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1. Investigation in yeast of novel variants in mitochondrial aminoacyl-tRNA synthetases WARS2, NARS2, and RARS2 genes associated with mitochondrial diseases;Human Molecular Genetics;2024-06-30
2. Physiological and engineered tRNA aminoacylation;WIREs RNA;2023-04-12
3. Response to Shen et al.;Genetics in Medicine;2022-02
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