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Journal Abstract Search
312 related items for PubMed ID: 32189241
1. Hearing impairment-associated KARS mutations lead to defects in aminoacylation of both cytoplasmic and mitochondrial tRNALys. Wang Y, Zhou JB, Zeng QY, Wu S, Xue MQ, Fang P, Wang ED, Zhou XL. Sci China Life Sci; 2020 Aug; 63(8):1227-1239. PubMed ID: 32189241 [Abstract] [Full Text] [Related]
4. Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency. Almalki A, Alston CL, Parker A, Simonic I, Mehta SG, He L, Reza M, Oliveira JM, Lightowlers RN, McFarland R, Taylor RW, Chrzanowska-Lightowlers ZM. Biochim Biophys Acta; 2014 Jan; 1842(1):56-64. PubMed ID: 24161539 [Abstract] [Full Text] [Related]
5. Association of mitochondrial Lysyl-tRNA synthetase with HIV-1 GagPol involves catalytic domain of the synthetase and transframe and integrase domains of Pol. Kobbi L, Octobre G, Dias J, Comisso M, Mirande M. J Mol Biol; 2011 Jul 29; 410(5):875-86. PubMed ID: 21763493 [Abstract] [Full Text] [Related]
6. Mutations in KARS cause a severe neurological and neurosensory disease with optic neuropathy. Scheidecker S, Bär S, Stoetzel C, Geoffroy V, Lannes B, Rinaldi B, Fischer F, Becker HD, Pelletier V, Pagan C, Acquaviva-Bourdain C, Kremer S, Mirande M, Tranchant C, Muller J, Friant S, Dollfus H. Hum Mutat; 2019 Oct 29; 40(10):1826-1840. PubMed ID: 31116475 [Abstract] [Full Text] [Related]
11. Mutations in KARS cause early-onset hearing loss and leukoencephalopathy: Potential pathogenic mechanism. Zhou XL, He LX, Yu LJ, Wang Y, Wang XJ, Wang ED, Yang T. Hum Mutat; 2017 Dec 29; 38(12):1740-1750. PubMed ID: 28887846 [Abstract] [Full Text] [Related]