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Journal Abstract Search

162 related items for PubMed ID: 11919191

  • 1. The 7472insC mitochondrial DNA mutation impairs the synthesis and extent of aminoacylation of tRNASer(UCN) but not its structure or rate of turnover.
    Toompuu M, Yasukawa T, Suzuki T, Hakkinen T, Spelbrink JN, Watanabe K, Jacobs HT.
    J Biol Chem; 2002 Jun 21; 277(25):22240-50. PubMed ID: 11919191
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  • 3. Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNASer(UCN) 7511A>G mutation.
    Fan W, Zheng J, Kong W, Cui L, Aishanjiang M, Yi Q, Wang M, Cang X, Tang X, Chen Y, Mo JQ, Sondheimer N, Ge W, Guan MX.
    J Biol Chem; 2019 Dec 13; 294(50):19292-19305. PubMed ID: 31685661
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  • 4. The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.
    Guan MX, Enriquez JA, Fischel-Ghodsian N, Puranam RS, Lin CP, Maw MA, Attardi G.
    Mol Cell Biol; 1998 Oct 13; 18(10):5868-79. PubMed ID: 9742104
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  • 7. Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafness.
    Li X, Fischel-Ghodsian N, Schwartz F, Yan Q, Friedman RA, Guan MX.
    Nucleic Acids Res; 2004 Oct 13; 32(3):867-77. PubMed ID: 14960712
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  • 8. The 7472insC mtDNA mutation impairs 5' and 3' processing of tRNA(Ser(UCN)).
    Toompuu M, Levinger LL, Nadal A, Gomez J, Jacobs HT.
    Biochem Biophys Res Commun; 2004 Sep 24; 322(3):803-13. PubMed ID: 15336535
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  • 9. A deafness-associated mitochondrial DNA mutation altered the tRNASer(UCN) metabolism and mitochondrial function.
    Xue L, Chen Y, Tang X, Yao J, Huang H, Wang M, Ye S, Wang M, Guan MX.
    Mitochondrion; 2019 May 24; 46():370-379. PubMed ID: 30336267
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  • 10. Biochemical characterization of the deafness-associated mitochondrial tRNASer(UCN) A7445G mutation in osteosarcoma cell cybrids.
    Li X, Zhang LS, Fischel-Ghodsian N, Guan MX.
    Biochem Biophys Res Commun; 2005 Mar 11; 328(2):491-8. PubMed ID: 15694374
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  • 11. Mytilus mitochondrial DNA contains a functional gene for a tRNASer(UCN) with a dihydrouridine arm-replacement loop and a pseudo-tRNASer(UCN) gene.
    Beagley CT, Okimoto R, Wolstenholme DR.
    Genetics; 1999 Jun 11; 152(2):641-52. PubMed ID: 10353906
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  • 16. A mitochondrial myopathy-associated tRNASer(UCN) 7453G>A mutation alters tRNA metabolism and mitochondrial function.
    Lin Y, Xu X, Wang W, Liu F, Zhao D, Li D, Ji K, Li W, Zhao Y, Yan C.
    Mitochondrion; 2021 Mar 11; 57():1-8. PubMed ID: 33279600
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  • 17. Mitochondrial tRNASer(UCN) 7471delC may be a novel mutation associated with maternally transmitted hypertension.
    Yang P, Wu P, Liu X, Feng J, Zheng S, Wang Y, Fan Z.
    Ir J Med Sci; 2020 May 11; 189(2):489-496. PubMed ID: 31776834
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  • 18. Translation activity of mitochondrial tRNA with unusual secondary structure.
    Hanada T, Suzuki T, Watanabe K.
    Nucleic Acids Symp Ser; 2000 May 11; (44):249-50. PubMed ID: 12903362
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  • 19. Asymmetrical effects of deafness-associated mitochondrial DNA 7516delA mutation on the processing of RNAs in the H-strand and L-strand polycistronic transcripts.
    Xiao Y, Wang M, He Q, Xu L, Zhang Q, Meng F, Jia Z, Zhang F, Wang H, Guan MX.
    Nucleic Acids Res; 2020 Nov 04; 48(19):11113-11129. PubMed ID: 33045734
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