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Journal Abstract Search

316 related items for PubMed ID: 33398350

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  • 2. A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function.
    Zhou M, Xue L, Chen Y, Li H, He Q, Wang B, Meng F, Wang M, Guan MX.
    J Biol Chem; 2018 Jan 26; 293(4):1425-1438. PubMed ID: 29222331
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  • 8. Isoleucylation properties of native human mitochondrial tRNAIle and tRNAIle transcripts. Implications for cardiomyopathy-related point mutations (4269, 4317) in the tRNAIle gene.
    Degoul F, Brulé H, Cepanec C, Helm M, Marsac C, Leroux J, Giegé R, Florentz C.
    Hum Mol Genet; 1998 Mar 26; 7(3):347-54. PubMed ID: 9466989
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  • 9. 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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  • 10. 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 13; 46():370-379. PubMed ID: 30336267
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  • 12. A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR).
    Zhou M, Wang M, Xue L, Lin Z, He Q, Shi W, Chen Y, Jin X, Li H, Jiang P, Guan MX.
    J Biol Chem; 2017 Aug 25; 292(34):13934-13946. PubMed ID: 28679533
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  • 14. [Mitochondrial tRNAIle A4317G mutation may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation].
    Liang LZ, Wu Y, Yang YL, Cai Q, Xiao HL, Zheng J, Zheng BJ, Tang XW, Zhu Y, Lu JX, Guan MX.
    Yi Chuan; 2013 Jun 25; 35(6):752-60. PubMed ID: 23774020
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  • 15. Deafness-associated tRNAPhe mutation impaired mitochondrial and cellular integrity.
    Chen X, Meng F, Chen C, Li S, Chou Z, Xu B, Mo JQ, Guo Y, Guan MX.
    J Biol Chem; 2024 May 25; 300(5):107235. PubMed ID: 38552739
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  • 18. A pathogenic point mutation reduces stability of mitochondrial mutant tRNA(Ile).
    Yasukawa T, Hino N, Suzuki T, Watanabe K, Ueda T, Ohta S.
    Nucleic Acids Res; 2000 Oct 01; 28(19):3779-84. PubMed ID: 11000270
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  • 19. Mitochondrial tRNAIle A4317G mutation may be associated with hearing impairment in a Han Chinese family.
    Cui Y, He DJ.
    Mol Med Rep; 2018 Dec 01; 18(6):5159-5165. PubMed ID: 30272361
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  • 20. A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction.
    Wang M, Liu H, Zheng J, Chen B, Zhou M, Fan W, Wang H, Liang X, Zhou X, Eriani G, Jiang P, Guan MX.
    J Biol Chem; 2016 Sep 30; 291(40):21029-21041. PubMed ID: 27519417
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