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Journal Abstract Search

291 related items for PubMed ID: 29222331

  • 1. 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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  • 2. A deafness-associated tRNA mutation caused pleiotropic effects on the m1G37 modification, processing, stability and aminoacylation of tRNAIle and mitochondrial translation.
    Meng F, Zhou M, Xiao Y, Mao X, Zheng J, Lin J, Lin T, Ye Z, Cang X, Fu Y, Wang M, Guan MX.
    Nucleic Acids Res; 2021 Jan 25; 49(2):1075-1093. PubMed ID: 33398350
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  • 3. A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function.
    Wang M, Peng Y, Zheng J, Zheng B, Jin X, Liu H, Wang Y, Tang X, Huang T, Jiang P, Guan MX.
    Nucleic Acids Res; 2016 Dec 15; 44(22):10974-10985. PubMed ID: 27536005
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  • 6. Clinical and genetic analysis of essential hypertension with mitochondrial tRNAMet 4435A>G and YARS2 mutation.
    Guo M, He Y, Chen A, Zhuang Z, Pan X, Guan M.
    Zhejiang Da Xue Xue Bao Yi Xue Ban; 2024 Apr 25; 53(2):184-193. PubMed ID: 38562030
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  • 8. Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree.
    Liu Y, Li R, Li Z, Wang XJ, Yang L, Wang S, Guan MX.
    Hypertension; 2009 Jun 25; 53(6):1083-90. PubMed ID: 19398658
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  • 9. The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree.
    Lu Z, Chen H, Meng Y, Wang Y, Xue L, Zhi S, Qiu Q, Yang L, Mo JQ, Guan MX.
    Eur J Hum Genet; 2011 Nov 25; 19(11):1181-6. PubMed ID: 21694735
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  • 11. Mechanistic insights into mitochondrial tRNAAla 3'-end metabolism deficiency.
    Ji Y, Nie Z, Meng F, Hu C, Chen H, Jin L, Chen M, Zhang M, Zhang J, Liang M, Wang M, Guan MX.
    J Biol Chem; 2021 Jul 25; 297(1):100816. PubMed ID: 34023389
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  • 13. 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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  • 14. A coronary artery disease-associated tRNAThr mutation altered mitochondrial function, apoptosis and angiogenesis.
    Jia Z, Zhang Y, Li Q, Ye Z, Liu Y, Fu C, Cang X, Wang M, Guan MX.
    Nucleic Acids Res; 2019 Feb 28; 47(4):2056-2074. PubMed ID: 30541130
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  • 15. Synthesis and properties of the anticodon stem-loop of human mitochondrial tRNAMet containing the disease-related G or m1G nucleosides at position 37.
    Podskoczyj K, Kulik K, Wasko J, Nawrot B, Suzuki T, Leszczynska G.
    Chem Commun (Camb); 2021 Nov 23; 57(93):12540-12543. PubMed ID: 34755158
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  • 16. Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation.
    Meng F, Cang X, Peng Y, Li R, Zhang Z, Li F, Fan Q, Guan AS, Fischel-Ghosian N, Zhao X, Guan MX.
    J Biol Chem; 2017 Feb 17; 292(7):2881-2892. PubMed ID: 28049726
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  • 17. Contribution of the tRNAIle 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation.
    Meng F, He Z, Tang X, Zheng J, Jin X, Zhu Y, Ren X, Zhou M, Wang M, Gong S, Mo JQ, Shu Q, Guan MX.
    J Biol Chem; 2018 Mar 02; 293(9):3321-3334. PubMed ID: 29348176
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