These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

188 related items for PubMed ID: 33045734

  • 21. Mitochondrial tRNA mutations associated with deafness.
    Zheng J, Ji Y, Guan MX.
    Mitochondrion; 2012 May; 12(3):406-13. PubMed ID: 22538251
    [Abstract] [Full Text] [Related]

  • 22. [Mutations of mitochondrial tRNASer(UCN) and their connection with hearing loss].
    Fan W, Tang X, Zheng B, Guan M, Xue L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb 10; 34(1):128-132. PubMed ID: 28186612
    [Abstract] [Full Text] [Related]

  • 23. 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
    [Abstract] [Full Text] [Related]

  • 24. Processing and editing of overlapping tRNAs in human mitochondria.
    Reichert A, Rothbauer U, Mörl M.
    J Biol Chem; 1998 Nov 27; 273(48):31977-84. PubMed ID: 9822669
    [Abstract] [Full Text] [Related]

  • 25. Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees.
    Chen B, Sun D, Yang L, Zhang C, Yang A, Zhu Y, Zhao J, Chen Y, Guan M, Wang X, Li R, Tang X, Wang J, Tao Z, Lu J, Guan MX.
    Am J Med Genet A; 2008 May 15; 146A(10):1248-58. PubMed ID: 18386806
    [Abstract] [Full Text] [Related]

  • 26. 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
    [Abstract] [Full Text] [Related]

  • 27. The effect on mitochondrial function of the tRNA Ser(UCN)/COI A7445G mtDNA point mutation associated with maternally-inherited sensorineural deafness.
    Hyslop SJ, James AM, Maw M, Fischel-Ghodsian N, Murphy MP.
    Biochem Mol Biol Int; 1997 Jul 30; 42(3):567-75. PubMed ID: 9247714
    [Abstract] [Full Text] [Related]

  • 28. 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
    [Abstract] [Full Text] [Related]

  • 29. Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.
    Yuan H, Qian Y, Xu Y, Cao J, Bai L, Shen W, Ji F, Zhang X, Kang D, Mo JQ, Greinwald JH, Han D, Zhai S, Young WY, Guan MX.
    Am J Med Genet A; 2005 Oct 01; 138A(2):133-40. PubMed ID: 16152638
    [Abstract] [Full Text] [Related]

  • 30. [Hearing loss may be associated with the novel mitochondrial tRNA(Asp) A7551G mutation in a Chinese family].
    Wu Y, Liang LZ, Xiao HL, Yang YL, Yu X, Zheng J, Fang F, Zheng BJ, Tang XW, Jin LJ, Guan MX.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2013 Dec 01; 48(12):978-84. PubMed ID: 24506995
    [Abstract] [Full Text] [Related]

  • 31. RNA processing in human mitochondria.
    Sanchez MI, Mercer TR, Davies SM, Shearwood AM, Nygård KK, Richman TR, Mattick JS, Rackham O, Filipovska A.
    Cell Cycle; 2011 Sep 01; 10(17):2904-16. PubMed ID: 21857155
    [Abstract] [Full Text] [Related]

  • 32. Deletion of Mtu1 (Trmu) in zebrafish revealed the essential role of tRNA modification in mitochondrial biogenesis and hearing function.
    Zhang Q, Zhang L, Chen D, He X, Yao S, Zhang Z, Chen Y, Guan MX.
    Nucleic Acids Res; 2018 Nov 16; 46(20):10930-10945. PubMed ID: 30137487
    [Abstract] [Full Text] [Related]

  • 33. 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 16; 57():1-8. PubMed ID: 33279600
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. 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
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. Additional copies of the mitochondrial Ef-Tu and aspartyl-tRNA synthetase genes can compensate for a mutation affecting the maturation of the mitochondrial tRNAAsp.
    Rinaldi T, Lande R, Bolotin-Fukuhara M, Frontali L.
    Curr Genet; 1997 Jun 28; 31(6):494-6. PubMed ID: 9211792
    [Abstract] [Full Text] [Related]

  • 40. The 3' addition of CCA to mitochondrial tRNASer(AGY) is specifically impaired in patients with mutations in the tRNA nucleotidyl transferase TRNT1.
    Sasarman F, Thiffault I, Weraarpachai W, Salomon S, Maftei C, Gauthier J, Ellazam B, Webb N, Antonicka H, Janer A, Brunel-Guitton C, Elpeleg O, Mitchell G, Shoubridge EA.
    Hum Mol Genet; 2015 May 15; 24(10):2841-7. PubMed ID: 25652405
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 10.