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Journal Abstract Search

322 related items for PubMed ID: 17659260

  • 21. Mitochondrial COI/tRNASer(UCN) G7444A mutation may be associated with aminoglycoside-induced and non-syndromic hearing impairment.
    Liu Q, Liu P, Ding Y, Dong XJ, Wang ZX, Qian YE, Wang Q, Yang GC.
    Mol Med Rep; 2015 Dec; 12(6):8176-8. PubMed ID: 26497601
    [Abstract] [Full Text] [Related]

  • 22. Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.
    Verhoeven K, Ensink RJ, Tiranti V, Huygen PL, Johnson DF, Schatteman I, Van Laer L, Verstreken M, Van de Heyning P, Fischel-Ghodsian N, Zeviani M, Cremers CW, Willems PJ, Van Camp G.
    Eur J Hum Genet; 1999 Jan; 7(1):45-51. PubMed ID: 10094190
    [Abstract] [Full Text] [Related]

  • 23. Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity.
    Guan MX.
    Mitochondrion; 2011 Mar; 11(2):237-45. PubMed ID: 21047563
    [Abstract] [Full Text] [Related]

  • 24. Mitochondrial COI/tRNASer(UCN) G7444A mutation may be associated with hearing impairment in a Han Chinese family.
    Ding Y, Xia BH, Teng YS, Zhuo GC, Leng JH.
    Int J Clin Exp Pathol; 2017 Mar; 10(9):9496-9502. PubMed ID: 31966824
    [Abstract] [Full Text] [Related]

  • 25. Mitochondrial tRNA(Ser(UCN)) variants in 2651 Han Chinese subjects with hearing loss.
    Tang X, Zheng J, Ying Z, Cai Z, Gao Y, He Z, Yu H, Yao J, Yang Y, Wang H, Chen Y, Guan MX.
    Mitochondrion; 2015 Jul; 23():17-24. PubMed ID: 25968158
    [Abstract] [Full Text] [Related]

  • 26. New polymorphic mtDNA restriction site in the 12S rRNA gene detected in Tunisian patients with non-syndromic hearing loss.
    Mkaouar-Rebai E, Tlili A, Masmoudi S, Charfeddine I, Fakhfakh F.
    Biochem Biophys Res Commun; 2008 May 09; 369(3):849-52. PubMed ID: 18325329
    [Abstract] [Full Text] [Related]

  • 27. Cochlear alterations in deaf and unaffected subjects carrying the deafness-associated A1555G mutation in the mitochondrial 12S rRNA gene.
    Bravo O, Ballana E, Estivill X.
    Biochem Biophys Res Commun; 2006 Jun 02; 344(2):511-6. PubMed ID: 16631122
    [Abstract] [Full Text] [Related]

  • 28. Deafness due to A1555G mitochondrial mutation without use of aminoglycoside.
    Matsunaga T, Kumanomido H, Shiroma M, Ohtsuka A, Asamura K, Usami S.
    Laryngoscope; 2004 Jun 02; 114(6):1085-91. PubMed ID: 15179218
    [Abstract] [Full Text] [Related]

  • 29. Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.
    Li Z, Li R, Chen J, Liao Z, Zhu Y, Qian Y, Xiong S, Heman-Ackah S, Wu J, Choo DI, Guan MX.
    Hum Genet; 2005 Jun 02; 117(1):9-15. PubMed ID: 15841390
    [Abstract] [Full Text] [Related]

  • 30. Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss.
    Gutiérrez Cortés N, Pertuiset C, Dumon E, Börlin M, Hebert-Chatelain E, Pierron D, Feldmann D, Jonard L, Marlin S, Letellier T, Rocher C.
    Hum Mutat; 2012 Apr 02; 33(4):681-9. PubMed ID: 22241583
    [Abstract] [Full Text] [Related]

  • 31. Hearing loss due to the mitochondrial A1555G mutation in Italian families.
    Casano RA, Bykhovskaya Y, Johnson DF, Hamon M, Torricelli F, Bigozzi M, Fischel-Ghodsian N.
    Am J Med Genet; 1998 Oct 12; 79(5):388-91. PubMed ID: 9779807
    [Abstract] [Full Text] [Related]

  • 32. Mitochondrial rRNA and tRNA and hearing function.
    Xing G, Chen Z, Cao X.
    Cell Res; 2007 Mar 12; 17(3):227-39. PubMed ID: 17199108
    [Abstract] [Full Text] [Related]

  • 33. Investigation of mitochondrial sequence variants associated with aminoglycoside-induced ototoxicity in South African TB patients on aminoglycosides.
    Human H, Hagen CM, de Jong G, Harris T, Lombard D, Christiansen M, Bardien S.
    Biochem Biophys Res Commun; 2010 Mar 19; 393(4):751-6. PubMed ID: 20171168
    [Abstract] [Full Text] [Related]

  • 34. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.
    Lévêque M, Marlin S, Jonard L, Procaccio V, Reynier P, Amati-Bonneau P, Baulande S, Pierron D, Lacombe D, Duriez F, Francannet C, Mom T, Journel H, Catros H, Drouin-Garraud V, Obstoy MF, Dollfus H, Eliot MM, Faivre L, Duvillard C, Couderc R, Garabedian EN, Petit C, Feldmann D, Denoyelle F.
    Eur J Hum Genet; 2007 Nov 19; 15(11):1145-55. PubMed ID: 17637808
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36. Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families.
    Wang X, Lu J, Zhu Y, Yang A, Yang L, Li R, Chen B, Qian Y, Tang X, Wang J, Zhang X, Guan MX.
    Pharmacogenet Genomics; 2008 Dec 19; 18(12):1059-70. PubMed ID: 18820594
    [Abstract] [Full Text] [Related]

  • 37.
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  • 38. Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss.
    Young WY, Zhao L, Qian Y, Li R, Chen J, Yuan H, Dai P, Zhai S, Han D, Guan MX.
    Am J Med Genet A; 2006 Oct 15; 140(20):2188-97. PubMed ID: 16955413
    [Abstract] [Full Text] [Related]

  • 39.
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  • 40. The Mitochondrial COI/tRNASER(UCN) G7444A Mutation may be Associated with Hearing Impairment in a Han Chinese Family.
    Y D, B-H X, Y-S T, G-C Z, J-H L.
    Balkan J Med Genet; 2017 Dec 15; 20(2):43-50. PubMed ID: 29876232
    [Abstract] [Full Text] [Related]

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