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Journal Abstract Search

370 related items for PubMed ID: 16631122

  • 21. MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene.
    Ballana E, Mercader JM, Fischel-Ghodsian N, Estivill X.
    BMC Med Genet; 2007 Dec 21; 8():81. PubMed ID: 18154640
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  • 23. Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation.
    Bykhovskaya Y, Mengesha E, Wang D, Yang H, Estivill X, Shohat M, Fischel-Ghodsian N.
    Mol Genet Metab; 2004 May 21; 82(1):27-32. PubMed ID: 15110318
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  • 24. Clinical and audiological follow up of a family with the 8363G>A mutation in the mitochondrial DNA.
    DiFabio R, Santorelli FM, Nola G, Cricchi F, Masi R, Ingrosso A, Fattori F, Carrozzo R, Vanacore N, Pierelli F, Ralli G, Casali C.
    Neuromuscul Disord; 2009 Apr 21; 19(4):291-6. PubMed ID: 19233651
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  • 28. Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.
    Young WY, Zhao L, Qian Y, Wang Q, Li N, Greinwald JH, Guan MX.
    Biochem Biophys Res Commun; 2005 Mar 25; 328(4):1244-51. PubMed ID: 15708009
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  • 29. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families.
    Dai P, Yuan Y, Huang D, Qian Y, Liu X, Han D, Yuan H, Wang X, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Sep 15; 348(1):200-5. PubMed ID: 16875663
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  • 30. [Prevalence of the A1555G MTDNA mutation in sporadic hearing-impaired patients without known history of aminoglycoside treatment].
    Morales Angulo C, Gallo-Terán J, Señaris B, Fontalva A, González-Aguado R, Fernández-Luna JL.
    Acta Otorrinolaringol Esp; 2011 Sep 15; 62(2):83-6. PubMed ID: 21129708
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  • 32. Audiological and radiological characteristics of a family with T961G mitochondrial mutation.
    Turchetta R, Mazzei F, Celani T, Cammeresi MG, Orlando MP, Altissimi G, de Vincentiis C, D'Ambrosio F, Messineo D, Ferraris A, Cianfrone G.
    Int J Audiol; 2012 Dec 15; 51(12):870-9. PubMed ID: 23013294
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  • 33. Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity.
    Xing G, Chen Z, Wei Q, Tian H, Li X, Zhou A, Bu X, Cao X.
    Biochem Biophys Res Commun; 2006 Aug 11; 346(4):1131-5. PubMed ID: 16782057
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  • 35. Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity.
    Guan MX.
    Mitochondrion; 2011 Mar 11; 11(2):237-45. PubMed ID: 21047563
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  • 37. [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 11; 35(6):752-60. PubMed ID: 23774020
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  • 38. Cochlear origin of hearing loss in MELAS syndrome.
    Sue CM, Lipsett LJ, Crimmins DS, Tsang CS, Boyages SC, Presgrave CM, Gibson WP, Byrne E, Morris JG.
    Ann Neurol; 1998 Mar 11; 43(3):350-9. PubMed ID: 9506552
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  • 40. 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
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