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Journal Abstract Search

191 related items for PubMed ID: 16650816

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  • 3. A mutation in mitochondrial 12S rRNA, A827G, in Argentinean family with hearing loss after aminoglycoside treatment.
    Chaig MR, Zernotti ME, Soria NW, Romero OF, Romero MF, Gerez NM.
    Biochem Biophys Res Commun; 2008 Apr 11; 368(3):631-6. PubMed ID: 18261986
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  • 4. [Mitochondrial 12S rRNA gene A827G in two pedigrees with nonsyndromic deafness].
    Chen ZB, Cao X, Xing GQ, Tian HQ, Zhou AD, Wei QU, Bu XK.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug 11; 23(4):415-8. PubMed ID: 16883529
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  • 6. Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family.
    Tang X, Li R, Zheng J, Cai Q, Zhang T, Gong S, Zheng W, He X, Zhu Y, Xue L, Yang A, Yang L, Lu J, Guan MX.
    Mol Genet Metab; 2010 May 11; 100(1):57-64. PubMed ID: 20153673
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  • 9. Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families.
    Wei Q, Xu D, Chen Z, Li H, Lu Y, Liu C, Bu X, Xing G, Cao X.
    Int J Audiol; 2013 Feb 11; 52(2):98-103. PubMed ID: 23237192
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  • 10. [Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss in five Han Chinese pedigrees].
    Zhang T, Chen BB, Zheng J, Gong SS, Zhang CQ, Lv JX, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug 11; 28(4):367-73. PubMed ID: 21811972
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  • 12. 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
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  • 14. Co-segregation of the T1095C with the A1555G mutation of the mitochondrial 12S rRNA gene in a patient with non-syndromic hearing loss.
    Dai D, Lu Y, Chen Z, Wei Q, Cao X, Xing G.
    Biochem Biophys Res Commun; 2008 Dec 26; 377(4):1152-5. PubMed ID: 18983818
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  • 15. [Mutation analysis of mitochondrial 12S rRNA gene G709A in a maternally inherited pedigree with non-syndromic deafness].
    Wei Q, Lu Y, Zhang Y, Chen Z, Xing G, Cao X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec 26; 26(6):610-4. PubMed ID: 19953480
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  • 17. Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation.
    Zhao L, Young WY, Li R, Wang Q, Qian Y, Guan MX.
    Biochem Biophys Res Commun; 2004 Dec 24; 325(4):1503-8. PubMed ID: 15555598
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  • 18. Unique penetrance of hearing loss in a five-generation Chinese family with the mitochondrial 12S rRNA 1555A > G mutation.
    Men M, Jiang L, Wang H, Liu Y, Hu Z, He C, Feng Y.
    Acta Otolaryngol; 2011 Sep 24; 131(9):970-5. PubMed ID: 21504270
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  • 19. 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 24; 18(12):1059-70. PubMed ID: 18820594
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  • 20. Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss.
    Yuan H, Chen J, Liu X, Cheng J, Wang X, Yang L, Yang S, Cao J, Kang D, Dai P, Zhai S, Han D, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2007 Oct 12; 362(1):94-100. PubMed ID: 17698030
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