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Journal Abstract Search

138 related items for PubMed ID: 17680545

  • 1. [Molecular genetic analysis of mitochondrial DNA C1494T mutation in non-syndromic hearing loss of Chinese population].
    Tian G, Liu YH, Ma YN, Li YJ, Zhang Y, Niu SL, Xu YE, Pei P, Wang ST, Bu DF, Du BR, Zhou X, Ke XM, Qi Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):464-6. PubMed ID: 17680545
    [Abstract] [Full Text] [Related]

  • 2. C1494T mitochondrial DNA mutation, hearing loss, and aminoglycosides antibiotics.
    Postal M, Palodeto B, Sartorato EL, Oliveira CA.
    Braz J Otorhinolaryngol; 2009 Aug; 75(6):884-7. PubMed ID: 20209292
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation.
    Wang Q, Li QZ, Han D, Zhao Y, Zhao L, Qian Y, Yuan H, Li R, Zhai S, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Feb 10; 340(2):583-8. PubMed ID: 16380089
    [Abstract] [Full Text] [Related]

  • 5. Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree.
    Chen T, Liu Q, Jiang L, Liu C, Ou Q.
    Genet Test Mol Biomarkers; 2013 Feb 10; 17(2):122-30. PubMed ID: 23256547
    [Abstract] [Full Text] [Related]

  • 6. 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 10; 52(2):98-103. PubMed ID: 23237192
    [Abstract] [Full Text] [Related]

  • 7. 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 10; 117(1):9-15. PubMed ID: 15841390
    [Abstract] [Full Text] [Related]

  • 8. Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation.
    Zhu Y, Li Q, Chen Z, Kun Y, Liu L, Liu X, Yuan H, Zhai S, Han D, Dai P.
    Mitochondrion; 2009 Nov 10; 9(6):418-28. PubMed ID: 19682603
    [Abstract] [Full Text] [Related]

  • 9. Screening for mitochondrial 12S rRNA C1494T mutation in 655 patients with non-syndromic hearing loss: An observational study.
    Gao Z, Yuan YS.
    Medicine (Baltimore); 2020 Mar 10; 99(13):e19373. PubMed ID: 32221064
    [Abstract] [Full Text] [Related]

  • 10. mtDNA mutation C1494T, haplogroup A, and hearing loss in Chinese.
    Wang CY, Kong QP, Yao YG, Zhang YP.
    Biochem Biophys Res Commun; 2006 Sep 22; 348(2):712-5. PubMed ID: 16890911
    [Abstract] [Full Text] [Related]

  • 11. Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.
    Chen J, Yang L, Yang A, Zhu Y, Zhao J, Sun D, Tao Z, Tang X, Wang J, Wang X, Tsushima A, Lan J, Li W, Wu F, Yuan Q, Ji J, Feng J, Wu C, Liao Z, Li Z, Greinwald JH, Lu J, Guan MX.
    Gene; 2007 Oct 15; 401(1-2):4-11. PubMed ID: 17698299
    [Abstract] [Full Text] [Related]

  • 12. Discrimination of A1555G and C1494T point mutations in the mitochondrial 12S rRNA gene by on/off switch.
    Guo ZF, Guo WS, Xiao L, Gao GQ, Lan F, Lu XG, Li K, Liao DF.
    Appl Biochem Biotechnol; 2012 Jan 15; 166(1):234-42. PubMed ID: 22068689
    [Abstract] [Full Text] [Related]

  • 13. Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.
    Zhao L, Wang Q, Qian Y, Li R, Cao J, Hart LC, Zhai S, Han D, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2005 Oct 28; 336(3):967-73. PubMed ID: 16168391
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. [Mitochondrial DNA G7444A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation].
    Yang AF, Zhu Y, Lu JX, Yang L, Zhao JY, Sun DM.
    Yi Chuan; 2008 Jun 09; 30(6):728-34. PubMed ID: 18550495
    [Abstract] [Full Text] [Related]

  • 16. [Mitochondrial DNA mutations and aminoglycoside antibiotics and hearing loss].
    Qu J, Wang J, Xu S.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov 09; 29(22):1936-40. PubMed ID: 26911053
    [Abstract] [Full Text] [Related]

  • 17. Screening for deafness-associated mitochondrial 12S rRNA mutations by using a multiplex allele-specific PCR method.
    Ding Y, Lang J, Zhang J, Xu J, Lin X, Lou X, Zheng H, Huai L.
    Biosci Rep; 2020 May 29; 40(5):. PubMed ID: 32400865
    [Abstract] [Full Text] [Related]

  • 18. [Characterization of two Chinese families with aminoglycoside-induced and nonsyndromic hearing loss both carrying a mitochondrial 12S rRNA 1494C>T mutation].
    Gong SS, Chen BB, Peng GH, Zheng J, Zhang T, Zheng BJ, Fang F, Zhang CQ, Lv JX, Guan MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug 29; 29(4):382-7. PubMed ID: 22875491
    [Abstract] [Full Text] [Related]

  • 19. Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese families.
    Zhu Y, Qian Y, Tang X, Wang J, Yang L, Liao Z, Li R, Ji J, Li Z, Chen J, Choo DI, Lu J, Guan MX.
    Biochem Biophys Res Commun; 2006 Apr 14; 342(3):843-50. PubMed ID: 16500624
    [Abstract] [Full Text] [Related]

  • 20. Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation.
    Tang X, Yang L, Zhu Y, Liao Z, Wang J, Qian Y, Tao Z, Hu L, Wu G, Lan J, Wang X, Ji J, Wu J, Ji Y, Feng J, Chen J, Li Z, Zhang X, Lu J, Guan MX.
    Gene; 2007 May 15; 393(1-2):11-9. PubMed ID: 17341440
    [Abstract] [Full Text] [Related]

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