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

155 related items for PubMed ID: 20209292

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

  • 2. [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]

  • 3. 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]

  • 4. [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 10; 29(22):1936-40. PubMed ID: 26911053
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Genetic susceptibility to aminoglycoside ototoxicity.
    Nguyen T, Jeyakumar A.
    Int J Pediatr Otorhinolaryngol; 2019 May 12; 120():15-19. PubMed ID: 30743189
    [Abstract] [Full Text] [Related]

  • 7. 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 12; 9(6):418-28. PubMed ID: 19682603
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. mtDNA mutations, hearing loss and aminoglycoside treatment in Mexicans.
    Meza G, Torres-Ruíz NM, Tirado-Gutiérrez C, Aguilera P.
    Braz J Otorhinolaryngol; 2011 Sep 22; 77(5):573-6. PubMed ID: 22030963
    [Abstract] [Full Text] [Related]

  • 10. 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 22; 117(1):9-15. PubMed ID: 15841390
    [Abstract] [Full Text] [Related]

  • 11. Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.
    Bindu LH, Reddy PP.
    Int J Audiol; 2008 Nov 22; 47(11):702-7. PubMed ID: 19031229
    [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 22; 166(1):234-42. PubMed ID: 22068689
    [Abstract] [Full Text] [Related]

  • 13. 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 22; 52(2):98-103. PubMed ID: 23237192
    [Abstract] [Full Text] [Related]

  • 14. 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 22; 99(13):e19373. PubMed ID: 32221064
    [Abstract] [Full Text] [Related]

  • 15. 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 22; 17(2):122-30. PubMed ID: 23256547
    [Abstract] [Full Text] [Related]

  • 16. Audiologic testing and molecular analysis of 12S rRNA in patients receiving aminoglycosides.
    Gürtler N, Schmuziger N, Kim Y, Mhatre AN, Jungi M, Lalwani AK.
    Laryngoscope; 2005 Apr 22; 115(4):640-4. PubMed ID: 15805873
    [Abstract] [Full Text] [Related]

  • 17. Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment.
    Ballana E, Morales E, Rabionet R, Montserrat B, Ventayol M, Bravo O, Gasparini P, Estivill X.
    Biochem Biophys Res Commun; 2006 Mar 24; 341(4):950-7. PubMed ID: 16458854
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss.
    Lu J, Li Z, Zhu Y, Yang A, Li R, Zheng J, Cai Q, Peng G, Zheng W, Tang X, Chen B, Chen J, Liao Z, Yang L, Li Y, You J, Ding Y, Yu H, Wang J, Sun D, Zhao J, Xue L, Wang J, Guan MX.
    Mitochondrion; 2010 Jun 15; 10(4):380-90. PubMed ID: 20100600
    [Abstract] [Full Text] [Related]

  • 20. [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 15; 29(4):382-7. PubMed ID: 22875491
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.