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286 related items for PubMed ID: 15805873

  • 21. Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C->T mutation in the mitochondrial 12S rRNA gene.
    Rodríguez-Ballesteros M, Olarte M, Aguirre LA, Galán F, Galán R, Vallejo LA, Navas C, Villamar M, Moreno-Pelayo MA, Moreno F, del Castillo I.
    J Med Genet; 2006 Nov; 43(11):e54. PubMed ID: 17085680
    [Abstract] [Full Text] [Related]

  • 22. Rapid mass screening method and counseling for the 1555A-->G mitochondrial mutation.
    Usami S, Abe S, Shinkawa H, Inoue Y, Yamaguchi T.
    J Hum Genet; 1999 Nov; 44(5):304-7. PubMed ID: 10496072
    [Abstract] [Full Text] [Related]

  • 23. 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; 166(1):234-42. PubMed ID: 22068689
    [Abstract] [Full Text] [Related]

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

  • 25. 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]

  • 26. Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.
    Kupka S, Tóth T, Wróbel M, Zeissler U, Szyfter W, Szyfter K, Niedzielska G, Bal J, Zenner HP, Sziklai I, Blin N, Pfister M.
    Hum Mutat; 2002 Mar 09; 19(3):308-9. PubMed ID: 11857751
    [Abstract] [Full Text] [Related]

  • 27. 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 09; 117(1):9-15. PubMed ID: 15841390
    [Abstract] [Full Text] [Related]

  • 28. Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.
    Kato T, Nishigaki Y, Noguchi Y, Ueno H, Hosoya H, Ito T, Kimura Y, Kitamura K, Tanaka M.
    J Hum Genet; 2010 Mar 09; 55(3):147-54. PubMed ID: 20111055
    [Abstract] [Full Text] [Related]

  • 29. Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics.
    Shen Z, Zheng J, Chen B, Peng G, Zhang T, Gong S, Zhu Y, Zhang C, Li R, Yang L, Zhou J, Cai T, Jin L, Lu J, Guan MX.
    J Transl Med; 2011 Jan 04; 9():4. PubMed ID: 21205314
    [Abstract] [Full Text] [Related]

  • 30. Topical gentamicin-induced hearing loss: a mitochondrial ribosomal RNA study of genetic susceptibility.
    Chen JM, Williamson PA, Hutchin T, Nedzelski JM, Cortopassi GA.
    Am J Otol; 1996 Nov 04; 17(6):850-2. PubMed ID: 8915412
    [Abstract] [Full Text] [Related]

  • 31. The contribution of the mitochondrial COI/tRNA(Ser(UCN)) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients.
    Rydzanicz M, Cywińska K, Wróbel M, Pollak A, Gawęcki W, Wojsyk-Banaszak I, Lechowicz U, Mueller-Malesińska M, Ołdak M, Płoski R, Skarżyński H, Szyfter K, Szyfter W.
    Mol Genet Metab; 2011 Nov 04; 104(1-2):153-9. PubMed ID: 21621438
    [Abstract] [Full Text] [Related]

  • 32.
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  • 33. Factors affecting sensitivity of distortion-product otoacoustic emissions to ototoxic hearing loss.
    Reavis KM, Phillips DS, Fausti SA, Gordon JS, Helt WJ, Wilmington D, Bratt GW, Konrad-Martin D.
    Ear Hear; 2008 Dec 04; 29(6):875-93. PubMed ID: 18753950
    [Abstract] [Full Text] [Related]

  • 34. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 04; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 35. C1494T mitochondrial DNA mutation, hearing loss, and aminoglycosides antibiotics.
    Postal M, Palodeto B, Sartorato EL, Oliveira CA.
    Braz J Otorhinolaryngol; 2009 Aug 04; 75(6):884-7. PubMed ID: 20209292
    [Abstract] [Full Text] [Related]

  • 36. Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss.
    Jin L, Yang A, Zhu Y, Zhao J, Wang X, Yang L, Sun D, Tao Z, Tsushima A, Wu G, Xu L, Chen C, Yi B, Cai J, Tang X, Wang J, Li D, Yuan Q, Liao Z, Chen J, Li Z, Lu J, Guan MX.
    Biochem Biophys Res Commun; 2007 Sep 14; 361(1):133-9. PubMed ID: 17659260
    [Abstract] [Full Text] [Related]

  • 37. 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 14; 10(4):380-90. PubMed ID: 20100600
    [Abstract] [Full Text] [Related]

  • 38. Mitochondrial 12S ribosomal RNA A1555G mutation associated with cardiomyopathy and hearing loss following high-dose chemotherapy and repeated aminoglycoside exposure.
    Skou AS, Tranebjærg L, Jensen T, Hasle H.
    J Pediatr; 2014 Feb 14; 164(2):413-5. PubMed ID: 24252789
    [Abstract] [Full Text] [Related]

  • 39. 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]

  • 40. 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
    [Abstract] [Full Text] [Related]

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