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

104 related items for PubMed ID: 34604960

  • 1. Pharmacogenetic screening of A1555G and C1494T mitochondrial mutations and the use of ototoxic drugs among Jordanians.
    Yehya A, Al-Trad B, Bani-Hmoud M, Rababa'h AM.
    Eur Rev Med Pharmacol Sci; 2021 Sep; 25(18):5684-5689. PubMed ID: 34604960
    [Abstract] [Full Text] [Related]

  • 2. [Modifier factors influencing the phenotypic manifestation of the deafness associated mitochondrial DNA mutations].
    YANG AF, ZHENG J, LV JX, GUAN MX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):165-71. PubMed ID: 21462128
    [Abstract] [Full Text] [Related]

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

  • 4. Study of mitochondrial DNA A1555G and C1494T mutations in a large cohort of women individuals.
    Wang L, Wang X, Cai X, Qiang R.
    Mitochondrial DNA A DNA Mapp Seq Anal; 2019 Mar; 30(2):222-225. PubMed ID: 29790807
    [Abstract] [Full Text] [Related]

  • 5. [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; 29(22):1936-40. PubMed ID: 26911053
    [Abstract] [Full Text] [Related]

  • 6. Screening of the mitochondrial A1555G mutation in patients with sensorineural hearing loss.
    Maniglia LP, Moreira BCL, da Silva MAOM, Piatto VB, Maniglia JV.
    Braz J Otorhinolaryngol; 2008 Nov; 74(5):731-736. PubMed ID: 19082356
    [Abstract] [Full Text] [Related]

  • 7. [Audiometric features of familial hearing impairment transmitted by mitochondrial inheritance (A1555G)].
    Morales Angulo C, Gallo Terán J, del Castillo I, Moreno Pelayo MA, García-Mantilla J, Moreno Herrero F.
    Acta Otorrinolaringol Esp; 2002 Nov; 53(9):641-8. PubMed ID: 12584878
    [Abstract] [Full Text] [Related]

  • 8. [Assessment of the risk of hearing loss in children with cystic fibrosis].
    Polyakov DP, Daikhes NA, Bazanova MV, Melyanovskaya YL.
    Vestn Otorinolaringol; 2024 Nov; 89(3):29-35. PubMed ID: 39104270
    [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; 99(13):e19373. PubMed ID: 32221064
    [Abstract] [Full Text] [Related]

  • 10. [Prevalence of common genetic mutations and clinical characteristics analysis in patients at different ages with nonsyndromic hearing impairment].
    Zhang CQ, Chen BB, Chen YY, Liu XJ, Zheng J, Gao JJ, Huang SY, Nan BY, Zhang YY, Yu X, Guan MX.
    Yi Chuan; 2013 Mar; 35(3):352-8. PubMed ID: 23575541
    [Abstract] [Full Text] [Related]

  • 11. Audiological and genetic features of the mtDNA mutations.
    Liu XZ, Angeli S, Ouyang XM, Liu W, Ke XM, Liu YH, Liu SX, Du LL, Deng XW, Yuan H, Yan D.
    Acta Otolaryngol; 2008 Jul; 128(7):732-8. PubMed ID: 18568513
    [Abstract] [Full Text] [Related]

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

  • 13. Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss.
    Moassass F, Al-Halabi B, Nweder MS, Al-Achkar W.
    Int J Pediatr Otorhinolaryngol; 2018 Oct; 113():110-114. PubMed ID: 30173967
    [Abstract] [Full Text] [Related]

  • 14. [Incidence of A1555G mutations in the mitochondrial DNA and 35delG in the GJB2 gene (connexin-26) in families with late onset non-syndromic sensorineural hearing loss from Cantabria].
    Gallo-Terán J, Morales-Angulo C, del Castillo I, Villamar M, Moreno-Pelayo MA, García-Mantilla J, Moreno F.
    Acta Otorrinolaringol Esp; 2002 Oct; 53(8):563-71. PubMed ID: 12530196
    [Abstract] [Full Text] [Related]

  • 15. 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; 115(4):640-4. PubMed ID: 15805873
    [Abstract] [Full Text] [Related]

  • 16. The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population.
    Ealy M, Lynch KA, Meyer NC, Smith RJ.
    Laryngoscope; 2011 Jun; 121(6):1184-6. PubMed ID: 21495045
    [Abstract] [Full Text] [Related]

  • 17. 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 Jun; 104(1-2):153-9. PubMed ID: 21621438
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. [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]

  • 20. 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]

    Page: [Next] [New Search]
    of 6.