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Journal Abstract Search

99 related items for PubMed ID: 24252789

  • 21.
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  • 23. Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity.
    Scrimshaw BJ, Faed JM, Tate WP, Yun K.
    J Hum Genet; 1999; 44(6):388-90. PubMed ID: 10570910
    [Abstract] [Full Text] [Related]

  • 24. Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity.
    Guan MX.
    Mitochondrion; 2011 Mar; 11(2):237-45. PubMed ID: 21047563
    [Abstract] [Full Text] [Related]

  • 25. 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]

  • 26. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides.
    Estivill X, Govea N, Barceló E, Badenas C, Romero E, Moral L, Scozzri R, D'Urbano L, Zeviani M, Torroni A.
    Am J Hum Genet; 1998 Jan; 62(1):27-35. PubMed ID: 9490575
    [Abstract] [Full Text] [Related]

  • 27. Prevalence of the mitochondrial DNA A1555G mutation in sensorineural deafness patients in island Southeast Asia.
    Malik SG, Pieter N, Sudoyo H, Kadir A, Marzuki S.
    J Hum Genet; 2003 Jan; 48(9):480-483. PubMed ID: 12955586
    [Abstract] [Full Text] [Related]

  • 28. Immunohistochemical and ultrastructural abnormalities in muscle from a patient with sensorineural hearing loss related to a 1555 A-to-G mitochondrial mutation.
    Kouzaki H, Suzuki M, Shimizu T.
    J Clin Neurosci; 2007 Jun; 14(6):603-7. PubMed ID: 16935512
    [Abstract] [Full Text] [Related]

  • 29. Interaction of aminoglycosides with human mitochondrial 12S rRNA carrying the deafness-associated mutation.
    Qian Y, Guan MX.
    Antimicrob Agents Chemother; 2009 Nov; 53(11):4612-8. PubMed ID: 19687236
    [Abstract] [Full Text] [Related]

  • 30. Normal hearing in a child with the m.1555A>G mutation despite repeated exposure to aminoglycosides. Has the penetrance of this pharmacogenetic interaction been overestimated?
    Al-Malky G, Suri R, Sirimanna T, Dawson SJ.
    Int J Pediatr Otorhinolaryngol; 2014 Jun; 78(6):969-73. PubMed ID: 24703164
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  • 31. 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 Jun; 74(5):731-736. PubMed ID: 19082356
    [Abstract] [Full Text] [Related]

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

  • 33. MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene.
    Ballana E, Mercader JM, Fischel-Ghodsian N, Estivill X.
    BMC Med Genet; 2007 Dec 21; 8():81. PubMed ID: 18154640
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  • 34.
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  • 35. [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 21; 28(2):165-71. PubMed ID: 21462128
    [Abstract] [Full Text] [Related]

  • 36. Myelocystocele-cloacal exstrophy in a pedigree with a mitochondrial 12S rRNA mutation, aminoglycoside-induced deafness, pigmentary disturbances, and spinal anomalies.
    Nye JS, Hayes EA, Amendola M, Vaughn D, Charrow J, McLone DG, Speer MC, Nance WE, Pandya A.
    Teratology; 2000 Mar 21; 61(3):165-71. PubMed ID: 10661905
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  • 37. Whole mitochondrial genome screening in two families with hearing loss: detection of a novel mutation in the 12S rRNA gene.
    Mkaouar-Rebai E, Fendri-Kriaa N, Louhichi N, Tlili A, Triki C, Ghorbel A, Masmoudi S, Fakhfakh F.
    Biosci Rep; 2010 Dec 21; 30(6):405-11. PubMed ID: 20055758
    [Abstract] [Full Text] [Related]

  • 38. Generation of an induced pluripotent stem cell line from a 39-year-old female patient with severe-to-profound non-syndromic sensorineural hearing loss and a A1555G mutation in the mitochondrial MTRNR1 gene.
    Hsu YH, Wu YT, Huang CY, Ho MC, Cheng YC, Syu SH, Lu HE, Chen YC, Tsai CL, Lin HC, Wei YH, Hsu YC, Hsieh PCH.
    Stem Cell Res; 2017 Dec 21; 25():245-249. PubMed ID: 29174977
    [Abstract] [Full Text] [Related]

  • 39. 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]

  • 40. The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence.
    Igumnova V, Veidemane L, Vīksna A, Capligina V, Zole E, Ranka R.
    J Hum Genet; 2019 Mar 15; 64(3):199-206. PubMed ID: 30523288
    [Abstract] [Full Text] [Related]

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