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Volumn 20, Issue 3, 1999, Pages 151-156

Inherited susceptibility to aminoglycoside ototoxicity: Genetic heterogeneity and clinical implications

Author keywords

[No Author keywords available]

Indexed keywords

AMINOGLYCOSIDE ANTIBIOTIC AGENT; CYTOSINE; DIHYDROSTREPTOMYCIN; DNA; MITOCHONDRIAL DNA; NUCLEOTIDE; RIBOSOME RNA; STREPTOMYCIN; THYMIDINE;

EID: 13044279515     PISSN: 01960709     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0196-0709(99)90062-5     Document Type: Article
Times cited : (122)

References (14)
  • 1
    • 0027226069 scopus 로고
    • Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness
    • Prezant TR, Agapian JV, Bohlman MC, et al: Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nat Genet 4:289-294, 1993
    • (1993) Nat Genet , vol.4 , pp. 289-294
    • Prezant, T.R.1    Agapian, J.V.2    Bohlman, M.C.3
  • 2
    • 0027218979 scopus 로고
    • A molecular basis for human hypersensitivity to aminoglycoside antibiotics
    • Hutchin T, Haworth I, Higashi K, et al: A molecular basis for human hypersensitivity to aminoglycoside antibiotics. Nucl Acids Res 21:4174-4179, 1993
    • (1993) Nucl Acids Res , vol.21 , pp. 4174-4179
    • Hutchin, T.1    Haworth, I.2    Higashi, K.3
  • 3
    • 0029916599 scopus 로고    scopus 로고
    • Nonsyndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairean pedigree
    • Matthijs G, Claes S, Longo-Mbenza B, et al: Nonsyndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairean pedigree. Eur J Hum Genet 4:46-51, 1996
    • (1996) Eur J Hum Genet , vol.4 , pp. 46-51
    • Matthijs, G.1    Claes, S.2    Longo-Mbenza, B.3
  • 4
    • 0031055387 scopus 로고    scopus 로고
    • Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity
    • Pandya A, Xia X, Radnaabazar J, et al: Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity. J Med Genet 34:169-172, 1997
    • (1997) J Med Genet , vol.34 , pp. 169-172
    • Pandya, A.1    Xia, X.2    Radnaabazar, J.3
  • 5
    • 0343852695 scopus 로고    scopus 로고
    • Two large Spanish pedigrees with non-syndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12SrRNA gene: Evidence of heteroplasmy
    • El-Schahawi M, deMunain L, Sarrazin AM, et al: Two large Spanish pedigrees with non-syndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12SrRNA gene: Evidence of heteroplasmy. Neurology 48:453-456, 1997
    • (1997) Neurology , vol.48 , pp. 453-456
    • El-Schahawi, M.1    DeMunain, L.2    Sarrazin, A.M.3
  • 6
    • 17344365276 scopus 로고    scopus 로고
    • Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment with aminoglycosides
    • Estivill X, Govea N, Barcelo A, et al: Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment with aminoglycosides. Am J Hum Genet 62:27-35, 1998
    • (1998) Am J Hum Genet , vol.62 , pp. 27-35
    • Estivill, X.1    Govea, N.2    Barcelo, A.3
  • 7
    • 0030974247 scopus 로고    scopus 로고
    • Mitochondrial gene mutations: A common predisposing factor in aminoglycoside ototoxicity
    • Fischel-Ghodsian N, Prezant TR, Chaltraw W, et al: Mitochondrial gene mutations: A common predisposing factor in aminoglycoside ototoxicity. Am J Otolaryngol 18:173-178, 1997
    • (1997) Am J Otolaryngol , vol.18 , pp. 173-178
    • Fischel-Ghodsian, N.1    Prezant, T.R.2    Chaltraw, W.3
  • 8
    • 0029003553 scopus 로고
    • Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside-induced deafness
    • Bacino CM, Prezant TR, Bu X, et al: Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside-induced deafness. Pharmacogenetics 5:165-172, 1995
    • (1995) Pharmacogenetics , vol.5 , pp. 165-172
    • Bacino, C.M.1    Prezant, T.R.2    Bu, X.3
  • 10
    • 0028847380 scopus 로고
    • Mitochondrial tRNA mutation associated with non-syndromic deafness
    • Fischel-Ghodsian N, Prezant TR, Fournier P, et al: Mitochondrial tRNA mutation associated with non-syndromic deafness. Am J Otolaryngol 16:403-408, 1995
    • (1995) Am J Otolaryngol , vol.16 , pp. 403-408
    • Fischel-Ghodsian, N.1    Prezant, T.R.2    Fournier, P.3
  • 11
    • 0345394974 scopus 로고    scopus 로고
    • Different penetrance of neurological symptoms associated with a mutation in the mitochondrial tRNA Ser(UCN) gene
    • in press
    • Verhoeven K, Ensink RJH, Tiranti V, et al: Different penetrance of neurological symptoms associated with a mutation in the mitochondrial tRNA Ser(UCN) gene. Eur J Hum Genet (in press)
    • Eur J Hum Genet
    • Verhoeven, K.1    Ensink, R.J.H.2    Tiranti, V.3
  • 12
    • 0027200741 scopus 로고
    • Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients
    • Shoffner JM, Brown MD, Torroni A, et al: Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients. Genomics 17:171-184, 1993
    • (1993) Genomics , vol.17 , pp. 171-184
    • Shoffner, J.M.1    Brown, M.D.2    Torroni, A.3
  • 13
    • 0023088802 scopus 로고
    • Length mutations in human mitochondrial DNA: Direct sequencing of enzymatically amplified DNA
    • Wrischnik LA, Higuchi RG, Stoneking M, et al: Length mutations in human mitochondrial DNA: Direct sequencing of enzymatically amplified DNA. Nucl Acids Res 15:529-542, 1987
    • (1987) Nucl Acids Res , vol.15 , pp. 529-542
    • Wrischnik, L.A.1    Higuchi, R.G.2    Stoneking, M.3
  • 14
    • 0030827973 scopus 로고    scopus 로고
    • Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness
    • Hamasaki K, Rando RR: Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness. Biochemistry 36:12323-12328, 1997
    • (1997) Biochemistry , vol.36 , pp. 12323-12328
    • Hamasaki, K.1    Rando, R.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.