메뉴 건너뛰기




Volumn 124, Issue 3, 2004, Pages 258-261

A novel mitochondrial mutation, 1556C → T, in a Japanese patient with streptomycin-induced tinnitus

Author keywords

1555A G; 1556C T; Aminoglycoside; Hearing loss; Mitochondrial mutation; Streptomycin; Tinnitus

Indexed keywords

STREPTOMYCIN;

EID: 2342572275     PISSN: 00016489     EISSN: None     Source Type: Journal    
DOI: 10.1080/00016480310015740     Document Type: Article
Times cited : (12)

References (20)
  • 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 1993; 4: 289-94.
    • (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. Nucleic Acids Res 1993; 21: 4174-9.
    • (1993) Nucleic Acids Res , vol.21 , pp. 4174-4179
    • Hutchin, T.1    Haworth, I.2    Higashi, K.3
  • 3
    • 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, Barceló 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 1998; 62: 27-35.
    • (1998) Am J Hum Genet , vol.62 , pp. 27-35
    • Estivill, X.1    Govea, N.2    Barceló, A.3
  • 4
    • 0029916599 scopus 로고    scopus 로고
    • Non-syndromic 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, Cassiman J-J. Non-syndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairean pedigree. Eur J Hum Genet 1996; 4: 46-51.
    • (1996) Eur J Hum Genet , vol.4 , pp. 46-51
    • Matthijs, G.1    Claes, S.2    Longo-Mbenza, B.3    Cassiman, J.-J.4
  • 5
    • 0027515721 scopus 로고
    • Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity
    • Fischel-Ghodsian N, Prezant TR, Bu X, Özatas S. Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity. Am J Otolaryngol 1993; 14: 399-403.
    • (1993) Am J Otolaryngol , vol.14 , pp. 399-403
    • Fischel-Ghodsian, N.1    Prezant, T.R.2    Bu, X.3    Özatas, S.4
  • 6
    • 0030974247 scopus 로고    scopus 로고
    • Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity
    • Fischel-Ghodsian N, Prezant TR, Chaltraw WE, et al. Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity. Am J Otolaryngol 1997; 18: 173-8.
    • (1997) Am J Otolaryngol , vol.18 , pp. 173-178
    • Fischel-Ghodsian, N.1    Prezant, T.R.2    Chaltraw, W.E.3
  • 7
    • 0032833546 scopus 로고    scopus 로고
    • Rapid mass screening method and counseling for the 1555A → G mitochondrial mutation
    • Usami S, Abe S, Shinkawa H, Inoue Y, Yamaguchi T. Rapid mass screening method and counseling for the 1555A → G mitochondrial mutation. J Hum Genet 1999; 44: 304-7.
    • (1999) J Hum Genet , vol.44 , pp. 304-307
    • Usami, S.1    Abe, S.2    Shinkawa, H.3    Inoue, Y.4    Yamaguchi, T.5
  • 8
    • 0031917201 scopus 로고    scopus 로고
    • Mitochondrial mutations and hearing loss: Paradigm for mitochondrial genetics
    • Fischel-Ghodsian N. Mitochondrial mutations and hearing loss: paradigm for mitochondrial genetics. Am J Hum Genet 1998; 62: 15-9.
    • (1998) Am J Hum Genet , vol.62 , pp. 15-19
    • Fischel-Ghodsian, N.1
  • 9
    • 0031004773 scopus 로고    scopus 로고
    • Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation
    • Usami S, Abe S, Kasai M, et al. Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation. Laryngoscope 1997; 107: 483-90.
    • (1997) Laryngoscope , vol.107 , pp. 483-490
    • Usami, S.1    Abe, S.2    Kasai, M.3
  • 10
    • 0032511738 scopus 로고    scopus 로고
    • Hearing loss due to the mitochondrial A1555G mutation in Italian families
    • Casano RA, Bykhovskaya Y, Johnson DF, et al. Hearing loss due to the mitochondrial A1555G mutation in Italian families. Am J Med Genet 1998; 79: 388-91.
    • (1998) Am J Med Genet , vol.79 , pp. 388-391
    • Casano, R.A.1    Bykhovskaya, Y.2    Johnson, D.F.3
  • 11
    • 0030806576 scopus 로고    scopus 로고
    • Familial streptomycin otoxicity in a South Africa family: A mitochondrial disorder
    • Gardner JC, Goliath R, Viljoen D, et al. Familial streptomycin otoxicity in a South Africa family: a mitochondrial disorder. J Med Genet 1997; 34: 904-6.
    • (1997) J Med Genet , vol.34 , pp. 904-906
    • Gardner, J.C.1    Goliath, R.2    Viljoen, D.3
  • 12
    • 0031765087 scopus 로고    scopus 로고
    • Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial mutation
    • Tono T, Ushisako Y, Kiyomizu K, et al. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial mutation. Am J Otol 1998; 19: 754-7.
    • (1998) Am J Otol , vol.19 , pp. 754-757
    • Tono, T.1    Ushisako, Y.2    Kiyomizu, K.3
  • 13
    • 0030016359 scopus 로고    scopus 로고
    • Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation
    • Guan M-X, Fischel-Ghodsian N, Attardi G. Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation. Hum Mol Genet 1996; 7: 963-71.
    • (1996) Hum Mol Genet , vol.7 , pp. 963-971
    • Guan, M.-X.1    Fischel-Ghodsian, N.2    Attardi, G.3
  • 14
    • 0021158357 scopus 로고
    • Structure of ribosomal RNA
    • Noller HF. Structure of ribosomal RNA. Ann Rev Biochem 1984; 53: 119-62.
    • (1984) Ann Rev Biochem , vol.53 , pp. 119-162
    • Noller, H.F.1
  • 17
    • 0023238983 scopus 로고
    • Interaction of antibiotics with functional sites in 16S ribosomal RNA
    • Moazed D, Noller HF. Interaction of antibiotics with functional sites in 16S ribosomal RNA. Nature 1987; 327: 389-94.
    • (1987) Nature , vol.327 , pp. 389-394
    • Moazed, D.1    Noller, H.F.2
  • 18
    • 0022916242 scopus 로고
    • Transfer RNA shields specific nucleotides in 16S ribosomal RNA from attack by chemical probes
    • Moazed D, Noller HF. Transfer RNA shields specific nucleotides in 16S ribosomal RNA from attack by chemical probes. Cell 1986; 47: 985-94.
    • (1986) Cell , vol.47 , pp. 985-994
    • Moazed, D.1    Noller, H.F.2
  • 19
    • 0032486097 scopus 로고    scopus 로고
    • Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation
    • Bykhovskaya Y, Shohat M, Ehrenman K, et al. Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation. Am J Med Genet 1998; 77: 421-6.
    • (1998) Am J Med Genet , vol.77 , pp. 421-426
    • Bykhovskaya, Y.1    Shohat, M.2    Ehrenman, K.3
  • 20
    • 0025040275 scopus 로고
    • Hearing in the elderly: The Framingham cohort, 1983-1985. Part I. Basic audiometric test results
    • Gates GA, Cooper Jr JC, Kannel WB, Miller NJ. Hearing in the elderly: the Framingham cohort, 1983-1985. Part I. Basic audiometric test results. Ear Hear 1990; 11: 247-56.
    • (1990) Ear Hear , vol.11 , pp. 247-256
    • Gates, G.A.1    Cooper Jr., J.C.2    Kannel, W.B.3    Miller, N.J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.