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Volumn 18, Issue 12, 2008, Pages 1095-1102

Frequency of mitochondrial 12S ribosomal RNA variants in an adult cystic fibrosis population

Author keywords

Aminoglycoside; Audiologic testing; Cystic flbrosis; Mitochondrial 12S ribosomal RNA; Mitochondrial genome; Ototoxicity

Indexed keywords

AZITHROMYCIN; COLISTIN; GENOMIC DNA; GENTAMICIN; MITOCHONDRIAL RNA; RNA 12S; TOBRAMYCIN;

EID: 57149134391     PISSN: 17446872     EISSN: 17446880     Source Type: Journal    
DOI: 10.1097/FPC.0b013e328312b072     Document Type: Article
Times cited : (21)

References (35)
  • 1
    • 0142043977 scopus 로고    scopus 로고
    • Pathophysiology and management of pulmonary infections in cystic fibrosis
    • Gibson RL, Burns JL, Ramsey BW. Pathophysiology and management of pulmonary infections in cystic fibrosis. Am J Respir Crit Care Med 2003; 168:918-951.
    • (2003) Am J Respir Crit Care Med , vol.168 , pp. 918-951
    • Gibson, R.L.1    Burns, J.L.2    Ramsey, B.W.3
  • 2
    • 0037027912 scopus 로고    scopus 로고
    • An overview of the pathogenesis of cystic fibrosis lung disease
    • Boucher RC. An overview of the pathogenesis of cystic fibrosis lung disease. Adv Drug Deliv Rev 2002; 54:1359-1371.
    • (2002) Adv Drug Deliv Rev , vol.54 , pp. 1359-1371
    • Boucher, R.C.1
  • 3
    • 0034745438 scopus 로고    scopus 로고
    • The neglected ion: HCO3
    • Quinton PM. The neglected ion: HCO3. Nat Med 2001; 7:292-293.
    • (2001) Nat Med , vol.7 , pp. 292-293
    • Quinton, P.M.1
  • 5
    • 0000043793 scopus 로고
    • Antimicrobial agents: Tetracyclines, chloramphenicol, erthromycin, and miscellaneous antibacterial agents
    • Oilman A, Rail A, Nies A, Taylor A, editors, 8th ed. New York: Pergamon Press;
    • Sande MA, Mandell GL.'Antimicrobial agents: tetracyclines, chloramphenicol, erthromycin, and miscellaneous antibacterial agents'. In: Oilman A, Rail A, Nies A, Taylor A, editors. Goodman and Oilman's, The pharmacological basis of therapeutics. 8th ed. New York: Pergamon Press; 1990. pp. 1117-1145.
    • (1990) Goodman and Oilman's, The pharmacological basis of therapeutics , pp. 1117-1145
    • Sande, M.A.1    Mandell, G.L.2
  • 6
    • 0032857844 scopus 로고    scopus 로고
    • Effects of chronic tobramycin treatment on distortion product otoacoustic emissions
    • Katbamna B, Homnick DN, Marks JH. Effects of chronic tobramycin treatment on distortion product otoacoustic emissions. Eur Hear 1999; 20:393-402.
    • (1999) Eur Hear , vol.20 , pp. 393-402
    • Katbamna, B.1    Homnick, D.N.2    Marks, J.H.3
  • 7
    • 0032168489 scopus 로고    scopus 로고
    • Sensorineural hearing loss caused by mitochondrial DNA mutations: Special reference to the 1555A>G mutation
    • quiz 434-435
    • Usami S, Abe S, Shinkawa H, Kimberling WJ. Sensorineural hearing loss caused by mitochondrial DNA mutations: special reference to the 1555A>G mutation. J Commun Disord 1998; 31:423-434; quiz 434-435.
    • (1998) J Commun Disord , vol.31 , pp. 423-434
    • Usami, S.1    Abe, S.2    Shinkawa, H.3    Kimberling, W.J.4
  • 8
    • 0031958231 scopus 로고    scopus 로고
    • Mitochondrial genetics and hearing loss: The missing link between genotype and phenotype
    • Fischel-Ghodsian N. Mitochondrial genetics and hearing loss: the missing link between genotype and phenotype. Proc Soc Exp Biol Med 1998; 218:1-6.
    • (1998) Proc Soc Exp Biol Med , vol.218 , pp. 1-6
    • Fischel-Ghodsian, N.1
  • 9
    • 0032796453 scopus 로고    scopus 로고
    • Genetic factors in aminoglycoside toxicity
    • Fischel-Ghodsian N. Genetic factors in aminoglycoside toxicity. Ann N Y Acad Sci 1999; 884:99-109.
    • (1999) Ann N Y Acad Sci , vol.884 , pp. 99-109
    • Fischel-Ghodsian, N.1
  • 10
    • 0027226069 scopus 로고
    • Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness
    • Prezant TR, Agapian JV, Bohlman MC, Bu X, Oztas S, Qiu WQ, et al. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nat Genet 1993; 4:289-294.
    • (1993) Nat Genet , vol.4 , pp. 289-294
    • Prezant, T.R.1    Agapian, J.V.2    Bohlman, M.C.3    Bu, X.4    Oztas, S.5    Qiu, W.Q.6
  • 12
    • 0347003512 scopus 로고    scopus 로고
    • Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel 1494C>T mutation in the MT-RNR1 gene in a large Chinese family
    • Zhao H, Li R, Wang Q, Van Q, Deng JH, Han D, et al. Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel 1494C>T mutation in the MT-RNR1 gene in a large Chinese family. Am J Hum Genet 2004; 74:139-152.
    • (2004) Am J Hum Genet , vol.74 , pp. 139-152
    • Zhao, H.1    Li, R.2    Wang, Q.3    Van, Q.4    Deng, J.H.5    Han, D.6
  • 13
    • 20344407298 scopus 로고    scopus 로고
    • Mutational analysis of the MT-RNR1 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, et al. Mutational analysis of the MT-RNR1 gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss. Hum Genet 2005; 117: 9-15.
    • (2005) Hum Genet , vol.117 , pp. 9-15
    • Li, Z.1    Li, R.2    Chen, J.3    Liao, Z.4    Zhu, Y.5    Qian, Y.6
  • 16
    • 8144221376 scopus 로고    scopus 로고
    • Phenotype of non-syndromic deafness associated with the mitochondrial 1555A>G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3
    • Bykhovskaya Y, Mengesha E, Wang D, Yang H, Estivill X, Shohat M, et al. Phenotype of non-syndromic deafness associated with the mitochondrial 1555A>G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3. Mol Genet Metab 2004; 83:199-206.
    • (2004) Mol Genet Metab , vol.83 , pp. 199-206
    • Bykhovskaya, Y.1    Mengesha, E.2    Wang, D.3    Yang, H.4    Estivill, X.5    Shohat, M.6
  • 17
    • 0000918182 scopus 로고
    • Preferred method for clinical determination of pure-tone thresholds
    • Carhart R, Jerger JJ. Preferred method for clinical determination of pure-tone thresholds. J Speech Hearing Disorders 1959; 24:330-345.
    • (1959) J Speech Hearing Disorders , vol.24 , pp. 330-345
    • Carhart, R.1    Jerger, J.J.2
  • 19
    • 0027968068 scopus 로고
    • Clustal W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
    • Thompson JD, Higgins DG, Gibson TJ. Clustal W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 1994; 22:4673-4680.
    • (1994) Nucleic Acids Res , vol.22 , pp. 4673-4680
    • Thompson, J.D.1    Higgins, D.G.2    Gibson, T.J.3
  • 20
    • 1842678661 scopus 로고    scopus 로고
    • Molecular pathogenetic mechanism of maternally inherited deafness
    • Guan MX. Molecular pathogenetic mechanism of maternally inherited deafness. Ann N Y Acad Sci 2004; 1011:259-271.
    • (2004) Ann N Y Acad Sci , vol.1011 , pp. 259-271
    • Guan, M.X.1
  • 21
    • 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; 62:15-19.
    • (1998) Am J Hum Genet , vol.62 , pp. 15-19
    • Fischel-Ghodsian, N.1
  • 23
    • 0033858002 scopus 로고    scopus 로고
    • A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity
    • Guan MX, Fischel-Ghodsian N, Attardi G. A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity. Hum Mol Genet 2000; 9:1787-1793.
    • (2000) Hum Mol Genet , vol.9 , pp. 1787-1793
    • Guan, M.X.1    Fischel-Ghodsian, N.2    Attardi, G.3
  • 26
    • 12344252667 scopus 로고    scopus 로고
    • New developments in our understanding of ototoxicity
    • discussion 16-17
    • Roland PS. New developments in our understanding of ototoxicity. Ear, Nose and Throat J 2004; 83:15-16; discussion 16-17.
    • (2004) Ear, Nose and Throat J , vol.83 , pp. 15-16
    • Roland, P.S.1
  • 29
    • 0032700610 scopus 로고    scopus 로고
    • Rapid identification of an 1555A>G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity
    • Scrimshaw BJ, Faed JM, Tate WP, Yun K. Rapid identification of an 1555A>G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity. J Hum Genet 1999; 44:388-390.
    • (1999) J Hum Genet , vol.44 , pp. 388-390
    • Scrimshaw, B.J.1    Faed, J.M.2    Tate, W.P.3    Yun, K.4
  • 31
    • 18344366125 scopus 로고    scopus 로고
    • Reduced median network analysis of complete mitochondrial DNA coding region sequences for the major African, Asian and European Haplogroups
    • Hernstadt C, Elson JL, Fahy E, Preston G, Turnbull DM, Anderson C, et al. Reduced median network analysis of complete mitochondrial DNA coding region sequences for the major African, Asian and European Haplogroups. Am J Hum Genet 2002; 70:1152-1171.
    • (2002) Am J Hum Genet , vol.70 , pp. 1152-1171
    • Hernstadt, C.1    Elson, J.L.2    Fahy, E.3    Preston, G.4    Turnbull, D.M.5    Anderson, C.6
  • 32
    • 29644446464 scopus 로고    scopus 로고
    • Clinical and molecular analysis of a four-generation Chinese family with amino-glycoside- induced and nonsyndromic hearing lose associated with the MT-RNR1 1494C>T mutation
    • Wang Q, Li QZ, Han D, Zhao Y, Zhao L, Qian Y, et al. Clinical and molecular analysis of a four-generation Chinese family with amino-glycoside- induced and nonsyndromic hearing lose associated with the MT-RNR1 1494C>T mutation. Biochem Biophys Res Commun 2006; 340:583-588.
    • (2006) Biochem Biophys Res Commun , vol.340 , pp. 583-588
    • Wang, Q.1    Li, Q.Z.2    Han, D.3    Zhao, Y.4    Zhao, L.5    Qian, Y.6
  • 33
    • 0029003553 scopus 로고
    • Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness
    • Bacino C, Prezant TR, Bu X, Foumier P, Fiachel-Ghodsian N. Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness. Pharmacogenetics 1995; 8:165-172.
    • (1995) Pharmacogenetics , vol.8 , pp. 165-172
    • Bacino, C.1    Prezant, T.R.2    Bu, X.3    Foumier, P.4    Fiachel-Ghodsian, N.5
  • 35
    • 19444371441 scopus 로고    scopus 로고
    • Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation
    • Kobayashi K, Oguchi T, Asamura K, Miyagawa M, Horai S, Abe S, et al. Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation. Auris Nasus Larynx 2006; 32:119-124.
    • (2006) Auris Nasus Larynx , vol.32 , pp. 119-124
    • Kobayashi, K.1    Oguchi, T.2    Asamura, K.3    Miyagawa, M.4    Horai, S.5    Abe, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.