-
1
-
-
0000043793
-
Antimicrobial agents
-
(8th edn). Gilman AG, Rall TW, Nies AS, Taylor P (Eds), Pergamon Press, Inc., Elmsford, NY, USA
-
Sande MA, Mandell GL: Antimicrobial agents. In: The Pharmacological Basis of Therapeutics (8th edn). Gilman AG, Rall TW, Nies AS, Taylor P (Eds), Pergamon Press, Inc., Elmsford, NY, USA 1098-1116 (1990).
-
(1990)
The Pharmacological Basis of Therapeutics
, pp. 1098-1116
-
-
Sande, M.A.1
Mandell, G.L.2
-
2
-
-
0029005340
-
Aminoglycosides
-
Lortholary O, Tod M, Cohen Y, Petitjean O: Aminoglycosides. Med. Clin. North Am. 79, 761-798 (1995).
-
(1995)
Med. Clin. North Am.
, vol.79
, pp. 761-798
-
-
Lortholary, O.1
Tod, M.2
Cohen, Y.3
Petitjean, O.4
-
3
-
-
0022618766
-
Aminoclycoside research 1975-1985: Prospects for development of improved agents
-
Price KE: Aminoclycoside research 1975-1985: prospects for development of improved agents. Antimicrobial Agents Chemother. 29, 543-548 (1986).
-
(1986)
Antimicrobial Agents Chemother.
, vol.29
, pp. 543-548
-
-
Price, K.E.1
-
4
-
-
0016276843
-
Ototoxicity with children caused by streptomycin
-
Prazic M, Salaj B: Ototoxicity with children caused by streptomycin. Audiology 14, 173-176 (1975).
-
(1975)
Audiology
, vol.14
, pp. 173-176
-
-
Prazic, M.1
Salaj, B.2
-
6
-
-
0021365039
-
Risk factors for the development of auditory toxicity in patients receiving aminoglycosides
-
Moore RD, Smith CR, Lietman PS: Risk factors for the development of auditory toxicity in patients receiving aminoglycosides. J. Infect. Dis. 149, 23-30 (1984).
-
(1984)
J. Infect. Dis.
, vol.149
, pp. 23-30
-
-
Moore, R.D.1
Smith, C.R.2
Lietman, P.S.3
-
7
-
-
0000771721
-
Streptomycin sulfate and dihydrostreptomycin toxicity. Behavioural and histopathologic studies
-
McGee TM, Olszewski J: Streptomycin sulfate and dihydrostreptomycin toxicity. Behavioural and histopathologic studies. Arch. Otolaryngol. 75, 295-311 (1962).
-
(1962)
Arch. Otolaryngol.
, vol.75
, pp. 295-311
-
-
McGee, T.M.1
Olszewski, J.2
-
8
-
-
0002945653
-
Structural damage of the organ of Corti and the vestibular epithelia caused by aminoglycoside antibiotics in the guinea-pig
-
Lerner SA, Matz GJ, Hawkins JE Jr (Eds), Little, Brown & Co., Boston, MA, USA
-
Wersall J: Structural damage of the organ of Corti and the vestibular epithelia caused by aminoglycoside antibiotics in the guinea-pig. In: Aminoglycoside Ototoxicity. Lerner SA, Matz GJ, Hawkins JE Jr (Eds), Little, Brown & Co., Boston, MA, USA 197-214 (1981).
-
(1981)
Aminoglycoside Ototoxicity
, pp. 197-214
-
-
Wersall, J.1
-
9
-
-
0023231026
-
Cochlear neural degeneration without hair cell loss in two patients with aminoglycoside ototoxicity
-
Hinojosa R, Lerner SA. Cochlear neural degeneration without hair cell loss in two patients with aminoglycoside ototoxicity. J. Infect. Dis. 156(3), 449-455 (1987).
-
(1987)
J. Infect. Dis.
, vol.156
, Issue.3
, pp. 449-455
-
-
Hinojosa, R.1
Lerner, S.A.2
-
10
-
-
0000782819
-
Site of action of streptomycin upon inner ear sensory cells
-
Duvall AJ, Wersall J: Site of action of streptomycin upon inner ear sensory cells. Acta Otolaryngol. 57, 581-598 (1964).
-
(1964)
Acta Otolaryngol.
, vol.57
, pp. 581-598
-
-
Duvall, A.J.1
Wersall, J.2
-
11
-
-
0016349423
-
Ototoxicite de la kanamycin au jour le jour. Etude experimentale en microscopie electronique
-
Darrouzet J, Guilhaume A: [Ototoxicite de la kanamycin au jour le jour. Etude experimentale en microscopie electronique.] Rev. Laryngol. Otol. Rhinol. 95, 601-621 (1974).
-
(1974)
Rev. Laryngol. Otol. Rhinol.
, vol.95
, pp. 601-621
-
-
Darrouzet, J.1
Guilhaume, A.2
-
13
-
-
0017645661
-
Effects of perilymphatic perfusion with neomycin on the cochlear microphonic potential in the guinea-pig
-
Nuttall AL, Marques DM, Lawrence M: Effects of perilymphatic perfusion with neomycin on the cochlear microphonic potential in the guinea-pig. Acta Otolaryngol. 83, 393-400 (1977).
-
(1977)
Acta Otolaryngol.
, vol.83
, pp. 393-400
-
-
Nuttall, A.L.1
Marques, D.M.2
Lawrence, M.3
-
14
-
-
0024535053
-
Blockage of the transduction channels of hair cells in the bullftog's sacculus by aminoglycoside antibiotics
-
Kroese ABA, Das A, Hudspeth AJ: Blockage of the transduction channels of hair cells in the bullftog's sacculus by aminoglycoside antibiotics. Hear. Res. 37, 203-217 (1989).
-
(1989)
Hear. Res.
, vol.37
, pp. 203-217
-
-
Kroese, A.B.A.1
Das, A.2
Hudspeth, A.J.3
-
15
-
-
0023153006
-
Dose-dependent changes in the rat cochlea following aminoglycoside intoxication. I. Physiological study
-
Puel JL, Lenoir M, Uziel A: Dose-dependent changes in the rat cochlea following aminoglycoside intoxication. I. Physiological study. Hear. Res. 26, 191-197 (1987).
-
(1987)
Hear. Res.
, vol.26
, pp. 191-197
-
-
Puel, J.L.1
Lenoir, M.2
Uziel, A.3
-
16
-
-
0013798626
-
A study of the relative concentrations of antibiotics in the blood, spinal fluid and perilymph in animals
-
Vrabec DP, Cody DT, Ulrich JA: A study of the relative concentrations of antibiotics in the blood, spinal fluid and perilymph in animals. Ann. Otol. Rhinol. Laryngol. 74, 689 (1965).
-
(1965)
Ann. Otol. Rhinol. Laryngol.
, vol.74
, pp. 689
-
-
Vrabec, D.P.1
Cody, D.T.2
Ulrich, J.A.3
-
17
-
-
0023918234
-
Pharmacokinetics of aminoglycoside antibiotics in blood, inner-ear fluids and tissues and their relationship to ototoxicity
-
Henley CM, Schacht J: Pharmacokinetics of aminoglycoside antibiotics in blood, inner-ear fluids and tissues and their relationship to ototoxicity. Audiology 27, 137-146 (1988).
-
(1988)
Audiology
, vol.27
, pp. 137-146
-
-
Henley, C.M.1
Schacht, J.2
-
18
-
-
0022640994
-
A review: Effects of noise and ototoxic drugs at the cellular level in the cochlea
-
Lim DJ: A review: effects of noise and ototoxic drugs at the cellular level in the cochlea. Am. J. Otolaryngol. 7, 73-99 (1986 ).
-
(1986)
Am. J. Otolaryngol.
, vol.7
, pp. 73-99
-
-
Lim, D.J.1
-
20
-
-
0023573969
-
Three molecular steps of aminoglycoside ototoxicity demonstrated in outer hair cells
-
Williams SE, Zenner HP, Schacht J: Three molecular steps of aminoglycoside ototoxicity demonstrated in outer hair cells. Hear. Res. 30, 11-18 (1987).
-
(1987)
Hear. Res.
, vol.30
, pp. 11-18
-
-
Williams, S.E.1
Zenner, H.P.2
Schacht, J.3
-
21
-
-
0017659506
-
Gentamicin-induced changes in RNA content in sensory and ganglionic cells in the hearing organ of the lizard Calotes versicolor: A cytochemical and morphological investigation
-
Jarlstedt J, Bagger-Sjoback D: Gentamicin-induced changes in RNA content in sensory and ganglionic cells in the hearing organ of the lizard Calotes versicolor: a cytochemical and morphological investigation. Acta Otolaryngol 84, 361-369 (1977).
-
(1977)
Acta Otolaryngol.
, vol.84
, pp. 361-369
-
-
Jarlstedt, J.1
Bagger-Sjoback, D.2
-
22
-
-
0017621924
-
Radioactive labelling of phospholipids and proteins by cochlear perfusion in the guinea-pig and the effect of neomycin
-
Stockhorst W, Schacht J: Radioactive labelling of phospholipids and proteins by cochlear perfusion in the guinea-pig and the eff-ect of neomycin. Acta Otolaryngol. 83, 401-409 (1977).
-
(1977)
Acta Otolaryngol.
, vol.83
, pp. 401-409
-
-
Stockhorst, W.1
Schacht, J.2
-
23
-
-
0030068133
-
Variable efficacy of radical scavengers and iron chelators to attenuate gentamycin ototoxicity in guinea pigs in vivo
-
Song BB, Schacht J: Variable efficacy of radical scavengers and iron chelators to attenuate gentamycin ototoxicity in guinea pigs in vivo. Hear. Res. 94, 87-93 (1996).
-
(1996)
Hear. Res.
, vol.94
, pp. 87-93
-
-
Song, B.B.1
Schacht, J.2
-
24
-
-
1842337282
-
Gene mutations in human haemoglobin: The chemical difference between normal and sickle cell haemoglobin
-
Ingram VM: Gene mutations in human haemoglobin: the chemical difference between normal and sickle cell haemoglobin. Nature 180, 326 (1957).
-
(1957)
Nature
, vol.180
, pp. 326
-
-
Ingram, V.M.1
-
25
-
-
0021346853
-
Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22
-
Groffen J, Stephenson JR, Heisterkamp N, de Klein A, Bartram CR, Grosveld G: Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22. Cell 36, 93-99 (1984).
-
(1984)
Cell
, vol.36
, pp. 93-99
-
-
Groffen, J.1
Stephenson, J.R.2
Heisterkamp, N.3
de Klein, A.4
Bartram, C.R.5
Grosveld, G.6
-
26
-
-
0025043959
-
The t(15;17) translocation of acute promyelocytic leukemia fuses the retinoic acid receptor α gene to a novel transcribed locus
-
de The H, Chomienne C, Lanotte M, Degos L, Dejean A. The t(15;17) translocation of acute promyelocytic leukemia fuses the retinoic acid receptor α gene to a novel transcribed locus. Nature 347, 558-561 (1990).
-
(1990)
Nature
, vol.347
, pp. 558-561
-
-
de The, H.1
Chomienne, C.2
Lanotte, M.3
Degos, L.4
Dejean, A.5
-
27
-
-
0025201879
-
All-trans retinoic acid as a differentiation therapy for acute promyelocytic leukemia. I. Clinical results
-
Castaigne S, Chomienne C, Daniel MT et al.: All- trans retinoic acid as a differentiation therapy for acute promyelocytic leukemia. I. Clinical results. Blood 76, 1704-1709 (1990).
-
(1990)
Blood
, vol.76
, pp. 1704-1709
-
-
Castaigne, S.1
Chomienne, C.2
Daniel, M.T.3
-
28
-
-
0037672877
-
Philadelphia chromosome-positive leukaemias: From basic mechanisms to molecular therapeutics
-
Kurzrock R, Kantarjian HM, Druker BJ, Talpaz M: Philadelphia chromosome-positive leukaemias: from basic mechanisms to molecular therapeutics. Ann. Internal Med. 138, 819-830 (2003).
-
(2003)
Ann. Internal Med.
, vol.138
, pp. 819-830
-
-
Kurzrock, R.1
Kantarjian, H.M.2
Druker, B.J.3
Talpaz, M.4
-
29
-
-
0001447272
-
Ototoxicity
-
(3rd edn). Paparella WM, Shumrick DA, Gluckman JL, Meyerhoff WL (Eds), W.B. Saunders Co., Philadelphia, PA, USA
-
Stringer SP, Meyerhoff WL, Wright CG: Ototoxicity. In: Otolaryngology (3rd edn). Paparella WM, Shumrick DA, Gluckman JL, Meyerhoff WL (Eds), W.B. Saunders Co., Philadelphia, PA, USA 1653-1669 (1991).
-
(1991)
Otolaryngology
, pp. 1653-1669
-
-
Stringer, S.P.1
Meyerhoff, W.L.2
Wright, C.G.3
-
30
-
-
0024360825
-
Unique inheritance of streptomycin-induced deafness
-
Higashi K: Unique inheritance of streptomycin-induced deafness. Clin. Genet. 35, 433-436 (1989).
-
(1989)
Clin. Genet.
, vol.35
, pp. 433-436
-
-
Higashi, K.1
-
32
-
-
0015120431
-
Familial incidence of streptomycin hearing loss and hereditary weakness of the cochlea
-
Tsuiki T, Murai S: Familial incidence of streptomycin hearing loss and hereditary weakness of the cochlea. Audiology 10, 315-322 (1971).
-
(1971)
Audiology
, vol.10
, pp. 315-322
-
-
Tsuiki, T.1
Murai, S.2
-
33
-
-
0003726761
-
-
W.B. Saunders Co., Philadelphia, PA, USA
-
Konigsmark BW, Gorlin RJ: Genetic and Metabolic Deafness W.B. Saunders Co., Philadelphia, PA, USA 364-365 (1976).
-
(1976)
Genetic and Metabolic Deafness
, pp. 364-365
-
-
Konigsmark, B.W.1
Gorlin, R.J.2
-
34
-
-
0025980075
-
Genetic aspects of antibiotic induced deafness: Mitochondrial inheritance
-
Hu D-N, Qiu W-Q, Wu B-T et al.: Genetic aspects of antibiotic induced deafness: mitochondrial inheritance. J. Med. Genet. 28, 79-83 (1991).
-
(1991)
J. Med. Genet.
, vol.28
, pp. 79-83
-
-
Hu, D.-N.1
Qiu, W.-Q.2
Wu, B.-T.3
-
35
-
-
0002520417
-
Animal models in the study of ototoxic hearing loss
-
Lerner SA, Matz GL, Hawkins JE Jr (Eds), Little, Brown and Co., Boston, MA, USA
-
Stebbins WC, McGinn CS, Feitosa AG et al.: Animal models in the study of ototoxic hearing loss. In: Aminoglycoside Ototoxicity. Lerner SA, Matz GL, Hawkins JE Jr (Eds), Little, Brown and Co., Boston, MA, USA, 5-25 (1981).
-
(1981)
Aminoglycoside Ototoxicity
, pp. 5-25
-
-
Stebbins, W.C.1
McGinn, C.S.2
Feitosa, A.G.3
-
36
-
-
0023579725
-
Decoding at the ribosomal A site: Antibiotics, misreading and energy of aminoacyl-tRNA binding
-
Hornig H, Woolley P, Luhrmann R. Decoding at the ribosomal A site: antibiotics, misreading and energy of aminoacyl-tRNA binding. Biochimie 69, 803-813 (1987).
-
(1987)
Biochimie
, vol.69
, pp. 803-813
-
-
Hornig, H.1
Woolley, P.2
Luhrmann, R.3
-
37
-
-
0014429801
-
Misreading of ribonucleic acid code words induced by aminoglycoside antibiotics
-
Davis J, Davis BD: Misreading of ribonucleic acid code words induced by aminoglycoside antibiotics. J. Biol. Chem. 243, 3312-3316 (1968).
-
(1968)
J. Biol. Chem.
, vol.243
, pp. 3312-3316
-
-
Davis, J.1
Davis, B.D.2
-
38
-
-
0025733603
-
Ribosomal RNA and translation
-
Noller HF: Ribosomal RNA and translation. Annu. Rev. Biochem. 60, 191-227 (1991).
-
(1991)
Annu. Rev. Biochem.
, vol.60
, pp. 191-227
-
-
Noller, H.F.1
-
39
-
-
0027226069
-
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
-
40
-
-
0023226742
-
Crosslinking of streptomycin to the 16S ribosomal RNA of Escherichia coli
-
Gravel M, Melancon P, Brakier-Gingras L: Crosslinking of streptomycin to the 16S ribosomal RNA of Escherichia coli. Biochemistry 26, 6227-6232 (1987).
-
(1987)
Biochemistry
, vol.26
, pp. 6227-6232
-
-
Gravel, M.1
Melancon, P.2
Brakier-Gingras, L.3
-
41
-
-
0019908820
-
Identification of the paromomycin-resistance mutation in the 15S rRNA gene of yeast mitochondria
-
Li M, Tzagaloff A, Underbrink-Lyon K, Martin NC: Identification of the paromomycin-resistance mutation in the 15S rRNA gene of yeast mitochondria. J. Biol. Chem. 257, 5921-5928 (1982).
-
(1982)
J. Biol. Chem.
, vol.257
, pp. 5921-5928
-
-
Li, M.1
Tzagaloff, A.2
Underbrink-Lyon, K.3
Martin, N.C.4
-
42
-
-
0021892944
-
The nucleotide sequence of the 17S ribosomal RNA gene of Tetrahymena thermophila and the identification of point mutations resulting in resistance to the antibiotics paromomycin and hygromycin
-
Spangler EA, Blackburn EH: The nucleotide sequence of the 17S ribosomal RNA gene of Tetrahymena thermophila and the identification of point mutations resulting in resistance to the antibiotics paromomycin and hygromycin. J. Biol. Chem. 260, 6334-6340 (1985).
-
(1985)
J. Biol. Chem.
, vol.260
, pp. 6334-6340
-
-
Spangler, E.A.1
Blackburn, E.H.2
-
43
-
-
0027218979
-
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. 21, 4174-4179 (1993).
-
(1993)
Nucleic Acids Res.
, vol.21
, pp. 4174-4179
-
-
Hutchin, T.1
Haworth, I.2
Higashi, K.3
-
44
-
-
0029916599
-
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. 4, 46-51 (1996).
-
(1996)
Eur. J. Hum. Genet.
, vol.4
, pp. 46-51
-
-
Matthijs, G.1
Claes, S.2
Longo-Mbenza, B.3
Cassiman, J.-J.4
-
45
-
-
0031055387
-
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
-
46
-
-
0343852695
-
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
-
47
-
-
17344365276
-
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
-
48
-
-
0032942192
-
Aminoglycoside induced deafness in an Israeli Jewish family with a mitochondrial ribosomal RNA gene mutation
-
Shohat M, Fischel-Ghodsian N, Legum C, Halpern GJ: Aminoglycoside induced deafness in an Israeli Jewish family with a mitochondrial ribosomal RNA gene mutation. Am. J. Otolaryngol. 20, 64-67 (1999).
-
(1999)
Am. J. Otolaryngol.
, vol.20
, pp. 64-67
-
-
Shohat, M.1
Fischel-Ghodsian, N.2
Legum, C.3
Halpern, G.J.4
-
49
-
-
0344167734
-
Cosegregation of C-insertion at position 961 with A1555G mutation of mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss
-
Li R, Xing G, Yan M et al: Cosegregation of C-insertion at position 961 with A1555G mutation of mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss. Am. J. Med. Genet. 124A, 113-117 (2004).
-
(2004)
Am. J. Med. Genet.
, vol.124 A
, pp. 113-117
-
-
Li, R.1
Xing, G.2
Yan, M.3
-
50
-
-
0027515721
-
Mitochondrial ribosomal RNA mutation associated with aminoglycoside ototoxicity
-
Fischel-Ghodsian N, Prezant TR, Bu X, Oztas S: Mitochondrial ribosomal RNA mutation associated with aminoglycoside ototoxicity. Am. J. Otolaryngol. 14, 399-403 (1993).
-
(1993)
Am. J. Otolaryngol.
, vol.14
, pp. 399-403
-
-
Fischel-Ghodsian, N.1
Prezant, T.R.2
Bu, X.3
Oztas, S.4
-
51
-
-
0030974247
-
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
-
52
-
-
0042828920
-
Heteroplasmy for the 1555A > G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss: Implications for genetic diagnosis and counseling
-
del Castillo FJ, Rodriguez-Ballesteros M, Martin Y et al. Heteroplasmy for the 1555A > G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss: implications for genetic diagnosis and counseling. J. Med. Genet. 40, 632-636 (2003).
-
(2003)
J. Med. Genet.
, vol.40
, pp. 632-636
-
-
del Castillo, F.J.1
Rodriguez-Ballesteros, M.2
Martin, Y.3
-
53
-
-
0032511738
-
Hearing loss due to the mitochondrial A1555G mutation in Italian families
-
Casano RAMS, Bykhovskaya Y, Johnson DF, Torricelli F, Bigozzi M, Fischel-Ghodsian N: Hearing loss due to the mitochondrial A1555G mutation in Italian families. Am. J. Med. Genet. 79, 388-391 (1998).
-
(1998)
Am. J. Med. Genet.
, vol.79
, pp. 388-391
-
-
Casano, R.A.M.S.1
Bykhovskaya, Y.2
Johnson, D.F.3
Torricelli, F.4
Bigozzi, M.5
Fischel-Ghodsian, N.6
-
54
-
-
0031958231
-
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. 218, 1-6 (1998).
-
(1998)
Proc. Soc. Exp. Biol. Med.
, vol.218
, pp. 1-6
-
-
Fischel-Ghodsian, N.1
-
55
-
-
0031917201
-
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. 62, 15-19 (1998).
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 15-19
-
-
Fischel-Ghodsian, N.1
-
56
-
-
0033911449
-
Candidate locus for a nuclear modifier gene for maternally inherited deafness
-
Bykhovskaya Y, Estivill X, Taylor K et al.: Candidate locus for a nuclear modifier gene for maternally inherited deafness. Am. J. Hum. Genet. 66, 1905-1910 (2000).
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1905-1910
-
-
Bykhovskaya, Y.1
Estivill, X.2
Taylor, K.3
-
57
-
-
18544371057
-
Linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness
-
Bykhovskaya Y, Yang H, Taylor K et al.: Linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness. Genet. Med. 3, 177-180 (2001).
-
(2001)
Genet. Med.
, vol.3
, pp. 177-180
-
-
Bykhovskaya, Y.1
Yang, H.2
Taylor, K.3
-
58
-
-
1942425120
-
Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation
-
Bykhovskaya Y, Mengesha E, Wang D et al.: Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation. Mol. Genet. Metab. 82, 27-32 (2004).
-
(2004)
Mol. Genet. Metab.
, vol.82
, pp. 27-32
-
-
Bykhovskaya, Y.1
Mengesha, E.2
Wang, D.3
-
59
-
-
8144221376
-
Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3
-
Bykhovskaya Y, Mengesha E, Wang D et al.: Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3. Mol. Genet. Metab. 83, 199-206 (2004).
-
(2004)
Mol. Genet. Metab.
, vol.83
, pp. 199-206
-
-
Bykhovskaya, Y.1
Mengesha, E.2
Wang, D.3
-
60
-
-
0037178851
-
Isolation and chanracterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12S rRNA A1555G mutation
-
Li X, Li R, Lin X, Guan MX: Isolation and chanracterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12S rRNA A1555G mutation. J. Biol. Chem. 277, 27256-27264 (2002).
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 27256-27264
-
-
Li, X.1
Li, R.2
Lin, X.3
Guan, M.X.4
-
61
-
-
0036837683
-
A human mitochondrial GTP binding protein related to tRNA modification may modulate the phenotypic expression of the deafness-associated mitochondrial 12S rRNA mutation
-
Li X, Guan MX: A human mitochondrial GTP binding protein related to tRNA modification may modulate the phenotypic expression of the deafness-associated mitochondrial 12S rRNA mutation. Mol. Cell. Biol. 22, 7701-7711 (2002).
-
(2002)
Mol. Cell. Biol.
, vol.22
, pp. 7701-7711
-
-
Li, X.1
Guan, M.X.2
-
62
-
-
0029003553
-
Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness
-
Bacino CM, Prezant TR, Bu X, Fournier P, Fischel-Ghodsian N: 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
Fournier, P.4
Fischel-Ghodsian, N.5
-
63
-
-
13044279515
-
Inherited susceptibility to aminoglycoside ototoxicity: Genetic heterogeneity and clinical implications
-
Casano RAMS, Johnson DF, Hamon M et al.: Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications. Am. J. Otolaryngol. 20, 151-156 (1999).
-
(1999)
Am. J. Otolaryngol.
, vol.20
, pp. 151-156
-
-
Casano, R.A.M.S.1
Johnson, D.F.2
Hamon, M.3
-
64
-
-
0036726578
-
Genetic susceptibility to aminoglycoside ototoxicity: How many are at risk?
-
Tang HY, Hutcheson E, Neill S, Drummond-Borg M, Speer M, Alford RL: Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk? Genet. Med. 4, 336-345 (2002).
-
(2002)
Genet. Med.
, vol.4
, pp. 336-345
-
-
Tang, H.Y.1
Hutcheson, E.2
Neill, S.3
Drummond-Borg, M.4
Speer, M.5
Alford, R.L.6
-
65
-
-
85028790817
-
Relative frequencies of the mitochondrial A1555G and 961 delT mutations in the 12SrRNA gene in a large sample of deaf probands from the United States
-
(Abstract)
-
Arnos K, Xia XJ, Norris G et al.: Relative frequencies of the mitochondrial A1555G and 961 delT mutations in the 12SrRNA gene in a large sample of deaf probands from the United States. Am. J. Hum. Genet. 73, 2196 (2003) (Abstract).
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 2196
-
-
Arnos, K.1
Xia, X.J.2
Norris, G.3
-
66
-
-
0347003512
-
Maternally inherited aminoglycoside-induced and non-syndromic deafness associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family
-
Zhao H, li R, Wang Q et al.: Maternally inherited aminoglycoside-induced and non-syndromic deafness associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family. Am. J. Hum. Genet. 74, 139-152 (2004).
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 139-152
-
-
Zhao, H.1
Li, R.2
Wang, Q.3
-
67
-
-
0033768121
-
A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness and neuropathy
-
Thyagarajan D, Bressman S, Bruno C et al.: A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness and neuropathy. Ann. Neurol. 48, 730-736 (2000).
-
(2000)
Ann. Neurol.
, vol.48
, pp. 730-736
-
-
Thyagarajan, D.1
Bressman, S.2
Bruno, C.3
-
68
-
-
0035131983
-
Maternally inherited deafness associated with a T1095C mutation in the mDNA
-
Tessa A, Giannotti A, Tieri L, Vilarinho L, Marotta G, Santorelli FM: Maternally inherited deafness associated with a T1095C mutation in the mDNA. Eur J. Hum. Genet. 9, 147-149 (2001).
-
(2001)
Eur J. Hum. Genet.
, vol.9
, pp. 147-149
-
-
Tessa, A.1
Giannotti, A.2
Tieri, L.3
Vilarinho, L.4
Marotta, G.5
Santorelli, F.M.6
-
69
-
-
8844236333
-
Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation
-
Zhao L, Young W-Y, Li R, Wang Q, Qian Y, Guan M-X: Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation. Biochem. Biophys. Red. Com. 325, 1503-1508 (2004).
-
(2004)
Biochem. Biophys. Red. Com.
, vol.325
, pp. 1503-1508
-
-
Zhao, L.1
Young, W.-Y.2
Li, R.3
Wang, Q.4
Qian, Y.5
Guan, M.-X.6
-
70
-
-
2342572275
-
A novel mitochondrial mutation, 1556C→T, in a Japanese patient with streptomycin-induced tinnitus
-
Tanimoto H, Nishio H, Matsuo M, Nibu K-I: A novel mitochondrial mutation, 1556C→T, in a Japanese patient with streptomycin-induced tinnitus. Acta Otolaryngol. 124, 258-261 (2004).
-
(2004)
Acta Otolaryngol.
, vol.124
, pp. 258-261
-
-
Tanimoto, H.1
Nishio, H.2
Matsuo, M.3
Nibu, K.-I.4
-
71
-
-
0027404833
-
Ultrastructural evidence for hair cell regeneration in the mammalian inner ear
-
Forge A, Li L, Corwin JT. Nevill G: Ultrastructural evidence for hair cell regeneration in the mammalian inner ear. Science 259, 1616-1619 (1993).
-
(1993)
Science
, vol.259
, pp. 1616-1619
-
-
Forge, A.1
Li, L.2
Corwin, J.T.3
Nevill, G.4
-
72
-
-
0027531639
-
Regenerative proliferation in inner ear sensory epithelia from adult guinea-pigs and humans
-
Warchol ME, Lambert PR, Goldstein BJ, Forge A, Corwin JT. Regenerative proliferation in inner ear sensory epithelia from adult guinea-pigs and humans. Science 259, 1619-1622 (1993).
-
(1993)
Science
, vol.259
, pp. 1619-1622
-
-
Warchol, M.E.1
Lambert, P.R.2
Goldstein, B.J.3
Forge, A.4
Corwin, J.T.5
-
73
-
-
0027222954
-
Retinoic acid stimulates regeneration of mammalian auditory hair cells
-
Lefebvre PP, Malgrange B, Staecker H, Moonen G, van de Water TR: Retinoic acid stimulates regeneration of mammalian auditory hair cells. Science 260, 692-695 (1993).
-
(1993)
Science
, vol.260
, pp. 692-695
-
-
Lefebvre, P.P.1
Malgrange, B.2
Staecker, H.3
Moonen, G.4
van de Water, T.R.5
-
74
-
-
0030460674
-
Identification of an overexpressed yeast gene which prevents aminoglycoside toxicity
-
Prezant TR, Chaltraw W. Fischel-Ghodsian N: Identification of an overexpressed yeast gene which prevents aminoglycoside toxicity. Microbiol. 142, 3407-3414 (1996).
-
(1996)
Microbiol.
, vol.142
, pp. 3407-3414
-
-
Prezant, T.R.1
Chaltraw, W.2
Fischel-Ghodsian, N.3
-
75
-
-
0031860647
-
Isolation of overexpressed yeast genes which prevent aminoglycoside ototoxicity
-
Johnson DF, Prezant TR, Lubavin B, Chaltraw WE, Fischel-Ghodsian N: Isolation of overexpressed yeast genes which prevent aminoglycoside ototoxicity. Hear. Res. 120, 62-68 (1998).
-
(1998)
Hear. Res.
, vol.120
, pp. 62-68
-
-
Johnson, D.F.1
Prezant, T.R.2
Lubavin, B.3
Chaltraw, W.E.4
Fischel-Ghodsian, N.5
-
76
-
-
0015450966
-
The genetics of bacterial ribosomes
-
Davies J, Nomura M: The genetics of bacterial ribosomes. Annu. Rev. Genet. 6, 203-234 (1972).
-
(1972)
Annu. Rev. Genet.
, vol.6
, pp. 203-234
-
-
Davies, J.1
Nomura, M.2
-
77
-
-
0016725415
-
Analysis of ribosomal proteins in streptomycin resistant and dependent mutants isolated from streptomycin independent Escherichia coli strains
-
Wittmann HG, Apirion D: Analysis of ribosomal proteins in streptomycin resistant and dependent mutants isolated from streptomycin independent Escherichia coli strains. Mol. Gen. Genet. 141, 331-341 (1975).
-
(1975)
Mol. Gen. Genet.
, vol.141
, pp. 331-341
-
-
Wittmann, H.G.1
Apirion, D.2
-
78
-
-
0016797562
-
Protein chemical studies on ribosomal proteins S4 and S12 from ram (ribosomal ambiguity) mutants of Escherichia coli
-
Van Acken U: Protein chemical studies on ribosomal proteins S4 and S12 from ram (ribosomal ambiguity) mutants of Escherichia coli. Mol. Gen. Genet. 140, 61-68 (1975).
-
(1975)
Mol. Gen. Genet.
, vol.140
, pp. 61-68
-
-
Van Acken, U.1
-
79
-
-
0026592739
-
Nam9 nuclear suppressor of mitochondrial ochre mutations in Saccharomyces cerevisiae codes for a protein homologous to S4 ribosomal proteins from chloroplasts, bacteria, and eukaryotes
-
Boguta M, Dmochowska A, Borsuk P et al.: Nam9 nuclear suppressor of mitochondrial ochre mutations in Saccharomyces cerevisiae codes for a protein homologous to S4 ribosomal proteins from chloroplasts, bacteria, and eukaryotes. Mol. Cell Biol. 12(1 , 402-412 (1992).
-
(1992)
Mol. Cell Biol.
, vol.12
, Issue.1
, pp. 402-412
-
-
Boguta, M.1
Dmochowska, A.2
Borsuk, P.3
-
80
-
-
0023663056
-
The tko locus, site of a behavioural mutation in D. melanogaster, codes for a protein homologous to prokaryotic ribosomal protein S12
-
Royden, CS, Pirrotta V, Jan LY. The tko locus, site of a behavioural mutation in D. melanogaster, codes for a protein homologous to prokaryotic ribosomal protein S12. Cell 51, 165-173 (1987).
-
(1987)
Cell
, vol.51
, pp. 165-173
-
-
Royden, C.S.1
Pirrotta, V.2
Jan, L.Y.3
-
81
-
-
0032531250
-
Cloning and characterization of the human mitochondrial ribosomal S12 gene
-
Johnson DF, Hamon M, Fischel-Ghodsian N: Cloning and characterization of the human mitochondrial ribosomal S12 gene. Genomics 52, 363-368 (1998).
-
(1998)
Genomics
, vol.52
, pp. 363-368
-
-
Johnson, D.F.1
Hamon, M.2
Fischel-Ghodsian, N.3
-
82
-
-
0030827973
-
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
-
83
-
-
0030016359
-
Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation
-
Guan MX, 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. 5, 963-972 (1996).
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 963-972
-
-
Guan, M.X.1
Fischel-Ghodsian, N.2
Attardi, G.3
-
84
-
-
0033858002
-
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. 9, 1787-1793 (2000).
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1787-1793
-
-
Guan, M.X.1
Fischel-Ghodsian, N.2
Attardi, G.3
-
86
-
-
0029832209
-
Audio-vestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosides
-
Braverman I, Jaber L, Levi H et al.: Audio-vestibular findings in patients with deafness caused by a mitochondrial susceptibility mutation and precipitated by an inherited nuclear mutation or aminoglycosides. Arch. Otolaryngol. Head Neck Surg. 122, 1001-1004 (1996).
-
(1996)
Arch. Otolaryngol. Head Neck Surg.
, vol.122
, pp. 1001-1004
-
-
Braverman, I.1
Jaber, L.2
Levi, H.3
-
87
-
-
0030778977
-
Protection from gentamicin ototoxicity by iron chelators in guinea-pig in vivo
-
Song BB, Anderson DJ, Schacht J: Protection from gentamicin ototoxicity by iron chelators in guinea-pig in vivo. J. Pharmacol. Exp. Ther. 282, 369-377 (1997).
-
(1997)
J. Pharmacol. Exp. Ther.
, vol.282
, pp. 369-377
-
-
Song, B.B.1
Anderson, D.J.2
Schacht, J.3
-
88
-
-
0029850284
-
N-Methyl-D-aspartate antagonists limit aminoglycoside antibiotic-induced hearing loss
-
Basile S, Huang J-M, Xie C, Webster D, Berlin C, Skolnick P: N-Methyl-D-aspartate antagonists limit aminoglycoside antibiotic-induced hearing loss. Nat. Med. 2, 1338-1343 (1996).
-
(1996)
Nat. Med.
, vol.2
, pp. 1338-1343
-
-
Basile, S.1
Huang, J.-M.2
Xie, C.3
Webster, D.4
Berlin, C.5
Skolnick, P.6
-
89
-
-
19144362852
-
Protection of auditory neurons from aminoglycoside toxicity by neurotrophin-3
-
Ernfors P, Duan ML, ElShamy WM, Canlon B: Protection of auditory neurons from aminoglycoside toxicity by neurotrophin-3. Nat. Med. 2, 463-467 (1996).
-
(1996)
Nat. Med.
, vol.2
, pp. 463-467
-
-
Ernfors, P.1
Duan, M.L.2
ElShamy, W.M.3
Canlon, B.4
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