Mitochondrial DNA Mutation (3243A→G,1555A→4G,7445A→G) in Noise-Induced
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Hong Young-Seoub
(Department of Preventive Medicine, College of Medicine, Dong-A University, Medical Research Center for Cancer Molecular Therapy)
Nishio Hisahide (Department of Public Health, Kobe University School of Medicine) Lee Myeong-Jin (Department of Public Health, Kobe University School of Medicine) Kwak Ki-Young (Department of Preventive Medicine, College of Medicine, Dong-A University, Medical Research Center for Cancer Molecular Therapy) Hwang Chan-Ho (Department of Otorhinolaryngology-Head and Neck Surgery, College of Medicine, Dong-A University) Shin Dong-Hoon (Department of Preventive Medicine, College of Medicine, Keimyung University) Kwak Jong-Young (Medical Research Center for Cancer Molecular Therapy, College of Medicine, Dong-A University) Lee Yong-Hwan (Department of Preventive Medicine, Kosin Medical College) Kim Jong-Min (Department of Anatomy and Cell Biology, College of Medicine, Dong-A University) Kim Joon-Youn (Department of Preventive Medicine, College of Medicine, Dong-A University, The Research Society of Environmental Genetic Epidemiology) |
1 | Chung, I. S., Shin, D. H. and Baek, W. K. 2000. Mitochondrial DNA A3243G mutation in noise-induced senso rineural hearing loss. Korean J Occup Environ Med 12(3), 319-326 |
2 | Wald, W. D. 1995. Endogenous factors related to susceptibility to damage from noise. Occupational Medicine, state of art review 10(3), 561-575 |
3 | Wallace, D. C. 1992. Disease for the mitochondrial DNA. Annu Rev Biochem 61, 1175-1212 DOI ScienceOn |
4 | Zenz, C. 1994. Occupational Medicine, St. Louis: Mosby Year Book, Inc |
5 | Ueda, N., Oshima, T., Ikeda, K., Abe, K., Aoki, M. and Takasaka, T. 1998. Mitochondrial DNA deletion is a predisposing cause for sensorineural hearing loss. Laryngoscope 108, 580-584 DOI ScienceOn |
6 | Usami, S., Abe, S. and Kasai, M. 1997. Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation. Laryngoscope 107, 483-90 DOI ScienceOn |
7 | Li, H-S., Hultcrantz, M. and Borg, E. 1993. Influence of age on noise induced permanent TSc in CBA/Ca and C57BL/ 6J mice. Audiology 195-204 |
8 | Odawara, M., Sasaki, K., Tachi, Y. and Yamashita, K. 1995. Selection of primers for detection of A to G mutation at nucleotide 3243 of the mitochondrial gene. Diabetologica 38, 377 DOI ScienceOn |
9 | Schindler, D. N., Jackler, R. K. and Robinson, S. T. 1997. Hearing loss. In: Ladou J, eds: Occupational and environmental medicine, 2nd edition, Appleton and Lange p 123-138 |
10 | Sevior, K. B., Hatamochi, A. and Stewart, I. A. 1998. Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness. Am J Med Genet 75, 170-185 |
11 | Thomas, A. W., Morgan, R., Majid, A., Rees, A. and Alcolado, J. C. 1995. Detection of mitochondrial DNA mutations in the patients with diabetes mellitus. Diabetologia 38, 376-379 DOI ScienceOn |
12 | Tamagawa, Y., Kitamura, K., Ishida, T., Hagiwara, H., Abe, K. and Nishizawa, M. 1996. Mitochondrial DNA mutation at nucleotide 1555 in a patient with bilateral sensorineural hearing loss of unknown etiology. Acta otolaryngol 116, 796-798 DOI ScienceOn |
13 | Taylor, W., Pearson, J. and Mair, A. 1965. Study of noise and hearing in jute weaving. J Acoust Soc Am 38, 113-120 DOI |
14 | Thalmann, I., Matshinsky, F. M. and Thalmann, R. 1970. Quantitative study of selected of selected enzymes involved in energy metabolism of the cochlear duct. Ann Otol 79, 12-17 |
15 | Li, H-S. 1992b Suppl. Genetic influence on susceptibility of the auditory system to aging and environmental factors. Scand Audiol 36, 1-39 |
16 | Li, H-S. and Borg, E. 1993. Auditory degeneration after acoustic trauma in two genotypes of mice. Hear Res 68, 19-27 DOI ScienceOn |
17 | Cody, A. R. and Robertson, D. 1983. Variability of noise- induced damage in the guinea pig cochlea: electrophisiology and morphological correlates after strictly controlled exposure. Hear Res 9, 55-70 DOI ScienceOn |
18 | Estivill, X., Govea, N. and Barcelo, A. 1998. 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 DOI ScienceOn |
19 | Goto, Y., Nonaka, I. and Horai, S. 1990. A mutation in the tRNALEU (UUR) gene associated with the MELAS subgroup of mitochondrial encephalopathies. Nature 348, 651- 653 DOI ScienceOn |
20 | Erway, L. C., Shiau, Y. W., Davis, R. R., and Krieg, E. F. 1996. Genetics of age-related loss in mice. Ⅲ. Susceptibility of inbred and F1 hybrid strains to noise-induced hearing loss. Hear Res 93, 181-187 DOI ScienceOn |
21 | Ikeda, K., Sunose, H. and Takasaka, T. 1994. Ion transport mechanisms in the outer hair cell of the mammalian cochlea. Prog Neurobiol 42, 703-737 DOI ScienceOn |
22 | Kelada, S. N., Eaton, D. L., Wang, S. S. and Khoury. 2003. The role of genetic polymorphism in environmental health. Environ Health Perspect 111, 1055-1065 DOI ScienceOn |
23 | Ladou, J. 1997. Occupational and environmental medicine Prentice-Hall International, Inc |
24 | Li, H-S. and Borg, E. 1991. Age related loss of auditory sensitivity in two mouse genotypes. Acta Otolaryngol 111, 827-834 DOI ScienceOn |
25 | Li, H-S. 1992a. Influence of Genotype and age on acute acoustic trauma and recovery in CBA/Ca and C57BL/6J mice. Acta Otolaryngol 112, 956-967 DOI ScienceOn |
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