Discrimination of A1555G and C1494T Point Mutations in the Mitochondrial 12S rRNA Gene by On/Off Switch-Reference-Cited by-同舟云学术

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Discrimination of A1555G and C1494T Point Mutations in the Mitochondrial 12S rRNA Gene by On/Off Switch

Published:2011-11-10 Issue:1 Volume:166 Page:234-242
ISSN:0273-2289
Container-title:Applied Biochemistry and Biotechnology
language:en
Short-container-title:Appl Biochem Biotechnol

Author:

Guo Zi-Fen,Guo Wu-Shuang,Xiao Li,Gao Guo-Qiang,Lan Fen,Lu Xue-Guan,Li Kai,Liao Duan-Fang

Publisher

Springer Science and Business Media LLC

Subject

Molecular Biology,Applied Microbiology and Biotechnology,Biochemistry,General Medicine,Bioengineering,Biotechnology

Link

http://link.springer.com/content/pdf/10.1007/s12010-011-9419-4.pdf

Reference13 articles.

1. Bindu, L. H., & Reddy, P. P. (2008). Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review. International Journal of Audiology, 47, 702–707.

2. Qian, Y., & Guan, M. X. (2009). Interaction of aminoglycosides with human mitochondrial 12S rRNA carrying the deafness-associated mutation. Antimicrobial Agents and Chemotherapy, 53, 4612–4618.

3. Prezant, T. R., Agapian, J. V., Bohlman, M. C., Bu, X., Oztas, S., Qiu, W. Q., et al. (1993). Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nature Genetics, 4, 289–294.

4. Guan, M. X. (2011). Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity. Mitochondrion, 11, 237–245.

5. Giordano, C., Pallotti, F., Walker, W. F., Checcarelli, N., Musumeci, O., Santorelli, F., et al. (2002). Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation. Biochemical and Biophysical Research Communications, 293, 521–529.

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