Characterization of the Kyoto Circling (KCI) Rat Carrying a Spontaneous Nonsense Mutation in the Protocadherin 15 (Pcdh15) Gene-Reference-Cited by-同舟云学术

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Characterization of the Kyoto Circling (KCI) Rat Carrying a Spontaneous Nonsense Mutation in the Protocadherin 15 (Pcdh15) Gene

Published:2009 Issue:1 Volume:58 Page:1-10
ISSN:1341-1357
Container-title:Experimental Animals
language:en
Short-container-title:Exp. Anim.

Author:

NAOI Kuniko¹²,KURAMOTO Takashi¹,KUWAMURA Yuki³,GOHMA Hiroshi¹,KUWAMURA Mitsuru⁴,SERIKAWA Tadao¹

Affiliation:

1. Institute of Laboratory Animals, Graduate School of Medicine, Kyoto University

2. Department of Medical Therapeutics, Molecular Therapeutics, Gifu Pharmaceutical University

3. Osaka Pathology Center, Drug Safety Research Laboratories, Shin Nippon Biomedical Laboratories, LTD.

4. Laboratory of Veterinary Pathology, Osaka Prefecture University

Publisher

Japanese Association for Laboratory Animal Science

Subject

General Veterinary,General Biochemistry, Genetics and Molecular Biology,Animal Science and Zoology,General Medicine

Link

http://www.jstage.jst.go.jp/article/expanim/58/1/58_1_1/_pdf

Reference18 articles.

1. 1. Ahituv, N. and Avraham, K.B. 2002. Mouse models for human deafness: current tools for new fashions. Trends Mol. Med. 8: 447-451.

2. 2. Ahmed, Z.M., Riazuddin, S., Bernstein, S.L., Ahmed, Z., Khan, S., Griffith, A.J., Morell, R.J., Friedman, T.B., Riazuddin, S., and Wilcox, E.R. 2001. Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. Am. J. Hum. Genet. 69: 25-34.

3. 3. Ahmed, Z.M., Riazuddin, S., Ahmad, J., Bernstein, S.L., Guo, Y., Sabar, M.F., Sieving, P., Riazuddin, S., Griffith, A.J., Friedman, T.B., Belyantseva, I.A., and Wilcox, E.R. 2003. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23. Hum. Mol. Genet. 12: 3215-3223.

4. 4. Alagramam, K.N., Zahorsky-Reeves, J., Wright, C.G., Pawlowski, K.S., Erway, L.C., Stubbs, L., and Woychik, R.P. 2000. Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer. Hear. Res. 148: 181-191.

5. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene

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