Advantages of a Mouse Model for Human Hearing Impairment-Reference-Cited by-同舟云学术

Advantages of a Mouse Model for Human Hearing Impairment

Published:2012 Issue:2 Volume:61 Page:85-98
ISSN:1341-1357
Container-title:Experimental Animals
language:en
Short-container-title:Exp. Anim.

Author:

Kikkawa Yoshiaki¹,Seki Yuta¹,Okumura Kazuhiro²,Ohshiba Yasuhiro¹³,Miyasaka Yuki¹³,Suzuki Sari¹⁴,Ozaki Mao¹⁴,Matsuoka Kunie¹,Noguchi Yoshihiro⁵,Yonekawa Hiromichi⁶

Affiliation:

1. Mammalian Genetics Project, Department of Genome Medicine, Tokyo Metropolitan Institute of Medical Science

2. Laboratory of Experimental Animals, Chiba Cancer Center Research Institute

3. Graduate School of Medical and Dental Sciences, Niigata University

4. Department of Bioproduction, Tokyo University of Agriculture

5. Department of Otolaryngology, Tokyo Medical and Dental University

6. Basic Research Center, Tokyo Metropolitan Institute of Medical Science

Publisher

Japanese Association for Laboratory Animal Science

Subject

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

Link

https://www.jstage.jst.go.jp/article/expanim/61/2/61_2_85/_pdf

Reference117 articles.

1. 1. Adato, A., Lefèvre, G., Delprat, B., Michel, V., Michalski, N., Chardenoux, S., Weil, D., El-Amraoui, A., and Petit, C. 2005. Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells. Hum. Mol. Genet. 14: 3921–3932.

2. 2. Adato, A., Michel, V., Kikkawa, Y., Reiners, J., Alagramam, K.N., Weil, D., Yonekawa, H., Wolfrum, U., El-Amraoui, A., and Petit, C. 2005. Interactions in the network of Usher syndrome type 1 proteins. Hum. Mol. Genet. 14: 347–356.

3. Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37

4. Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F

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

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