Rat Mutations cvd and hob with Cerebellar Malformations Map to Chromosome 2-Reference-Cited by-同舟云学术

Rat Mutations cvd and hob with Cerebellar Malformations Map to Chromosome 2

Published:2004 Issue:1 Volume:53 Page:21-26
ISSN:1341-1357
Container-title:Experimental Animals
language:en
Short-container-title:Exp. Anim.

Author:

KUWAMURA Mitsuru¹,ANDO Yosuke²,TAKADA Akiko¹,KANEHARA Toshiko¹,YAMATE Jyoji¹,KOTANI Takao¹,TAKESHITA Shigehito²,KANBORI Miyuki²,KITADA Kazuhiro³,SERIKAWA Tadao³

Affiliation:

1. Laboratory of Veterinary Pathology, Graduate School of Agriculture and Biological Sciences, Osaka Prefecture University

2. Medicinal Safety Research Laboratories, Sankyo Co., Ltd.

3. Institute of Laboratory Animals, Graduate School of Medicine, Kyoto 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/53/1/53_1_21/_pdf

Reference19 articles.

1. The mouse rostral cerebellar malformation gene encodes an UNC-5-like protein

2. 2. Ausubel, F.M., Brent, R., Kingston, R.E., Moore, D.D., Seidman, J.G., Smith, J.A., and Struhl, K. 1993. Current Protocols in Molecular Biology. (New York: Wiley Interscience).

3. DANDY-WALKER SYNDROME AND AGENESIS OF THE CEREBELLAR VERMIS: DIAGNOSTIC PROBLEMS AND GENETIC COUNSELLING

4. Rostral cerebellar malformation (rcm/rcm): A murine mutant to study regionalization of the cerebellum

5. Granule Cells and Cerebellar Boundaries: Analysis ofUnc5h3Mutant Chimeras

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1. Rat neurological mutations cerebellar vermis defect and hobble are caused by mutations in the netrin-1 receptor gene Unc5h3;Molecular Brain Research;2004-03