A Deletion in the Endothelin-B Receptor Gene is Responsible for the Waardenburg Syndrome-Like Phenotypes of WS4 Mice-Reference-Cited by-同舟云学术

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A Deletion in the Endothelin-B Receptor Gene is Responsible for the Waardenburg Syndrome-Like Phenotypes of WS4 Mice

Published:2006 Issue:5 Volume:55 Page:491-495
ISSN:1341-1357
Container-title:Experimental Animals
language:en
Short-container-title:Exp. Anim.

Author:

OHTANI Shin¹²,SHINKAI Yusuke¹³,HORIBE Akio¹,KATAYAMA Kentaro¹,TSUJI Takehito¹,MATSUSHIMA Yoshibumi⁴,TACHIBANA Masayoshi⁴,KUNIEDA Tetsuo¹

Affiliation:

1. Graduate School of Natural Science and Technology, Okayama University

2. National Institute of Neuroscience, National Center of Neurology and Psychiatry

3. Institute of Advanced Technology, Kinki University

4. Saitama Cancer Center, Research Institute

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/55/5/55_5_491/_pdf

Reference13 articles.

1. 1. Attié, T., Till, M., Pelet, A., Amiel, J., Edery, P., Boutrand, L., Munnich, A., and Lyonnet, S. 1995. Mol. Genet. 4: 2407-2409.

2. Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons

3. 3. Bzymek, M. and Lovett, S.T. 2001. Genetics 158: 527-540.

4. Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)

5. 5. Game, L., Bergounioux, J., Close, J.P., Marzouka, B.E., and Thein, S.L. 2003. Br. J. Haematol. 123: 154-159.

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1. Genetic characterization of a patient with an unusual presentation of Waardenburg syndrome Type 4 and retinoblastoma;Pediatric Blood & Cancer;2020-07-16

2. From single nucleotide substitutions up to chromosomal deletions: genetic cause of leucism-associated disorders in animals;BERL MUNCH TIERARZTL;2016

3. High-incidence spontaneous tumors in JF1/Ms mice: relevance of hypomorphic germline mutation and subsequent promoter methylation of Ednrb;Journal of Cancer Research and Clinical Oncology;2013-11-06

4. Malformation syndromes;Rennie & Roberton's Textbook of Neonatology;2012

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