Genetic mutation of <i>Frem3</i> does not causeFraser syndrome in mice-Reference-Cited by-同舟云学术

Genetic mutation of Frem3 does not causeFraser syndrome in mice

Published:2020 Issue:1 Volume:69 Page:104-109
ISSN:1341-1357
Container-title:Experimental Animals
language:en
Short-container-title:Exp. Anim.

Author:

Kiyozumi Daiji¹²,Mori Masashi¹²,Kodani Mayo¹³,Ikawa Masahito¹²³⁴⁵

Affiliation:

1. Research Institute for Microbial Diseases, 3-1 Yamadaoka, Suita, Osaka 565-0871, Japan

2. Immunology Frontier Research Center, 3-1 Yamadaoka, Suita, Osaka 565-0871, Japan

3. Graduate School of Pharmaceutical Sciences, 3-1 Yamadaoka, Suita, Osaka 565-0871, Japan

4. Graduate School of Medicine, Osaka University, 3-1 Yamadaoka, Suita, Osaka 565-0871, Japan

5. The Institute of Medical Science, The University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan

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/69/1/69_19-0088/_pdf

Reference15 articles.

1. 1. Alazami A.M., Shaheen R., Alzahrani F., Snape K., Saggar A., Brinkmann B., Bavi P., Al-Gazali L.I. and Alkuraya F.S. 2009. FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndrome. Am. J. Hum. Genet. 85: 414–418.

2. 2. Darling S. and Gossler A. 1994. A mouse model for Fraser syndrome? Clin. Dysmorphol. 3: 91–95.

3. 3. Jadeja S., Smyth I., Pitera J.E., Taylor M.S., van Haelst M., Bentley E., McGregor L., Hopkins J., Chalepakis G., Philip N., Perez Aytes A., Watt F.M., Darling S.M., Jackson I., Woolf A.S. and Scambler P.J. 2005. Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs. Nat. Genet. 37: 520–525.

4. 4. Kiyozumi D., Sugimoto N., Nakano I. and Sekiguchi K. 2007. Frem3, a member of the 12 CSPG repeats-containing extracellular matrix protein family, is a basement membrane protein with tissue distribution patterns distinct from those of Fras1, Frem2, and QBRICK/Frem1. Matrix Biol. 26: 456–462.

5. 5. Kiyozumi D., Sugimoto N. and Sekiguchi K. 2006. Breakdown of the reciprocal stabilization of QBRICK/Frem1, Fras1, and Frem2 at the basement membrane provokes Fraser syndrome-like defects. Proc. Natl. Acad. Sci. USA 103: 11981–11986.

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