Craniofacial abnormality with skeletal dysplasia in mice lacking chondroitin sulfate N-acetylgalactosaminyltransferase-1-Reference-Cited by-同舟云学术

Craniofacial abnormality with skeletal dysplasia in mice lacking chondroitin sulfate N-acetylgalactosaminyltransferase-1

Published:2018-11-20 Issue:1 Volume:8 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Ida-Yonemochi Hiroko,Morita Wataru,Sugiura Nobuo,Kawakami Ryosuke,Morioka Yuki,Takeuchi Yuka,Sato Toshiya^ORCID,Shibata Shunichi,Watanabe Hideto,Imamura Takeshi,Igarashi Michihiro,Ohshima Hayato^ORCID,Takeuchi Kosei^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-018-35412-5.pdf

Reference55 articles.

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3. Grobe, K. Cerebral hypoplasia and craniofacial defects in mice lacking heparan sulfate Ndst1 gene function. Development 132, 3777–3786 (2005).

4. Eames, B. F. et al. UDP xylose synthase 1 is required for morphogenesis and histogenesis of the craniofacial skeleton. Dev. Biol. 341, 400–415 (2010).

5. Ida-Yonemochi, H. et al. Morphogenetic roles of perlecan in the tooth enamel organ: An analysis of overexpression using transgenic mice. Matrix Biol. 30, 379–388 (2011).

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