Craniosynostosis in transgenic mice overexpressing Nell-1-Reference-Cited by-同舟云学术

Craniosynostosis in transgenic mice overexpressing Nell-1

Published:2002-09-15 Issue:6 Volume:110 Page:861-870
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Zhang Xinli,Kuroda Shun’ichi,Carpenter Dale,Nishimura Ichiro,Soo Chia,Moats Rex,Iida Keisuke,Wisner Eric,Hu Fei-Ya,Miao Steve,Beanes Steve,Dang Catherine,Vastardis Heleni,Longaker Michael,Tanizawa Katsuyuki,Kanayama Norihiro,Saito Naoaki,Ting Kang

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference22 articles.

1. Abnormal bone growth and selective translational regulation in basic fibroblast growth factor (FGF-2) transgenic mice.

2. Crouzon-like craniofacial dysmorphology in the mouse is caused by an insertional mutation at theFgf3/Fgf4 locus

3. A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

4. Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull.

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