Perlecan, the Multidomain Heparan Sulfate Proteoglycan of Basement Membranes, Is also a Prominent Component of the Cartilaginous Primordia in the Developing Human Fetal Spine
Author:
Affiliation:
1. The Institute of Bone and Joint Research, The University of Sydney (Department of Surgery), at the Royal North Shore Hospital of Sydney, St. Leonards, Australia
2. Biomics Research Services, Homebush, Australia
Publisher
SAGE Publications
Subject
Histology,Anatomy
Link
http://journals.sagepub.com/doi/pdf/10.1177/002215540305101010
Reference72 articles.
1. Structural and Functional Mutations of the Perlecan Gene Cause Schwartz-Jampel Syndrome, with Myotonic Myopathy and Chondrodysplasia
2. Perlecan is essential for cartilage and cephalic development
3. Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene
4. Dyssegmental dysplasia, Silverman-Handmaker type: Unexpected role of perlecan in cartilage development
5. Perlecan, basal lamina proteoglycan, promotes basic fibroblast growth factor-receptor binding, mitogenesis, and angiogenesis
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