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pubmed-article:12042245pubmed:dateCreated2002-6-3lld:pubmed
pubmed-article:12042245pubmed:abstractTextThe proteoglycans, especially the large chondroitin sulfate proteoglycan aggrecan, have long been viewed as important components of the extracellular matrix of cartilage. The drastic change in expression during differentiation from mesenchyme to cartilage, the loss of tissue integrity associated with proteoglycan degradation in several disease processes and, most important, the demonstration of abnormalities in proteoglycan production concomitant with the aberrant growth patterns exhibited by the brachymorphic mouse, the cartilage matrix deficient mouse, and the nanomelic chick provide the strongest evidence that the proteoglycan aggrecan is essential during differentiation and for maintenance of the skeletal elements. More recently, mutations associated with proteoglycans other than aggrecan, especially the heparan sulfate proteoglycans, glypican and perlecan, suggest an important role for these molecules in skeletal development as well. This review focuses on the molecular bases of the hereditary proteoglycan defects in animal models, as well as of some human chondrodysplasias, that collectively are providing a better understanding of the role of proteoglycans in the development and maintenance of the skeletal elements.lld:pubmed
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pubmed-article:12042245pubmed:authorpubmed-author:SchwartzNancy...lld:pubmed
pubmed-article:12042245pubmed:authorpubmed-author:DomowiczMiria...lld:pubmed
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pubmed-article:12042245pubmed:volume12lld:pubmed
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pubmed-article:12042245pubmed:pagination57R-68Rlld:pubmed
pubmed-article:12042245pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:12042245pubmed:year2002lld:pubmed
pubmed-article:12042245pubmed:articleTitleChondrodysplasias due to proteoglycan defects.lld:pubmed
pubmed-article:12042245pubmed:affiliationDepartment of Pediatrics, University of Chicago, MC 5058, 5826 S. Maryland Ave., Chicago, IL 60637, USA.lld:pubmed
pubmed-article:12042245pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12042245pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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