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dyssegmental dysplasia, silverman-handmaker type
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HSPG2
Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia
Mapping of binding sites for nidogens, fibulin-2, fibronectin and heparin to different IG modules of perlecan
Binding of mouse and human fibulin-2 to extracellular matrix ligands
The protein core of the proteoglycan perlecan binds specifically to fibroblast growth factor-7
Fibroblast growth factor-binding protein is a novel partner for perlecan protein core
Binding of perlecan to transthyretin in vitro
Cloning of human heparan sulfate proteoglycan core protein, assignment of the gene (HSPG2) to 1p36.1----p35 and identification of a BamHI restriction fragment length polymorphism
Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia
Perlecan: a gem of a proteoglycan
Changes in perlecan during chondrocyte differentiation in the fetal bovine rib growth plate
Chondrogenic activity of the heparan sulfate proteoglycan perlecan maps to the N-terminal domain I
Perlecan is a component of cartilage matrix and promotes chondrocyte attachment
Formation of heparan sulfate or chondroitin/dermatan sulfate on recombinant domain I of mouse perlecan expressed in Chinese hamster ovary cells
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