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注意:仅列出部分参考文献,下载原文获取全部文献信息。Discovery and characterization of a novel inhibitor of matrix metalloprotease-13 that reduces cartilage damage in vivo without joint fibroplasia side effects
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ADAMTS-1-knockout mice do not exhibit abnormalities in aggrecan turnover in vitro or in vivo
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ADAMTS5 is the major aggrecanase in mouse cartilage in vivo and in vitro
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Proprotein convertase furin interacts with and cleaves pro-ADAMTS4 (aggrecanase-1) in the trans-Golgi network
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ADAMTS4 (aggrecanase-1) activation on the cell surface involves C-terminal cleavage by glycosylphosphatidyl inositol-anchored membrane type 4-matrix metalloproteinase and binding of the activated proteinase to chondroitin sulfate and heparan sulfate on syndecan-1
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Characterization of and osteoarthritis susceptibility in ADAMTS-4-knockout mice
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Cleavage of von Willebrand factor requires the spacer domain of the metalloprotease ADAMTS13
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Identification of the 183RWTNNFREY191 region as a critical segment of matrix metalloproteinase 1 for the expression of collagenolytic activity
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The thrombospondin motif of aggrecanase-1 (ADAMTS-4) is critical for aggrecan substrate recognition and cleavage
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ADAMTS-1 cleaves a cartilage proteoglycan, aggrecan
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