LEADER 03514nam 22006015 450 001 9910298450403321 005 20200706065213.0 010 $a3-319-08717-7 024 7 $a10.1007/978-3-319-08717-7 035 $a(CKB)3710000000463525 035 $a(EBL)3568369 035 $a(SSID)ssj0001546630 035 $a(PQKBManifestationID)16140851 035 $a(PQKBTitleCode)TC0001546630 035 $a(PQKBWorkID)14796171 035 $a(PQKB)11245199 035 $a(DE-He213)978-3-319-08717-7 035 $a(MiAaPQ)EBC3568369 035 $a(PPN)188455523 035 $a(EXLCZ)993710000000463525 100 $a20150813d2015 u| 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aADAMTS13 $eBiology and Disease /$fedited by George M. Rodgers 205 $a1st ed. 2015. 210 1$aCham :$cSpringer International Publishing :$cImprint: Springer,$d2015. 215 $a1 online resource (193 p.) 300 $aDescription based upon print version of record. 311 $a3-319-08716-9 320 $aIncludes bibliographical references and index. 327 $a1. A13: Structure and function -- 2. A13: The von Willebrand factor cleaving protease -- 3. A13: Angiogenesis and other biologic activities -- 4. A13:  Assays -- 5. Inherited A13 deficiency (Upshaw-Schulman Syndrome) -- 6. Acquired A13 deficiency (TTP) -- 7. Related thrombotic microangiopathies -- 8. Future directions. 330 $aThis comprehensive volume discusses the protease ADAMTS13, summarizing the current status of basic and clinical research. The nine authoritative chapters begin with a historical perspective followed by exploration of the biochemistry and structure-function relationships of ADAMTS13 as well as its normal function in hemostasis (cleavage of von Willebrand factor). Emerging research themes for ADAMTS13 are covered, including its potential role in angiogenesis and other aspects of cell biology. Additional topics include laboratory assays for ADAMTS13, inherited ADAMTS13 deficiency, and acquired ADAMTS13 deficiency. A chapter on related thrombotic microangiopathic (TMA) disorders examines the differences between TMAs associated with ADAMTS13 deficiency and those not associated with ADAMTS13 deficiency. A final chapter reviews the preliminary information on emerging aspects of ADAMTS13, such as the status of recombinant ADAMTS13 products and their potential utility.   Comprehensive in its exploration of the ADAMTS13 protease in disease, ADAMTS13: Biology and Disease is a significant resource for clinical hematologists, transfusion medicine physicians, and researchers interested in hemostasis, vascular biology, biochemistry, and metalloproteases. 606 $aProteomics 606 $aHematology 606 $aCell biology 606 $aProteomics$3https://scigraph.springernature.com/ontologies/product-market-codes/L1403X 606 $aHematology$3https://scigraph.springernature.com/ontologies/product-market-codes/H3307X 606 $aCell Biology$3https://scigraph.springernature.com/ontologies/product-market-codes/L16008 615 0$aProteomics. 615 0$aHematology. 615 0$aCell biology. 615 14$aProteomics. 615 24$aHematology. 615 24$aCell Biology. 676 $a570 702 $aRodgers$b George M$4edt$4http://id.loc.gov/vocabulary/relators/edt 906 $aBOOK 912 $a9910298450403321 996 $aADAMTS13$92528867 997 $aUNINA