| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2015PLoSO..1022931D |
| P356 | DOI | 10.1371/JOURNAL.PONE.0122931 |
| P932 | PMC publication ID | 4388381 |
| P698 | PubMed publication ID | 25849793 |
| P5875 | ResearchGate publication ID | 276890061 |
| P50 | author | David Ginsburg | Q56192322 |
| Colin Kretz | Q59698524 | ||
| P2093 | author name string | Nidhi Agrawal | |
| Andrew Yee | |||
| Karl C Desch | |||
| Jane Cheng | |||
| Robert Gildersleeve | |||
| Kristin Metzger | |||
| P2860 | cites work | Localization of vitronectin binding domain in plasminogen activator inhibitor-1. | Q54633160 |
| Use of a mouse model to elucidate the phenotypic effects of the von Willebrand factor cleavage mutants, Y1605A/M1606A and R1597W. | Q55332935 | ||
| Localization of ADAMTS13 to the stellate cells of human liver | Q58119522 | ||
| The genetic map of the filamentous bacteriophage f1 | Q69184510 | ||
| New Tn10 derivatives for transposon mutagenesis and for construction of lacZ operon fusions by transposition | Q72413204 | ||
| Factor VIII accelerates proteolytic cleavage of von Willebrand factor by ADAMTS13. | Q36677173 | ||
| Extensive contacts between ADAMTS13 exosites and von Willebrand factor domain A2 contribute to substrate specificity | Q36843699 | ||
| Distinguishing the specificities of closely related proteases. Role of P3 in substrate and inhibitor discrimination between tissue-type plasminogen activator and urokinase. | Q36867219 | ||
| ADAMTS13 is expressed in hepatic stellate cells | Q36950896 | ||
| Binding of platelet glycoprotein Ibalpha to von Willebrand factor domain A1 stimulates the cleavage of the adjacent domain A2 by ADAMTS13. | Q36986074 | ||
| Production, crystallization and preliminary crystallographic analysis of an exosite-containing fragment of human von Willebrand factor-cleaving proteinase ADAMTS13. | Q37250107 | ||
| Crystal structures of the noncatalytic domains of ADAMTS13 reveal multiple discontinuous exosites for von Willebrand factor | Q37428907 | ||
| N-linked glycosylation of VWF modulates its interaction with ADAMTS13. | Q40059074 | ||
| Impaired intracellular transport produced by a subset of type IIA von Willebrand disease mutations | Q41635614 | ||
| Mechanoenzymatic cleavage of the ultralarge vascular protein von Willebrand factor | Q42013734 | ||
| Modifying murine von Willebrand factor A1 domain for in vivo assessment of human platelet therapies | Q46847132 | ||
| Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization | Q48377892 | ||
| Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura | Q24291691 | ||
| Inducible secretion of large, biologically potent von Willebrand factor multimers | Q24296142 | ||
| Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura | Q24651320 | ||
| ADAMTS13 turns 3 | Q28240324 | ||
| Identification of strain-specific variants of mouse Adamts13 gene encoding von Willebrand factor-cleaving protease | Q28588904 | ||
| Allosteric activation of ADAMTS13 by von Willebrand factor. | Q29568910 | ||
| Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura | Q33339170 | ||
| VWF73, a region from D1596 to R1668 of von Willebrand factor, provides a minimal substrate for ADAMTS-13 | Q33356956 | ||
| An IAP retrotransposon in the mouse ADAMTS13 gene creates ADAMTS13 variant proteins that are less effective in cleaving von Willebrand factor multimers | Q33374872 | ||
| Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura | Q33481821 | ||
| A von Willebrand factor fragment containing the D'D3 domains is sufficient to stabilize coagulation factor VIII in mice | Q33917215 | ||
| Shear stress enhances the proteolysis of von Willebrand factor in normal plasma | Q34060639 | ||
| Unraveling the scissile bond: how ADAMTS13 recognizes and cleaves von Willebrand factor. | Q34196324 | ||
| Bacteriophage lambda cloning system for the construction of directional cDNA libraries | Q34631721 | ||
| Mechanism of von Willebrand factor scissile bond cleavage by a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13). | Q35105077 | ||
| Exosite interactions contribute to tension-induced cleavage of von Willebrand factor by the antithrombotic ADAMTS13 metalloprotease | Q35193294 | ||
| Light chain of factor VIII is sufficient for accelerating cleavage of von Willebrand factor by ADAMTS13 metalloprotease | Q36294654 | ||
| Mechanisms by which von Willebrand disease mutations destabilize the A2 domain | Q36647297 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | phage display | Q896217 |
| P304 | page(s) | e0122931 | |
| P577 | publication date | 2015-04-07 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Probing ADAMTS13 substrate specificity using phage display | |
| P478 | volume | 10 |
| Q50135856 | ADAMTS-13 and von Willebrand factor: a dynamic duo. |
| Q41946735 | Conformational quiescence of ADAMTS-13 prevents proteolytic promiscuity |
| Q49172247 | High throughput protease profiling comprehensively defines active site specificity for thrombin and ADAMTS13. |
| Q37733182 | Influences of ABO blood group, age and gender on plasma coagulation factor VIII, fibrinogen, von Willebrand factor and ADAMTS13 levels in a Chinese population. |
| Q36309980 | Mapping the Substrate Recognition Landscapes of Metalloproteases Using Comprehensive Mutagenesis. |
| Q35690203 | Massively parallel enzyme kinetics reveals the substrate recognition landscape of the metalloprotease ADAMTS13. |
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