메뉴 건너뛰기




Volumn 14, Issue 2, 2001, Pages 257-279

Structure of von Willebrand factor and its function in platelet adhesion and thrombus formation

Author keywords

Adhesion; Aggregation; Haemostasis; Platelet; Thrombosis; von Willebrand factor

Indexed keywords

BLOOD CLOTTING FACTOR 8; FIBRIN; MEMBRANE RECEPTOR; PLASMA PROTEIN; POLYMER; PROCOAGULANT; PROTEIN SUBUNIT; PROTEINASE; VON WILLEBRAND FACTOR;

EID: 0034919227     PISSN: 15216926     EISSN: None     Source Type: Journal    
DOI: 10.1053/beha.2001.0133     Document Type: Article
Times cited : (154)

References (105)
  • 1
  • 6
    • 0001982603 scopus 로고
    • Electron microscopy of von Willebrand factor
    • Zimmerman TS & Ruggeri ZM (eds) Coagulation and Bleeding Disorders. The Role of Factor VIII and von Willebrand Factor, New York: Marcel Dekker
    • (1989) , pp. 181-193
    • Fowler, W.E.1    Fretto, L.J.2
  • 14
    • 0019958149 scopus 로고
    • Multimeric composition of factor VIII/von Willebrand factor following administration of DDAVP: Implications for pathophysiology and therapy of von Willebrand's disease subtypes
    • (1982) Blood , vol.59 , pp. 1272-1278
    • Ruggeri, Z.M.1    Mannucci, P.M.2    Federici, A.B.3
  • 16
    • 0029925856 scopus 로고    scopus 로고
    • Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis
    • (1996) Blood , vol.87 , pp. 4223-4234
    • Furlan, M.1    Robles, R.2    Lammle, B.3
  • 17
    • 0029878123 scopus 로고    scopus 로고
    • Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion
    • (1996) Blood , vol.87 , pp. 4235-4244
    • Tsai, H.M.1
  • 18
    • 0030973267 scopus 로고    scopus 로고
    • Deficient activity of von Willebrand factor - Cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura
    • (1997) Blood , vol.89 , pp. 3097-3103
    • Furlan, M.1    Robles, R.2    Solenthaler, M.3
  • 32
    • 0030905830 scopus 로고    scopus 로고
    • Patient with type 2N von Willebrand disease is heterozygous for a new mutation: Gly22Glu. Demonstration of a defective expression of the second allele by the use of monoclonal antibodies
    • (1997) Blood , vol.89 , pp. 3263-3269
    • Gu, J.1    Jorieux, S.2    Lavergne, J.M.3
  • 33
    • 0028201807 scopus 로고
    • A revised classification of von Willebrand disease. For the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
    • (1994) Thrombosis and Haemostasis , vol.71 , pp. 520-525
    • Sadler, J.E.1
  • 51
    • 0026442717 scopus 로고
    • Identification of aspartic acid 514 through glutamic acid 542 as a glycoprotein Ib-IX complex receptor recognition sequence in von Willebrand factor. Mechanisms of modulation of von Willebrand factor by ristocetin and botrocetin
    • (1992) Biochemistry , vol.31 , pp. 11144-11151
    • Berndt, M.C.1    Ward, C.M.2    Booth, W.J.3
  • 58
    • 0024353508 scopus 로고
    • Role of botrocetin in platelet agglutination: Formation of an activated complex of botrocetin and von Willebrand factor
    • (1989) Blood , vol.74 , pp. 1031-1035
    • Read, M.S.1    Smith, S.V.2    Lamb, M.A.3
  • 71
    • 0023666065 scopus 로고
    • Integrins: A family of cell surface receptors
    • (1987) Cell , vol.48 , pp. 549-554
    • Hynes, R.O.1
  • 72
    • 0026770377 scopus 로고
    • Integrins: Versatility, modulation and signaling in cell adhesion
    • (1992) Cell , vol.69 , pp. 11-25
    • Hynes, R.O.1
  • 74
    • 0023938680 scopus 로고
    • Generation and characterization of peptide-specific antibodies that inhibit von Willebrand factor binding to GP IIb-IIIa without interacting with other adhesive molecules: Selectivity is conferred by Pro 1743 and residues adjacent to the sequence Arg 1744-Gly1745-Asp1746
    • (1988) Journal of Biological Chemistry , vol.263 , pp. 7500-7505
    • Berliner, S.1    Niiya, K.2    Roberts, J.R.3
  • 79
    • 0026066834 scopus 로고
    • The binding domain of von Willebrand factor to sulfatides is distinct from those interacting with glycoprotein Ib, heparin, and collagen and resides between amino acid residues Leu 512 and Lys 673
    • (1991) Blood , vol.78 , pp. 2310-2317
    • Christophe, O.1    Obert, B.2    Meyer, D.3
  • 81
    • 0025238515 scopus 로고
    • Multimer size dependence of von Willebrand factor binding to crosslinked or noncrosslinked fibrin
    • (1990) Blood , vol.75 , pp. 1460-1465
    • Ribes, J.A.1    Francis, C.W.2
  • 87
    • 0002106819 scopus 로고
    • Rheology of thrombosis
    • Colman RW, Hirsh J, Marder VJ et al. (eds) Basic Principles and Clinical Practice, Philadelphia: JB Lippincott
    • (1987) Hemostasis and Thrombosis , pp. 1111-1122
    • Leonard, E.F.1
  • 98
    • 0020320790 scopus 로고
    • Adenosine diphosphate induces binding of von Willebrand factor to human platelets
    • (1982) Nature , vol.297 , pp. 154-156
    • Fujimoto, T.1    Hawinger, J.2
  • 103


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.