메뉴 건너뛰기




Volumn 8, Issue 6, 2010, Pages 1273-1280

Accelerated clearance alone explains ultra-large multimers in von Willebrand disease Vicenza

Author keywords

Clearance; Von Willebrand disease; Von Willebrand factor

Indexed keywords

BLOOD CLOTTING FACTOR 8; DESMOPRESSIN; POLYMER; VON WILLEBRAND FACTOR;

EID: 77954466579     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2010.03753.x     Document Type: Article
Times cited : (25)

References (24)
  • 7
    • 0036624746 scopus 로고    scopus 로고
    • The elusive pathogenesis of von Willebrand disease Vicenza
    • author reply 4
    • Castaman G, Rodeghiero F, Mannucci PM. The elusive pathogenesis of von Willebrand disease Vicenza. Blood 2002, 99:4243-4. author reply 4
    • (2002) Blood , vol.99 , pp. 4243-4244
    • Castaman, G.1    Rodeghiero, F.2    Mannucci, P.M.3
  • 9
    • 0023392945 scopus 로고
    • High-efficiency transformation of mammalian cells by plasmid DNA
    • Chen C, Okayama H. High-efficiency transformation of mammalian cells by plasmid DNA. Mol Cell Biol 1987, 7:2745-52.
    • (1987) Mol Cell Biol , vol.7 , pp. 2745-2752
    • Chen, C.1    Okayama, H.2
  • 10
    • 0029042992 scopus 로고
    • Identification of amino acid residues essential for von Willebrand factor binding to platelet glycoprotein Ib. Charged-to-alanine scanning mutagenesis of the A1 domain of human von Willebrand factor
    • Matsushita T, Sadler JE. Identification of amino acid residues essential for von Willebrand factor binding to platelet glycoprotein Ib. Charged-to-alanine scanning mutagenesis of the A1 domain of human von Willebrand factor. J Biol Chem 1995, 270:13406-14.
    • (1995) J Biol Chem , vol.270 , pp. 13406-13414
    • Matsushita, T.1    Sadler, J.E.2
  • 11
    • 0026630044 scopus 로고
    • Impaired intracellular transport produced by a subset of type IIA von Willebrand disease mutations
    • Lyons SE, Bruck ME, Bowie EJ, Ginsburg D. Impaired intracellular transport produced by a subset of type IIA von Willebrand disease mutations. J Biol Chem 1992, 267:4424-30.
    • (1992) J Biol Chem , vol.267 , pp. 4424-4430
    • Lyons, S.E.1    Bruck, M.E.2    Bowie, E.J.3    Ginsburg, D.4
  • 12
    • 0025607976 scopus 로고
    • Multimeric analysis of von Willebrand factor by molecular sieving electrophoresis in sodium dodecyl sulphate agarose gel
    • Raines G, Aumann H, Sykes S, Street A. Multimeric analysis of von Willebrand factor by molecular sieving electrophoresis in sodium dodecyl sulphate agarose gel. Thromb Res 1990, 60:201-12.
    • (1990) Thromb Res , vol.60 , pp. 201-212
    • Raines, G.1    Aumann, H.2    Sykes, S.3    Street, A.4
  • 14
    • 1842530336 scopus 로고    scopus 로고
    • An experimental model to study the in vivo survival of von Willebrand factor. Basic aspects and application to the R1205H mutation
    • Lenting PJ, Westein E, Terraube V, Ribba AS, Huizinga EG, Meyer D, de Groot PG, Denis CV. An experimental model to study the in vivo survival of von Willebrand factor. Basic aspects and application to the R1205H mutation. J Biol Chem 2004, 279:12102-9.
    • (2004) J Biol Chem , vol.279 , pp. 12102-12109
    • Lenting, P.J.1    Westein, E.2    Terraube, V.3    Ribba, A.S.4    Huizinga, E.G.5    Meyer, D.6    de Groot, P.G.7    Denis, C.V.8
  • 15
    • 77954517045 scopus 로고    scopus 로고
    • Modeling VWF catabolism predicts the multimer pattern and subunit degradation in VWD Vicenza, type 1, type 2A, and healthy controls after DDAVP infusion
    • Gézsi A, Mohl A, Sallai K, Nagy E, Szabó T, Sadler JE, Bodó I. Modeling VWF catabolism predicts the multimer pattern and subunit degradation in VWD Vicenza, type 1, type 2A, and healthy controls after DDAVP infusion. J Thromb Haemost 2005, 3:P1476.
    • (2005) J Thromb Haemost , vol.3
    • Gézsi, A.1    Mohl, A.2    Sallai, K.3    Nagy, E.4    Szabó, T.5    Sadler, J.E.6    Bodó, I.7
  • 16
    • 0033865397 scopus 로고    scopus 로고
    • An additional unique candidate mutation (G2470A; M740I) in the original families with von Willebrand disease type 2 M Vicenza and the G3864A (R1205H) mutation
    • Castaman G, Missiaglia E, Federici AB, Schneppenheim R, Rodeghiero F. An additional unique candidate mutation (G2470A; M740I) in the original families with von Willebrand disease type 2 M Vicenza and the G3864A (R1205H) mutation. Thromb Haemost 2000, 84:350-1.
    • (2000) Thromb Haemost , vol.84 , pp. 350-351
    • Castaman, G.1    Missiaglia, E.2    Federici, A.B.3    Schneppenheim, R.4    Rodeghiero, F.5
  • 21
    • 1242338729 scopus 로고    scopus 로고
    • Increased clearance of von Willebrand factor antigen post-DDAVP in Type 1 von Willebrand disease: is it a potential pathogenic process?
    • Brown SA, Eldridge A, Collins PW, Bowen DJ. Increased clearance of von Willebrand factor antigen post-DDAVP in Type 1 von Willebrand disease: is it a potential pathogenic process? J Thromb Haemost 2003, 1:1714-7.
    • (2003) J Thromb Haemost , vol.1 , pp. 1714-1717
    • Brown, S.A.1    Eldridge, A.2    Collins, P.W.3    Bowen, D.J.4
  • 22
    • 0023921265 scopus 로고
    • Hyper-responsiveness to DDAVP for patients with type I von Willebrand's disease and normal intra-platelet von Willebrand factor
    • Rodeghiero F, Castaman G, Di Bona E, Ruggeri M, Lombardi R, Mannucci PM. Hyper-responsiveness to DDAVP for patients with type I von Willebrand's disease and normal intra-platelet von Willebrand factor. Eur J Haematol 1988, 40:163-7.
    • (1988) Eur J Haematol , vol.40 , pp. 163-167
    • Rodeghiero, F.1    Castaman, G.2    Di Bona, E.3    Ruggeri, M.4    Lombardi, R.5    Mannucci, P.M.6
  • 23
    • 34250767667 scopus 로고    scopus 로고
    • Clearance mechanisms of von Willebrand factor and factor VIII
    • Lenting PJ, Vans CJ, Denis CV. Clearance mechanisms of von Willebrand factor and factor VIII. J Thromb Haemost 2007, 5:1353-60.
    • (2007) J Thromb Haemost , vol.5 , pp. 1353-1360
    • Lenting, P.J.1    Vans, C.J.2    Denis, C.V.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.