메뉴 건너뛰기




Volumn 22, Issue 3, 2000, Pages 269-275

Interactions between von willebrand factor and factor viii: Where did they first meet

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 8; COMPLEMENTARY DNA; DESMOPRESSIN ACETATE; RECOMBINANT BLOOD CLOTTING FACTOR 8; VON WILLEBRAND FACTOR;

EID: 0034455182     PISSN: 01928562     EISSN: None     Source Type: Journal    
DOI: 10.1097/00043426-200005000-00017     Document Type: Article
Times cited : (35)

References (27)
  • 1
    • 0014499005 scopus 로고
    • Hemophilia in the Talmud and Rabbinic writings.
    • Rosner F. Hemophilia in the Talmud and Rabbinic writings. Ann Intern Med 1969;70:833.
    • (1969) Ann Intern Med , vol.70 , pp. 833
    • Rosner, F.1
  • 2
    • 85026182045 scopus 로고    scopus 로고
    • Brinkhous KM. A short history of hemophilia, with some comments on the word "hemophilia". In: Brinkhous KM, Hemker HC, eds. Handbook of Hemophilia. New York: American Elsevier, 1975:3-20.
    • Brinkhous KM. A short history of hemophilia, with some comments on the word "hemophilia". In: Brinkhous KM, Hemker HC, eds. Handbook of Hemophilia. New York: American Elsevier, 1975:3-20.
  • 3
    • 0001063498 scopus 로고
    • On a method of determining the condition of blood coagulability for clinical and experimental purposes, and on the effect of the administration of calcium salts in hemophilia and actual or threatened hemorrhage.
    • Wright AE. On a method of determining the condition of blood coagulability for clinical and experimental purposes, and on the effect of the administration of calcium salts in hemophilia and actual or threatened hemorrhage. Br Med J 1893;2:223.
    • (1893) Br Med J , vol.2 , pp. 223
    • Wright, A.E.1
  • 5
    • 0014976247 scopus 로고
    • Immunologic differentiation of classic hemophilia (factor VIII deficiency) and von Willebrand's disease with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and on an acquired circulating anticoagulant against antihemophilic factor.
    • Zimmerman TS, Ratnoff OD, Powell AE. Immunologic differentiation of classic hemophilia (factor VIII deficiency) and von Willebrand's disease with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and on an acquired circulating anticoagulant against antihemophilic factor. J Clin Invest 1971;50:244-54.
    • (1971) J Clin Invest , vol.50 , pp. 244-54
    • Zimmerman, T.S.1    Ratnoff, O.D.2    Powell, A.E.3
  • 6
    • 0015247223 scopus 로고
    • Ristocetin: A new tool in the investigation of platelet.
    • Howard MA, Firkin BG. Ristocetin: A new tool in the investigation of platelet. Thromb Diath Haemorrhagica 1971;26:362-369.
    • (1971) Thromb Diath Haemorrhagica , vol.26 , pp. 362-369
    • Howard, M.A.1    Firkin, B.G.2
  • 7
    • 0015923364 scopus 로고
    • von Willebrand factor: Dissociation from antihemophilic factor procoagulant activity.
    • Weiss HJ, Hoyer IW. von Willebrand factor: Dissociation from antihemophilic factor procoagulant activity. Science 1973;182:1149-1151.
    • (1973) Science , vol.182 , pp. 1149-1151
    • Weiss, H.J.1    Hoyer, I.W.2
  • 8
    • 0021677942 scopus 로고
    • Structure of human factor VIII.
    • Vehar GA, Keyt V, Eaton D, et al. Structure of human factor VIII. Nature 1984;312:337-42.
    • (1984) Nature , vol.312 , pp. 337-42
    • Vehar, G.A.1    Keyt, V.2    Eaton, D.3
  • 9
    • 0029550056 scopus 로고
    • Structure and function of Factor VIII.
    • Lollar P. Structure and function of Factor VIII. Adv Exp Med Biol 1995;386:3-17.
    • (1995) Adv Exp Med Biol , vol.386 , pp. 3-17
    • Lollar, P.1
  • 10
    • 0028043332 scopus 로고
    • Role of the B domain for factor VIII and factor V expression and function.
    • Pittman DD, Marquette KA, Kaufman RJ. Role of the B domain for factor VIII and factor V expression and function. Blood 1994;84:4214-25.
    • (1994) Blood , vol.84 , pp. 4214-25
    • Pittman, D.D.1    Marquette, K.A.2    Kaufman, R.J.3
  • 12
    • 0017889090 scopus 로고
    • von Willebrand's disease antigen II: A new plasma and platelet antigen deficient in severe von Willebrand's disease.
    • Montgomery RR, Zimmerman TS. von Willebrand's disease antigen II: A new plasma and platelet antigen deficient in severe von Willebrand's disease. J Clin Invest 1978;61:1498.
    • (1978) J Clin Invest , vol.61 , pp. 1498
    • Montgomery, R.R.1    Zimmerman, T.S.2
  • 13
    • 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.
    • Furlan M, Robles R, Lamie B. Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis. Blood 1996;87:4223-34.
    • (1996) Blood , vol.87 , pp. 4223-34
    • Furlan, M.1    Robles, R.2    Lamie, B.3
  • 14
    • 0026045281 scopus 로고
    • Structure and function of von Willebrand factor: relationship to von Willebrand's disease.
    • Ruggeri ZM. Structure and function of von Willebrand factor: relationship to von Willebrand's disease. Mayo Clin Proc 1991;66:847-61.
    • (1991) Mayo Clin Proc , vol.66 , pp. 847-61
    • Ruggeri, Z.M.1
  • 15
    • 0026567524 scopus 로고
    • Clinical and biologic evaluation in von Willebrand's disease of a von Willebrand factor concentrate with low factor VIII activity.
    • Goudemand J, Mazurier C, Marey Am Caron C, Coupez B, Mizon P, Goudemand M. Clinical and biologic evaluation in von Willebrand's disease of a von Willebrand factor concentrate with low factor VIII activity. Br J Haematol 1992;80(2):214-21.
    • (1992) Br J Haematol , vol.80 , Issue.2 , pp. 214-21
    • Goudemand, J.1    Mazurier, C.2    Marey Am Caron, C.3    Coupez, B.4    Mizon, P.5    Goudemand, M.6
  • 16
    • 0013849103 scopus 로고
    • Haemophilia A with apparently autosomal dominant inheritance. Evidence for a second autosomal locus involved in factor 8 production.
    • Hensen A, Mattern MJ, Loeliger EA. Haemophilia A with apparently autosomal dominant inheritance. Evidence for a second autosomal locus involved in factor 8 production. Thromb Diath Haemorrhagica 1965;14:341-5.
    • (1965) Thromb Diath Haemorrhagica , vol.14 , pp. 341-5
    • Hensen, A.1    Mattern, M.J.2    Loeliger, E.A.3
  • 17
    • 0015994570 scopus 로고
    • "Autosomal hemophilia": a variant of von Willebrand's disease.
    • Weltkamp JJ, van Tilburg NH. "Autosomal hemophilia": a variant of von Willebrand's disease. Br J Haematol 1974;26:141-52.
    • (1974) Br J Haematol , vol.26 , pp. 141-52
    • Weltkamp, J.J.1    van Tilburg, N.H.2
  • 18
    • 0019947580 scopus 로고
    • A variant of von Willebrand's disease with abnormal expression factor VIII procoagulant activity.
    • Montgomery RR, Hathaway WE, Johnson J, Jacobson L. A variant of von Willebrand's disease with abnormal expression factor VIII procoagulant activity. Blood 1982;60:201-7.
    • (1982) Blood , vol.60 , pp. 201-7
    • Montgomery, R.R.1    Hathaway, W.E.2    Johnson, J.3    Jacobson, L.4
  • 19
    • 4244008849 scopus 로고
    • Mazurier C. The "Normandy" variant of von Willebrand disease: characterization.
    • Jorieux S, Mercier B, Oukfir D. Mazurier C. The "Normandy" variant of von Willebrand disease: characterization. Blood 1991;77:1937-41.
    • (1991) Blood , vol.77 , pp. 1937-41
    • Jorieux, S.1    Mercier, B.2    Oukfir, D.3
  • 20
    • 0026002404 scopus 로고
    • Abnormal binding of factor VIII is linked with the substitution of Gln for Arg91 in von Willebrand factor in a variant form of von Willebrand disease.
    • 91 in von Willebrand factor in a variant form of von Willebrand disease. J Biol Chem 1991;266:19146-9.
    • (1991) J Biol Chem , vol.266 , pp. 19146-9
    • Kroner, A.1    Friedman, K.D.2    Fahs, S.A.3    Scott, J.P.4    Montgomery, R.R.5
  • 21
    • 0025766750 scopus 로고
    • Molecular characterization of a unique von Willebrand disease variant. A novel mutation affecting von Willebrand factor/factor VIII interaction.
    • Cacheris PM, Nichols WC, Ginsburg D. Molecular characterization of a unique von Willebrand disease variant. A novel mutation affecting von Willebrand factor/factor VIII interaction. J Biol Chem 1991;266:13499-502.
    • (1991) J Biol Chem , vol.266 , pp. 13499-502
    • Cacheris, P.M.1    Nichols, W.C.2    Ginsburg, D.3
  • 22
    • 0025817840 scopus 로고
    • The "Normandy" variant of von Willebrand disease: characterization of a point mutation in the von Willebrand factor gene.
    • Gaucher C, Jorieux S, Mercier B, Oufir D, Mazurier C. The "Normandy" variant of von Willebrand disease: characterization of a point mutation in the von Willebrand factor gene. Blood 1991;77:1937-41.
    • (1991) Blood , vol.77 , pp. 1937-41
    • Gaucher, C.1    Jorieux, S.2    Mercier, B.3    Oufir, D.4    Mazurier, C.5
  • 23
    • 0025837733 scopus 로고
    • Identification of two point mutations in the von Willebrand factor gene of three families with the "Normandy" variant of von Willebrand disease.
    • Gaucher C, Mercier B, Jorieux S, Oufkir D, Mazurier C. Identification of two point mutations in the von Willebrand factor gene of three families with the "Normandy" variant of von Willebrand disease. Br J Haematol 1991;78:506-14.
    • (1991) Br J Haematol , vol.78 , pp. 506-14
    • Gaucher, C.1    Mercier, B.2    Jorieux, S.3    Oufkir, D.4    Mazurier, C.5
  • 24
    • 0030040896 scopus 로고    scopus 로고
    • The defective interaction between von Willebrand factor and factor VIII in a patient with type 1 von Willebrand disease is caused by substitution of Arg19 and His54 in mature von Willebrand factor.
    • Kroner PA, Foster PA, Fahs SA, Montgomery RR. The defective interaction between von Willebrand factor and factor VIII in a patient with type 1 von Willebrand disease is caused by substitution of Arg19 and His54 in mature von Willebrand factor. Blood 1996;87:1013-21.
    • (1996) Blood , vol.87 , pp. 1013-21
    • Kroner, P.A.1    Foster, P.A.2    Fahs, S.A.3    Montgomery, R.R.4
  • 25
    • 0024597022 scopus 로고
    • Effect of von Willebrand factor coexpression on the synthesis and secretion of factor VIII in Chinese hamster ovary cells.
    • Kaufman RJ, Wasley LC, Davies MV, Wise RJ, Israel DI, Dorner AJ. Effect of von Willebrand factor coexpression on the synthesis and secretion of factor VIII in Chinese hamster ovary cells. Mol Cell Biol 1989;9:1233-42.
    • (1989) Mol Cell Biol , vol.9 , pp. 1233-42
    • Kaufman, R.J.1    Wasley, L.C.2    Davies, M.V.3    Wise, R.J.4    Israel, D.I.5    Dorner, A.J.6
  • 26
    • 0025777063 scopus 로고
    • von Willebrand factor biosynthesis and processing.
    • Mayadas TN, Wagner DD. von Willebrand factor biosynthesis and processing. Ann NY Acad Sci 1991;614:153-66.
    • (1991) Ann NY Acad Sci , vol.614 , pp. 153-66
    • Mayadas, T.N.1    Wagner, D.D.2
  • 27
    • 0026762462 scopus 로고
    • Biological regulation of factor VII activity.
    • Kaufman RJ. Biological regulation of factor VII activity. Annu Rev Med 1992;43:325-39.
    • (1992) Annu Rev Med , vol.43 , pp. 325-39
    • Kaufman, R.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.