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Volumn 17, Issue 6, 2012, Pages 350-354

Homozygous FVII deficiencies with different reactivity towards tissue thromboplastins of different origin

Author keywords

FVII activity discrepancies; FVII deficiency; Tissue thromboplastins

Indexed keywords

BLOOD CLOTTING FACTOR 7; RECOMBINANT THROMBOPLASTIN; THROMBOPLASTIN;

EID: 84869752243     PISSN: 10245332     EISSN: 16078454     Source Type: Journal    
DOI: 10.1179/1024533212Z.000000000144     Document Type: Article
Times cited : (10)

References (28)
  • 1
    • 0036040213 scopus 로고    scopus 로고
    • Factor VII deficiency
    • Perry DJ. Factor VII deficiency. Br J Haematol. 2002;118(3): 689-700.
    • (2002) Br J Haematol , vol.118 , Issue.3 , pp. 689-700
    • Perry, D.J.1
  • 2
    • 0018192517 scopus 로고
    • Factor VII Padua: A congenital coagulation disorder due to an abnormal factor VII with a peculiar activation pattern
    • Girolami A, Fabris F, Dal Bo Zanon R, Ghiotto G, Burul A. Factor VII Padua: a congenital coagulation disorder due to an abnormal factor VII with a peculiar activation pattern. J Lab Clin Med. 1978;91:387-95.
    • (1978) J Lab Clin Med , vol.91 , pp. 387-395
    • Girolami, A.1    Fabris, F.2    Dal Bo Zanon, R.3    Ghiotto, G.4    Burul, A.5
  • 4
    • 78650175151 scopus 로고
    • Variant coagulation factors X and VII with point mutations in a highly conserved motif in the substrate binding pocket. Comparative molecular modelling
    • abstract
    • James HL, Kumar A, Girolami A, Hubbard J, Fair DS. Variant coagulation factors X and VII with point mutations in a highly conserved motif in the substrate binding pocket. Comparative molecular modelling. Thromb Haemost. 1991;65(Suppl.):932 (abstract).
    • (1991) Thromb Haemost , vol.65 , Issue.SUPPL , pp. 932
    • James, H.L.1    Kumar, A.2    Girolami, A.3    Hubbard, J.4    Fair, D.S.5
  • 5
    • 0025871447 scopus 로고
    • Purification and characterization of factor VII 304-Gln: A variant molecule with reduced activity isolated from a clinically unaffected male
    • O'Brien DP, Gale KM, Anderson JS, McVey JH, Miller GJ, Meade TW, et al. Purification and characterization of factor VII 304-Gln: a variant molecule with reduced activity isolated from a clinically unaffected male. Blood. 1991;78:132-40.
    • (1991) Blood , vol.78 , pp. 132-140
    • O'Brien, D.P.1    Gale, K.M.2    Anderson, J.S.3    McVey, J.H.4    Miller, G.J.5    Meade, T.W.6
  • 6
    • 0027528846 scopus 로고
    • The dysfunction of coagulation factor VII Padua results from substitution of arginine-304 by glutamine
    • James HL, Girolami A, Hubbard JG, Kumar A, Fair DS. The dysfunction of coagulation factor VII Padua results from substitution of arginine-304 by glutamine. Biochim Biophys Acta. 1993;1172:301-5.
    • (1993) Biochim Biophys Acta , vol.1172 , pp. 301-305
    • James, H.L.1    Girolami, A.2    Hubbard, J.G.3    Kumar, A.4    Fair, D.S.5
  • 7
    • 4243270455 scopus 로고
    • The molecular defect in factor VII Detroit is due to substitution of Arg (304) by Glu
    • abstract
    • Shurafa MS, Kumar A, Fair DS, James HL. The molecular defect in factor VII Detroit is due to substitution of Arg (304) by Glu. FASEB J. 1993;7:115 (abstract).
    • (1993) FASEB J , vol.7 , pp. 115
    • Shurafa, M.S.1    Kumar, A.2    Fair, D.S.3    James, H.L.4
  • 9
    • 75649089326 scopus 로고    scopus 로고
    • Source of tissue factor leading to discrepant plasma FVII levels in eight FVII-deficient patients of African origin
    • P-M-002
    • Horellou MH, Chalendard J, Juin F, Conard J, Gouault-Heilmann M, Tapon-Bretaudière J. Source of tissue factor leading to discrepant plasma FVII levels in eight FVII-deficient patients of African origin. J Thromb Haemost. 2007;5(Suppl. 2): P-M-002.
    • (2007) J Thromb Haemost , vol.5 , Issue.SUPPL. 2
    • Horellou, M.H.1    Chalendard, J.2    Juin, F.3    Conard, J.4    Gouault-Heilmann, M.5    Tapon-Bretaudière, J.6
  • 11
    • 77957750989 scopus 로고    scopus 로고
    • Diagnosis of FVII Padua (Arg304Gln) by means of simple clotting tests
    • Girolami A, Bert de Marinis G, Bonamigo E. Diagnosis of FVII Padua (Arg304Gln) by means of simple clotting tests. Clin Chim Acta. 2010;411:2107-8.
    • (2010) Clin Chim Acta , vol.411 , pp. 2107-2108
    • Girolami, A.1    de Marinis, B.G.2    Bonamigo, E.3
  • 12
    • 78449254568 scopus 로고    scopus 로고
    • Ox-brain versus rabbit brain thromboplastin assays are the best tool for a preliminary diagnosis of the Arg304Gln FVII defect (FVII Padua)
    • Girolami A. Ox-brain versus rabbit brain thromboplastin assays are the best tool for a preliminary diagnosis of the Arg304Gln FVII defect (FVII Padua). Acta Haematol. 2010;124:229-34.
    • (2010) Acta Haematol , vol.124 , pp. 229-234
    • Girolami, A.1
  • 13
    • 0028988004 scopus 로고
    • Factor VII Shinjo: A dysfunctional factor VII variant homozygous for the substitution Gln for Arg at position 79
    • Takamiya O, Abe S, Yoshioka A, Nakajima K, McVey JH, Tuddenham EG. Factor VII Shinjo: a dysfunctional factor VII variant homozygous for the substitution Gln for Arg at position 79. Haemostasis. 1995;25:89-97.
    • (1995) Haemostasis , vol.25 , pp. 89-97
    • Takamiya, O.1    Abe, S.2    Yoshioka, A.3    Nakajima, K.4    McVey, J.H.5    Tuddenham, E.G.6
  • 14
    • 0031721547 scopus 로고    scopus 로고
    • Dysfunctional factor VII variant (FVII Tondabayashi) with R79Q: Determination of mutated site with monoclonal anti-human factor VII antibody (B101/B1)
    • Takamiya O, Takeuchi S. Dysfunctional factor VII variant (FVII Tondabayashi) with R79Q: determination of mutated site with monoclonal anti-human factor VII antibody (B101/B1). Clin Chem. 1998;44:1993-5.
    • (1998) Clin Chem , vol.44 , pp. 1993-1995
    • Takamiya, O.1    Takeuchi, S.2
  • 15
    • 0001904524 scopus 로고    scopus 로고
    • The blood coagulation factors: Their complementary DNA, genes and expression
    • Colman RW, Hirsh J, Marder VJ, Clower AW, George JN, Goldhaber S, (eds.), 5th ed. Philadelphia: Lippincott Williams and Wilkins
    • Greenberg DL, Davie EW. The blood coagulation factors: their complementary DNA, genes and expression. In: Colman RW, Hirsh J, Marder VJ, Clower AW, George JN, Goldhaber S, (eds.) Hemostasis and thrombosis. 5th ed. Philadelphia: Lippincott Williams and Wilkins; 2006. p. 21.
    • (2006) Hemostasis and Thrombosis , pp. 21
    • Greenberg, D.L.1    Davie, E.W.2
  • 16
    • 0029992658 scopus 로고    scopus 로고
    • Identification of surface residues mediating tissue factor binding and catalytic function of the serine protease factor VIIa
    • Dickinson CD, Kelly CR, Ruf W. Identification of surface residues mediating tissue factor binding and catalytic function of the serine protease factor VIIa. Proc Natl Acad Sci USA. 1996;93: 14379-84.
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 14379-14384
    • Dickinson, C.D.1    Kelly, C.R.2    Ruf, W.3
  • 17
    • 0028263506 scopus 로고
    • Severe factor VII deficiency caused by mutations abolishing the cleavage site for activation and altering binding to tissue factor
    • Chaing S, Clarke B, Sridhara S, Chu K, Friedman P, VanDusen W, et al. Severe factor VII deficiency caused by mutations abolishing the cleavage site for activation and altering binding to tissue factor. Blood. 1994;83:3524-35.
    • (1994) Blood , vol.83 , pp. 3524-3535
    • Chaing, S.1    Clarke, B.2    Sridhara, S.3    Chu, K.4    Friedman, P.5    Vandusen, W.6
  • 18
    • 0026501320 scopus 로고
    • The first epidermal growth factor domain of human coagulation factor VII is essential for binding with tissue factor
    • Clarke BJ, Ofosu FA, Sridhara S, Bona RD, Rickles FR, Blajchman MA. The first epidermal growth factor domain of human coagulation factor VII is essential for binding with tissue factor. FEBS Lett. 1992;298:206-10.
    • (1992) FEBS Lett , vol.298 , pp. 206-210
    • Clarke, B.J.1    Ofosu, F.A.2    Sridhara, S.3    Bona, R.D.4    Rickles, F.R.5    Blajchman, M.A.6
  • 19
    • 0028003934 scopus 로고
    • Surface plasmon resonance studies of the interaction between factor VII and tissue factor. Demonstration of defective tissue factor binding in a variant FVII molecule (FVII-R79Q)
    • O'Brien DP, Kemball-Cook G, Hutchinson AM, Martin DM, Johnson DJ, Byfield PG, et al. Surface plasmon resonance studies of the interaction between factor VII and tissue factor. Demonstration of defective tissue factor binding in a variant FVII molecule (FVII-R79Q). Biochemistry. 1994;33: 14162-9.
    • (1994) Biochemistry , vol.33 , pp. 14162-14169
    • O'Brien, D.P.1    Kemball-Cook, G.2    Hutchinson, A.M.3    Martin, D.M.4    Johnson, D.J.5    Byfield, P.G.6
  • 20
    • 0028305158 scopus 로고
    • Molecular defects in CRM+factor VII deficiencies: Modelling of missense mutations in the catalytic domain of FVII
    • Bernardi F, Liney DL, Patracchini P, Gemmati D, Legnani C, Arcieri P, et al. Molecular defects in CRM+factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII. Br J Haematol. 1994;86:610-8.
    • (1994) Br J Haematol , vol.86 , pp. 610-618
    • Bernardi, F.1    Liney, D.L.2    Patracchini, P.3    Gemmati, D.4    Legnani, C.5    Arcieri, P.6
  • 21
    • 0028340150 scopus 로고
    • Impaired human tissue factor-mediated activity in blood clotting factor VII Nagoya (Arg304→Trp). Evidence that a region in the catalytic domain of factor VII is important for the association with tissue factor
    • Matsushita T, Kojima T, Emi N, Takahashi I, Saito H. Impaired human tissue factor-mediated activity in blood clotting factor VII Nagoya (Arg304→Trp). Evidence that a region in the catalytic domain of factor VII is important for the association with tissue factor. J Biol Chem. 1994;269: 7355-63.
    • (1994) J Biol Chem , vol.269 , pp. 7355-7363
    • Matsushita, T.1    Kojima, T.2    Emi, N.3    Takahashi, I.4    Saito, H.5
  • 22
    • 0033867990 scopus 로고    scopus 로고
    • Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiency
    • Peyvandi F, Jenkins PV, Mannucci PM, Billio A, Zeinali S, Perkins SJ, et al. Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiency. Thromb Haemost. 2000; 84:250-7.
    • (2000) Thromb Haemost , vol.84 , pp. 250-257
    • Peyvandi, F.1    Jenkins, P.V.2    Mannucci, P.M.3    Billio, A.4    Zeinali, S.5    Perkins, S.J.6
  • 23
    • 63049094038 scopus 로고    scopus 로고
    • Greifswald factor FVII deficiency study group. Factor VII deficiency: Clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene
    • Herrmann FH, Wulff K, Auerswald G, Schulman S, Astermark J, Batorova A, et al. Greifswald factor FVII deficiency study group. Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene. Haemophilia. 2009;15:267-80.
    • (2009) Haemophilia , vol.15 , pp. 267-280
    • Herrmann, F.H.1    Wulff, K.2    Auerswald, G.3    Schulman, S.4    Astermark, J.5    Batorova, A.6
  • 25
    • 0029866660 scopus 로고    scopus 로고
    • Factor VII G331D: A variant molecule involving replacement of a residue in the substrate-binding region of the catalytic domain
    • Zheng DQ, Shurafa M, James HL. Factor VII G331D: a variant molecule involving replacement of a residue in the substrate-binding region of the catalytic domain. Blood Coagul Fibrinolysis. 1996;7:93-6.
    • (1996) Blood Coagul Fibrinolysis , vol.7 , pp. 93-96
    • Zheng, D.Q.1    Shurafa, M.2    James, H.L.3
  • 27
    • 27844481104 scopus 로고    scopus 로고
    • Potential predictors of bleeding risk in inherited factor VII deficiency. Clinical, biological and molecular criteria
    • Giansily-Blaizot M, Schved JF. Potential predictors of bleeding risk in inherited factor VII deficiency. Clinical, biological and molecular criteria. Thromb Haemost. 2005;94:901-6.
    • (2005) Thromb Haemost , vol.94 , pp. 901-906
    • Giansily-Blaizot, M.1    Schved, J.F.2
  • 28
    • 0027309429 scopus 로고
    • Recombinant thromboplastin is slightly more sensitive to factor VII Padua than standard thromboplastins of human origin
    • Girolami A, Sartori MT, Steffan A, Fadin MA. Recombinant thromboplastin is slightly more sensitive to factor VII Padua than standard thromboplastins of human origin. Blood Coagul Fibrinolysis. 1993;4:497-8.
    • (1993) Blood Coagul Fibrinolysis , vol.4 , pp. 497-498
    • Girolami, A.1    Sartori, M.T.2    Steffan, A.3    Fadin, M.A.4


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