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Volumn 126, Issue 1, 2006, Pages 128-132

Asymptomatic factor VII deficiency in African Americans

Author keywords

Blood banking; Clinical pathology; Coagulation; Molecular diagnostics; Transfusion medicine

Indexed keywords

ADENINE NUCLEOTIDE; AMINO ACID; ARGININE; BLOOD CLOTTING FACTOR 7; GLUTAMINE; GUANINE NUCLEOTIDE; THROMBOPLASTIN;

EID: 33745774573     PISSN: 00029173     EISSN: None     Source Type: Journal    
DOI: 10.1309/36HQ36ETU7K8MUXT     Document Type: Article
Times cited : (13)

References (23)
  • 1
    • 0034917278 scopus 로고    scopus 로고
    • Tissue factor: An enzyme cofactor and a true receptor
    • Morrissey JH. Tissue factor: an enzyme cofactor and a true receptor. Thromb Haemost. 2001;6:66-74.
    • (2001) Thromb Haemost , vol.6 , pp. 66-74
    • Morrissey, J.H.1
  • 2
    • 0004330552 scopus 로고
    • Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation
    • O'Hara PJ, Grant FJ, Haldeman BA, et al. Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation. Proc Natl Acad Sci U S A. 1987;84:5158-5162.
    • (1987) Proc Natl Acad Sci U S A , vol.84 , pp. 5158-5162
    • O'Hara, P.J.1    Grant, F.J.2    Haldeman, B.A.3
  • 3
    • 20144382370 scopus 로고    scopus 로고
    • Clinical phenotypes and factor VII genotype in congenital factor VII deficiency
    • Mariani GM, Herrmann FH, Dolce A, et al. Clinical phenotypes and factor VII genotype in congenital factor VII deficiency. Thromb Haemost. 2005;93:481-487.
    • (2005) Thromb Haemost , vol.93 , pp. 481-487
    • Mariani, G.M.1    Herrmann, F.H.2    Dolce, A.3
  • 5
    • 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, et al. Factor VII Padua: a congenital coagulation disorder due to an abnormal factor VII with a peculiar activation pattern. J Lab Clin Med. 1978;91:387-395.
    • (1978) J Lab Clin Med , vol.91 , pp. 387-395
    • Girolami, A.1    Fabris, F.2    Dal Bo Zanon, R.3
  • 6
    • 24044551334 scopus 로고    scopus 로고
    • Mild factor VII deficiency due to heterozygosis is not associated with a bleeding tendency
    • Girolami A, Vettore S, Bortoletto E, et al. Mild factor VII deficiency due to heterozygosis is not associated with a bleeding tendency [letter]. Blood Coagul Fibrinolysis. 2005;16:459-460.
    • (2005) Blood Coagul Fibrinolysis , vol.16 , pp. 459-460
    • Girolami, A.1    Vettore, S.2    Bortoletto, E.3
  • 7
    • 0027528846 scopus 로고
    • The dysfunction of coagulation factor VIIPadua results from substitution of arginine-304 by glutamine
    • James HL, Girolami A, Hubbard JG, et al. The dysfunction of coagulation factor VIIPadua results from substitution of arginine-304 by glutamine. Biochim Biophys Acta. 1993;1172:301-305.
    • (1993) Biochim Biophys Acta , vol.1172 , pp. 301-305
    • James, H.L.1    Girolami, A.2    Hubbard, J.G.3
  • 8
    • 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, et al. Purification and characterization of factor VII 304-Gln: a variant molecule with reduced activity isolated from a clinically unaffected male. Blood. 1991;78:132-140.
    • (1991) Blood , vol.78 , pp. 132-140
    • O'Brien, D.P.1    Gale, K.M.2    Anderson, J.S.3
  • 9
    • 0022410305 scopus 로고
    • Hereditary factor VII deficiency: Heterogeneity defined by combined functional and immunochemical analysis
    • Triplett DA, Brandt JT, Batard MA, et al. Hereditary factor VII deficiency: heterogeneity defined by combined functional and immunochemical analysis. Blood. 1985;66:1284-1287.
    • (1985) Blood , vol.66 , pp. 1284-1287
    • Triplett, D.A.1    Brandt, J.T.2    Batard, M.A.3
  • 10
    • 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, et al. Severe factor VII deficiency caused by mutations abolishing the cleavage site for activation and altering binding to tissue factor. Blood. 1994;83:3524-3535.
    • (1994) Blood , vol.83 , pp. 3524-3535
    • Chaing, S.1    Clarke, B.2    Sridhara, S.3
  • 11
    • 10444250971 scopus 로고    scopus 로고
    • Characterization of mild coagulation factor VII deficiency: Activity and clearance of the Arg315Trp and Arg315Lys variants in the Cys310-Cys329 loop (c170s)
    • Furlan Freguia C, Toso R, Pollak ES, et al. Characterization of mild coagulation factor VII deficiency: activity and clearance of the Arg315Trp and Arg315Lys variants in the Cys310-Cys329 loop (c170s). Haematologica. 2004;89:1504-1509.
    • (2004) Haematologica , vol.89 , pp. 1504-1509
    • Furlan Freguia, C.1    Toso, R.2    Pollak, E.S.3
  • 12
    • 0035165403 scopus 로고    scopus 로고
    • Factor VII deficiency and the FVII mutation database
    • McVey JH, Boswell E, Mumford AD, et al. Factor VII deficiency and the FVII mutation database. Hum Mutat. 2001;17:3-17.
    • (2001) Hum Mutat , vol.17 , pp. 3-17
    • McVey, J.H.1    Boswell, E.2    Mumford, A.D.3
  • 13
    • 0027938159 scopus 로고
    • African-American factor VII-deficient variants in Georgia (FVII variants)
    • Krauss JS, Matthews A, Oliver J, et al. African-American factor VII-deficient variants in Georgia (FVII variants). Am J Hematol. 1994;47:239-241.
    • (1994) Am J Hematol , vol.47 , pp. 239-241
    • Krauss, J.S.1    Matthews, A.2    Oliver, J.3
  • 14
    • 13244275116 scopus 로고    scopus 로고
    • Lack of bleeding in patients with severe factor VII deficiency
    • Barnett JM, Demel KC, Mega AE, et al. Lack of bleeding in patients with severe factor VII deficiency. Am J Hematol. 2005;78:134-137.
    • (2005) Am J Hematol , vol.78 , pp. 134-137
    • Barnett, J.M.1    Demel, K.C.2    Mega, A.E.3
  • 15
    • 0023902762 scopus 로고
    • Factor VII activity and antigen in a patient with abnormal factor VII
    • Takamiya O, Funahashi S, Kinoshita S, et al. Factor VII activity and antigen in a patient with abnormal factor VII. Clin Lab Haematol. 1988;10:159-165.
    • (1988) Clin Lab Haematol , vol.10 , pp. 159-165
    • Takamiya, O.1    Funahashi, S.2    Kinoshita, S.3
  • 16
    • 0029153854 scopus 로고
    • Inherited factor VII deficiency: Genetics and molecular pathology
    • Tuddenham EG, Pemberton S, Cooper DN. Inherited factor VII deficiency: genetics and molecular pathology. Thromb Haemost. 1995;74:313-321.
    • (1995) Thromb Haemost , vol.74 , pp. 313-321
    • Tuddenham, E.G.1    Pemberton, S.2    Cooper, D.N.3
  • 17
    • 0038395711 scopus 로고    scopus 로고
    • Prevalence of factor VII deficiency and molecular characterization of the F7 gene in Brazilian patients
    • Rodrigues DN, Siqueira LH, Galizoni AM, et al. Prevalence of factor VII deficiency and molecular characterization of the F7 gene in Brazilian patients. Blood Coagul Fibrinolysis. 2003;14:289-292.
    • (2003) Blood Coagul Fibrinolysis , vol.14 , pp. 289-292
    • Rodrigues, D.N.1    Siqueira, L.H.2    Galizoni, A.M.3
  • 18
    • 0028316109 scopus 로고
    • The rates of G:C→T:A and G:C→C:G transversions at CpG dinucleotides in the human factor IX gene
    • Ketterling RP, Vielhaber E, Sommer SS. The rates of G:C→T:A and G:C→C:G transversions at CpG dinucleotides in the human factor IX gene. Am J Hum Genet. 1994;54:831-835.
    • (1994) Am J Hum Genet , vol.54 , pp. 831-835
    • Ketterling, R.P.1    Vielhaber, E.2    Sommer, S.S.3
  • 19
    • 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 U S A. 1996;93:14379-14384.
    • (1996) Proc Natl Acad Sci U S A , vol.93 , pp. 14379-14384
    • Dickinson, C.D.1    Kelly, C.R.2    Ruf, W.3
  • 20
    • 4444370350 scopus 로고    scopus 로고
    • Comparison among natural (Arg304Gln, Arg304Trp) and artificial (Arg290His, Arg290Lys) mutations in coagulation factor VII loops
    • Furlan Freguia C, Toso R, Pinotti M, et al. Comparison among natural (Arg304Gln, Arg304Trp) and artificial (Arg290His, Arg290Lys) mutations in coagulation factor VII loops. J Thromb Haemost. 2003;1:2455-2457.
    • (2003) J Thromb Haemost , vol.1 , pp. 2455-2457
    • Furlan Freguia, C.1    Toso, R.2    Pinotti, M.3
  • 21
    • 0029926396 scopus 로고    scopus 로고
    • The crystal structure of the complex of blood coagulation factor VIIa with soluble tissue factor
    • Banner DW, D'Arcy A, Chene C, et al. The crystal structure of the complex of blood coagulation factor VIIa with soluble tissue factor. Nature. 1996;380:41-46.
    • (1996) Nature , vol.380 , pp. 41-46
    • Banner, D.W.1    D'Arcy, A.2    Chene, C.3
  • 22
    • 0002720981 scopus 로고    scopus 로고
    • Inherited disorders of prothrombin conversion
    • Colman R, Marder VJ, Clowes AW, et al, eds. Philadelphia, PA: Lippincott Williams & Wilkins;
    • Roberts HR, Escobar MA. Inherited disorders of prothrombin conversion. In: Colman R, Marder VJ, Clowes AW, et al, eds. Hemostosis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:928-930.
    • (2006) Hemostosis and Thrombosis: Basic Principles and Clinical Practice 5th Ed. , pp. 928-930
    • Roberts, H.R.1    Escobar, M.A.2
  • 23
    • 0029560352 scopus 로고
    • Prophylaxis and therapy with factor VII concentrate (human) immuno, vapor heated in patients with congenital factor VII deficiency: A summary of case reports
    • Cohen LJ, McWilliams NB, Neuberg R, et al. Prophylaxis and therapy with factor VII concentrate (human) immuno, vapor heated in patients with congenital factor VII deficiency: a summary of case reports. Am J Hematol. 1995;50:269-276.
    • (1995) Am J Hematol , vol.50 , pp. 269-276
    • Cohen, L.J.1    McWilliams, N.B.2    Neuberg, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.