-
1
-
-
0034917278
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
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