-
1
-
-
0027446268
-
Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C
-
Dahlback B, Carlsson M, Sevensson PJ. Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C. Proc Natl Acad Sci USA 1993; 90: 1004-1008.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 1004-1008
-
-
Dahlback, B.1
Carlsson, M.2
Sevensson, P.J.3
-
2
-
-
0028314865
-
Mutation in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koeleman BPC, Koster T et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994; 369: 64-67.
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koeleman, B.P.C.2
Koster, T.3
-
3
-
-
0031868874
-
Genetic polymorphisms and risk of coronary artery disease
-
Murata M, Kawano K, Matsubara Y, Ishikawa K, Watanabe G, Watanabe K, Ikeda Y. Genetic polymorphisms and risk of coronary artery disease. Semin Thromb Haemost 1998; 24: 245-250.
-
(1998)
Semin Thromb Haemost
, vol.24
, pp. 245-250
-
-
Murata, M.1
Kawano, K.2
Matsubara, Y.3
Ishikawa, K.4
Watanabe, G.5
Watanabe, K.6
Ikeda, Y.7
-
4
-
-
0027447258
-
Inherited predisposition to thrombosis
-
Miletich JP, Prescott SM, White R, Majerus PW, Bovill EG. Inherited predisposition to thrombosis. Cell 1993; 72: 477-480.
-
(1993)
Cell
, vol.72
, pp. 477-480
-
-
Miletich, J.P.1
Prescott, S.M.2
White, R.3
Majerus, P.W.4
Bovill, E.G.5
-
5
-
-
0030809467
-
Clinical relevance of polymorphic markers of arterial thrombosis
-
Di Minno G, Gradone E, Margaglione M. Clinical relevance of polymorphic markers of arterial thrombosis. Thromb Haemost 1997; 78: 462-466.
-
(1997)
Thromb Haemost
, vol.78
, pp. 462-466
-
-
Di Minno, G.1
Gradone, E.2
Margaglione, M.3
-
8
-
-
0015295415
-
The diagnosis of deep vein thrombosis using the 1251-fibrinogen test
-
Kakkar W. The diagnosis of deep vein thrombosis using the 1251-fibrinogen test. Arch Surg 1972; 104: 152-159.
-
(1972)
Arch Surg
, vol.104
, pp. 152-159
-
-
Kakkar, W.1
-
9
-
-
0016175746
-
Failure of low dose heparin to prevent deep vein thrombosis after hip-replacement arthroplasty
-
Hampson WGJ, Harris FC, Lucas HK, Roberts PH, McCall IW, Jackson PC, Powell NL, Staddon GE. Failure of low dose heparin to prevent deep vein thrombosis after hip-replacement arthroplasty. Lancet 1974; 5: 795-797.
-
(1974)
Lancet
, vol.5
, pp. 795-797
-
-
Hampson, W.G.J.1
Harris, F.C.2
Lucas, H.K.3
Roberts, P.H.4
McCall, I.W.5
Jackson, P.C.6
Powell, N.L.7
Staddon, G.E.8
-
11
-
-
0030560928
-
Low prevalence of activated protein C resistance and coagulation factor V Arg506 to Gln mutation among Japanese patients with various forms of thrombosis and normal individuals
-
Zama T, Murata M, Ono F et al. Low prevalence of activated protein C resistance and coagulation factor V Arg506 to Gln mutation among Japanese patients with various forms of thrombosis and normal individuals. Int J Hematol 1996; 65: 71-78.
-
(1996)
Int J Hematol
, vol.65
, pp. 71-78
-
-
Zama, T.1
Murata, M.2
Ono, F.3
-
12
-
-
0031618374
-
Frequencies of prothrombin 20210 G/A mutation may be different among races - Studies on Japanese populations with various forms of thrombotic disorders and healthy subjects
-
Isshiki I, Murata M, Watanabe R et al. Frequencies of prothrombin 20210 G/A mutation may be different among races - studies on Japanese populations with various forms of thrombotic disorders and healthy subjects. Blood Coagul Fibrinolysis 1998; 9: 105-106.
-
(1998)
Blood Coagul Fibrinolysis
, vol.9
, pp. 105-106
-
-
Isshiki, I.1
Murata, M.2
Watanabe, R.3
-
13
-
-
0029993061
-
Genotyping of the human platelet antigen systems 1 through 5 by multiplex polymerase chain reaction and ligationbased typing
-
Legler TJ, Kohler M, Mayr WR, Panzer S, Ohto H and Fischer GF. Genotyping of the human platelet antigen systems 1 through 5 by multiplex polymerase chain reaction and ligationbased typing. Transfusion 1996; 36: 426-431.
-
(1996)
Transfusion
, vol.36
, pp. 426-431
-
-
Legler, T.J.1
Kohler, M.2
Mayr, W.R.3
Panzer, S.4
Ohto, H.5
Fischer, G.F.6
-
14
-
-
0030731403
-
Coronary artery disease and polymorphisms in a receptor mediating shear stress-dependent platelet activation
-
Murata M, Matsubara Y, Kawano K et al. Coronary artery disease and polymorphisms in a receptor mediating shear stress-dependent platelet activation. Circulation 1997; 96: 3281-3286.
-
(1997)
Circulation
, vol.96
, pp. 3281-3286
-
-
Murata, M.1
Matsubara, Y.2
Kawano, K.3
-
15
-
-
0027125530
-
The pathogenesis of coronary artery disease and the acute coronary syndromes
-
Fuster V, Badimon L, Badimon JJ, and Chesebro JH. The pathogenesis of coronary artery disease and the acute coronary syndromes. N Engl J Med 1992; 356: 242-250.
-
(1992)
N Engl J Med
, vol.356
, pp. 242-250
-
-
Fuster, V.1
Badimon, L.2
Badimon, J.J.3
Chesebro, J.H.4
-
16
-
-
0031657877
-
The role of platelets in ischemic stroke
-
del Zoppo GJ. The role of platelets in ischemic stroke. Neurology 1998; 51(3 Suppl 3): S9-14.
-
(1998)
Neurology
, vol.51
, Issue.3 SUPPL. 3
-
-
Del Zoppo, G.J.1
-
17
-
-
0031721148
-
Therapeutic inhibition of platelet function in stroke
-
Harker LA. Therapeutic inhibition of platelet function in stroke. Cerebrovasc Dis 1998; 8 Suppl 5: 8-18.
-
(1998)
Cerebrovasc Dis
, vol.8
, Issue.5 SUPPL.
, pp. 8-18
-
-
Harker, L.A.1
-
18
-
-
0023155614
-
Shear-induced platelet aggregation requires von Willebrand factor and platelet glycoproteins Ib and IIb-IIIa
-
Peterson DM, Stathopoulos NA, Giorgio TD, Hellumus JD, Moake JL. Shear-induced platelet aggregation requires von Willebrand factor and platelet glycoproteins Ib and IIb-IIIa. Blood 1987; 69: 625-628.
-
(1987)
Blood
, vol.69
, pp. 625-628
-
-
Peterson, D.M.1
Stathopoulos, N.A.2
Giorgio, T.D.3
Hellumus, J.D.4
Moake, J.L.5
-
19
-
-
0025732428
-
The role of von Willebrand factor and fibrinogen in platelet aggregation under varying shear stress
-
Ikeda Y, Handa M, Kawano K et al. The role of von Willebrand factor and fibrinogen in platelet aggregation under varying shear stress. J Clin Invest 1991; 87: 1234-1240.
-
(1991)
J Clin Invest
, vol.87
, pp. 1234-1240
-
-
Ikeda, Y.1
Handa, M.2
Kawano, K.3
-
20
-
-
0028979497
-
The α2β1 integrin: A collagen receptor on platelets and other cells
-
Santoro SA, Zutter MM. The α2β1 integrin: A collagen receptor on platelets and other cells. Thromb Haemost 1995; 74: 813.
-
(1995)
Thromb Haemost
, vol.74
, pp. 813
-
-
Santoro, S.A.1
Zutter, M.M.2
-
21
-
-
0030792541
-
Platelet adhesion to collagen: An update
-
Sixma JJ, Zanten GH, Huizinga EG, van der Plas RM, Verkley M, Wu YP, Gros P, de Groot PG. Platelet adhesion to collagen: an update. Thromb Haemost 1997; 78: 434.
-
(1997)
Thromb Haemost
, vol.78
, pp. 434
-
-
Sixma, J.J.1
Zanten, G.H.2
Huizinga, E.G.3
Van Der Plas, R.M.4
Verkley, M.5
Wu, Y.P.6
Gros, P.7
De Groot, P.G.8
-
22
-
-
0030742897
-
Platelet receptor for collagen
-
Moroi M, Jung SM. Platelet receptor for collagen. Thromb Haemost 1997; 78: 439.
-
(1997)
Thromb Haemost
, vol.78
, pp. 439
-
-
Moroi, M.1
Jung, S.M.2
-
23
-
-
0028274014
-
The platelet glycoprotein Ib-IX complex
-
Lopez JA. The platelet glycoprotein Ib-IX complex. Blood Coagul Fibrinolysis 1994; 5: 97-119.
-
(1994)
Blood Coagul Fibrinolysis
, vol.5
, pp. 97-119
-
-
Lopez, J.A.1
-
24
-
-
0030742894
-
Platelet GPIb-V-IX complex
-
Clemetson KJ. Platelet GPIb-V-IX complex. Thromb Haemost 1997; 78: 266-270.
-
(1997)
Thromb Haemost
, vol.78
, pp. 266-270
-
-
Clemetson, K.J.1
-
26
-
-
0026610362
-
NH2-terminal globular domain of human platelet glycoprotein Ibα has a methionine 145/threonine145 amino acid polymorphism, which is associated with the HPA-2 (Ko) alloantigens
-
Kuijpers RWAM, Faber NM, Cuypers HThM Ouwehand WH and von dem Borne AEGKr. NH2-terminal globular domain of human platelet glycoprotein Ibα has a methionine 145/threonine145 amino acid polymorphism, which is associated with the HPA-2 (Ko) alloantigens. J Clin Invest 1992; 89: 381-384.
-
(1992)
J Clin Invest
, vol.89
, pp. 381-384
-
-
Kuijpers, R.W.A.M.1
Faber, N.M.2
Cuypers, H.Th.M.3
Ouwehand, W.H.4
Von Dem Borne, A.E.G.Kr.5
-
27
-
-
0026720406
-
Genetic and structural characterization of an amino acid dimorphism in glycoprotein Ibα involved in platelet transfusion refractoriness
-
Murata M, Furihata K, Ishida F, Russell SR, Ware J and Ruggeri ZM. Genetic and structural characterization of an amino acid dimorphism in glycoprotein Ibα involved in platelet transfusion refractoriness. Blood 1992; 79: 3086-3090.
-
(1992)
Blood
, vol.79
, pp. 3086-3090
-
-
Murata, M.1
Furihata, K.2
Ishida, F.3
Russell, S.R.4
Ware, J.5
Ruggeri, Z.M.6
-
28
-
-
0026655919
-
Polymorphism of human glycoprotein Ib alpha results from a variable number of tandem repeats of a 13-amino acid sequence in the mucin-like macroglycopeptide region. Structure/function implications
-
Lopez JA, Ludwig EH, McCarthy BJ. Polymorphism of human glycoprotein Ib alpha results from a variable number of tandem repeats of a 13-amino acid sequence in the mucin-like macroglycopeptide region. Structure/function implications. J Biol Chem 1992; 267: 10055-10056.
-
(1992)
J Biol Chem
, vol.267
, pp. 10055-10056
-
-
Lopez, J.A.1
Ludwig, E.H.2
McCarthy, B.J.3
-
29
-
-
0033168684
-
Kozak sequence polymorphism of the glycoprotein (GP) Ib alpha gene is a major determinant of the plasma membrane levels of the platelet GP Ib-IX-V complex
-
Afshar-Kharghan V, Li CQ, Khoshnevis-Asl M, Lopez JA. Kozak sequence polymorphism of the glycoprotein (GP) Ib alpha gene is a major determinant of the plasma membrane levels of the platelet GP Ib-IX-V complex. Blood 1999; 94(1): 186-191.
-
(1999)
Blood
, vol.94
, Issue.1
, pp. 186-191
-
-
Afshar-Kharghan, V.1
Li, C.Q.2
Khoshnevis-Asl, M.3
Lopez, J.A.4
-
30
-
-
0032532036
-
Polymorphisms of platelet membrane glycoprotein Ib associated with arterial thrombotic disease
-
Gonzalez-Conejero R, Lozano ML, Rivera J et al. Polymorphisms of platelet membrane glycoprotein Ib associated with arterial thrombotic disease. Blood 1998; 92(8): 2771-1776.
-
(1998)
Blood
, vol.92
, Issue.8
, pp. 2771-11776
-
-
Gonzalez-Conejero, R.1
Lozano, M.L.2
Rivera, J.3
-
31
-
-
0030793970
-
Polymorphisms of the human platelet antigens HPA-1, HPA-2, HPA-3, and HPA-5 on the platelet receptors for fibrinogen (GPIIb/IIIa), von Willebrand factor (GPIb/IX), and collagen (GPIa/IIa) are not correlated with an increased risk for stroke
-
Carlsson LE, Greinacher A, Spitzer C, Walther R, Kessler C. Polymorphisms of the human platelet antigens HPA-1, HPA-2, HPA-3, and HPA-5 on the platelet receptors for fibrinogen (GPIIb/IIIa), von Willebrand factor (GPIb/IX), and collagen (GPIa/IIa) are not correlated with an increased risk for stroke. Stroke 1997; 28: 1392-1395.
-
(1997)
Stroke
, vol.28
, pp. 1392-1395
-
-
Carlsson, L.E.1
Greinacher, A.2
Spitzer, C.3
Walther, R.4
Kessler, C.5
-
32
-
-
0031878376
-
Platelet GPIIIa P1A1 and GPIb variable number of tandem repeat polymorphisms and markers of platelet activation in acute stroke
-
Carter AM, Catto AJ, Bamford JM, Grant PJ. Platelet GPIIIa P1A1 and GPIb variable number of tandem repeat polymorphisms and markers of platelet activation in acute stroke. Arterioscler Thromb Vasc Biol 1998; 18: 1124-1131.
-
(1998)
Arterioscler Thromb Vasc Biol
, vol.18
, pp. 1124-1131
-
-
Carter, A.M.1
Catto, A.J.2
Bamford, J.M.3
Grant, P.J.4
-
33
-
-
0033980198
-
Association between platelet glycoprotein Ibα genotype and ischemic cerebrovascular disease
-
Sonoda A, Murata M, Ito D et al. Association between platelet glycoprotein Ibα genotype and ischemic cerebrovascular disease. Stroke 2000; 31: 493-497.
-
(2000)
Stroke
, vol.31
, pp. 493-497
-
-
Sonoda, A.1
Murata, M.2
Ito, D.3
-
34
-
-
0029840990
-
Frequency and functional relevance of genetic threonin145/methionin145 dimorphism in platelet glycoprotein Ibα in an Italian population
-
Mazzucato M, Pradella P, De Angelis V, Stefan A, De Marco L. Frequency and functional relevance of genetic threonin145/methionin145 dimorphism in platelet glycoprotein Ibα in an Italian population. Transfusion 1996; 6: 891-894.
-
(1996)
Transfusion
, vol.6
, pp. 891-894
-
-
Mazzucato, M.1
Pradella, P.2
De Angelis, V.3
Stefan, A.4
De Marco, L.5
-
35
-
-
0033983970
-
Threonine-145/Methionine-145 variants of baculovirus produced recombinant ligand binding domain of GPIbα express HPA-2 epitopes and show equal binding of von Willebrand factor
-
Li CQ, Garner SF, Davies J, Smethurst PA, Wardell MR, Ouwehand WH. Threonine-145/Methionine-145 variants of baculovirus produced recombinant ligand binding domain of GPIbα express HPA-2 epitopes and show equal binding of von Willebrand factor. Blood 2000; 95: 205-211.
-
(2000)
Blood
, vol.95
, pp. 205-211
-
-
Li, C.Q.1
Garner, S.F.2
Davies, J.3
Smethurst, P.A.4
Wardell, M.R.5
Ouwehand, W.H.6
-
36
-
-
0033966464
-
A common polymorphism flanking the ATG initiation codon of GPIbα does not affect expression and is not a major risk factor for arterial thrombosis
-
Corral J, Lozano ML, Gonzalez-Conejero R et al. A common polymorphism flanking the ATG initiation codon of GPIbα does not affect expression and is not a major risk factor for arterial thrombosis. Thromb Haemost 2000; 83: 23-28.
-
(2000)
Thromb Haemost
, vol.83
, pp. 23-28
-
-
Corral, J.1
Lozano, M.L.2
Gonzalez-Conejero, R.3
-
37
-
-
0030942489
-
Heredity variation in platelet integrin a2bl density is associated with two silent polymorphisms in the a2 gene coding sequence
-
Kunicki TJ, Kritzik M, Annis DS, Nugent DJ. Heredity variation in platelet integrin a2bl density is associated with two silent polymorphisms in the a2 gene coding sequence. Blood 1997; 89: 1939.
-
(1997)
Blood
, vol.89
, pp. 1939
-
-
Kunicki, T.J.1
Kritzik, M.2
Annis, D.S.3
Nugent, D.J.4
-
38
-
-
0032173427
-
Nucleotide polymorphism in the a2 gene define multiple alleles that are associated with differences in platelet a2b1 density
-
Kritzik M, Savage B, Nugent DJ, Santoso S, Ruggeri ZM, Kunicki TJ. Nucleotide polymorphism in the a2 gene define multiple alleles that are associated with differences in platelet a2b1 density. Blood 1998; 92: 1.
-
(1998)
Blood
, vol.92
, pp. 1
-
-
Kritzik, M.1
Savage, B.2
Nugent, D.J.3
Santoso, S.4
Ruggeri, Z.M.5
Kunicki, T.J.6
-
39
-
-
0031725671
-
Analysis of platelet glycoprotein Ia (alpha2 integrin) allele frequencies in three North American populations reveals genetic association between nucleotide 807C/T and amino acid 505 Glu/Lys (HPA-5) dimorphisms
-
Reiner AP, Aramaki KM, Teramura G, Gaur L. Analysis of platelet glycoprotein Ia (alpha2 integrin) allele frequencies in three North American populations reveals genetic association between nucleotide 807C/T and amino acid 505 Glu/Lys (HPA-5) dimorphisms. Thromb Haemost 1998; 80: 449.
-
(1998)
Thromb Haemost
, vol.80
, pp. 449
-
-
Reiner, A.P.1
Aramaki, K.M.2
Teramura, G.3
Gaur, L.4
-
40
-
-
0033137302
-
The alpha2 gene coding sequence T807/A873 of the platelet collagen receptor integrin alpha2betal might be a genetic risk factor for the development of stroke in younger patients
-
Carlsson LE, Santoso S, Spitzer C, Kessler C, Greinacher A. The alpha2 gene coding sequence T807/A873 of the platelet collagen receptor integrin alpha2betal might be a genetic risk factor for the development of stroke in younger patients. Blood 1999; 93: 3583.
-
(1999)
Blood
, vol.93
, pp. 3583
-
-
Carlsson, L.E.1
Santoso, S.2
Spitzer, C.3
Kessler, C.4
Greinacher, A.5
-
41
-
-
0033561354
-
Association of the platelet glycoprotein Ia C807T gene polymorphism with nonfatal myocardial infarction in younger patients
-
Santoso S, Kunicki TJ, Kroll H, Haberbosch W, Gardemann A. Association of the platelet glycoprotein Ia C807T gene polymorphism with nonfatal myocardial infarction in younger patients. Blood 1999; 93: 2449.
-
(1999)
Blood
, vol.93
, pp. 2449
-
-
Santoso, S.1
Kunicki, T.J.2
Kroll, H.3
Haberbosch, W.4
Gardemann, A.5
-
42
-
-
0001218842
-
Association of two silent polymorphisms of platelet glycoprotein Ia/IIa receptor with risk of myocardial infarction: A case-control study
-
Moshfegh K, Wuillemin WA, Redondo M et al. Association of two silent polymorphisms of platelet glycoprotein Ia/IIa receptor with risk of myocardial infarction: A case-control study. Lancet 1999; 353: 351.
-
(1999)
Lancet
, vol.353
, pp. 351
-
-
Moshfegh, K.1
Wuillemin, W.A.2
Redondo, M.3
-
43
-
-
0034161315
-
Association between diabetic retinopathy and genetic variations in α2β1 Integrin, a platelet receptor for collagen
-
Matsubara Y, Murata M, Maruyama T et al. Association between diabetic retinopathy and genetic variations in α2β1 Integrin, a platelet receptor for collagen. Blood 2000; 95: 1560-1564.
-
(2000)
Blood
, vol.95
, pp. 1560-1564
-
-
Matsubara, Y.1
Murata, M.2
Maruyama, T.3
-
44
-
-
0029875770
-
A polymorphism of platelet glycoprotein receptor as an inhierited risk factor for coronary thrombosis
-
Weiss EJ, Bray PF, Tayback M et al. A polymorphism of platelet glycoprotein receptor as an inhierited risk factor for coronary thrombosis. N Engl J Med 1996; 334: 1090-1094.
-
(1996)
N Engl J Med
, vol.334
, pp. 1090-1094
-
-
Weiss, E.J.1
Bray, P.F.2
Tayback, M.3
-
45
-
-
0030614495
-
PIA1/A2 polymorphism of platelet glycoprotein Ilia and risks of myocardial infarction, stroke, and venous thrombosis
-
Ridker PM Hennekens CH Schmitz C, Stampfer MJ and Lindpaintner K. PIA1/A2 polymorphism of platelet glycoprotein Ilia and risks of myocardial infarction, stroke, and venous thrombosis. Lancet 1997; 349: 385-388.
-
(1997)
Lancet
, vol.349
, pp. 385-388
-
-
Ridker, P.M.1
Hennekens, C.H.2
Schmitz, C.3
Stampfer, M.J.4
Lindpaintner, K.5
-
46
-
-
0032916837
-
Increased platelet aggregability associated with platelet GPIIIa P1A2 polymorphism. The Framingham offspring study
-
Feng D, Lindpaintner K, Larson D et al. Increased platelet aggregability associated with platelet GPIIIa P1A2 polymorphism. The Framingham offspring study. Arterioscler Thromb Vasc Biol 1999; 19: 1142-1147.
-
(1999)
Arterioscler Thromb Vasc Biol
, vol.19
, pp. 1142-1147
-
-
Feng, D.1
Lindpaintner, K.2
Larson, D.3
-
47
-
-
0008461416
-
The P1A1 alloantigen does not alter the affinity of GPIIb-IIIa for fibrinogen or RGD-containing peptides
-
Bennet JS, Vilarire G, Catella-Lawson F, Rut AR, Fitzgerald G. The P1A1 alloantigen does not alter the affinity of GPIIb-IIIa for fibrinogen or RGD-containing peptides. Blood 90: 154a, 1997.
-
(1997)
Blood
, vol.90
-
-
Bennet, J.S.1
Vilarire, G.2
Catella-Lawson, F.3
Rut, A.R.4
Fitzgerald, G.5
-
48
-
-
0032565146
-
P1A2 polymorphism and efficacy of aspirin
-
Cook GE, Bray PF, Hamlington J, Pham DM, GoldschmidtClermont PJ. P1A2 polymorphism and efficacy of aspirin. Lancet 1998; 351: 1353.
-
(1998)
Lancet
, vol.351
, pp. 1353
-
-
Cook, G.E.1
Bray, P.F.2
Hamlington, J.3
Pham, D.M.4
Goldschmidtclermont, P.J.5
-
49
-
-
0028961636
-
European Atherosclerosis Research Study: Genotype at the fibrinogen locus (G-455-A beta gene) is associated with differences in plasma fibrinogen levels in young men and women from different regions in Europe: evidence for gender-genotype-environment interaction
-
Humphries SE, Ye S, Talmud P, Bara L, Wilhelmsen L, Tiret L European Atherosclerosis Research Study: genotype at the fibrinogen locus (G-455-A beta gene) is associated with differences in plasma fibrinogen levels in young men and women from different regions in Europe: evidence for gender-genotype-environment interaction. Arterioscler Thromb Vasc Biol 1995; 15: 96-104.
-
(1995)
Arterioscler Thromb Vasc Biol
, vol.15
, pp. 96-104
-
-
Humphries, S.E.1
Ye, S.2
Talmud, P.3
Bara, L.4
Wilhelmsen, L.5
Tiret, L.6
-
50
-
-
0029850530
-
A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
-
Poort, SR, Rosendaal FR, Restina PH and Bertina RM. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996; 88: 3698-3703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Restina, P.H.3
Bertina, R.M.4
-
51
-
-
0030921663
-
A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women
-
Rosendaal FR, Siscovick DS, Schwartz SM, Psaty BM, Raghunathan TE, Vos HL. A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women. Blood 1997; 90: 1747-1750.
-
(1997)
Blood
, vol.90
, pp. 1747-1750
-
-
Rosendaal, F.R.1
Siscovick, D.S.2
Schwartz, S.M.3
Psaty, B.M.4
Raghunathan, T.E.5
Vos, H.L.6
-
52
-
-
0028810738
-
World distribution of factor V Leiden
-
Rees DC, Cox M, Clegg JB. World distribution of factor V Leiden. Lancet 1995; 346: 1133-1134.
-
(1995)
Lancet
, vol.346
, pp. 1133-1134
-
-
Rees, D.C.1
Cox, M.2
Clegg, J.B.3
-
53
-
-
9044243754
-
Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasma
-
Bernardi F, Marchetti G, Pinotti M et al. Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasma. Arterioscler Thromb Vasc Biol 1996; 16:72-76.
-
(1996)
Arterioscler Thromb Vasc Biol
, vol.16
, pp. 72-76
-
-
Bernardi, F.1
Marchetti, G.2
Pinotti, M.3
-
54
-
-
0029875176
-
Factor VII polymorphism, factor VII: C levels and features of insulin resistance in non-insulin-dependent diabetes mellitus
-
Heywood DM, Mansfield MW and Grant PJ. Factor VII polymorphism, factor VII: C levels and features of insulin resistance in non-insulin-dependent diabetes mellitus. Thromb Haemostas 1996; 75: 401-406.
-
(1996)
Thromb Haemostas
, vol.75
, pp. 401-406
-
-
Heywood, D.M.1
Mansfield, M.W.2
Grant, P.J.3
-
55
-
-
0032495540
-
Polymorphisms in the coagulation factor VII gene and the risk of myocardial infarction
-
Iacoviello L, Castelnuovo AD, Knijff P et al. Polymorphisms in the coagulation factor VII gene and the risk of myocardial infarction. N Engl J Med 1998; 338: 79-85.
-
(1998)
N Engl J Med
, vol.338
, pp. 79-85
-
-
Iacoviello, L.1
Castelnuovo, A.D.2
Knijff, P.3
-
56
-
-
0032521229
-
A common genetic polymorphism (46 C to T substitution) in the 5′-untranslated region of the coagulation factor XII gene is associated with low translation efficiency and decrease in plasma factor XII level
-
Kanaji T, Okamura T, Osaki K, Kuroiwa M, Shimoda K, Hamasaki M, Niho Y. A common genetic polymorphism (46 C to T substitution) in the 5′-untranslated region of the coagulation factor XII gene is associated with low translation efficiency and decrease in plasma factor XII level. Blood 1998; 91:2010-2014.
-
(1998)
Blood
, vol.91
, pp. 2010-2014
-
-
Kanaji, T.1
Okamura, T.2
Osaki, K.3
Kuroiwa, M.4
Shimoda, K.5
Hamasaki, M.6
Niho, Y.7
-
57
-
-
0033621940
-
Genotype distribution of the 46C/T polymorphism of coagulation factor XII in the Japanese population: Absence of its association with ischemic cerebrovascular disease
-
Oguchi S, Ito D, Murata M et al. Genotype distribution of the 46C/T polymorphism of coagulation factor XII in the Japanese population: absence of its association with ischemic cerebrovascular disease. Thromb Haemost 2000; 83: 178-179.
-
(2000)
Thromb Haemost
, vol.83
, pp. 178-179
-
-
Oguchi, S.1
Ito, D.2
Murata, M.3
-
58
-
-
0019845596
-
Reduced titer of Hageman factor (Factor XII) in Orientals
-
Gordon EM, Donaldson VH, Saito H, Su E, Ratnoff OD. Reduced titer of Hageman factor (Factor XII) in Orientals. Ann Intern Med 1981; 95: 697-700.
-
(1981)
Ann Intern Med
, vol.95
, pp. 697-700
-
-
Gordon, E.M.1
Donaldson, V.H.2
Saito, H.3
Su, E.4
Ratnoff, O.D.5
-
59
-
-
0031443535
-
Risk of coronary heart disease and activation of factor XII in middleaged men
-
Miller GJ, Esnouf MP, Burgess AI, Cooper JA, Mitchell JP. Risk of coronary heart disease and activation of factor XII in middleaged men. Arterioscler Thromb Vasc Biol 1997; 17: 2103-2106.
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 2103-2106
-
-
Miller, G.J.1
Esnouf, M.P.2
Burgess, A.I.3
Cooper, J.A.4
Mitchell, J.P.5
-
60
-
-
0034072826
-
Activated factor XII levels are dependent on factor XII46C/T genotypes and factor XII zymogen levels, and are associated with vascular risk factors in patients and healthy subjects
-
in press
-
Ishii K, Oguchi S, Murata M et al. Activated factor XII levels are dependent on factor XII46C/T genotypes and factor XII zymogen levels, and are associated with vascular risk factors in patients and healthy subjects. Blood Coagul Fibrinolysis 2000; (in press).
-
(2000)
Blood Coagul Fibrinolysis
-
-
Ishii, K.1
Oguchi, S.2
Murata, M.3
-
61
-
-
0031963827
-
Association of a common polymorphism in the factor XIII gene with myocardial infarction
-
Kohler HP, Stickland MH, Ossei-Gerning N, Carter A, Mikkola H, Grant PJ. Association of a common polymorphism in the factor XIII gene with myocardial infarction. Thromb Haemost 1998; 79: 8-13.
-
(1998)
Thromb Haemost
, vol.79
, pp. 8-13
-
-
Kohler, H.P.1
Stickland, M.H.2
Ossei-Gerning, N.3
Carter, A.4
Mikkola, H.5
Grant, P.J.6
-
62
-
-
0032945056
-
Association of a common polymorphism in the factor XIII gene with venous thrombosis
-
Catto AJ, Kohler HP, Coore J, Mansfield MW, Stickland MH, Grant PJ. Association of a common polymorphism in the factor XIII gene with venous thrombosis. Blood 1999; 93: 906-908.
-
(1999)
Blood
, vol.93
, pp. 906-908
-
-
Catto, A.J.1
Kohler, H.P.2
Coore, J.3
Mansfield, M.W.4
Stickland, M.H.5
Grant, P.J.6
-
63
-
-
0032904240
-
Genotype/phenotype correlations for factor XIII: Specific normal polymorphisms are associated with high or low factor XIII specific activity
-
Anwar R, Gallivan L, Edmonds SD, Markham AR Genotype/phenotype correlations for factor XIII: specific normal polymorphisms are associated with high or low factor XIII specific activity. Blood 1999; 93: 897-905.
-
(1999)
Blood
, vol.93
, pp. 897-905
-
-
Anwar, R.1
Gallivan, L.2
Edmonds, S.D.3
Markham, A.R.4
-
64
-
-
0028882653
-
Plasminogen activator inhibitor-1 (PAI-1) promotor polymorphism and coronary artery disease in non-insulin-dependent diabetes
-
Mansfield MW, Stickland MH, Grant PJ. Plasminogen activator inhibitor-1 (PAI-1) promotor polymorphism and coronary artery disease in non-insulin-dependent diabetes. Thromb Haemost 1995; 74: 1032-1034.
-
(1995)
Thromb Haemost
, vol.74
, pp. 1032-1034
-
-
Mansfield, M.W.1
Stickland, M.H.2
Grant, P.J.3
-
65
-
-
0031283145
-
A 192Arg variant of the human paraoxonase (HUMPONA) gene polymorphisms is associated with the increased risk for coronary artery disease in the Japanese
-
Zama T, Murata M, Matsubara Y et al. A 192Arg variant of the human paraoxonase (HUMPONA) gene polymorphisms is associated with the increased risk for coronary artery disease in the Japanese. Arterioscler Thromb Vasc Biol 1997; 17: 3565-3569.
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 3565-3569
-
-
Zama, T.1
Murata, M.2
Matsubara, Y.3
-
66
-
-
0033614734
-
C(-260)-T polymorphism in the promoter of the CD 14 monocyte receptor gene as the risk factor for myocardial infarction
-
Hubacek JA, Pit'fha J, Skodava Z, Stanek V, Poledne R. C(-260)-T polymorphism in the promoter of the CD 14 monocyte receptor gene as the risk factor for myocardial infarction. Circulation 1999; 99: 3218-3220.
-
(1999)
Circulation
, vol.99
, pp. 3218-3220
-
-
Hubacek, J.A.1
Pit'fha, J.2
Skodava, Z.3
Stanek, V.4
Poledne, R.5
-
67
-
-
0032949577
-
A new promoter polymorphism in the gene of lipopolysaccharide receptor CD 14 is associated with expired myocardial infarction in patients with low atherosclerotic risk profile
-
Unkelbach K, Gardemann A, Kostrzewa M, Philipp M, Tillmanns H, Haberbosch W. A new promoter polymorphism in the gene of lipopolysaccharide receptor CD 14 is associated with expired myocardial infarction in patients with low atherosclerotic risk profile. Arterioscler Thromb Vasc Biol 1999; 19: 932-938.
-
(1999)
Arterioscler Thromb Vasc Biol
, vol.19
, pp. 932-938
-
-
Unkelbach, K.1
Gardemann, A.2
Kostrzewa, M.3
Philipp, M.4
Tillmanns, H.5
Haberbosch, W.6
-
68
-
-
0343527886
-
C242T polymorphism of NADPH oxidase p22 phox gene and ischemic cerebrovascular disease in the Japanese population
-
Ito D, Murata M, Watanabe K, Yoshida T, Saito I, Tanahashi N, Fukuuchi Y. C242T polymorphism of NADPH oxidase p22 phox gene and ischemic cerebrovascular disease in the Japanese population. Stroke 2000; 31: 936-939.
-
(2000)
Stroke
, vol.31
, pp. 936-939
-
-
Ito, D.1
Murata, M.2
Watanabe, K.3
Yoshida, T.4
Saito, I.5
Tanahashi, N.6
Fukuuchi, Y.7
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