-
1
-
-
0034161456
-
Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease
-
Lane DA, Grant PJ. Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease. Blood 2000; 95:1517-1532.
-
(2000)
Blood
, vol.95
, pp. 1517-1532
-
-
Lane, D.A.1
Grant, P.J.2
-
2
-
-
0023197647
-
The broad substrate specificity of human angiotensin i converting enzyme
-
Skidgel RA, Erdos EG. The broad substrate specificity of human angiotensin I converting enzyme. Clin Exp Hypertens A 1987; 9:243-259.
-
(1987)
Clin Exp Hypertens A
, vol.9
, pp. 243-259
-
-
Skidgel, R.A.1
Erdos, E.G.2
-
3
-
-
33745017730
-
ACE polymorphisms
-
Sayed-Tabatabaei FA, Oostra BA, Isaacs A, van Duijn CM, Witteman JC. ACE polymorphisms. Circ Res 2006; 98:1123-1133.
-
(2006)
Circ Res
, vol.98
, pp. 1123-1133
-
-
Sayed-Tabatabaei, F.A.1
Oostra, B.A.2
Isaacs, A.3
Van Duijn, C.M.4
Witteman, J.C.5
-
4
-
-
0036713993
-
High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity
-
Soubrier F, Martin S, Alonso A, Visvikis S, Tiret L, Matsuda F, et al. High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity. Eur J Hum Genet 2002; 10:553-561.
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 553-561
-
-
Soubrier, F.1
Martin, S.2
Alonso, A.3
Visvikis, S.4
Tiret, L.5
Matsuda, F.6
-
5
-
-
0025165779
-
An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels
-
Rigat B, Hubert C, Alhenc-Gelas F, Cambien F, Corvol P, Soubrier F. An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels. J Clin Invest 1990; 86:1343-1346.
-
(1990)
J Clin Invest
, vol.86
, pp. 1343-1346
-
-
Rigat, B.1
Hubert, C.2
Alhenc-Gelas, F.3
Cambien, F.4
Corvol, P.5
Soubrier, F.6
-
6
-
-
29344445008
-
The relationship between ACE insertion/deletion polymorphism and coronary artery disease with or without myocardial infarction
-
Seckin D, Ilhan N, Ozbay Y. The relationship between ACE insertion/deletion polymorphism and coronary artery disease with or without myocardial infarction. Clin Biochem 2006; 39:50-54.
-
(2006)
Clin Biochem
, vol.39
, pp. 50-54
-
-
Seckin, D.1
Ilhan, N.2
Ozbay, Y.3
-
7
-
-
33646465604
-
The incidence of some angiotensin-1 converting enzyme gene alleles in patients with coronary heart disease
-
Istrati VF, Butorov IV, Manea DV, Ikim AA, Barbakar NI, Kalenich OS, et al. The incidence of some angiotensin-1 converting enzyme gene alleles in patients with coronary heart disease. Klin Med (Mosk) 2006; 84:22-24.
-
(2006)
Klin Med (Mosk)
, vol.84
, pp. 22-24
-
-
Istrati, V.F.1
Butorov, I.V.2
Manea, D.V.3
Ikim, A.A.4
Barbakar, N.I.5
Kalenich, O.S.6
-
9
-
-
0027468144
-
The angiotensin I converting enzyme gene and predisposition to high blood pressure
-
Harrap SB, Davidson HR, Connor JM, Soubrier F, Corvol P, Fraser R, et al. The angiotensin I converting enzyme gene and predisposition to high blood pressure. Hypertension 1993; 21:455-460. (Pubitemid 23095158)
-
(1993)
Hypertension
, vol.21
, Issue.4
, pp. 455-460
-
-
Harrap, S.B.1
Davidson, H.R.2
Connor, J.M.3
Soubrier, F.4
Corvol, P.5
Fraser, R.6
Foy, C.J.W.7
Watt, G.C.M.8
-
11
-
-
33644540513
-
Evaluation of the angiotensin-converting enzyme insertion/deletion polymorphism and the risk of ischaemic stroke
-
Tuncer N, Tuglular S, KiliçG, Sazci A, Us O, Kara I. Evaluation of the angiotensin-converting enzyme insertion/deletion polymorphism and the risk of ischaemic stroke. J Clin Neurosci 2006; 13:224-227.
-
(2006)
J Clin Neurosci
, vol.13
, pp. 224-227
-
-
Tuncer, N.1
Tuglular, S.2
Kiliçg Sazci, A.3
Us, O.4
Kara, I.5
-
12
-
-
33646348716
-
Hyperhomocysteinaemia, methylenetetrahydrofolate reductase polymorphism and risk of coronary artery disease
-
DOI 10.1258/000456306776865232
-
Kerkeni M, Addad F, Chauffert M, Myara A, Gerhardt M, Chevenne D, et al. Hyperhomocysteinaemia, methylenetetrahydrofolate reductase polymorphism and risk of coronary artery disease. Ann Clin Biochem 2006; 43:200-206. (Pubitemid 43668152)
-
(2006)
Annals of Clinical Biochemistry
, vol.43
, Issue.3
, pp. 200-206
-
-
Kerkeni, M.1
Addad, F.2
Chauffert, M.3
Myara, A.4
Gerhardt, M.5
Chevenne, D.6
Trivin, F.7
Farhat, M.B.8
Miled, A.9
Maaroufi, K.10
-
13
-
-
4143111407
-
C677 T polymorphism of the methylenetetrahydrofolate reductase gene is a risk factor of adverse events after coronary revascularization
-
Botto N, Andreassi MG, Rizza A, Berti S, Bevilacqua S, Federici C, et al. C677 T polymorphism of the methylenetetrahydrofolate reductase gene is a risk factor of adverse events after coronary revascularization. Int J Cardiol 2004; 96:341-345.
-
(2004)
Int J Cardiol
, vol.96
, pp. 341-345
-
-
Botto, N.1
Andreassi, M.G.2
Rizza, A.3
Berti, S.4
Bevilacqua, S.5
Federici, C.6
-
14
-
-
27644488218
-
Prevalence of genetic risk factors for coronary artery disease in Corsica island (France)
-
Falchi A, Giovannoni L, Piras IS, Calo CM, Moral P, Vona G, et al. Prevalence of genetic risk factors for coronary artery disease in Corsica island (France). Exp Mol Pathol 2005; 79:210-213.
-
(2005)
Exp Mol Pathol
, vol.79
, pp. 210-213
-
-
Falchi, A.1
Giovannoni, L.2
Piras, I.S.3
Calo, C.M.4
Moral, P.5
Vona, G.6
-
15
-
-
24944545722
-
Association of MTRRA66G polymorphism (but not of MTHFR C677 T and A1298C, MTRA2756G, TCN C776G) with homocysteine and coronary artery disease in the French population
-
Gueant-Rodriguez RM, Gué ant JL, Viola M, Tramoy D, Gaeta F, Romano A. Association of MTRRA66G polymorphism (but not of MTHFR C677 T and A1298C, MTRA2756G, TCN C776G) with homocysteine and coronary artery disease in the French population. Thromb Haemost 2005; 94:510-515.
-
(2005)
Thromb Haemost
, vol.94
, pp. 510-515
-
-
Gueant-Rodriguez, R.M.1
Guéant, J.L.2
Viola, M.3
Tramoy, D.4
Gaeta, F.5
Romano, A.6
-
16
-
-
0036223658
-
Homocysteine and methylenetetrahydrofolate reductase genotype: Association with risk of coronary heart disease and relation to inflammatory, hemostatic, and lipid parameters
-
Rothenbacher D, Fischer HG, Hoffmeister A, Hoffmann MM, März W, Bode G, et al. Homocysteine and methylenetetrahydrofolate reductase genotype: association with risk of coronary heart disease and relation to inflammatory, hemostatic, and lipid parameters. Atherosclerosis 2002; 162:193-200.
-
(2002)
Atherosclerosis
, vol.162
, pp. 193-200
-
-
Rothenbacher, D.1
Fischer, H.G.2
Hoffmeister, A.3
Hoffmann, M.M.4
März, W.5
Bode, G.6
-
17
-
-
0026016865
-
Genetic variation at the plasminogen activator inhibitor-1 locus is associated with altered levels of plasma plasminogen activator inhibitor-1 activity
-
Dawson S, Hamsten A,Wiman B, Henney A, Humphries S. Genetic variation at the plasminogen activator inhibitor-1 locus is associated with altered levels of plasma plasminogen activator inhibitor-1 activity. Arterioscler Thromb 1991; 11:183-190.
-
(1991)
Arterioscler Thromb
, vol.11
, pp. 183-190
-
-
Dawson, S.1
Hamsten, A.2
Wiman, B.3
Henney, A.4
Humphries, S.5
-
18
-
-
16944367480
-
Five frequent polymorphisms, of the PAI-1 gene: Lack of association between genotypes, PAI activity, and triglyceride levels in a healthy population
-
Henry M, Chomiki N, Scarabin PY, Alessi MC, Peiretti F, Arveiler D, et al. Five frequent polymorphisms, of the PAI-1 gene: lack of association between genotypes, PAI activity, and triglyceride levels in a healthy population. Arterioscler Thromb Vasc Biol 1997; 17:851-858.
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 851-858
-
-
Henry, M.1
Chomiki, N.2
Scarabin, P.Y.3
Alessi, M.C.4
Peiretti, F.5
Arveiler, D.6
-
19
-
-
0042381668
-
Plasminogen activator inhibitor 1 (PAI-1) 1334G/A genetic polymorphism in colorectal cancer
-
Smolarz B, Romanowicz-Makowska H, Kulig A. Plasminogen activator inhibitor 1 (PAI-1) 1334G/A genetic polymorphism in colorectal cancer. Acta Biochim Pol 2003; 50:489-495.
-
(2003)
Acta Biochim Pol
, vol.50
, pp. 489-495
-
-
Smolarz, B.1
Romanowicz-Makowska, H.2
Kulig, A.3
-
20
-
-
0033933395
-
Plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism, coronary thrombosis, and myocardial infarction in middle-aged Finnish men who died suddenly
-
Mikkelsson J, Perola M,Wartiovaara U, Peltonen L, Palotie A, Penttilä A, et al. Plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism, coronary thrombosis, and myocardial infarction in middle-aged Finnish men who died suddenly. Thromb Haemost 2000; 84:78-82.
-
(2000)
Thromb Haemost
, vol.84
, pp. 78-82
-
-
Mikkelsson, J.1
Perola, M.2
Wartiovaara, U.3
Peltonen, L.4
Palotie, A.5
Penttilä, A.6
-
21
-
-
0033951954
-
Genetic polymorphisms and coronary artery disease in the south of France
-
Canavy I, Henry M, Morange PE, Tiret L, Poirier O, Ebagosti A, et al. Genetic polymorphisms and coronary artery disease in the south of France. Thromb Haemost 2000; 83:212-216.
-
(2000)
Thromb Haemost
, vol.83
, pp. 212-216
-
-
Canavy, I.1
Henry, M.2
Morange, P.E.3
Tiret, L.4
Poirier, O.5
Ebagosti, A.6
-
22
-
-
0028314865
-
Mutation in blood coagulation factor v associated with resistance to activated protein C
-
Bertina RM, Koeleman BP, Koster T, Rosendaal FR, Dirven RJ, de Ronde H, 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.2
Koster, T.3
Rosendaal, F.R.4
Dirven, R.J.5
De Ronde, H.6
-
23
-
-
1242272118
-
Coexistence of prothrombic risk factors and its relation to left ventricular thrombus in acute myocardial infarction
-
Ucar F, Celik S, Ovali E, Karti SS, Pakdemir A, Yilmaz M, et al. Coexistence of prothrombic risk factors and its relation to left ventricular thrombus in acute myocardial infarction. Acta Cardiol 2004; 59:33-39.
-
(2004)
Acta Cardiol
, vol.59
, pp. 33-39
-
-
Ucar, F.1
Celik, S.2
Ovali, E.3
Karti, S.S.4
Pakdemir, A.5
Yilmaz, M.6
-
24
-
-
33646907966
-
Valvular aortic stenosis: Disease severity and timing of intervention
-
Otto CM. Valvular aortic stenosis: disease severity and timing of intervention. J Am Coll Cardiol 2006; 47:2141-2151.
-
(2006)
J Am Coll Cardiol
, vol.47
, pp. 2141-2151
-
-
Otto, C.M.1
-
25
-
-
27844449987
-
Does the angiotensin-converting enzyme (ACE) gene insertion/deletion polymorphism modify the response to ACE inhibitor therapy? A systematic review
-
Scharplatz M, Puhan MA, Steurer J, Perna A, Bachmann LM. Does the angiotensin-converting enzyme (ACE) gene insertion/deletion polymorphism modify the response to ACE inhibitor therapy? A systematic review. Curr Control Trials Cardiovasc Med 2005; 6:16.
-
(2005)
Curr Control Trials Cardiovasc Med
, vol.6
, pp. 16
-
-
Scharplatz, M.1
Puhan, M.A.2
Steurer, J.3
Perna, A.4
Bachmann, L.M.5
-
26
-
-
0033571722
-
Lack of association of a common polymorphism of the plasminogen activator inhibitor-1 gene with coronary artery disease and myocardial infarction
-
Anderson JL, Muhlestein JB, Habashi J, Carlquist JF, Bair TL, Elmer SP, et al. Lack of association of a common polymorphism of the plasminogen activator inhibitor-1 gene with coronary artery disease and myocardial infarction. J Am Coll Cardiol 1999; 34:1778-1783.
-
(1999)
J Am Coll Cardiol
, vol.34
, pp. 1778-1783
-
-
Anderson, J.L.1
Muhlestein, J.B.2
Habashi, J.3
Carlquist, J.F.4
Bair, T.L.5
Elmer, S.P.6
-
27
-
-
0036796224
-
Prevalence of two thrombophilia predisposing mutations: Factor v G1691A (R506Q; Leiden) and prothrombin G20210A, among healthy Lebanese
-
Tamim H, Finan RR, Almawi WY. Prevalence of two thrombophilia predisposing mutations: factor V G1691A (R506Q; Leiden) and prothrombin G20210A, among healthy Lebanese. Thromb Haemost 2002; 88:691-692.
-
(2002)
Thromb Haemost
, vol.88
, pp. 691-692
-
-
Tamim, H.1
Finan, R.R.2
Almawi, W.Y.3
-
28
-
-
33646075437
-
Predictors of coronary artery disease in the Lebanese population
-
Abchee A, Puzantian H, Azar ST, Shbaklo H, Nasrallah A, Sawaya FJ, et al. Predictors of coronary artery disease in the Lebanese population. Thromb Res 2006; 117:631-637.
-
(2006)
Thromb Res
, vol.117
, pp. 631-637
-
-
Abchee, A.1
Puzantian, H.2
Azar, S.T.3
Shbaklo, H.4
Nasrallah, A.5
Sawaya, F.J.6
-
29
-
-
0029314388
-
Angiotensin-I converting enzyme genotype DD is a risk factor for coronary artery disease
-
Beohar N, Damaraju S, Prather A, Yu QT, Raizner A, Kleiman NS, et al. Angiotensin-I converting enzyme genotype DD is a risk factor for coronary artery disease. J Investig Med 1995; 43:275-280.
-
(1995)
J Investig Med
, vol.43
, pp. 275-280
-
-
Beohar, N.1
Damaraju, S.2
Prather, A.3
Yu, Q.T.4
Raizner, A.5
Kleiman, N.S.6
-
30
-
-
0034979086
-
Differences in frequency of the deletion polymorphism of the angiotensin-convertingënzyme gene in different ethnic groups
-
Mathew J, Basheeruddin K, Prabhakar S. Differences in frequency of the deletion polymorphism of the angiotensin-convertingënzyme gene in different ethnic groups. Angiology 2001; 52:375-379.
-
(2001)
Angiology
, vol.52
, pp. 375-379
-
-
Mathew, J.1
Basheeruddin, K.2
Prabhakar, S.3
|