-
1
-
-
0025801573
-
A frequent thrombomodulin amino acid dimorphism is not associated with thrombophilia
-
van der Velden P.A., Krommenhoek-Van Es T., Allaart C.F., Bertina R.M., Reitsma P.H. A frequent thrombomodulin amino acid dimorphism is not associated with thrombophilia. Thromb Haemost. 65:1991;511-513.
-
(1991)
Thromb Haemost
, vol.65
, pp. 511-513
-
-
Van Der Velden, P.A.1
Krommenhoek-Van Es, T.2
Allaart, C.F.3
Bertina, R.M.4
Reitsma, P.H.5
-
2
-
-
0028954459
-
The first mutation identified in the thrombomodulin gene in a 45-year-old man presenting with thromboembolic disease
-
Öhlin A.K., Marlar R.A. The first mutation identified in the thrombomodulin gene in a 45-year-old man presenting with thromboembolic disease. Blood. 85:1995;330-336.
-
(1995)
Blood
, vol.85
, pp. 330-336
-
-
Öhlin, A.K.1
Marlar, R.A.2
-
3
-
-
1842413039
-
A novel thrombomodulin gene mutation in a patient suffering from sagittal sinus thrombosis
-
Norlund L., Zöller B., Öhlin A.K. A novel thrombomodulin gene mutation in a patient suffering from sagittal sinus thrombosis. Thromb Haemost. 78:1997;1164-1166.
-
(1997)
Thromb Haemost
, vol.78
, pp. 1164-1166
-
-
Norlund, L.1
Zöller, B.2
Öhlin, A.K.3
-
4
-
-
0030855091
-
Thrombomodulin gene mutations associated with myocardial infarction
-
Ireland H., Kunz G., Kyriakoulis K., Stubbs P.J., Lane D.A. Thrombomodulin gene mutations associated with myocardial infarction. Circulation. 96:1997;15-18.
-
(1997)
Circulation
, vol.96
, pp. 15-18
-
-
Ireland, H.1
Kunz, G.2
Kyriakoulis, K.3
Stubbs, P.J.4
Lane, D.A.5
-
5
-
-
0000321079
-
Functional significance of G-33A promoter mutation of thrombomodulin gene and its influence on plasma soluble thrombomodulin level in patients with coronary artery disease
-
(abstr)
-
Li Y.H., Chen J.H., Chang B.Y., Lin J.C., Wu H.L., Shi G.Y., Tsai W.C., Chao T.H., Tsai L.M., Lin L.J. Functional significance of G-33A promoter mutation of thrombomodulin gene and its influence on plasma soluble thrombomodulin level in patients with coronary artery disease. (abstr) J Am Coll Cardiol. 35:2000;259A.
-
(2000)
J Am Coll Cardiol
, vol.35
-
-
Li, Y.H.1
Chen, J.H.2
Chang, B.Y.3
Lin, J.C.4
Wu, H.L.5
Shi, G.Y.6
Tsai, W.C.7
Chao, T.H.8
Tsai, L.M.9
Lin, L.J.10
-
6
-
-
0036801821
-
Characterization of thrombomodulin gene mutations of 5′-regulatory region
-
Nakazawa F., Koyama T., Shibamiya A., Hirosawa S. Characterization of thrombomodulin gene mutations of 5′-regulatory region. Atherosclerosis. 164:2002;385-387.
-
(2002)
Atherosclerosis
, vol.164
, pp. 385-387
-
-
Nakazawa, F.1
Koyama, T.2
Shibamiya, A.3
Hirosawa, S.4
-
7
-
-
0036145726
-
Synergistic effect of thrombomodulin promoter -33G/A polymorphism and smoking on the onset of acute myocardial infarction
-
Li Y.H., Chen J.H., Tsai W.C., Chao T.H., Guo H.R., Tsai L.M., Wu H.L., Shi G.Y. Synergistic effect of thrombomodulin promoter -33G/A polymorphism and smoking on the onset of acute myocardial infarction. Thromb Haemost. 87:2002;86-91.
-
(2002)
Thromb Haemost
, vol.87
, pp. 86-91
-
-
Li, Y.H.1
Chen, J.H.2
Tsai, W.C.3
Chao, T.H.4
Guo, H.R.5
Tsai, L.M.6
Wu, H.L.7
Shi, G.Y.8
-
8
-
-
0035991108
-
Association of G-33A polymorphism in the thrombomodulin gene with myocardial infarction in Koreans
-
Park H.Y., Nabika T., Jang Y., Kwon H.M., Cho S.Y., Masuda J. Association of G-33A polymorphism in the thrombomodulin gene with myocardial infarction in Koreans. Hypertens Res Clin Exp. 25:2002;389-394.
-
(2002)
Hypertens Res Clin Exp
, vol.25
, pp. 389-394
-
-
Park, H.Y.1
Nabika, T.2
Jang, Y.3
Kwon, H.M.4
Cho, S.Y.5
Masuda, J.6
-
9
-
-
0031056791
-
A common thrombomodulin amino acid dimorphism is associated with myocardial infarction
-
Norlund L., Holm J., Öhlin A.K. A common thrombomodulin amino acid dimorphism is associated with myocardial infarction. Thromb Haemost. 77:1997;248-251.
-
(1997)
Thromb Haemost
, vol.77
, pp. 248-251
-
-
Norlund, L.1
Holm, J.2
Öhlin, A.K.3
-
10
-
-
0035853133
-
Thrombomodulin Ala455Val polymorphism and risk of coronary heart disease
-
Wu K.K., Aleksic N., Ahn C., Boerwinkle E., Folsom A.R., Juneja H. Thrombomodulin Ala455Val polymorphism and risk of coronary heart disease. Circulation. 103:2001;1386-1389.
-
(2001)
Circulation
, vol.103
, pp. 1386-1389
-
-
Wu, K.K.1
Aleksic, N.2
Ahn, C.3
Boerwinkle, E.4
Folsom, A.R.5
Juneja, H.6
-
11
-
-
0032893645
-
Mutations in promoter region of thrombomodulin and venous thromboembolic disease
-
Le Flem L., Picard V., Emmerich J., Gandrille S., Fiessinger J., Aiach M., Alhenc-Gelas M. Mutations in promoter region of thrombomodulin and venous thromboembolic disease. Arterioscler Thromb Vasc Biol. 19:1999;1098-1104.
-
(1999)
Arterioscler Thromb Vasc Biol
, vol.19
, pp. 1098-1104
-
-
Le Flem, L.1
Picard, V.2
Emmerich, J.3
Gandrille, S.4
Fiessinger, J.5
Aiach, M.6
Alhenc-Gelas, M.7
-
12
-
-
0033434025
-
Peroxisome proliferator-activated receptor γ C161→T polymorphism and coronary artery disease
-
Wang X.L., Oosterhof J., Duarte N. Peroxisome proliferator-activated receptor γ C161→T polymorphism and coronary artery disease. Cardiovasc Res. 44:1999;588-594.
-
(1999)
Cardiovasc Res
, vol.44
, pp. 588-594
-
-
Wang, X.L.1
Oosterhof, J.2
Duarte, N.3
-
13
-
-
0031912333
-
A genetic polymorphism of the peroxisome proliferator-activated receptor γ gene influences plasma leptin levels in obese humans
-
Meirhaeghe A., Fajas L., Helbecque N., Cottel D., Lebel P., Dallongeville J., Deeb S., Auwerx J., Amouyel P. A genetic polymorphism of the peroxisome proliferator-activated receptor γ gene influences plasma leptin levels in obese humans. Hum Mol Genet. 7:1998;435-440.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 435-440
-
-
Meirhaeghe, A.1
Fajas, L.2
Helbecque, N.3
Cottel, D.4
Lebel, P.5
Dallongeville, J.6
Deeb, S.7
Auwerx, J.8
Amouyel, P.9
-
14
-
-
85030931060
-
Homozygous mutation of C161→T polymorphism in the exon 6 of peroxisome proliferator-activated receptor γ gene is associated with onset of premature myocardial infarction
-
(abstr)
-
Chao T.H., Li Y.H., Chen J.H., Wu H.L., Shi G.Y. Homozygous mutation of C161→T polymorphism in the exon 6 of peroxisome proliferator-activated receptor γ gene is associated with onset of premature myocardial infarction. (abstr) J Am Coll Cardiol. 41:2003;381A.
-
(2003)
J Am Coll Cardiol
, vol.41
-
-
Chao, T.H.1
Li, Y.H.2
Chen, J.H.3
Wu, H.L.4
Shi, G.Y.5
-
15
-
-
0033452690
-
Analysis of thrombomodulin gene polymorphism in women with severe early onset preclampsia
-
Nakabayashi M., Yamamoto S., Suzuki K. Analysis of thrombomodulin gene polymorphism in women with severe early onset preclampsia. Semin Thromb Hemost. 25:1999;475-479.
-
(1999)
Semin Thromb Hemost
, vol.25
, pp. 475-479
-
-
Nakabayashi, M.1
Yamamoto, S.2
Suzuki, K.3
|