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Results: 1 to 20 of 105

1.

Identification and characterization of a thrombomodulin gene mutation coding for an elongated protein with reduced expression in a kindred with myocardial infarction.

Kunz G, Ireland HA, Stubbs PJ, Kahan M, Coulton GC, Lane DA.

Blood. 2000 Jan 15;95(2):569-76.

PMID:
10627464
[PubMed - indexed for MEDLINE]
Free Article
2.

A mutation in the thrombomodulin gene, 127G to A coding for Ala25Thr, and the risk of myocardial infarction in men.

Doggen CJ, Kunz G, Rosendaal FR, Lane DA, Vos HL, Stubbs PJ, Manger Cats V, Ireland H.

Thromb Haemost. 1998 Nov;80(5):743-8.

PMID:
9843165
[PubMed - indexed for MEDLINE]
3.
4.

Synergistic effect of thrombomodulin promoter -33G/A polymorphism and smoking on the onset of acute myocardial infarction.

Li YH, Chen JH, Tsai WC, Chao TH, Guo HR, Tsai LM, Wu HL, Shi GY.

Thromb Haemost. 2002 Jan;87(1):86-91.

PMID:
11848462
[PubMed - indexed for MEDLINE]
5.

A common thrombomodulin amino acid dimorphism is associated with myocardial infarction.

Norlund L, Holm J, Zöller B, Ohlin AK.

Thromb Haemost. 1997 Feb;77(2):248-51.

PMID:
9157575
[PubMed - indexed for MEDLINE]
6.

Directed search for thrombomodulin gene mutations.

Ireland H, Kyriakoulis K, Kunz G, Lane DA.

Haemostasis. 1996 Oct;26 Suppl 4:227-32.

PMID:
8979128
[PubMed - indexed for MEDLINE]
7.

Naturally occurring mutations in the thrombomodulin gene leading to impaired expression and function.

Kunz G, Ohlin AK, Adami A, Zöller B, Svensson P, Lane DA.

Blood. 2002 May 15;99(10):3646-53.

PMID:
11986219
[PubMed - indexed for MEDLINE]
Free Article
8.

Thrombomodulin gene mutations associated with myocardial infarction.

Ireland H, Kunz G, Kyriakoulis K, Stubbs PJ, Lane DA.

Circulation. 1997 Jul 1;96(1):15-8.

PMID:
9236408
[PubMed - indexed for MEDLINE]
Free Article
9.

G-33A mutation in the promoter region of thrombomodulin gene and its association with coronary artery disease and plasma soluble thrombomodulin levels.

Li YH, Chen JH, Wu HL, Shi GY, Huang HC, Chao TH, Tsai WC, Tsai LM, Guo HR, Wu WS, Chen ZC.

Am J Cardiol. 2000 Jan 1;85(1):8-12.

PMID:
11078228
[PubMed - indexed for MEDLINE]
10.

Stable expression of a secretable deletion mutant of recombinant human thrombomodulin in mammalian cells.

Parkinson JF, Grinnell BW, Moore RE, Hoskins J, Vlahos CJ, Bang NU.

J Biol Chem. 1990 Jul 25;265(21):12602-10.

PMID:
2165069
[PubMed - indexed for MEDLINE]
Free Article
11.

Genetic variation in the human thrombomodulin promoter locus and prognosis after acute coronary syndrome.

Ohlin AK, Holm J, Hillarp A.

Thromb Res. 2004;113(5):319-26.

PMID:
15183044
[PubMed - indexed for MEDLINE]
12.

A novel thrombomodulin gene mutation in a patient suffering from sagittal sinus thrombosis.

Norlund L, Zöller B, Ohlin AK.

Thromb Haemost. 1997 Oct;78(4):1164-6.

PMID:
9364978
[PubMed - indexed for MEDLINE]
13.

Elements of the primary structure of thrombomodulin required for efficient thrombin-activable fibrinolysis inhibitor activation.

Wang W, Nagashima M, Schneider M, Morser J, Nesheim M.

J Biol Chem. 2000 Jul 28;275(30):22942-7.

PMID:
10801821
[PubMed - indexed for MEDLINE]
Free Article
14.

Association of G-33A polymorphism in the thrombomodulin gene with myocardial infarction in Koreans.

Park HY, Nabika T, Jang Y, Kwon HM, Cho SY, Masuda J.

Hypertens Res. 2002 May;25(3):389-94.

PMID:
12135317
[PubMed - indexed for MEDLINE]
Free Article
15.

Thrombomodulin with the Asp468Tyr mutation is expressed on the cell surface with normal cofactor activity for protein C activation.

Nakazawa F, Koyama T, Saito T, Shibakura M, Yoshinaga H, Chung DH, Kamiyama R, Hirosawa S.

Br J Haematol. 1999 Aug;106(2):416-20.

PMID:
10460600
[PubMed - indexed for MEDLINE]
16.

Low Mpl receptor expression in a pedigree with familial platelet disorder with predisposition to acute myelogenous leukemia and a novel AML1 mutation.

Heller PG, Glembotsky AC, Gandhi MJ, Cummings CL, Pirola CJ, Marta RF, Kornblihtt LI, Drachman JG, Molinas FC.

Blood. 2005 Jun 15;105(12):4664-70. Epub 2005 Mar 1.

PMID:
15741216
[PubMed - indexed for MEDLINE]
Free Article
17.

Impaired secretion of the elongated mutant of protein C (protein C-Nagoya). Molecular and cellular basis for hereditary protein C deficiency.

Yamamoto K, Tanimoto M, Emi N, Matsushita T, Takamatsu J, Saito H.

J Clin Invest. 1992 Dec;90(6):2439-46.

PMID:
1469096
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Functional mutation in the promoter region of thrombomodulin gene in relation to carotid atherosclerosis.

Li YH, Chen CH, Yeh PS, Lin HJ, Chang BI, Lin JC, Guo HR, Wu HL, Shi GY, Lai ML, Chen JH.

Atherosclerosis. 2001 Feb 15;154(3):713-9.

PMID:
11257274
[PubMed - indexed for MEDLINE]
19.

Replication protein A1 reduces transcription of the endothelial nitric oxide synthase gene containing a -786T-->C mutation associated with coronary spastic angina.

Miyamoto Y, Saito Y, Nakayama M, Shimasaki Y, Yoshimura T, Yoshimura M, Harada M, Kajiyama N, Kishimoto I, Kuwahara K, Hino J, Ogawa E, Hamanaka I, Kamitani S, Takahashi N, Kawakami R, Kangawa K, Yasue H, Nakao K.

Hum Mol Genet. 2000 Nov 1;9(18):2629-37.

PMID:
11063722
[PubMed - indexed for MEDLINE]
Free Article
20.

The amino terminal lectin-like domain of thrombomodulin is required for constitutive endocytosis.

Conway EM, Pollefeyt S, Collen D, Steiner-Mosonyi M.

Blood. 1997 Jan 15;89(2):652-61.

PMID:
9002969
[PubMed - indexed for MEDLINE]
Free Article

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