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Items: 1 to 20 of 93

2.

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
3.

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
4.

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
5.

Thrombomodulin gene defects in families with thromboembolic disease--a report on four families.

Ohlin AK, Marlar RA.

Thromb Haemost. 1999 Mar;81(3):338-44.

PMID:
10102456
6.
7.

Thrombomodulin promoter mutations, venous thrombosis, and varicose veins.

Le Flem L, Mennen L, Aubry ML, Aiach M, Scarabin PY, Emmerich J, Alhenc-Gelas M.

Arterioscler Thromb Vasc Biol. 2001 Mar;21(3):445-51.

8.

One novel and one recurrent mutation in the PROS1 gene cause type I protein S deficiency in patients with pulmonary embolism associated with deep vein thrombosis.

Mizukami K, Nakabayashi T, Naitoh S, Takeda M, Tarumi T, Mizoguchi I, Ieko M, Koike T.

Am J Hematol. 2006 Oct;81(10):787-97.

9.
10.

Directed search for thrombomodulin gene mutations.

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

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

PMID:
8979128
11.

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.

12.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
13.

Probing the activation of protein C by the thrombin-thrombomodulin complex using structural analysis, site-directed mutagenesis, and computer modeling.

Knobe KE, Berntsdotter A, Shen L, Morser J, Dahlbäck B, Villoutreix BO.

Proteins. 1999 May 1;35(2):218-34.

PMID:
10223294
14.

Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.

Ma L, Wang H, Chen J, Jin W, Liu L, Ban B, Shen J, Hua Z, Chai J.

Chin Med J (Engl). 2000 Feb;113(2):111-6.

PMID:
11775531
15.

Thrombomodulin gene variations and thromboembolic disease.

Ohlin AK, Norlund L, Marlar RA.

Thromb Haemost. 1997 Jul;78(1):396-400. Review.

PMID:
9198186
16.

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
17.

Hereditary protein C deficiency associated with mutations in exon IX of the protein C gene.

Doig RG, Begley CG, McGrath KM.

Thromb Haemost. 1994 Aug;72(2):203-8.

PMID:
7831652
18.

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
19.

An efficient strategy for detection of known and new mutations of the CYP2D6 gene using single strand conformation polymorphism analysis.

Broly F, Marez D, Sabbagh N, Legrand M, Millecamps S, Lo Guidice JM, Boone P, Meyer UA.

Pharmacogenetics. 1995 Dec;5(6):373-84.

PMID:
8747409
20.

Thrombomodulin gene polymorphisms or haplotypes as potential risk factors for venous thromboembolism: a population-based case-control study.

Heit JA, Petterson TM, Owen WG, Burke JP, DE Andrade M, Melton LJ 3rd.

J Thromb Haemost. 2005 Apr;3(4):710-7.

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