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C Lecut

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Articles 6
Citations 82
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Recent Articles
1.
Delierneux C, Donis N, Servais L, Wera O, Lecut C, Vandereyken M, et al.
J Thromb Haemost . 2017 Mar; 15(5):983-997. PMID: 28296036
Summary: Background Synthetic phosphorothioate-modified CpG oligodeoxynucleotides (ODNs) show potent immunostimulatory properties that are widely exploited in clinical trials of anticancer treatment. Unexpectedly, a recent study indicated that CpG ODNs activate...
2.
Onselaer M, Oury C, Hunter R, Eeckhoudt S, Barile N, Lecut C, et al.
J Thromb Haemost . 2014 Mar; 12(6):973-86. PMID: 24655923
Background: Platelet activation requires sweeping morphologic changes, supported by contraction and remodeling of the platelet actin cytoskeleton. In various other cell types, AMP-activated protein kinase (AMPK) controls the phosphorylation state...
3.
Lecut C, Faccinetto C, Delierneux C, van Oerle R, Spronk H, Evans R, et al.
J Thromb Haemost . 2012 Jan; 10(3):453-65. PMID: 22212928
Background: In sepsis, extracellular ATP, secreted by activated platelets and leukocytes, may contribute to the crosstalk between hemostasis and inflammation. Previously, we showed that, in addition to their role in...
4.
Lecut C, Feeney L, Kingsbury G, Hopkins J, Lanza F, Gachet C, et al.
J Thromb Haemost . 2003 Dec; 1(12):2653-62. PMID: 14675102
Platelet interactions with adhesive ligands exposed at sites of vascular injury initiate the normal hemostatic response but may also lead to arterial thrombosis. Platelet membrane glycoprotein (GP)VI is a key...
5.
Lagrue-Lak-Hal A, Debili N, Kingbury G, Lecut C, Le Couedic J, Villeval J, et al.
J Biol Chem . 2001 Mar; 276(18):15316-25. PMID: 11278467
In this report, the expression and function of the platelet collagen receptor glycoprotein VI (GPVI) were studied in human megakaryocytes during differentiation and maturation of mobilized blood and cord blood...
6.
Mounier C, Luchetta P, Lecut C, Koduri R, Faure G, Lambeau G, et al.
Eur J Biochem . 2000 Aug; 267(16):4960-9. PMID: 10931177
Human secreted group IIA phospholipase A2 (hGIIA) was reported to inhibit prothrombinase activity because of binding to factor Xa. This study further shows that hGIIA and its catalytically inactive H48Q...