Van Geet C - Search Results

1

Unravelling the disease mechanism for TSPYL1 deficiency.

Buyse G, Di Michele M, Wijgaerts A, Louwette S, Wittevrongel C, Thys C, Downes K, Ceulemans B, Van Esch H, Van Geet C, Freson K. Buyse G, et al. Among authors: van esch h, van geet c. Hum Mol Genet. 2020 Dec 18;29(20):3431-3442. doi: 10.1093/hmg/ddaa233. Hum Mol Genet. 2020. PMID: 33075815 Free article.

2

Different substitutions at residue D218 of the X-linked transcription factor GATA1 lead to altered clinical severity of macrothrombocytopenia and anemia and are associated with variable skewed X inactivation.

Freson K, Matthijs G, Thys C, Mariën P, Hoylaerts MF, Vermylen J, Van Geet C. Freson K, et al. Among authors: van geet c. Hum Mol Genet. 2002 Jan 15;11(2):147-52. doi: 10.1093/hmg/11.2.147. Hum Mol Genet. 2002. PMID: 11809723 Free article.

3

Pseudohypoparathyroidism type Ib with disturbed imprinting in the GNAS1 cluster and Gsalpha deficiency in platelets.

Freson K, Thys C, Wittevrongel C, Proesmans W, Hoylaerts MF, Vermylen J, Van Geet C. Freson K, et al. Among authors: van geet c. Hum Mol Genet. 2002 Oct 15;11(22):2741-50. doi: 10.1093/hmg/11.22.2741. Hum Mol Genet. 2002. PMID: 12374764

4

Molecular cloning and characterization of the GATA1 cofactor human FOG1 and assessment of its binding to GATA1 proteins carrying D218 substitutions.

Freson K, Thys C, Wittewrongel C, Vermylen J, Hoylaerts MF, Van Geet C. Freson K, et al. Among authors: van geet c. Hum Genet. 2003 Jan;112(1):42-9. doi: 10.1007/s00439-002-0832-1. Epub 2002 Oct 16. Hum Genet. 2003. PMID: 12483298

5

Functional polymorphisms in the paternally expressed XLalphas and its cofactor ALEX decrease their mutual interaction and enhance receptor-mediated cAMP formation.

Freson K, Jaeken J, Van Helvoirt M, de Zegher F, Wittevrongel C, Thys C, Hoylaerts MF, Vermylen J, Van Geet C. Freson K, et al. Among authors: van helvoirt m, van geet c. Hum Mol Genet. 2003 May 15;12(10):1121-30. doi: 10.1093/hmg/ddg130. Hum Mol Genet. 2003. PMID: 12719376

6

The pituitary adenylate cyclase-activating polypeptide is a physiological inhibitor of platelet activation.

Freson K, Hashimoto H, Thys C, Wittevrongel C, Danloy S, Morita Y, Shintani N, Tomiyama Y, Vermylen J, Hoylaerts MF, Baba A, Van Geet C. Freson K, et al. Among authors: van geet c. J Clin Invest. 2004 Mar;113(6):905-12. doi: 10.1172/JCI19252. J Clin Invest. 2004. PMID: 15067323 Free PMC article.

7

The TUBB1 Q43P functional polymorphism reduces the risk of cardiovascular disease in men by modulating platelet function and structure.

Freson K, De Vos R, Wittevrongel C, Thys C, Defoor J, Vanhees L, Vermylen J, Peerlinck K, Van Geet C. Freson K, et al. Among authors: van geet c. Blood. 2005 Oct 1;106(7):2356-62. doi: 10.1182/blood-2005-02-0723. Epub 2005 Jun 14. Blood. 2005. PMID: 15956286 Free article.

8

Mechanisms of action and targets for actual and future antiplatelet drugs.

Freson K, Thys C, Wittevrongel C, Van Geet C. Freson K, et al. Among authors: van geet c. Mini Rev Med Chem. 2006 Jun;6(6):719-26. doi: 10.2174/138955706777435661. Mini Rev Med Chem. 2006. PMID: 16787383 Review.

9

-391 C to G substitution in the regulator of G-protein signalling-2 promoter increases susceptibility to the metabolic syndrome in white European men: consistency between molecular and epidemiological studies.

Freson K, Stolarz K, Aerts R, Brand E, Brand-Herrmann SM, Kawecka-Jaszcz K, Kuznetsova T, Tikhonoff V, Thijs L, Vermylen J, Staessen JA, Van Geet C; European Project on Genes in Hypertension Investigators. Freson K, et al. Among authors: van geet c. J Hypertens. 2007 Jan;25(1):117-25. doi: 10.1097/HJH.0b013e3280109c6c. J Hypertens. 2007. PMID: 17143182 Free article.

10

Increased Gs signalling in platelets and impaired collagen activation, due to a defect in the dystrophin gene, result in increased blood loss during spinal surgery.

Labarque V, Freson K, Thys C, Wittevrongel C, Hoylaerts MF, De Vos R, Goemans N, Van Geet C. Labarque V, et al. Among authors: van geet c. Hum Mol Genet. 2008 Feb 1;17(3):357-66. doi: 10.1093/hmg/ddm312. Epub 2007 Nov 1. Hum Mol Genet. 2008. PMID: 17981813

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