1 - 25 of 73 results for author:"Reitsma P.H." in Literature citations
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| Modulation of mouse coagulation gene transcription following acute in vivo delivery of synthetic small interfering RNAs targeting HNF4alpha and C/EBPalpha. Safdar H., Cheung K.L., Vos H.L., Gonzalez F.J., Reitsma P.H., Inoue Y., van Vlijmen B.J. PLoS ONE 7:e38104-e38104(2012) · Mapped (2) |
| Biogenesis of Weibel-Palade bodies in von Willebrand's disease variants with impaired von Willebrand factor intrachain or interchain disulfide bond formation. Wang J.W., Groeneveld D.J., Cosemans G., Dirven R.J., Valentijn K.M., Voorberg J., Reitsma P.H., Eikenboom J. Haematologica 97:859-866(2012) · Mapped (6) |
| Evolutionary conservation of the tissue factor disulfide bonds and identification of a possible oxidoreductase binding motif. van den Hengel L.G., van den Berg Y.W., Reitsma P.H., Bos M.H., Versteeg H.H. J. Thromb. Haemost. 10:161-162(2012) · Mapped (5) |
| Haplotypes of VKORC1, NQO1 and GGCX, their effect on activity levels of vitamin K-dependent coagulation factors, and the risk of venous thrombosis. de Visser M.C., Roshani S., Rutten J.W., van Hylckama Vlieg A., Vos H.L., Rosendaal F.R., Reitsma P.H. Thromb. Haemost. 106:563-565(2011) · Mapped (15) |
| Intracellular storage and regulated secretion of von Willebrand factor in quantitative von Willebrand disease. Wang J.W., Valentijn K.M., de Boer H.C., Dirven R.J., van Zonneveld A.J., Koster A.J., Voorberg J., Reitsma P.H., Eikenboom J. J. Biol. Chem. 286:24180-24188(2011) · Mapped (6) |
| High levels of protein C are determined by PROCR haplotype 3. Pintao M.C., Roshani S., de Visser M.C., Tieken C., Tanck M.W., Wichers I.M., Meijers J.C., Rosendaal F.R., Middeldorp S., Reitsma P.H. J. Thromb. Haemost. 9:969-976(2011) · Mapped (21) |
| Gene variants associated with venous thrombosis: confirmation in the MEGA study. Arellano A.R., Bezemer I.D., Tong C.H., Catanese J.J., Devlin J.J., Reitsma P.H., Bare L.A., Rosendaal F.R. J. Thromb. Haemost. 8:1132-1134(2010) · Mapped (105) |
| Alternatively spliced tissue factor induces angiogenesis through integrin ligation. van den Berg Y.W., van den Hengel L.G., Myers H.R., Ayachi O., Jordanova E., Ruf W., Spek C.A., Reitsma P.H., Bogdanov V.Y., Versteeg H.H. Proc. Natl. Acad. Sci. U.S.A. 106:19497-19502(2009) · Mapped (3) |
| Genetic variants associated with deep vein thrombosis: the F11 locus. Li Y., Bezemer I.D., Rowland C.M., Tong C.H., Arellano A.R., Catanese J.J., Devlin J.J., Reitsma P.H., Bare L.A., Rosendaal F.R. J. Thromb. Haemost. 7:1802-1808(2009) · Mapped (6) |
| Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency. Pintao M.C., Garcia A.A., Borgel D., Alhenc-Gelas M., Spek C.A., de Visser M.C., Gandrille S., Reitsma P.H. Hum. Genet. 126:449-456(2009) · Mapped (28) |
| F9 Malmo, factor IX and deep vein thrombosis. Bezemer I.D., Arellano A.R., Tong C.H., Rowland C.M., Ireland H.A., Bauer K.A., Catanese J., Reitsma P.H., Doggen C.J., Devlin J.J. et al. Haematologica 94:693-699(2009) · Mapped (49) |
| Coagulation factor Xa inhibits cancer cell migration via protease-activated receptor-1 activation. Borensztajn K., Bijlsma M.F., Reitsma P.H., Peppelenbosch M.P., Spek C.A. Thromb. Res. 124:219-225(2009) · Mapped (3) |
| Polymorphisms in the protein C gene as risk factor for venous thrombosis. Pomp E.R., Doggen C.J., Vos H.L., Reitsma P.H., Rosendaal F.R. Thromb. Haemost. 101:62-67(2009) · Mapped (33) |
| Characterization of the intracellular signalling capacity of natural FXa mutants with reduced pro-coagulant activity. Monti M., Borensztajn K.S., Pinotti M., Canella A., Branchini A., Marchetti G., Reitsma P.H., Bernardi F., Spek C.A. Thromb. Res. 123:914-918(2009) · Mapped (3) |
| Haplotypes of the interleukin-1 receptor antagonist gene, interleukin-1 receptor antagonist mRNA levels and the risk of myocardial infarction. van Minkelen R., Wettinger S.B., de Visser M.C., Vos H.L., Reitsma P.H., Rosendaal F.R., Bertina R.M., Doggen C.J. Atherosclerosis 203:201-205(2009) · Mapped (2) |
| PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations. Ten Kate M.K., Platteel M., Mulder R., Terpstra P., Nicolaes G.A., Reitsma P.H., van der Steege G., van der Meer J. Hum. Mutat. 29:939-947(2008) · Mapped (28) |
| Gene variants associated with deep vein thrombosis. Bezemer I.D., Bare L.A., Doggen C.J., Arellano A.R., Tong C., Rowland C.M., Catanese J., Young B.A., Reitsma P.H., Devlin J.J. et al. JAMA 299:1306-1314(2008) · Mapped (15) |
| ADAMTS-13, von Willebrand factor and related parameters in severe sepsis and septic shock. Kremer Hovinga J.A., Zeerleder S., Kessler P., Romani de Wit T., van Mourik J.A., Hack C.E., ten Cate H., Reitsma P.H., Wuillemin W.A., Lammle B. J. Thromb. Haemost. 5:2284-2290(2007) · Mapped (6) |
| VKORC1 gene variation and venous thrombosis: 'another one bites the dust'? Reitsma P.H. J. Thromb. Haemost. 5:2017-2019(2007) · Mapped (2) |
| Protease-activated receptor-4 inhibition protects from multiorgan failure in a murine model of systemic inflammation. Slofstra S.H., Bijlsma M.F., Groot A.P., Reitsma P.H., Lindhout T., ten Cate H., Spek C.A. Blood 110:3176-3182(2007) · Mapped (2) |
| Gene expression profiling identifies C/EBPdelta as a candidate regulator of endotoxin-induced disseminated intravascular coagulation. Slofstra S.H., Groot A.P., Obdeijn M.H., Reitsma P.H., ten Cate H., Spek C.A. Am. J. Respir. Crit. Care Med. 176:602-609(2007) · Mapped (4) |
| Coagulation factor Xa drives tumor cells into apoptosis through BH3-only protein Bim up-regulation. Borensztajn K.S., Bijlsma M.F., Groot A.P., Bruggemann L.W., Versteeg H.H., Reitsma P.H., Peppelenbosch M.P., Spek C.A. Exp. Cell Res. 313:2622-2633(2007) · Mapped (3) |
| Fibrinogen plasma levels modify the association between the factor XIII Val34Leu variant and risk of coronary artery disease: the EPIC-Norfolk prospective population study. Boekholdt S.M., Sandhu M.S., Wareham N.J., Luben R., Reitsma P.H., Khaw K.T. J. Thromb. Haemost. 4:2204-2209(2006) · Mapped (10) |
| Alternatively spliced tissue factor in mice: induction by Streptococcus pneumoniae. Bruggemann L.W., Drijfhout J.W., Reitsma P.H., Spek C.A. J. Thromb. Haemost. 4:918-920(2006) · Mapped (3) |
| Common variants of multiple genes that control reverse cholesterol transport together explain only a minor part of the variation of HDL cholesterol levels. Boekholdt S.M., Souverein O.W., Tanck M.W., Hovingh G.K., Kuivenhoven J.A., Peters R.I., Jansen H., Schiffers P.M., van der Wall E.E., Doevendans P.A. et al. Clin. Genet. 69:263-270(2006) · Mapped (46) |