Search Results - "VAN MARION, V."

Objective data on DNA success rates can aid the selection process of crime samples for analysis by rapid mobile DNA technologies by Mapes, A.A, Kloosterman, A.D, Poot, C.J. de, Marion, V. van

“…Highlights • Rapid-DNA systems are still insufficient for analysis of minimal traces. Bloodstains and cigarette ends show potential for Rapid-DNA analysis. •…”
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von Willebrand factor and its propeptide: the influence of secretion and clearance on protein levels and the risk of venous thrombosis by NOSSENT, A. Y., VAN MARION, V., VAN TILBURG, N. H., ROSENDAAL, F. R., BERTINA, R. M., VAN MOURIK, J. A., EIKENBOOM, H. C. J.

“…Background and objectives: Elevated levels of factor (F)VIII are associated with an increased risk of thrombosis. FVIII levels are determined mainly by von…”
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Fibrinogen Aα Thr312Ala polymorphism is associated with chronic thromboembolic pulmonary hypertension by SUNTHARALINGAM, J, GOLDSMITH, K, VAN MARION, V, LONG, L, TREACY, C. M, DUDBRIDGE, F, TOSHNER, M. R, PEPKE-ZABA, J, EIKENBOOM, J. C. J, MORRELL, N. W

“…Although chronic thromboembolic pulmonary hypertension (CTEPH) is characterised by the persistence of organised thrombus, few pro-thrombotic risk factors have…”
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Genome‐wide linkage scan in affected sibling pairs identifies novel susceptibility region for venous thromboembolism: Genetics In Familial Thrombosis study by Visser, M.C.H., Minkelen, R., Marion, V., Heijer, M., Eikenboom, J., Vos, H.L., Slagboom, P.E., Houwing‐Duistermaat, J.J., Rosendaal, F.R., Bertina, R.M.

“…Summary Background Venous thromboembolism (VTE) is a multicausal disorder involving environmental and genetic risk factors. In many thrombophilic families the…”
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Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD by EIKENBOOM, J., VAN MARION, V., PUTTER, H., GOODEVE, A., RODEGHIERO, F., CASTAMAN, G., FEDERICI, A. B., BATLLE, J., MEYER, D., MAZURIER, C., GOUDEMAND, J., SCHNEPPENHEIM, R., BUDDE, U., INGERSLEV, J., VORLOVA, Z., HABART, D., HOLMBERG, L., LETHAGEN, S., PASI, J., HILL, F., PEAKE, I.

“…Background: von Willebrand disease (VWD) type 1 is a congenital bleeding disorder caused by genetic defects in the von Willebrand factor (VWF) gene and…”
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Haplotypes of the EPCR gene, plasma sEPCR levels and the risk of deep venous thrombosis by Uitte De Willige, S., Van Marion, V., Rosendaal, F. R., Vos, H. L., De Visser, M. C. H., Bertina, R. M.

“…Background: Binding of protein C (PC) to the endothelial cell PC receptor (EPCR) stimulates PC activation by increasing the affinity of PC for the…”
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IN FOCUS: von Willebrand factor and its propeptide: the influence of secretion and clearance on protein levels and the risk of venous thrombosis by Nossent, A Y, Van Marion, V, Van Tilburg, NH, Rosendaal, FR, Bertina, R M, Van Mourik, JA, Eikenboom, HCJ

“…Background and objectives: Elevated levels of factor (F)VIII are associated with an increased risk of thrombosis. FVIII levels are determined mainly by von…”
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Fibrinogen Aalpha Thr312Ala polymorphism is associated with chronic thromboembolic pulmonary hypertension by Suntharalingam, J, Goldsmith, K, van Marion, V, Long, L, Treacy, C M, Dudbridge, F, Toshner, M R, Pepke-Zaba, J, Eikenboom, J C J, Morrell, N W

“…Although chronic thromboembolic pulmonary hypertension (CTEPH) is characterised by the persistence of organised thrombus, few pro-thrombotic risk factors have…”
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Fibrinogen A{alpha} Thr312Ala polymorphism is associated with chronic thromboembolic pulmonary hypertension by Suntharalingam, J, Goldsmith, K, van Marion, V, Long, L, Treacy, C. M, Dudbridge, F, Toshner, M. R, Pepke-Zaba, J, Eikenboom, J. C. J, Morrell, N. W

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