Search Results - "Wiesmeijer, Karien C"

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  1. 1

    A rapid assay for on-site monitoring of infliximab trough levels: a feasibility study by Corstjens, Paul L. A. M., Fidder, Herma H., Wiesmeijer, Karien C., de Dood, Claudia J., Rispens, Theo, Wolbink, Gert-Jan, Hommes, Daniel W., Tanke, Hans J.

    Published in Analytical and bioanalytical chemistry (01-09-2013)
    “…Monitoring levels of biologicals against tumor necrosis factor (TNF) has been suggested to improve therapeutic outcomes in inflammatory bowel diseases (IBDs)…”
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    Journal Article
  2. 2

    BMP Receptor Inhibition Enhances Tissue Repair in Endoglin Heterozygous Mice by Bakker, Wineke, Dingenouts, Calinda K E, Lodder, Kirsten, Wiesmeijer, Karien C, de Jong, Alwin, Kurakula, Kondababu, Mager, Hans-Jurgen J, Smits, Anke M, de Vries, Margreet R, Quax, Paul H A, Goumans, Marie José T H

    “…Hereditary hemorrhagic telangiectasia type 1 (HHT1) is a severe vascular disorder caused by mutations in the TGFβ/BMP co-receptor . Endoglin haploinsufficiency…”
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    Journal Article
  3. 3

    Inhibiting DPP4 in a mouse model of HHT1 results in a shift towards regenerative macrophages and reduces fibrosis after myocardial infarction by Dingenouts, Calinda K E, Bakker, Wineke, Lodder, Kirsten, Wiesmeijer, Karien C, Moerkamp, Asja T, Maring, Janita A, Arthur, Helen M, Smits, Anke M, Goumans, Marie-José

    Published in PloS one (18-12-2017)
    “…Hereditary Hemorrhagic Telangiectasia type-1 (HHT1) is a genetic vascular disorder caused by haploinsufficiency of the TGFβ co-receptor endoglin. Dysfunctional…”
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    Journal Article
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    Lateral flow assay for simultaneous detection of cellular- and humoral immune responses by Corstjens, Paul L.A.M., de Dood, Claudia J., van der Ploeg-van Schip, Jolien J., Wiesmeijer, Karien C., Riuttamäki, Terhi, van Meijgaarden, Krista E., Spencer, John S., Tanke, Hans J., Ottenhoff, Tom H.M., Geluk, Annemieke

    Published in Clinical biochemistry (01-10-2011)
    “…The development of a cytokine detection assay suitable for detection of multiple biomarkers for improved diagnosis of mycobacterial diseases. A lateral flow…”
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  8. 8

    Prenatal diagnosis of trisomy 13 on fetal cells obtained from maternal blood after minor enrichment by Oosterwijk, Jan C., Mesker, Wilma E., Ouwerkerk-Van Velzen, Maria C. M., Knepflé, Cecile F. H. M., Wiesmeijer, Karien C., Beverstock, Geoffrey C., Van Ommen, Gert-Jan B., Tanke, Hans J., Kanhai, Humphrey H. H.

    Published in Prenatal diagnosis (01-10-1998)
    “…In a pilot study to establish fetal nucleated red blood cell (NRBC) detection in maternal blood, trisomy 13 was diagnosed by FISH analysis at 11 weeks'…”
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