Search Results - "de Kievit, Peggy"

Rapid, high sensitivity, point-of-care test for cardiac troponin based on optomagnetic biosensor by Dittmer, Wendy U., Evers, Toon H., Hardeman, Willie M., Huijnen, Willeke, Kamps, Rick, de Kievit, Peggy, Neijzen, Jaap H.M., Nieuwenhuis, Jeroen H., Sijbers, Mara J.J., Dekkers, Dave W.C., Hefti, Marco H., Martens, Mike F.W.C.

“…We present a prototype handheld device based on a newly developed optomagnetic technology for the sensitive detection of cardiac troponin I (cTnI) in a…”
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Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere by van der Maarel, Silvère M, Lemmers, Richard J.L.F, de Kievit, Peggy, Sandkuijl, Lodewijk, Padberg, George W, van Ommen, Gert-Jan B, Frants, Rune R

“…Contractions in the polymorphic D4Z4 repeat array of subtelomere 4qter cause autosomal dominant facioscapulohumeral muscular dystrophy in humans. A polymorphic…”
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Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis by Lemmers, Richard J. L. F., De Kievit, Peggy, van geel, Michel, van der Wielen, Michiel J.R., Bakker, Egbert, Padberg, George W., Frants, Rune R., Van Der Maarel, Silvère M.

“…Facioscapulohumeral muscular dystrophy is caused by partial deletion of the D4Z4 repeat array on chromosome 4q35. Genetic diagnosis is based on sizing of this…”
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Quantitative assessment of a novel flow-through porous microarray for the rapid analysis of gene expression profiles by Wu, Ying, de Kievit, Peggy, Vahlkamp, Lars, Pijnenburg, Dirk, Smit, Maarten, Dankers, Martijn, Melchers, Diana, Stax, Martijn, Boender, Piet J., Ingham, Colin, Bastiaensen, Niek, de Wijn, Rik, van Alewijk, Dirk, van Damme, Henk, Raap, Anton K., Chan, Alan B., van Beuningen, Rinie

“…A novel microarray system that utilizes a porous aluminum-oxide substrate and flow-through incubation has been developed for rapid molecular biological…”
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