Výsledky vyhledávání - Rutger Meinsma

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  1. 1
    Increased risk of grade IV neutropenia after administration of 5‐fluorouracil due to a dihydropyrimidine dehydrogenase deficiency: High prevalence of the IVS14+1g>a mutation

    Increased risk of grade IV neutropenia after administration of 5‐fluorouracil due to a dihydropyrimidine dehydrogenase deficiency: High prevalence of the IVS14+1g>a mutation Autor André B. P. Kuilenburg, Rutger Meinsma, Lida Zoetekouw, Albert H. Gennip

    Vydáno 2002
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  2. 2
    Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicity

    Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicity Autor André B. P. Kuilenburg, P. Vreken, L.V.A.M. Beex, Rutger Meinsma, Henk van Lenthe, Ronney A. De Abreu, Albert H. Gennip

    Vydáno 1997
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  3. 3
    Novel disease-causing mutations in the dihydropyrimidine dehydrogenase gene interpreted by analysis of the three-dimensional protein structure

    Novel disease-causing mutations in the dihydropyrimidine dehydrogenase gene interpreted by analysis of the three-dimensional protein structure Autor André B. P. Kuilenburg, Doreen Dobritzsch, Rutger Meinsma, Janet Haasjes, Hans R. Waterham, Małgorzata J.M. Nowaczyk, George Maropoulos, Guido Hein, Hermann Kalhoff, J M Kirk, Holger BAASKE, Anne Aukett, John A. Duley, K. P. Ward, Ylva Lindqvist, Albert H. Gennip

    Vydáno 2002
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  4. 4
    Intragenic deletions and a deep intronic mutation affecting pre-mRNA splicing in the dihydropyrimidine dehydrogenase gene as novel mechanisms causing 5-fluorouracil toxicity

    Intragenic deletions and a deep intronic mutation affecting pre-mRNA splicing in the dihydropyrimidine dehydrogenase gene as novel mechanisms causing 5-fluorouracil toxicity Autor André B. P. Kuilenburg, Judith Meijer, Adri N. Mul, Rutger Meinsma, Veronika Schmid, Doreen Dobritzsch, Raoul C. M. Hennekam, Marcel M.A.M. Mannens, Marion Kiechle, Marie‐Christine Etienne‐Grimaldi, Heinz‐Josef Klümpen, Jan Gerard Maring, Veerle A. Derleyn, Ed Maartense, G. Milano, Raymon Vijzelaar, Eva Groß

    Vydáno 2010
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  5. 5
    Analysis of severely affected patients with dihydropyrimidine dehydrogenase deficiency reveals large intragenic rearrangements of DPYD and a de novo interstitial deletion del(1)(p13.3p21.3)

    Analysis of severely affected patients with dihydropyrimidine dehydrogenase deficiency reveals large intragenic rearrangements of DPYD and a de novo interstitial deletion del(1)(p1... Autor André B. P. Kuilenburg, Judith Meijer, Adri N. Mul, Raoul C. M. Hennekam, J.M.N. Hoovers, Christine de Die‐Smulders, Christian Weber, Andrea Mori, Jörgen Bierau, Brian Fowler, Klaus Macke, Jörn Oliver Sass, Rutger Meinsma, Julia B. Hennermann, Peter Miny, Lida Zoetekouw, Raymon Vijzelaar, Joost Nicolai, Bauke Ylstra, M. Estela Rubio‐Gozalbo

    Vydáno 2009
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  6. 6
    Dihydropyrimidinase deficiency: Phenotype, genotype and structural consequences in 17 patients

    Dihydropyrimidinase deficiency: Phenotype, genotype and structural consequences in 17 patients Autor André B. P. Kuilenburg, Doreen Dobritzsch, Judith Meijer, Rutger Meinsma, Jean‐François Benoist, Birgit Assmann, Susanne Schubert‐Bast, Georg F. Hoffmann, Marinus Durán, Maaike C. de Vries, G Kurlemann, François Eyskens, Lawrence Greed, Jörn Oliver Sass, Karl Otfried Schwab, A Sewell, John H. Walter, Andreas Hahn, Lida Zoetekouw, Antònia Ribes, Suzanne Lind, Raoul C. M. Hennekam

    Vydáno 2010
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