نتائج البحث - Ralph W.H. Gottschalk

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  1. 1
    Keratinocyte Gene Expression Profiles Discriminate Sensitizing and Irritating Compounds

    Keratinocyte Gene Expression Profiles Discriminate Sensitizing and Irritating Compounds حسب Rob J. Vandebriel, Jeroen L.A. Pennings, Kirsten A. Baken, Tessa E. Pronk, André Boorsma, Ralph W.H. Gottschalk, Henk Van Loveren

    منشور في 2010
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  2. 2
    Differential Gene Expression in Human Peripheral Blood Mononuclear Cells Induced by Cigarette Smoke and Its Constituents

    Differential Gene Expression in Human Peripheral Blood Mononuclear Cells Induced by Cigarette Smoke and Its Constituents حسب Danitsja M. van Leeuwen, Ralph W.H. Gottschalk, Marcel H. van Herwijnen, E.J.C. Moonen, Jos Kleinjans, Joost H.M. van Delft

    منشور في 2005
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  3. 3
    Discrimination for Genotoxic and Nongenotoxic Carcinogens by Gene Expression Profiling in Primary Mouse Hepatocytes Improves with Exposure Time

    Discrimination for Genotoxic and Nongenotoxic Carcinogens by Gene Expression Profiling in Primary Mouse Hepatocytes Improves with Exposure Time حسب Karen Mathijs, Karen Brauers, Danyel Jennen, André Boorsma, Marcel H. M. van Herwijnen, Ralph W.H. Gottschalk, Jos Kleinjans, Joost H.M. van Delft

    منشور في 2009
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  4. 4
    Cigarette smoke-induced differential gene expression in blood cells from monozygotic twin pairs

    Cigarette smoke-induced differential gene expression in blood cells from monozygotic twin pairs حسب Danitsja M. van Leeuwen, Ebienus van Agen, Ralph W.H. Gottschalk, Robert Vlietinck, Marij Gielen, Marcel H. M. van Herwijnen, L.M. Maas, Jos Kleinjans, Joost H.M. van Delft

    منشور في 2006
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  5. 5
    Impact of multiple genetic polymorphisms on effects of a 4-week blueberry juice intervention on ex vivo induced lymphocytic DNA damage in human volunteers

    Impact of multiple genetic polymorphisms on effects of a 4-week blueberry juice intervention on ex vivo induced lymphocytic DNA damage in human volunteers حسب Lonneke C. Wilms, Agnes W. Boots, Vincent C. J. de Boer, Lou M. Maas, Daniëlle Pachen, Ralph W.H. Gottschalk, Hans B. Ketelslegers, Roger Godschalk, Guido R.M.M. Haenen, Frederik‐Jan van Schooten, Jos Kleinjans

    منشور في 2007
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  6. 6
    Genetic Variants of Methyl Metabolizing Enzymes and Epigenetic Regulators: Associations with Promoter CpG Island Hypermethylation in Colorectal Cancer

    Genetic Variants of Methyl Metabolizing Enzymes and Epigenetic Regulators: Associations with Promoter CpG Island Hypermethylation in Colorectal Cancer حسب Stefan de Vogel, Kristien Wouters, Ralph W.H. Gottschalk, Frederik‐Jan van Schooten, Anton F.P.M. de Goeij, Adriaan P. de Bruı̈ne, Royle A. Goldbohm, Piet A. van den Brandt, Matty P. Weijenberg, Manon van Engeland

    منشور في 2009
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  7. 7
    Toxicogenomic Profiles in Relation to Maternal Immunotoxic Exposure and Immune Functionality in Newborns

    Toxicogenomic Profiles in Relation to Maternal Immunotoxic Exposure and Immune Functionality in Newborns حسب Kevin Hochstenbach, Danitsja M. van Leeuwen, Hans Gmuender, Ralph W.H. Gottschalk, Solvor B. Stølevik, Unni C. Nygaard, Martinus Løvik, Berit Granum, Ellen Namork, Helle Margrete Meltzer, Jos Kleinjans, Joost H.M. van Delft, Henk Van Loveren

    منشور في 2012
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  8. 8
    Mitochondrial DNA copy number in colorectal cancer: between tissue comparisons, clinicopathological characteristics and survival

    Mitochondrial DNA copy number in colorectal cancer: between tissue comparisons, clinicopathological characteristics and survival حسب Frits van Osch, A.M. Voets, Leo J. Schouten, Ralph W.H. Gottschalk, Colinda C.J.M. Simons, Manon van Engeland, Marjolein H.F.M. Lentjes, Piet A. van den Brandt, Hubert J.M. Smeets, Matty P. Weijenberg

    منشور في 2015
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  9. 9
    Novel SLC25A32 mutation in a patient with a severe neuromuscular phenotype

    Novel SLC25A32 mutation in a patient with a severe neuromuscular phenotype حسب Debby M.E.I. Hellebrekers, Suzanne C.E.H. Sallevelt, Tom E. J. Theunissen, Alexandra T.M. Hendrickx, Ralph W.H. Gottschalk, Janneke G. J. Hoeijmakers, Daphna D.J. Habets, Jörgen Bierau, Kees Schoonderwoerd, Hubert J.M. Smeets

    منشور في 2017
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  10. 10
    Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause

    Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause حسب Tom E. J. Theunissen, Minh Nguyen, Rick Kamps, Alexandra T.M. Hendrickx, Suzanne C.E.H. Sallevelt, Ralph W.H. Gottschalk, Chantal Calis, Alphons P. M. Stassen, Bart de Koning, Elvira N. M. Mulder-Den Hartog, Kees Schoonderwoerd, Sabine A. Fuchs, Yvonne Hilhorst‐Hofstee, Marjolein Visser, Jo Vanoevelen, Radek Szklarczyk, Mike Gerards, I.F.M. de Coo, Debby M.E.I. Hellebrekers, Hubert J.M. Smeets

    منشور في 2018
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