Search Results - Debby M.E.I. Hellebrekers

  • Showing 1 - 15 results of 15
Refine Results
  1. 1
    Methylation-Specific PCR Unraveled

    Methylation-Specific PCR Unraveled by Sarah Derks, Marjolein H.F.M. Lentjes, Debby M.E.I. Hellebrekers, Adriaan P. de Bruı̈ne, James G. Herman, Manon van Engeland

    Published 2004
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  2. 2
    Design of Nonpeptidic Topomimetics of Antiangiogenic Proteins With Antitumor Activities

    Design of Nonpeptidic Topomimetics of Antiangiogenic Proteins With Antitumor Activities by Ruud P.M. Dings, Xuemei Chen, Debby M.E.I. Hellebrekers, Loes I. van Eijk, Ying Zhang, Thomas R. Hoye, Arjan W. Griffioen, Kevin H. Mayo

    Published 2006
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  3. 3
    Identification of Epigenetically Silenced Genes in Tumor Endothelial Cells

    Identification of Epigenetically Silenced Genes in Tumor Endothelial Cells by Debby M.E.I. Hellebrekers, Veerle Melotte, Emmanuelle Viré, Elise Langenkamp, Grietje Molema, François Fuks, James G. Herman, Wim Van Criekinge, Arjan W. Griffioen, Manon van Engeland

    Published 2007
    Get full text
    Artigo
    Save to List
    Saved in:
  4. 4
    Angiostatic activity of DNA methyltransferase inhibitors

    Angiostatic activity of DNA methyltransferase inhibitors by Debby M.E.I. Hellebrekers, Kam-Wing Jair, Emmanuelle Viré, Sayaka Eguchi, Nicole Hoebers, Mario F. Fraga, Manel Esteller, François Fuks, Stephen B. Baylin, Manon van Engeland, Arjan W. Griffioen

    Published 2006
    Get full text
    Artigo
    Save to List
    Saved in:
  5. 5
    Epigenetic Regulation of Tumor Endothelial Cell Anergy: Silencing of Intercellular Adhesion Molecule-1 by Histone Modifications

    Epigenetic Regulation of Tumor Endothelial Cell Anergy: Silencing of Intercellular Adhesion Molecule-1 by Histone Modifications by Debby M.E.I. Hellebrekers, Karolien Castermans, Emmanuelle Viré, Ruud P.M. Dings, Nicole Hoebers, Kevin H. Mayo, Mirjam G.A. oude Egbrink, Grietje Molema, François Fuks, Manon van Engeland, Arjan W. Griffioen

    Published 2006
    Get full text
    Artigo
    Save to List
    Saved in:
  6. 6
    Novel SLC25A32 mutation in a patient with a severe neuromuscular phenotype

    Novel SLC25A32 mutation in a patient with a severe neuromuscular phenotype by 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

    Published 2017
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  7. 7
    Defective NDUFA9 as a novel cause of neonatally fatal complex I disease

    Defective NDUFA9 as a novel cause of neonatally fatal complex I disease by B.J.C. van den Bosch, Mike Gerards, Wim J. Sluiter, Alexander P.A. Stegmann, Eveline Jongen, Debby M.E.I. Hellebrekers, Renske Oegema, Ellen Lambrichs, Holger Prokisch, Katharina Danhauser, Kees Schoonderwoerd, I.F.M. de Coo, Hubert J.M. Smeets

    Published 2011
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  8. 8
    De novo mtDNA point mutations are common and have a low recurrence risk

    De novo mtDNA point mutations are common and have a low recurrence risk by Suzanne C.E.H. Sallevelt, Christine de Die‐Smulders, Alexandra T.M. Hendrickx, Debby M.E.I. Hellebrekers, I.F.M. de Coo, Charlotte L. Alston, Charlotte V. Y. Knowles, Robert W. Taylor, Robert McFarland, Hubert J.M. Smeets

    Published 2016
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  9. 9
    GATA4 and GATA5 are Potential Tumor Suppressors and Biomarkers in Colorectal Cancer

    GATA4 and GATA5 are Potential Tumor Suppressors and Biomarkers in Colorectal Cancer by Debby M.E.I. Hellebrekers, Marjolein H.F.M. Lentjes, Sandra M. van den Bosch, Veerle Melotte, Kristien Wouters, Kathleen L.J. Daenen, Kim M. Smits, Yoshimitsu Akiyama, Yasuhito Yuasa, Silvia Sanduleanu, Carolina A.J. Khalid-de Bakker, Daisy Jonkers, Matty P. Weijenberg, Joost Louwagie, Wim Van Criekinge, Beatriz Carvalho, Gerrit A. Meijer, Stephen B. Baylin, James G. Herman, Adriaan P. de Bruı̈ne, Manon van Engeland

    Published 2009
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  10. 10
    N-Myc Downstream-Regulated Gene 4 ( NDRG4 ): A Candidate Tumor Suppressor Gene and Potential Biomarker for Colorectal Cancer

    N-Myc Downstream-Regulated Gene 4 ( NDRG4 ): A Candidate Tumor Suppressor Gene and Potential Biomarker for Colorectal Cancer by Veerle Melotte, Marjolein H.F.M. Lentjes, Sandra M. van den Bosch, Debby M.E.I. Hellebrekers, Joep P.J. de Hoon, Kristien Wouters, Kathleen L.J. Daenen, Iris Partouns-Hendriks, Filip Stessels, Joost Louwagie, Kim M. Smits, Matty P. Weijenberg, Silvia Sanduleanu, Carolina A.J. Khalid-de Bakker, Frank A. Oort, Gerrit A. Meijer, Daisy Jonkers, James G. Herman, Adriaan P. de Bruı̈ne, Manon van Engeland

    Published 2009
    Get full text
    Artigo
    Save to List
    Saved in:
  11. 11
    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 by 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

    Published 2018
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  12. 12
    A mutation update for the <i>FLNC</i> gene in myopathies and cardiomyopathies

    A mutation update for the <i>FLNC</i> gene in myopathies and cardiomyopathies by Job A.J. Verdonschot, Els K. Vanhoutte, Godelieve R.F. Claes, Apollonia T. J. M. Helderman‐van den Enden, Janneke G. J. Hoeijmakers, Debby M.E.I. Hellebrekers, Amber de Haan, Imke Christiaans, Ronald H. Lekanne Deprez, Hanne M. Boen, Emeline M. Van Craenenbroeck, Bart Loeys, Yvonne M. Hoedemaekers, Carlo Marcelis, Marlies Kempers, Esther Brusse, Jaap I. van Waning, Annette F. Baas, Dennis Dooijes, Folkert W. Asselbergs, Daniela Q.C.M. Barge‐Schaapveld, Pieter Koopman, Arthur van den Wijngaard, Stéphane Heymans, Ingrid P.C. Krapels, Han G. Brunner

    Published 2020
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  13. 13
    Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing

    Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing by A Janssen, Rebekka M. Koeck, Rick Essers, Ping Cao, Wanwisa van Dijk, Marion Drüsedau, Jeroen Meekels, Burcu Yaldiz, Maartje van de Vorst, Bart de Koning, Debby M.E.I. Hellebrekers, Servi J.C. Stevens, Su Ming Sun, Malou Heijligers, Sonja A. de Munnik, Chris M.J. van Uum, Juul Achten, Lars Hamers, Marjan Naghdi, Lisenka E.L.M. Vissers, Ron J T van Golde, Guido de Wert, Jos Dreesen, Christine de Die‐Smulders, Edith Coonen, Han G. Brunner, Arthur van den Wijngaard, Aimée Paulussen, Masoud Zamani Esteki

    Published 2024
    Get full text
    Artigo
    Save to List
    Saved in:
  14. 14
    Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans

    Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans by Thuy-Linh Le, Louise Galmiche, J Levý, Pim Suwannarat, Debby M.E.I. Hellebrekers, Khomgrit Morarach, Franck Boismoreau, Tom E. J. Theunissen, Mathilde Lefebvre, Anna Pelet, Jéléna Martinovic, A. Gélot, Fabien Guimiot, Amanda Calleroz, Cyril Gitiaux, Marie Hully, Olivier Goulet, Christophe Chardot, Séverine Drunat, Yline Capri, Christine Bôle‐Feysot, Patrick Nitschké, Sandra Whalen, L. Mouthon, Holly E. Babcock, Robert M.W. Hofstra, Irenaeus F.M. de Coo, Anne‐Claude Tabet, Thierry Jo Molina, Boris Keren, Alice Brooks, Hubert J.M. Smeets, Ulrika Marklund, Christopher T. Gordon, Stanislas Lyonnet, Jeanne Amiel, Nadège Bondurand

    Published 2021
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  15. 15
    Genome sequencing as a generic diagnostic strategy for rare disease

    Genome sequencing as a generic diagnostic strategy for rare disease by Gaby Schobers, Ronny Derks, Amber den Ouden, Hilde Swinkels, Jeroen van Reeuwijk, Ermanno Bosgoed, Dorien Lugtenberg, Su Ming Sun, Jordi Corominas Galbany, Marjan M. Weiss, Marinus J. Blok, Richelle A. C. M. Olde Keizer, Tom Hofste, Debby M.E.I. Hellebrekers, Nicole de Leeuw, Alexander P.A. Stegmann, Erik‐Jan Kamsteeg, Aimée Paulussen, Marjolijn J. L. Ligtenberg, Xiangqun Zheng-Bradley, John F. Peden, Alejandra Gutierrez, Adam Pullen, Thomas J. Payne, Christian Gilissen, Arthur van den Wijngaard, Han G. Brunner, Marcel Nelen, Helger G. Yntema, Lisenka E.L.M. Vissers

    Published 2024
    Get full text Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: