Resultados de búsqueda - Michiel Adriaens

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  1. 1
    Computational modelling of cancerous mutations in the EGFR/ERK signalling pathway

    Computational modelling of cancerous mutations in the EGFR/ERK signalling pathway por Richard Orton, Michiel Adriaens, Amélie Gormand, Oliver Sturm, Walter Kölch, David Gilbert

    Publicado 2009
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  2. 2
    The public road to high-quality curated biological pathways

    The public road to high-quality curated biological pathways por Michiel Adriaens, Magali Jaillard, Andra Waagmeester, Susan L. Coort, Alexander R. Pico, Chris T. Evelo

    Publicado 2008
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  3. 3
    Mapping of lamin A- and progerin-interacting genome regions

    Mapping of lamin A- and progerin-interacting genome regions por Nard Kubben, Michiel Adriaens, Wouter Meuleman, Jan Willem Voncken, Bas van Steensel, Tom Misteli

    Publicado 2012
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  4. 4
    Fetuin B is related to cytokine/chemokine and insulin signaling in adipose tissue and plasma in humans

    Fetuin B is related to cytokine/chemokine and insulin signaling in adipose tissue and plasma in humans por E. Kemper, Gijs H. Goossens, Ellen E. Blaak, Michiel Adriaens, Ruth C. R. Meex

    Publicado 2025
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  5. 5
    User-friendly solutions for microarray quality control and pre-processing on ArrayAnalysis.org

    User-friendly solutions for microarray quality control and pre-processing on ArrayAnalysis.org por Lars Eijssen, Magali Jaillard, Michiel Adriaens, Stan Gaj, Philip J. de Groot, Michael Müller, Chris T. Evelo

    Publicado 2013
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  6. 6
    From SNPs to pathways: Biological interpretation of type 2 diabetes (T2DM) genome wide association study (GWAS) results

    From SNPs to pathways: Biological interpretation of type 2 diabetes (T2DM) genome wide association study (GWAS) results por Elisa Cirillo, Martina Kutmon, Manuel A. González Hernández, Tom Hooimeijer, Michiel Adriaens, Lars Eijssen, Laurence D. Parnell, Susan L. Coort, Chris T. Evelo

    Publicado 2018
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  7. 7
    Hypoxia increases genome-wide bivalent epigenetic marking by specific gain of H3K27me3

    Hypoxia increases genome-wide bivalent epigenetic marking by specific gain of H3K27me3 por Peggy Prickaerts, Michiel Adriaens, Twan van den Beucken, Elizabeth Koch, Ludwig J. Dubois, Vivian E.H. Dahlmans, Caroline Gits, Chris T. Evelo, Michelle Chan‐Seng‐Yue, Bradly G. Wouters, Jan Willem Voncken

    Publicado 2016
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  8. 8
    Genome-Wide Identification of Expression Quantitative Trait Loci (eQTLs) in Human Heart

    Genome-Wide Identification of Expression Quantitative Trait Loci (eQTLs) in Human Heart por Tamara T. Koopmann, Michiel Adriaens, Perry D. Moerland, Roos F. Marsman, Marinda Westerveld, Sean Lal, Taifang Zhang, Christine Q. Simmons, István Baczkó, Cristobal G. dos Remedios, Nanette H. Bishopric, András Varró, Alfred L. George, Elisabeth M. Lodder, Connie R. Bezzina

    Publicado 2014
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  9. 9
    Genome-Wide Polyadenylation Maps Reveal Dynamic mRNA 3′-End Formation in the Failing Human Heart

    Genome-Wide Polyadenylation Maps Reveal Dynamic mRNA 3′-End Formation in the Failing Human Heart por Esther E. Creemers, Amira Bawazeer, Alejandro P. Ugalde, Hanneke W. M. van Deutekom, Ingeborg van der Made, Nina E. de Groot, Michiel Adriaens, Stuart A. Cook, Connie R. Bezzina, Norbert Hübner, Jolanda van der Velden, Ran Elkon, Reuven Agami, Yigal M. Pinto

    Publicado 2015
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  10. 10
    Phenotypic clustering of dilated cardiomyopathy patients highlights important pathophysiological differences

    Phenotypic clustering of dilated cardiomyopathy patients highlights important pathophysiological differences por Job A.J. Verdonschot, Marco Merlo, Fernándo Domínguez, Ping Wang, Michiel T.H.M. Henkens, Michiel Adriaens, Mark R. Hazebroek, Marco Masè, Luis Escobar-López, Rafael Cobas Paz, Kasper Derks, Arthur van den Wijngaard, Ingrid P.C. Krapels, Han G. Brunner, Gianfranco Sinagra, Pablo García‐Pavía, Stéphane Heymans

    Publicado 2020
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  11. 11
    Hypoxia promotes stem cell phenotypes and poor prognosis through epigenetic regulation of DICER

    Hypoxia promotes stem cell phenotypes and poor prognosis through epigenetic regulation of DICER por Twan van den Beucken, Elizabeth Koch, Kenneth C. Chu, Rajesha Rupaimoole, Peggy Prickaerts, Michiel Adriaens, Jan Willem Voncken, Adrian L. Harris, Francesca M. Buffa, Syed Haider, Maud H. W. Starmans, Cindy Q. Yao, Mircea Ivan, Cristina Ivan, Chad V. Pecot, Paul C. Boutros, Anil K. Sood, Marianne Koritzinsky, Bradly G. Wouters

    Publicado 2014
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  12. 12
    Cardiometabolic health improvements upon dietary intervention are driven by tissue-specific insulin resistance phenotype: A precision nutrition trial

    Cardiometabolic health improvements upon dietary intervention are driven by tissue-specific insulin resistance phenotype: A precision nutrition trial por Inez Trouwborst, Anouk Gijbels, Kelly M. Jardon, Els Siebelink, Gabby B. Hul, Lisa Wanders, Balázs Erdős, Szabolcs Péter, Cécile M. Singh‐Povel, Johan de Vogel‐van den Bosch, Michiel Adriaens, Ilja C.W. Arts, Dick H. J. Thijssen, Edith J. M. Feskens, Gijs H. Goossens, Lydia A. Afman, Ellen E. Blaak

    Publicado 2023
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  13. 13
    Coxsackie and Adenovirus Receptor Is a Modifier of Cardiac Conduction and Arrhythmia Vulnerability in the Setting of Myocardial Ischemia

    Coxsackie and Adenovirus Receptor Is a Modifier of Cardiac Conduction and Arrhythmia Vulnerability in the Setting of Myocardial Ischemia por Roos F. Marsman, Connie R. Bezzina, Fabian Freiberg, Arie O. Verkerk, Michiel Adriaens, Svitlana Podliesna, Chen Chen, Bettina Purfürst, Bastian Spallek, Tamara T. Koopmann, István Baczkó, Cristobal G. dos Remedios, Alfred L. George, Nanette H. Bishopric, Elisabeth M. Lodder, Jacques M.T. de Bakker, Robert Fischer, Ruben Coronel, Arthur A.M. Wilde, Michael Gotthardt, Carol Ann Remme

    Publicado 2013
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  14. 14
    A common genetic variant within SCN10A modulates cardiac SCN5A expression

    A common genetic variant within SCN10A modulates cardiac SCN5A expression por Malou van den Boogaard, Scott Smemo, Ozanna Burnicka-Turek, David E. Arnolds, Harmen J.G. van de Werken, Petra Klous, David McKean, Jochen D. Muehlschlegel, Julia Moosmann, Okan Toka, Xinan Yang, Tamara T. Koopmann, Michiel Adriaens, Connie R. Bezzina, Wouter de Laat, Christine E. Seidman, J.G. Seidman, Vincent M. Christoffels, Marcelo A. Nóbrega, Phil Barnett, Ivan P. Moskowitz

    Publicado 2014
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  15. 15
    Subcutaneous Adipose Tissue and Systemic Inflammation Are Associated With Peripheral but Not Hepatic Insulin Resistance in Humans

    Subcutaneous Adipose Tissue and Systemic Inflammation Are Associated With Peripheral but Not Hepatic Insulin Resistance in Humans por Birgitta W. van der Kolk, Marianthi Kalafati, Michiel Adriaens, Marleen M. J. van Greevenbroek, Nicole Vogelzangs, Wim H. M. Saris, Arne Astrup, Armand Valsesia, Dominique Langin, Carla Kallen, Simone J.P.M. Eussen, Casper G. Schalkwijk, Coen D.A. Stehouwer, Gijs H. Goossens, Ilja C.W. Arts, Johan W. E. Jocken, Chris T. Evelo, Ellen E. Blaak

    Publicado 2019
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  16. 16
    Subclassification of obesity for precision prediction of cardiometabolic diseases

    Subclassification of obesity for precision prediction of cardiometabolic diseases por Daniel Coral, Femke Smit, Ali Farzaneh, Alexander Gieswinkel, Juan Fernández Tajes, Thomas Sparsø, Carl Delfin, Pierre Bauvin, Kan Wang, Marinella Temprosa, Diederik De Cock, Jordi Blanch, José Manuel Fernández‐Real, Rafel Ramos, M. Kamran Ikram, Maria F. Gomez, Maryam Kavousi, Marina Panova‐Noeva, Philipp S. Wild, Carla Kallen, Michiel Adriaens, Marleen M. J. van Greevenbroek, Ilja C.W. Arts, Carel W. le Roux, Fariba Ahmadizar, Timothy M. Frayling, Giuseppe N. Giordano, Ewan R. Pearson, Paul W. Franks

    Publicado 2024
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  17. 17
    Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy

    Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy por Matthias Heinig, Michiel Adriaens, Sebastian Schäfer, Hanneke W. M. van Deutekom, Elisabeth M. Lodder, James S. Ware, Valentin Schneider-Lunitz, Leanne E. Felkin, Esther E. Creemers, Benjamin Meder, Hugo A. Katus, Frank Rühle, Monika Stoll, François Cambien, Eric Villard, Philippe Charron, András Varró, Nanette H. Bishopric, Alfred L. George, Cristobal G. dos Remedios, Aida Moreno‐Moral, Francesco Pesce, Anja Bauerfeind, Franz Rüschendorf, Carola Rintisch, Enrico Petretto, Paul J.R. Barton, Stuart A. Cook, Yigal M. Pinto, Connie R. Bezzina, Norbert Hübner

    Publicado 2017
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  18. 18
    Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

    Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 por Heather J. Cordell, Jamie Bentham, Ana Töpf, Diana Zélénika, Simon Heath, Chrysovalanto Mamasoula, Catherine Cosgrove, Gillian M. Blue, Javier T Granados-Riveron, Kerry Setchfield, Chris Thornborough, Jeroen Breckpot, Rachel Soemedi, Ruairidh Martin, Thahira Rahman, Darroch Hall, Klaartje van Engelen, Antoon F.M. Moorman, A. H. Zwinderman, Phil Barnett, Tamara T. Koopmann, Michiel Adriaens, András Varró, Alfred L. George, C. Dos Remedios, Nanette H. Bishopric, Connie R. Bezzina, John O’Sullivan, Marc Gewillig, Frances Bu’Lock, David S. Winlaw, Shoumo Bhattacharya, Koenraad Devriendt, J. David Brook, Barbara J.M. Mulder, Seema Mital, Alex V. Postma, G.M. Lathrop, Martin Farrall, Judith A. Goodship, Bernard Keavney

    Publicado 2013
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  19. 19
    52 Genetic Loci Influencing Myocardial Mass

    52 Genetic Loci Influencing Myocardial Mass por Pim van der Harst, Jessica van Setten, Niek Verweij, Georg Vogler, Lude Franke, Matthew T. Maurano, Xinchen Wang, Irene Mateo Leach, Mark Eijgelsheim, Nona Sotoodehnia, Caroline Hayward, Rossella Sorice, Osorio Meirelles, Leo‐Pekka Lyytikäinen, Ozren Polašek, Toshiko Tanaka, Dan E. Arking, Sheila Ulivi, Stella Trompet, Martina Müller‐Nurasyid, Albert V. Smith, Marcus Dörr, Kathleen F. Kerr, Jared W. Magnani, Fabiola Del Greco M, Weihua Zhang, Ilja M. Nolte, Claudia Silva, Sandosh Padmanabhan, Vinicius Tragante, Tõnu Esko, Gonçalo R. Abecasis, Michiel Adriaens, Karl Andersen, Phil Barnett, Joshua C. Bis, Rolf Bodmer, Brendan M. Buckley, Harry Campbell, Megan V. Cannon, Aravinda Chakravarti, Lin Y. Chen, Alessandro Delitala, Richard B. Devereux, Pieter A. Doevendans, Anna F. Dominiczak, Luigi Ferrucci, Ian Ford, Christian Gieger, Tamara B. Harris, Eric Haugen, Matthias Heinig, Dena Hernandez, Hans L. Hillege, Joel N. Hirschhorn, Albert Hofman, Norbert Hübner, Shih-Jen Hwang, Alfonso Iorio, Mika Kähönen, Manolis Kellis, Ivana Kolčić, Ishminder K. Kooner, Jaspal S. Kooner, Jan A. Kors, Edward G. Lakatta, Kasper Lage, Lenore J. Launer, Daniel Levy, Alicia Lundby, Peter W. Macfarlane, Dalit May, Thomas Meitinger, Andres Metspalu, Stefania Nappo, Silvia Naitza, Shane Neph, Alex S. Nord, Teresa Nutile, Peter M. Okin, Jesper V. Olsen, Ben A. Oostra, Josef Penninger, L Pennacchio, Tune H. Pers, Siegfried Perz, Annette Peters, Yigal M. Pinto, Arne Pfeufer, Maria Grazia Pilia, Peter P. Pramstaller, Bram P. Prins, Olli T. Raitakari, Soumya Raychaudhuri, Kenneth Rice, Elizabeth J. Rossin, Jerome I. Rotter, Sebastian Schäfer, David Schlessinger, Carsten Oliver Schmidt

    Publicado 2016
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