Association between the DTNBP1 gene and intelligence: a case-control study in young patients with schizophrenia and related disorders and unaffected siblings

Por Zinkstok, Janneke R, de Wilde, Odette, van Amelsvoort, Therese AMJ, Tanck, Michael W, Baas, Frank, Linszen, Don H
Publicado em 2007

Soluble ST2 plasma concentrations predict mortality in severe sepsis

Por Hoogerwerf, Jacobien J., Tanck, Michael W. T., van Zoelen, Marieke A. D., Wittebole, Xavier, Laterre, Pierre-François, van der Poll, Tom
Publicado em 2010

HIV-1 Disease Progression Is Associated with Bile-Salt Stimulated Lipase (BSSL) Gene Polymorphism

Por Stax, Martijn J., Kootstra, Neeltje A., van 't Wout, Angélique B., Tanck, Michael W. T., Bakker, Margreet, Pollakis, Georgios, Paxton, William A.
Publicado em 2012

ABCG5/G8 polymorphisms and markers of cholesterol metabolism: systematic review and meta-analysis

Por Jakulj, Lily, Vissers, Maud N., Tanck, Michael W. T., Hutten, Barbara A., Stellaard, Frans, Kastelein, John J. P., Dallinga-Thie, Geesje M.
Publicado em 2010

Binding of Human Milk to Pathogen Receptor DC-SIGN Varies with Bile Salt-Stimulated Lipase (BSSL) Gene Polymorphism

Por Stax, Martijn J., Naarding, Marloes A., Tanck, Michael W. T., Lindquist, Susanne, Hernell, Olle, Lyle, Robert, Brandtzaeg, Per, Eggesbø, Merete, Pollakis, Georgios, Paxton, William A.
Publicado em 2011

SNPs Identified as Modulators of ECG Traits in the General Population Do Not Markedly Affect ECG Traits during Acute Myocardial Infarction nor Ventricular Fibrillation Risk in This...

Por Pazoki, Raha, de Jong, Jonas S.S.G., Marsman, Roos F., Bruinsma, Nienke, Dekker, Lukas R. C., Wilde, Arthur A. M., Bezzina, Connie R., Tanck, Michael W. T.
Publicado em 2013

Mannose-binding lectin-associated serine protease 2 (MASP-2) contributes to poor disease outcome in humans and mice with pneumococcal meningitis

Por Kasanmoentalib, E. Soemirien, Valls Seron, Mercedes, Ferwerda, Bart, Tanck, Michael W., Zwinderman, Aeilko H., Baas, Frank, van der Ende, Arie, Brouwer, Matthijs C., van de Beek, Diederik
Publicado no J Neuroinflammation (2017)

Receptor for Advanced Glycation End Products (RAGE) Serves a Protective Role during Klebsiella pneumoniae - Induced Pneumonia

Por Achouiti, Ahmed, de Vos, Alex F., van ‘t Veer, Cornelis, Florquin, Sandrine, Tanck, Michael W., Nawroth, Peter P., Bierhaus, Angelika, van der Poll, Tom, van Zoelen, Marieke A. D.
Publicado no PLoS One (2016)

Both Paraoxonase-1 Genotype and Activity Do Not Predict the Risk of Future Coronary Artery Disease; the EPIC-Norfolk Prospective Population Study

Por Birjmohun, Rakesh S., Vergeer, Menno, Stroes, Erik S. G., Sandhu, Manjinder S., Ricketts, Sally L., Tanck, Michael W., Wareham, Nicholas J., Jukema, J. Wouter, Kastelein, John J. P., Khaw, Kay-Tee, Boekholdt, S. Matthijs
Publicado em 2009

Dissection of a Quantitative Trait Locus for PR Interval Duration Identifies Tnni3k as a Novel Modulator of Cardiac Conduction

Por Lodder, Elisabeth M., Scicluna, Brendon P., Milano, Annalisa, Sun, Albert Y., Tang, Hao, Remme, Carol Ann, Moerland, Perry D., Tanck, Michael W. T., Pitt, Geoffrey S., Marchuk, Douglas A., Bezzina, Connie R.
Publicado em 2012

Erratum to: Mannose-binding lectin-associated serine protease 2 (MASP-2) contributes to poor disease outcome in humans and mice with pneumococcal meningitis

Por Kasanmoentalib, E. Soemirien, Seron, Mercedes Valls, Ferwerda, Bart, Tanck, Michael W., Zwinderman, Aeilko H., Baas, Frank, van der Ende, Arie, Schwaeble, William J., Brouwer, Matthijs C., van de Beek, Diederik
Publicado no J Neuroinflammation (2017)

Hyperglycemia enhances coagulation and reduces neutrophil degranulation, whereas hyperinsulinemia inhibits fibrinolysis during human endotoxemia

Por Stegenga, Michiel E., van der Crabben, Saskia N., Blümer, Regje M. E., Levi, Marcel, Meijers, Joost C. M., Serlie, Mireille J., Tanck, Michael W. T., Sauerwein, Hans P., van der Poll, Tom
Publicado em 2008

The Angio-Fibrotic Switch of VEGF and CTGF in Proliferative Diabetic Retinopathy

Por Kuiper, Esther J., Van Nieuwenhoven, Frans A., de Smet, Marc D., van Meurs, Jan C., Tanck, Michael W., Oliver, Noelynn, Klaassen, Ingeborg, Van Noorden, Cornelis J. F., Goldschmeding, Roel, Schlingemann, Reinier O.
Publicado em 2008

V-akt murine thymoma viral oncogene homolog 3 (AKT3) contributes to poor disease outcome in humans and mice with pneumococcal meningitis

Por Valls Serón, Mercedes, Ferwerda, Bart, Engelen-Lee, JooYeon, Geldhoff, Madelijn, Jaspers, Valery, Zwinderman, Aeilko H., Tanck, Michael W., Baas, Frank, van der Ende, Arie, Brouwer, Matthijs C., van de Beek, Diederik
Publicado no Acta Neuropathol Commun (2016)

Chemokine Ligand 2 Genetic Variants, serum MCP-1 Levels and the Risk of Coronary Artery Disease

Por van Wijk, Diederik F., van Leuven, Sander I., Sandhu, Manjinder S., Tanck, Michael W., Hutten, Barbara A., Wareham, Nicholas J., Kastelein, John J.P., Stroes, Erik S.G., MBBChir, Kay-Tee Khaw, Boekholdt, S. Matthijs
Publicado em 2010

Haplotype-Sharing Analysis Implicates Chromosome 7q36 Harboring DPP6 in Familial Idiopathic Ventricular Fibrillation

Por Alders, Marielle, Koopmann, Tamara T., Christiaans, Imke, Postema, Pieter G., Beekman, Leander, Tanck, Michael W.T., Zeppenfeld, Katja, Loh, Peter, Koch, Karel T., Demolombe, Sophie, Mannens, Marcel M.A.M., Bezzina, Connie R., Wilde, Arthur A.M.
Publicado em 2009

Common genetic variants do not associate with CAD in familial hypercholesterolemia

Por van Iperen, Erik P A, Sivapalaratnam, Suthesh, Boekholdt, S Matthijs, Hovingh, G Kees, Maiwald, Stephanie, Tanck, Michael W, Soranzo, Nicole, Stephens, Jonathan C, Sambrook, Jennifer G, Levi, Marcel, Ouwehand, Willem H, Kastelein, John JP, Trip, Mieke D, Zwinderman, Aeilko H
Publicado em 2014

Variants in the 3′ untranslated region of the KCNQ1-encoded K(v)7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner...

Por Amin, Ahmad S., Giudicessi, John R., Tijsen, Anke J., Spanjaart, Anne M., Reckman, Yolan J., Klemens, Christine A., Tanck, Michael W., Kapplinger, Jamie D., Hofman, Nynke, Sinner, Moritz F., Müller, Martina, Wijnen, Wino J., Tan, Hanno L., Bezzina, Connie R., Creemers, Esther E., Wilde, Arthur A. M., Ackerman, Michael J., Pinto, Yigal M.
Publicado em 2012

Ext1 heterozygosity causes a modest effect on postprandial lipid clearance in humans

Por Mooij, Hans L., Bernelot Moens, Sophie J., Gordts, Philip L. S. M., Stanford, Kristin I., Foley, Erin M., van den Boogert, Marjolein A. W., Witjes, Julia J., Hassing, H. Carlijne, Tanck, Michael W., van de Sande, Michiel A. J., Levels, J. Han, Kastelein, John J. P., Stroes, Erik S. G., Dallinga-Thie, Geesje M., Esko, Jeff D., Nieuwdorp, Max
Publicado no J Lipid Res (2015)

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

Por Kolder, Iris C.R.M., Tanck, Michael W.T., Postema, Pieter G., Barc, Julien, Sinner, Moritz F., Zumhagen, Sven, Husemann, Anja, Stallmeyer, Birgit, Koopmann, Tamara T., Hofman, Nynke, Pfeufer, Arne, Lichtner, Peter, Meitinger, Thomas, Beckmann, Britt M., Myerburg, Robert J., Bishopric, Nanette H., Roden, Dan M., Kääb, Stefan, Wilde, Arthur A.M., Schott, Jean-Jacques, Schulze-Bahr, Eric, Bezzina, Connie R.
Publicado no Circ Cardiovasc Genet (2015)