P. Tuijnenburg MD

MD P. Tuijnenburg

Position: Research Associate
Main activities: Research
Specialisation: Primary Immunodeficiencies, B cells
Focus of research: Investigating the cellular phenotype and function of lymphocytes in primary immunodeficiencies and determine normal B cell development and differentiation in healthy individuals.

Amsterdam UMC Research Institutes

AMC departments

Tuijnenburg Paul, Lango Allen Hana, Burns Siobhan O., Greene Daniel, Jansen Machiel H., Staples Emily, Stephens Jonathan, Carss Keren J., Biasci Daniele, Baxendale Helen, Thomas Moira, Chandra Anita, Kiani-Alikhan Sorena, Longhurst Hilary J., Seneviratne Suranjith L., Oksenhendler Eric, Simeoni Ilenia, de Bree Godelieve J., Tool Anton T. J., van Leeuwen Ester M. M., Ebberink Eduard H. T. M., Meijer Alexander B., Tuna Salih, Whitehorn Deborah, Brown Matthew, Turro Ernest, Thrasher Adrian J., Smith Kenneth G. C., Thaventhiran James E., Kuijpers Taco W. Loss of function NFKB1 variants are the most common monogenic cause of CVID in Europeans Journal of allergy and clinical immunology 2018;142 (4):1285-1296 [PubMed]
Oud Machteld M., Tuijnenburg Paul, Hempel Maja, van Vlies Naomi, Ren Zemin, Ferdinandusse Sacha, Jansen Machiel H., Santer René, Johannsen Jessika, Bacchelli Chiara, Alders Marielle, Li Rui, Davies Rosalind, Dupuis Lucie, Cale Catherine M., Wanders Ronald J. A., Pals Steven T., Ocaka Louise, James Chela, Müller Ingo, Lehmberg Kai, Strom Tim, Engels Hartmut, Williams Hywel J., Beales Phil, Roepman Ronald, Dias Patricia, Brunner Han G., Cobben Jan-Maarten, Hall Christine, Hartley Taila, Le Quesne Stabej Polona, Mendoza-Londono Roberto, Davies E. Graham, de Sousa Sérgio B., Lessel Davor, Arts Heleen H., Kuijpers Taco W. Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome American journal of human genetics 2017;100 (2):281-296 [PubMed]