foto

P. Tuijnenburg MD

Position
PhD student
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.

Key publications
  • Tuijnenburg P, Lango Allen H, Burns SO, Greene D, Jansen MH, Staples E, Stephens J, Carss KJ, Biasci D, Baxendale H, Thomas M, Chandra A, Kiani-Alikhan S, Longhurst HJ, Seneviratne SL, Oksenhendler E, Simeoni I, de Bree GJ, Tool ATJ, van Leeuwen EMM, Ebberink EHTM, Meijer AB, Tuna S, Whitehorn D, Brown M, Turro E, Thrasher AJ, Smith KGC, Thaventhiran JE, Kuijpers TW [Contributors: Adhya Z, Alachkar H, Anantharachagan A, Antrobus R, Arumugakani G, Bacchelli C, Baxendale H, Bethune C, Bibi S, Boardman B, Booth C, Browning M, Brownlie M, Burns S, Chandra A, Clifford H, Cooper N, Davies S, Dempster J, Devlin L, Doffinger R, Drewe E, Edgar D, Egner W, El-Shanawany T, Gaspar B, Ghurye R, Gilmour K, Goddard S, Gordins P, Grigoriadou S, Hackett S, Hague R, Harper L, Hayman G, Herwadkar A, Hughes S, Huissoon A, Jolles S, Jones J, Kelleher P, Klein N, Kuijpers T, Kumararatne D, Laffan J, Lango Allen H, Lear S, Longhurst H, Lorenzo L, Maimaris J, Manson A, McDermott E, Millar H, Mistry A, Morrisson V, Murng S, Nasir I, Nejentsev S, Noorani S, Oksenhendler E, Ponsford M, Qasim W, Quinn E, Quinti I, Richter A, Samarghitean C, Sargur R, Savic S, Seneviratne S, Sewall C, Shackley F, Simeoni I, Smith KGC, Staples E, Stauss H, Steele C, Thaventhiran J, Thomas M, Thrasher A, Welch S, Willcocks L, Workman S, Worth A, Yeatman N, Yong P, Ashford S, Bradley J, Fletcher D, Hammerton T, James R, Kingston N, Ouwehand W, Penkett C, Raymond FL, Stirrups K, Veltman M, Young T, Brown M, Clements-Brod N, Davis J, Dewhurst E, Erwood M, Frary A, Linger R, Martin J, Papadia S, Rehnstrom K, Astle W, Attwood A, Bleda M, Carss K, Daugherty L, Deevi S, Graf S, Greene D, Halmagyi C, Haimel M, Hu F, Matser V, Meacham S, Megy K, Shamardina O, Titterton C, Tuna S, Turro E, Yu P, von Ziegenweldt J, Furnell A, Mapeta R, Staines S, Stephens J, Whitehorn D, Rayner-Matthews P, Watt C]] , Loss-of-function nuclear factor kappa B subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans. J ALLERGY CLIN IMMUN 2018;142 (4):1285-1296 [PubMed]
  • Oud MM, Tuijnenburg P, Hempel M, van Vlies N, Ren Z, Ferdinandusse S, Jansen MH, Santer R, Johannsen J, Bacchelli C, Alders M, Li R, Davies R, Dupuis L, Cale CM, Wanders RJA, Pals ST, Ocaka L, James C, Müller I, Lehmberg K, Strom T, Engels H, Williams HJ, Beales P, Roepman R, Dias P, Brunner HG, Cobben JM, Hall C, Hartley T, Le Quesne Stabej P, Mendoza-Londono R, Davies EG, de Sousa SB, Lessel D, Arts HH, Kuijpers TW, Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome. AM J HUM GENET 2017;100 (2):281-296 [PubMed]
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