Researcher
Delfien Bogaert
- Disciplines:Palliative care and end-of-life care, Laboratory medicine, Other translational sciences, Regenerative medicine, Nursing, Other clinical sciences, Other basic sciences, Other paramedical sciences, Other health sciences, Other medical and health sciences
Affiliations
- Department of Internal medicine (Department)
Member
From1 Oct 2013 → 30 Sep 2017
Projects
1 - 1 of 1
- Use of an integrative classification system and next-generation sequencing strategies for gene identification in common variable immunodeficiency disorder (CVID).From1 Oct 2013 → 30 Sep 2017Funding: FWO fellowships, BOF - Other initiatives
Publications
21 - 30 of 52
- Ikaros family zinc finger 1 regulates dendritic cell development and function in humans(2018)Volume: 48
Authors: U. Cytlak, A. Resteu, Delfien Bogaert, H. S. Kuehn, T. Altmann, A. Gennery, G. Jackson, A. Kumanovics, Melissa Dullaers, J. Reichenbach, et al.
Pages: 189 - 189 - A novel IKAROS haploinsufficiency kindred with unexpectedly late and variable B-cell maturation defects(2018)
Authors: Delfien Bogaert, Hye Sun Kuehn, Katherine R Calvo, Arnaud Vanlander, Marieke De Bruyne, Urszula Cytlak, Venetia Bigley, Frans De Baets, Sergio D Rosenzweig, Filomeen Haerynck, et al.
Pages: 432 - 435 - A CARD9 founder mutation disrupts NF-κB signaling by inhibiting BCL10 and MALT1 recruitment and signalosome formation(2018)
Authors: Marieke De Bruyne, Levi Hoste, Delfien Bogaert, Lien Van den Bossche, Eef Parthoens, Mélanie Migaud, Deborah Konopnicki, Jean Cyr Yombi, Ana Alves de Medeiros, Lieve Brochez, et al.
- Primary antibody deficiencies from bedside to bench : the role of molecular diagnostics(2018)
Authors: Delfien Bogaert
Number of pages: 1 - Molecular diagnosis of Common Variable Immunodeficiency and related antibody disorders : an integrated immunological and genetic approach(2018)
Authors: Delfien Bogaert
Pages: 38 - 39 - A novel LPS-responsive beige-like anchor protein (LRBA) mutation presents with normal cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and overactive TH17 immunity(2018)
Authors: Marieke De Bruyne, Delfien Bogaert, Lien Van den Bossche, Lisa Roels, Els van de Vijver, Ann Driessen, Marielle van Gijn, Laura Gámez-Diaz, Bodo Grimbacher, Filomeen Haerynck, et al.
Pages: 1968 - 1971 - Early-onset primary antibody deficiency resembling common variable immunodeficiency challenges the diagnosis of Wiedeman-Steiner and Roifman syndromes(2017)
Authors: Delfien Bogaert, Melissa Dullaers, Hye Sun Kuehn, Julie E Niemela, Hans De Wilde, Sarah De Schryver, Marieke De Bruyne, Frans De Baets, Sergio D Rosenzweig, Filomeen Haerynck
- Molecular genetics of common variable immunodeficiency(2017)
Authors: Delfien Bogaert, Melissa Dullaers, Elfride De Baere, Filomeen Haerynck
Number of pages: 1 - To B or not to B matured : a novel IKAROS haploinsufficiency kindred with unexpectedly late and variable B cell maturation defects(2017)
Authors: Delfien Bogaert, Hye Sun Kuehn, Katherine Calvo, Arnaud Vanlander, Marieke De Bruyne, Urszula Cytlak, Venetia Bigley, Frans De Baets, Sergio Rosenzweig, Filomeen Haerynck, et al.
Number of pages: 1 - Molecular diagnosis of Common Variable Immunodeficiency and related antibody disorders : an integrated immunological and genetic approach(2017)
Authors: Delfien Bogaert