Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Delfien J. Bogaert"'
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/436bccef86fe4f9980ee19089d6b4fee
Autor:
Manfred Fliegauf, Matias Kinnunen, Sara Posadas-Cantera, Nadezhda Camacho-Ordonez, Hassan Abolhassani, Laia Alsina, Faranaz Atschekzei, Delfien J. Bogaert, Siobhan O. Burns, Joseph A. Church, Gregor Dückers, Alexandra F. Freeman, Lennart Hammarström, Leif Gunnar Hanitsch, Tessa Kerre, Robin Kobbe, Svetlana O. Sharapova, Kathrin Siepermann, Carsten Speckmann, Sophie Steiner, Nisha Verma, Jolan E. Walter, Emma Westermann-Clark, Sigune Goldacker, Klaus Warnatz, Markku Varjosalo, Bodo Grimbacher
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Most of the currently known heterozygous pathogenic NFKB1 (Nuclear factor kappa B subunit 1) variants comprise deleterious defects such as severe truncations, internal deletions, and frameshift variants. Collectively, these represent the most frequen
Externí odkaz:
https://doaj.org/article/d9245bd92ea94ce499ebc30f5a9fab14
Autor:
Delfien J. Bogaert, Melissa Dullaers, Hye Sun Kuehn, Bart P. Leroy, Julie E. Niemela, Hans De Wilde, Sarah De Schryver, Marieke De Bruyne, Frauke Coppieters, Bart N. Lambrecht, Frans De Baets, Sergio D. Rosenzweig, Elfride De Baere, Filomeen Haerynck
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Abstract Syndromic primary immunodeficiencies are rare genetic disorders that affect both the immune system and other organ systems. More often, the immune defect is not the major clinical problem and is sometimes only recognized after a diagnosis ha
Externí odkaz:
https://doaj.org/article/f68a77738ec346f0b26833713134e241
Autor:
Annelies Emmaneel, Delfien J. Bogaert, Sofie Van Gassen, Simon J. Tavernier, Melissa Dullaers, Filomeen Haerynck, Yvan Saeys
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Common variable immunodeficiency (CVID) is one of the most frequently diagnosed primary antibody deficiencies (PADs), a group of disorders characterized by a decrease in one or more immunoglobulin (sub)classes and/or impaired antibody responses cause
Externí odkaz:
https://doaj.org/article/a959fc49fb094dddbdb6939d452789f2
Autor:
Marieke De Bruyne, Levi Hoste, Delfien J. Bogaert, Lien Van den Bossche, Simon J. Tavernier, Eef Parthoens, Mélanie Migaud, Deborah Konopnicki, Jean Cyr Yombi, Bart N. Lambrecht, Sabine van Daele, Ana Karina Alves de Medeiros, Lieve Brochez, Rudi Beyaert, Elfride De Baere, Anne Puel, Jean-Laurent Casanova, Jean-Christophe Goffard, Savvas N. Savvides, Filomeen Haerynck, Jens Staal, Melissa Dullaers
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Background: Inherited CARD9 deficiency constitutes a primary immunodeficiency predisposing uniquely to chronic and invasive fungal infections. Certain mutations are shown to negatively impact CARD9 protein expression and/or NF-κB activation, but the
Externí odkaz:
https://doaj.org/article/0ba87f23952c42b5b2b177471ecb035f
Autor:
Manfred, Fliegauf, Matias, Kinnunen, Sara, Posadas-Cantera, Nadezhda, Camacho-Ordonez, Hassan, Abolhassani, Laia, Alsina, Faranaz, Atschekzei, Delfien J, Bogaert, Siobhan O, Burns, Joseph A, Church, Gregor, Dückers, Alexandra F, Freeman, Lennart, Hammarström, Leif Gunnar, Hanitsch, Tessa, Kerre, Robin, Kobbe, Svetlana O, Sharapova, Kathrin, Siepermann, Carsten, Speckmann, Sophie, Steiner, Nisha, Verma, Jolan E, Walter, Emma, Westermann-Clark, Sigune, Goldacker, Klaus, Warnatz, Markku, Varjosalo, Bodo, Grimbacher
Publikováno v:
Frontiers in immunology. 13
Most of the currently known heterozygous pathogenic