Martin de Boer
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Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease
HMP D Roos, M de Boer, F Kuribayashi, C Meischl, R S Weening, A W Segal, A ...
Blood 87 (5), 1663-81, 1996
Human neutrophil immunodeficiency syndrome is associated with an inhibitory Rac2 mutation
DR Ambruso, C Knall, AN Abell, J Panepinto, A Kurkchubasche, ...
Proceedings of the National Academy of Sciences 97 (9), 4654-4659, 2000
Leukocyte adhesion deficiency type 1 (LAD-1)/variant. A novel immunodeficiency syndrome characterized by dysfunctional beta2 integrins.
TW Kuijpers, RA Van Lier, D Hamann, M de Boer, LY Thung, RS Weening, ...
The Journal of clinical investigation 100 (7), 1725-1733, 1997
LAD-1/variant syndrome is caused by mutations in FERMT3
TW Kuijpers, E van de Vijver, MAJ Weterman, M de Boer, ATJ Tool, ...
Blood 113 (19), 4740-4746, 2009
Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura
WB Breunis, E van Mirre, M Bruin, J Geissler, M de Boer, M Peters, ...
Blood 111 (3), 1029-1038, 2008
[8] Purification and cryopreservation of phagocytes from human blood
D Roos, M de Boer
Methods in enzymology 132, 225-243, 1986
Hematologically important mutations: X-linked chronic granulomatous disease (third update)
D Roos, DB Kuhns, A Maddalena, J Roesler, JA Lopez, T Ariga, T Avcin, ...
Blood Cells, Molecules, and Diseases 45 (3), 246-265, 2010
Copy number variation at the FCGR locus includes FCGR3A, FCGR2C and FCGR3B but not FCGR2A and FCGR2B
WB Breunis, E van Mirre, J Geissler, N Laddach, G Wolbink, ...
Human mutation 30 (5), E640-E650, 2009
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)
D Roos, DB Kuhns, A Maddalena, J Bustamante, C Kannengiesser, ...
Blood Cells, Molecules, and Diseases 44 (4), 291-299, 2010
Interaction between human neutrophils and zymosan particles: the role of opsonins and divalent cations.
D Roos, AA Bot, ML Van Schaik, M De Boer, MR Daha
The Journal of Immunology 126 (2), 433-440, 1981
Molecular diagnosis of chronic granulomatous disease
D Roos, M de Boer
Clinical & Experimental Immunology 175 (2), 139-149, 2014
Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients
MY Köker, Y Camcıoğlu, K Van Leeuwen, SŞ Kılıç, I Barlan, M Yılmaz, ...
Journal of allergy and clinical immunology 132 (5), 1156-1163. e5, 2013
Hematologically important mutations: leukocyte adhesion deficiency (first update)
E Van De Vijver, A Maddalena, Ö Sanal, SM Holland, G Uzel, ...
Blood Cells, Molecules, and Diseases 48 (1), 53-61, 2012
Evidence consistent with human L1 retrotransposition in maternal meiosis I
B Brouha, C Meischl, E Ostertag, M De Boer, Y Zhang, H Neijens, D Roos, ...
The American Journal of Human Genetics 71 (2), 327-336, 2002
Specific leukotriene formation by purified human eosinophils and neutrophils
J Verhagen, PLB Bruynzeel, JA Koedam, G Aryan Wassink, M de Boer, ...
FEBS letters 168 (1), 23-28, 1984
Point mutations in the β-subunit of cytochrome b558 leading to X-linked chronic granulomatous disease
BGJM Bolscher, M de Boer, A de Klein, RS Weening, D Roos
Blood 77 (11), 2482-2487, 1991
Metabolic comparison between basophils and other leukocytes from human blood.
M De Boer, D Roos
The Journal of Immunology 136 (9), 3447-3454, 1986
Prevalence, genetics and clinical presentation of chronic granulomatous disease in Sweden
A Åhlin, M De Boer, D Roos, J Leusen, CIE Smith, U Sundin, H Rabbani, ...
Acta paediatrica 84 (12), 1386-1394, 1995
A point mutation in gp91-phox of cytochrome b558 of the human NADPH oxidase leading to defective translocation of the cytosolic proteins p47-phox and p67-phox.
JH Leusen, M de Boer, BG Bolscher, PM Hilarius, RS Weening, HD Ochs, ...
The Journal of clinical investigation 93 (5), 2120-2126, 1994
Epac1‐Rap1 signaling regulates monocyte adhesion and chemotaxis
MJ Lorenowicz, J van Gils, M de Boer, PL Hordijk, M Fernandez‐Borja
Journal of leukocyte biology 80 (6), 1542-1552, 2006
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