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M. de Boer
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Journal Articles

Four novel mutations in the gene encoding gp91- phox of human NADPH oxidase: consequences for oxidase assembly

J. H. W. Leusen, C. Meischl, M. H. M. Eppink, P. M. Hilarius, M. de Boer, R. S. Weening, A. Åhlin, L. Sanders, D. Goldblatt, H. Skopczynska, E. Bernatowska, J. Palmblad, A. J. Verhoeven, W. J. H. van Berkel, D. Roos
Journal: Blood
Blood (2000) 95 (2): 666–673.
https://doi.org/10.1182/blood.V95.2.666
Published: 2000
Journal Articles

Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease

D Roos, M de Boer, F Kuribayashi, C Meischl, RS Weening, AW Segal, A Ahlin, K Nemet, JP Hossle, E Bernatowska-Matuszkiewicz, H Middleton-Price
Journal: Blood
Blood (1996) 87 (5): 1663–1681.
https://doi.org/10.1182/blood.V87.5.1663.1663
Published: 1996
Journal Articles

Autosomal recessive chronic granulomatous disease with absence of the 67-kD cytosolic NADPH oxidase component: identification of mutation and detection of carriers

M de Boer, PM Hilarius-Stokman, JP Hossle, AJ Verhoeven, N Graf, RT Kenney, R Seger, D Roos
Journal: Blood
Blood (1994) 83 (2): 531–536.
https://doi.org/10.1182/blood.V83.2.531.531
Published: 1994
Journal Articles

Synergy between cyclosporin A and a monoclonal antibody to B7 in blocking alloantigen-induced T-cell activation

SW Van Gool, JL Ceuppens, H Walter, M de Boer
Journal: Blood
Blood (1994) 83 (1): 176–183.
https://doi.org/10.1182/blood.V83.1.176.176
Published: 1994
Journal Articles

The B7/BB1 antigen is expressed by Reed-Sternberg cells of Hodgkin's disease and contributes to the stimulating capacity of Hodgkin's disease-derived cell lines

J Delabie, JL Ceuppens, P Vandenberghe, M de Boer, L Coorevits, C De Wolf- Peeters
Journal: Blood
Blood (1993) 82 (9): 2845–2852.
https://doi.org/10.1182/blood.V82.9.2845.2845
Published: 1993
Journal Articles

A novel syndrome of severe neutrophil dysfunction: unresponsiveness confined to chemotaxin-induced functions

D Roos, TW Kuijpers, F Mascart-Lemone, L Koenderman, M de Boer, R van Zwieten, AJ Verhoeven
Journal: Blood
Blood (1993) 81 (10): 2735–2743.
https://doi.org/10.1182/blood.V81.10.2735.2735
Published: 1993
Journal Articles

Splice site mutations are a common cause of X-linked chronic granulomatous disease

M de Boer, BG Bolscher, MC Dinauer, SH Orkin, CI Smith, A Ahlin, RS Weening, D Roos
Journal: Blood
Blood (1992) 80 (6): 1553–1558.
https://doi.org/10.1182/blood.V80.6.1553.1553
Published: 1992
Journal Articles

Point mutations in the beta-subunit of cytochrome b558 leading to X- linked chronic granulomatous disease

BG Bolscher, M de Boer, A de Klein, RS Weening, D Roos
Journal: Blood
Blood (1991) 77 (11): 2482–2487.
https://doi.org/10.1182/blood.V77.11.2482.2482
Published: 1991
Journal Articles

Immunologic detection of endothelial cells in human whole blood

R Sbarbati, M de Boer, M Marzilli, M Scarlattini, G Rossi, JA van Mourik
Journal: Blood
Blood (1991) 77 (4): 764–769.
https://doi.org/10.1182/blood.V77.4.764.764
Published: 1991