受强制性开放获取政策约束的文章 - Martin de Boer了解详情
无法在其他位置公开访问的文章：1 篇
Rhizopus oryzae skin infection treated with posaconazole in a boy with chronic granulomatous disease
JG Wildenbeest, MW Oomen, RJ Brüggemann, M de Boer, Y Bijleveld, ...
The Pediatric infectious disease journal 29 (6), 578, 2010
强制性开放获取政策： US National Institutes of Health
可在其他位置公开访问的文章：18 篇
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
强制性开放获取政策： US National Institutes of Health
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
强制性开放获取政策： US National Institutes of Health
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
强制性开放获取政策： US National Institutes of Health
Combined immunodeficiency with severe inflammation and allergy caused by ARPC1B deficiency
TW Kuijpers, ATJ Tool, I van der Bijl, M de Boer, M Van Houdt, ...
Journal of Allergy and Clinical Immunology 140 (1), 273-277. e10, 2017
强制性开放获取政策： Cancer Research UK
Inherited p40phox deficiency differs from classic chronic granulomatous disease
A Van De Geer, A Nieto-Patlán, DB Kuhns, ATJ Tool, AA Arias, M Bouaziz, ...
The Journal of clinical investigation 128 (9), 3957-3975, 2018
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research …
Molecular basis of glutathione reductase deficiency in human blood cells
NM Kamerbeek, R van Zwieten, M de Boer, G Morren, H Vuil, N Bannink, ...
Blood 109 (8), 3560-3566, 2007
强制性开放获取政策： German Research Foundation
Extensive Ethnic Variation and Linkage Disequilibrium at the FCGR2/3 Locus: Different Genetic Associations Revealed in Kawasaki Disease
SQ Nagelkerke, CE Tacke, WB Breunis, MWT Tanck, J Geissler, E Png, ...
Frontiers in immunology 10, 185, 2019
强制性开放获取政策： Royal Netherlands Academy of Arts and Sciences
Genetic variation of human neutrophil Fcγ receptors and SIRPα in antibody‐dependent cellular cytotoxicity towards cancer cells
LW Treffers, XW Zhao, J van der Heijden, SQ Nagelkerke, DJ van Rees, ...
European journal of immunology 48 (2), 344-354, 2018
强制性开放获取政策： Dutch Cancer Society
Hematologically important mutations: the autosomal forms of chronic granulomatous disease (third update)
D Roos, K Van Leeuwen, AP Hsu, DL Priel, A Begtrup, R Brandon, ...
Blood Cells, Molecules, and Diseases 92, 102596, 2021
强制性开放获取政策： US National Institutes of Health, Scientific and Technological Research …
MKL1 deficiency results in a severe neutrophil motility defect due to impaired actin polymerization
EGG Sprenkeler, SSV Henriet, ATJ Tool, IC Kreft, I van der Bijl, CEM Aarts, ...
Blood, The Journal of the American Society of Hematology 135 (24), 2171-2181, 2020
强制性开放获取政策： European Commission, Netherlands Organisation for Health Research and …
Defective AP-3-dependent VAMP8 trafficking impairs Weibel-Palade body exocytosis in Hermansky-Pudlak Syndrome type 2 blood outgrowth endothelial cells
E Karampini, M Schillemans, M Hofman, F van Alphen, M de Boer, ...
Haematologica 104 (10), 2091, 2019
强制性开放获取政策： European Hematology Association, Netherlands
Nonallelic homologous recombination of the FCGR2/3 locus results in copy number variation and novel chimeric FCGR2 genes with aberrant functional expression
MBTWK S Q Nagelkerke, C E Tacke, W B Breunis, J Geissler, J W R Sins, B ...
Genes and Immunity, 2015
强制性开放获取政策： Royal Netherlands Academy of Arts and Sciences
Rapid genetic analysis of X-linked chronic granulomatous disease by high-resolution melting
HR Hill, NH Augustine, RJ Pryor, GH Reed, JD Bagnato, AE Tebo, ...
The Journal of Molecular Diagnostics 12 (3), 368-376, 2010
强制性开放获取政策： US National Institutes of Health
Hermansky–Pudlak syndrome type 2: Aberrant pre‐mRNA splicing and mislocalization of granule proteins in neutrophils
M de Boer, K van Leeuwen, J Geissler, F van Alphen, E de Vries, ...
Human mutation 38 (10), 1402-1411, 2017
强制性开放获取政策： US National Institutes of Health
Alternative trafficking of Weibel‐Palade body proteins in CRISPR/Cas9‐engineered von Willebrand factor–deficient blood outgrowth endothelial cells
M Schillemans, M Kat, J Westeneng, A Gangaev, M Hofman, B Nota, ...
Research and practice in thrombosis and haemostasis 3 (4), 718-732, 2019
强制性开放获取政策： European Hematology Association, Netherlands
Identification of genetic biomarkers for alloimmunization in sickle cell disease
SM Meinderts, JJ Gerritsma, JWR Sins, M de Boer, K van Leeuwen, ...
British journal of haematology 186 (6), 887-899, 2019
强制性开放获取政策： Agence Nationale de la Recherche
Two CGD families with a hypomorphic mutation in the activation domain of p67phox
D Roos, JD van Buul, ATJ Tool, JD Matute, CM Marchal, BH Hayee, ...
Journal of clinical & cellular immunology 5 (3), 2014
强制性开放获取政策： US National Institutes of Health
Complex medical history of a patient with a compound heterozygous mutation in C1QC
R Lubbers, LJJ Beaart-van de Voorde, K van Leeuwen, M de Boer, ...
Lupus 28 (10), 1255-1260, 2019
强制性开放获取政策： Netherlands Organisation for Scientific Research, Netherlands Organisation …
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