Dirk Roos

Q: What Schools Are Affiliated With Dirk Roos

Dirk Roos is affiliated with the following schools: University of Amsterdam, Nagasaki University, Tel Aviv University, Eindhoven University of Technology, Delft University of Technology, University of Pennsylvania

Dirk Roos's AcademicInfluence.com Rankings

Dirk Roos

Computer Science

#3643

World Rank

#3827

Historical Rank

Artificial Intelligence

#701

World Rank

#712

Historical Rank

Database

#965

World Rank

#1014

Historical Rank

computer-science Degrees

Download Badge

Computer Science

Dirk Roos's Degrees

PhD Computer Science University of Amsterdam
Masters Artificial Intelligence University of Amsterdam
Bachelors Computer Science University of Amsterdam

Similar Degrees You Can Earn

Why Is Dirk Roos Influential?

(Suggest an Edit or Addition)

(See a Problem?)

Dirk Roos's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Complement and immunoglobulins stimulate superoxide production by human leukocytes independently of phagocytosis. (1975) (713)
Chronic Granulomatous Disease: The European Experience (2009) (623)
Neutrophils: Between Host Defence, Immune Modulation, and Tissue Injury (2015) (521)
Human neutrophil immunodeficiency syndrome is associated with an inhibitory Rac2 mutation. (2000) (466)
Membrane surface antigen expression on neutrophils: a reappraisal of the use of surface markers for neutrophil activation. (1991) (460)
Human neutrophils lose their surface Fc gamma RIII and acquire Annexin V binding sites during apoptosis in vitro. (1995) (454)
Fc gammaRIIIa-158V/F polymorphism influences the binding of IgG by natural killer cell Fc gammaRIIIa, independently of the Fc gammaRIIIa-48L/R/H phenotype. (1997) (442)
The Pi-linked receptor FcRIII is released on stimulation of neutrophils (1988) (409)
Monitoring human basophil activation via CD63 monoclonal antibody 435. (1991) (380)
Oxidative killing of microbes by neutrophils. (2003) (354)
Brominating oxidants generated by human eosinophils. (1986) (335)
Functional characterization of mitochondria in neutrophils: a role restricted to apoptosis (2004) (334)
Cleavage of CXCR1 on neutrophils disables bacterial killing in cystic fibrosis lung disease (2007) (328)
Single-cell Raman and fluorescence microscopy reveal the association of lipid bodies with phagosomes in leukocytes. (2005) (297)
Changes in the carbohydrate metabolism of mitogenically stimulated human peripheral lymphocytes. I. Stimulation by phytohaemagglutinin. (1970) (271)
Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease. (1996) (270)
Invasive fungal infection and impaired neutrophil killing in human CARD9 deficiency. (2013) (256)
Quantitative aspects of the production of superoxide radicals by phagocytizing human granulocytes. (1975) (248)
Hematologically important mutations: X-linked chronic granulomatous disease (third update). (1997) (234)
Vascular-endothelial-cadherin modulates endothelial monolayer permeability. (1999) (233)
Leukocyte adhesion deficiency type 1 (LAD-1)/variant. A novel immunodeficiency syndrome characterized by dysfunctional beta2 integrins. (1997) (224)
Neutrophil Fc gamma RIIIb deficiency, nature, and clinical consequences: a study of 21 individuals from 14 families. (1995) (222)
Neutrophil migration across monolayers of cytokine-prestimulated endothelial cells: a role for platelet-activating factor and IL-8 (1992) (221)
LAD-1/variant syndrome is caused by mutations in FERMT3. (2009) (219)
CXCR2 mediates NADPH oxidase–independent neutrophil extracellular trap formation in cystic fibrosis airway inflammation (2010) (216)
Characterization and quantification of the peroxidase in human monocytes. (1978) (214)
Purification and cryopreservation of phagocytes from human blood. (1986) (211)
Oxygen consumption of phagocytizing cells in human leukocyte and granulocyte preparations: a comparative study. (1974) (209)
Platelet activation during preparation of platelet concentrates: a comparison of the platelet‐rich plasma and the buffy coat methods (1990) (208)
Infiltrated Neutrophils Acquire Novel Chemokine Receptor Expression and Chemokine Responsiveness in Chronic Inflammatory Lung Diseases (2008) (205)
Functional activity of enucleated human polymorphonuclear leukocytes (1983) (203)
Granulocyte colony-stimulating factor administration to healthy volunteers: analysis of the immediate activating effects on circulating neutrophils. (1994) (201)
Neutrophil and monocyte adherence to and migration across monolayers of cytokine-activated endothelial cells: the contribution of CD18, ELAM-1, and VLA-4. (1991) (199)
Differences in oxygen metabolism of phagocytosing monocytes and neutrophils. (1978) (198)
The 40-kDa Fc gamma receptor (FcRII) on human neutrophils is essential for the IgG-induced respiratory burst and IgG-induced phagocytosis. (1989) (194)
Production of hydrogen peroxide by phagocytizing human granulocytes. (1975) (194)
Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease (1996) (190)
Neutrophils Kill Antibody-Opsonized Cancer Cells by Trogoptosis. (2018) (189)
Human NLRP3 inflammasome activation is Nox1-4 independent. (2010) (188)
Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura. (2008) (184)
Actin filament polymerization regulates gliding motility by apicomplexan parasites. (2003) (183)
Soluble Fc gamma receptor III in human plasma originates from release by neutrophils. (1990) (182)
Detection of platelet activation with monoclonal antibodies and flow cytometry. Changes during platelet storage (1990) (176)
Increased Nox2 expression in human cardiomyocytes after acute myocardial infarction (2003) (175)
Reactive oxygen species are required for the phagocytosis of myelin by macrophages (1998) (173)
Biallelic neutrophil Na-antigen system is associated with a polymorphism on the phospho-inositol-linked Fc gamma receptor III (CD16). (1990) (171)
Complement receptor 3, not Dectin-1, is the major receptor on human neutrophils for beta-glucan-bearing particles. (2009) (171)
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update). (2000) (170)
Characterization of two monoclonal antibodies against cytochrome b558 of human neutrophils. (1989) (169)
Neutrophil activation in sickle cell disease (1999) (168)
Granulocyte colony-stimulating factor inhibits the mitochondria-dependent activation of caspase-3 in neutrophils. (2002) (168)
CD66 nonspecific cross-reacting antigens are involved in neutrophil adherence to cytokine-activated endothelial cells (1992) (167)
Copy number variation at the FCGR locus includes FCGR3A, FCGR2C and FCGR3B but not FCGR2A and FCGR2B (2009) (166)
Effect of tumor necrosis factor-induced integrin activation on Fc gamma receptor II-mediated signal transduction: relevance for activation of neutrophils by anti-proteinase 3 or anti-myeloperoxidase antibodies. (1995) (164)
Changes in the carbohydrate metabolism of mitogenically stimulated human peripheral lymphocytes. II. Relative importance of glycolysis and oxidative phosphorylation on phytohaemagglutinin stimulation. (1973) (163)
Role of endothelial leukocyte adhesion molecule-1 and platelet-activating factor in neutrophil adherence to IL-1-prestimulated endothelial cells. Endothelial leukocyte adhesion molecule-1-mediated CD18 activation. (1991) (159)
Evidence for small intracellular vesicles in human blood phagocytes containing cytochrome b558 and the adhesion molecule CD11b/CD18. (1993) (155)
Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. (2013) (146)
The Genetic Basis of Chronic Granulomatous Disease (1994) (144)
Hematologically important mutations: leukocyte adhesion deficiency (first update). (2012) (144)
γ-β-Thalassaemia studies showing that deletion of the γ- and δ-genes influences β-globin gene expression in man (1980) (144)
Two independent killing mechanisms of Candida albicans by human neutrophils: evidence from innate immunity defects. (2014) (142)
Phosphatidylinositol-linked FcRIII mediates exocytosis of neutrophil granule proteins, but does not mediate initiation of the respiratory burst. (1990) (141)
Mitochondrial Membrane Potential in Human Neutrophils Is Maintained by Complex III Activity in the Absence of Supercomplex Organisation (2008) (139)
Molecular diagnosis of chronic granulomatous disease (2014) (138)
Divergent effects of tumor necrosis factor α on apoptosis of human neutrophils (2001) (138)
Protection of phagocytic leukocytes by endogenous glutathione: studies in a family with glutathione reductase deficiency. (1979) (136)
Current Concepts of Hyperinflammation in Chronic Granulomatous Disease (2011) (134)
Tumor necrosis factor α induces a caspase-independent death pathway in human neutrophils (2003) (134)
Interactions between the components of the human NADPH oxidase: intrigues in the phox family. (1996) (132)
Human Neutrophils Use Different Mechanisms To Kill Aspergillus fumigatus Conidia and Hyphae: Evidence from Phagocyte Defects (2016) (131)
Intracellular expression of reactive oxygen species-generating NADPH oxidase NOX4 in normal and cancer thyroid tissues. (2010) (130)
Deficient alternative complement pathway activation due to factor D deficiency by 2 novel mutations in the complement factor D gene in a family with meningococcal infections. (2006) (130)
Perilesional neurochemical changes in focal epilepsies (1996) (127)
Maternal genomic neutrophil FcRIII deficiency leading to neonatal isoimmune neutropenia. (1990) (126)
Refractive index sensing of green fluorescent proteins in living cells using fluorescence lifetime imaging microscopy. (2008) (126)
Binding characteristics of dimeric IgG subclass complexes to human neutrophils. (1989) (124)
Interaction between human neutrophils and zymosan particles: the role of opsonins and divalent cations. (1981) (124)
Rapid genotyping of blood group antigens by multiplex polymerase chain reaction and DNA microarray hybridization (2005) (117)
Evidence consistent with human L1 retrotransposition in maternal meiosis I. (2002) (115)
Nucleotide profiles of normal human blood cells determined by high-performance liquid chromatography. (1985) (111)
Effect of acute hyperglycaemia and/or hyperinsulinaemia on proinflammatory gene expression, cytokine production and neutrophil function in humans (2008) (111)
Metabolic comparison between basophils and other leukocytes from human blood. (1986) (109)
Apoptosis of Neutrophils (2003) (109)
Cutting Edge: Infection by the Agent of Human Granulocytic Ehrlichiosis Prevents the Respiratory Burst by Down-Regulating gp91phox1 (2000) (109)
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. (1994) (108)
Natural history and early diagnosis of LAD-1/variant syndrome. (2007) (108)
The Fc gamma RIIIA-158F allele is a risk factor for systemic lupus erythematosus (1998) (107)
Familial deficiency of glutathione reductase in human blood cells. (1976) (107)
Chronic granulomatous disease. (2016) (107)
Divergent effects of tumor necrosis factor alpha on apoptosis of human neutrophils. (2000) (107)
Assembly and activation of the NADPH:O2 oxidoreductase in human neutrophils after stimulation with phorbol myristate acetate. (1990) (106)
156Pro-->Gln substitution in the light chain of cytochrome b558 of the human NADPH oxidase (p22-phox) leads to defective translocation of the cytosolic proteins p47-phox and p67-phox (1994) (105)
A new exon created by intronic insertion of a rearranged LINE-1 element as the cause of chronic granulomatous disease (2000) (105)
Protection of human neutrophils by endogenous catalase: studies with cells from catalase-deficient individuals. (1980) (105)
Purified protein kinase C phosphorylates a 47-kDa protein in control neutrophil cytoplasts but not in neutrophil cytoplasts from patients with the autosomal form of chronic granulomatous disease. (1988) (104)
Neutrophils in Barth syndrome (BTHS) avidly bind annexin-V in the absence of apoptosis. (2004) (104)
A family with complement factor D deficiency. (2001) (103)
Prevalence, genetics and clinical presentation of chronic granulomatous disease in Sweden (1995) (101)
Changes in the carbohydrate metabolism of mitogenically stimulated human peripheral lymphocytes. 3. Stimulation by tuberculin and allogeneic cells. (1973) (101)
Apoptotic neutrophils in the circulation of patients with glycogen storage disease type 1b (GSD1b). (2003) (101)
Repression of rac2 mRNA Expression by Anaplasma phagocytophila Is Essential to the Inhibition of Superoxide Production and Bacterial Proliferation1 (2002) (100)
A triallelic Fc gamma receptor type IIIA polymorphism influences the binding of human IgG by NK cell Fc gamma RIIIa. (1996) (99)
Limitations on the use of dihydrorhodamine 123 for flow cytometric analysis of the neutrophil respiratory burst. (1996) (99)
Inborn defects in the antioxidant systems of human red blood cells. (2014) (99)
Point mutations in the beta-subunit of cytochrome b558 leading to X-linked chronic granulomatous disease. (1991) (97)
FcγRIIIB Gene Duplication: Evidence for Presence and Expression of Three Distinct FcγRIIIB Genes in NA(1+,2+)SH(+) Individuals (1998) (97)
How neutrophils kill fungi (2016) (97)
Primary immunodeficiency mutation databases. (2001) (94)
PU.1 as an essential activator for the expression of gp91(phox) gene in human peripheral neutrophils, monocytes, and B lymphocytes. (1998) (94)
Apoptosis of neutrophils (2004) (92)
NADPH oxidase(s): new source(s) of reactive oxygen species in the vascular system? (2002) (91)
Extracellular proton release by stimulated neutrophils. (1981) (91)
TLR Expression on Neutrophils at the Pulmonary Site of Infection: TLR1/TLR2-Mediated Up-Regulation of TLR5 Expression in Cystic Fibrosis Lung Disease1 (2008) (91)
Chronic granulomatous disease in Israel: clinical, functional and molecular studies of 38 patients. (2008) (90)
Hematologic abnormalities in Shwachman Diamond syndrome: lack of genotype-phenotype relationship. (2005) (89)
Phagocytosing human neutrophils inactivate their own granular enzymes. (1981) (89)
Cytokine-activated endothelial cells internalize E-selectin into a lysosomal compartment of vesiculotubular shape. A tubulin-driven process. (1994) (86)
Molecular basis and enzymatic properties of glucose 6-phosphate dehydrogenase volendam, leading to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections. (1999) (85)
Disturbed interaction of p21-rac with mutated p67-phox causes chronic granulomatous disease (1996) (84)
Combined immunodeficiency with severe inflammation and allergy caused by ARPC1B deficiency. (2017) (84)
Synergism between eosinophil cationic protein and oxygen metabolites in killing of schistosomula of Schistosoma mansoni. (1987) (84)
Ficoll-isopaque gradients for the determination of density distributions of human blood lymphocytes and other reticulo-endothelial cells. (1974) (84)
Continuous therapy with sulfamethoxazole-trimethoprim in patients with chronic granulomatous disease. (1983) (83)
1-O-hexadecyl-2-Q-methylglycerol, a novel inhibitor of protein kinase C, inhibits the respiratory burst in human neutrophils. (1989) (83)
Location of the Epitope for 7D5, a Monoclonal Antibody Raised against Human Flavocytochrome b558, to the Extracellular Peptide Portion of Primate gp91phox (2001) (82)
Unusual late presentation of X-linked chronic granulomatous disease in an adult female with a somatic mosaic for a novel mutation in CYBB. (2005) (82)
Interactions between the components of the human NADPH oxidase: a review about the intrigues in the phox family. (1996) (81)
Hematologically important mutations: leukocyte adhesion deficiency. (2001) (81)
Bid Truncation, Bid/Bax Targeting to the Mitochondria, and Caspase Activation Associated with Neutrophil Apoptosis Are Inhibited by Granulocyte Colony-Stimulating Factor (2004) (81)
Dual mechanisms in priming of the chemoattractant-induced respiratory burst in human granulocytes. A Ca2+-dependent and a Ca2+-independent route. (1989) (80)
Intracellular Chemical Imaging of Heme-Containing Enzymes Involved in Innate Immunity Using Resonance Raman Microscopy (2004) (80)
Purification and partial characterization of the b-type cytochrome from human polymorphonuclear leukocytes. (1985) (79)
A phosphoprotein of Mr 47,000, defective in autosomal chronic granulomatous disease, copurifies with one of two soluble components required for NADPH:O2 oxidoreductase activity in human neutrophils. (1989) (78)
Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patients (2017) (77)
Interactions between the cytosolic components p47phox and p67phox of the human neutrophil NADPH oxidase that are not required for activation in the cell-free system (1995) (77)
X-CGDbase: a database of X-CGD-causing mutations. (1996) (77)
C-reactive protein enhances IgG-mediated phagocyte responses and thrombocytopenia. (2015) (76)
Cytochrome b deficiency in an autosomal form of chronic granulomatous disease. A third form of chronic granulomatous disease recognized by monocyte hybridization. (1985) (76)
Activation of AP-1 through reactive oxygen species by angiotensin II in rat cardiomyocytes. (2005) (75)
Complementation in monocyte hybrids revealing genetic heterogeneity in chronic granulomatous disease (1984) (73)
Pathogenesis of diseases associated with antineutrophil cytoplasm autoantibodies. (2004) (73)
Inherited p40phox deficiency differs from classic chronic granulomatous disease (2018) (72)
Dynamics of Transcription Regulation in Human Bone Marrow Myeloid Differentiation to Mature Blood Neutrophils (2018) (71)
Mannan-binding lectin (MBL)-mediated opsonization is enhanced by the alternative pathway amplification loop. (2006) (71)
Differential activation of human basophils by anti‐IgE and formyl‐methionyl‐leucylphenylalanine. Indications for protein kinase C‐dependent and ‐independent activation pathways (1991) (71)
Mannose-Binding Lectin (MBL) Facilitates Opsonophagocytosis of Yeasts but Not of Bacteria despite MBL Binding1 (2008) (71)
Neutrophil Fc-gamma receptors: a two-way bridge in the immune system. (1990) (70)
Heterotypic FcγR Clusters Evoke a Synergistic Ca2+ Response in Human Neutrophils (*) (1995) (69)
Studies on the incorporation of precursors into purine and pyrimidine nucleotides via 'de novo' and 'salvage' pathways in normal lymphocytes and lymphoblastic cell-line cells. (1989) (69)
Influence of tyrosine phosphorylation on protein interaction with FcγRIIa (1997) (68)
Association of all three types of Fc gamma R (CD64, CD32, and CD16) with a gamma-chain homodimer in cultured human monocytes. (1993) (67)
Effect of ascorbate on abnormal neutrophil, platelet and lymphocytic function in a patient with the Chediak-Higashi syndrome. (1981) (65)
Anion-exchange high performance liquid chromatography method for the quantitation of nucleotides in human blood cells. (1985) (65)
Intramitochondrial serine protease activity of Omi/HtrA2 is required for caspase-independent cell death of human neutrophils (2004) (63)
Defective initiation of the metabolic stimulation in phagocytizing granulocytes: a new congenital defect. (1976) (63)
β 1 integrin activation on human neutrophils promotes β 2 integrin‐mediated adhesion to fibronectin (2001) (63)
Evidence for transformation-related increase in CTP synthetase activity in situ in human lymphoblastic leukemia. (1993) (62)
Characterization of four CD18 mutants in leucocyte adhesion deficient (LAD) patients with differential capacities to support expression and function of the CD11/CD18 integrins LFA‐1, Mac‐1 and p150,95 (2001) (62)
Neutrophil migration across monolayers of resting or cytokine-activated endothelial cells. Role of intracellular calcium changes and fusion of specific granules with the plasma membrane. (1992) (62)
Sequential migration of neutrophils across monolayers of endothelial and epithelial cells (2000) (62)
Chronic granulomatous disease with partial deficiency of cytochrome b 558 and incomplete respiratory burst: variants of the X‐linked, cytochrome b 558–negative form of the disease (1992) (60)
Clinical differences in chronic granulomatous disease in patients with cytochrome b-negative or cytochrome b-positive neutrophils. (1985) (60)
Continuous Translocation of Rac2 and the NADPH Oxidase Component p67phox during Phagocytosis* (2004) (60)
Tumor necrosis factor alpha induces a caspase-independent death pathway in human neutrophils. (2003) (60)
Copy number variation of the activating FCGR 2 C gene predisposes to idiopathic thrombocytopenic purpura (2008) (59)
Expression of myeloperoxidase (MPO) by neutrophils is necessary for their activation by anti‐neutrophil cytoplasm autoantibodies (ANCA) against MPO (2003) (59)
Oxygen Intermediates and the Microbicidal Event (1980) (58)
Immunologic studies with LFA-1- and Mo1-deficient lymphocytes from a patient with recurrent bacterial infections. (1985) (58)
Homocysteine-Induced Apoptosis in Endothelial Cells Coincides With Nuclear NOX2 and Peri-nuclear NOX4 Activity (2011) (58)
Cytochrome b, flavins, and ubiquinone-50 in enucleated human neutrophils (polymorphonuclear leukocyte cytoplasts). (1984) (58)
Gene-scan method for the recognition of carriers and patients with p47(phox)-deficient autosomal recessive chronic granulomatous disease. (2001) (58)
Intracellular events in anti-IgE nonreleasing human basophils. (1992) (58)
Dysregulation of innate immune receptors on neutrophils in chronic granulomatous disease. (2008) (57)
Soluble Fc-y Receptor Ill in Human Plasma Originates from Release by Neutrophils (57)
A missense mutation in the heavy subunit of gamma-glutamylcysteine synthetase gene causes hemolytic anemia. (2000) (57)
Priming of the respiratory burst in human eosinophils is accompanied by changes in signal transduction. (1990) (57)
Polarized secretion of interleukin-8 by human mesothelial cells: a role in neutrophil migration. (1995) (56)
The plasma concentration of soluble Fc‐gamma RIII is related to production of neutrophils (1994) (56)
Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox). (1992) (56)
Parenteral lipids modulate leukocyte phenotypes in whole blood, depending on their fatty acid composition. (2005) (56)
Tyrosine phosphorylation-dependent activation of phosphatidylinositide 3-kinase occurs upstream of Ca2+-signalling induced by Fcgamma receptor cross-linking in human neutrophils. (1997) (56)
Large-scale purification and cryopreservation of human monocytes. (1981) (55)
fMet-Leu-Phe-induced activation of phospholipase D in human neutrophils. Dependence on changes in cytosolic free Ca2+ concentration and relation with respiratory burst activation. (1991) (55)
Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase (2006) (55)
Ischemia induces nuclear NOX2 expression in cardiomyocytes and subsequently activates apoptosis (2006) (55)
Human eosinophils express, relative to other circulating leukocytes, large amounts of secretory 14-kD phospholipase A2. (1998) (55)
Granulocytes without degranulation: neutrophil function in granule-depleted cytoplasts. (1983) (55)
Seven new mutations in the nicotinamide adenine dinucleotide reduced-cytochrome b(5) reductase gene leading to methemoglobinemia type I. (2001) (55)
Deconjugation kinetics of glucuronidated phase II flavonoid metabolites by beta-glucuronidase from neutrophils. (2010) (55)
Neutrophil responsiveness to IgG, as determined by fixed ratios of mRNA levels for activating and inhibitory FcgammaRII (CD32), is stable over time and unaffected by cytokines. (2006) (54)
Eosinophils do respond to fMLP. (1987) (54)
Changes in the levels of glutathione in phagocytosing human neutrophils. (1980) (54)
Characterization of the peroxidase in human eosinophils. (1980) (53)
Continuous cell activation is necessary for stable interaction of complement receptor type 3 with its counter‐structure in the aggregation response of human neutrophils (1990) (53)
Delayed but functional neutrophil extracellular trap formation in neonates. (2009) (53)
Different proteolytic mechanisms involved in FcγRIIIb shedding from human neutrophils (2001) (53)
Leukocyte adhesion deficiency-type 1 (LAD-1)/variant: A novel immunodeficiency syndrome characterized by dysfunctional β2 integrins (1997) (52)
Hematologically important mutations: X-linked chronic granulomatous disease (second update). (2001) (52)
Characterization of the interaction of human eosinophils and neutrophils with opsonized particles. (1985) (52)
Homocysteine affects cardiomyocyte viability: concentration-dependent effects on reversible flip-flop, apoptosis and necrosis (2007) (52)
Transmigration of human neutrophils across airway epithelial cell monolayers is preferentially in the physiologic basolateral-to-apical direction. (1996) (51)
Heterogeneity in Chronic Granulomatous Disease Detected With an Improved Nitroblue Tetrazolium Slide Test (1986) (51)
Neutrophil Transmigration across Monolayers of Endothelial Cells and Airway Epithelial Cells Is Regulated by Different Mechanisms a (1996) (51)
Medium-chain, triglyceride-containing lipid emulsions increase human neutrophil beta2 integrin expression, adhesion, and degranulation. (2000) (51)
Granulocyte concentrates: prolonged functional capacity during storage in the presence of phenotypic changes (2008) (50)
Localization of the low-Mr subunit of cytochrome b558 in human blood phagocytes by immunoelectron microscopy. (1990) (50)
Monitoring of platelet morphology during storage of platelet concentrates (1989) (49)
The activity of one soluble component of the cell-free NADPH:O2 oxidoreductase of human neutrophils depends on guanosine 5'-O-(3-thio)triphosphate. (1990) (49)
Fc gamma receptors of phagocytes. (1995) (48)
A novel splice variant of FcγRIIa: a risk factor for anaphylaxis in patients with hypogammaglobulinemia. (2013) (48)
Autosomal recessive chronic granulomatous disease with absence of the 67-kD cytosolic NADPH oxidase component: identification of mutation and detection of carriers. (1994) (48)
Triple role of platelet-activating factor in eosinophil migration across monolayers of lung epithelial cells: eosinophil chemoattractant and priming agent and epithelial cell activator. (1998) (47)
The Fc gammaRIIIA-158F allele is a risk factor for systemic lupus erythematosus. (1998) (47)
Molecular basis of glutathione reductase deficiency in human blood cells. (2007) (47)
Splice site mutations are a common cause of X-linked chronic granulomatous disease (1992) (46)
Induction of neutrophil FC-gamma receptor I expression can be used as a marker for biologic activity of recombinant interferon-gamma in vivo. (1991) (46)
Defects in the oxidative killing of microorganisms by phagocytic leukocytes. (1978) (46)
An analysis of genetic variation across the MBL2 locus in Dutch Caucasians indicates that 3′ haplotypes could modify circulating levels of mannose-binding lectin (2005) (45)
The molecular basis of chronic granulomatous disease (2004) (45)
Functional Epitope on Human Neutrophil Flavocytochrome b5581 (2003) (45)
Interference of PR3‐ANCA with the enzymatic activity of PR3: differences in patients during active disease or remission of Wegener's granulomatosis (2002) (44)
Four novel mutations in the gene encoding gp91-phox of human NADPH oxidase: consequences for oxidase assembly. (2000) (44)
Leukocyte membrane adhesion proteins LFA-1, CR3 and p150,95: a review of functional and regulatory aspects. (1989) (44)
Genetic analysis of patients with leukocyte adhesion deficiency: genomic sequencing reveals otherwise undetectable mutations. (2002) (44)
Innate immune receptors on neutrophils and their role in chronic lung disease (2009) (44)
Cross-linking of the carcinoembryonic antigen-like glycoproteins CD66 and CD67 induces neutrophil aggregation. (1993) (43)
Therapeutic strategy in p47-phox deficient chronic granulomatous disease presenting as inflammatory bowel disease. (2010) (43)
Killing of schistosomula by taurine chloramine and taurine bromamine. (1987) (43)
NA‐phenotype‐dependent differences in neutrophil FcγRIIIb expression cause differences in plasma levels of soluble FcγRIII (1996) (43)
Calcium signalling is altered in myeloid cells with a deficiency in NADPH oxidase activity (2003) (42)
A single dose of granulocyte-macrophage colony-stimulating factor induces systemic interleukin-8 release and neutrophil activation in healthy volunteers. (1996) (42)
Application of a human multidrug transporter (ABCG2) variant as selectable marker in gene transfer to progenitor cells. (2003) (41)
The Rh complex exports ammonium from human red blood cells (2003) (41)
Distinct adhesive properties of granulocytes and monocytes to endothelial cells under static and stirred conditions. (1990) (40)
Fc gamma RIIIB gene duplication: evidence for presence and expression of three distinct Fc gamma RIIIB genes in NA(1+,2+)SH(+) individuals. (1998) (40)
A patient with nucleoside phosphorylase deficiency, selective t-cell deficiency, and autoimmune hemolytic anemia. (1978) (40)
Bactericidal action of eosinophils from normal human blood (1986) (39)
Deletion of leucine 61 in glucose-6-phosphate dehydrogenase leads to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections. (2002) (39)
Granulocyte-macrophage colony-stimulating factor, interleukin-3 (IL-3), and IL-5 greatly enhance the interaction of human eosinophils with opsonized particles by changing the affinity of complement receptor type 3. (1994) (38)
Eosinophils isolated with two different methods show different characteristics of activation. (1995) (38)
Clinical and laboratory work-up of patients with neutrophil shortage or dysfunction. (1999) (38)
Immunocytochemical discovery of the 22- to 23-Kd subunit of cytochrome b558 at the surface of human peripheral phagocytes. (1988) (38)
Primary Immunodeficiency Caused by an Exonized Retroposed Gene Copy Inserted in the CYBB Gene (2014) (38)
Effect of cytochalasin B on the oxidative metabolism of human peripheral blood granulocytes. (1976) (38)
Oxidative killing of microorganisms by phagocytic cells (1977) (37)
Complement Receptor 3 and Toll-Like Receptor 4 Act Sequentially in Uptake and Intracellular Killing of Unopsonized Salmonella enterica Serovar Typhimurium by Human Neutrophils (2007) (37)
Release of azurophilic granule contents in fMLP-stimulated neutrophils requires two activation signals, one of which is a rise in cytosolic free Ca2+. (1991) (37)
A three‐dimensional model system to study the interactions between human leukocytes and endothelial cells (1990) (37)
The Respiratory Burst of Phagocytic Leucocytes (1991) (37)
Purification of eosinophils from normal human blood, preparation of eosinoplasts and characterization of their functional response to various stimuli. (1987) (36)
Stimulation of human basophils results in homotypic aggregation. A response independent of degranulation. (1993) (36)
Neutrophil adherence to and migration across monolayers of human peritoneal mesothelial cells. The role of mesothelium in the influx of neutrophils during peritonitis. (1996) (36)
15 – Oxidative Stress in Human Neutrophilic Granulocytes: Host Defence and Self-Defence (1985) (36)
Plasma levels of mannan-binding lectin in relation to periodontitis and smoking. (2005) (35)
Effect of phytohaemagglutinin on the carbohydrate metabolism of human blood lymphocytes after inhibition of the oxidative phosphorylation. (1973) (35)
Excretion of superoxide by phagocytes measured with cytochrome c entrapped in resealed erythrocyte ghosts. (1984) (35)
Inherited Glutathione Reductase Deficiency and Plasmodium falciparum Malaria—A Case Study (2009) (35)
Effects of structurally different lipid emulsions on human neutrophil migration. (1999) (35)
Soluble Fc gamma RIIIa is present in plasma and is derived from natural killer cells. (1994) (35)
Characterization of two subsets of human T gamma cells. (1982) (34)
The 47-kDa protein involved in the NADPH:O2 oxidoreductase activity of human neutrophils is phosphorylated by cyclic AMP-dependent protein kinase without induction of a respiratory burst. (1988) (34)
SIRPα controls the activity of the phagocyte NADPH oxidase by restricting the expression of gp91(phox). (2012) (34)
Detection of carriers of the autosomal form of chronic granulomatous disease. (1988) (33)
[Paroxysmal nocturnal hemoglobinuria]. (1992) (33)
Kinetics and mechanism of the bactericidal action of human neutrophils against Escherichia coli (1984) (33)
The protective role of glutathione (1979) (33)
Mutations of chronic granulomatous disease in Turkish families (2007) (32)
Point mutations in the promoter region of the CYBB gene leading to mild chronic granulomatous disease (2000) (32)
In vitro Evaluation of Buffy‐Coat‐Derived Platelet Concentrates Stored in a Synthetic Medium 1 (1991) (32)
Impaired killing of Candida albicans by granulocytes mobilized for transfusion purposes: a role for granule components (2016) (32)
Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutations (2009) (32)
Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous disease (2009) (31)
Immunodeficiency mutation databases (1996) (31)
Priming of human eosinophils by platelet-activating factor enhances the number of cells able to bind and respond to opsonized particles. (1992) (31)
Imbalance in the nucleotide pools of myeloid leukemia cells and HL-60 cells: correlation with cell-cycle phase, proliferation, differentiation, and transformation. (1987) (31)
Actin Polymerization Induces Shedding of FcγRIIIb (CD16) from Human Neutrophils (1999) (31)
Organelle-depleted human neutrophil cytoplasts used to study fmet-leu-phe receptor modulation and cell function. (1984) (31)
Resonance Raman imaging of the NADPH oxidase subunit cytochrome b558 in single neutrophilic granulocytes. (2003) (31)
The involvement of oxygen radicals in microbicidal mechanisms of leukocytes and macrophages (1991) (31)
Hyper-reactive PMNs in FcγRIIa 131 H/H genotype periodontitis patients (2007) (31)
Clinical value of soluble IgG Fc receptor type III in plasma from patients with chronic idiopathic neutropenia. (1998) (30)
Detection of gp91-phox precursor protein in B-cell lines from patients with X-linked chronic granulomatous disease as an indicator for mutations impairing cytochrome b558 biosynthesis. (1996) (30)
Skewing of X‐chromosome inactivation in three generations of carriers with X‐linked chronic granulomatous disease within one family (2006) (30)
Functional analysis of two-amino acid substitutions in gp91phox in a patient with X-linked flavocytochrome b558-positive chronic granulomatous disease by means of transgenic PLB-985 cells (2004) (30)
Beta1 integrin activation on human neutrophils promotes beta2 integrin-mediated adhesion to fibronectin. (2001) (30)
Growth factors G-CSF and GM-CSF differentially preserve chemotaxis of neutrophils aging in vitro. (2007) (29)
Mannose-Binding Lectin (MBL) Substitution: Recovery of Opsonic Function In Vivo Lags behind MBL Serum Levels1 (2009) (29)
Characteristics of CR3-mediated aggregation in human eosinophils: effect of priming by platelet-activating factor. (1991) (29)
Some enzymatic characteristics of eosinophil peroxidase from patients with eosinophilia and from healthy donors (1981) (28)
H9c2 cardiomyoblasts produce thyroid hormone. (2008) (28)
Expression and intracellular localization of the human N-acetylmuramyl-L-alanine amidase, a bacterial cell wall-degrading enzyme. (1997) (28)
T lymphocyte characteristics in bone marrow-transplanted patients. I. Changes in biochemical properties that correlate with the immunologic reconstitution. (1981) (28)
An improved method for the purification of basophilic granulocytes from human blood. (1992) (28)
Regulation and kinetics of platelet‐activating factor and leukotriene C4 synthesis by activated human basophils (2003) (28)
Platelet‐activating factor (PAF) acts as an intercellular messenger in the changes of cytosolic free Ca2+ in human neutrophils induced by opsonized particles (1989) (28)
Nicotinamide-adenine dinucleotide phosphate oxidase assembly and activation in EBV-transformed B lymphoblastoid cell lines of normal and chronic granulomatous disease patients. (1998) (27)
The effect of salmeterol and nimesulide on chemotaxis and synthesis of PAF and LTC4 by human eosinophils. (1996) (27)
The Oxidative Metabolism of Monocytes (1980) (27)
Imbalance in the ribonucleotide pools of lymphoid cells from acute lymphoblastic leukemia patients. (1986) (27)
Involvement of a metalloprotease in the shedding of human neutrophil Fc gammaRIIIB. (1997) (27)
Involvement of Fcγ receptors and β2 integrins in neutrophil activation by anti‐proteinase‐3 or anti‐myeloperoxidase antibodies (2003) (27)
Influence of corticosteroids on human polymorphonuclear leukocyte function in vitro (1976) (27)
Enzyme analysis of lymphoproliferative diseases: a useful addition to cell surface phenotyping. (1983) (27)
Prenatal diagnosis in two families with autosomal, p47phox‐deficient chronic granulomatous disease due to a novel point mutation in NCF1 (2002) (27)
The anti-FcγRIII MAb 3G8 induces neutrophil activation via a cooperative action of FcγRIIIb and FcγRIIa (1997) (26)
Stored Platelets Release Nucleotides as Inhibitors of Platelet Function (1992) (26)
The Release of Hydrogen Peroxide from Mononuclear Phagocytes and its Role in Extracellular Cytolysis (1980) (26)
Epitope identification for human neutrophil flavocytochrome b monoclonals 48 and 449 (2000) (25)
Mechanisms regulating eosinophil extravasation in asthma. (1996) (25)
Priming by tumor necrosis factor‐α of human neutrophil NADPH‐oxidase activity induced by anti‐proteinase‐3 or anti‐myeloperoxidase antibodies (2006) (25)
Diurnal Fluctuation of Leukocyte G6PD Activity. A Possible Explanation for the Normal Neutrophil Bactericidal Activity and the Low Incidence of Pyogenic Infections in Patients with Severe G6PD Deficiency in Israel (2004) (24)
Depletion of Dense Granule Nucleotides during Storage of Human Platelets (1990) (24)
Acute lymphoblastic leukemia in a patient with chronic granulomatous disease and a novel mutation in CYBB: First report (2005) (24)
Influence of peroperative lavage solutions on peritoneal defence mechanisms in vitro. (1999) (24)
Hyper-reactive PMNs in FcgammaRIIa 131 H/H genotype periodontitis patients. (2007) (23)
Oxidative metabolism of mononuclear phagocytes (1980) (23)
Degranulation of human basophils by picomolar concentrations of IL-3, IL-5, or granulocyte-macrophage colony-stimulating factor. (1998) (23)
Rapid genetic analysis of x-linked chronic granulomatous disease by high-resolution melting. (2010) (23)
1,2‐Diacylglycerol accumulation in human neutrophils does not correlate with respiratory burst activation (1989) (23)
Characterization of hereditary partial myeloperoxidase deficiency. (1982) (23)
Lessons Learned from Phagocytic Function Studies in a Large Cohort of Patients with Recurrent Infections (2012) (23)
[Hemoglobinopathies and thalassemias]. (1982) (23)
A rapid turbidimetric assay of phagocytosis and serum opsonizing capacity. (1989) (23)
Peritoneal interleukin-8 in acute appendicitis. (1996) (22)
Release of platelet-activating factor is important for the respiratory burst induced in human eosinophils by opsonized particles. (1992) (22)
Complement fragments C3b and iC3b coupled to latex induce a respiratory burst in human neutrophils. (1990) (22)
The role of basophils in allergic disease. (1996) (21)
Alu‐repeat–induced deletions within the NCF2 gene causing p67‐phox–deficient chronic granulomatous disease (CGD) (2010) (21)
Different unequal cross-over events between NCF1 and its pseudogenes in autosomal p47(phox)-deficient chronic granulomatous disease. (2013) (21)
Glutathione-dependent dehydroascorbate reduction: a determinant of dehydroascorbate uptake by human polymorphonuclear leukocytes. (1980) (21)
Chronic Granulomatous Disease: A 25-Year Patient Registry Based on a Multistep Diagnostic Procedure, from the Referral Center for Primary Immunodeficiencies in Greece (2013) (21)
Phagocytosis and degradation of DNA‐anti‐DNA complexes by human phagocytes I. Assay conditions, quantitative aspects and differences between human blood monocytes and neutrophils (1981) (21)
The impact of platelet‐activating factor (PAF)‐like mediators on the functional activity of neutrophils: anti‐inflammatory effects of human PAF‐acetylhydrolase (2001) (21)
Endogenous catalase protects human blood phagocytes against oxidative damage by extracellularly generated hydrogen peroxide. (1980) (21)
Hermansky–Pudlak syndrome type 2: Aberrant pre‐mRNA splicing and mislocalization of granule proteins in neutrophils (2017) (21)
Visceral Leishmaniasis and Other Severe Infections in an Adult Patient with p47-phox-Deficient Chronic Granulomatous Disease (2000) (20)
A novel mutation in the DIA1 gene in a patient with methemoglobinemia type II (2005) (20)
β-Globin mutation detection by tagged single-base extension and hybridization to universal glass and flow-through microarrays (2004) (20)
Isolation and partial characterization of a novel subset of human T lymphocytes defined by monoclonal antibodies. (1982) (20)
Cytotoxic Activity of Human Monocytes Towards Sensitized Red Cells is not Dependent on the Generation of Reactive Oxygen Species (1979) (20)
FcγRIIIa-158V/F polymorphism influences the binding of IgG by NK cell FcγRIIIa, independent of the FcγRIIIa-48L/R/H phenotype (1997) (19)
Activation of Human Granulocytes by Intravenous Immunoglobulin Preparations Is Mediated by FcγRII and FcγRIII Receptors (2000) (19)
Development of systemic lupus erythematosus in a young child affected with chronic granulomatous disease following withdrawal of treatment with interferon-gamma. (2003) (19)
Tyrosine phosphorylation of a gamma-chain homodimer associated with Fc gamma RIII (CD16) in cultured human monocytes. (1993) (19)
Splice site mutations are a common cause of X-linked chronic granulomatous disease. (1992) (19)
Pyruvate kinase and the "high ATP syndrome". (1984) (19)
Chronic Granulomatous Disease. (2019) (19)
Characterization of physically different human T-cell subsets with monoclonal antibodies and biochemical markers. (1981) (19)
Molecular Basis of Autosomal Recessive Chronic Granulomatous Disease in Iran (2010) (19)
Common Infections and Target Organs Associated with Chronic Granulomatous Disease in Iran (2019) (18)
A Novel Syndrome of Severe Neutrophil Dysfunction: Unresponsiveness Confined to Chemotaxin-Induced Functions (1993) (18)
Mannose-Binding Lectin (MBL) Substitution: Recovery of Opsonic Function In Vivo Lags behind MBL Serum Levels (2009) (18)
Extensive Variation in Gene Copy Number at the Killer Immunoglobulin-Like Receptor Locus in Humans (2013) (18)
Decreased redox state in red blood cells from patients with sarcoidosis. (2002) (18)
An EPR study of myeloperoxidase in human granulocytes. (1976) (17)
Isopycnic centrifugation of antigen-activated human blood lymphocytes in the early phase of in vitro stimulation. (1974) (17)
Actin polymerization induces shedding of FcgammaRIIIb (CD16) from human neutrophils. (1999) (17)
Celiac disease and pulmonary hemosiderosis in a patient with chronic granulomatous disease (2004) (17)
Release of Superoxide Anion by Macrophages: Effect of in Vivo or in Vitro Priming (1980) (17)
Kinetics and mechanism of the bactericidal action of human neutrophils against Escherichia coli. (1984) (17)
Increased Nox 2 expression in human cardiomyocytes after acute myocardial infarction (2003) (17)
Functional and genetic characterization of two extremely rare cases of Williams–Beuren Syndrome associated with chronic granulomatous disease (2013) (17)
Basophils from patients with allergic asthma show a primed phenotype. (1999) (17)
Lymphadenopathy After BCG Vaccination in a Child with Chronic Granulomatous Disease (2004) (17)
A 40‐base‐pair duplication in the gp91‐phox gene leading to X‐linked chronic granulomatous disease (1993) (16)
In vivo destruction of erythrocytes by complement-binding and non-complement-binding antibodies. (1980) (16)
gamma-beta-Thalassaemia studies showing that deletion of the gamma- and delta-genes influences beta-globin gene expression in man. (1980) (16)
Interleukin-5 Potentiates Sulfidopeptide Leukotriene Production by Human Eosinophils (1994) (16)
An easy, specific and sensitive assay for the determination of the catalase activity of human blood cells. (1980) (16)
Recurrent pyoderma gangrenosum and cystic acne associated with leucocyte adhesion deficiency due to novel mutations in ITGB2: successful treatment with infliximab and adalimumab. (2015) (16)
T FcRIIIA158F allele is a risk factor for systemic lupus erythematosus (1998) (16)
G→T transition at cDNA nt 110 (K37Q) in the PKLR (pyruvate kinase) gene is the molecular basis of a case of hereditary increase of red blood cell ATP (1997) (15)
Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1 (2013) (15)
Retraction: CXCR2 mediates NADPH oxidase–independent neutrophil extracellular trap formation in cystic fibrosis airway inflammation (2011) (15)
Phospholipase D-derived phosphatidic acid is involved in the activation of the CD11b/CD18 integrin in human eosinophils. (1999) (14)
Influence of tyrosine phosphorylation on protein interaction with FcgammaRIIa. (1997) (14)
Dose-response of lymphocyte carbohydrate metabolism to phytohaemagglutinin. (1972) (14)
Characterization of the peroxidase in human eosinophils. (1980) (13)
Genetical Analysis of All Danish Patients Diagnosed with Chronic Granulomatous Disease (2012) (13)
Biallelic Neutrophil Na-Antigen System Is Associated With a Polymorphism on the Phospho-Inositol-Linked Fcy Receptor 111 (CD16) (2003) (13)
Low beta-adrenergic receptor concentration on human thymocytes. (1983) (13)
Neutrophils enhance eosinophil migration across monolayers of lung epithelial cells (2001) (12)
Single-cell optical imaging of the phagocyte NADPH oxidase. (2006) (12)
Preparation and cryopreservation of cytoplasts from human phagocytes. (1986) (12)
PU . 1 as an essential activator for the expression of gp 91 phox gene in human peripheral neutrophils , monocytes , and B lymphocytes ( gene expression y chronic granulomatous disease ) (1998) (12)
Expression and Intracellular Localization of the Human N-acetylmuramyl-L- alanine Amidase, a Bacterial Cell Wall - Degrading Enzyme (1997) (11)
Somatic triple mosaicism in a carrier of X-linked chronic granulomatous disease. (1998) (11)
Erratum to: Chronic Granulomatous Disease: A 25-Year Patient Registry Based on a Multistep Diagnostic Procedure, from the Referral Center for Primary Immunodeficiencies in Greece (2013) (11)
A novel syndrome of severe neutrophil dysfunction: unresponsiveness confined to chemotaxin-induced functions. (1993) (11)
Sensitive on-line radioactivity measurements with a heterogeneous flow-cell: application to lymphoid cell ribonucleotides separated by high-performance liquid chromatography. (1987) (11)
Lipid effects on neutrophil calcium signaling induced by opsonized particles: platelet activating factor is only part of the story. (2004) (11)
Stimulus secretion coupling in human basophilic granulocytes (1993) (11)
activation of caspase-3 in neutrophils Granulocyte colony-stimulating factor inhibits the mitochondria-dependent (2013) (11)
A founder effect for p47(phox)Trp193Ter chronic granulomatous disease in Kavkazi Jews. (2015) (11)
Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update). (2021) (11)
Involvement of Fcgamma receptors and beta2 integrins in neutrophil activation by anti-proteinase-3 or anti-myeloperoxidase antibodies. (2003) (11)
Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girl. (1999) (10)
Hematologically important mutations: X-linked chronic granulomatous disease (fourth update). (2021) (10)
Two CGD Families with a Hypomorphic Mutation in the Activation Domain of p67phox. (2014) (10)
Mutation in an exonic splicing enhancer site causing chronic granulomatous disease. (2017) (10)
NA-phenotype-dependent differences in neutrophil Fc gamma RIIIb expression cause differences in plasma levels of soluble Fc gamma RIII. (1996) (10)
Effect of interferon‐γ, in vitro and in vivo, on mRNA levels of phagocyte oxidase components (1996) (10)
A donor splice site mutation in intron 1 of CYBA, leading to chronic granulomatous disease. (2005) (9)
Two X-Linked Chronic Granulomatous Disease Patients with Unusual NADPH Oxidase Properties (2011) (9)
Purine and pyrimidine metabolism of normal and leukemic lymphocytes. (1989) (9)
Very early onset inflammatory bowel disease: Investigation of the IL-10 signaling pathway in Iranian children. (2017) (9)
Cytotoxic activity of human monocytes towards sensitized red cells is not dependent on the generation of reactive oxygen species. (1979) (9)
Chronic granulomatous disease: mutations in cytochrome b558. (1993) (9)
Protection of human neutrophils against oxidative damage (1980) (8)
Detection of gp 91-phox precursor protein in B-cell lines from patients with X-linked chronic granulomatous disease as an indicator for mutations impairing cytochrome b 558 biosynthesis (1996) (8)
Congenital deficiency of leukocyte-adherence glycoproteins: a familial defect. (1987) (8)
Changes in the carbohydrate metabolism of mitogenically stimulated human peripheral lymphocytes. 3. Stimulation by tuberculin and allogenic cells. (1973) (8)
Generation of reactive oxygen species by phagocytes (1992) (8)
Gene mutations responsible for primary immunodeficiency disorders: A report from the first primary immunodeficiency biobank in Iran (2016) (8)
Proinflammatory cytokine response toward fungi but not bacteria in chronic granulomatous disease. (2016) (8)
Cryopreservation of enucleated human neutrophils (PMN cytoplasts) (1984) (8)
Differential mechanisms in the stimulus-secretion coupling in human basophils: Evidence for a protein-kinase-C-dependent and a protein-kinase-C-independent route (1990) (8)
A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation (2009) (8)
Genetic Characteristics, Infectious, and Noninfectious Manifestations of 32 Patients with Chronic Granulomatous Disease (2020) (7)
Identification of allele-specific p22-phox mutations in a compound heterozygous patient with chronic granulomatous disease by mismatch PCR and restriction enzyme analysis (1994) (7)
Activation of human granulocytes by intravenous immunoglobulin preparations is mediated by FcgammaRII and FcgammaRIII receptors. (2000) (7)
The anti-Fc gamma RIII mAb 3G8 induces neutrophil activation via a cooperative actin of Fc gamma RIIIb and Fc gamma RIIa. (1997) (7)
Neutrophils: the Power Within (2004) (7)
Postmortem diagnosis of chronic granulomatous disease: how worthwhile is it? (2005) (7)
The search for a genetic defect in Polish patients with chronic granulomatous disease. (2004) (7)
An adult autosomal recessive chronic granulomatous disease patient with pulmonary Aspergillus terreus infection (2018) (6)
Genetic Analysis of 13 Iranian Families With Leukocyte Adhesion Deficiency Type 1 (2019) (6)
Mutations in cis that affect mRNA synthesis, processing and translation. (2021) (6)
A metabolic comparison between human blood monocytes and neutrophils. (1979) (6)
Loss of Thrombin-Induced Ca2+ Mobilization in a Subpopulation of Platelets during Storage (1991) (6)
Molecular events during phagocyte stimulation. (1981) (6)
Comparison between the chromate inhibition test and a cytochemical method for the determination of glucose-6-phosphate dehydrogenase deficiency in erythrocytes. (1989) (6)
Phosphatidyl-inositol-linked CD14 is involved in priming of human neutrophils by lipopolysaccharide (LPS), but not in the inactivation of LPS. (1994) (6)
Dissociation of phagocytosis, metabolic stimulation and lysosomal enzyme release in human leukocytes (1976) (6)
Mutation characterization and heterodimer analysis of patients with leukocyte adhesion deficiency: Including one novel mutation. (2017) (6)
FcgRIIIB Gene Duplication: Evidence for Presence and Expression of Three Distinct FcgRIIIB Genes in NA(11,21)SH(1) Individuals (1998) (6)
A novel polymorphism in the coding region of CYBB, the human gp91-phox gene (1996) (6)
Leukocyte extravasation: mechanisms and consequences. (1993) (6)
H 9 c 2 cardiomyoblasts produce thyroid hormone (2008) (5)
Effects of Oxygen on Metabolic Patterns and Endocytosis of Macrophages (1980) (5)
Phagocytosis and degradation of DNA-anti-DNA complexes by human phagocytes: influence of the antibody class. (1982) (5)
Adenosine Receptors on Human T Lymphocytes and Human Thymocytes (1986) (5)
Abnormal nucleotide pattern in the eosinophils of a patient with acute lymphoblastic leukemia associated with eosinophilia. (1986) (5)
Fc-gamma receptors: mediators, targets and markers of disease. (1991) (5)
Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe Experience (2021) (5)
411 Charaterization of the role of Ca2+ in the stimulation of human basophilic granulocytes (1991) (5)
Reactivity differences among human T cells from blood and lymphoid organs, analysed by limiting dilution: correlation with specific gravity and binding of peanut lectin. (1981) (5)
Clinical and laboratory findings in patients with leukocyte adhesion deficiency type I: A multicenter study in Turkey (2021) (5)
Restoration of the neutrophil chemotactic responsiveness by levamisole treatment in patients with recurrent infections, eczema and hyperimmunoglobulinaemia E (1977) (5)
Membrane Dynamics and Organization of the Phagocyte NADPH Oxidase in PLB-985 Cells (2020) (5)
Successful treatment with percutaneous transhepatic alcoholization of a liver abscess in a child with chronic granulomatous disease. (2011) (5)
Phagocytosis and degradation of DNA-antiDNA complexes by human phagocytes. Influence of rheumatoid factors. (1981) (5)
Disturbed Interaction of p 21-rac with Mutated p 67-phox Causes Chronic Granulomatous Disease (2003) (5)
Membrane surface antigen expression on human monocytes: changes during purification, in vitro activation and transmigration across monolayers of endothelial cells (1992) (5)
A false-carrier state for the c.579G>A mutation in the NCF1 gene in Ashkenazi Jews (2018) (5)
NAD(P)H oxidase in the failing human heart. (2003) (4)
Neutrophils, eosinophils, and basophils in the skin immune system (1997) (4)
Prenatal diagnosis of chronic granulomatous disease in a male fetus. (2009) (4)
Nimesulide Inhibits Platelet-Activating Factor Synthesis in Activated Human Neutrophils (2012) (4)
RIIIa, Independently of the Fc γ Killer Cell Fc RIIIa-158V/F Polymorphism Influences the Binding of IgG by Natural γ Fc (2013) (4)
Oxidative damage to lysosomal enzymes in human phagocytosing neutrophils. (1982) (4)
[Determination of spectrin in erythrocytes: an important aid in the diagnosis of hereditary spherocytosis]. (1995) (4)
Response: Adherence to the LAD variant form (2007) (4)
Analysis of Chronic Granulomatous Disease in the Kavkazi Population in Israel Reveals Phenotypic Heterogeneity in Patients with the Same NCF1 mutation (c.579G>A) (2018) (4)
Pyrimidine 5'-nucleotidase deficiency: improved detection of carriers. (1989) (4)
Chronic granulomatous disease of childhood: an unusual cause of recurrent uncommon infections in a 61‐year‐old man (2011) (4)
Inhibited by Granulocyte Associated with Neutrophil Apoptosis Are Mitochondria, and Caspase Activation Bid Truncation, Bid/Bax Targeting to the (2013) (4)
Alu repeat-induced deletions in chronic granulomatous disease: a cause not only for p67-phox, but also for p47-phox deficiency (2013) (4)
Activation of cryptic splice sites in three patients with chronic granulomatous disease (2019) (4)
Phenylglyoxal is not a selective inhibitor of phagocytosis. (1979) (4)
Neutrophil antigens, from bench to bedside. (1995) (4)
NUCLEOSIDE-PHOSPHORYLASE DEFICIENCY, AUTOIMMUNE HAEMOLYTIC ANAE MIA AND SELECTIVE T-CELL DEFICIENCY (1978) (3)
[Hemolytic anemia caused by pyrimidine-5'-nucleotidase deficiency]. (1988) (3)
Cytokine-prestimulated Endothelial Cells: A RoleforPlateletActivating Factor and IL-8 (1992) (3)
CD18, ELAM-1, and VLA-4 of monolayers of cytokine-activated endothelial cells: the contribution Neutrophil and monocyte adherence to and migration across (2011) (3)
Deficiency of pyrimidine 5′-nucleotidase in human leukocytes (1989) (3)
Influence of Complement Components on the Size and the Opsonization of DNA‐Anti‐DNA Complexes (1982) (3)
Rare Duplication or Deletion of Exons 6, 7 and 8 in CYBB Leading to X-Linked Chronic Granulomatous Disease in Two Patients from Different Families (2012) (3)
Innate immunity — phagocytes, natural killer cells and the complement system (2005) (3)
Limited influence of the mesothelium on the influx of monocytes into the peritoneal cavity (1996) (3)
Familial deficiency of granulocyte bactericidal capacity associated with growth retardation. (1978) (3)
Discrepancies in the oxygen balance of whole human neutrophils and neutrophil homogenates. (1982) (3)
Interference of PR3-ANCA with the enzymatic activity of PR3 (2002) (3)
Mannose-Binding Lectin ( MBL ) Facilitates Opsonophagocytosis of Yeasts but Not of Bacteria despite MBL Binding 1 (2008) (3)
The Respiratory Burst and the NADPH Oxidase of Phagocytic Leukocytes (1988) (3)
A sensitive mechanized determination of ATP+ADP. (1973) (2)
Pro-myeloperoxidase, a target antigen for antineutrophil cytoplasm autoantibodies: comment on the article by Russell et al. (2002) (2)
The Oxygen Metabolism of Human Blood Monocytes and Neutrophils (1980) (2)
Complement and phagocytes - A complicated interaction. (2015) (2)
[Chronic granulomatous disease (CGD): dysfunction of the neutrophil granulocyte NADPH-oxidase enzyme system]. (1997) (2)
Invasive fungal infection and impaired neutrophil killing in human CARD 9 deficiency Running title : CARD 9 deficiency in neutrophils (2013) (2)
The Fc gamma RIIIA-158F is a risk factor for systemic lupus erythematosus. (1997) (2)
Cytotoxicity of Human Monocytes Against Sensitized Erythrocytes (1980) (2)
Retrotransposable genetic elements causing neutrophil defects (2018) (2)
Cryopreservation of enucleated human neutrophils (PMN cytoplasts). (1984) (2)
Recombinant human interferon-gamma treatment in severe leucocyte adhesion deficiency. (1992) (1)
Hematologically important mutations: Leukocyte adhesion deficiency (second update). (2023) (1)
Raman microscopy of phagocytosis: shedding light on macrophage foam cell formation (2006) (1)
Characterization of 4 New Mutations in the CYBB Gene in 10 Iranian Families With X-linked Chronic Granulomatous Disease (2018) (1)
SIRP alpha controls phagocyte NADPH oxidase function by limiting the expression of gp91(phox) (2010) (1)
Imbalance in Nucleotide Pools of Myeloid Leukemia Cells and HL-60 Cells: Correlation with Cell Cycle Phase, Cell Proliferation and Differentiation (1985) (1)
Male X-chromosome mosaicism leading to carrier phenotype and inheritance of chronic granulomatous disease. (2018) (1)
[Chronic granulomatous disease. Clinical symptoms and biochemical background]. (1976) (1)
Gene Duplication : Evidence for Presence and Expression of Three Distinct Fc g RIIIB Genes in NA ( 1 1 , 2 1 ) SH ( 1 ) Individuals By (1998) (1)
[Molecular-genetic studies of carrier stage of glucose-6-phosphate dehydrogenase deficiency]. (1994) (1)
Haemolytic disease of the newborn and chronic anaemia induced by gamma beta thalassaemia in a Dutch family. (1981) (1)
CHARACTERIZATION OF THE O2¯/H2O2-GENERATING SYSTEM IN HUMAN NEUTROPHILS (1984) (1)
[Hemolytic disease of the newborn and chronic hypochromic microcytic anemia in one family: gamma-delta-beta thalassemia]. (1981) (1)
Recombinant human interferon-γ treatment in severe leucocyte adhesion deficiency (1992) (1)
Homocysteine-Induced Apoptosis in Endothelial Cells Coincides With Nuclear NOX2 and Peri-nuclear NOX4 Activity (2011) (1)
UvA-DARE ( Digital Academic Repository ) Evidence consistent with human L 1 retrotransposition in maternal meiosis (2002) (1)
Genetic mutations and clinical presentation of chronic granulomatous disease (1997) (1)
X-linked chronic granulomatous disease, a useful database (1998) (1)
Granulocytes without degranulation: neutrophil function in granule-depleted neutroplasts. (1983) (1)
RELATION BETWEEN RECEPTOR BINDING, PHAGOCYTOSIS AND EFFECTOR FUNCTION OF HUMAN POLYMORPHONUCLEAR LEUKOCYTES (1976) (1)
NADPH Oxidases in the Heart (2006) (1)
Comments on J Clin Immunol (2014) 34:633–641 DOI 10.1007/s10875-014-0061-0 (2016) (1)
Developments in the treatment of patients with chronic granulomatous disease. (1988) (1)
Fcγ Receptors of Myeloid Cells (1993) (1)
Formation of reactive oxygen species by phagocytic cells: functions and dysfunctions. (1988) (1)
Clinical value of soluble IgG Fc receptor type III (sFcγRIII) in plasma from patients with neutropenia (1997) (1)
Characterization of two novel mutations in IL-12R signaling in MSMD patients. (2019) (1)
Human neutrophil membrane fluidity after incubation in structurally different lipid emulsions (2000) (1)
Depletion of intracellular Ca2+ stores in human basophils permits histamine release upon treatment with IL-3, IL-5 or GM-CSF (1997) (0)
Neutrophil Functional Disorders (2017) (0)
NADPHH oxidase(s): new source(s) of reactive oxygen speciess in the vascular system? (2007) (0)
CYBB an adult female with a somatic mosaic for a novel mutation in Unusual late presentation of X-linked chronic granulomatous disease in (2013) (0)
Chemokine Responsiveness in Chronic Chemokine Receptor Expression and Infiltrated Neutrophils Acquire Novel (2008) (0)
Epithelial Cell Activator Chemoattractant and Priming Agent and Lung Epithelial Cells : Eosinophil Eosinophil Migration Across Monolayers of Triple Role of Platelet-Activating Factor in (1998) (0)
[Molecular genetic studies in alpha-thalassemia]. (1992) (0)
Lessons Learned from Phagocytic Function Studies in a Large Cohort of Patients with Recurrent Infections (2011) (0)
RESTORATION OF NEUTROPHIL CHEMOTACTIC RESPONSIVENESS BY LEVAMISOLE TREATMENT IN PATIENTS WITH THE HYPER-IgE SYNDROME (1979) (0)
Functional Consequences of Genetic Variation across the Entire MBL2 Locus: Possible Identification of 3′ SNPs That Could Modify Circulating Levels of MBL. (2004) (0)
Binding of MoAbs of the endothelial workshop panel to resting and activated human HUVEC, platelets and neutrophilic granulocytes (1993) (0)
Rare Duplication or Deletion of Exons 6, 7 and 8 in CYBB Leading to X-Linked Chronic Granulomatous Disease in Two Patients from Different Families (2012) (0)
Structural Heterogeneity of Human NK Lymphocyte FcRIII Associated with the Biallelic System NA1/NA21 (1990) (0)
Mannose-Binding Lectin ( MBL ) Substitution : Recovery of Opsonic Function In Vivo Lags behind MBL Serum Levels 1 (2009) (0)
PECAM-1 is implicated in Transendothelial Migration of Neutrophils, but not of Eosinophils (2011) (0)
[Clinical symptoms, diagnosis and treatment of phagocyte dysfunction]. (1987) (0)
Possible role of a metalloprotease in the shedding of neutrophil Fc gamma IIIb [Abstract] (1996) (0)
Decreased leukocyte phagocytosis in patients with liver metastases (1998) (0)
82 PURINE AND PYRIMIDINE METABOLISM OF NORMAL AND LEUKEMIC CELLS (1988) (0)
Eosinophils and Platelet-Activating Factor (2019) (0)
Introduction to the special issue on NEUTROPHILS of the European Journal of Clinical Investigation (2018) (0)
ACTIVATION OF fa INTEGRINS INCREASES APOPTOSIS OF CYTOKINE-TREATED HUMAN NEUTROPHILS (2009) (0)
ADENOSINE RECEPTORS ON HUMAN T LYMPHOCYTES AND HUMAN THYMOCYTES: 55 (1985) (0)
Disease Somatic Triple Mosaicism in a Carrier of X-Linked Chronic Granulomatous (2012) (0)
LAD III versus LAD I variant. Authors' reply (2007) (0)
Polymorphisms of FcγRIIIa on NK cells and macrophages (1998) (0)
Quantitative detection of NADPH oxidase in live neutrophilic granulocytes by Raman cytometry (2006) (0)
A defect in the initiation of the metabolic stimulation during phagocytosis of human granulocytes (1976) (0)
Hypocalcemia persisting after surgery of benign thyroid diseases – A follow-up of 281 patients (2015) (0)
Analysis of Chronic Granulomatous Disease in the Kavkazi Population in Israel Reveals Phenotypic Heterogeneity in Patients with the Same NCF1 mutation (c.579G>A) (2018) (0)
Confocal Raman microscopy of cytochrome b558 in single neutrophilic granulocytes (2003) (0)
Single-Cell Raman Microscopy: Shedding Light on Innate Immunity (2004) (0)
Chapter 3 The inhibitory receptor SIRP α limits phagocyte NADPH oxidase activity by controlling gp 91 phox expression (2011) (0)
Involvement of ELAM-1 in monocyte adherence to and migration across IL-1-stimulated endothelial cell monolayers (1992) (0)
A Dutch family with Hb Atlanta [beta 75(E19)Leu-->Pro]. (1996) (0)
Incubation in Lipofundin® stimulates the early respiratory burst of human neutrophils compared to Intralipid® and structured fat emulsion 73403® (1998) (0)
Studies on the neutrophil NADPH oxidase (2007) (0)
Short title: NOX4 in human thyroid (2009) (0)
Erratum to: Chronic Granulomatous Disease: A 25-Year Patient Registry Based on a Multistep Diagnostic Procedure, from the Referral Center for Primary Immunodeficiencies in Greece (2014) (0)
PHAGOCYTOSIS OF DNA-ANTI-DNA COMPLEXES BY HUMAN PMN VIA Fc AND C3 RECEPTOR (1976) (0)
Preconceptional screening for carriers of haemoglobinopathies and/or cystic fibrosis, dependent on ethnic background: feasibility of a combined offer in the Dutch population (2002) (0)
DISEASE WITH THE USE OF THE POLYMERASE CHAIN REACTION X-LINKED CHRONIC GRANULOMATOUS (1992) (0)
idiopathic thrombocytopenic purpura gene predisposes to FCGR2C Copy number variation of the activating (2013) (0)
Chronic granulomatous disease in Israel: clinical, functional and molecular studies of 43 patients (2009) (0)
Correlation between genetic profile, serum levels and functionality of the polymorphic complement protein C4 (2007) (0)
Chronic granulomatous disease caused by a partly exonised retroposed TMF1 gene copy inserted into the CYBB gene. (2011) (0)
UvA-DARE ( Digital Academic Repository ) Chronic granulomatous disease : the European experience (2009) (0)
ROLE OF GLUTATHIONE IN PHAGOCYTE HOST DEFENSE MECHANISMS (1978) (0)
reductase gene leading to methemoglobinemia type I 5 b cytochrome - Seven new mutations in the nicotinamide adenine dinucleotide reduced (2013) (0)
FERMT3 LAD-1/variant syndrome is caused by mutations in (2013) (0)
Three different NCF2 mutations in five consanguineous families from Turkey resulting in autosomal recessive chronic granulomatous disease (2008) (0)
A Novel Deletion in FERMT3 Causes LAD-III in a Turkish Family (2023) (0)
Bacterial Proliferation Inhibition of Superoxide Production and Is Essential to the Anaplasma phagocytophila mRNA Expression by rac 2 Repression of and Erol Fikrig (2002) (0)
A Dutch Fay with Hb Atlanta [β75(E19)Leu → Pr0] (1996) (0)
Lipofundin® increases in vitro adhesion molecule expression, degranulation and binding capacity of human neutrophils, contrary to Intralipid® and structured Fat Emulsion 73403® (1998) (0)
Leukocyte membrane determinants regulating immune reactivity : proceedings of the Tenth Leukocyte Culture Conference, held in Amsterdam, The Netherlands, September 10-13, 1975 (1976) (0)
Involvement of Reactive Oxygen Species in Angiotensin II-Induced Cardiac Hypertrophy in Neonatal Rat Ventricular Myocytes (2005) (0)
LAD III versus LAD I variant - Response (2007) (0)
Chronic granulomatous disease due to different mutations in patients from the same consanguineous extended family (2018) (0)
Association of FC Γ Receptor Polymorphisms in Kawasaki Disease (2003) (0)
UvA-DARE ( Digital Academic Repository ) A family with complement factor D deficiency (2001) (0)
376 Increased Nox2 expression in human cardiomyocytes after AMI (2003) (0)
An Alu-repeat-induced deletion within the NCF2 gene leads to the expression of shortened p67-phox protein lacking TPR4 motif and thereby to chronic granulomatous disease (2008) (0)
Running title: CARD9 deficiency in neutrophils (2016) (0)
FcRn, the neonatal IgG-Fc receptor, analysis of functional expression in several cell lines (1999) (0)
Septic Granulomatosis - a Chameleon: Tumor, Lung Malformation or Immunodeficiency? (2015) (0)
UvA-DARE ( Digital Academic Repository ) Mitochondria in neutrophil apoptosis (2009) (0)
Live-cell microscopy on the pagocyte NADPH oxidase using fluorescent protein chimeras of gp91phox, p67phox, and Rac2. (2007) (0)
genotype-phenotype relationship Hematologic abnormalities in Shwachman Diamond syndrome: lack of (2013) (0)
Gin Substitution in the Light Chain of Cytochrome bsss of the Human N A D P H Oxidase ( p 22-phox ) Leads to Defective Translocation of the Cytosofic Proteins p 47-phox and p 67-phox By (2003) (0)
IMBALANCE IN NUCLEOTIDE POOLS OF MYELOID LEUKEMIA CELLS AND HL-60 CELLS: CORRELATION WITH CELL CYCLE PHASE,CELL PROLIFERATION AND DIFFERENTIATION: 53 (1985) (0)
CONTAMINATING LEUKOCYTES INFLUENCE THE STORAGE CONDITIONS OF PLATELET CONCENTRATES (1987) (0)
Somatic hybridization of monocytes: a method to study the genetic heterogeneity of chronic granulomatous disease and the molecular composition of the phagocyte oxidase system (1985) (0)
The development of a human lung microvascular endothelial cell line (1997) (0)
The role of reactive oxygen species in the phagocytosis of myelin (1998) (0)
Gp91 phox-homologs in cardiomyocytes: a putative novel source of reactive oxygen species. Molecular and functional characterization in rat and human cardiomyocytes (2002) (0)
Raman Cytometry : Quantitative determination by Raman microspectroscopy of cytochrome b558 in neutrophilic granulocytes (2006) (0)
Confocal Raman imaging of cytochrome b558 in single neutrophils (2004) (0)
Comments on J Clin Immunol (2014) 34:633–641 DOI 10.1007/s10875-014-0061-0 (2016) (0)
Analysis of functional defects in CGD by confocal microscopy (2002) (0)
UvA-DARE ( Digital Academic Repository ) Neutrophil cell death : mechanisms and regulation (2009) (0)
family with meningococcal infections a deficiency by two novel mutations in the Complement Factor D gene in Deficient alternative complement pathway activation due to factor D (2013) (0)
Proton Release by Stimulated Neutrophils (1981) (0)
C-Reactive Protein enhances antibody-mediated platelet destruction (2014) (0)
Letter: Granulocyte function and opsonins. (1975) (0)
granulomatous disease Splice site mutations are a common cause of X-linked chronic (2011) (0)
Epigenomic and functional dynamics of human bone marrow myeloid differentiation to mature blood neutrophils (2018) (0)
Phenomenon of highly selective interaction between human neutrophils (PMN) and staphylococci (1997) (0)
Modulation of anti-GBM-glomerulonephritis in rats by fibronectin CS1-peptides (1997) (0)
Physiology and Pathophysiology of Human Neutrophils (1985) (0)
Disease Patients Lines of Normal and Chronic Granulomatous in EBV-Transformed B Lymphoblastoid Cell Phosphate Oxidase Assembly and Activation Nicotinamide-Adenine Dinucleotide (1998) (0)
UvA-DARE ( Digital Academic Repository ) FcgammaRIIIb shedding from human neutrophils (2017) (0)
Single-Cell Raman Microscopy: Shedding Blue and Red Light on Phagocytosis (2004) (0)
, L . oxidase : consequences for oxidase assembly of human NADPH phox Four novel mutations in the gene encoding gp 91 (2000) (0)
Resonance Raman Imaging of Cytochrome b558 in Single Neutrophils (2003) (0)
UvA-DARE ( Digital Academic Repository ) The role of mannose-binding lectin in vitro and in vivo (2008) (0)
Neutrophils Bind to Endothelial Leukocyte-Adhesion Molecule-1 through a Sialidase-Sensitive Mechanism1 (1991) (0)
Chronic Granulomatous Disease: A 25-Year Patient Registry Based on a Multistep Diagnostic Procedure, from the Referral Center for Primary Immunodeficiencies in Greece (2013) (0)
UvA-DARE ( Digital Academic Repository ) Tyrosine phosphorylation-dependent activation of phosphatidylinositide 3-kinase occurs upstream of CA 2 +-signalling induced by Fcgamma receptor cross-linking in human neutrophils (1997) (0)
Human neutrophil membrane fluidity after incubation in structuraily different lipid emusions: a fluorescence polarization study (1999) (0)
[An opsonin-independent strain of Staphylococcus epidermidis]. (1997) (0)
Sequential migration of granulocytes across monolayers of endothelial and lung epithelial cells: a new model for inflammatory processes in the lung (2001) (0)
Mannose-binding lectin (MBL) binding during opsonization is not indicative for its role in phagocytosis (2007) (0)
Lung Epithelial Cells: Eosinophil Eosinophil Migration Across Monolayers of Triple Role of Platelet-Activating Factor in (1998) (0)
Single-cell Raman microscopy of lipid bodies in neutrophils and PLB985 cells (2005) (0)
Recurrent skin abscesses in a female X‐linked chronic granulomatous disease carrier (2020) (0)
Uridine fluxes in healthy proliferating T-lymphocytes, MOLT-3 T-ALL cell-line cells and differentiated MOLT-3 cells. (1991) (0)
Primary immunodeficiency (PP-051) (2010) (0)
Respiratory Burst by Down-Regulating Human Granulocytic Ehrlichiosis Prevents Cutting Edge : Infection by the Agent of (2000) (0)
Allogeneic hematopoietic stem cell transplantation (2017) (0)
Natural history and early diagnosis of LAD 1/variant syndrome. Commentary (2007) (0)
41 THE EFFECT OF ASCORBATE ON SEVERAL BLOOD CELL FUNCTIONS IN THE CHEDIAK-HIGASHI SYNDROME (1979) (0)

This paper list is powered by the following services:

What Schools Are Affiliated With Dirk Roos?

Dirk Roos is affiliated with the following schools:

Dirk Roos's Academic­Influence.com Rankings

Dirk Roos's Degrees

Similar Degrees You Can Earn

Why Is Dirk Roos Influential?

Dirk Roos's Published Works

Published Works

What Schools Are Affiliated With Dirk Roos?

Dirk Roos's AcademicInfluence.com Rankings