dr. Melissa Dullaers
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The transcriptome of lung tumor-infiltrating dendritic cells reveals a tumor-supporting phenotype and a microRNA signature with negative impact on clinical outcome
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Haematopoietic prolyl hydroxylase-1 deficiency promotes M2 macrophage polarization and is both necessary and sufficient to protect against experimental colitis
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Inflammasomes in inflammatory disease
(2016) EUROPEAN JOURNAL OF CLINICAL INVESTIGATION. In European Journal of Clinical Investigation 46(Supplement 1). p.99-99 -
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
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Chronic and invasive fungal infections in a family with CARD9 deficiency (vol 36, pg 204, 2016)
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CVID, isolated IgG deficiency and isolated IgG subclass deficiency : clinical features and B cell maturation of the Ghent cohort
(2016) -
RC3H1 mutation with increased ICOS expression causes an autoinflammatory syndrome
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JAK2 deficiency as a novel cause of impaired Th17 immunity
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The immunophenotypical landscape of patients with primary antibody deficiencies and their asymptomatic first-degree relatives : arguments for a multifactorial aetiology
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Recurrent cutaneous abscesses as the presenting manifestation of STAT1 gain-of-function mutation