Suchergebnisse - "Tuijnenburg, Paul"

PubPharm (14)

1

Targeting NF-κB signaling in B cells as a potential new treatment modality for ANCA-associated vasculitis

enthalten in: Journal of autoimmunity | 2024

von Merino-Vico, A. | van Hamburg, J. | Tuijnenburg, P. | +19

2

Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

enthalten in: The Journal of allergy and clinical immunology | 2020

von Lorenzini, T. | Fliegauf, M. | Klammer, N. | +173

ErratumIn: J Allergy Clin Immunol. 2021 Nov;148(5):1345. - PMID 34743834

3

Publisher Correction : Whole-genome sequencing of a sporadic primary immunodeficiency cohort

enthalten in: Nature | 2020

von Thaventhiran, J. | Lango Allen, H. | Burren, O. | +157

ErratumFor: Nature. 2020 Jul;583(7814):90-95. - PMID 32499645

4

Whole-genome sequencing of a sporadic primary immunodeficiency cohort

enthalten in: Nature | 2020

von Thaventhiran, J. | Lango Allen, H. | Burren, O. | +157

ErratumIn: Nature. 2020 Aug;584(7819):E2. - PMID 32678341

5

Whole genome sequencing of a sporadic primary immunodeficiency cohort

enthalten in: bioRxiv.org | 2020

von Thaventhiran, J. | Allen, H. | Burren, O. | +56

6

High-throughput compound screen reveals mTOR inhibitors as potential therapeutics to reduce (auto)antibody production by human plasma cells

enthalten in: European journal of immunology | 2020

von Tuijnenburg, P. | Aan de Kerk, D. | Jansen, M. | +5

7

High‐throughput compound screen reveals mTOR inhibitors as potential therapeutics to reduce (auto)antibody production by human plasma cells

enthalten in: European Journal of Immunology | 2020

von Tuijnenburg, P. | aan de Kerk, D. | Jansen, M. | +5

8

Pathogenic NFKB2 variant in the ankyrin repeat domain (R635X) causes a variable antibody deficiency

enthalten in: Clinical immunology (Orlando, Fla.) | 2019

von Tuijnenburg, P. | Lango Allen, H. | de Bree, G. | +9

9

A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency

enthalten in: The Journal of allergy and clinical immunology | 2019

von Volpi, S. | Cicalese, M. | Tuijnenburg, P. | +49

10

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

enthalten in: The Journal of allergy and clinical immunology | 2018

von Tuijnenburg, P. | Lango Allen, H. | Burns, S. | +128

CommentIn: J Allergy Clin Immunol. 2018 Oct;142(4):1062-1065. - PMID 30165054