Paul Tuijnenburg

Amsterdam, NH, Netherlands

Last Updated: 09/26/2026

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Found 11 publications

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

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

Journal: Journal of autoimmunity

Published: July 18, 2023

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

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

Journal: Nature

Published: July 18, 2020

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

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

Journal: The Journal of allergy and clinical immunology

Published: July 08, 2019

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

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

Journal: European journal of immunology

Published: May 08, 2019

Whole-genome sequencing of a sporadic primary immunodeficiency cohort.

Whole-genome sequencing of a sporadic primary immunodeficiency cohort.

Journal: Nature

Published: December 01, 2018

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

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

Journal: Clinical immunology (Orlando, Fla.)

Published: November 06, 2018

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

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

Journal: The Journal of allergy and clinical immunology

Published: September 10, 2018

The TNF Receptor Superfamily-NF-κB Axis Is Critical to Maintain Effector Regulatory T Cells in Lymphoid and Non-lymphoid Tissues.

The TNF Receptor Superfamily-NF-κB Axis Is Critical to Maintain Effector Regulatory T Cells in Lymphoid and Non-lymphoid Tissues.

Journal: Cell reports

Published: May 09, 2017

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

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

Journal: The Journal of allergy and clinical immunology

Published: April 13, 2017

Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome.

Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome.

Journal: American journal of human genetics

Published: November 01, 2016

Humoral Immunodeficiency with Hypotonia, Feeding Difficulties, Enteropathy, and Mild Eczema Caused by a Classical FOXP3 Mutation.

Humoral Immunodeficiency with Hypotonia, Feeding Difficulties, Enteropathy, and Mild Eczema Caused by a Classical FOXP3 Mutation.

Journal: Frontiers in pediatrics

Published: October 28, 2016

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Last Updated: 09/26/2026