Selket Delafontaine

Leuven, VLG, Belgium

Last Updated: 09/26/2026

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Found 24 publications

Correction: Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Correction: Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Journal: The Journal of experimental medicine
Published: January 09, 2026

ADA2-deficient cells exhibit increased levels of cell death and metabolic disturbances.

ADA2-deficient cells exhibit increased levels of cell death and metabolic disturbances.

Journal: Cell death discovery
Published: August 02, 2025

Oncostatin M silence and neopeptide: the value of exploring patients with rare inherited bone marrow failure.

Oncostatin M silence and neopeptide: the value of exploring patients with rare inherited bone marrow failure.

Journal: The Journal of clinical investigation
Published: March 17, 2025

Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Journal: The Journal of experimental medicine
Published: March 05, 2025

Inhibition of lysosomal degradation increases expression of mutant ADA2 in DADA2 monocytes.

Inhibition of lysosomal degradation increases expression of mutant ADA2 in DADA2 monocytes.

Journal: The Journal of allergy and clinical immunology
Published: February 17, 2025

Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Journal: medRxiv : the preprint server for health sciences
Published: December 23, 2024

Human ADA2 Deficiency: Ten Years Later.

Human ADA2 Deficiency: Ten Years Later.

Journal: Current allergy and asthma reports
Published: June 26, 2024

Autoinflammatory patients with Golgi-trapped CDC42 exhibit intracellular trafficking defects leading to STING hyperactivation and ER stress.

Autoinflammatory patients with Golgi-trapped CDC42 exhibit intracellular trafficking defects leading to STING hyperactivation and ER stress.

Journal: Nature communications
Published: January 26, 2024

Inborn errors of immunity: A field without frontiers.

Inborn errors of immunity: A field without frontiers.

Journal: Immunological reviews
Published: December 08, 2023

Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome.

Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome.

Journal: Journal of clinical immunology
Published: October 06, 2023

A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutations.

A new severe congenital neutropenia syndrome associated with autosomal recessive COPZ1 mutations.

Journal: Blood
Published: September 19, 2023

Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children.

Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children.

Journal: Science (New York, N.Y.)
Published: December 20, 2022
Showing 1-12 of 24

Last Updated: 09/26/2026