Marie-celine Deau

Illkirch-graffenstaden, France

Last Updated: 09/26/2026

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Found 12 publications

APDS treatment in Germany: decision criteria, costs and contribution of leniolisib to outcomes.

APDS treatment in Germany: decision criteria, costs and contribution of leniolisib to outcomes.

Journal: Frontiers in immunology
Published: March 30, 2026

LRBA deficiency impairs autophagy and contributes to enhanced antigen presentation and T-cell dysregulation.

LRBA deficiency impairs autophagy and contributes to enhanced antigen presentation and T-cell dysregulation.

Journal: EMBO reports
Published: December 16, 2024

Helios represses megakaryocyte priming in hematopoietic stem and progenitor cells.

Helios represses megakaryocyte priming in hematopoietic stem and progenitor cells.

Journal: The Journal of experimental medicine
Published: October 30, 2020

Large deletions of the 5' region of IKZF1 lead to haploinsufficiency in B-cell precursor acute lymphoblastic leukaemia.

Large deletions of the 5' region of IKZF1 lead to haploinsufficiency in B-cell precursor acute lymphoblastic leukaemia.

Journal: British journal of haematology
Published: January 31, 2019

Loss of ARHGEF1 causes a human primary antibody deficiency.

Loss of ARHGEF1 causes a human primary antibody deficiency.

Journal: The Journal of clinical investigation
Published: February 15, 2018

Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1).

Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1).

Journal: Haematologica
Published: April 22, 2017

MYB-GATA1 fusion promotes basophilic leukaemia: involvement of interleukin-33 and nerve growth factor receptors.

MYB-GATA1 fusion promotes basophilic leukaemia: involvement of interleukin-33 and nerve growth factor receptors.

Journal: The Journal of pathology
Published: July 18, 2016

Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study.

Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study.

Journal: The Journal of allergy and clinical immunology
Published: October 13, 2015

Hyper-activated PI3K-δ in immunodeficiency.

Hyper-activated PI3K-δ in immunodeficiency.

Journal: Oncotarget
Published: August 20, 2015

A human immunodeficiency caused by mutations in the PIK3R1 gene.

A human immunodeficiency caused by mutations in the PIK3R1 gene.

Journal: The Journal of clinical investigation
Published: April 02, 2015

An inherited immunoglobulin class-switch recombination deficiency associated with a defect in the INO80 chromatin remodeling complex.

An inherited immunoglobulin class-switch recombination deficiency associated with a defect in the INO80 chromatin remodeling complex.

Journal: The Journal of allergy and clinical immunology
Published: June 24, 2014

A human immunodeficiency caused by mutations in the PIK3R1 gene.

A human immunodeficiency caused by mutations in the PIK3R1 gene.

Journal: The Journal of clinical investigation
Published: February 19, 2014
Showing 1-12 of 12

Last Updated: 09/26/2026