Aude Magerus-Chatinet

Paris, France

Last Updated: 09/26/2026

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Found 19 publications

Soluble CD95L triggers Caspase-10-driven reactive oxygen species production in neutrophils and aggravates anti-neutrophil cytoplasmic antibody-vasculitis.

Soluble CD95L triggers Caspase-10-driven reactive oxygen species production in neutrophils and aggravates anti-neutrophil cytoplasmic antibody-vasculitis.

Journal: Nature communications

Published: July 03, 2025

Study of the potential role of CASPASE-10 mutations in the development of autoimmune lymphoproliferative syndrome.

Study of the potential role of CASPASE-10 mutations in the development of autoimmune lymphoproliferative syndrome.

Journal: Cell death & disease

Published: October 13, 2023

The genetic landscape of the FAS pathway deficiencies.

The genetic landscape of the FAS pathway deficiencies.

Journal: Biomedical journal

Published: April 10, 2021

Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes.

Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes.

Journal: Blood

Published: November 20, 2018

Chronic granulomatous skin lesions leading to a diagnosis of TAP1 deficiency syndrome.

Chronic granulomatous skin lesions leading to a diagnosis of TAP1 deficiency syndrome.

Journal: Pediatric dermatology

Published: September 07, 2018

The Autoimmune Lymphoproliferative Syndrome with Defective FAS or FAS-Ligand Functions.

The Autoimmune Lymphoproliferative Syndrome with Defective FAS or FAS-Ligand Functions.

Journal: Journal of clinical immunology

Published: November 10, 2017

Autoimmune Lymphoproliferative Syndrome-FAS Patients Have an Abnormal Regulatory T Cell (Treg) Phenotype but Display Normal Natural Treg-Suppressive Function on T Cell Proliferation.

Autoimmune Lymphoproliferative Syndrome-FAS Patients Have an Abnormal Regulatory T Cell (Treg) Phenotype but Display Normal Natural Treg-Suppressive Function on T Cell Proliferation.

Journal: Frontiers in immunology

Published: September 05, 2017

Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations.

Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations.

Journal: Clinical immunology (Orlando, Fla.)

Published: August 18, 2017

Lymphadenopathy driven by TCR-Vγ8Vδ1 T-cell expansion in FAS-related autoimmune lymphoproliferative syndrome.

Lymphadenopathy driven by TCR-Vγ8Vδ1 T-cell expansion in FAS-related autoimmune lymphoproliferative syndrome.

Journal: Blood advances

Published: March 05, 2017

In Vitro Evaluation of the Apoptosis Function in Human Activated T Cells.

In Vitro Evaluation of the Apoptosis Function in Human Activated T Cells.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: January 13, 2017

Evolution of disease activity and biomarkers on and off rapamycin in 28 patients with autoimmune lymphoproliferative syndrome.

Evolution of disease activity and biomarkers on and off rapamycin in 28 patients with autoimmune lymphoproliferative syndrome.

Journal: Haematologica

Published: October 30, 2016

LRBA deficiency with autoimmunity and early onset chronic erosive polyarthritis.

LRBA deficiency with autoimmunity and early onset chronic erosive polyarthritis.

Journal: Clinical immunology (Orlando, Fla.)

Published: February 04, 2016

Showing 1-12 of 19

Last Updated: 09/26/2026