Isabelle Andre

Paris, France

Last Updated: 09/26/2026

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Found 30 publications

Ex vivo-generated lymphoid progenitors encompass both T cell and innate lymphoid cell fates.

Ex vivo-generated lymphoid progenitors encompass both T cell and innate lymphoid cell fates.

Journal: Frontiers in immunology

Published: April 24, 2025

Ex vivo T-lymphopoiesis assays assisting corrective treatment choice for genetically undefined T-lymphocytopenia.

Ex vivo T-lymphopoiesis assays assisting corrective treatment choice for genetically undefined T-lymphocytopenia.

Journal: Clinical immunology (Orlando, Fla.)

Published: December 23, 2024

Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function.

Somatic deficiency of the human E3 ubiquitin ligase CBL in leukocytes impairs B cell but not T cell development and function.

Journal: Nature immunology

Published: December 16, 2024

Feeder-cell-free system for ex vivo production of natural killer cells from cord blood hematopoietic stem and progenitor cells.

Feeder-cell-free system for ex vivo production of natural killer cells from cord blood hematopoietic stem and progenitor cells.

Journal: Frontiers in immunology

Published: November 20, 2024

Restoration of T and B Cell Differentiation after RAG1 Gene Transfer in Human RAG1 Defective Hematopoietic Stem Cells.

Restoration of T and B Cell Differentiation after RAG1 Gene Transfer in Human RAG1 Defective Hematopoietic Stem Cells.

Journal: Biomedicines

Published: April 12, 2024

Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation.

Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation.

Journal: The Journal of clinical investigation

Published: April 02, 2024

Human oncostatin M deficiency underlies an inherited severe bone marrow failure syndrome.

Human oncostatin M deficiency underlies an inherited severe bone marrow failure syndrome.

Journal: The Journal of clinical investigation

Published: March 08, 2024

Comprehensive Genetic Profiling Reveals Frequent Alterations of Driver Genes on the X Chromosome in Extranodal NK/T-cell Lymphoma.

Comprehensive Genetic Profiling Reveals Frequent Alterations of Driver Genes on the X Chromosome in Extranodal NK/T-cell Lymphoma.

Journal: Cancer research

Published: January 11, 2024

Mutations from patients with IPEX ported to mice reveal different patterns of FoxP3 and Treg dysfunction.

Mutations from patients with IPEX ported to mice reveal different patterns of FoxP3 and Treg dysfunction.

Journal: Cell reports

Published: March 27, 2023

Author Correction to: T-lymphoid progenitor-based immunotherapies: clinical perspectives for one and all.

Author Correction to: T-lymphoid progenitor-based immunotherapies: clinical perspectives for one and all.

Journal: Cellular & molecular immunology

Published: November 14, 2022

T-lymphoid progenitor-based immunotherapies: clinical perspectives for one and all.

T-lymphoid progenitor-based immunotherapies: clinical perspectives for one and all.

Journal: Cellular & molecular immunology

Published: September 01, 2022

A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiency.

A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiency.

Journal: The Journal of experimental medicine

Published: July 28, 2022

Showing 1-12 of 30

Last Updated: 09/26/2026