Raphaël Carapito

University of Strasbourg

France

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Articles (10)

Year:

2023

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2023

Year:

2023

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2023

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2023

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2022

Year:

2022

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2022

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2022

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2022

Collaborators (22)

Erik Nelson

Associate Professor

University of Illinois at Urbana-Champaign

UNITED STATES

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Lionel Apetoh

UNITED STATES

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Jose Trenado Álvarez

Profesor médico asociado

University of Barcelona

SPAIN

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philippe georgel

Inserm u1183

FRANCE

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Yasutoshi KIDO

Osaka University

JAPAN

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Agnès Linglart

FRANCE

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Takaki Asano

Assistant professor

Hiroshima University

JAPAN

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Marton Keszei

Karolinska Institutet

SWEDEN

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celine verstuyft

Full Professor of Pharmacology

FRANCE

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Peng Zhang

Rockefeller University

UNITED STATES

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Toby Lawrence

King’s College London

UNITED KINGDOM

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Eric D'Ortenzio

Head

INSERM

FRANCE

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Federica Sallusto

SWITZERLAND

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Satoshi Okada

Professor

Hiroshima University

JAPAN

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Lionel Lamhaut

INSERM

FRANCE

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Trine Hyrup Mogensen

Aarhus University

DENMARK

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Yurdagul Uzunhan

Sorbonne Université

FRANCE

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Frédérique Végran

Université de Franche-Comté

FRANCE

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Lisa Westerberg

Karolinska Institutet

SWEDEN

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Pauline Soulas-Sprauel

Professor/Hospital practitioner (PU-PH)

University of Strasbourg

FRANCE

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Teresa Auguet

SPAIN

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Seiamak Bahram

Professor of Immunology

University of Strasbourg

FRANCE

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Raphaël Carapito

Research Interests

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Articles (10)

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

Human IL-23 is essential for IFN-γ–dependent immunity to mycobacteria

Investigating Chemokine-Matrix Networks in Breast Cancer: Tenascin-C Sets the Tone for CCL2

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.

Infiltrating CD8+ T cells and M2 macrophages are retained in tumor matrix tracks enriched in low tension fibronectin fibers.

Dicer1 deficient mice exhibit premature aging and metabolic perturbations in adipocytes

CD4 T cell-intrinsic STING signaling controls the differentiation and effector functions of TH1 and TH9 cells

A gain-of-function variant in the Wiskott-Aldrich syndrome gene is associated with a MYH9-related disease-like syndrome

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.

Fc receptors and the diversity of antibody responses to HIV infection and vaccination.

Collaborators (22)

Erik Nelson

Lionel Apetoh

Jose Trenado Álvarez

philippe georgel

Yasutoshi KIDO

Agnès Linglart

Takaki Asano

Marton Keszei

celine verstuyft

Peng Zhang

Toby Lawrence

Eric D'Ortenzio

Federica Sallusto

Satoshi Okada

Lionel Lamhaut

Trine Hyrup Mogensen

Yurdagul Uzunhan

Frédérique Végran

Lisa Westerberg

Pauline Soulas-Sprauel

Teresa Auguet

Seiamak Bahram

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