jeanpierre de villartay

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INSERM

France

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Recent Grants

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Certaines Leucémies Lymphoides Chroniques (LLC) sont elles une forme de déficit immunitaire héréditaire? (CLL-DIP)

Open Date: 2022-01-01

Close Date: 2024-12-01

Grant: Close

Approches interdisciplinaires des processus oncogéniques et perspectives thérapeutiques : Apports à l’oncologie de la physique, de la chimie et des sciences de l’ingénieur

Open Date: 2021-11-01

Close Date: 2024-10-01

Grant: Close

Caractérisation génétique d'une cohorte de LLC familiales

Open Date: 2019-05-01

Close Date: 2020-05-01

Grant: Close

Consequences of DNA repair and telomere defects on the function of the Immune System: application to CVID and immune deficiencies with dysmorphic syndromes

Open Date: 2014-01-01

Close Date: 2017-12-31

Grant: Close

Structure and function of human NHEJ multiprotein complexes

Open Date: 2012-09-01

Close Date: 2015-08-31

Articles (11)

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2024

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2021

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2021

Université Paris Cité

FRANCE

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Adam Handel

University of Oxford

UNITED KINGDOM

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jeanpierre de villartay

Research Interests

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Contact this professor

Recent Grants

Articles (11)

Characterization of novel mutations in the TEL-patch domain of the telomeric factor TPP1 associated with telomere biology disorders.

Autoimmunity and immunodeficiency associated with monoallelic LIG4 mutations via haploinsufficiency.

Brief Report: T-Cell Receptor α Repertoire Diversity at Birth After in utero Exposure to HIV Integrase Strand-Transfer Inhibitors.

Base-editing-mediated dissection of a γ-globin cis-regulatory element for the therapeutic reactivation of fetal hemoglobin expression.

Lymphoma as an Exclusion Criteria for CVID Diagnosis Revisited.

Radiosensitivity in patients affected by ARPC1B deficiency: a new disease trait?

Inborn errors of immunity caused by defects in the DNA damage response pathways: Importance of minimizing treatment-related genotoxicity.

Inherited human Apollo deficiency causes severe bone marrow failure and developmental defects.

An XRCC4 mutant mouse, a model for human X4 syndrome, reveals interplays with Xlf, PAXX, and ATM in lymphoid development.

Somatic genetic rescue of a germline ribosome assembly defect.

Indispensable epigenetic control of thymic epithelial cell development and function by polycomb repressive complex 2.

Collaborators (13)

Ignazia Prigione

Despina Moshous

Fabien Touzot

Norberto Escudero Urquijo

Anne Chalumeau

Patrick Revy

Jean-Paul Concordet

Georg Hollander

Isabelle Callebaut

Shengjiang Tan

Stephen Daley

Annarita Miccio

Adam Handel

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