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Blood|April 15, 2006
Competition within the early B-cell compartment conditions B-cell reconstitution after hematopoietic stem cell transplantation in nonirradiated recipientsAllen Liu, Christian A J Vosshenrich, Chantal Lagresle-Peyrou, et al.
The Journal of Allergy and Clinical Immunology|March 4, 2014
The BLNK adaptor protein has a nonredundant role in human B-cell differentiationChantal Lagresle-Peyrou, Michèle Millili, Sonia Luce, et al.
Blood Advances|February 9, 2021
Adenylate kinase 2 expression and addiction in T-ALLNabih Maslah, Mehdi Latiri, Vahid Asnafi, et al.
Blood Advances|January 4, 2018
Gene transfer into hematopoietic stem cells reduces HLH manifestations in a murine model of Munc13-4 deficiencyTayebeh Soheili, Amandine Durand, Fernando E Sepulveda, et al.
Stem Cells (Dayton, Ohio)|June 13, 2012
Human T-lymphoid progenitors generated in a feeder-cell-free Delta-like-4 culture system promote T-cell reconstitution in NOD/SCID/γc(-/-) miceChristian Reimann, Emmanuelle Six, Liliane Dal-Cortivo, et al.
Nucleic Acids Research|April 16, 2008
DNA bar coding and pyrosequencing to analyze adverse events in therapeutic gene transferGary P Wang, Alexandrine Garrigue, Angela Ciuffi, et al.
Haematologica|January 11, 2020
A gain-of-function RAC2 mutation is associated with bone-marrow hypoplasia and an autosomal dominant form of severe combined immunodeficiencyChantal Lagresle-Peyrou, Aurélien Olichon, Hanem Sadek, et al.
Frontiers in Immunology|March 7, 2025
Feeder-cell-free system for <i>ex vivo</i> production of natural killer cells from cord blood hematopoietic stem and progenitor cellsMarta Martin Corredera, Juliette Paillet, Pierre Gaudeaux, et al.
Molecular Therapy. Methods & Clinical Development|November 14, 2019
Biosafety Studies of a Clinically Applicable Lentiviral Vector for the Gene Therapy of Artemis-SCIDSabine Charrier, Chantal Lagresle-Peyrou, Valentina Poletti, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 29, 2008
Restoration of human B-cell differentiation into NOD-SCID mice engrafted with gene-corrected CD34+ cells isolated from Artemis or RAG1-deficient patientsChantal Lagresle-Peyrou, Fatine Benjelloun, Christophe Hue, et al.
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