, décembre 2022 — De novo generation of the NPM-ALK fusion recapitulates the pleiotropic phenotypes of ALK+ ALCL pathogenesis and reveals the ROR2 receptor as target for tumor cells. Molecular Cancer vol. 21, n° 1, dir. {BioMed Central} p. 65
, novembre 2022 — Base-editing-mediated dissection of a γ-globin cis-regulatory element for the therapeutic reactivation of fetal hemoglobin expression. Nature Communications vol. 13, n° 1, p. 6618
, juin 2022 — Disease modeling by efficient genome editing using a near PAM-less base editor in vivo. Nature Communications vol. 13, n° 1, dir. {Nature Publishing Group} p. 3435
, octobre 2021 — Unraveling Ewing Sarcoma Tumorigenesis Originating from Patient-Derived Mesenchymal Stem Cells. Cancer Research vol. 81, n° 19, dir. {American Association for Cancer Research} p. 4994-5006
, octobre 2021 — Recent Progress in Genome Editing for Gene Therapy Applications: The French Perspective. Human Gene Therapy vol. 32, 19-20, dir. {Mary Ann Liebert} p. 1059-1075
, février 2020 — Editing a \gamma-globin repressor binding site restores fetal hemoglobin synthesis and corrects the sickle cell disease phenotype. Science Advances vol. 6, n° 7, dir. {American Association for the Advancement of Science (AAAS)} eaay9392
, 2019 — Differential Requirements for the RAD51 Paralogs in Genome Repair and Maintenance in Human Cells. PLoS Genetics vol. 15, n° 10, dir. {Public Library of Science} e1008355
, décembre 2018 — High doses of CRISPR/Cas9 ribonucleoprotein efficiently induce gene knockout with low mosaicism in the hydrozoan Clytia hemisphaerica through microhomology-mediated deletion. Scientific Reports vol. 8, n° 1, dir. {Nature Publishing Group}
, juillet 2018 — The Xenopus tadpole: an in vivo model to screen drugs favoring remyelination. Multiple Sclerosis Journal vol. 24, n° 11, dir. {SAGE Publications} p. 1421-1432
, avril 2018 — Generation of Rag1 and Il2rg immunodeficient rats and application to humanization studies. , , Poster
, 2018 — Chromosomal Translocation Formation Is Sufficient to Produce Fusion Circular RNAs Specific to Patient Tumor Cells. iScience vol. 5, , dir. {Elsevier} p. 19-29
, 2018 — CtIP fusion to Cas9 enhances transgene integration by homology-dependent repair. Nature Communications vol. 9, n° 1, dir. {Nature Publishing Group}
, 2018 — Generation of Immunodeficient Rats With Rag1 and Il2rg Gene Deletions and Human Tissue Grafting Models. Transplantation vol. 102, n° 8, dir. {Lippincott, Williams \& Wilkins} p. 1271-1278
, novembre 2017 — Generation of gene-edited rats by delivery of CRISPR/Cas9 protein and donor DNA into intact zygotes using electroporation. Scientific Reports vol. 7, n° 1, dir. {Nature Publishing Group} p. 16554
, janvier 2017 — CRISPR-Cas9: A revolution in genome editing in rheumatic diseases. Joint Bone Spine vol. 84, n° 1, dir. {Elsevier Masson} p. 1-4
, juin 2016 — The human DNA ends proteome uncovers an unexpected entanglement of functional pathways. Nucleic Acids Research vol. 44, n° 10, dir. {Oxford University Press} p. 4721-4733
, mars 2016 — Improved Genome Editing Efficiency and Flexibility Using Modified Oligonucleotides with TALEN and CRISPR-Cas9 Nucleases.. Cell Reports vol. 14, n° 9, dir. {Elsevier Inc} p. 2263-72
, 2016 — « Genome Editing in Rats Using TALE Nucleases » in TALENs. Methods in Molecular Biology.. , , p. 245-259
, décembre 2015 — Genome Editing and Dialogic Responsibility: “What’s in a Name?”. American Journal of Bioethics vol. 15, n° 12, dir. {Taylor \& Francis (Routledge)} p. 54-57
, octobre 2015 — Homology-directed repair in rodent zygotes using Cas9 and TALEN engineered proteins. Scientific Reports vol. 5, , dir. {Nature Publishing Group} p. 14410