, August 2014 — Efficient gene targeting by homology-directed repair in rat zygotes using TALE nucleases. Genome Research vol. 24, n° 8, dir. {Cold Spring Harbor Laboratory Press} p. 1371-1383
, August 2014 — Gene targeting in rats using transcription activator-like effector nucleases. Methods vol. 69, n° 1, dir. {Elsevier} p. 102-107
, December 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}
, July 2008 — Triplex-forming oligonucleotide-orthophenanthroline conjugates for efficient targeted genome modification.. Proceedings of the National Academy of Sciences of the United States of
America vol. 105, n° 28, dir. {National Academy of Sciences} p. 9576-81
, July 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
, 2007 — A hybrid CMV-H1 construct improves efficiency of PEI-delivered shRNA in the mouse brain.. Nucleic Acids Research vol. 35, n° 9, dir. {Oxford University Press} e65
, February 2005 — Lipid-mediated siRNA delivery down-regulates exogenous gene expression in the mouse brain at picomolar levels.. The Journal of Gene Medicine vol. 7, n° 2, dir. {Wiley} p. 198-207
, February 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
, 2018 — Chromosomal Translocation Formation Is Sufficient to Produce Fusion Circular RNAs Specific to Patient Tumor Cells. iScience vol. 5, , dir. {Elsevier} p. 19-29
, December 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
, June 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
, November 2012 — Flavin Conjugates for Delivery of Peptide Nucleic Acids. ChemBioChem vol. 13, n° 17, dir. {Wiley-VCH Verlag}
, October 2015 — Homology-directed repair in rodent zygotes using Cas9 and TALEN engineered proteins. Scientific Reports vol. 5, , dir. {Nature Publishing Group} p. 14410
, 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
, November 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
, 2016 — « Genome Editing in Rats Using TALE Nucleases » in TALENs. Methods in Molecular Biology.. , , p. 245-259
, January 2017 — CRISPR-Cas9: A revolution in genome editing in rheumatic diseases. Joint Bone Spine vol. 84, n° 1, dir. {Elsevier Masson} p. 1-4
, March 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
, 2014 — Characterization of Dystrophin Deficient Rats: A New Model for Duchenne Muscular Dystrophy. PLoS ONE vol. 9, n° 10, dir. {Public Library of Science} 13 p.