A. Crénéguy

Hepatic lentiviral gene transfer prevents the long-term onset of hepatic tumours of glycogen storage disease type 1a in mice.

G. Mithieux, N. Ferry, S. Gaillard, 2015, Human molecular genetics.

Multiplex CRISPR/Cas9 system impairs HCMV replication by excising an essential viral gene

J. Gergen, I. Anegon, E. Verhoeyen, 2018, PloS one.

Highly efficient in vitro and in vivo delivery of functional RNAs using new versatile MS2-chimeric retrovirus-like particles

Philippe Leboulch, Nicolas Martin, P. Ravassard, 2015, Molecular therapy. Methods & clinical development.

Efficient Generation of Myostatin Knock-Out Sheep Using CRISPR/Cas9 Technology and Microinjection into Zygotes

L. Tesson, I. Anegon, A. Crénéguy, 2015, PloS one.

Surface expression of the hRSV nucleoprotein impairs immunological synapse formation with T cells

Michael Loran Dustin, M. Cammer, A. Kalergis, 2014, Proceedings of the National Academy of Sciences.

Homology-directed repair in rodent zygotes using Cas9 and TALEN engineered proteins

D. Gauguier, J. Concordet, S. Remy, 2015, Scientific Reports.

Surface expression of the hRSV nucleoprotein impairs immunological synapse formation with T cells

Michael Loran Dustin, M. Cammer, A. Kalergis, 2014, Proceedings of the National Academy of Sciences.