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Genomics|November 30, 2005
A knock-in mouse model of congenital erythropoietic porphyriaC Ged, M Mendez, E Robert, et al.
Gene Therapy|June 6, 1998
Rapid analysis and efficient selection of human transduced primitive hematopoietic cells using the humanized S65T green fluorescent proteinF Mazurier, F Moreau-Gaudry, V Maguer-Satta, et al.
Gene Therapy|April 26, 2001
Successful therapeutic effect in a mouse model of erythropoietic protoporphyria by partial genetic correction and fluorescence-based selection of hematopoietic cellsA Fontanellas, M Mendez, F Mazurier, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 11, 2001
Gene therapy of a mouse model of protoporphyria with a self-inactivating erythroid-specific lentiviral vector without preselectionE Richard, M Mendez, F Mazurier, et al.
The British Journal of Dermatology|July 24, 2012
Congenital erythropoietic porphyria: a single-observer clinical study of 29 casesR P Katugampola, M N Badminton, A Y Finlay, et al.
The British Journal of Dermatology|July 19, 2012
A management algorithm for congenital erythropoietic porphyria derived from a study of 29 casesR P Katugampola, A V Anstey, A Y Finlay, et al.
Nature Communications|August 14, 2021
CRISPR-Cas9 globin editing can induce megabase-scale copy-neutral losses of heterozygosity in hematopoietic cellsJ Boutin, J Rosier, D Cappellen, et al.
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