Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Grégory Cédrone"'
Autor:
Sabine Charrier, Chantal Lagresle-Peyrou, Valentina Poletti, Michael Rothe, Grégory Cédrone, Bernard Gjata, Fulvio Mavilio, Alain Fischer, Axel Schambach, Jean-Pierre de Villartay, Marina Cavazzana, Salima Hacein-Bey-Abina, Anne Galy
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 15, Iss , Pp 232-245 (2019)
Genetic deficiency of the nuclease DCLRE1C/Artemis causes radiosensitive severe combined immunodeficiency (RS-SCID) with lack of peripheral T and B cells and increased sensitivity to ionizing radiations. Gene therapy based on transplanting autologous
Externí odkaz:
https://doaj.org/article/3824403f1c8443e1b57c5921ed3b19ae
Autor:
Grégory Cédrone, Alain Fischer, Sabine Charrier, Axel Schambach, Michael Rothe, Chantal Lagresle-Peyrou, Bernard Gjata, Salima Hacein-Bey-Abina, Jean-Pierre de Villartay, Fulvio Mavilio, Anne Galy, Valentina Poletti, Marina Cavazzana
Publikováno v:
Mol Ther Methods Clin Dev
Mol Ther Methods Clin Dev, 2019, 15, pp.232-245. ⟨10.1016/j.omtm.2019.08.014⟩
Molecular Therapy. Methods & Clinical Development
Molecular Therapy-Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 15, Iss, Pp 232-245 (2019)
Mol Ther Methods Clin Dev, 2019, 15, pp.232-245. ⟨10.1016/j.omtm.2019.08.014⟩
Molecular Therapy. Methods & Clinical Development
Molecular Therapy-Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 15, Iss, Pp 232-245 (2019)
Genetic deficiency of the nuclease DCLRE1C/Artemis causes radiosensitive severe combined immunodeficiency (RS-SCID) with lack of peripheral T and B cells and increased sensitivity to ionizing radiations. Gene therapy based on transplanting autologous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95eb6abbec6734dd7e1265579a3a67bb
https://hal.archives-ouvertes.fr/hal-02880790
https://hal.archives-ouvertes.fr/hal-02880790
Autor:
Sabine Charrier, Michael Blundell, Gregory Cédrone, Fawzia Louache, William Vainchenker, Adrian J. Thrasher, Anne Galy
Publikováno v:
Haematologica, Vol 98, Iss 8 (2013)
The Wiskott-Aldrich syndrome protein is an essential cytoskeleton regulator found in cells of the hematopoietic lineage and controls the motility of leukocytes. The impact of WAS gene deficiency on the mobilization of hematopoietic progenitor/stem ce
Externí odkaz:
https://doaj.org/article/cd49dbcf1c44494894b00ee0a08857c0