Human adenylate kinase 2 deficiency causes a profound haematopoietic defect associated with sensorineural deafness

Por Lagresle-Peyrou, Chantal, Six, Emmanuelle M., Picard, Capucine, Rieux-Laucat, Frédéric, Michel, Vincent, Ditadi, Andrea, Chappedelaine, Corinne Demerens-de, Morillon, Estelle, Valensi, Françoise, Simon-Stoos, Karen L., Mullikin, James C., Noroski, Lenora M., Besse, Céline, Wulffraat, Nicolas M., Ferster, Alina, Abecasis, Manuel M., Calvo, Fabien, Petit, Christine, Candotti, Fabio, Abel, Laurent, Fischer, Alain, Cavazzana-Calvo, Marina
Publicado em 2008

Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1

Por Hacein-Bey-Abina, Salima, Garrigue, Alexandrine, Wang, Gary P., Soulier, Jean, Lim, Annick, Morillon, Estelle, Clappier, Emmanuelle, Caccavelli, Laure, Delabesse, Eric, Beldjord, Kheira, Asnafi, Vahid, MacIntyre, Elizabeth, Dal Cortivo, Liliane, Radford, Isabelle, Brousse, Nicole, Sigaux, François, Moshous, Despina, Hauer, Julia, Borkhardt, Arndt, Belohradsky, Bernd H., Wintergerst, Uwe, Velez, Maria C., Leiva, Lily, Sorensen, Ricardo, Wulffraat, Nicolas, Blanche, Stéphane, Bushman, Frederic D., Fischer, Alain, Cavazzana-Calvo, Marina
Publicado em 2008