Gene Therapy in a Patient with Sickle Cell Disease von Ribeil, Jean-Antoine, Hacein-Bey-Abina, Salima, Payen, Emmanuel, Magnani, Alessandra, Semeraro, Michaela, Magrin, Elisa, Caccavelli, Laure, Neven, Benedicte, Bourget, Philippe, El Nemer, Wassim, Bartolucci, Pablo, Weber, Leslie, Puy, Hervé, Meritet, Jean-François, Grevent, David, Beuzard, Yves, Chrétien, Stany, Lefebvre, Thibaud, Ross, Robert W, Negre, Olivier, Veres, Gabor, Sandler, Laura, Soni, Sandeep, de Montalembert, Mariane, Blanche, Stéphane, Leboulch, Philippe, Cavazzana, Marina

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Gene Therapy in Patients with Transfusion-Dependent β-Thalassemia von Thompson, Alexis A, Walters, Mark C, Kwiatkowski, Janet, Rasko, John E.J, Ribeil, Jean-Antoine, Hongeng, Suradej, Magrin, Elisa, Schiller, Gary J, Payen, Emmanuel, Semeraro, Michaela, Moshous, Despina, Lefrere, Francois, Puy, Hervé, Bourget, Philippe, Magnani, Alessandra, Caccavelli, Laure, Diana, Jean-Sébastien, Suarez, Felipe, Monpoux, Fabrice, Brousse, Valentine, Poirot, Catherine, Brouzes, Chantal, Meritet, Jean-François, Pondarré, Corinne, Beuzard, Yves, Chrétien, Stany, Lefebvre, Thibaud, Teachey, David T, Anurathapan, Usanarat, Ho, P. Joy, von Kalle, Christof, Kletzel, Morris, Vichinsky, Elliott, Soni, Sandeep, Veres, Gabor, Negre, Olivier, Ross, Robert W, Davidson, David, Petrusich, Alexandria, Sandler, Laura, Asmal, Mohammed, Hermine, Olivier, De Montalembert, Mariane, Hacein-Bey-Abina, Salima, Blanche, Stéphane, Leboulch, Philippe, Cavazzana, Marina

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A Modified γ-Retrovirus Vector for X-Linked Severe Combined Immunodeficiency von Hacein-Bey-Abina, Salima, Pai, Sung-Yun, Gaspar, H. Bobby, Armant, Myriam, Berry, Charles C, Blanche, Stephane, Bleesing, Jack, Blondeau, Johanna, de Boer, Helen, Buckland, Karen F, Caccavelli, Laure, Cros, Guilhem, De Oliveira, Satiro, Fernández, Karen S, Guo, Dongjing, Harris, Chad E, Hopkins, Gregory, Lehmann, Leslie E, Lim, Annick, London, Wendy B, van der Loo, Johannes C.M, Malani, Nirav, Male, Frances, Malik, Punam, Marinovic, M. Angélica, McNicol, Anne-Marie, Moshous, Despina, Neven, Benedicte, Oleastro, Matías, Picard, Capucine, Ritz, Jerome, Rivat, Christine, Schambach, Axel, Shaw, Kit L, Sherman, Eric A, Silberstein, Leslie E, Six, Emmanuelle, Touzot, Fabien, Tsytsykova, Alla, Xu-Bayford, Jinhua, Baum, Christopher, Bushman, Frederic D, Fischer, Alain, Kohn, Donald B, Filipovich, Alexandra H, Notarangelo, Luigi D, Cavazzana, Marina, Williams, David A, Thrasher, Adrian J

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Human immunodeficiency virus–driven expansion of CD4+CD25+ regulatory T cells, which suppress HIV-specific CD4 T-cell responses in HIV-infected patients von Weiss, Laurence, Donkova-Petrini, Vladimira, Caccavelli, Laure, Balbo, Michèle, Carbonneil, Cédric, Levy, Yves

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Thyroid Hormone Inhibits the Human Prolactin Gene Promoter by Interfering with Activating Protein-1 and Estrogen Stimulations von Pernasetti, Flavia, Caccavelli, Laure, Van de Weerdt, Cécile, Martial, Joseph A, Muller, Marc

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Alteration of Gα Subunits mRNA Levels in Bromocriptine Resistant Prolactinomas von Caccavelli, L., Morange-Ramos, I., Kordon, C., Jaquet, P., Enjalbert, A.

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Transcription Factor AP1 Is Involved in Basal and Okadaic Acid-Stimulated Activity of the Human PRL Promoter von Caccavelli, Laure, Manfroid, Isabelle, Martial, Joseph A, Muller, Marc

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Neonatal induction and maintenance of tolerance to Th2-induced immune manifestations in rats von Field, A.C, Caccavelli, L, Fillion, J, Kuhn, J, Mandet, C, Bellon, B

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Regulatory CD8+ T Cells Control Neonatal Tolerance to a Th2-Mediated Autoimmunity von Field, Anne-Christine, Caccavelli, Laure, Bloch, Marie-Francoise, Bellon, Blanche

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Hematopoietic Stem Cell Gene Therapy with Lentiviral Vector in X-linked Adrenoleukodystrophy von Cartie, N, Hacein-Bey-Abina, S, Bartholomae, C, Veres, G, Schmidt, M, Kutschera, I, Vidaud, M, Dal-Cortivo, L, Caccavelli, L, Malhaoui, N, Kiermer, V, Mittelstaedt, D, Bellesme, C, Audat, F

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Polyclonal distribution of lentiviral vector integration sites in gene therapy for x-adrenoleukodystrophy von Bartholomae, C, Cartier-Lacave, N, Hacein-Bey-Abina, S, Veres, G, Kutschera, I, Vidaud, M, Dal-Cortivo, L, Caccavelli, L, Mahlaoui, N, Kiermer, V, Mittelstaedt, D, Bellesme, C, Lahlou, N, Lefrere, F

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Regulatory CD8 super(+) T Cells Control Neonatal Tolerance to a Th2-Mediated Autoimmunity von Field, A-C, Caccavelli, L, Bloch, M-F, Bellon, B

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Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis von Cabrera-Serrano, M, Caccavelli, L, Savarese, M, Vihola, A, Jokela, M, Johari, M, Capiod, T, Madrange, M, Bugiardini, E, Brady, S, Quinlivan, R, Merve, A, Scalco, R, Hilton-Jones, D, Houlden, H, Ibrahim Aydin, H, Ceylaner, S, Vockley, J, Taylor, RL, Folland, C, Kelly, A, Goullee, H, Ylikallio, E, Auranen, M, Tyynismaa, H, Udd, B, Forrest, ARR, Davis, MR, Bratkovic, D, Manton, N, Robertson, T, McCombe, P, Laing, NG, Phillips, L, de Lonlay, P, Ravenscroft, G

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Normal IgG protects against acute graft‐versus‐host disease by targeting CD4+CD134+ donor alloreactive T cells von Caccavelli, Laure, Field, Anne‐Christine, Betin, Virginie, Dreillard, Laetitia, Belair, Marie‐France, Bloch, Marie‐Françoise, Bruneval, Patrick, Kazatchkine, Michel, Bellon, Blanche

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Neonatal induction of tolerance to T(h)2-mediated autoimmunity in rats von Field, A C, Caccavelli, L, Fillion, J, Kuhn, J, Mandet, C, Druet, P, Bellon, B

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Clonal tracking in gene therapy patients reveals a diversity of human hematopoietic differentiation programs von Six, E, Guilloux, A, Denis, A, Lecoules, A, Magnani, A, Vilette, R, Male, F, Cagnard, N, Delville, M, Magrin, E, Caccavelli, L, Roudaut, C, Plantier, C, Sobrino, S, Gregg, J, Nobles, CL, Everett, JK, Hacein-Bey-Abina, S, Galy, A, Fischer, A, Thrasher, AJ, André, I, Cavazzana, M, Bushman, F

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Neonatal induction of tolerance to T sub(h)2-mediated autoimmunity in rats von Field, A-C, Caccavelli, L, Fillion, J, Kuhn, J, Mandet, C, Druet, P, Bellon, B

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Normal IgG protects against acute graft-versus-host disease by targeting CD4 super(+)CD134 super(+) donor alloreactive T cells von Caccavelli, L, Field, A-C, Betin, V, Dreillard, L, Belair, M-F, Bloch, M-F, Bruneval, P, Kazatchkine, M, Bellon, B

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A Diversity of Human Hematopoietic Differentiation Programs Identified Through In Vivo Tracking of Hematopoiesis in Wiskott-Aldrich Syndrome Patients von Six, E, Lecoules, A, Caccavelli, L, Nobles, C, Male, F, Magnani, A, Roudaut, C, Plantier, C, Magrin, E, Cagnard, N, Hacein-Bey-Abina, S, Galy, A, Thrasher, AJ, Andre-Schmutz, I, Guilloux, A, Berry, CC, Bushman, FD, Cavazzana, M

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Récepteurs membranaires et protéines de couplage dans les cellules adénohypophysaires von Cussac, D., Caccavelli, L., Pellegrini, I., Audinot, V., Jaquet, P., Enjalberti, A.

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