Lymphopoiesis in transgenic mice over-expressing Artemis von Rivera-Munoz, P, Abramowski, V, Jacquot, S, André, P, Charrier, S, Lipson-Ruffert, K, Fischer, A, Galy, A, Cavazzana, M, de Villartay, J-P

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V(D)J and immunoglobulin class switch recombinations: a paradigm to study the regulation of DNA end-joining von Soulas-Sprauel, P, Rivera-Munoz, P, Malivert, L, Le Guyader, G, Abramowski, V, Revy, P, de Villartay, J-P

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Variable correction of Artemis deficiency by I-Sce1-meganuclease-assisted homologous recombination in murine hematopoietic stem cells von Rivière, J, Hauer, J, Poirot, L, Brochet, J, Souque, P, Mollier, K, Gouble, A, Charneau, P, Fischer, A, Pâques, F, de Villartay, J-P, Cavazzana, M

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Artemis, a Novel DNA Double-Strand Break Repair/V(D)J Recombination Protein, Is Mutated in Human Severe Combined Immune Deficiency von Moshous, Despina, Callebaut, Isabelle, de Chasseval, Régina, Corneo, Barbara, Cavazzana-Calvo, Marina, Le Deist, Françoise, Tezcan, Ilhan, Sanal, Ozden, Bertrand, Yves, Philippe, Noel, Fischer, Alain, de Villartay, Jean-Pierre

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Mutations in Fas Associated with Human Lymphoproliferative Syndrome and Autoimmunity von Rieux-Laucat, F., Le Deist, F., Hivroz, C., Roberts, I. A. G., Debatin, K. M., Fischer, A., de Villartay, J. P.

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A new gene involved in DNA double-strand break repair and V(D)J recombination is located on human chromosome 10p von MOSHOUS, D, LANYING LI, DE CHASSEVAL, R, PHILIPPE, N, JABADO, N, COWAN, M. J, FISCHER, A, DE VILLARTAY, J.-P

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Sustained Correction of X-Linked Severe Combined Immunodeficiency by ex Vivo Gene Therapy von Hacein-Bey-Abina, Salima, Le Deist, Françoise, Carlier, Frédérique, Bouneaud, Cécile, Hue, Christophe, De Villartay, Jean-Pierre, Thrasher, Adrian J, Wulffraat, Nicolas, Sorensen, Ricardo, Dupuis-Girod, Sophie, Fischer, Alain, Davies, E. Graham, Kuis, Wietse, Leiva, Lilly, Cavazzana-Calvo, Marina

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Metallo‐β‐lactamase fold within nucleic acids processing enzymes: the β‐CASP family von Callebaut, Isabelle, Moshous, Despina, Mornon, Jean‐Paul, de Villartay, Jean‐Pierre

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Reduced immunoglobulin gene diversity in patients with Cornelia de Lange syndrome von Björkman, Andrea, Du, Likun, van der Burg, Mirjam, Cormier-Daire, Valerie, Borck, Guntram, Pié, Juan, Anderlid, Britt-Marie, Hammarström, Lennart, Ström, Lena, de Villartay, Jean-Pierre, Kipling, David, Dunn Walters, Deborah, Pan-Hammarström, Qiang

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A human severe combined immunodeficiency (SCID) condition with increased sensitivity to ionizing radiations and impaired V(D)J rearrangements defines a new DNA recombination/repair... von Nicolas, N, Moshous, D, Cavazzana-Calvo, M, Papadopoulo, D, de Chasseval, R, Le Deist, F, Fischer, A, de Villartay, J P

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A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection von de Villartay, Jean-Pierre, Lim, Annick, Al-Mousa, Hamoud, Dupont, Sophie, Déchanet-Merville, Julie, Coumau-Gatbois, Edith, Gougeon, Marie-Lise, Lemainque, Arnaud, Eidenschenk, Céline, Jouanguy, Emmanuelle, Abel, Laurent, Casanova, Jean-Laurent, Fischer, Alain, Le Deist, Françoise

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Lymphoproliferative syndrome with autoimmunity : A possible genetic basis for dominant expression of the clinical manifestations von RIEUX-LAUCAT, F, BLACHERE, S, CHAPEL, H, NIELSEN, S, BERRAH, M, FISCHER, A, LE DEIST, F, DANIELAN, S, DE VILLARTAY, J. P, OLEASTRO, M, SOLARY, E, BADER-MEUNIER, B, ARKWRIGHT, P, PONDARE, C, BERNAUDIN, F

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Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B–severe combined immune deficiency or Omenn syndrome von Corneo, Barbara, Moshous, Despina, Güngör, Tayfun, Wulffraat, Nicolas, Philippet, Pierre, Deist, Françoise Le, Fischer, Alain, de Villartay, Jean-Pierre

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A Founder Mutation in Artemis, an SNM1-Like Protein, Causes SCID in Athabascan-Speaking Native Americans von Li, Lanying, Moshous, Despina, Zhou, Yungui, Wang, Junhua, Xie, Gang, Salido, Eduardo, Hu, Diana, de Villartay, Jean-Pierre, Cowan, Morton J

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T early alpha (TEA) regulates initial TCRVAJA rearrangements and leads to TCRJA coincidence von Mauvieux, Laurent, Villey, Isabelle, de Villartay, Jean‐Pierre

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Deletion of the human T-cell receptor δ-gene by a site-specific recombination von de Villartay, Jean-Pierre, Hockett Coran, Richard D. David, Korsmeyer, Stanley J, Cohen, David I

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The metallo-beta-lactamase/beta-CASP domain of Artemis constitutes the catalytic core for V(D)J recombination von Poinsignon, Catherine, Moshous, Despina, Callebaut, Isabelle, de Chasseval, Régina, Villey, Isabelle, de Villartay, Jean-Pierre

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Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiency von CAVAZZANA-CALVO, M, LE DEIST, F, DE SAINT BASILE, G, PAPADOPOULO, D, DE VILLARTAY, J. P, FISCHER, A

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A case report of a patient with microcephaly, facial dysmorphism, chromosomal radiosensitivity and telomere length alterations closely resembling “Nijmegen breakage syndrome” pheno... von Berardinelli, F, di Masi, A, Salvatore, M, Banerjee, S, Myung, K, De Villartay, J.P, Revy, P, Plebani, A, Soresina, A, Taruscio, D, Tanzarella, C, Antoccia, A

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The mechanisms of immune diversification and their disorders von Fischer, Alain, Durandy, Anne, de Villartay, Jean-Pierre

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