IL4I1 Accelerates the Expansion of Effector CD8 + T Cells at the Expense of Memory Precursors by Increasing the Threshold of T-Cell Activation by Puiffe, Marie-Line, Dupont, Aurélie, Sako, Nouhoum, Gatineau, Jérôme, Cohen, José L, Mestivier, Denis, Lebon, Agnès, Prévost-Blondel, Armelle, Castellano, Flavia, Molinier-Frenkel, Valérie

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Reduced nighttime transpiration is a relevant breeding target for high water-use efficiency in grapevine by Coupel-Ledru, Aude, Lebon, Eric, Christophe, Angélique, Gallo, Agustina, Gago, Pilar, Pantin, Florent, Doligez, Agnès, Simonneau, Thierry

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Nonpathogenic SIV infection of African green monkeys induces a strong but rapidly controlled type I IFN response by Jacquelin, Béatrice, Mayau, Véronique, Targat, Brice, Liovat, Anne-Sophie, Kunkel, Désirée, Petitjean, Gaël, Dillies, Marie-Agnès, Roques, Pierre, Butor, Cécile, Silvestri, Guido, Giavedoni, Luis D, Lebon, Pierre, Barré-Sinoussi, Françoise, Benecke, Arndt, Müller-Trutwin, Michaela C

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Genetic variation in a grapevine progeny (Vitis vinifera L. cvs Grenache×Syrah) reveals inconsistencies between maintenance of daytime leaf water potential and response of transpir... by Coupel-Ledru, Aude, Lebon, Éric, Christophe, Angélique, Doligez, Agnès, Cabrera-Bosquet, Llorenç, Péchier, Philippe, Hamard, Philippe, This, Patrice, Simonneau, Thierry

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Long-term outcome of imatinib 400 mg compared to imatinib 600 mg or imatinib 400 mg daily in combination with cytarabine or pegylated interferon alpha 2a for chronic myeloid leukae... by Guilhot, Francois, Rigal-Huguet, Françoise, Guilhot, Joëlle, Guerci-Bresler, Agnès-Paule, Maloisel, Frédéric, Rea, Delphine, Coiteux, Valérie, Gardembas, Martine, Berthou, Christian, Vekhoff, Anne, Jourdan, Eric, Berger, Marc, Fouillard, Loïc, Alexis, Magda, Legros, Laurence, Rousselot, Philippe, Delmer, Alain, Lenain, Pascal, Escoffre Barbe, Martine, Gyan, Emmanuel, Bulabois, Claude-Eric, Dubruille, Viviane, Joly, Bertrand, Pollet, Bertrand, Cony-Makhoul, Pascale, Johnson-Ansah, Hyacinthe, Mercier, Melanie, Caillot, Denis, Charbonnier, Aude, Kiladjian, Jean-Jacques, Chapiro, Jacques, Penot, Amélie, Dorvaux, Véronique, Vaida, Iona, Santagostino, Alberto, Roy, Lydia, Zerazhi, Hacene, Deconinck, Eric, Maisonneuve, Herve, Plantier, Isabelle, Lebon, Delphine, Arkam, Yazid, Cambier, Nathalie, Ghomari, Kamel, Miclea, Jean-Michel, Glaisner, Sylvie, Cayuela, Jean-Michel, Chomel, Jean-Claude, Muller, Marc, Lhermitte, Ludovic, Delord, Marc, Preudhomme, Claude, Etienne, Gabriel, Mahon, François-Xavier, Nicolini, Franck- Emmanuel

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PIEZO1 activation delays erythroid differentiation of normal and hereditary xerocytosis-derived human progenitor cells by Caulier, Alexis, Jankovsky, Nicolas, Demont, Yohann, Ouled-Haddou, Hakim, Demagny, Julien, Guitton, Corinne, Merlusca, Lavinia, Lebon, Delphine, Vong, Pascal, Aubry, Aurélien, Lahary, Agnès, Rose, Christian, Gréaume, Sandrine, Cardon, Emilie, Platon, Jessica, Ouadid-Ahidouch, Halima, Rochette, Jacques, Marolleau, Jean-Pierre, Picard, Véronique, Garçon, Loïc

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Coronavirus 229E-Related Pneumonia in Immunocompromised Patients by Pene, Frédéric, Merlat, Annabelle, Vabret, Astrid, Rozenberg, Flore, Buzyn, Agnès, Dreyfus, François, Cariou, Alain, Freymuth, François, Lebon, Pierre

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Single-Unit Transfusion Is Non Inferior to Double Unit Transfusion in Patients with Hematological Disorders Receiving Allogeneic or Autologous Bone Marrow Transplant or Induction C... by Chantepie, Sylvain, Mear, Jean-Baptiste, Briant, Anais R, Vilque, Jean-Pierre, Gac, Anne-Claire, Cheze, Stephane, Girault, Stephane, Turlure, Pascal, Marolleau, Jean-Pierre, Lebon, Delphine, Charbonnier, Amandine, Jardin, Fabrice, Lenain, Pascal, Peyro Saint Paul, Laure, Abonnet, Véronique, Dutheil, Jean-Jacques, Chene, Yannick, Bazin, Agnès, Reman, Oumedaly, Parienti, Jean-Jacques

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Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number Variations by Cárdenas-de-la-Parra, Alonso, Martin-Brevet, Sandra, Moreau, Clara, Rodriguez-Herreros, Borja, Fonov, Vladimir S., Maillard, Anne M., Zürcher, Nicole R., Addor, Marie-Claude, Andrieux, Joris, Arveiler, Benoît, Baujatm, Geneviève, Sloan-Bénan, Frédérique, Belfiore, Marco, Bonneau, Dominique, Bouquillon, Sonia, Boute, Odile, Brusco, Alfredo, Busa, Tiffany, Caberg, Jean-Hubert, Campion, Dominique, Colombert, Vanessa, Cordier, Marie-Pierre, David, Albert, Debray, François-Guillaume, Delrue, Marie-Ange, Doco-Fenzy, Martine, Dunkhase-Heinl, Ulrike, Edery, Patrick, Fagerberg, Christina, Faivre, Laurence, Forzano, Francesca, Genevieve, David, Gérard, Marion, Giachino, Daniela, Guichet, Agnès, Guillin, Olivier, Héron, Delphine, Isidor, Bertrand, Jacquette, Aurélia, Jaillard, Sylvie, Journel, Hubert, Keren, Boris, Lacombe, Didier, Lebon, Sébastien, Le Caignec, Cédric, Lemaître, Marie-Pierre, Lespinasse, James, Mathieu-Dramart, Michèle, Mercier, Sandra, Mignot, Cyril, Missirian, Chantal, Petit, Florence, Pilekær Sørensen, Kristina, Pinson, Lucile, Plessis, Ghislaine, Prieur, Fabienne, Rooryck-Thambo, Caroline, Rossi, Massimiliano, Sanlaville, Damien, Schlott Kristiansen, Britta, Schluth-Bolard, Caroline, Till, Marianne, Van Haelst, Mieke, Van Maldergem, Lionel, Hadjikhani, Nouchine, Beckmann, Jacques S., Reymond, Alexandre, Draganski, Bogdan, Jacquemont, Sébastien, Collins, D. Louis

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Diphtheria, tetanus, poliomyelitis, yellow fever and hepatitis B seroprevalence among HIV1-infected migrants. Results from the ANRS VIHVO vaccine sub-study by Mullaert, Jimmy, Abgrall, Sophie, Lele, Nathalie, Batteux, Frederic, Slama, Lilia Ben, Meritet, Jean-Francois, Lebon, Pierre, Bouchaud, Olivier, Grabar, Sophie, Launay, Odile

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A novel recurrent mitochondrial DNA mutation in ND3 gene is associated with isolated complex I deficiency causing Leigh syndrome and dystonia by Sarzi, Emmanuelle, Brown, Michael D., Lebon, Sophie, Chretien, Dominique, Munnich, Arnold, Rotig, Agnès, Procaccio, Vincent

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The spectrum of systemic involvement in adults presenting with renal lesion and mitochondrial tRNA(Leu) gene mutation by Guéry, Bruno, Choukroun, Gabriel, Noël, Laure-Hélène, Clavel, Pierre, Rötig, Agnès, Lebon, Sophie, Rustin, Pierre, Bellané-Chantelot, Christine, Mougenot, Béatrice, Grünfeld, Jean-Pierre, Chauveau, Dominique

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Type I interferon as a stimulus for cross-priming by Le Bon, Agnès, Tough, David F

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Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey by Briggs, Tracy A., Rice, Gillian I., Adib, Navid, Ades, Lesley, Barete, Stephane, Baskar, Kannan, Baudouin, Veronique, Cebeci, Ayse N., Clapuyt, Philippe, Coman, David, De Somer, Lien, Finezilber, Yael, Frydman, Moshe, Guven, Ayla, Heritier, Sébastien, Karall, Daniela, Kulkarni, Muralidhar L., Lebon, Pierre, Levitt, David, Le Merrer, Martine, Linglart, Agnes, Livingston, John H., Navarro, Vincent, Okenfuss, Ericka, Puel, Anne, Revencu, Nicole, Scholl-Bürgi, Sabine, Vivarelli, Marina, Wouters, Carine, Bader-Meunier, Brigitte, Crow, Yanick J.

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Assay of mitochondrial respiratory chain complex I in human lymphocytes and cultured skin fibroblasts by Chretien, Dominique, Bénit, Paule, Chol, Marie, Lebon, Sophie, Rötig, Agnès, Munnich, Arnold, Rustin, Pierre

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A novel mutation in the human complex I NDUFS7 subunit associated with Leigh syndrome by Lebon, Sophie, Rodriguez, Diana, Bridoux, Delphine, Zerrad, Amal, Rötig, Agnès, Munnich, Arnold, Legrand, Alain, Slama, Abdelhamid

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Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey by Briggs, Tracy A., Rice, Gillian I., Adib, Navid, Ades, Lesley, Barete, Stephane, Baskar, Kannan, Baudouin, Veronique, Cebeci, Ayse N., Clapuyt, Philippe, Coman, David, De Somer, Lien, Finezilber, Yael, Frydman, Moshe, Guven, Ayla, Heritier, Sébastien, Karall, Daniela, Kulkarni, Muralidhar L., Lebon, Pierre, Levitt, David, Le Merrer, Martine, Linglart, Agnes, Livingston, John H., Navarro, Vincent, Okenfuss, Ericka, Puel, Anne, Revencu, Nicole, Scholl-Bürgi, Sabine, Vivarelli, Marina, Wouters, Carine, Bader-Meunier, Brigitte, Crow, Yanick J.

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Molecular diagnostics of mitochondrial disorders by Rötig, Agnès, Lebon, Sophie, Zinovieva, Elena, Mollet, Julie, Sarzi, Emmanuelle, Bonnefont, Jean-Paul, Munnich, Arnold

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A novel mutation of the NDUFS7 gene leads to activation of a cryptic exon and impaired assembly of mitochondrial complex I in a patient with Leigh syndrome by Lebon, Sophie, Minai, Limor, Chretien, Dominique, Corcos, Johanna, Serre, Valérie, Kadhom, Noman, Steffann, Julie, Pauchard, Jean-Yves, Munnich, Arnold, Bonnefont, Jean-Paul, Rötig, Agnès

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Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonse... by BENIT, Paule, STEFFANN, Julie, MUNNICH, Arnold, RÖTIG, Agnès, LEBON, Sophie, CHRETIEN, Dominique, KADHOM, Noman, DE LONLAY, Pascale, GOLDENBERG, Alice, DUMEZ, Yves, DOMMERGUES, Marc, RUSTIN, Pierre

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