检索结果 - Wassila Carpentier

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  1. 1
    Limitations of IL-2 and Rapamycin in Immunotherapy of Type 1 Diabetes

    Limitations of IL-2 and Rapamycin in Immunotherapy of Type 1 Diabetes 由 Audrey Baeyens, Louis Pérol, Gwladys Fourcade, Nicolas Cagnard, Wassila Carpentier, Janine Woytschak, Onur Boyman, Agnès Hartemann, Eliane Piaggio

    出版 2013
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  2. 2
    Expansion of Functionally Anergic CD21−/low Marginal Zone-like B Cell Clones in Hepatitis C Virus Infection-Related Autoimmunity

    Expansion of Functionally Anergic CD21−/low Marginal Zone-like B Cell Clones in Hepatitis C Virus Infection-Related Autoimmunity 由 Benjamin Terrier, Florence Joly, Thomas Vazquez, Philippe Benech, Michèlle Rosenzwajg, Wassila Carpentier, Marlène Garrido, Pascale Ghillani‐Dalbin, David Klatzmann, P. Cacoub, David Saadoun

    出版 2011
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  3. 3
    Patterns of chromosomal copy-number alterations in intrahepatic cholangiocarcinoma

    Patterns of chromosomal copy-number alterations in intrahepatic cholangiocarcinoma 由 Cyril Dalmasso, Wassila Carpentier, Catherine Guettier, Sophie Camilleri‐Bröet, Wyllians Vendramini Borelli, Cedália Rosane Campos dos Santos, Denis Castaing, Jean‐Charles Duclos‐Vallée, Philippe Broët

    出版 2015
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  4. 4
    Gene Expression Analyses Identify Narp Contribution in the Development of l-DOPA-Induced Dyskinesia

    Gene Expression Analyses Identify Narp Contribution in the Development of l-DOPA-Induced Dyskinesia 由 Fanny Charbonnier‐Beaupel, Marion Malerbi, Cristina Alcacer, Khadija Tahiri, Wassila Carpentier, Chuansong Wang, Matthew J. During, Desheng Xu, Paul F. Worley, Jean‐Antoine Girault, Denis Hervé, Jean‐Christophe Corvol

    出版 2015
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  5. 5
    Pathogenic T cells have a paradoxical protective effect in murine autoimmune diabetes by boosting Tregs

    Pathogenic T cells have a paradoxical protective effect in murine autoimmune diabetes by boosting Tregs 由 Yenkel Grinberg‐Bleyer, David Saadoun, Audrey Baeyens, Fabienne Billiard, Jérémie D. Goldstein, Sylvie Grégoire, Gaëlle Martin, Rima Elhage, Nicolas Dérian, Wassila Carpentier, Gilles Marodon, David Klatzmann, Eliane Piaggio, Benoı̂t L. Salomon

    出版 2010
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  6. 6
    IL-2 reverses established type 1 diabetes in NOD mice by a local effect on pancreatic regulatory T cells

    IL-2 reverses established type 1 diabetes in NOD mice by a local effect on pancreatic regulatory T cells 由 Yenkel Grinberg‐Bleyer, Audrey Baeyens, Sylvaine You, Rima Elhage, Gwladys Fourcade, Sylvie Grégoire, Nicolas Cagnard, Wassila Carpentier, Qizhi Tang, Jeffrey A. Bluestone, Lucienne Chatenoud, David Klatzmann, Benoı̂t L. Salomon, Eliane Piaggio

    出版 2010
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  7. 7
    <i>CRB1</i> mutations in inherited retinal dystrophies

    <i>CRB1</i> mutations in inherited retinal dystrophies 由 Kinga M. Bujakowska, Isabelle Audo, Saddek Mohand‐Saïd, Marie‐Elise Lancelot, Aline Antonio, Aurore Germain, Thierry Léveillard, Mélanie Letexier, Jean‐Paul Saraiva, Christine Lonjou, Wassila Carpentier, José‐Alain Sahel, Shomi S. Bhattacharya, Christina Zeitz

    出版 2011
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  8. 8
    Restoration of regulatory and effector T cell balance and B cell homeostasis in systemic lupus erythematosus patients through vitamin D supplementation

    Restoration of regulatory and effector T cell balance and B cell homeostasis in systemic lupus erythematosus patients through vitamin D supplementation 由 Benjamin Terrier, Nicolas Dérian, Y. Schoindre, Wahiba Chaara, Guillaume Géri, Noël Zahr, K. Mariampillai, Michèlle Rosenzwajg, Wassila Carpentier, Lucile Musset, Jean‐Charles Piette, Adrien Six, David Klatzmann, David Saadoun, P. Cacoub, N. Costedoat‐Chalumeau

    出版 2012
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  9. 9
    CX3CR1 deficiency promotes muscle repair and regeneration by enhancing macrophage ApoE production

    CX3CR1 deficiency promotes muscle repair and regeneration by enhancing macrophage ApoE production 由 Ludovic Arnold, Hélène Perrin, Camille Baudesson de Chanville, Marielle Saclier, Patricia Hermand, Lucie Poupel, Elodie Guyon, Fabrice Licata, Wassila Carpentier, José Vilar, Rémi Mounier, Bénédicte Chazaud, Nora Benhabilès, Alexandre Boissonnas, Béhazine Combadière, Christophe Combadière

    出版 2015
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  10. 10
    Distinct Genetic Loci Control Plasma HIV-RNA and Cellular HIV-DNA Levels in HIV-1 Infection: The ANRS Genome Wide Association 01 Study

    Distinct Genetic Loci Control Plasma HIV-RNA and Cellular HIV-DNA Levels in HIV-1 Infection: The ANRS Genome Wide Association 01 Study 由 Cyril Dalmasso, Wassila Carpentier, Laurence Meyer, Christine Rouzioux, Cécile Goujard, Marie‐Laure Chaix, Olivier Lambotte, Véronique Avettand-Fènoël, Sigrid Le Clerc, Laurent Denis, Christiane Deveau, Faroudy Boufassa, Patrice Debré, Jean‐François Delfraissy, Philippe Broët, Ioannis Théodorou

    出版 2008
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  11. 11
    A Genome-Wide Association Study in Caucasian Women Points Out a Putative Role of the STXBP5L Gene in Facial Photoaging

    A Genome-Wide Association Study in Caucasian Women Points Out a Putative Role of the STXBP5L Gene in Facial Photoaging 由 Sigrid Le Clerc, Lieng Taing, Khaled Ezzedine, Julie Latreille, Olivier Delaneau, Toufik Labib, Cédric Coulonges, Anne Bernard, Safa Melak, Wassila Carpentier, Denis Malvy, Randa Jdid, Pilar Galán, Serge Herçberg, Frédérique Morizot, Christiane Guinot, Erwin Tschachler, J F Zagury

    出版 2012
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  12. 12
    Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability

    Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability 由 Tangui Le Guen, Laurent Jullien, Fabien Touzot, Michael Schertzer, Laetitia Gaillard, Mylène Perderiset, Wassila Carpentier, Patrick Nitschké, Capucine Pïcard, Gérard Couillault, Jean Soulier, Alain Fischer, Isabelle Callebaut, Nada Jabado, Arturo Londoño‐Vallejo, Jean‐Pierre de Villartay, Patrick Revy

    出版 2013
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  13. 13
    Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation

    Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation 由 Despina Moshous, Emmanuel Martin, Wassila Carpentier, Apiradee Lim, Isabelle Callebaut, Danielle Canioni, Fabian Hauck, Jacek Majewski, Jeremy Schwartzentruber, Patrick Nitschké, Nicolas Sirvent, Pierre Frange, Capucine Pïcard, Stéphane Blanche, Patrick Revy, Alain Fischer, Sylvain Latour, Nada Jabado, Jean‐Pierre de Villartay

    出版 2013
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  14. 14
    RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects

    RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects 由 Marc Jeanpierre, G. Macé, Mélanie Parisot, Vincent Morinière, A. Pawtowsky, Max E. Benabou, Jéléna Martinovic, Jeanne Amiel, Tania Attié‐Bitach, Anne‐Lise Delezoide, Philippe Loget, Patricia Blanchet, Dominique Gaillard, M. Gonzalés, Wassila Carpentier, Patrick Nitschké, Frédéric Torès, Laurence Heidet, Corinne Antignac, Rémi Salomon

    出版 2011
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  15. 15
    An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation

    An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation 由 Tangui Le Guen, Fabien Touzot, Isabelle André‐Schmutz, Chantal Lagresle‐Peyrou, Benoît France, Laëtitia Kermasson, Nathalie Lambert, Capucine Pïcard, Patrick Nitschké, Wassila Carpentier, Christine Bôle‐Feysot, Apiradee Lim, Marina Cavazzana, Isabelle Callebaut, Jean Soulier, Nada Jabado, Alain Fischer, Jean‐Pierre de Villartay, Patrick Revy

    出版 2015
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  16. 16
    KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations

    KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations 由 Stephan Klebe, Alexander Lossos, Hamid Azzedine, Emeline Mundwiller, Ruth Sheffer, Marion Gaussen, Cécilia Marelli, Magdalena Nawara, Wassila Carpentier, Vincent Meyer, Agnès Rastetter, Elodie Martin, Delphine Bouteiller, Laurent Orlando, Gàbor Gyapay, Khalid H. El-Hachimi, Bat-El Zimmerman, Moriya Gamliel, Adel Misk, Israela Lerer, Alexis Brice, Alexandra Durr, Giovanni Stévanin

    出版 2012
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  17. 17
    Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

    Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females 由 Christel Depienne, Delphine Bouteiller, Boris Keren, Emmanuel Cheuret, Karine Poirier, Oriane Trouillard, B Benyahia, Chloé Quēlin, Wassila Carpentier, Sophie Julia, Alexandra Afenjar, Agnès Gautier, François Rivier, Sophie Meyer, Patrick Berquin, Marie Hélias, Isabelle Py, Serge Rivera, Nadia Bahi‐Buisson, Isabelle Gourfinkel‐An, Cécile Cazeneuve, Merle Ruberg, Alexis Brice, Rima Nabbout, Eric Leguern

    出版 2009
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  18. 18
    Genomewide Association Study of an AIDS‐Nonprogression Cohort Emphasizes the Role Played by<i>HLA</i>Genes (ANRS Genomewide Association Study 02)

    Genomewide Association Study of an AIDS‐Nonprogression Cohort Emphasizes the Role Played by<i>HLA</i>Genes (ANRS Genomewide Association Study 02) 由 Sophie Limou, Sigrid Le Clerc, Cédric Coulonges, Wassila Carpentier, Christian Dina, Olivier Delaneau, Taoufik Labib, Lieng Taing, Robert Sladek, Christiane Deveau, Rojo Ratsimandresy, Matthieu Montès, Jean‐Louis Spadoni, Jean‐Daniel Lelièvre, Yves Lévy, Amu Therwath, François Schächter, Fumihiko Matsuda, Marta Gut, Philippe Froguel, Jean‐François Delfraissy, Serge Herçberg, Jean‐François Zagury

    出版 2008
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  19. 19
    Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human

    Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human 由 Michel Kielar, Françoise Phan Dinh Tuy, Sara Bizzotto, Cécile Lebrand, Camino de Juan Romero, Karine Poirier, Renske Oegema, Grazia M.S. Mancini, Nadia Bahi‐Buisson, Robert Olaso, Anne‐Gaëlle Le Moing, Katia Boutourlinsky, Dominique Boucher, Wassila Carpentier, Patrick Berquin, Jean‐François Deleuze, Richard Belvindrah, Vı́ctor Borrell, Egbert Welker, Jamel Chelly, Alexandre Croquelois, Fiona Francis

    出版 2014
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  20. 20
    RAD51 Haploinsufficiency Causes Congenital Mirror Movements in Humans

    RAD51 Haploinsufficiency Causes Congenital Mirror Movements in Humans 由 Christel Depienne, Delphine Bouteiller, Aurélie Méneret, S. Billot, Sergiu Groppa, Stephan Klebe, Fanny Charbonnier‐Beaupel, Jean‐Christophe Corvol, Jean‐Paul Saraiva, Norbert Brueggemann, Kailash P. Bhatia, M. Cincotta, Vanessa Brochard, Constance Flamand‐Roze, Wassila Carpentier, Sabine Meunier, Yannick Marie, Marion Gaussen, Giovanni Stévanin, Rosine Wehrlé, Marie Vidailhet, Christine Klein, Isabelle Dusart, Alexis Brice, Emmanuel Roze

    出版 2012
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