Որոնման արդյունքները - Patrick Revy
- Ցուցադրվում են 1 - 20 արդյունքները 45
- Գնացեք Հաջորդ էջ
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The Block in Immunoglobulin Class Switch Recombination Caused by Activation-Induced Cytidine Deaminase Deficiency Occurs Prior to the Generation of DNA Double Strand Breaks in Swit... Nadia Catalan, Françoise Selz, Kohsuke Imai, Patrick Revy, Alain Fischer, Anne Durandy
Հրապարակվել է 2003Artigo -
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Cernunnos Interacts with the XRCC4·DNA-ligase IV Complex and Is Homologous to the Yeast Nonhomologous End-joining Factor Nej1 Isabelle Callebaut, Laurent Malivert, Alain Fischer, Jean‐Paul Mornon, Patrick Revy, Jean‐Pierre de Villartay
Հրապարակվել է 2006Artigo -
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Human RTEL1 Interacts with KPNB1 (Importin β) and NUP153 and Connects Nuclear Import to Nuclear Envelope Stability in S-Phase Michael Schertzer, Laurent Jullien, André Luiz Pinto Santos, Rodrigo T. Calado, Patrick Revy, Arturo Londoño‐Vallejo
Հրապարակվել է 2023Artigo -
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TGF-β1 Prevents the Noncognate Maturation of Human Dendritic Langerhans Cells Frédéric Geissmann, Patrick Revy, Armelle Régnault, Yves Lepelletier, Michel Dy, Nicole Brousse, Sebastián Amigorena, Olivier Hermine, Anne Durandy
Հրապարակվել է 1999Artigo -
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Function of Apollo (SNM1B) at telomere highlighted by a splice variant identified in a patient with Hoyeraal–Hreidarsson syndrome Fabien Touzot, Isabelle Callebaut, Jean Soulier, Laetitia Gaillard, Chantal Azerrad, Anne Durandy, Alain Fischer, Jean‐Pierre de Villartay, Patrick Revy
Հրապարակվել է 2010Artigo -
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RAG2 and XLF/Cernunnos interplay reveals a novel role for the RAG complex in DNA repair Chloé Lescale, Vincent Abramowski, Marie Bedora-Faure, Valentine Murigneux, Gabriella Vera, David B. Roth, Patrick Revy, Jean‐Pierre de Villartay, Ludovic Deriano
Հրապարակվել է 2016Artigo -
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Interferon-γ –Receptor Deficiency in an Infant with Fatal Bacille Calmette–Guérin Infection Emmanuelle Jouanguy, Frédéric Altare, Salma Lamhamedi, Patrick Revy, Jean‐François Emile, Melanie J. Newport, Michael Levin, Stéphane Blanche, Eric Seboun, Alain Fischer, Jean‐Laurent Casanova
Հրապարակվել է 1996Artigo -
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Cernunnos Deficiency Reduces Thymocyte Life Span and Alters the T Cell Repertoire in Mice and Humans Gabriella Vera, Paola Rivera-Muñoz, Vincent Abramowski, Laurent Malivert, Apiradee Lim, Christine Bôle‐Feysot, Christelle Martin, Benoît Florkin, Sylvain Latour, Patrick Revy, Jean‐Pierre de Villartay
Հրապարակվել է 2012Artigo -
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Abnormal CD40-mediated activation pathway in B lymphocytes from patients with hyper-IgM syndrome and normal CD40 ligand expression. Anne Durandy, Claire Hivroz, Fabienne Mazerolles, Claudine Schiff, Frédéric Bernard, Emmanuelle Jouanguy, Patrick Revy, James P. Di Santo, J F Gauchat, J Y Bonnefoy, Jean‐Laurent Casanova, A Fischer
Հրապարակվել է 1997Artigo -
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Hyper-IgM syndrome type 4 with a B lymphocyte–intrinsic selective deficiency in Ig class-switch recombination Kohsuke Imai, Nadia Catalan, Alessandro Plebani, László Maródi, Özden Sanal, Satoru Kumaki, Vasantha Nagendran, Philip Wood, Catherine Glastre, F. Sarrot-Reynauld, Olivier Hermine, Monique Forveille, Patrick Revy, Alain Fischer, Anne Durandy
Հրապարակվել է 2003Artigo -
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A nonsense mutation in the DNA repair factor Hebo causes mild bone marrow failure and microcephaly Shu Zhang, Corinne Pondarré, Gaëlle Pennarun, Hélène Labussière‐Wallet, Gabriella Vera, Benoît France, Marie Chansel, Isabelle Rouvet, Patrick Revy, Bernard S. López, Jean Soulier, Pascale Bertrand, Isabelle Callebaut, Jean‐Pierre de Villartay
Հրապարակվել է 2016Artigo -
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Bloom syndrome protein restrains innate immune sensing of micronuclei by cGAS Matthieu Gratia, Mathieu P. Rodero, Cécile Conrad, Elias Bou Samra, Mathieu Maurin, Gillian Rice, Darragh Duffy, Patrick Revy, Florence Petit, Russell C. Dale, Yanick J. Crow, Mounira Amor-Guéret, Nicolas Manel
Հրապարակվել է 2019Artigo -
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Structural characterization of filaments formed by human Xrcc4–Cernunnos/XLF complex involved in nonhomologous DNA end-joining Virginie Ropars, Pascal Drevet, Pierre Legrand, Sonia Baconnais, Jérémy Amram, Guilhem Faure, José A. Márquez, Olivier Piétrement, Raphaël Guérois, Isabelle Callebaut, Éric Le Cam, Patrick Revy, Jean‐Pierre de Villartay, Jean‐Baptiste Charbonnier
Հրապարակվել է 2011Artigo -
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PAXX and Xlf interplay revealed by impaired CNS development and immunodeficiency of double KO mice Vincent Abramowski, Etienne Olivier, Ramy Elsaid, Junjie Yang, Aurélie Berland, Laëtitia Kermasson, Benoît Roch, Stefania Musilli, Jean-Paul Moussu, Karelia Lipson-Ruffert, Patrick Revy, Ana Cumano, François D. Boussin, Jean‐Pierre de Villartay
Հրապարակվել է 2017Artigo -
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Cernunnos, a Novel Nonhomologous End-Joining Factor, Is Mutated in Human Immunodeficiency with Microcephaly Dietke Buck, Laurent Malivert, Régina de Chasseval, Anne Barraud, Marie‐Claude Fondanèche, Özden Sanal, Alessandro Plebani, Jean-Louis Stéphan, Markus Hufnagel, Françoise Le Deist, Alain Fischer, Anne Durandy, Jean‐Pierre de Villartay, Patrick Revy
Հրապարակվել է 2006Artigo -
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Heterozygous<i>RTEL1</i>mutations are associated with familial pulmonary fibrosis Caroline Kannengiesser, Raphaël Borie, Christelle Ménard, Marion Réocreux, Patrick Nitschké, Steven Gazal, Hervé Mal, Camille Taillé, Jacques Cadranel, Hilario Nunès, Dominique Valeyre, J.-F. Cordier, Isabelle Callebaut, Cathérine Boileau, Vincent Cottin, Bernard Grandchamp, Patrick Revy, Bruno Crestani
Հրապարակվել է 2015Artigo -
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Primary Microcephaly, Impaired DNA Replication, and Genomic Instability Caused by Compound Heterozygous<i>ATR</i>Mutations Houda Benhelli‐Mokrani, Laetitia Gaillard, Patricia Biasutto, Tangui Le Guen, Fabien Touzot, Nadia Vasquez, Jun Komatsu, Emmanuel Conseiller, Capucine Pïcard, Éliane Gluckman, Christine Francannet, Alain Fischer, Anne Durandy, Jean Soulier, Jean‐Pierre de Villartay, Marina Cavazzana, Patrick Revy
Հրապարակվել է 2012Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Genetics
Gene
Cell biology
DNA
Mutation
Immunology
Immune system
Telomere
DNA damage
Medicine
Molecular biology
DNA repair
Phenotype
Cancer research
Antibody
Microcephaly
Transcription factor
B cell
DNA repair protein XRCC4
Dyskeratosis congenita
Missense mutation
Non-homologous end joining
RNA
T cell
Chemistry
DNA mismatch repair
Genome instability
Haematopoiesis
Recombination