Výsledky vyhledávání - Angélique Pichot

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  1. 1
    Platelets favor the outgrowth of established metastases

    Platelets favor the outgrowth of established metastases Autor María Jesús García-León, Cristina Liboni, Vincent Mittelheisser, Louis Bochler, Gautier Follain, Clarisse Mouriaux, Ignacio Busnelli, Annabel Larnicol, Florent Colin, Marina Peralta, Naël Osmani, Valentin Gensbittel, Catherine Bourdon, Rafael Samaniego, Angélique Pichot, Nicodème Paul, Anne Molitor, Raphaël Carapito, Martine Jandrot‐Perrus, Olivier Lefèbvre, P Mangin, Jacky G. Goetz

    Vydáno 2024
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  2. 2
    <i>NCKAP1L</i>defects lead to a novel syndrome combining immunodeficiency, lymphoproliferation, and hyperinflammation

    <i>NCKAP1L</i>defects lead to a novel syndrome combining immunodeficiency, lymphoproliferation, and hyperinflammation Autor Carla N. Castro, Michèlle Rosenzwajg, Raphaël Carapito, Mohammad Shahrooei, Martina Konantz, Amjad Khan, Zhichao Miao, Miriam Groß, Thibaud Tranchant, Mirjana Radosavljevic, Nicodème Paul, Tristan Stemmelen, Fabien Pitoiset, Aurélie Hirschler, Benoît Nespola, Anne Molitor, Véronique Rolli, Angélique Pichot, Laura Faletti, Bruno Rinaldi, Sylvie Friant, Mark Mednikov, Hatice Karaüzüm, M. Javad Aman, Christine Carapito, Claudia Lengerke, Vahid Ziaee, Wafaa Eyaid, Stephan Ehl, Fayhan Alroqi, Nima Parvaneh, Seiamak Bahram

    Vydáno 2020
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  3. 3
    Hemodynamic Forces Tune the Arrest, Adhesion, and Extravasation of Circulating Tumor Cells

    Hemodynamic Forces Tune the Arrest, Adhesion, and Extravasation of Circulating Tumor Cells Autor Gautier Follain, Naël Osmani, Ana Sofia Azevedo, Guillaume Allio, Luc Mercier, Matthia A. Karreman, Gergely Solecki, María Jesús García-León, Olivier Lefèbvre, Nina Fekonja, Claudia Hille, Vincent Chabannes, Guillaume Dollé, Thibaut Métivet, François Der Hovsepian, Christophe Prud'Homme, Angélique Pichot, Nicodème Paul, Raphaël Carapito, Seiamak Bahram, Bernhard Ruthensteiner, André Kemmling, Susanne Siemonsen, Tanja Schneider, Jens Fiehler, Markus Glatzel, Frank Winkler, Yannick Schwab, Klaus Pantel, Sébastien Harlepp, Jacky G. Goetz

    Vydáno 2018
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  4. 4
    Peripheral positioning of lysosomes supports melanoma aggressiveness

    Peripheral positioning of lysosomes supports melanoma aggressiveness Autor Kateřina Jeřábková, Marina Peralta, Kuang-Jing Huang, Antoine Mousson, Clara Bourgeat Maudru, Louis Bochler, Ignacio Busnelli, Rabia Karali, Hélène Justiniano, Lucian-Mihai Lisii, Philippe Carl, Vincent Mittelheisser, Nandini Asokan, Annabel Larnicol, Olivier Lefèbvre, Hugo Lachuer, Angélique Pichot, Tristan Stemmelen, Anne Molitor, Léa Scheid, Quentin Frenger, Frédéric Gros, Aurélie Hirschler, François Delalande, Émilie Sick, Raphaël Carapito, Christine Carapito, Dan Lipsker, Kristine Schauer, Philippe Rondé, Vincent Hyenne, Jacky G. Goetz

    Vydáno 2025
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  5. 5
    The MHC class I MICA gene is a histocompatibility antigen in kidney transplantation

    The MHC class I MICA gene is a histocompatibility antigen in kidney transplantation Autor Raphaël Carapito, Ismaïl Aouadi, Martin Verniquet, Meiggie Untrau, Angélique Pichot, Thomas Beaudrey, Xavier Bassand, Sébastien Meyer, Loic Faucher, Juliane Posson, Aurore Morlon, И. В. Котова, Florent Delbos, Alexandre Walencik, Alice Aarnink, Anne Kennel, Caroline Suberbielle, Jean‐Luc Taupin, Benedict M. Matern, Eric Spierings, Nicolas Congy‐Jolivet, Arnaud Essaydi, Peggy Perrin, Antoine Blancher, Dominique Charron, Nezih Cereb, Myriam Maumy‐Bertrand, Frédèric Bertrand, Valérie Garrigue, Vincent Pernin, Laurent Weekers, Maarten Naesens, Nassim Kamar, Christophe Legendre, Denis Glotz, Sophie Caillard, Marc Ladrière, Magali Giral, Dany Anglicheau, Caner Süsal, Seiamak Bahram

    Vydáno 2022
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  6. 6
    Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond–like features

    Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond–like features Autor Raphaël Carapito, Martina Konantz, Catherine Paillard, Zhichao Miao, Angélique Pichot, Magalie S. Leduc, Yaping Yang, Katie Bergstrom, Donald H. Mahoney, Deborah L. Shardy, Ghada Alsaleh, Lydie Naegely, Aline Kolmer, Nicodème Paul, Antoine Hanauer, Véronique Rolli, Joëlle S. Müller, Elisa Alghisi, Loïc Sauteur, Cécile Macquin, Aurore Morlon, Consuelo Sebastia Sancho, Patrizia Amati‐Bonneau, Vincent Procaccio, Anne‐Laure Mosca‐Boidron, Nathalie Marle, Naël Osmani, Olivier Lefèbvre, Jacky G. Goetz, Şule Ünal, Nurten Akarsu, Mirjana Radosavljevic, Marie‐Pierre Chenard, Fanny Rialland, Audrey Grain, Marie C. Béné, Marion Eveillard, Marie Vincent, Julien Guy, Laurence Faivre, Christel Thauvin‐Robinet, Julien Thévenon, Kasiani C. Myers, Mark D. Fleming, Akiko Shimamura, Elodie Bottollier-Lemallaz, Éric Westhof, Claudia Lengerke, Bertrand Isidor, Seiamak Bahram

    Vydáno 2017
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  7. 7
    Matching for the nonconventional MHC-I MICA gene significantly reduces the incidence of acute and chronic GVHD

    Matching for the nonconventional MHC-I MICA gene significantly reduces the incidence of acute and chronic GVHD Autor Raphaël Carapito, Nicolas Jung, Marius Kwemou, Meiggie Untrau, Sandra Michel, Angélique Pichot, Gaëlle Giacometti, Cécile Macquin, W. Ilias, Aurore Morlon, Irina Kotova, Petya Apostolova, Annette Schmitt‐Graeff, Anne Cesbron, Katia Gagne, Machteld Oudshoorn, Bronno van der Holt, Myriam Labalette, Eric Spierings, Christophe Picard, Pascale Loiseau, Ryad Tamouza, Antoine Toubert, A. Parissiadis, Valérie Dubois, Xavier Lafarge, Myriam Maumy‐Bertrand, Frédèric Bertrand, Luca Vago, Fabio Ciceri, Catherine Paillard, Sergi Querol, Jorge Sierra, Katharina Fleischhauer, Arnon Nagler, Myriam Labopin, Hidetoshi Inoko, Peter A. von dem Borne, Jürgen Kuball, Masao Ôta, Yoshihiko Katsuyama, Mauricette Michallet, Bruno Lioure, Régis Peffault de Latour, Didier Blaise, Jan J. Cornelissen, Ibrahim Yakoub‐Agha, Frans H.J. Claas, Philippe Moreau, Nöel Milpied, Dominique Charron, Mohamad Mohty, Robert Zeiser, Gerard Socié, Seiamak Bahram

    Vydáno 2016
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  8. 8
    ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder

    ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder Autor Raphaël Carapito, Ekaterina L. Ivanova, Aurore Morlon, Linyan Meng, Anne Molitor, Éva Erdmann, Bruno Kieffer, Angélique Pichot, Lydie Naegely, Aline Kolmer, Nicodème Paul, Antoine Hanauer, Frédéric Tran Mau‐Them, Nolwenn Jean‐Marçais, Susan M. Hiatt, Gregory M. Cooper, Tatiana Tvrdik, Alison M. Muir, Clémantine Dimartino, Maya Chopra, Jeanne Amiel, Christopher T. Gordon, Fabien Dutreux, Aurore Garde, Christel Thauvin‐Robinet, Xia Wang, Magalie S. Leduc, Meredith Phillips, Heather P. Crawford, Mary K. Kukolich, David Hunt, Victoria Harrison, Mira Kharbanda, Robert Śmigiel, Nina B. Gold, Christina Hung, David Viskochil, Sarah Dugan, Pınar Bayrak‐Toydemir, Géraldine Joly‐Helas, Anne‐Marie Guerrot, Caroline Schluth–Bolard, Marlène Rio, Ingrid M. Wentzensen, Kirsty McWalter, Rhonda E. Schnur, Andrea M. Lewis, Seema R. Lalani, Noël Mensah-Bonsu, Jocelyn Céraline, Zijie Sun, Rafał Płoski, Carlos A. Bacino, Heather C. Mefford, Laurence Faivre, Olaf A. Bodamer, Jamel Chelly, Bertrand Isidor, Seiamak Bahram

    Vydáno 2019
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  9. 9
    Identification of driver genes for critical forms of COVID-19 in a deeply phenotyped young patient cohort

    Identification of driver genes for critical forms of COVID-19 in a deeply phenotyped young patient cohort Autor Raphaël Carapito, Richard Y. Li, Julie Helms, Christine Carapito, Sharvari Gujja, Véronique Rolli, Raony Guimaraes, Jose Malagon-Lopez, Perrine Spinnhirny, Alexandre Lederle, Razieh Mohseninia, Aurélie Hirschler, Leslie Muller, Paul Bastard, Adrian Gervais, Qian Zhang, François Danion, Yvon Ruch, Maleka Schenck, Olivier Collange, Thiên‐Nga Chamaraux‐Tran, Anne Molitor, Angélique Pichot, Alice Bernard, Ouria Tahar, Sabrina Bibi-Triki, Haiguo Wu, Nicodème Paul, Sylvain Mayeur, Annabel Larnicol, Géraldine Laumond, Julia Frappier, Sylvie Schmidt, Antoine Hanauer, Cécile Macquin, Tristan Stemmelen, Michael Simons, Xavier Mariette, Olivier Hermine, Samira Fafi‐Kremer, B. Goichot, Bernard Drénou, Khaldoun Kuteifan, Julien Pottecher, Paul‐Michel Mertès, Shweta Kailasan, M. Javad Aman, Elisa Pin, Peter Nilsson, Anne Thomas, Alain Viari, Damien Sanlaville, Francis Schneider, Jean Sibilia, Pierre‐Louis Tharaux, Jean‐Laurent Casanova, Yves Hansmann, Daniel A. Lidar, Mirjana Radosavljevic, Jeffrey R. Gulcher, Ferhat Meziani, Christiane Moog, Thomas W. Chittenden, Seiamak Bahram

    Vydáno 2021
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  10. 10
    Identification of driver genes for severe forms of COVID-19 in a deeply phenotyped young patient cohort

    Identification of driver genes for severe forms of COVID-19 in a deeply phenotyped young patient cohort Autor Raphaël Carapito, Richard Li, Julie Helms, Christine Carapito, Sharvari Gujja, Véronique Rolli, Raony Guimaraes, Jose Malagon-Lopez, Perrine Spinnhirny, Razieh Mohseninia, Aurélie Hirschler, Leslie Muller, Paul Bastard, Adrian Gervais, Qian Zhang, François Danion, Yvon Ruch, Maleka Schenck-Dhif, Olivier Collange, Thiên‐Nga Chamaraux‐Tran, Anne Molitor, Angélique Pichot, Alice Bernard, Ouria Tahar, Sabrina Bibi-Triki, Haiguo Wu, Nicodème Paul, Sylvain Mayeur, Annabel Larnicol, Géraldine Laumond, Julia Frappier, Sylvie Schmidt, Antoine Hanauer, Cécile Macquin, Tristan Stemmelen, Michael Simons, Xavier Mariette, Olivier Hermine, Samira Fafi‐Kremer, B. Goichot, Bernard Drénou, Khaldoun Kuteifan, Julien Pottecher, Paul‐Michel Mertès, Shweta Kailasan, M. Javad Aman, Elisa Pin, Peter Nilsson, Anne Thomas, Alain Viari, Damien Sanlaville, Francis Schneider, Jean Sibilia, Pierre‐Louis Tharaux, Jean-Laurent Casanova, Yves Hansmann, Daniel A. Lidar, Mirjana Radosavljevic, Jeffrey R. Gulcher, Ferhat Meziani, Christiane Moog, Thomas W. Chittenden, Seiamak Bahram

    Vydáno 2021
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