Canlyniadau Chwilio - Mohammed Zarhrate

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  1. 1
    Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation

    Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation gan Aude Magérus‐Chatinet, Bénédicte Neven, Marie–Claude Stolzenberg, Cécile Daussy, Peter D. Arkwright, Nina Lanzarotti, Catherine Schaffner, Sophie Cluet-Dennetiere, Filomeen Haerynck, Gérard Michel, Christine Bôle‐Feysot, Mohammed Zarhrate, Isabelle Radford‐Weiss, Serge Romana, Capucine Pïcard, Alain Fischer, Frédéric Rieux‐Laucat

    Cyhoeddwyd 2010
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  2. 2
    Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans

    Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans gan Camille Humbert, Flora Silbermann, Bharti Morar, Mélanie Parisot, Mohammed Zarhrate, Cécile Masson, Frédéric Torès, Patricia Blanchet, Marie-José Perez, Yuliya Petrov, Philippe Khau Van Kien, J. Roume, Brigitte Leroy, Olivier Gribouval, Luba Kalaydjieva, Laurence Heidet, Rémi Salomon, Corinne Antignac, Alexandre Benmerah, Sophie Saunier, Marc Jeanpierre

    Cyhoeddwyd 2014
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  3. 3
    PIK3CA inhibition in models of proliferative glomerulonephritis and lupus nephritis

    PIK3CA inhibition in models of proliferative glomerulonephritis and lupus nephritis gan Junna Yamaguchi, Pierre Isnard, Noémie Robil, Pierre de la Grange, Clément Hoguin, Alain Schmitt, Aurélie Hummel, Jérôme Mégret, Nicolas Goudin, Marine Luka, Mickaël Ménager, Cécile Masson, Mohammed Zarhrate, Christine Bôle‐Feysot, Michalina Janiszewska, Kornélia Polyák, Julien Dairou, Sara Baldassari, Stéphanie Baulac, Christine Broissand, Christophe Legendre, Fabiola Terzi, Guillaume Canaud

    Cyhoeddwyd 2024
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  4. 4
    Human <scp>ALPI</scp> deficiency causes inflammatory bowel disease and highlights a key mechanism of gut homeostasis

    Human <scp>ALPI</scp> deficiency causes inflammatory bowel disease and highlights a key mechanism of gut homeostasis gan Marianna Parlato, Fabienne Charbit‐Henrion, Jie Pan, Claudio Romano, Rémi Duclaux‐Loras, Marie‐Hélène Le Du, Neil Warner, Paola Francalanci, Julie Bruneau, Marc Bras, Mohammed Zarhrate, Bernadette Bègue, Nicolas Guégan, Sabine Rakotobé, Nathalie Kapel, Paola De Angelis, Anne M. Griffiths, Karoline Fiedler, Eileen Crowley, Frank M. Ruemmele, Aleixo M. Muise, Nadine Cerf‐Bensussan

    Cyhoeddwyd 2018
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  5. 5
    Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes

    Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes gan Jérôme Hadjadj, Nathalie Aladjidi, Helder Fernandes, Guy Leverger, Aude Magérus‐Chatinet, Fabienne Mazerolles, Marie–Claude Stolzenberg, Sidonie Jacques, Capucine Pïcard, Jérémie Rosain, Cécile Fourrage, Sylvain Hanein, Mohammed Zarhrate, Marlène Pasquet, Wadih Abou Chahla, Vincent Barlogis, Yves Bertrand, Isabelle Pellier, Elodie Colomb Bottollier, Fanny Fouyssac, Pascale Blouin, Caroline Thomas, Nathalie Cheikh, Éric Doré, Corinne Pondarré, Dominique Plantaz, Éric Jeziorski, Frédéric Millot, Nicolas Garcelon, Stéphane Ducassou, Yves Pérel, Thierry Leblanc, Bénédicte Neven, Alain Fischer, Frédéric Rieux‐Laucat

    Cyhoeddwyd 2019
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  6. 6
    Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization

    Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization gan Albane A. Bizet, Anita Becker-Heck, Rebecca Ryan, Kristina Weber, Emilie Filhol, Pauline Krug, Jan Halbritter, Marion Delous, Marie-Christine Lasbennes, Bolan Linghu, Edward J. Oakeley, Mohammed Zarhrate, Patrick Nitschké, Meriem Garfa-Traoré, Fabrizio C. Serluca, Fan Yang, Tewis Bouwmeester, Lucile Pinson, Élisabeth Cassuto, Philippe Dubot, Neveen A. Soliman, José‐Alain Sahel, Rémi Salomon, Iain A. Drummond, Marie‐Claire Gubler, Corinne Antignac, Salah‐Dine Chibout, Joseph D. Szustakowski, Friedhelm Hildebrandt, Esben Lorentzen, Andreas W. Sailer, Alexandre Benmerah, Pierre Saint-Mézard, Sophie Saunier

    Cyhoeddwyd 2015
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  7. 7
    Somatic genetic rescue of a germline ribosome assembly defect

    Somatic genetic rescue of a germline ribosome assembly defect gan Shengjiang Tan, Laëtitia Kermasson, Christine Hilcenko, Vasileios Kargas, David Traynor, Ahmed Z. Boukerrou, Norberto Escudero-Urquijo, Alexandre Faille, Alexis Bertrand, Maxim Rossmann, Beatriz Goyenechea, Jin Li, Jonathan Moreil, Olivier Alibeu, Blandine Beaupain, Christine Bôle‐Feysot, Stefano Fumagalli, Sophie Kaltenbach, Jean-Alain Martignoles, Cécile Masson, Patrick Nitschké, Mélanie Parisot, Aurore Pouliet, Isabelle Radford‐Weiss, Frédéric Torès, Jean‐Pierre de Villartay, Mohammed Zarhrate, Ai Ling Koh, Kong Boo Phua, Bruno Reversade, Peter J. Bond, Christine Bellanné‐Chantelot, Isabelle Callebaut, François Delhommeau, Jean Donadieu, Alan J. Warren, Patrick Revy

    Cyhoeddwyd 2021
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  8. 8
    Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in <i>STAT2</i>

    Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in <i>STAT2</i> gan C.J. Duncan, Benjamin Thompson, Rui Chen, Gillian Rice, Florian Gothe, D. F. Young, Simon C. Lovell, Victoria G. Shuttleworth, Vicky Brocklebank, Bronte M. Corner, Andrew Skelton, Vincent Bondet, Jonathan Coxhead, Darragh Duffy, Cécile Fourrage, John H. Livingston, Julija Pavaine, Edmund Cheesman, Stephania Bitetti, Angela Grainger, Meghan Acres, Barbara A. Innes, Aneta Mikulášová, Ruyue Sun, Rafiqul Hussain, Ronnie Wright, Robert Wynn, Mohammed Zarhrate, Leo Zeef, Katrina Wood, Stephen Hughes, Claire L. Harris, Karin R. Engelhardt, Yanick J. Crow, Richard E. Randall, David Kavanagh, Sophie Hambleton, Tracy A. Briggs

    Cyhoeddwyd 2019
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  9. 9
    A monocyte/dendritic cell molecular signature of SARS-CoV-2-related multisystem inflammatory syndrome in children with severe myocarditis

    A monocyte/dendritic cell molecular signature of SARS-CoV-2-related multisystem inflammatory syndrome in children with severe myocarditis gan Camille de Cevins, Marine Luka, Nikaïa Smith, Sonia Meynier, Aude Magérus‐Chatinet, Francesco Carbone, Víctor Paredes, Laura Barnabei, Maxime Batignes, Alexandre Boullé, Marie–Claude Stolzenberg, Brieuc P. Pérot, Bruno Charbit, Tinhinane Fali, Vithura Pirabakaran, Boris Sorin, Quentin Riller, Ghaith Abdessalem, Maxime Beretta, Ludivine Grzelak, Pedro Gonçalves, James P. Di Santo, Hugo Mouquet, Olivier Schwartz, Mohammed Zarhrate, Mélanie Parisot, Christine Bôle‐Feysot, Cécile Masson, Nicolas Cagnard, Aurélien Corneau, Camille Brunaud, Shen‐Ying Zhang, Jean‐Laurent Casanova, Brigitte Bader‐Meunier, Julien Haroche, Isabelle Melki, Mathie Lorrot, Mehdi Oualha, Florence Moulin, Damien Bonnet, Zahra Belhadjer, Marianne Leruez, Slimane Allali, Christèle Gras‐Le Guen, Loïc de Pontual, Alain Fischer, Darragh Duffy, Frédéric Rieux‐Laucat, Julie Toubiana, Mickaël M. Ménager

    Cyhoeddwyd 2021
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  10. 10
    Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy

    Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy gan Vivien Béziat, Franck Rapaport, Jiafen Hu, Matthias Titeux, Mathilde Bonnet des Claustres, Mathieu Bourgey, Heather Griffin, Élise Bandet, S. Cindy, Roya Sherkat, Hassan Rokni‐Zadeh, David M. Louis, Majid Changi‐Ashtiani, Ottavia M. Delmonte, Toshiaki Fukushima, Tanwir Habib, Andrea Guennoun, Taushif Khan, Noemi Bender, Mahbuba Rahman, Frédégonde About, Rui Yang, Geetha Rao, Claire Rouzaud, Jingwei Li, Debra A. Shearer, Karla K. Balogh, Fatima Al Ali, Manar Ata, Soroosh Dabiri, Mana Momenilandi, Justine Nammour, Marie-Alexandra Alyanakian, Marianne Leruez‐Ville, David Guenat, Marie Materna, Léa Marcot, Natasha Vladikine, Christine Soret, Hassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, Jouni Uitto, Émilie Catherinot, Shadi Sadat Navabi, Mohammed Zarhrate, David T. Woodley, Mohamed Jeljeli, Thomas Abraham, Serkan Belkaya, Lazaro Lorenzo, Jérémie Rosain, Mousa Bayat, Fanny Lanternier, Olivier Lortholary, Faramarz Zakavi, Philippe Gros, Gérard Orth, Laurent Abel, Jean‐Luc Prétet, Sylvie Fraitag, Emmanuelle Jouanguy, Mark M. Davis, Stuart G. Tangye, Luigi D. Notarangelo, Nico Marr, Tim Waterboer, David Langlais, John Doorbar, Alain Hovnanian, Neil D. Christensen, Xavier Bossuyt, Mohammad Shahrooei, Jean‐Laurent Casanova

    Cyhoeddwyd 2021
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