Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Marie Temple"'
Autor:
David Rombaut, Carine Lefèvre, Tony Rached, Sabrina Bondu, Anne Letessier, Raphael M. Mangione, Batoul Farhat, Auriane Lesieur-Pasquier, Daisy Castillo-Guzman, Ismael Boussaid, Chloé Friedrich, Aurore Tourville, Magali De Carvalho, Françoise Levavasseur, Marjorie Leduc, Morgane Le Gall, Sarah Battault, Marie Temple, Alexandre Houy, Didier Bouscary, Lise Willems, Sophie Park, Sophie Raynaud, Thomas Cluzeau, Emmanuelle Clappier, Pierre Fenaux, Lionel Adès, Raphael Margueron, Michel Wassef, Samar Alsafadi, Nicolas Chapuis, Olivier Kosmider, Eric Solary, Angelos Constantinou, Marc-Henri Stern, Nathalie Droin, Benoit Palancade, Benoit Miotto, Frédéric Chédin, Michaela Fontenay
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-20 (2024)
Abstract Myelodysplastic syndromes (MDS) with mutated SF3B1 gene present features including a favourable outcome distinct from MDS with mutations in other splicing factor genes SRSF2 or U2AF1. Molecular bases of these divergences are poorly understoo
Externí odkaz:
https://doaj.org/article/123566d884df484c9b7e6a5d549470f7
Publikováno v:
Molecular Ecology.
Publikováno v:
British Journal of Haematology
British Journal of Haematology, 2023, ⟨10.1111/bjh.18826⟩
British Journal of Haematology, 2023, ⟨10.1111/bjh.18826⟩
International audience; Obinutuzumab (GA101) is a humanized anti-CD20 monoclonal antibody used in the treatment of B-cell malignancies. Under rare occasions, obinutuzumab may induce acute and severe thrombocytopenia. However, little is known about th
Autor:
Chloé Friedrich, Loria Zalmaï, Juliette Gay, Marie Magdeleine Coude, Clotilde Bravetti, Romain Vazquez, Marie Temple, Eugénie Duroyon, Luc Darnige, Justine Decroocq, Anne Sophie Alary, Olivier Kosmider
Publikováno v:
International Journal of Laboratory Hematology. 44:928-933
Autor:
Chloé, Friedrich, Loria, Zalmaï, Juliette, Gay, Marie Magdeleine, Coude, Clotilde, Bravetti, Romain, Vazquez, Marie, Temple, Eugénie, Duroyon, Luc, Darnige, Justine, Decroocq, Anne Sophie, Alary, Olivier, Kosmider
Publikováno v:
International journal of laboratory hematologyREFERENCES. 44(5)
The additional sex combs like 1 (ASXL1) gene is frequently mutated in a number of haematological neoplasms. The c.1934dupG, known to be the most common alteration in ASXL1, is associated with poor clinical outcome. A systematic determination of ASXL1
Autor:
Victoria Raggueneau, François Mignon, Ernesto Diaz-Flores, Claire Flaujac, Mehrsa Koukabi, Marie Temple, Philippe Rousselot, Benjamin Manéglier, Jennifer Osman, Fabrice Bruneel, Floriane Devaux, Alix Greder-Belan, Stéphanie Marque-Juillet, Rémy Favre, Jérôme Lambert, Reza Azarian, Véronique Hentgen, Delphine Bridoux
Publikováno v:
British Journal of Haematology
British Journal of Haematology, Wiley, 2020, 190 (5), pp.718-722. ⟨10.1111/bjh.16943⟩
British Journal of Haematology, Wiley, 2020, 190 (5), pp.718-722. ⟨10.1111/bjh.16943⟩
International audience; Complementary tools are warranted to increase the sensitivity of the initial testing for COVID-19. We identified a specific ‘sandglass’ aspect on the white blood cell scattergram of COVID-19 patients reflecting the presenc
Autor:
Marie Temple, Charles Marchionini, Bérénice Schell, Théophile Cocherie, Audrey Sabbagh, Amandine Caillault, Clémentine Moulin, Inès Rezzoug, Floriane Devaux, Hélène Vantomme, Edouard Le Guillou, Lorra Monpierre, Pauline Thiebot, Laurence Pacot, Eve-Marie Walle, Céline Mory, Lise Larcher
Publikováno v:
Annales de Biologie Clinique. 78:211-222
Autor:
Olivier Kosmider, Céline Possémé, Marie Templé, Aurélien Corneau, Francesco Carbone, Eugénie Duroyon, Paul Breillat, Twinu-Wilson Chirayath, Bénédicte Oules, Pierre Sohier, Marine Luka, Camille Gobeaux, Estibaliz Lazaro, Roderau Outh, Guillaume Le Guenno, François Lifermann, Marie Berleur, Melchior Le Mene, Chloé Friedrich, Cédric Lenormand, Thierry Weitten, Vivien Guillotin, Barbara Burroni, Jeremy Boussier, Lise Willems, Selim Aractingi, Léa Dionet, Pierre-Louis Tharaux, Béatrice Vergier, Pierre Raynaud, Hang-Korng Ea, Mickael Ménager, Darragh Duffy, Benjamin Terrier
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-17 (2024)
Abstract Acquired mutations in the UBA1 gene were recently identified in patients with severe adult-onset auto-inflammatory syndrome called VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic). However, the precise physiological and clini
Externí odkaz:
https://doaj.org/article/1c0de64cb1ab4953a41137e4248834bd
Autor:
Estelle Balducci, Sophie Kaltenbach, Patrick Villarese, Eugénie Duroyon, Loria Zalmai, Chloé Friedrich, Felipe Suarez, Ambroise Marcais, Didier Bouscary, Justine Decroocq, Rudy Birsen, Michaëla Fontenay, Marie Templé, Chantal Brouzes, Aurore Touzart, Thomas Steimlé, Agata Cieslak, Ludovic Lhermitte, Carole Almire, Nicolas Chapuis, Olivier Hermine, Vahid Asnafi, Olivier Kosmider, Lucile Couronné
Publikováno v:
Blood Cancer Journal, Vol 12, Iss 9, Pp 1-4 (2022)
Externí odkaz:
https://doaj.org/article/87432a0ce3c84ceea234e0dc50e3058c
Autor:
Natacha Johnson, Marie Templé, Chloe Friedrich, Lise Willems, Rudy Birsen, Marguerite Vignon, Paul Deschamps, Patricia Franchi, Johanna Mondesir, Benedicte Deau-Fischer, Elsa Miekoutima, Ismaël Boussaid, Nicolas Chapuis, Olivier Kosmider, Didier Bouscary, Jerome Tamburini, Justine Decroocq
Publikováno v:
Haematologica, Vol 108, Iss 10 (2023)
Externí odkaz:
https://doaj.org/article/2abb127402f94d7c938ea21ea52a9c4d