Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Sabrina Bondu"'
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
Autor:
Meriem Ladli, Cyrielle Richard, Lilia Cantero Aguilar, Sarah Ducamp, Sabrina Bondu, Pierre Sujobert, Jérôme Tamburini, Catherine Lacombe, Nabih Azar, Marc Foretz, Yael Zermati, Patrick Mayeux, Benoit Viollet, Frédérique Verdier
Publikováno v:
Haematologica, Vol 104, Iss 5 (2019)
AMP-activated protein kinase (AMPK) is a heterotrimeric complex containing α, β, and γ subunits involved in maintaining integrity and survival of murine red blood cells. Indeed, Ampk α1−/−, Ampk β1−/− and Ampk γ1−/− mice develop hem
Externí odkaz:
https://doaj.org/article/a9a0e307e321463b82d48aac27127b72
Autor:
David Rombaut, Carine Lefevre, Batoul Farhat, Sabrina Bondu, Anne Letessier, Auriane Lesieur-Pasquier, Daisy Castillo-Guzman, Marjorie Leduc, Emilie-Fleur Gautier, Virginie Chesnais, Alice Rousseau, Ismael Boussaid, Sarah Battault, Alexandre Houy, Didier Bouscary, Lise Willems, Nicolas Chapuis, Sophie Park, Sophie Raynaud, Thomas Cluzeau, Emmanuelle Clappier, Pierre Fenaux, Lionel Ades, Eric Solary, Raphael Margueron, Michel Wassef, Olivier Kosmider, Samar Alsafadi, Nathalie Droin, Angelos Constantinou, Marc-Henri Stern, Benoit Miotto, Frederic Chedin, Michaela Fontenay
Publikováno v:
Blood. 140:215-216
Autor:
Eva de Berranger, Olivier Mir, Angelo Paci, Véronique Kemmel, Philippe Bourget, Claire Galambrun, Virginie Gandemer, Charlotte Jubert, Christelle Dufour, Despina Moshous, Vianney Poinsignon, Bénédicte Devictor, Laurent Nguyen, Laura Faivre, Jean-Hugues Dalle, Gilles Vassal, Aurélie Pétain, J.P. Vannier, Sabrina Bondu, Sophie Broutin, Bénédicte Neven
Publikováno v:
Pediatric bloodcancerREFERENCES. 67(10)
BACKGROUND Busulfan (Bu) is the cornerstone of conditioning regimens prior to hematopoietic stem cell transplantation, widely used in both adults and children for the treatment of malignant and nonmalignant diseases. Despite an intravenous formulatio
Autor:
Nabih Azar, Sarah Ducamp, Pierre Sujobert, Catherine Lacombe, Frédérique Verdier, Cyrielle Richard, Patrick Mayeux, Yael Zermati, Meriem Ladli, Marc Foretz, Sabrina Bondu, Lilia Cantero Aguilar, Benoit Viollet, Jerome Tamburini
Publikováno v:
Haematologica
Haematologica, Ferrata Storti Foundation, 2019, 104 (5), pp.907-918. ⟨10.3324/haematol.2018.191403⟩
Haematologica, Ferrata Storti Foundation, 2019, 104 (5), pp.907-918. ⟨10.3324/haematol.2018.191403⟩
International audience; AMP-activated protein kinase (AMPK) is a heterotrimeric complex containing α, β, and γ subunits involved in maintaining integrity and survival of murine red blood cells. Indeed, Ampk α1-/- , Ampk β1-/- and Ampk γ1-/- mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9707f483a50a7f03c2f13031c4d50691
https://hal.archives-ouvertes.fr/hal-02348833/document
https://hal.archives-ouvertes.fr/hal-02348833/document
Autor:
Lionel Ades, Sabrina Bondu, Aspasia Stamatoullas, François Guillonneau, Zoubida Karim, Thomas Cluzeau, Mathilde Hunault, Raphaël Margueron, Elizabeta Nemeth, Grace Jung, Olivier Kosmider, Michel Wassef, Nathalie Droin, Ismael Boussaid, Carine Lefevre, Patrick Mayeux, Emmanuel Gyan, Susann Winter, Alexandre Houy, Anne-Sophie Alary, Alice Rousseau, Léon Kautz, Didier Bouscary, Thibaud Lefebvre, Valeria Santini, Marc-Henri Stern, Tomas Ganz, Abderrahmane Bousta, Uwe Platzbecker, Hervé Puy, Samar Alsafadi, Anne Sophie Kubasch, Prunelle Perrier, David Rombaut, Sophie Park, Andrea Toma, Sophie Kaltenbach, Nicolas Cagnard, Michaela Fontenay
Publikováno v:
Science Translational Medicine
Science Translational Medicine, 2019, 11 (500), pp.eaav5467. ⟨10.1126/scitranslmed.aav5467⟩
Science Translational Medicine, American Association for the Advancement of Science, 2019, 11 (500), pp.eaav5467. ⟨10.1126/scitranslmed.aav5467⟩
Science Translational Medicine, 2019, 11 (500), pp.eaav5467. ⟨10.1126/scitranslmed.aav5467⟩
Science Translational Medicine, American Association for the Advancement of Science, 2019, 11 (500), pp.eaav5467. ⟨10.1126/scitranslmed.aav5467⟩
International audience; Myelodysplastic syndromes (MDS) with ring sideroblasts are hematopoietic stem cell disorders with erythroid dysplasia and mutations in the SF3B1 splicing factor gene. Patients with MDS with SF3B1 mutations often accumulate exc
Autor:
Sabrina, Bondu, Anne-Sophie, Alary, Carine, Lefèvre, Alexandre, Houy, Grace, Jung, Thibaud, Lefebvre, David, Rombaut, Ismael, Boussaid, Abderrahmane, Bousta, François, Guillonneau, Prunelle, Perrier, Samar, Alsafadi, Michel, Wassef, Raphaël, Margueron, Alice, Rousseau, Nathalie, Droin, Nicolas, Cagnard, Sophie, Kaltenbach, Susann, Winter, Anne-Sophie, Kubasch, Didier, Bouscary, Valeria, Santini, Andrea, Toma, Mathilde, Hunault, Aspasia, Stamatoullas, Emmanuel, Gyan, Thomas, Cluzeau, Uwe, Platzbecker, Lionel, Adès, Hervé, Puy, Marc-Henri, Stern, Zoubida, Karim, Patrick, Mayeux, Elizabeta, Nemeth, Sophie, Park, Tomas, Ganz, Léon, Kautz, Olivier, Kosmider, Michaëla, Fontenay
Publikováno v:
Sci Transl Med
Myelodysplastic syndromes (MDS) with ring sideroblasts are hematopoietic stem cell disorders with erythroid dysplasia and mutations in the SF3B1 splicing factor gene. MDS patients with SF3B1 mutations often accumulate excessive tissue iron, even in t
Publikováno v:
Current opinion in hematology. 24(3)
Myelodysplastic syndromes (MDS) are heterogeneous diseases of the hematopoietic stem cell in the elderly. Anemia is the main symptom that mostly correlates with dysplastic erythropoiesis in the bone marrow. We will review the recent advances in under
Autor:
M'Boyba Diop, Carine Lefevre, Sophie Raynaud, Nicolas Chapuis, Marie-Laure Arcangeli, Meyling Cheok, Lise Willems, Laurence Legros, Evelyne Lauret, Caroline Delette, Virginie Chesnais, Didier Bouscary, Sabrina Bondu, Alice Rousseau, Hélène Guermouche, Olivier A. Bernard, Michaela Fontenay, Françoise Pflumio, Olivier Kosmider
Publikováno v:
ResearcherID
Myelodysplastic syndromes (MDSs) are hematopoietic stem cell disorders in which recurrent mutations define clonal hematopoiesis. The origin of the phenotypic diversity of non-del(5q) MDS remains unclear. Here, we investigated the clonal architecture
Autor:
Carine Lefevre, Sabrina Bondu, Marc-Henri Stern, Olivier Kosmider, Nicolas Cagnard, Michaela Fontenay, Alexandre Houy, Delphine G. Bernard, Abderrahmane Bousta
Publikováno v:
Blood. 128:1972-1972
Introduction SF3B1 hotspot mutations are associated with various cancers like uveal melanoma, chronic lymphocytic leukemia and myelodysplastic syndrome with ring sideroblasts (MDS-RS). These mutations affect RNA splicing by the use of alternative bra