Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Camille Debord"'
Autor:
Pierre Peterlin, Marie C. Béné, Maxime Jullien, Thierry Guillaume, Amandine Le Bourgeois, Alice Garnier, Camille Debord, Marion Eveillard, Patrice Chevallier
Publikováno v:
eJHaem, Vol 4, Iss 4, Pp 1089-1095 (2023)
Abstract In this monocentric prospective study, the influence on long‐term outcomes of peripheral blood levels of monocytic‐myeloid‐derived suppressive cells (M‐MDSC) was investigated in 56 patients with acute leukemia (myeloid n = 47; lympho
Externí odkaz:
https://doaj.org/article/8ba3e1e2649e436eb537937b373ae19a
Autor:
Pierre Peterlin, Joelle Gaschet, Thierry Guillaume, Alice Garnier, Marion Eveillard, Amandine Le Bourgeois, Michel Cherel, Camille Debord, Yannick Le Bris, Olivier Theisen, Catherine Godon, Béatrice Mahé, Viviane Dubruille, Soraya Wuilleme, Cyrille Touzeau, Thomas Gastinne, Nicolas Blin, Anne Lok, Benoît Tessoulin, Steven Le Gouill, Philippe Moreau, Marie‐C Béné, Patrice Chevallier
Publikováno v:
Cancer Medicine, Vol 10, Iss 2, Pp 642-648 (2021)
Abstract The aim of this study was to assess the potential impact of the kinetics of serum levels of seven cytokines during induction in acute myeloid leukemia (AML) patients. Indeed, the role of cytokines, in the pathophysiology and response to ther
Externí odkaz:
https://doaj.org/article/489f420bf9c943fa9f0afed8b3326dca
Autor:
Dorothée Selimoglu-Buet, Julie Rivière, Hussein Ghamlouch, Laura Bencheikh, Catherine Lacout, Margot Morabito, M’boyba Diop, Guillaume Meurice, Marie Breckler, Aurélie Chauveau, Camille Debord, Franck Debeurme, Raphael Itzykson, Nicolas Chapuis, Christophe Willekens, Orianne Wagner-Ballon, Olivier A. Bernard, Nathalie Droin, Eric Solary
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-17 (2018)
A decrease in the fraction of non-classical monocytes is a hallmark of chronic myelomonocytic leukaemia. Taking advantage of this abnormal situation, the authors identify a mechanistic link between miR-150 and TET3 as being involved in monocyte subse
Externí odkaz:
https://doaj.org/article/5d55187610e84c0189ca6173abd8c67a
Autor:
Sophie Vantyghem, Pierre Peterlin, Sylvain Thépot, Audrey Ménard, Viviane Dubruille, Camille Debord, Thierry Guillaume, Alice Garnier, Amandine Le Bourgeois, Soraya Wuilleme, Catherine Godon, Olivier Theisen, Marion Eveillard, Jacques Delaunay, Hervé Maisonneuve, Nadine Morineau, Bruno Villemagne, Stéphane Vigouroux, François Subiger, Elsa Lestang, Marion Loirat, Anne Parcelier, Pascal Godmer, Mélanie Mercier, Adrien Trebouet, Damien Luque Paz, Ronan Le Calloch, Lenaig Le Clech, Céline Bossard, Anne Moreau, Valérie Ugo, Mathilde Hunault, Philippe Moreau, Steven Le Gouill, Patrice Chevallier, Marie C. Béné, Yannick Le Bris
Publikováno v:
Haematologica, Vol 106, Iss 3 (2020)
Next-generation sequencing (NGS) is used to investigate the presence of somatic mutations. The utility of incorporating routine sequencing to guide diagnosis and therapeutic decisions remains unclear. We report the findings of an observational, multi
Externí odkaz:
https://doaj.org/article/ea9169a7f0b249b4b36236d800d823a7
Publikováno v:
Platelets, Vol 32, Iss 1, Pp 144-145 (2021)
Externí odkaz:
https://doaj.org/article/756fdeff071d4cfeb21373fa72564d62
Autor:
Pierre Peterlin, Joelle Gaschet, Thierry Guillaume, Alice Garnier, Marion Eveillard, Amandine Le Bourgeois, Michel Cherel, Camille Debord, Yannick Le Bris, Olivier Theisen, Béatrice Mahé, Viviane Dubruille, Catherine Godon, Nelly Robillard, Soraya Wuilleme, Cyrille Touzeau, Thomas Gastinne, Nicolas Blin, Anne Lok, Antoine Bonnet, Steven Le Gouill, Philippe Moreau, Marie-C Béné, Patrice Chevallier
Publikováno v:
Haematologica, Vol 104, Iss 6 (2019)
Externí odkaz:
https://doaj.org/article/b5fa4d12e9e64b99890e497d18c7581e
Autor:
Valérie Bardet, Orianne Wagner-Ballon, Julien Guy, Céline Morvan, Camille Debord, Franck Trimoreau, Emmanuel Benayoun, Nicolas Chapuis, Nicolas Freynet, Cédric Rossi, Stéphanie Mathis, Marie-Pierre Gourin, Andréa Toma, Marie C. Béné, Jean Feuillard, Estelle Guérin
Publikováno v:
Haematologica, Vol 100, Iss 4 (2015)
Although numerous recent publications have demonstrated interest in multiparameter flow cytometry in the investigation of myelodysplastic disorders, it is perceived by many laboratory hematologists as difficult and expensive, requiring a high level o
Externí odkaz:
https://doaj.org/article/d29b8b0070154b93a9ed72ab30e24414
Autor:
Pierre Peterlin, Camille Debord, Marion Eveillard, Alice Garnier, Amandine Le Bourgeois, Thierry Guillaume, Maxime Jullien, Marie C. Béné, Patrice Chevallier
Publikováno v:
Journal of Cellular and Molecular Medicine. 26:5486-5492
Myeloid Derived Suppressive Cells (MDSC) are capable to suppress innate and adaptive immune responses, thus favouring solid cancer progression. However, little is known about the role of MDSC in acute myeloid leukaemia (AML). In this monocentric pros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62232747a39eaebbcda3cce1a55ab716
https://doi.org/10.1111/jcmm.17576
https://doi.org/10.1111/jcmm.17576
Autor:
Julia Guillou, Alice de Pellegars, Florence Porcheret, Véronique Frémeaux-Bacchi, Emma Allain-Launay, Camille Debord, Manon Denis, Yann Péréon, Christine Barnérias, Isabelle Desguerre, Gwenaëlle Roussey, Sandra Mercier
Publikováno v:
Blood Advances. 6:4266-4270
Adeno-associated virus (AAV) gene therapies are highly promising, such as the onasemnogene abeparvovec (Zolgensma) in spinal muscle atrophy (SMA). We report the first case of fatal systemic thrombotic microangiopathy (TMA) following onasemnogene abep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e09659c665eb0a757bbda768ebeb8911
https://doi.org/10.1182/bloodadvances.2021006419
https://doi.org/10.1182/bloodadvances.2021006419
Autor:
Audrey Grain, adeline normand, caroline Thomas, camille debord, olivier pichon, Marie Bene, Marion Eveillard, olivier theisen
A three-year-old girl with a history of epilepsy seizures was diagnosed with acute lymphoblastic leukemia. A comprehensive genetic study of blast cells led to the discovery of a constitutional deletion of the PCDH19 gene. This description underlines
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de8e13bb4c7683b330505c0d5c58bd0e
https://doi.org/10.22541/au.166363923.37968168/v1
https://doi.org/10.22541/au.166363923.37968168/v1
