Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Michaël, Dussiot"'
Autor:
Julien Demagny, Camille Roussel, Maïlys Le Guyader, Eric Guiheneuf, Véronique Harrivel, Thomas Boyer, Momar Diouf, Michaël Dussiot, Yohann Demont, Loïc Garçon
Publikováno v:
EBioMedicine, Vol 83, Iss , Pp 104209- (2022)
Summary: Background: Schistocyte counts are a cornerstone of the diagnosis of thrombotic microangiopathy syndrome (TMA). Their manual quantification is complex and alternative automated methods suffer from pitfalls that limit their use. We report a m
Externí odkaz:
https://doaj.org/article/ddc21e42b1544d48b2a77fde1d004541
Autor:
Mickaël Marin, Sandy Peltier, Youcef Hadjou, Sonia Georgeault, Michaël Dussiot, Camille Roussel, Olivier Hermine, Philippe Roingeard, Pierre A. Buffet, Pascal Amireault
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Refrigerated storage of red cell concentrates before transfusion is associated with progressive alterations of red blood cells (RBC). Small RBC (type III echinocytes, sphero-echinocytes, and spherocytes) defined as storage-induced micro-erythrocytes
Externí odkaz:
https://doaj.org/article/964a0c6e16fa4d3eb48e021a9fcdb45a
Autor:
Laura Bencheikh, M’Boyba Khadija Diop, Julie Rivière, Aygun Imanci, Gerard Pierron, Sylvie Souquere, Audrey Naimo, Margot Morabito, Michaël Dussiot, Frédéric De Leeuw, Camille Lobry, Eric Solary, Nathalie Droin
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
Receptor tyrosine kinases localize to the cell surface and have been suggested to also have nuclear function. Here the authors provide evidence that Colony Stimulating Factor-1 Receptor (CSF-1R) migrates to the nucleus upon CSF-1 stimulation in monoc
Externí odkaz:
https://doaj.org/article/087012bf40e543c99b57671485f865ff
Autor:
Lucie Dupuis, Margaux Chauvet, Emmanuelle Bourdelier, Michaël Dussiot, Nadia Belmatoug, Caroline Le Van Kim, Arnaud Chêne, Mélanie Franco
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 14, p 7640 (2022)
Gaucher disease (GD) is caused by glucocerebrosidase deficiency leading to the accumulation of sphingolipids in macrophages named “Gaucher’s Cells”. These cells are characterized by deregulated expression of cell surface markers, abnormal secre
Externí odkaz:
https://doaj.org/article/d40cf1732b7f44ef9d97361a8feb6f05
Autor:
Sara El Hoss, Sylvie Cochet, Auria Godard, Hongxia Yan, Michaël Dussiot, Giacomo Frati, Bénédicte Boutonnat-Faucher, Sandrine Laurance, Olivier Renaud, Laure Joseph, Annarita Miccio, Valentine Brousse, Mohandas Narla, Wassim El Nemer
Publikováno v:
Haematologica, Vol 106, Iss 10 (2020)
While ineffective erythropoiesis has long been recognized as a key contributor to anemia in thalassemia, its role in anemia of sickle cell disease (SCD) has not been critically explored. Using in vitro and in vivo derived human erythroblasts we asses
Externí odkaz:
https://doaj.org/article/aaaa847b38394956a803db1d63a540dd
Autor:
Marc Gastou, Sarah Rio, Michaël Dussiot, Narjesse Karboul, Hélène Moniz, Thierry Leblanc, Margaux Sevin, Patrick Gonin, Jérome Larghéro, Carmen Garrido, Anupama Narla, Narla Mohandas, William Vainchenker, Olivier Hermine, Eric Solary, Lydie Da Costa
Publikováno v:
Blood Advances, Vol 1, Iss 22, Pp 1959-1976 (2017)
Abstract: Diamond-Blackfan anemia (DBA) is a rare congenital bone marrow failure syndrome that exhibits an erythroid-specific phenotype. In at least 70% of cases, DBA is related to a haploinsufficient germ line mutation in a ribosomal protein (RP) ge
Externí odkaz:
https://doaj.org/article/29a79bc7c51841ca8afd6c4fd7f2d674
Autor:
Flavia Guillem, Michaël Dussiot, Elia Colin, Thunwarat Suriyun, Jean Benoit Arlet, Nicolas Goudin, Guillaume Marcion, Renaud Seigneuric, Sebastien Causse, Patrick Gonin, Marc Gastou, Marc Deloger, Julien Rossignol, Mathilde Lamarque, Zakia Belaid Choucair, Emilie Fleur Gautier, Sarah Ducamp, Julie Vandekerckhove, Ivan C. Moura, Thiago Trovati Maciel, Carmen Garrido, Xiuli An, Patrick Mayeux, Narla Mohandas, Geneviève Courtois, Olivier Hermine
Publikováno v:
Haematologica, Vol 105, Iss 9 (2019)
β-thalassemia major (β-TM) is an inherited hemoglobinopathy caused by a quantitative defect in the synthesis of β-globin chains of hemoglobin, leading to the accumulation of free a-globin chains that aggregate and cause ineffective erythropoiesis.
Externí odkaz:
https://doaj.org/article/9c8681ff1975469eabfa5bbd4e3b3606
Autor:
Yuta Ito, Amira Marouf, Yasunori Kogure, Junji Koya, Mariko Tabata, Yuki Saito, Sumito Shingaki, Mitsuhiro Yuasa, Kentaro Yamaguchi, Julie Bruneau, Manon Vavasseur, Michaël Dussiot, Isabelle Andre, Akshay Joshi, Chantal Lagresle-Peyrou, Aude Magerus, Sammara Chaubard, David Lavergne, Emmanuel Bachy, Erika Brunet, Virginie Fataccioli, Chantal Brouzes, Camille Laurent, Laurence De Leval, Alexandra Traverse-Glehen, Céline Bossard, Marie Parrens, Véronique Meignin, Laure Philippe, Julien Rossignol, Felipe Suarez, Jean-Marie Michot, Olivier Tournilhac, Christine Bole-Feysot, Patrick Nitschke, Bruno Tesson, Cécile Laurent, Thierry Jo Molina, Vahid Asnafi, Sachiko Tsukita, Koji Izutsu, Hiroaki Miyoshi, Seiji Sakata, Akito Dobashi, Kengo Takeuchi, Koichi Ohshima, Philippe Gaulard, Arnaud Jaccard, Seishi Ogawa, Olivier Hermine, Keisuke Kataoka, Lucile Couronne
Publikováno v:
Blood. 140:1737-1739
Autor:
Manon Bardyn, Jingkui Chen, Michaël Dussiot, David Crettaz, Lucas Schmid, Emmanuel Längst, Pascal Amireault, Jean-Daniel Tissot, Mario Jolicoeur, Michel Prudent
Publikováno v:
Metabolites, Vol 10, Iss 6, p 226 (2020)
After blood donation, the red blood cells (RBCs) for transfusion are generally isolated by centrifugation and then filtrated and supplemented with additive solution. The consecutive changes of the extracellular environment participate to the occurren
Externí odkaz:
https://doaj.org/article/f02268a1d1a942a49446c21d6a1f1c9d
Publikováno v:
Haematologica, Vol 103, Iss 10 (2018)
Externí odkaz:
https://doaj.org/article/f3a582a6bd754a839f95e7a1071c640c