Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Frédéric Galactéros"'
Autor:
Pablo Bartolucci, Léonard Féasson, Céline Schwalm, Frédéric Galactéros, Christophe Hourdé, Laurent Messonnier, Barnabas Gellen, Louise Deldicque, Angèle N. Merlet, Marc Francaux
Publikováno v:
American journal of hematology, Vol. 95, no.11, p. 1257-1268 (2020)
Sickle cell disease (SCD) patients display skeletal muscle hypotrophy, altered oxidative capacity, exercise intolerance and poor quality of life. We previously demonstrated that moderate-intensity endurance training is beneficial for improving muscle
Autor:
Anne-Laure Pham Hung D'Alexandry D'Orengiani, Pablo Bartolucci, Daniel E. Bauer, Thomas Pincez, R. Coleman Lindsley, Simon Lee, Yann Ilboudo, Michael Preuss, Guillaume Lettre, Ruth J. F. Loos, Frédéric Galactéros, Philippe Joly
Publikováno v:
Blood
Autor:
Cornelis L. Harteveld, Joanne Traeger-Synodinos, Jennichjen Slomp, Christina Vrettou, Sharda Bisoen, Maaike Verschuren, Nicolette S. den Hollander, Jeanet A.C. ter Huurne, Ahlem Achour, Gijs W. E. Santen, Frédéric Galactéros, Claudia A. L. Ruivenkamp, Rianne Schaap, Rob Castel, Tamara T. Koopmann, Serge Pissard, Sandra G.J. Arkesteijn, Anneliese Grimbergen, Jeroen Knijnenburg, Frank Baas, Linda Vijfhuizen
Publikováno v:
Blood, 136(15), 1789-1793. American Society of Hematology
Autor:
Pablo Bartolucci, Seth L. Alper, Guillaume Lettre, Marie Trudel, Carlo Brugnara, Alicia Rivera, Yann Ilboudo, Josepha-Clara Sedzro, Mélissa Beaudoin, Frédéric Galactéros
Publikováno v:
Blood Cells, Molecules, and Diseases. 65:60-65
Deoxy-hemoglobin S polymerization into rigid fibers is the direct cause of the clinical sequelae observed in sickle cell disease (SCD). The rate of polymerization of sickle hemoglobin is determined primarily by intracellular hemoglobin concentration,
Autor:
Yukio Nakamura, Jing Zeng, Abdullah Kutlar, Luca Pinello, Emily Stern, Ryo Kurita, Partha Pratim Das, Guillaume Lettre, Yuxuan Wu, Colin A. McKenzie, Yann Ilboudo, Marvin Reid, Stuart H. Orkin, Guo-Cheng Yuan, Matthew C. Canver, Frédéric Galactéros, Samuel Lessard, Diane D. Chen, Austen J. Needleman, Carlo Brugnara, Daniel E. Bauer, Mitchel A. Cole
Publikováno v:
Nature genetics
Cas9-mediated, high-throughput, saturating in situ mutagenesis permits fine-mapping of function across genomic segments. Disease- and trait-associated variants from genome-wide association studies largely cluster in regulatory DNA. Here we demonstrat
Autor:
Philippe Chadebech, Marie-Amélie de Ménorval, Gwellaouen Bodivit, Armand Mekontso-Dessap, Sadaf Pakdaman, Alicia Jouard, Frédéric Galactéros, Philippe Bierling, Anoosha Habibi, France Pirenne
Publikováno v:
Transfusion. 56:1730-1738
BACKGROUND The transfusion of red blood cell (RBC) concentrates is the main treatment for acute vaso-occlusive symptoms in sickle cell disease (SCD). Units of packed RBCs (pRBCs) must retain optimal characteristics for transfusion throughout the stor
Autor:
Armand Mekontso-Dessap, Pablo Bartolucci, Claire Rieux, T. Peyrard, Frédéric Galactéros, Joëlle Nataf, Philippe Chadebech, Anoosha Habibi, Btissam Chami, Philippe Bierling, Clara Ibanez
Publikováno v:
Transfusion. 56:1828-1833
BACKGROUND Delayed hemolytic transfusion reaction (DHTR) is a life-threatening condition in sickle cell disease (SCD) patients that is frequently complicated by hyperhemolysis. Antibodies resulting from antigen disparity between donors of European an
Autor:
Nicolas Hebert, Rakotoson Marie Georgine, Gwellaouen Bodivit, Etienne Audureau, Nadia Oubaya, Sadaf Pakdaman, Mehdi Sakka, Gaetana Di Liberto, Philippe Chadebech, Benoît Vingert, France Pirenne, Frédéric Galactéros, Marie Cambot, Pablo Bartolucci
Publikováno v:
Blood. 134:1008-1008
Introduction: Fetal hemoglobin (HbF) expression is a major modulator of sickle cell disease (SCD) severity by decreasing the HbS polymerization. However, the distribution of HbF in red blood cells (RBC) is heterogeneous in SCD patients. In the hypoth
Autor:
Frédéric Galactéros, Carlo Brugnara, Pablo Bartolucci, Guillaume Lettre, Melanie E. Garrett, Marilyn J. Telen, Yann Ilboudo, Allison E. Ashley-Koch
Publikováno v:
American journal of hematology. 93(11)
Autor:
Aline Floch, Dominique Gien, Christophe Tournamille, Btissam Chami, Anoosha Habibi, Frédéric Galactéros, Philippe Bierling, Rachid Djoudi, Corinne Pondarré, Thierry Peyrard, France Pirenne
Publikováno v:
Transfusion
Transfusion, Wiley, 2018, 58 (6), pp.1527-1535. ⟨10.1111/trf.14633⟩
Transfusion, Wiley, 2018, 58 (6), pp.1527-1535. ⟨10.1111/trf.14633⟩
International audience; BACKGROUND : Sickle cell disease (SCD) patients undergo multiple red blood cell (RBC) transfusions and are regularly exposed to low‐prevalence (LP) antigens specific to individuals of African descent. This study evaluated th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af28ed172039924cc6fc6054e8affca1
https://hal.archives-ouvertes.fr/hal-02936930
https://hal.archives-ouvertes.fr/hal-02936930