Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Claudine Lapoumeroulie"'
Autor:
Valentine Brousse, Yves Colin, Catia Pereira, Cecile Arnaud, Marie Helene Odièvre, Anne Boutemy, Corinne Guitton, Mariane de Montalembert, Claudine Lapouméroulie, Julien Picot, Caroline Le Van Kim, Wassim El Nemer
Publikováno v:
EBioMedicine, Vol 2, Iss 2, Pp 154-157 (2015)
Sickle cell anaemia (SCA) results from a single mutation in the β globin gene. It is seldom symptomatic in the first semester of life. We analysed the expression pattern of 9 adhesion molecules on red blood cells, in a cohort of 54 SCA and 17 non-SC
Externí odkaz:
https://doaj.org/article/68773e3548734306bb42a7a40d3203b1
Autor:
Sandrine Laurance, Pauline Lansiaux, François-Xavier Pellay, Michelle Hauchecorne, Arndt Benecke, Jacques Elion, Claudine Lapoumeroulie
Publikováno v:
Haematologica, Vol 96, Iss 4 (2011)
Background All the cellular partners of the vascular system and especially endothelial cells are involved in the pathophysiology of the vasoocclusive crises associated with sickle cell disease. In sickle cell disease, circulating cells adhere abnorma
Externí odkaz:
https://doaj.org/article/1ae5be375b4c4547b085d9762d9bb84b
Autor:
Aurélie Claes, Philippe Connes, Maryse Etienne-Julan, Marie-Dominique Hardy-Dessources, Yohann Garnier, Régine Hierso, Nathalie Lemonne, Claudine Lapoumeroulie, Marc Romana, Wassim El Nemer, Marie Garnier, Séverine Ferdinand, Kizzy-Clara Cita
Publikováno v:
Blood
Blood, American Society of Hematology, 2020, 136 (2), pp.247-256. ⟨10.1182/blood.2020004853⟩
Blood, American Society of Hematology, 2020, 136 (2), pp.247-256. ⟨10.1182/blood.2020004853⟩
International audience; Plasma MPs released during crisis in SS patients increase endothelial ICAM-1 levels and neutrophil adhesion. l HU treatment lowers PS exposure on MPs, which abolishes their proinflammatory properties. Microparticles (MPs) are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::672e493c4ae2cd4e28752d876cb63e06
https://pubmed.ncbi.nlm.nih.gov/32645168
https://pubmed.ncbi.nlm.nih.gov/32645168
Autor:
Jacques Elion, Marie-Dominique Hardy-Dessources, Sara El Hoss, Régine Hierso, Nathalie Lemonne, Keyne Charlot, Philippe Connes, Claudine Lapoumeroulie, Marc Romana, Caroline Le Van Kim
Publikováno v:
British Journal of Haematology
British Journal of Haematology, Wiley, 2018, 185 (5), pp.991-994. ⟨10.1111/bjh.15686⟩
British Journal of Haematology, Wiley, 2019, 185 (5), pp.991-994. ⟨10.1111/bjh.15686⟩
British Journal of Haematology, Wiley, In press
British Journal of Haematology, Wiley, 2018, 185 (5), pp.991-994. ⟨10.1111/bjh.15686⟩
British Journal of Haematology, Wiley, 2019, 185 (5), pp.991-994. ⟨10.1111/bjh.15686⟩
British Journal of Haematology, Wiley, In press
International audience; Painful vaso-occlusive crisis (VOC) represents the most frequent complication encountered by SCA patients. In animal models, increased red blood cell (RBC) adhesion to the endothelium has been demonstrated to initiate VOC by i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e210fa105295bc652dd403d463ea1c78
https://hal-univ-lyon1.archives-ouvertes.fr/hal-02461231
https://hal-univ-lyon1.archives-ouvertes.fr/hal-02461231
Autor:
Pierre A. Buffet, Narla Mohandas, Valentine Brousse, Véronique Picard, Caroline Le Van Kim, Catia Pereira, Corinne Guitton, Chantal Brouzes, Sara El Hoss, Cécile Arnaud, Claudine Lapoumeroulie, Stephan Menzel, Thao Nguyen-Khoa, Wassim El Nemer, Mariane de Montalembert, Kate Gardner, Serge Pissard, Yves Colin-Aronovicz, Béatrice Pellegrino, Marie Hélène Odièvre-Montanié, Micheline Maier-Redelsperger, Françoise Bernaudin, Caroline Elie, Naïm Bouazza, David Mames
Publikováno v:
American Journal of Hematology
American Journal of Hematology, Wiley, 2018, 93 (11), pp.1411-1419. ⟨10.1002/ajh.25260⟩
American Journal of Hematology, Wiley, 2018, 93 (11), pp.1411-1419. ⟨10.1002/ajh.25260⟩
In order to identify very early prognostic factors that can provide insights into subsequent clinical complications, we performed a comprehensive longitudinal multi-center cohort study on 57 infants with sickle cell anemia (55 SS; 2 Sβ°) during the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6d90d55943824a7ee5a256ef1f52475
https://hal.archives-ouvertes.fr/hal-02416879
https://hal.archives-ouvertes.fr/hal-02416879
Autor:
Maria Alejandra Lizarralde Iragorri, Bruno Le Pioufle, Alexander Rodrigo Ferreira, Jacques Elion, Ana Cristina Silva Pinto, Claudine Lapoumeroulie, Yann Lamarre, Tieying Xu, Simone Kashima, Valentine Brousse, Dimas Tadeu Covas, Sara El Hoss, Wassim El Nemer, Yves Colin, Olivier Français, Caroline Le Van Kim, Sophie D. Lefevre, Michael Dussiot
Publikováno v:
Lab on a Chip
Lab on a Chip, Royal Society of Chemistry, 2018, 18 (19), pp.2975-2984. ⟨10.1039/C8LC00637G⟩
Lab on a Chip, 2018, 18 (19), pp.2975-2984. ⟨10.1039/C8LC00637G⟩
Lab on a Chip, Royal Society of Chemistry, 2018, 18 (19), pp.2975-2984. ⟨10.1039/C8LC00637G⟩
Lab on a Chip, 2018, 18 (19), pp.2975-2984. ⟨10.1039/C8LC00637G⟩
The human red blood cell is a biconcave disc of 6-8 × 2 μm that is highly elastic. This capacity to deform enables it to stretch while circulating through narrow capillaries to ensure its main function of gas exchange. Red cell shape and deformabil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27aec27147620cce7db47e8aa6178429
https://hal.archives-ouvertes.fr/hal-01875109
https://hal.archives-ouvertes.fr/hal-01875109
Autor:
Frédéric B. Piel, Lisa Langabeer, Jeannette Klein, Claudine Lapoumeroulie, Carolina Backman Johansson, Giovanna Russo, Kwaku Ohene-Frempong, Baba Inusa, Rachel Yahyaoui, Catherine Badens, Michael Angastiniotis, José L Marín Soria, Ralph Fingerhut, Charles Turner, Léon Tshilolo, Jacques Elion, Corrina McMahon, Elena Dulín, Ana Marcão, Celeste Bento, Yvonne Daniel, Markus Schmugge, Marina García-Morín, Raffaella Colombatti, Laura Sainati, Marianne de Montalembert, Stephan Lobitz, Patrick Ducoroy, Bichr Allaf, Ute Holtkamp, Duran Canatan, Marelle J. Bouva, John James, Jean-Marc Périni, Donatella Venturelli, Allison Streetly, Elena Cela, Paul Telfer, Claudia Frömmel, Marina Kleanthous, Matthew R.M. Charlton, Laura Vilarinho, Cathy Coppinger, Béatrice Gulbis, Joachim B. Kunz
Publikováno v:
British Journal of Haematology
British journal of haematology, 183 (4
British journal of haematology, 183 (4
Sickle Cell Disease (SCD) is an increasing global health problem and presents significant challenges to European health care systems. Newborn screening (NBS) for SCD enables early initiation of preventive measures and has contributed to a reduction i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abcbc87bf672e09e4efdc017ccaa8189
http://hdl.handle.net/11577/3353238
http://hdl.handle.net/11577/3353238
Autor:
Sandrine Laurance, Vicky Chaar, Jacques Elion, Claudine Lapoumeroulie, Wassim El Nemer, Maria De Grandis, Yves Colin, Sylvie Cochet, Caroline Le Van Kim
Publikováno v:
Journal of Biological Chemistry. 289:11512-11521
Vaso-occlusive crises are the main acute complication in sickle cell disease. They are initiated by abnormal adhesion of circulating blood cells to vascular endothelium of the microcirculation. Several interactions involving an intricate network of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f86c957b843cb44f7350ecd7d06e0e9
https://doi.org/10.1074/jbc.m113.506121
https://doi.org/10.1074/jbc.m113.506121
Autor:
Anil Pathare, David Dennison, S. Al-Maamari, Shoaib Al-Zadjali, Claudine Lapoumeroulie, S. Alkindi, Ibtisam Elnour, Salem Al-Tamemi, R. Krishnamoorthy
Publikováno v:
Clinical Genetics. 87:185-189
Chronic granulomatous disease (CGD), a rare inherited disorder of the innate immune system, results from mutations in any one of the five genes encoding the subunits of the nicotinamide adenine dinucleotide phosphate-oxidase (NADPH) oxidase enzyme, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed8e319d0397cc5ab6cab688f148f2d4
https://doi.org/10.1111/cge.12351
https://doi.org/10.1111/cge.12351
Autor:
Mor Diaw, Lucile Offredo, Pierre-Louis Tharaux, Olivier Blanc Brude, Xavier Jouven, Brigitte Ranque, Philippe Connes, Marc Romana, Yves Colin Aronovicz, Dapa A. Diallo, Abdoul Karim Dembele, Claudine Lapoumeroulie, Diop Saliou, Caroline Le Van Kim
Publikováno v:
Blood. 134:2310-2310
Although most individuals with sickle cell disease (SCD) live in sub-Saharan Africa, the history of the disease in this continent remains largely unknown. SCD is characterized by chronic hemolytic anemia, acute-vaso occlusive events and progressive v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f34b249e22da401348501a29d341f77
https://doi.org/10.1182/blood-2019-126713
https://doi.org/10.1182/blood-2019-126713