Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Odile Bournier"'
Autor:
Clément d’Audigier, Eric Pasmant, Odile Bournier, Yves Laurian, Marie Claude Guillin, Annie Bezeaud
Publikováno v:
Haematologica, Vol 93, Iss 5 (2008)
Externí odkaz:
https://doaj.org/article/4dcf2031dd124a42953cd982892a4606
Autor:
Odile Bournier, Arlette Darfeuille-Michaud, Christel Neut, Jean-Claude Marie, José Luis, Hanane Boukemara, Pham My-Chan Dang, Laurent Dubuquoy, Viviana Marzaioli, Jamel El-Benna, Imen Elatrech
Publikováno v:
Inflammatory Bowel Diseases. 21:1018-1026
Background: Increased reactive oxygen species (ROS) production is associated with inflamed ileal lesions in Crohn’s disease colonized by pathogenic adherent–invasive Escherichia coli LF82. We investigated whether such ileal bacteria can modulate
Autor:
Odile Bournier, Yolande Kroviarski, Maya Debbabi, Marie-Anne Gougerot-Pocidalo, Jamel El-Benna, Pham My-Chan Dang
Publikováno v:
The FASEB Journal. 27:1733-1748
Reactive oxygen species (ROS) production by NADPH oxidase 1 (NOX1), which is mainly expressed in colon epithelial cells, requires the membrane-bound component p22(PHOX) and the cytosolic partners NOX organizer 1 (NOXO1), NOX activator 1 (NOXA1), and
Autor:
Jan Frystyk, Alan Flyvbjerg, Jamel El Benna, Margarita Hurtado-Nedelec, Gilles Hayem, Benoit Marion-Gaber, Odile Bournier, Marie-Anne Gougerot-Pocidalo, Jean-Claude Marie, Pia Chedid
Publikováno v:
Chedid, P, Hurtado-Nedelec, M, Marion-Gaber, B, Bournier, O, Hayem, G, Gougerot-Pocidalo, M-A, Frystyk, J, Flyvbjerg, A, El Benna, J & Marie, J-C 2012, ' Adiponectin and its globular fragment differentially modulate the oxidative burst of primary human phagocytes ', American Journal of Pathology, vol. 180, no. 2, pp. 682-92 . https://doi.org/10.1016/j.ajpath.2011.10.013
Adiponectin (Acrp30) belongs to the family of C1q/tumor necrosis factor α (TNFα)-related proteins. Acrp30 circulates as multimers of high, middle, and low molecular weight. In this study, we detected Acrp30 and its globular fragment (gAcrp30) in sy
Autor:
Gilles Hayem, James S. Malter, Marie Anne Gougerot-Pocidalo, Odile Bournier, Aghleb Bartegi, Ping K. Lu, Pham My-Chan Dang, Xiao Zhen Zhou, Riad Arabi Derkawi, Silvia Ciappelloni, Houssam Raad, Tarek Boussetta, Yolande Kroviarski, Jamel El-Benna
Publikováno v:
Blood. 116:5795-5802
Neutrophils play a key role in host defense by releasing reactive oxygen species (ROS). However, excessive ROS production by neutrophil nicotinamide adenine dinucleotide phosphate (NADPH) oxidase can damage bystander tissues, thereby contributing to
Autor:
Björn Rotter, Marie Christine Lecomte, Gaël Nicolas, Yolande Kroviarski, Odile Bournier, Didier Dhermy
Publikováno v:
Biology of the Cell. 98:279-293
Background information. The α- and β-spectrin chains constitute the filaments of the spectrin-based skeleton, which was first identified in erythrocytes. The discovery of analogous structures at plasma membranes of eukaryotic cells has led to inves
Publikováno v:
Biochemical Journal. 388:631-638
The spectrin-based membrane skeleton, a multi-protein scaffold attached to diverse cellular membranes, is presumed to be involved in the stabilization of membranes, the establishment of membrane domains as well as in vesicle trafficking and nuclear f
Autor:
Odile Bournier, J. Steen-Johnsen, Didier Dhermy, Bernard Grandchamp, Gilles Hetet, Gil Tchernia, T. Cynober
Publikováno v:
Clinical & Laboratory Haematology. 22:329-336
We studied a recessive hereditary spherocytosis (HS) family from Norway in which all four children had haemolytic spherocytosis while spectrin (Sp) deficiency was detected in the proband. Molecular analysis demonstrated that all affected children had
Autor:
Odile Bournier, Dominique Bibas, Jean-Luc Harousseau, Bernard Grandchamp, Colette Galand, Didier Dhermy, Isabelle Devaux, M. Garbarz
Publikováno v:
British Journal of Haematology. 100:90-98
We studied a family with autosomal dominant hereditary spherocytosis (HS) associated with a mild spectrin deficiency. Linkage analysis using two microsatellite markers (D14S63 and D14S271) very close to the beta-spectrin gene (SPTB) showed that HS co
Autor:
Odile Bournier, Bernard G. Forget, Sylvie Leborgne, Colette Galand, H. Gautero, Clement Glele-Kakai, Isabelle Devaux, Didier Dhermy, Marie-Christine Lecomte, Patrick G. Gallagher, M. Garbarz, Isidore Zohoun
Publikováno v:
British Journal of Haematology. 95:57-66
We studied an African population in Benin and discovered an unexpectedly high frequency (1.6%) of hereditary elliptocytosis (HE) among the 1447 subjects studied. In approximately two-thirds of HE individuals we identified molecular defects, primarily