NOXO1 phosphorylation on serine 154 is critical for optimal NADPH oxidase 1 assembly and activation von Debbabi, Maya, Kroviarski, Yolande, Bournier, Odile, Gougerot‐Pocidalo, Marie‐Anne, El‐Benna, Jamel, Dang, Pham My‐Chan

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Tyrosine Phosphorylation Regulates Alpha II Spectrin Cleavage by Calpain von Nicolas, Gaël, Fournier, Catherine M., Galand, Colette, Malbert-Colas, Laurence, Bournier, Odile, Kroviarski, Yolande, Bourgeois, Monique, Camonis, Jacques H., Dhermy, Didier, Grandchamp, Bernard, Lecomte, Marie-Christine

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A natural variant with a point mutation resulting in a homozygous Arg to His substitution at position 388 in prothrombin von D'AUDIGIER, Clément, PASMANT, Eric, BOURNIER, Odile, LAURIAN, Yves, GUILLIN, Marie Claude, BEZEAUD, Annie

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The prolyl isomerase Pin1 acts as a novel molecular switch for TNF-α–induced priming of the NADPH oxidase in human neutrophils von Boussetta, Tarek, Gougerot-Pocidalo, Marie-Anne, Hayem, Gilles, Ciappelloni, Silvia, Raad, Houssam, Arabi Derkawi, Riad, Bournier, Odile, Kroviarski, Yolande, Zhou, Xiao Zhen, Malter, James S., Lu, Ping K., Bartegi, Aghleb, Dang, Pham My-Chan, El-Benna, Jamel

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Adiponectin and Its Globular Fragment Differentially Modulate the Oxidative Burst of Primary Human Phagocytes von Chedid, Pia, Hurtado-Nedelec, Margarita, Marion-Gaber, Benoit, Bournier, Odile, Hayem, Gilles, Gougerot-Pocidalo, Marie-Anne, Frystyk, Jan, Flyvbjerg, Alan, El Benna, Jamel, Marie, Jean-Claude

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Escherichia coli LF82 differentially regulates ROS production and mucin expression in intestinal epithelial T84 cells: implication of NOX1 von Elatrech, Imen, Marzaioli, Viviana, Boukemara, Hanane, Bournier, Odile, Neut, Christel, Darfeuille-Michaud, Arlette, Luis, José, Dubuquoy, Laurent, El-Benna, Jamel, My-Chan Dang, Pham, Marie, Jean-Claude

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Escherichia coli LF82 Differentially Regulates ROS Production and Mucin Expression in Intestinal Epithelial T84 Cells von Elatrech, Imen, Marzaioli, Viviana, Boukemara, Hanane, Bournier, Odile, Neut, Christel, Darfeuille-Michaud, Arlette, Luis, José, Dubuquoy, Laurent, El-Benna, Jamel, Dang, Pham My-Chan, Marie, Jean-Claude

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Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects von Dhermy, Didier, Galand, Colette, Bournier, Odile, Boulanger, Laurent, Cynober, Thérèse, Schismanoff, Pierre Olivier, Bursaux, Elisabeth, Tchernia Boivin, Gil, Pierre, Garbarz, Michel

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αII-Spectrin interacts with Tes and EVL, two actin-binding proteins located at cell contacts von ROTTER, Björn, BOURNIER, Odile, NICOLAS, Gael, DHERMY, Didier, LECOMTE, Marie-Christine

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Spectrin interacts with EVL (Enabled/vasodilator-stimulated phosphoprotein-like protein), a protein involved in actin polymerization von Bournier, Odile, Kroviarski, Yolande, Rotter, Björn, Nicolas, Gaël, Lecomte, Marie C., Dhermy, Didier

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The red blood cell band 3 variant (band 3Bicetrel: R490C) associated with dominant hereditary spherocytosis causes defective membrane targeting of the molecule and a dominant negat... von Didier Dhermy, Odile Bournier, Monique Bourgeois, Bernard Grandchamp

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Coinheritance of alpha-and beta-spectrin gene mutations in a case of hereditary elliptocytosis von Dhermy, D, Galand, C, Bournier, O, King, M J, Cynober, T, Roberts, I, Kanyike, F, Adekile, A

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AlphaII-spectrin interacts with Tes and EVL, two actin-binding proteins located at cell contacts von Rotter, Björn, Bournier, Odile, Nicolas, Gael, Dhermy, Didier, Lecomte, Marie-Christine

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A 5′ splice region G → C mutation in exon 3 of the human β‐spectrin gene leads to decreased levels of β‐spectrin mRNA and is responsible for dominant hereditary spherocytosis (spec... von Garbarz, Michel, Galand, Colette, Bibas, Dominique, Bournier, Odile, Devaux, Isabelle, Harousseau, Jean‐Luc, Grandchamp, Bernard, Dhermy, Didier

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Hereditary Spherocytosis with Spectrin Deficiency Related to Null Mutations of the β-Spectrin Gene von Dhermy, Didier, Galand, Colette, Bournier, Odile, Cynober, Thérèse, Méchinaud, Françoise, Tchemia, Gil, Garbarz, Michel

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Hereditary pyropoikilocytosis and elliptocytosis in a white french family with the spectrin αI/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the sp... von GARBARZ, M, LECOMTE, M.-C, FORGET, B. G, BOIVIN, P, DHERMY, D, FEO, C, DEVAUX, I, PICAT, C, LEFEBVRE, C, GALIBERT, F, GAUTERO, H, BOURNIER, O, GALAND, C

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Interaction of Spectrin with the Low Molecular Weight Phosphotyrosine Phosphatese (LMW-PTP) von Lecomte, Marie-Christine, Nicolas, Gaël, Fournier, Catherine, Galand, Colette, Malbert-Colas, Laurence, Bournier, Odile, Dhermy, Didier, Grandchamps, Bernard

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Purification of erythrocyte protein 4.1 by selective interaction with inositol hexaphosphate von El Ouggouti, Soumaya, Bournier, Odile, Boivin, Pierre, Bertrand, Olivier, Dhermy, Didier

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A New Abnormal Variant of Spectrin in Black Patients With Hereditary Elliptocytosis von Lecomte, Marie-Christine, Dhermy, Didier, Solis, Constance, Ester, Anna, Féo, Claude, Gautero, Huguette, Bournier, Odile, Boivin, Pierre

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A natural variant with a point mutation resulting in a homozygous Arg to His substitution at position 388 in prothrombin von d'Audigier, Clément, Pasmant, Eric, Bournier, Odile, Laurian, Yves, Guillin, Marie Claude, Bezeaud, Annie

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