Search Results - "Bournier, Odile"

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

“…Reactive oxygen species (ROS) production by NADPH oxidase 1 (NOX1), which is mainly expressed in colon epithelial cells, requires the membrane‐bound component…”
Get full text

Tyrosine Phosphorylation Regulates Alpha II Spectrin Cleavage by Calpain by 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

“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
Get full text

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

Get full text

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

“…Among 80 hereditary spherocytosis (HS) kindreds studied using denaturing electrophoretic separation of solubilized eythrocyte membrane proteins, we recognized…”
Get full text

The prolyl isomerase Pin1 acts as a novel molecular switch for TNF-α–induced priming of the NADPH oxidase in human neutrophils by 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

“…Neutrophils play a key role in host defense by releasing reactive oxygen species (ROS). However, excessive ROS production by neutrophil nicotinamide adenine…”
Get full text

Adiponectin and Its Globular Fragment Differentially Modulate the Oxidative Burst of Primary Human Phagocytes by 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

“…Adiponectin (Acrp30) belongs to the family of C1q/tumor necrosis factor α (TNFα)-related proteins. Acrp30 circulates as multimers of high, middle, and low…”
Get full text

Escherichia coli LF82 differentially regulates ROS production and mucin expression in intestinal epithelial T84 cells: implication of NOX1 by 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

“…Increased reactive oxygen species (ROS) production is associated with inflamed ileal lesions in Crohn's disease colonized by pathogenic adherent-invasive…”
Get full text

The red blood cell band 3 variant (band 3Biceêtrel:R490C) associated with dominant hereditary spherocytosis causes defective membrane targeting of the molecule and a dominant negative effect by Dhermy, D, Burnier, O, Bourgeois, M, Grandchamp, B

“…Hereditary spherocytosis (HS), a common human inherited haemolytic anaemia, is associated with partial deficiency of different erythrocyte membrane proteins…”
Get more information

Escherichia coli LF82 Differentially Regulates ROS Production and Mucin Expression in Intestinal Epithelial T84 Cells by 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

“…Background: Increased reactive oxygen species (ROS) production is associated with inflamed ileal lesions in Crohn’s disease colonized by pathogenic…”
Get full text

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

“…The spectrin-based membrane skeleton, a multi-protein scaffold attached to diverse cellular membranes, is presumed to be involved in the stabilization of…”
Get full text

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

“…Background information. The α‐ and β‐spectrin chains constitute the filaments of the spectrin‐based skeleton, which was first identified in erythrocytes. The…”
Get full text

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

“…The spectrin-based membrane skeleton, a multi-protein scaffold attached to diverse cellular membranes, is presumed to be involved in the stabilization of…”
Get full text

Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin by Glele-Kakai, C, Garbarz, M, Lecomte, M C, Leborgne, S, Galand, C, Bournier, O, Devaux, I, Gautero, H, Zohoun, I, Gallagher, P G, Forget, B G, Dhermy, D

“…We studied an African population in Benin and discovered an unexpectedly high frequency (1.6%) of hereditary elliptocytosis (HE) among the 1447 subjects…”
Get more information

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

Get full text

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 (spectrin Guemene‐Penfao) by Garbarz, Michel, Galand, Colette, Bibas, Dominique, Bournier, Odile, Devaux, Isabelle, Harousseau, Jean‐Luc, Grandchamp, Bernard, Dhermy, Didier

“…We studied a family with autosomal dominant hereditary spherocytosis (HS) associated with a mild spectrin deficiency. Linkage analysis using two microsatellite…”
Get full text

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

“…Spectrin deficiency is the most common deficiency found in HS. It is heterogeneous in terms of clinical expression, inheritance (dominant or recessive) and…”
Get full text

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 spectrin αI domain by 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

“…We describe a white French family in which 12 subjects presented with hereditary elliptocytosis (HE) or hereditary pyropoikilocytosis (HPP). Eight of these…”
Get full text

Purification of erythrocyte protein 4.1 by selective interaction with inositol hexaphosphate by el Ouggouti, S, Bournier, O, Boivin, P, Bertrand, O, Dhermy, D

“…Protein 4.1 is a multifunctional structural protein occupying a strategic position in the erythrocyte membrane. It is present in the erythrocyte membrane…”
Get more information

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

“…Seven black patients with mild hereditary elliptocytosis (HE) from five unrelated families were studied. The erythrocytes of these patients exhibited an…”
Get full text

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

Get full text