Search Results - "Urbach, Valérie"

Specialized proresolving mediator resolvin E1 corrects the altered cystic fibrosis nasal epithelium cilia beating dynamics by Briottet, Maëlle, Sy, Khadeeja, London, Charlie, Aissat, Abdel, Shum, Mickael, Escabasse, Virginie, Louis, Bruno, Urbach, Valérie

“…In cystic fibrosis (CF), impaired mucociliary clearance leads to chronic infection and inflammation. However, cilia beating features in a CF altered…”
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The Impact of Air Pollution on the Course of Cystic Fibrosis: A Review by Blayac, Marion, Coll, Patrice, Urbach, Valérie, Fanen, Pascale, Epaud, Ralph, Lanone, Sophie

“…Cystic fibrosis (CF) is a lethal and widespread autosomal recessive disorder affecting over 80,000 people worldwide. It is caused by mutations of the gene,…”
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Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis by Simonin, Juliette, Bille, Emmanuelle, Crambert, Gilles, Noel, Sabrina, Dreano, Elise, Edwards, Aurélie, Hatton, Aurélie, Pranke, Iwona, Villeret, Bérengère, Cottart, Charles-Henry, Vrel, Jean-Patrick, Urbach, Valérie, Baatallah, Nesrine, Hinzpeter, Alexandre, Golec, Anita, Touqui, Lhousseine, Nassif, Xavier, Galietta, Luis J. V, Planelles, Gabrielle, Sallenave, Jean-Michel, Edelman, Aleksander, Sermet-Gaudelus, Isabelle

“…Cystic fibrosis (CF) is caused by defective Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein. Morbidity is mainly due to early airway…”
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Optimization of 3D islet-like cluster derived from human pluripotent stem cells: an efficient in vitro differentiation protocol by Ghorbani-Dalini, Sadegh, Azarpira, Negar, Hossein Sangtarash, Mohammad, Urbach, Valérie, Yaghobi, Ramin, Reza Soleimanpour-Lichaei, Hamid, Sarshar, Meysam

“…•This study presents a protocol that differentiates hiPSC into 3D glucose-responsive insulin-producing islet-like cluster.•This differentiation protocol…”
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DHA, RvD1, RvD5, and MaR1 reduce human coronary arteries contractions induced by PGE2 by Bouhadoun, Amel, Manikpurage, Hasanga D., Deschildre, Catherine, Zalghout, Sara, Dubourdeau, Marc, Urbach, Valérie, Ho-Tin-Noe, Benoît, Deschamps, Lydia, Michel, Jean-Baptiste, Longrois, Dan, Norel, Xavier

“…In patients with coronary artery disease (CAD), plasma levels of pro-inflammatory lipid mediators such as PGE2 and TxA2 are increased. They could increase…”
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Lipoxin A4 stimulates calcium-activated chloride currents and increases airway surface liquid height in normal and cystic fibrosis airway epithelia by Verrière, Valia, Higgins, Gerard, Al-Alawi, Mazen, Costello, Richard W, McNally, Paul, Chiron, Raphaël, Harvey, Brian J, Urbach, Valérie

“…Cystic Fibrosis (CF) is a genetic disease characterised by a deficit in epithelial Cl(-) secretion which in the lung leads to airway dehydration and a reduced…”
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Author Correction: Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis by Simonin, Juliette, Bille, Emmanuelle, Crambert, Gilles, Noel, Sabrina, Dreano, Elise, Edwards, Aurélie, Hatton, Aurélie, Pranke, Iwona, Villeret, Bérengère, Cottart, Charles-Henry, Vrel, Jean-Patrick, Urbach, Valérie, Baatallah, Nesrine, Hinzpeter, Alexandre, Golec, Anita, Touqui, Lhousseine, Nassif, Xavier, Galietta, Luis J. V., Planelles, Gabrielle, Sallenave, Jean-Michel, Edelman, Aleksander, Sermet-Gaudelus, Isabelle

“…An amendment to this paper has been published and can be accessed via a link at the top of the paper…”
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Physiological Impact of Abnormal Lipoxin A 4 Production on Cystic Fibrosis Airway Epithelium and Therapeutic Potential by Higgins, Gerard, Ringholz, Fiona, Buchanan, Paul, McNally, Paul, Urbach, Valérie

“…Lipoxin A 4 has been described as a major signal for the resolution of inflammation and is abnormally produced in the lungs of patients with cystic fibrosis…”
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Physiological Impact of Abnormal Lipoxin A4 Production on Cystic Fibrosis Airway Epithelium and Therapeutic Potential by Urbach, Valérie, McNally, Paul, Buchanan, Paul, Ringholz, Fiona, Higgins, Gerard

“…Lipoxin A4 has been described as a major signal for the resolution of inflammation and is abnormally produced in the lungs of patients with cystic fibrosis…”
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Sexual dimorphism and oestrogen regulation of KCNE3 expression modulates the functional properties of KCNQ1 K+ channels by Alzamora, Rodrigo, O’Mahony, Fiona, Bustos, Viviana, Rapetti‐Mauss, Raphael, Urbach, Valérie, Cid, L. Pablo, Sepúlveda, Francisco V., Harvey, Brian J.

“…Non‐Technical Summary  High levels of oestrogen are known to cause fluid retention in fertile females. It is thought that the increase in body fluid volume is…”
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An unexpected effect of TNF-α on F508del-CFTR maturation and function [version 2; peer review: 2 approved] by Bitam, Sara, Pranke, Iwona, Hollenhorst, Monika, Servel, Nathalie, Moquereau, Christelle, Tondelier, Danielle, Hatton, Aurélie, Urbach, Valérie, Sermet-Gaudelus, Isabelle, Hinzpeter, Alexandre, Edelman, Aleksander

“…Cystic fibrosis (CF) is a multifactorial disease caused by mutations in the cystic fibrosis transmembrane conductance regulator gene ( CFTR), which encodes a…”
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Specialized Pro-Resolving Lipid Mediators in Cystic Fibrosis by Philippe, Réginald, Urbach, Valerie

“…In cystic fibrosis (CF), impaired airway surface hydration (ASL) and mucociliary clearance that promote chronic bacterial colonization, persistent…”
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Lipoxin A4 and interleukin-8 levels in cystic fibrosis sputum after antibiotherapy by Chiron, Raphaël, Grumbach, Y. Yaël, Quynh, Nga V.T, Verriere, Valia, Urbach, Valérie

“…Abstract Antibiotics are largely prescribed for cystic fibrosis (CF) respiratory exacerbations. Effects of antibiotics on the inflammatory profile of the…”
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Rapid Effects of Dexamethasone on Intracellular pH and Na+/H+ Exchanger Activity in Human Bronchial Epithelial Cells by Verrière, Valia A., Hynes, Darina, Faherty, Sheila, Devaney, James, Bousquet, Jean, Harvey, Brian J., Urbach, Valérie

“…Glucocorticoids have been shown to produce rapid nongenomic responses in airway epithelia. By using an intracellular pH (pHi) spectrofluorescence imaging…”
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Physiological levels of lipoxin A 4 inhibit ENaC and restore airway surface liquid height in cystic fibrosis bronchial epithelium by Al-Alawi, Mazen, Buchanan, Paul, Verriere, Valia, Higgins, Gerard, McCabe, Olive, Costello, Richard W., McNally, Paul, Urbach, Valérie, Harvey, Brian J.

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The Role of Specialized Pro-Resolving Mediators in Cystic Fibrosis Airways Disease by Briottet, Maelle, Shum, Mickael, Urbach, Valerie

“…Cystic Fibrosis (CF) is a recessive genetic disease due to mutations of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene encoding the CFTR…”
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Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators by Pranke, Iwona M., Hatton, Aurélie, Simonin, Juliette, Jais, Jean Philippe, Le Pimpec-Barthes, Françoise, Carsin, Ania, Bonnette, Pierre, Fayon, Michael, Stremler-Le Bel, Nathalie, Grenet, Dominique, Thumerel, Matthieu, Mazenq, Julie, Urbach, Valerie, Mesbahi, Myriam, Girodon-Boulandet, Emanuelle, Hinzpeter, Alexandre, Edelman, Aleksander, Sermet-Gaudelus, Isabelle

“…Clinical studies with modulators of the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) protein have demonstrated that functional restoration of the…”
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CF Patients’ Airway Epithelium and Sex Contribute to Biosynthesis Defects of Pro-Resolving Lipids by Shum, Mickael, London, Charlie M., Briottet, Maelle, Sy, Khadeeja Adam, Baillif, Vincent, Philippe, Reginald, Zare, Abdolhossein, Ghorbani-Dalini, Sadegh, Remus, Natacha, Tarze, Agathe, Escabasse, Virginie, Epaud, Ralph, Dubourdeau, Marc, Urbach, Valerie

“…Specialized pro-resolving lipid mediators (SPMs) as lipoxins (LX), resolvins (Rv), protectins (PD) and maresins (MaR) promote the resolution of inflammation…”
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An unexpected effect of TNF-α on F508del-CFTR maturation and function by Bitam, Sara, Pranke, Iwona, Hollenhorst, Monika, Servel, Nathalie, Moquereau, Christelle, Tondelier, Danielle, Hatton, Aurélie, Urbach, Valérie, Sermet-Gaudelus, Isabelle, Hinzpeter, Alexandre, Edelman, Aleksander

“…Cystic fibrosis (CF) is a multifactorial disease caused by mutations in the cystic fibrosis transmembrane conductance regulator gene ( CFTR), which encodes a…”
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LXA4 stimulates ZO-1 expression and transepithelial electrical resistance in human airway epithelial (16HBE14o-) cells by Grumbach, Yael, Quynh, Nga Vu Thi, Chiron, Raphaël, Urbach, Valérie

“…Lipoxin A(4) (LXA(4)) is a biologically active eicosanoid produced in human airways that displays anti-inflammatory properties. In cystic fibrosis and severe…”
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