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Florian Bossard

Showing results (1-10 of 8) with videos related to

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Human Gene Therapy|November 2, 2005
Amphiphilic block copolymers promote gene delivery in vivo to pathological skeletal musclesPeggy Richard, Florian Bossard, Lea Desigaux, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|January 24, 2007
NHE-RF1 protein rescues DeltaF508-CFTR functionFlorian Bossard, Amal Robay, Gilles Toumaniantz, et al.
American Journal of Respiratory Cell and Molecular Biology|March 6, 2010
β1, β2, and β3 adrenoceptors and Na+/H+ exchanger regulatory factor 1 expression in human bronchi and their modifications in cystic fibrosisFlorian Bossard, Emilie Silantieff, Emmanuelle Lavazais-Blancou, et al.
Journal of Cell Science|April 13, 2019
Transcytosis maintains CFTR apical polarity in the face of constitutive and mutation-induced basolateral missortingAurélien Bidaud-Meynard, Florian Bossard, Andrea Schnúr, et al.
Molecular Biology of the Cell|May 8, 2009
Revisiting the role of cystic fibrosis transmembrane conductance regulator and counterion permeability in the pH regulation of endocytic organellesHerve Barriere, Miklos Bagdany, Florian Bossard, et al.
Molecular Biology of the Cell|September 14, 2012
Proinflammatory cytokine secretion is suppressed by TMEM16A or CFTR channel activity in human cystic fibrosis bronchial epitheliaGuido Veit, Florian Bossard, Julie Goepp, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 21, 2007
Discovery of alpha-aminoazaheterocycle-methylglyoxal adducts as a new class of high-affinity inhibitors of cystic fibrosis transmembrane conductance regulator chloride channelsChristel Routaboul, Caroline Norez, Patricia Melin, et al.
Cell|January 24, 2012
Correction of both NBD1 energetics and domain interface is required to restore ΔF508 CFTR folding and functionWael M Rabeh, Florian Bossard, Haijin Xu, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Human Gene Therapy|November 2, 2005
Amphiphilic block copolymers promote gene delivery in vivo to pathological skeletal musclesPeggy Richard, Florian Bossard, Lea Desigaux, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|January 24, 2007
NHE-RF1 protein rescues DeltaF508-CFTR functionFlorian Bossard, Amal Robay, Gilles Toumaniantz, et al.
American Journal of Respiratory Cell and Molecular Biology|March 6, 2010
β1, β2, and β3 adrenoceptors and Na+/H+ exchanger regulatory factor 1 expression in human bronchi and their modifications in cystic fibrosisFlorian Bossard, Emilie Silantieff, Emmanuelle Lavazais-Blancou, et al.
Journal of Cell Science|April 13, 2019
Transcytosis maintains CFTR apical polarity in the face of constitutive and mutation-induced basolateral missortingAurélien Bidaud-Meynard, Florian Bossard, Andrea Schnúr, et al.
Molecular Biology of the Cell|May 8, 2009
Revisiting the role of cystic fibrosis transmembrane conductance regulator and counterion permeability in the pH regulation of endocytic organellesHerve Barriere, Miklos Bagdany, Florian Bossard, et al.
Molecular Biology of the Cell|September 14, 2012
Proinflammatory cytokine secretion is suppressed by TMEM16A or CFTR channel activity in human cystic fibrosis bronchial epitheliaGuido Veit, Florian Bossard, Julie Goepp, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 21, 2007
Discovery of alpha-aminoazaheterocycle-methylglyoxal adducts as a new class of high-affinity inhibitors of cystic fibrosis transmembrane conductance regulator chloride channelsChristel Routaboul, Caroline Norez, Patricia Melin, et al.
Cell|January 24, 2012
Correction of both NBD1 energetics and domain interface is required to restore ΔF508 CFTR folding and functionWael M Rabeh, Florian Bossard, Haijin Xu, et al.
Pageof 1