Search research articles
Contact Us
Filters
Showing results (1-10 of 8) with videos related to
Page
of 1
Sort By:
Human Gene Therapy
|
November 2, 2005
Amphiphilic block copolymers promote gene delivery in vivo to pathological skeletal muscles
Peggy 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 function
Florian 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 fibrosis
Florian 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 missorting
Aurélien 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 organelles
Herve 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 epithelia
Guido 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 channels
Christel 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 function
Wael M Rabeh, Florian Bossard, Haijin Xu, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Human Gene Therapy
|
November 2, 2005
Amphiphilic block copolymers promote gene delivery in vivo to pathological skeletal muscles
Peggy 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 function
Florian 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 fibrosis
Florian 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 missorting
Aurélien 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 organelles
Herve 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 epithelia
Guido 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 channels
Christel 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 function
Wael M Rabeh, Florian Bossard, Haijin Xu, et al.
Page
of 1