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The Journal of Pediatrics
|
February 20, 2007
Nasal potential difference in cystic fibrosis diagnosis of very young children
Isabelle Sermet-Gaudelus, Emmanuelle Girodon, Frédéric Huet, et al.
International Journal of Molecular Sciences
|
December 23, 2022
Acting on the CFTR Membrane-Spanning Domains Interface Rescues Some Misfolded Mutants
Nesrine Baatallah, Ahmad Elbahnsi, Benoit Chevalier, et al.
The Journal of Biological Chemistry
|
November 18, 2006
Membrane cholesterol content modulates ClC-2 gating and sensitivity to oxidative stress
Alexandre Hinzpeter, Janine Fritsch, Florence Borot, et al.
Molecular Therapy. Nucleic Acids
|
June 24, 2015
Liposome-based Formulation for Intracellular Delivery of Functional Proteins
Benoît Chatin, Mathieu Mével, Julie Devallière, et al.
British Journal of Pharmacology
|
March 4, 2011
Resveratrol rescues cAMP-dependent anionic transport in the cystic fibrosis pancreatic cell line CFPAC1
Nabila Hamdaoui, Maryvonne Baudoin-Legros, Mairead Kelly, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 18, 2015
Finding new drugs to enhance anion secretion in cystic fibrosis: Toward suitable systems for better drug screening. Report on the pre-conference meeting to the 12th ECFS Basic Science Conference, Albufeira, 25-28 March 2015
Alan S Verkman, Aleksander Edelman, Margarida Amaral, et al.
F1000Research
|
November 27, 2015
An unexpected effect of TNF-α on F508del-CFTR maturation and function
Sara Bitam, Iwona Pranke, Monika Hollenhorst, et al.
Plos One
|
October 1, 2014
Proteomic analysis of nasal epithelial cells from cystic fibrosis patients
Ludovic Jeanson, Ida Chiara Guerrera, Jean-François Papon, et al.
American Journal of Respiratory and Critical Care Medicine
|
October 18, 2018
Might Brushed Nasal Cells Be a Surrogate for CFTR Modulator Clinical Response?
Iwona Pranke, Aurelie Hatton, Alexandra Masson, et al.
Human Mutation
|
March 19, 2005
Misprocessing of the CFTR protein leads to mild cystic fibrosis phenotype
Jérôme Clain, Jacqueline Lehmann-Che, Ingrid Duguépéroux, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 108) with videos related to
Sort By:
Page
of 11
The Journal of Pediatrics
|
February 20, 2007
Nasal potential difference in cystic fibrosis diagnosis of very young children
Isabelle Sermet-Gaudelus, Emmanuelle Girodon, Frédéric Huet, et al.
International Journal of Molecular Sciences
|
December 23, 2022
Acting on the CFTR Membrane-Spanning Domains Interface Rescues Some Misfolded Mutants
Nesrine Baatallah, Ahmad Elbahnsi, Benoit Chevalier, et al.
The Journal of Biological Chemistry
|
November 18, 2006
Membrane cholesterol content modulates ClC-2 gating and sensitivity to oxidative stress
Alexandre Hinzpeter, Janine Fritsch, Florence Borot, et al.
Molecular Therapy. Nucleic Acids
|
June 24, 2015
Liposome-based Formulation for Intracellular Delivery of Functional Proteins
Benoît Chatin, Mathieu Mével, Julie Devallière, et al.
British Journal of Pharmacology
|
March 4, 2011
Resveratrol rescues cAMP-dependent anionic transport in the cystic fibrosis pancreatic cell line CFPAC1
Nabila Hamdaoui, Maryvonne Baudoin-Legros, Mairead Kelly, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 18, 2015
Finding new drugs to enhance anion secretion in cystic fibrosis: Toward suitable systems for better drug screening. Report on the pre-conference meeting to the 12th ECFS Basic Science Conference, Albufeira, 25-28 March 2015
Alan S Verkman, Aleksander Edelman, Margarida Amaral, et al.
F1000Research
|
November 27, 2015
An unexpected effect of TNF-α on F508del-CFTR maturation and function
Sara Bitam, Iwona Pranke, Monika Hollenhorst, et al.
Plos One
|
October 1, 2014
Proteomic analysis of nasal epithelial cells from cystic fibrosis patients
Ludovic Jeanson, Ida Chiara Guerrera, Jean-François Papon, et al.
American Journal of Respiratory and Critical Care Medicine
|
October 18, 2018
Might Brushed Nasal Cells Be a Surrogate for CFTR Modulator Clinical Response?
Iwona Pranke, Aurelie Hatton, Alexandra Masson, et al.
Human Mutation
|
March 19, 2005
Misprocessing of the CFTR protein leads to mild cystic fibrosis phenotype
Jérôme Clain, Jacqueline Lehmann-Che, Ingrid Duguépéroux, et al.
Page
of 11