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Publications by Kaisa Thorell

Bicarbonate and Functional CFTR Channel Are Required for Proper Mucin Secretion and Link Cystic Fibrosis With Its Mucus Phenotype

Journal of Experimental Medicine
MedicineAllergyImmunology
2012English

Correction: Rapid Evolution of Distinct Helicobacter Pylori Subpopulations in the Americas

PLoS Genetics
EvolutionEcologyGeneticsMolecular BiologyCancer ResearchSystematicsBehavior
2017English

Related publications

Cystic Fibrosis: Impaired Bicarbonate Secretion and Mucoviscidosis

The Lancet
Medicine
2008English

CFTR: Cystic Fibrosis and Beyond

European Respiratory Journal
MedicinePulmonaryRespiratory Medicine
2014English

Correction: Mechanisms of CFTR Functional Variants That Impair Regulated Bicarbonate Permeation and Increase Risk for Pancreatitis but Not for Cystic Fibrosis

PLoS Genetics
EvolutionEcologyGeneticsMolecular BiologyCancer ResearchSystematicsBehavior
2014English

Recent Progress in CFTR Interactome Mapping and Its Importance for Cystic Fibrosis

Frontiers in Pharmacology
Pharmacology
2018English

Is Cystic Fibrosis Mucus Abnormal?

Pediatric Research
Child HealthPediatricsPerinatology
1981English

Curcumin Cross-Links Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Polypeptides and Potentiates CFTR Channel Activity by Distinct Mechanisms

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2009English

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2015English

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

Science-Business eXchange
2012English

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

Science-Business eXchange
2013English

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