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Publications by Gianni Mastella
Chloride Conductance and Genetic Background Modulate the Cystic Fibrosis Phenotype of ΔF508 Homozygous Twins and Siblings
Journal of Clinical Investigation
Medicine
Related publications
Genotype/Phenotype Association in Cystic Fibrosis: Analyses of the ΔF508, R553X, and 3905insT Mutations
Pediatric Research
Child Health
Pediatrics
Perinatology
Functional Stability of Rescued ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator in Airway Epithelial Cells
American Journal of Respiratory Cell and Molecular Biology
Respiratory Medicine
Pulmonary
Clinical Biochemistry
Cell Biology
Molecular Biology
Identification and Regulation of the Cystic Fibrosis Transmembrane Conductance Regulator-Generated Chloride Channel.
Journal of Clinical Investigation
Medicine
Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)-Mediated Residual Chloride Secretion Does Not Protect Against Early Chronic Pseudomonas Aeruginosa Infection in F508del Homozygous Cystic Fibrosis Patients
Pediatric Research
Child Health
Pediatrics
Perinatology
Vitamin C Controls the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A Missense Cystic Fibrosis Transmembrane Conductance Regulator Mutation With Variable Phenotype
Pediatrics
Child Health
Pediatrics
Perinatology
Gating of Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channels by Adenosine Triphosphate Hydrolysis
Journal of General Physiology
Physiology
A Single Conductance Pore for Chloride Ions Formed by Two Cystic Fibrosis Transmembrane Conductance Regulator Molecules
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Cystic Fibrosis Transmembrane Conductance Regulator and Adenosine Triphosphate
Science
Multidisciplinary
Philosophy of Science
History
