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Publications by Michele Ettorre
Impaired CFTR Function in Mild Cystic Fibrosis Associated With the S977f/T5TG12complex Allele in Trans With F508del Mutation
Journal of Cystic Fibrosis
Child Health
Pulmonary
Pediatrics
Perinatology
Respiratory Medicine
Related publications
The Cystic Fibrosis F508del Mutation in Crohn's Disease
Journal of Cystic Fibrosis
Child Health
Pulmonary
Pediatrics
Perinatology
Respiratory Medicine
CFTR F508del Mutation and 5T Allele in Patients With Chronic Pancreatitis and Pancreatic Adenocarcinoma
Acta chirurgica iugoslavica
Thymosin Α-1 Does Not Correct F508del-CFTR in Cystic Fibrosis Airway Epithelia
JCI insight
Medicine
Cysteamine Re-Establishes the Clearance of Pseudomonas Aeruginosa by Macrophages Bearing the Cystic Fibrosis-Relevant F508del-CFTR Mutation
Cell Death and Disease
Molecular Neuroscience
Immunology
Cell Biology
Cancer Research
Cellular
Medicine
Thymosin Α-1 Does Not Correct F508del-CFTR in Cystic Fibrosis Airway Epithelia
JCI insight
Medicine
Cystic Fibrosis Transmembrane Regulator (CFTR) Delta F508 Mutation and 5T Allele in Patients With Chronic Pancreatitis and Exocrine Pancreatic Cancer
Gut
Gastroenterology
Prs16 - Modeled Survival Gains of Patients With Cystic Fibrosis (Cf) Aged ≥12 Years Heterozygous for F508del-CFTR and a Residual Function Mutation (F508del/Rf) Treated With the Cf Transmembrane Conductance Regulator Modulator (Cftrm) Tezacaftor/Ivacaftor (Tez/Iva)
Value in Health
Medicine
Health Policy
Public Health
Occupational Health
Environmental
Phenotypic Expression of the p.Leu1077Pro CFTR Mutation in Sicilian Cystic Fibrosis Patients
BMC Research Notes
Biochemistry
Medicine
Genetics
Molecular Biology
Nine Cystic Fibrosis Patients Homozygous for the CFTR Nonsense Mutation R1162X Have Mild or Moderate Lung Disease.
Journal of Medical Genetics
Genetics
