PREVALENCE, FUNCTION AND TREATMENT OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR GENE MUTATIONS IN BRONCHIECTASIS PATIENTS

Project

PREVALENCE, FUNCTION AND TREATMENT OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR GENE MUTATIONS IN BRONCHIECTASIS PATIENTS

Academic Signature
Overview

Il servizio di classificazione ACADEMIC SIGNATURE è IN BETA TESTING e i risultati potrebbero non essere corretti

Academic Signature (8)

Cystic Fibrosis Transmembrane Conductance Regulator

ATP-Binding Cassette, Sub-Family C Proteins

Bronchiectasis

Bronchial Diseases

Cystic Fibrosis Transmembrane Conductance Regulator

Chloride Channels

Cystic Fibrosis

Genetic Diseases, Inborn

Cystic Fibrosis

Infant, Newborn, Diseases

Cystic Fibrosis

Prevalence

Cystic Fibrosis

Pancreatic Diseases

Contributors

BLASI FRANCESCO BRUNO ARTURO Scientific Manager

Departments involved

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti Principale

Type

PRIN2022 - PRIN bando 2022

Funder

MINISTERO DELL'UNIVERSITA' E DELLA RICERCA

External Organization Funding Organization

Date/time interval

October 16, 2023 - February 17, 2026

Project duration

28 months