Cystic fibrosis (CF) is a monogenetic disease caused by the mutation of CFTR, a cAMP-regulated Cl− channel expressing at the apical plasma membrane (PM) of epithelia.
Shogo Taniguchi +5 more
doaj +1 more source
Development of CpG-Depleted CFTR Plasmid-Based Nanoparticles for Nonviral Gene Therapy in Lung Cystic Fibrosis Disease. [PDF]
Qiu B +6 more
europepmc +1 more source
Distinct CFTR Mutation Spectrum and Atypical Clinical Presentations in Chinese Patients with Cystic Fibrosis. [PDF]
Wang Z +6 more
europepmc +1 more source
RFFL-mediated protein quality control limits functional rescue of TRID-CFTR modulator combination therapy for cystic fibrosis nonsense mutations. [PDF]
Tateishi H +3 more
europepmc +1 more source
Large variations in total and allele-specific transcript expression in a disease mutation-independent manner. [PDF]
Freyberg M +13 more
europepmc +1 more source
Tracking early cystic fibrosis in the new era. [PDF]
Anagnostopoulou P, Rovira-Amigo S.
europepmc +1 more source
Cutaneous Symptoms of Cystic Fibrosis: A Narrative Review. [PDF]
Piątkiewicz M +4 more
europepmc +1 more source
Clinical characteristics of pulmonary non-tuberculous mycobacterial disease with <i>CFTR</i> variants in the Japanese population. [PDF]
Nagao G +16 more
europepmc +1 more source
Decoding liver injury in cystic fibrosis: How to tell drug-induced liver injury from cystic fibrosis liver disease. [PDF]
Lee J +11 more
europepmc +1 more source

