The distribution and role of the CFTR protein in the intracellular compartments
A Lukasiak, M Zajac - Membranes, 2021 - mdpi.com
Cystic fibrosis is a hereditary disease that mainly affects secretory organs in humans. It is
caused by mutations in the gene encoding CFTR with the most common phenylalanine …
caused by mutations in the gene encoding CFTR with the most common phenylalanine …
CFTR chloride channel activity modulates the mitochondrial morphology in cultured epithelial cells
R García, C Falduti, M Clauzure, R Jara… - … International Journal of …, 2021 - Elsevier
The impairment of the CFTR channel activity, a cAMP-activated chloride (Cl−) channel
responsible for cystic fibrosis (CF), has been associated with a variety of mitochondrial …
responsible for cystic fibrosis (CF), has been associated with a variety of mitochondrial …
Oxidative Stress in Antibiotic Toxic Optic Neuropathy Mimicking Acute LHON in a Patient with Exacerbation of Cystic Fibrosis
L Kovač, M Volk, M Šuštar Habjan, M Hawlina - Stresses, 2023 - mdpi.com
The striking similarity of disc edema without leakage on fluorescein angiography, which is
pathognomonic of Leber hereditary optic neuropathy (LHON), was present in a patient with …
pathognomonic of Leber hereditary optic neuropathy (LHON), was present in a patient with …