Advances in anion transport by synthetic supramolecular systems are discussed in this
article. Developments in the design of discrete molecular carriers for anions and …

Anionic species are omnipresent and involved in many important biological processes. A
large number of artificial anion receptors has therefore been developed. Some of these are …

Lipid bilayer membranes form compartments requisite for life. Interfacing supramolecular
systems, including receptors, catalysts, signal transducers and ion transporters, enables the …

Defective anion transport is a hallmark of the genetic disease cystic fibrosis (CF). One
approach to restore anion transport to CF cells utilises alternative pathways for …

Motivated by their potential biological applications, anion receptors are increasingly
explored as transmembrane transporters for anions. The vast majority of the reported anion …

The cystic fibrosis (CF) lung disease is due to the lack/dysfunction of the CF Transmembrane
Conductance Regulator (CFTR), a chloride channel expressed by epithelial cells as the …

Cystic fibrosis (CF) is a life-shortening monogenic disease caused by mutations in the gene
encoding the CF transmembrane conductance regulator (CFTR) protein, an anion channel …

Several life‐threatening diseases, also known as 'Channelopathies' are linked to
irregularities in ion transport proteins. Significant research efforts have fostered the …

Cystic fibrosis is a hereditary disease that originates from mutations in the epithelial chloride
channel CFTR. Whereas established therapies for the treatment of cystic fibrosis target …

Malassezia is a lipophilic unicellular fungus that is able, under specific conditions, to cause
severe cutaneous and systemic diseases in predisposed subjects. This review is divided …