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Article

A rapid membrane potential assay to monitor CFTR function and inhibition.

Journal of biomolecular screening - 1 Oct 2013

Maitra Rangan, Sivashanmugam Perumal, Warner Keith

Abstract excerpt

The cystic fibrosis transmembrane conductance regulator (CFTR) protein is an important regulator of ion transport and fluid secretion in humans. Mutations to CFTR cause cystic fibrosis, which is a common recessive genetic disorder in Caucasians. Involvement of CFTR has been noted in other importa...

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Source

Identifiers

PMID: 23653393
DOI: 10.1177/1087057113488420

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23653393-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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