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Article

Cystic fibrosis transmembrane conductance regulator expression in human spinal and sympathetic ganglia.

Laboratory investigation; a journal of technical methods and pathology - 1 Jun 2009

Niu Na, Zhang Jie, Guo Yong, Yang Chunzhang, Gu Jiang

Abstract excerpt

Cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel protein, and mutations of its gene cause cystic fibrosis. CFTR is known to be expressed in epithelial cells of the respiratory, digestive and reproductive tracts. It is also present in rat neurons and heart ganglion cells. In humans, it is expressed in the hypothalamus, but has not been identified in other parts of the human nervous...

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Identifiers

PMID: 19333236
DOI: 10.1038/labinvest.2009.28

Genes

CFTR

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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