Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Homology of pendrin, sodium-iodide symporter and apical iodide transporter.

Frontiers in bioscience (Landmark edition) - 1 Jun 2018

Benvenga Salvatore, Guarneri Fabrizio

Abstract excerpt

We observed local homology between human pendrin and sodium/iodide symporter (NIS), that was absent in the NIS-homologous sodium/monocarboxylate transporter or apical iodide transporter (AIT) which, however, does not transport iodide. Thus, we analyzed the full proteins. They shared 63 identical and 66 similar residues (overall homology 14.4%, but 21% when omitting intervening sequences of 15 or more residues)....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Goiter, Nodular
Share to Hearing Loss, Sensorineural
Share to Hypothyroidism

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Iodides

Share to Ion Transport

Share to Monocarboxylic Acid Transporters

Share to Sulfate Transporters

Share to Symporters

Source

Identifiers

PMID: 29772533
DOI: 10.2741/4677

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Homology of pendrin, sodium-iodide symporter and apical iodide transporter.PMID 29772533Read ↗

Clinical and molecular characteristics of Pendred syndrome.Semantic proximity Read ↗

Pendred syndrome.Semantic proximity Read ↗

Genetics and phenomics of Pendred syndrome.Semantic proximity Read ↗

Pendred syndrome.Semantic proximity Read ↗

[Pendrin: physiology, molecular biology and clinical importance].Semantic proximity Read ↗

The role of pendrin in iodide regulation.Semantic proximity Read ↗

Pendred's Syndrome: Identification of the Genetic Defect a Century After Its RecognitionSemantic proximity Read ↗

The Pendred syndrome gene encodes a chloride-iodide transport proteinSemantic proximity Read ↗

Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4).Semantic proximity Read ↗

Mutations in the Pendred Syndrome (PDS/SLC26A) Gene: An Increasingly Complex Phenotypic Spectrum From Goiter to Thyroid HypoplasiaSemantic proximity Read ↗

Iodide handling disorders (NIS, TPO, TG, IYD).Semantic proximity Read ↗

Analysis of cellular localization and function of carboxy-terminal mutants of pendrin.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.