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Article

[The thyroid as a model for molecular mechanisms in genetic diseases].

Medicina - 1 Jan 2005

Rivolta Carina M, Moya Christian M, Esperante Sebastian A, Gutnisky Viviana J, Varela Viviana, Targovnik Hector M

Abstract excerpt

Thyroid diseases constitute a heterogeneous collection of abnormalities associated with mutations in genes responsible for the development of thyroid: thyroid transcription factor-1 (TTF-1), thyroid transcriptions factor-2 (TTF-2) and PAX8, or in one of the genes coding for the proteins involved in thyroid hormone biosynthesis such as thyroglobulin (TG), thyroperoxidase (TPO), hydrogen peroxide-generating system...

Read the complete abstract on PubMed

Topics

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Share to Congenital Hypothyroidism
Share to DUOX2 gene
Share to Goiter

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hyperthyroidism

Share to Iodide Peroxidase

Share to Mutation

Share to Receptors, Thyrotropin

Share to Thyroid Hormones

Source

Identifiers

PMID: 16042141

Genes

DUOX2
TPO
PAX8

Provenance

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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