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

Up to date with human thyroglobulin

1 Aug 2001

Abstract excerpt

The coding region of the human thyroglobulin (TG) mRNA has been resequenced, and comparison with the TG sequence originally published in 1987 showed many variations. All of the variations were validated in 20--40 other alleles, and this resulted in the revision of 41 nucleotide positions. This review presents the revised wild-type human TG sequence, including all known exon/exon boundaries and additional data on...

Read the complete abstract on PubMed

Topics

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

Share to RNA and protein synthesis mechanisms
Share to Thyroid Cancer Diagnosis and Treatment
Share to Thyroid Disorders and Treatments

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

Source

Identifiers

PMID: 11479128
DOI: 10.1677/joe.0.1700307

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Up to date with human thyroglobulinPMID 11479128Read ↗

The revised 8307 base pair coding sequence of human thyroglobulin transiently expressed in eukaryotic cells.Semantic proximity Read ↗

Molecular advances in thyroglobulin disorders.Semantic proximity Read ↗

Structure and genetic variants of thyroglobulin: Pathophysiological implications.Semantic proximity Read ↗

A novel mutation in intron 11 donor splice site, responsible of a rare genotype in thyroglobulin gene by altering the pre-mRNA splincing process. Cell expression and bioinformatic analysis.Semantic proximity Read ↗

Clinical, Biochemical, and Molecular Genetic Characterization of Two Patients with Congenital Hypothyroidism Harboring Novel Compound Heterozygous Variants in the Thyroglobulin GeneSemantic proximity Read ↗

Naturally occurring mutations in the thyroglobulin gene.Semantic proximity Read ↗

Thyroglobulin gene mutations in congenital hypothyroidism.Semantic proximity Read ↗

Genetics and phenomics of hypothyroidism and goiter due to thyroglobulin mutations.Semantic proximity Read ↗

[Thyroglobulin gene abnormalities].Semantic proximity Read ↗

[Thyroglobulin gene abnormalities].Semantic proximity Read ↗

Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism.Semantic proximity Read ↗

Thyroglobulin From Molecular and Cellular Biology to Clinical Endocrinology.Semantic proximity Read ↗

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