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

Genetic studies on human thyroxine-binding globulin (TBG).

Human genetics - 1 Mar 1990

Luckenbach C, Kömpf J, Ritter H

Abstract excerpt

An enzyme immunoassay technique combined with Western blotting is described to demonstrate thyroxine-binding globulin (TBG) by isoelectric focusing in thin-layer polyacrylamide gels with 8 mol/l urea. Quantitative evaluation was by laser densitometry. No genetic charge variants of TBG were encoun...

Topics

Electrophoresis, Polyacrylamide Gel
Female
Humans
Isoelectric Focusing
Male
Pedigree
Phenotype
Thyroxine-Binding Proteins

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 2106478
DOI: 10.1007/BF00196237

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-2106478-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 9 closest

Genetic studies on human thyroxine-binding globulin (TBG).PMID 2106478Read ↗

Thyroxine-binding globulin: organization of the gene and variants.Semantic proximity Read ↗

Partial deficiency of thyroxine-binding globulin-Allentown is due to a mutation in the signal peptide.Semantic proximity Read ↗

An additional carbohydrate chain in the variant thyroxine-binding globulin-Gary (TBGAsn-96) impairs its secretion.Semantic proximity Read ↗

Complete thyroxine-binding globulin (TBG) deficiency caused by a single nucleotide deletion in the TBG gene.Semantic proximity Read ↗

Complete thyroxine-binding globulin (TBG) deficiency in two families without mutations in coding or promoter regions of the TBG genes: in vitro demonstration of exon skipping.Semantic proximity Read ↗

Molecular analysis of the human vitamin D binding protein (group specific component, Gc) in tuberous sclerosis complex (TSC).Semantic proximity Read ↗

Two novel variants in the thyroxine-binding globulin (TBG) gene behind the diagnosis of TBG deficiency.Semantic proximity Read ↗

Characterization of the thyroxine-binding site of thyroxine-binding globulin by site-directed mutagenesis.Semantic proximity Read ↗

Thyroxine-binding globulin variant (TBG-Kumamoto): identification of a point mutation and genotype analysis of its family.Semantic proximity Read ↗

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