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

Characterization of bovine TGM1 and exclusion as candidate gene for ichthyosis in Chianina.

The Journal of heredity - 1 Jan 2000

Dardano Sabrina, Gandolfi Barbara, Parma Pietro, Polli Michele, Bighignoli Barbara, Strillacci Maria G, Cozzi Maria C, Molteni Luciano, Longeri Maria

Abstract excerpt

Ichthyosis is a heterogeneous group of keratinization disorders reported both in human and animals. Two rare, inherited forms have been reported in cattle, both characterized by autosomal recessive transmission. Because mutations of transglutaminase 1 (TGM1) gene are associated with autosomal rec...

Read the complete abstract on PubMed

Topics

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

Share to Cattle
Share to Genetic Linkage
Share to Ichthyosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Polymorphism, Genetic

Share to Transglutaminases

Source

Identifiers

PMID: 18165261
DOI: 10.1093/jhered/esm101

Genes

TGM1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-18165261-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Characterization of bovine TGM1 and exclusion as candidate gene for ichthyosis in Chianina.PMID 18165261Read ↗

A frameshift insertion in FA2H causes a recessively inherited form of ichthyosis congenita in Chianina cattle.Semantic proximity Read ↗

High prevalence of autosomal recessive congenital ichthyosis in a Mexican population caused by a new mutation in the TGM1 gene: epidemiological evidence of a founder effect.Semantic proximity Read ↗

Novel transglutaminase 1 mutations in patients affected by lamellar ichthyosis.Semantic proximity Read ↗

Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosis.Semantic proximity Read ↗

Autosomal recessive lamellar ichthyosis: identification of a new mutation in transglutaminase 1 and evidence for genetic heterogeneity.Semantic proximity Read ↗

Identification and In Silico Analysis of a Homozygous Nonsense Variant in TGM1 Gene Segregating with Congenital Ichthyosis in a Consanguineous Family.Semantic proximity Read ↗

Sequencing of ABCA12 gene in severe congenital skin diseaseSemantic proximity Read ↗

Prenatal exclusion of lamellar ichthyosis based on identification of two new mutations in the transglutaminase 1 gene.Semantic proximity Read ↗

Ichthyosis in Chianina cattle.Semantic proximity Read ↗

Haplotype association and mutation analysis of the transglutaminase 1 gene for prenatal exclusion of lamellar ichthyosis.Semantic proximity Read ↗

Novel TGM1 Gene Mutation in a Japanese Patient with Bathing Suit Ichthyosis.Semantic proximity Read ↗

Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from Norway.Semantic proximity Read ↗

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