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

Canine TCOF1; cloning, chromosome assignment and genetic analysis in dogs with different head types.

Mammalian genome : official journal of the International Mammalian Genome Society - 1 Aug 2001

Haworth K E, Islam I, Breen M, Putt W, Makrinou E, Binns M, Hopkinson D, Edwards Y

Abstract excerpt

We describe the construction of a dog embryonic head/neck cDNA library and the isolation of the dog homolog of the Treacher Collins Syndrome gene, TCOF1. The protein shows a similar three-domain structure to that described for human TCOF1, but the dog gene lacks exon 10 and contains two exons not present in the human sequence. In addition, exon 19 is differentially spliced in the dog. How these structural...

Read the complete abstract on PubMed

Topics

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

Share to Animals, Domestic
Share to Breeding

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes

Share to DNA, Complementary

Share to Gene Library

Share to In Situ Hybridization, Fluorescence

Share to Phosphoproteins

Source

Identifiers

PMID: 11471057
DOI: 10.1007/s00335-001-3011-0

Genes

TCOF1

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Canine TCOF1; cloning, chromosome assignment and genetic analysis in dogs with different head types.PMID 11471057Read ↗

TCOF1 T/Ser variant and brachycephaly in dogs.Semantic proximity Read ↗

Gross deletions in TCOF1 are a cause of Treacher–Collins–Franceschetti syndromeSemantic proximity Read ↗

A Novel Missense Variant in the TCOF1 Gene in one Chinese Case With Treacher Collins Syndrome.Semantic proximity Read ↗

TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region.Semantic proximity Read ↗

Fishing the molecular bases of Treacher Collins syndrome.Semantic proximity Read ↗

A De Novo Mutation Destroys the Central Repeated Domain of TCOF1 in a Chinese Family with Treacher Collins SyndromeSemantic proximity Read ↗

Novel mutations of TCOF1 gene in European patients with Treacher Collins syndrome.Semantic proximity Read ↗

Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients.Semantic proximity Read ↗

Tcof1-Related Molecular Networks in Treacher Collins Syndrome.Semantic proximity Read ↗

Identification of mutations in TCOF1: use of molecular analysis in the pre- and postnatal diagnosis of Treacher Collins syndrome.Semantic proximity Read ↗

Mutational Analysis of TCOF1, GSC, and HOXA2 in Patients With Treacher Collins Syndrome.Semantic proximity Read ↗

Mutational analysis of the TCOF1 gene in 11 Japanese patients with Treacher Collins Syndrome and mechanism of mutagenesis.Semantic proximity Read ↗

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