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

Of hairless mice and men: the genetic basis of congenital alopecia universalis/congenital atrichia.

Journal of cutaneous medicine and surgery - 1 Oct 1999

Bale S J

Abstract excerpt

BACKGROUND: Mouse models of human diseases help identify gene defects. OBJECTIVE: The methods of homozygosity mapping and mouse/human homology to identify genes are reviewed. The genotype/phenotype correlation in two clinical entities with mutations in the human hairless gene are discussed. METHODS: The example of the hairless mouse's contribution to our knowledge of hereditary alopecia is used, and the utility...

Read the complete abstract on PubMed

Topics

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

Share to Alopecia
Share to Chromosome Mapping
Share to Consanguinity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Disease Models, Animal

Share to Genotype

Share to Homozygote

Share to Mice, Hairless

Source

Identifiers

PMID: 10575161
DOI: 10.1177/120347549900300607

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Of hairless mice and men: the genetic basis of congenital alopecia universalis/congenital atrichia.PMID 10575161Read ↗

Mouse models for human hair loss disordersSemantic proximity Read ↗

[Mutation of the human hairless gene in atrichia universalis].Semantic proximity Read ↗

Inherited mouse mutations: models for the study of alopecia.Semantic proximity Read ↗

Molecular basis of congenital atrichia in humans and mice.Semantic proximity Read ↗

Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: an update.Semantic proximity Read ↗

Alopecia areata: updates from the mouse perspective.Semantic proximity Read ↗

Alopecia universalis associated with a mutation in the human hairless gene.Semantic proximity Read ↗

The molecular basis of congenital atrichia in humans and mice: mutations in the hairless gene.Semantic proximity Read ↗

Molecular and functional aspects of the hairless (hr) gene in laboratory rodents and humans.Semantic proximity Read ↗

A novel nonsense mutation and polymorphisms in the mouse hairless gene.Semantic proximity Read ↗

Inherited disorders of the skin in human and mouse: from development to differentiation.Semantic proximity Read ↗

Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice.Semantic proximity Read ↗

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