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

Mouse homologues of human hereditary disease.

Journal of medical genetics - 1 Jan 1994

Searle A G, Edwards J H, Hall J G

Abstract excerpt

Details are given of 214 loci known to be associated with human hereditary disease, which have been mapped on both human and mouse chromosomes. Forty two of these have pathological variants in both species; in general the mouse variants are similar in their effects to the corresponding human ones...

Topics

Animals
Chromosome Mapping
Genetic Diseases, Inborn
Genetic Variation
Humans
Mice
Proto-Oncogene Mas
Proto-Oncogenes
Species Specificity

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8151633
DOI: 10.1136/jmg.31.1.1
PMCID: PMC1049593

Genes

DMD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8151633-2026-08-30.1. 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 · 12 closest

Mouse homologues of human hereditary disease.PMID 8151633Read ↗

Mouse models of human familial cancer syndromes.Semantic proximity Read ↗

ENU mutagenesis in the mouse: application to human genetic disease.Semantic proximity Read ↗

Mouse mutations and human disorders are paired.Semantic proximity Read ↗

Mutagenesis strategies for identifying novel loci associated with disease phenotypes.Semantic proximity Read ↗

Mouse models of human single gene disorders. I: Nontransgenic mice.Semantic proximity Read ↗

The dysmorphic human-mouse homology database (DHMHD): an interactive World-Wide Web resource for gene mapping.Semantic proximity Read ↗

A phenotype map of the mouse X chromosome: models for human X-linked disease.Semantic proximity Read ↗

Large-scale production of mouse phenotypes: the search for animal models for inherited diseases in humans.Semantic proximity Read ↗

[Characterization of ENU-mutant mice. Animal models for human diseases using morphological and molecular methods].Semantic proximity Read ↗

Modelling human regulatory variation in mouse: finding the function in genome-wide association studies and whole-genome sequencing.Semantic proximity Read ↗

Hypomorphic mutation of the mouse Huntington’s disease gene orthologueSemantic proximity Read ↗

Mouse model for somatic mutation at the HPRT gene: molecular and cellular analyses.Semantic proximity Read ↗

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