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

Jimpy(msd) mouse mutation and connatal Pelizaeus-Merzbacher disease.

American journal of medical genetics - 3 Feb 1998

Yamamoto T, Nanba E, Zhang H, Sasaki M, Komaki H, Takeshita K

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Central Nervous System Diseases
Share to Demyelinating Diseases
Share to Diffuse Cerebral Sclerosis of Schilder
Share to Disease Models, Animal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Infant

Share to Myelin Proteolipid Protein

Source

Identifiers

PMID: 9482656

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

Jimpy(msd) mouse mutation and connatal Pelizaeus-Merzbacher disease.PMID 9482656Read ↗

Genetic diseases and gene knockouts reveal diverse connexin functions.Semantic proximity Read ↗

Pathologic and Phenotypic Alterations in a Mouse Expressing a Connexin47 Missense Mutation That Causes Pelizaeus-Merzbacher–Like Disease in HumansSemantic proximity Read ↗

Jimpy-4J mouse has a missense mutation in exon 2 of the Plp gene.Semantic proximity Read ↗

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

A severe connatal form of Pelizaeus Merzbacher disease in a Czech boy caused by a novel mutation (725C>A, Ala242Glu) at the 'jimpy(msd) codon' in the PLP gene.Semantic proximity Read ↗

Connexin-caused genetic diseases and corresponding mouse models.Semantic proximity Read ↗

What has the mdx mouse model of duchenne muscular dystrophy contributed to our understanding of this disease?Semantic proximity Read ↗

Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans.Semantic proximity Read ↗

The neurological mouse mutations jittery and hesitant are allelic and map to the region of mouse chromosome 10 homologous to 19p13.3.Semantic proximity Read ↗

Gene disruption of Mfsd8 in mice provides the first animal model for CLN7 diseaseSemantic proximity Read ↗

Uncoupling of hypomyelination and glial cell death by a mutation in the proteolipid protein gene.Semantic proximity Read ↗

The Moonwalker mouse: new insights into TRPC3 function, cerebellar development, and ataxia.Semantic proximity Read ↗

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