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

Hypomyelinated pt mutant rabbit as a new model of Pelizeaus-Merzbacher disease.

Neurologia i neurochirurgia polska - 1 Jan 1996

Sypecka J, Domańska-Janik 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 Demyelinating Diseases
Share to Diffuse Cerebral Sclerosis of Schilder
Share to Disease Models, Animal
Share to Exons

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Phenotype

Share to Point Mutation

Share to Rabbits

Share to X Chromosome

Source

Identifiers

PMID: 9100242

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hypomyelinated pt mutant rabbit as a new model of Pelizeaus-Merzbacher disease.PMID 9100242Read ↗

Rabbit paralytic tremor phenotype--a plp1 gene mutation as a model of human Pelizaeus-Merzbacher disease.Semantic proximity Read ↗

Myelin proteolipid protein mutation in the rabbit: a new model of Pelizaeus-Merzbacher disease.Semantic proximity Read ↗

Phenotypic diversity resulting from a point mutation.Semantic proximity Read ↗

Paralytic tremor (pt): a new allele of the proteolipid protein gene in rabbits.Semantic proximity Read ↗

Developmental expression of major myelin proteins in hypomyelinated pt mutant rabbit.Semantic proximity Read ↗

[I. Prolegomena to experimental studies on hereditary disease of the nervous system on a "pt" rabbit model].Semantic proximity Read ↗

pt point mutation in plp gene results in hyperexpression of MOG in hypomyelinated rabbit.Semantic proximity Read ↗

Dysmyelination in mice and the proteolipid protein gene family.Semantic proximity Read ↗

Proteolipid/DM-20 proteins bearing the paralytic tremor mutation in peripheral nerves and transfected Cos-7 cells.Semantic proximity Read ↗

Degree of Hypomyelination and Magnetic Resonance Spectroscopy Findings in Patients with Pelizaeus Merzbacher PhenotypeSemantic proximity Read ↗

Expression of myelin-specific proteins during development of normal and hypomyelinated Paralytic tremor mutant rabbits. II. Studies on the purified myelin.Semantic proximity Read ↗

Paralytic tremor (pt) rabbit: a sex-linked mutation affecting proteolipid protein-gene expression.Semantic proximity Read ↗

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