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

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

Brain research - 22 Oct 1993

Tosic M, Dolivo M, Amiguet P, Domanska-Janik K, Matthieu J M

Abstract excerpt

Paralytic tremor (pt) is a neurological sex-linked recessive mutation in rabbits which is characterized by a coarse body tremor and limb paresis. Morphological studies showed that this mutation affects CNS myelination. Although the number of oligodendrocytes is not reduced, myelination is slower, irregular and defective. We have made a biochemical and molecular analysis of 4-wk-old mutant and normal rabbits. The...

Read the complete abstract on PubMed

Topics

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

Share to Gene Expression
Share to Genetic Linkage
Share to Mutation

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

Share to Myelin Proteins

Share to Rabbits

Share to RNA, Messenger

Share to Tremor

Share to X Chromosome

Source

Identifiers

PMID: 8275312
DOI: 10.1016/0006-8993(93)91073-2

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

Paralytic tremor (pt) rabbit: a sex-linked mutation affecting proteolipid protein-gene expression.PMID 8275312Read ↗

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

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

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

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

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

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

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

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

Calcium-activated neutral protease (CANP) in normal and dysmyelinating mutant paralytic tremor rabbit myelin.Semantic proximity Read ↗

Intracellular transport of the DM-20 bearing shaking pup (shp) mutation and its possible phenotypic consequences.Semantic proximity Read ↗

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

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