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

Cerebellar vermis defect: a new neurological mutation in the rat.

The Journal of heredity - 1 Jan 2000

Kuwamura M, Yoshida T, Ishida A, Tsudzuki M, Yamate J, Kotani T, Sakuma S

Abstract excerpt

A new neurological rat mutation showing hind-leg paralysis, cerebellar vermis defect, and cerebellar cortical dysplasia was named "cerebellar vermis defect" (CVD). Pathologically, affected animals already had a small-sized cerebellum in newborns and started to show hind-leg paralysis at approximately 14 days of age. The CVD rat was fertile in both sexes. Genetic analysis indicated that the CVD character is...

Read the complete abstract on PubMed

Topics

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

Share to Cerebellum
Share to Crosses, Genetic
Share to Hindlimb

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

Share to Mutation

Share to Paralysis

Share to Rats, Inbred Lew

Source

Identifiers

PMID: 8830096
DOI: 10.1093/oxfordjournals.jhered.a022976

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

Cerebellar vermis defect: a new neurological mutation in the rat.PMID 8830096Read ↗

Rat neurological mutations cerebellar vermis defect and hobble are caused by mutations in the netrin-1 receptor gene Unc5h3.Semantic proximity Read ↗

Rat mutations cvd and hob with cerebellar malformations map to chromosome 2.Semantic proximity Read ↗

Rostral cerebellar malformation, (rcm): a new recessive mutation on chromosome 3 of the mouse.Semantic proximity Read ↗

Hyperspiny Purkinje cell, a new neurological mutation in the mouse.Semantic proximity Read ↗

Mutations in <i>VLDLR</i> as a Cause for Autosomal Recessive Cerebellar Ataxia With Mental Retardation (Dysequilibrium Syndrome)Semantic proximity Read ↗

Cerebellar vermis aplasia: patient report and exclusion of the candidate genes EN2 and ZIC1.Semantic proximity Read ↗

A new rat model of creatine transporter deficiency reveals behavioral disorder and altered brain metabolism.Semantic proximity Read ↗

Cerebellar vermis hypoplasia - non progressive congenital ataxia: clinical and radiological findings in a pair of siblings.Semantic proximity Read ↗

Congenital quiver, an inherited neurological defect in the chicken.Semantic proximity Read ↗

Phenotypic characterization of spontaneously mutated rats showing lethal dwarfism and epilepsy.Semantic proximity Read ↗

A new neurological mutant rat with symmetrical calcification of Purkinje cells in cerebellum.Semantic proximity Read ↗

Cell death and neurodegeneration in the postnatal development of cerebellar vermis in normal and Reeler miceSemantic proximity Read ↗

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