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

Detection of the reelin breakpoint in reeler mice.

Brain research. Molecular brain research - 1 Jul 1996

D'Arcangelo G, Miao G G, Curran T

Abstract excerpt

Disruption of the reelin gene by partial deletion causes the neurological phenotype known as reeler. Here we report the cloning and sequencing of the reelin breakpoint region from the Jackson reeler strain (rl). Based on this sequence, we developed a polymerase chain reaction screen that allows the identification of mutant mice prior to the appearance of the phenotype. The assay also permits discrimination of...

Read the complete abstract on PubMed

Topics

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

Share to DNA, Complementary
Share to Mice
Share to Mice, Inbred Strains

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

Share to Base Sequence

Share to Mice, Neurologic Mutants

Share to Molecular Sequence Data

Share to Mutation

Source

Identifiers

PMID: 8804731
DOI: 10.1016/0169-328x(96)00046-0

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

Detection of the reelin breakpoint in reeler mice.PMID 8804731Read ↗

A reeler mutant mouse with a new, spontaneous mutation in the reelin gene.Semantic proximity Read ↗

High-resolution genetic map and YAC contig around the mouse neurological locus reeler.Semantic proximity Read ↗

Isolation of an allele of reeler by insertional mutagenesis.Semantic proximity Read ↗

A protein related to extracellular matrix proteins deleted in the mouse mutant reeler.Semantic proximity Read ↗

A truncated Reelin protein is produced but not secreted in the 'Orleans' reeler mutation (Reln[rl-Orl]).Semantic proximity Read ↗

The phenotypic characteristics of heterozygous reeler mouse.Semantic proximity Read ↗

Rat neurological disease creeping is caused by a mutation in the reelin gene.Semantic proximity Read ↗

Expression of reelin, the gene responsible for the reeler mutation, in embryonic development and adulthood in the mouse.Semantic proximity Read ↗

The <em>Reeler</em> Mouse: A Translational Model of Human Neurological Conditions or Simply a Good Tool for Better Understanding Neurodevelopment?Semantic proximity Read ↗

Birthdate and cell marker analysis of scrambler: a novel mutation affecting cortical development with a reeler-like phenotype.Semantic proximity Read ↗

Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of reelin.Semantic proximity Read ↗

Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice.Semantic proximity Read ↗

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