Rat neurological disease creeping is caused by a mutation in the reelin gene (Q28569118)

31 January 2017

title

Rat neurological disease creeping is caused by a mutation in the reelin gene (English)

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31 January 2017

Norihide Yokoi

1

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31 January 2017

Misako Namae

2

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31 January 2017

He-Yao Wang

3

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31 January 2017

Ken Kojima

4

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31 January 2017

Masanori Fuse

5

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31 January 2017

Kazuki Yasuda

6

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31 January 2017

Tadao Serikawa

7

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31 January 2017

Susumu Seino

8

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31 January 2017

Kajuro Komeda

9

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31 January 2017

publication date

10 April 2003

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31 January 2017

published in

Molecular Brain Research

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31 January 2017

volume

112

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31 January 2017

issue

1-2

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31 January 2017

page(s)

1–7

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Shaking rat Kawasaki (SRK): a new neurological mutant rat in the Wistar strain

31 January 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

A YAC contig containing the reeler locus with preliminary characterization of candidate gene fragments

1 reference

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7 January 2021

Mechanisms of Cortical Development: A View From Mutations in Mice

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7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Reelin is a ligand for lipoprotein receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Reelin is a secreted glycoprotein recognized by the CR-50 monoclonal antibody.

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

The human reelin gene: isolation, sequencing, and mapping on chromosome 7.

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Two new mutants, ‘trembler’ and ‘reeler’, with neurological actions in the house mouse (Mus musculus L.)

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Chlorambucil-induced mutations in mice recovered in homozygotes

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Events governing organization of postmigratory neurons: studies on brain development in normal and reeler mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Gender effect on Purkinje cell loss in the cerebellum of the heterozygous reeler mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Direct binding of Reelin to VLDL receptor and ApoE receptor 2 induces tyrosine phosphorylation of disabled-1 and modulates tau phosphorylation

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

The reeler gene encodes a protein with an EGF-like motif expressed by pioneer neurons

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

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7 January 2021

Mouse disabled (mDab1): a Src binding protein implicated in neuronal development

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7 January 2021

High-resolution genetic map and YAC contig around the mouse neurological locus reeler.

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7 January 2021

Mutant mice with scrambled brains: understanding the signaling pathways that control cell positioning in the CNS.

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7 January 2021

Genomic organization of the mouse reelin gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Reln(rl-Alb2), an allele of reeler isolated from a chlorambucil screen, is due to an IAP insertion with exon skipping

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Proteins of the CNR family are multiple receptors for Reelin

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Expression of reelin in adult mammalian blood, liver, pituitary pars intermedia, and adrenal chromaffin cells

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Dysfunction of the Orleans reeler gene arising from exon skipping due to transposition of a full-length copy of an active L1 sequence into the skipped exon

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

The phenotypic characteristics of heterozygous reeler mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

Genetic mapping of the rat mutation creeping and evaluation of its positional candidate gene reelin

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2802%2900650-2

7 January 2021

10.1016/S0169-328X(02)00650-2

Identifiers

DOI

0 references

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