(Q52171405)

26 April 2018

title

The disabled 1 gene is disrupted by a replacement with L1 fragment in yotari mice. (English)

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26 April 2018

author name string

Kojima T

series ordinal

1

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26 April 2018

Nakajima K

series ordinal

2

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26 April 2018

Mikoshiba K

series ordinal

3

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26 April 2018

publication date

1 January 2000

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26 April 2018

published in

Molecular Brain Research

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26 April 2018

volume

75

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26 April 2018

issue

1

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26 April 2018

page(s)

121-127

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26 April 2018

Regional and cellular patterns of reelin mRNA expression in the forebrain of the developing and adult mouse.

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

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Neocortical histogenesis in normal and reeler mice: a developmental study based upon [3H]thymidine autoradiography.

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7 January 2021

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

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7 January 2021

Rapid amplification of a retrotransposon subfamily is evolving the mouse genome

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7 January 2021

Target sites for the transposition of rat long interspersed repeated DNA elements (LINEs) are not random

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7 January 2021

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

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7 January 2021

A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion

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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

Neuronal position in the developing brain is regulated by mouse disabled-1

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7 January 2021

Reelin-induced tyrosine [corrected] phosphorylation of disabled 1 during neuronal positioning

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7 January 2021

Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man.

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7 January 2021

The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequences

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7 January 2021

Reverse transcription of R2Bm RNA is primed by a nick at the chromosomal target site: a mechanism for non-LTR retrotransposition

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7 January 2021

Anatomical, Physiological and biochemical studies of the cerebellum fromreelermutant mouse

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7 January 2021

Ataxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-trisphosphate receptor.

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7 January 2021

Morphological and Biochemical Studies on the Cerebral Cortex from Reeler Mutant Mice: Development of Cortical Layers and Metabolic Mapping by the Deoxyglucose Method

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7 January 2021

Developmental studies on the cerebellum from reeler mutant mouse in vivo and in vitro.

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7 January 2021

Distribution of a reeler gene-related antigen in the developing cerebellum: an immunohistochemical study with an allogeneic antibody CR-50 on normal and reeler mice.

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7 January 2021

High frequency retrotransposition in cultured mammalian cells

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7 January 2021

A catalogue of splice junction sequences

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7 January 2021

Disruption of hippocampal development in vivo by CR-50 mAb against reelin

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7 January 2021

Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy

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7 January 2021

The reeler gene-associated antigen on Cajal-Retzius neurons is a crucial molecule for laminar organization of cortical neurons.

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7 January 2021

Reelin mRNA expression during mouse brain development

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7 January 2021

Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice

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7 January 2021

The morphology of the hippocampus and dentate gyrus in normal and reeler mice

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7 January 2021

Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration

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7 January 2021

Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse

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7 January 2021

A novel neurological mutant mouse, yotari, which exhibits reeler-like phenotype but expresses CR-50 antigen/reelin

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7 January 2021

10.1016/S0169-328X(99)00313-7

Identifiers

DOI

1 reference

26 April 2018

1 reference

26 April 2018