(Q28141045)

GOA release 2020-03-11

author name string

Y T Kwon

1

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A Gupta

2

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Y Zhou

3

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M Nikolic

4

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L H Tsai

Genetic malformations of the human cerebral cortex

5

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language of work or name

English

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publication date

6 April 2000

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published in

Current Biology

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volume

10

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page(s)

363-72

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issue

7

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cites work

1 reference

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

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

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

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

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

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

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Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death

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Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality

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The cdk5/p35 kinase is essential for neurite outgrowth during neuronal differentiation

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Neuronal cdc2-like kinase

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Neurite outgrowth in response to transfected N-CAM and N-cadherin reveals fundamental differences in neuronal responsiveness to CAMs

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A role for the cadherin family of cell adhesion molecules in hippocampal long-term potentiation

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Biochemical and cellular effects of roscovitine, a potent and selective inhibitor of the cyclin-dependent kinases cdc2, cdk2 and cdk5.

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Cadherin-mediated cell-cell adhesion is perturbed by v-src tyrosine phosphorylation in metastatic fibroblasts

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7 January 2021

Proteins of the CNR family are multiple receptors for Reelin

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Distinct functions of alpha3 and alpha(v) integrin receptors in neuronal migration and laminar organization of the cerebral cortex.

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7 January 2021

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