Epilepsy and brain abnormalities in mice lacking the Otx1 gene (Q34400653)

1 August 2017

title

Epilepsy and brain abnormalities in mice lacking the Otx1 gene (English)

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1 August 2017

F Tuorto

5

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Antonio Simeone

object named as

A Simeone

8

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author name string

D Acampora

1

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1 August 2017

S Mazan

2

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V Avantaggiato

3

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1 August 2017

P Barone

4

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1 August 2017

Y Lallemand

6

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P Brûlet

7

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1 August 2017

language of work or name

English

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publication date

1 October 1996

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1 August 2017

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1 August 2017

volume

14

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1 August 2017

issue

2

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1 August 2017

page(s)

218-222

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Nested expression domains of four homeobox genes in developing rostral brain

1 August 2017

cites work

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21 January 2018

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The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain

21 January 2018

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Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.

21 January 2018

1 reference

Developmental defects in brain segmentation caused by mutations of the homeobox genes orthodenticle and empty spiracles in Drosophila

21 January 2018

1 reference

21 January 2018

Targeting epilepsy genes

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Localization of a gene for partial epilepsy to chromosome 10q

21 January 2018

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Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2

21 January 2018

1 reference

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

21 January 2018

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Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development

21 January 2018

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The embryonic vertebrate forebrain: the prosomeric model.

21 January 2018

1 reference

7 January 2021

Expression patterns of the homeo box-containing genes En-1 and En-2 and the proto-oncogene int-1 diverge during mouse development.

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7 January 2021

Subtle Cerebellar Phenotype in Mice Homozygous for a Targeted Deletion of the En-2 Homeobox

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7 January 2021

Otx1 and Otx2 define layers and regions in developing cerebral cortex and cerebellum.

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7 January 2021

Neuropathological findings in primary generalized epilepsy: a study of eight cases

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7 January 2021

Abnormalities of gyration, heterotopias, tuberous sclerosis, focal cortical dysplasia, microdysgenesis, dysembryoplastic neuroepithelial tumour and dysgenesis of the archicortex in epilepsy. Clinical, EEG and neuroimaging features in 100 adult patie

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7 January 2021

Targeted replacement of the homeobox gene Hox-3.1 by the Escherichia coli lacZ in mouse chimeric embryos

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7 January 2021

Identifiers

DOI

10.1038/NG1096-218

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1 August 2017

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