(Q48071134)

8 February 2018

title

Epileptic seizures caused by inactivation of a novel gene, jerky, related to centromere binding protein-B in transgenic mice (English)

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8 February 2018

author name string

Toth M

1

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8 February 2018

Grimsby J

2

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8 February 2018

Buzsaki G

3

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8 February 2018

Donovan GP

4

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8 February 2018

language of work or name

English

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publication date

1 September 1995

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8 February 2018

published in

Nature Genetics

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8 February 2018

volume

11

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8 February 2018

issue

1

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8 February 2018

page(s)

71-75

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8 February 2018

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

cites work

1 reference

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

21 January 2018

1 reference

Localization of a gene for partial epilepsy to chromosome 10q

21 January 2018

1 reference

Eating disorder and epilepsy in mice lacking 5-HT2c serotonin receptors

21 January 2018

1 reference

Modification of seizure activity by electrical stimulation. II. Motor seizure

21 January 2018

1 reference

Basic local alignment search tool

21 January 2018

1 reference

Molecular cloning of cDNA for CENP-B, the major human centromere autoantigen

21 January 2018

1 reference

A human centromere protein, CENP-B, has a DNA binding domain containing four potential alpha helices at the NH2 terminus, which is separable from dimerizing activity

21 January 2018

1 reference

Stargazer: a new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures.

21 January 2018

1 reference

Conversion of the lac repressor into an allosterically regulated transcriptional activator for mammalian cells

21 January 2018

1 reference

A nonsense mutation in the alpha4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI)

21 January 2018

1 reference

7 January 2021

Linkage studies in progressive myoclonus epilepsy: Unverricht-Lundborg and Lafora's diseases

1 reference

7 January 2021

The chromosome 6p epilepsy locus: exploring mode of inheritance and heterogeneity through linkage analysis

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7 January 2021

Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6.

1 reference

7 January 2021

Ceruloplasmin gene defect associated with epilepsy in EL mice

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7 January 2021

Differentiation is induced in three-dimensional cultures of brain cells immortalized by the LAP mammalian regulatory system

1 reference

7 January 2021

Maps from two interspecific backcross DNA panels available as a community genetic mapping resource

1 reference

7 January 2021

Localization of thyrotropin-releasing hormone receptor and thyrotroph embryonic factor on mouse Chromosome 15

1 reference

7 January 2021

The pogo transposable element family of Drosophila melanogaster

1 reference

7 January 2021

Characterisation of PDC2, a gene necessary for high level expression of pyruvate decarboxylase structural genes in Saccharomyces cerevisiae

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7 January 2021

A single gene error of noradrenergic axon growth synchronizes central neurones

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7 January 2021

Cellular and molecular basis of epilepsy.

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7 January 2021

Identifiers

DOI

10.1038/NG0995-71

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8 February 2018

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8 February 2018