(Q33748748)

29 July 2017

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title

Detecting genes in new and old mouse models for epilepsy: a prospectus through the magnifying glass (English)

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29 July 2017

Frankel WN

1

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29 July 2017

1 September 1999

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29 July 2017

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29 July 2017

36

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29 July 2017

2-3

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29 July 2017

97-110

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Ca2+-dependent regulation in neuronal gene expression

29 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Mouse models of genetic disease: new approaches, new paradigms.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Cerebellar circuitry is activated during convulsive episodes in the tottering (tg/tg) mutant mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Secretory phospholipase Pla2g2a confers resistance to intestinal tumorigenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Cloning, mRNA expression, and chromosomal mapping of mouse and human preprocortistatin

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

1 reference

7 January 2021

Mapping murine loci for seizure response to kainic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Enhanced aspartate release related to epilepsy in (EL) mice

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Enhanced aspartate release from hippocampal slices of epileptic (El) mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Absence epilepsy in tottering mutant mice is associated with calcium channel defects

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Taking stock of complex trait genetics in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Congenic strains reveal effects of the epilepsy quantitative trait locus, El2, separate from other El loci

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

New seizure frequency QTL and the complex genetics of epilepsy in EL mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Purkinje cell loss from alternating sagittal zones in the cerebellum of leaner mutant mice

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Anticonvulsant sensitivity of absence seizures in the tottering mutant mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Cerebellar cell degeneration in the leaner mutant mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Positional cloning of the mouse circadian clock gene

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Genetic and physical maps of the stargazer locus on mouse chromosome 15

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Genetics of spike-wave discharges in the electroencephalogram (EEG) of the WAG/Rij inbred rat strain: a classical mendelian crossbreeding study

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Molecular characterization of a neuronal low-voltage-activated T-type calcium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Cerebellar brain-derived neurotrophic factor-TrkB defect associated with impairment of eyeblink conditioning in Stargazer mutant mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Developmental analysis of hippocampal mossy fiber outgrowth in a mutant mouse with inherited spike-wave seizures.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Chemical mutagenesis and fine-structure functional analysis of the mouse genome

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Genes for epilepsy mapped in the mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Functional genomics in the mouse: phenotype-based mutagenesis screens

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Genetic heterogeneity for the development of audiogenic seizures in mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

Mice lacking tissue non-specific alkaline phosphatase die from seizures due to defective metabolism of vitamin B-6.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900044-3

7 January 2021

10.1016/S0920-1211(99)00044-3

Identifiers

DOI

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29 July 2017

1 reference

PubMed ID

10515158