Motor disturbances in mice with deficiency of the sodium channel gene Scn8a show features of human dystonia (Q44760138)

6 December 2017

Motor disturbances in mice with deficiency of the sodium channel gene Scn8a show features of human dystonia (English)

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6 December 2017

Melanie Hamann

1

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6 December 2017

Miriam H Meisler

series ordinal

2

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6 December 2017

Angelika Richter

series ordinal

3

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6 December 2017

language of work or name

English

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publication date

1 December 2003

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6 December 2017

Experimental Neurology

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6 December 2017

184

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6 December 2017

2

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6 December 2017

830-838

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Dopamine transmission in DYT1 dystonia: a biochemical and autoradiographical study

6 December 2017

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https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Sodium channel Na(v)1.6 is localized at nodes of ranvier, dendrites, and synapses

7 January 2021

1 reference

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Paroxysmal dyskinesias: clinical features and classification

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Hereditary motor end-plate disease in the mouse: light and electron microscopic studies

7 January 2021

1 reference

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The sodium channel Scn8a is the major contributor to the postnatal developmental increase of sodium current density in spinal motoneurons.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Differences in anxiety-related behaviours and in sensitivity to diazepam in inbred and outbred strains of mice.

7 January 2021

1 reference

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Paroxysmal kinesigenic choreoathetosis: a report of 26 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Na(v)1.6).

7 January 2021

1 reference

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Voltage-gated sodium channels in epilepsy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Mutation detection in the med and medJ alleles of the sodium channel Scn8a. Unusual splicing due to a minor class AT-AC intron.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Atypical presentation of dopa-responsive dystonia: generalized hypotonia and proximal weakness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

The neuronal channelopathies

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

D1/D5 dopamine receptor activation differentially modulates rapidly inactivating and persistent sodium currents in prefrontal cortex pyramidal neurons.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Sodium channels and neurological disease: insights from Scn8a mutations in the mouse

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Identification of epilepsy genes in human and mouse

7 January 2021

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Immunocytochemical characterization of catecholaminergic neurons in the rat striatum following dopamine-depleting lesions

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Tyrosine hydroxylase immunoreactivity and [3H]WIN 35,428 binding to the dopamine transporter in a hamster model of idiopathic paroxysmal dystonia.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Corneal kindling in mice: behavioral and pharmacological differences to conventional kindling.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Channelopathies: ion channel disorders of muscle as a paradigm for paroxysmal disorders of the nervous system

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Altered subthreshold sodium currents and disrupted firing patterns in Purkinje neurons of Scn8a mutant mice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Pathology of idiopathic dystonia: findings from genetic animal models

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

The novel antiepileptic drug, lamotrigine, exerts prodystonic effects in a mutant hamster model of generalized dystonia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Prodystonic effects of riluzole in an animal model of idiopathic dystonia related to decreased total power in the red nucleus?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Classification and definition of disorders causing hypertonia in childhood

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

A novel, abundant sodium channel expressed in neurons and glia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Actions of adenosine A2A receptor antagonist KW-6002 on drug-induced catalepsy and hypokinesia caused by reserpine or MPTP

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Inherited muscle and nerve diseases in mice: a tabulation with commentary

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Sodium currents in striatal neurons from dystonic dt(sz) hamsters: altered response to lamotrigine

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Research opportunities in dystonia: National Institute of Neurological Disorders and Stroke workshop summary.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Mutational and biochemical analysis of dopamine in dystonia: evidence for decreased dopamine D2 receptor inhibition

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

Stereological methods for estimating the total number of neurons and synapses: issues of precision and bias

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-4886%2803%2900290-5

10.1016/S0014-4886(03)00290-5

7 January 2021

Identifiers

DOI

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6 December 2017

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