Distinct phenotypes in zebrafish models of human startle disease. - Wikidata - awgldk - TriplyDB

Distinct phenotypes in zebrafish models of human startle disease.

Distinct phenotypes in zebrafish models of human startle disease.

http://www.wikidata.org/entity/Q37679180

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Defects of the Glycinergic Synapse in Zebrafish.The impact of human hyperekplexia mutations on glycine receptor structure and function Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis.An E3-ligase-based method for ablating inhibitory synapses Structure/Function Studies of the α4 Subunit Reveal Evolutionary Loss of a GlyR Subtype Involved in Startle and Escape Responses.Spatial patterning of excitatory and inhibitory neuropil territories during spinal circuit development.Functional Consequences of the Postnatal Switch From Neonatal to Mutant Adult Glycine Receptor α1 Subunits in the Shaky Mouse Model of Startle Disease.Characterization of the Zebrafish Glycine Receptor Family Reveals Insights Into Glycine Receptor Structure Function and Stoichiometry

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Distinct phenotypes in zebrafish models of human startle disease.

http://www.wikidata.org/entity/Q37679180

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 09 September 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Distinct phenotypes in zebrafish models of human startle disease.

@en

Distinct phenotypes in zebrafish models of human startle disease.

@nl

type

label

Distinct phenotypes in zebrafish models of human startle disease.

@en

Distinct phenotypes in zebrafish models of human startle disease.

@nl

prefLabel

Distinct phenotypes in zebrafish models of human startle disease.

@en

Distinct phenotypes in zebrafish models of human startle disease.

@nl

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J.NBD.2013.09.002

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Neurobiology of Disease

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Distinct phenotypes in zebrafish models of human startle disease.

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Julia E Dallman

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Lisa R Ganser

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Qing Yan

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Robert Kozol

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P2860

Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB)

A missense mutation in the gene encoding the alpha 1 subunit of the inhibitory glycine receptor in the spasmodic mouse

Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia

Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease.

A method and server for predicting damaging missense mutations

Stages of embryonic development of the zebrafish

Primer3 on the WWW for general users and for biologist programmers

GABA: a pioneer transmitter that excites immature neurons and generates primitive oscillations

Glycine receptor heterogeneity in rat spinal cord during postnatal development

Altered inhibitory synaptic transmission in superficial dorsal horn neurones in spastic and oscillator mice

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139-151

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scholarly article

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10.1016/J.NBD.2013.09.002

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60

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Robert J. Harvey

Victoria M James

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2013-09-09T00:00:00Z

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256540361

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24029548

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3972633

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