A genetic interaction network model of a complex neurological disease. - Wikidata - thesis-toulmin - TriplyDB

A genetic interaction network model of a complex neurological disease.

A genetic interaction network model of a complex neurological disease.

http://www.wikidata.org/entity/Q34559798

about

SWDreader: a wavelet-based algorithm using spectral phase to characterize spike-wave morphological variation in genetic models of absence epilepsy.Weak Epistasis Generally Stabilizes Phenotypes in a Mouse Intercross.The detection and characterization of pleiotropy: discovery, progress, and promise.Network approaches to systems biology analysis of complex disease: integrative methods for multi-omics data.An Analytic Solution to the Computation of Power and Sample Size for Genetic Association Studies under a Pleiotropic Mode of Inheritance.Differential molecular and behavioural alterations in mouse models of GABRG2 haploinsufficiency versus dominant negative mutations associated with human epilepsy Mapping of quantitative trait loci for grain yield and its components in a US popular winter wheat TAM 111 using 90K SNPs.

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P2860

A genetic interaction network model of a complex neurological disease.

http://www.wikidata.org/entity/Q34559798

description

2014 nî lūn-bûn

@nan

2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

A genetic interaction network model of a complex neurological disease.

@ast

A genetic interaction network model of a complex neurological disease.

@en

A genetic interaction network model of a complex neurological disease.

@nl

type

label

A genetic interaction network model of a complex neurological disease.

@ast

A genetic interaction network model of a complex neurological disease.

@en

A genetic interaction network model of a complex neurological disease.

@nl

prefLabel

A genetic interaction network model of a complex neurological disease.

@ast

A genetic interaction network model of a complex neurological disease.

@en

A genetic interaction network model of a complex neurological disease.

@nl

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Genes, Brain and Behavior

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A genetic interaction network model of a complex neurological disease.

@en

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A L Tyler

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B J Beyer

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G W Carter

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T C McGarr

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W N Frankel

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P2860

Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures

Association between genetic variation of CACNA1H and childhood absence epilepsy

Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation

New variants in the CACNA1H gene identified in childhood absence epilepsy

R/qtl: QTL mapping in experimental crosses

Cloned glutamate receptors

Reduced cortical inhibition in a mouse model of familial childhood absence epilepsy.

Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4

Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice.

Childhood absence epilepsy: genes, channels, neurons and networks.

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831-840

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10.1111/GBB.12178

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