Increased seizure susceptibility and cortical malformation in beta-catenin mutant mice.

Increased seizure susceptibility and cortical malformation in beta-catenin mutant mice.

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http://www.wikidata.org/entity/Q47284702
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features.Altered dendritic morphology of Purkinje cells in Dyt1 ΔGAG knock-in and purkinje cell-specific Dyt1 conditional knockout mice.Motor deficits and decreased striatal dopamine receptor 2 binding activity in the striatum-specific Dyt1 conditional knockout miceAbnormal nuclear envelope in the cerebellar Purkinje cells and impaired motor learning in DYT11 myoclonus-dystonia mouse modelsMultilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C.Neural crest-derived mesenchymal cells require Wnt signaling for their development and drive invagination of the telencephalic midlineAbnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse modelsImproved motor performance in Dyt1 ΔGAG heterozygous knock-in mice by cerebellar Purkinje-cell specific Dyt1 conditional knocking-outCurrent models and future directions for understanding the neural circuitries of maternal behaviors in rodents.Deciphering the function of canonical Wnt signals in development and disease: conditional loss- and gain-of-function mutations of beta-catenin in mice.The Role of Wnt/β-Catenin Signaling Pathway in Disrupted Hippocampal Neurogenesis of Temporal Lobe Epilepsy: A Potential Therapeutic Target?APC conditional knock-out mouse is a model of infantile spasms with elevated neuronal β-catenin levels, neonatal spasms, and chronic seizures.De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.Recombinant inbreeding in mice reveals thresholds in embryonic corpus callosum development.GSK3 and β-catenin determines functional expression of sodium channels at the axon initial segment.l-Carnitine Modulates Epileptic Seizures in Pentylenetetrazole-Kindled Rats via Suppression of Apoptosis and Autophagy and Upregulation of Hsp70.
P2860

Increased seizure susceptibility and cortical malformation in beta-catenin mutant mice.

Item
http://www.wikidata.org/entity/Q47284702
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
Increased seizure susceptibility and cortical malformation in beta-catenin mutant mice.
@en
Increased seizure susceptibility and cortical malformation in beta-catenin mutant mice.
@nl
type
label
Increased seizure susceptibility and cortical malformation in beta-catenin mutant mice.
@en
Increased seizure susceptibility and cortical malformation in beta-catenin mutant mice.
@nl
prefLabel
Increased seizure susceptibility and cortical malformation in beta-catenin mutant mice.
@en
Increased seizure susceptibility and cortical malformation in beta-catenin mutant mice.
@nl
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P50
P577
P698
P356
P1433
P1476
Increased seizure susceptibility and cortical malformation in beta-catenin mutant mice.
@en
P2093
P304
P31
P356
10.1016/J.BBRC.2004.05.204
P407
P433
P478
P50
P577
P698