Abnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse models - Wikidata - awgldk - TriplyDB

Abnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse models

Abnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse models

http://www.wikidata.org/entity/Q35688598

about

Enhanced hippocampal long-term potentiation and fear memory in Btbd9 mutant mice Striatal cholinergic dysfunction as a unifying theme in the pathophysiology of dystonia Alteration of striatal dopaminergic neurotransmission in a mouse model of DYT11 myoclonus-dystonia.Behavioral and electrophysiological characterization of Dyt1 heterozygous knockout mice.Improved motor performance in Dyt1 ΔGAG heterozygous knock-in mice by cerebellar Purkinje-cell specific Dyt1 conditional knocking-out Recent advances in the molecular pathogenesis of dystonia-plus syndromes and heredodegenerative dystonias.Engineering animal models of dystonia Genetic Aspects of Myoclonus-Dystonia Syndrome (MDS).Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndrome.Electromyographic evidence in support of a knock-in mouse model of DYT1 Dystonia.Unusual α-synuclein and cerebellar pathologies in a case of hereditary myoclonus-dystonia without SGCE mutation.How Many Types of Dystonia? Pathophysiological Considerations.

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Abnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse models

http://www.wikidata.org/entity/Q35688598

description

2011 nî lūn-bûn

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2011年の論文

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2011年論文

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2011年論文

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2011年论文

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name

Abnormal nuclear envelopes in ...... yoclonus-dystonia mouse models

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Abnormal nuclear envelopes in ...... yoclonus-dystonia mouse models

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type

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Abnormal nuclear envelopes in ...... yoclonus-dystonia mouse models

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Human Molecular Genetics

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Abnormal nuclear envelopes in ...... yoclonus-dystonia mouse models

@en

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Fumiaki Yokoi

http://www.w3.org/2001/XMLSchema#string

Mai T Dang

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Tong Zhou

http://www.w3.org/2001/XMLSchema#string

P2860

Human epsilon-sarcoglycan is highly related to alpha-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene

epsilon-Sarcoglycan, a broadly expressed homologue of the gene mutated in limb-girdle muscular dystrophy 2D

TorsinA binds the KASH domain of nesprins and participates in linkage between nuclear envelope and cytoskeleton

Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia

Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia

Site-specific DNA recombination in mammalian cells by the Cre recombinase of bacteriophage P1

Nuclear envelope proteins and associated diseases

The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted

PDZ domains and the organization of supramolecular complexes

Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome

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916-925

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scholarly article

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10.1093/HMG/DDR528

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4

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21

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2011-11-11T00:00:00Z

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51789518

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22080833

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corpus striatum

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3263984

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