Behavioral Responses in Animal Model of Congenital Muscular Dystrophy 1D.

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Alterations of GABAergic Neuron-Associated Extracellular Matrix and Synaptic Responses in -Heterozygous Mice Subjected to Prenatal Stress

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Behavioral Responses in Animal Model of Congenital Muscular Dystrophy 1D.

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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Behavioral Responses in Animal Model of Congenital Muscular Dystrophy 1D.

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Behavioral Responses in Animal Model of Congenital Muscular Dystrophy 1D.

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type

Item

label

Behavioral Responses in Animal Model of Congenital Muscular Dystrophy 1D.

@en

Behavioral Responses in Animal Model of Congenital Muscular Dystrophy 1D.

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Behavioral Responses in Animal Model of Congenital Muscular Dystrophy 1D.

@en

Behavioral Responses in Animal Model of Congenital Muscular Dystrophy 1D.

@nl

P1476

Behavioral Responses in Animal Model of Congenital Muscular Dystrophy 1D.

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Aryadnne L Schactae

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Clarissa M Comim

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Diogo Dominguini

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Francielle Mina

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

Jaime A Soares

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

João Quevedo

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

Letícia Ventura

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

Viviane Freiberger

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P2860

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1

Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan

Glycosylation defects: a new mechanism for muscular dystrophy?

Validation of open:closed arm entries in an elevated plus-maze as a measure of anxiety in the rat

Human brain malformations and their lessons for neuronal migration.

Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene.

Breaches of the pial basement membrane are associated with defective dentate gyrus development in mouse models of congenital muscular dystrophies

Clinical, pathologic, and mutational spectrum of dystroglycanopathy caused by LARGE mutations.

Psychiatric and cognitive phenotype in children and adolescents with myotonic dystrophy.

Dystroglycanopathies: coming into focus.

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s12035-014-9024-y

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402-407

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scholarly article

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10.1007/S12035-014-9024-Y

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Mariz Vainzof

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2014-12-03T00:00:00Z

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25465243

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Behavioral Responses in Animal Model of Congenital Muscular Dystrophy 1D.

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Behavioral Responses in Animal Model of Congenital Muscular Dystrophy 1D.

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P1433

P1476

P2093

P2860

P2888

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P433

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P577

P698

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P1433

P1476

P2093

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P2888

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P356

P433

P478

P50

P577

P698