Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour. - Wikidata - awgldk - TriplyDB

Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour.

Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour.

http://www.wikidata.org/entity/Q36632504

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Myotonic Dystrophies: State of the Art of New Therapeutic Developments for the CNS.Tractography reveals diffuse white matter abnormalities in Myotonic Dystrophy Type 1 Targeting DMPK with Antisense Oligonucleotide Improves Muscle Strength in Myotonic Dystrophy Type 1 Mice Consensus brain-derived protein, extraction protocol for the study of human and murine brain proteome using both 2D-DIGE and mini 2DE immunoblotting.RNA-protein interactions in unstable microsatellite diseases.Sense and Antisense DMPK RNA Foci Accumulate in DM1 Tissues during Development Synaptic protein dysregulation in myotonic dystrophy type 1: Disease neuropathogenesis beyond missplicing Sleep-Wake Cycle and Daytime Sleepiness in the Myotonic Dystrophies Understanding the molecular consequences of inherited muscular dystrophies: advancements through proteomic experimentation.Myotonic dystrophy is not only a disease affecting the muscles, it is also a CNS disorder.Reduced cytoplasmic MBNL1 is an early event in a brain-specific mouse model of myotonic dystrophy.Altered levels of the splicing factor muscleblind modifies cerebral cortical function in mouse models of myotonic dystrophy.Epiretinal membrane: a treatable cause of visual disability in myotonic dystrophy type 1.

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Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour.

http://www.wikidata.org/entity/Q36632504

description

2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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2013年论文

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2013年论文

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name

Myotonic dystrophy CTG expansi ...... nsmission and mouse behaviour.

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Myotonic dystrophy CTG expansi ...... nsmission and mouse behaviour.

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type

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Myotonic dystrophy CTG expansi ...... nsmission and mouse behaviour.

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Myotonic dystrophy CTG expansi ...... nsmission and mouse behaviour.

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prefLabel

Myotonic dystrophy CTG expansi ...... nsmission and mouse behaviour.

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Myotonic dystrophy CTG expansi ...... nsmission and mouse behaviour.

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Myotonic dystrophy CTG expansi ...... nsmission and mouse behaviour.

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Aline Huguet

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Annie Nicole

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Bruno Buisson

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Bulmaro Cisneros

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Caroline Chevarin

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Céline Guiraud-Dogan

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Elodie Marciniak

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Esther Steidl

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Fabrice Trovero

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Friedrich Metzger

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Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy

The synaptic vesicle cycle

Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy

Muscleblind-like 2-mediated alternative splicing in the developing brain and dysregulation in myotonic dystrophy

The neuropsychopharmacology of fronto-executive function: monoaminergic modulation

Elevation of RNA-binding protein CUGBP1 is an early event in an inducible heart-specific mouse model of myotonic dystrophy

Chronic mild stress (CMS) in mice: of anhedonia, 'anomalous anxiolysis' and activity

The small GTP-binding protein Rab3A regulates a late step in synaptic vesicle fusion

RNA CUG repeats sequester CUGBP1 and alter protein levels and activity of CUGBP1

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

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957-970

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10.1093/BRAIN/AWS367

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Pt 3

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136

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