Brain pathology of spinocerebellar ataxias. - Wikidata - awgldk - TriplyDB

Brain pathology of spinocerebellar ataxias.

Brain pathology of spinocerebellar ataxias.

http://www.wikidata.org/entity/Q34298978

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Molecular Pathological Classification of Neurodegenerative Diseases: Turning towards Precision Medicine 'Essential tremor' or 'the essential tremors': is this one disease or a family of diseases?Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24 Motor Dysfunctions and Neuropathology in Mouse Models of Spinocerebellar Ataxia Type 2: A Comprehensive Review Parkinsonism in spinocerebellar ataxia An miRNA-mediated therapy for SCA6 blocks IRES-driven translation of the CACNA1A second cistron Metabolic Profiling and Phenotyping of Central Nervous System Diseases: Metabolites Bring Insights into Brain Dysfunctions.Structural and Functional Magnetic Resonance Imaging of the Cerebellum: Considerations for Assessing Cerebellar Ataxias.Sensory and motor cortex function contributes to symptom severity in spinocerebellar ataxia type 6.A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking.Evaluation of Antisense Oligonucleotides Targeting ATXN3 in SCA3 Mouse Models Climbing fiber-Purkinje cell synaptic pathology in tremor and cerebellar degenerative diseases.Torpedo formation and Purkinje cell loss: modeling their relationship in cerebellar disease.Huntington's disease (HD): degeneration of select nuclei, widespread occurrence of neuronal nuclear and axonal inclusions in the brainstem.In vivo evidence for mTORC2-mediated actin cytoskeleton rearrangement in neurons Cerebellar soluble mutant ataxin-3 level decreases during disease progression in Spinocerebellar Ataxia Type 3 mice A knockin mouse model of spinocerebellar ataxia type 3 exhibits prominent aggregate pathology and aberrant splicing of the disease gene transcript.Progression of brain atrophy in spinocerebellar ataxia type 2: a longitudinal tensor-based morphometry study.Clinical analysis of adult-onset spinocerebellar ataxias in Thailand.Distinct transduction profiles in the CNS via three injection routes of AAV9 and the application to generation of a neurodegenerative mouse model.Quantitative evaluation of human cerebellum-dependent motor learning through prism adaptation of hand-reaching movement.The role for alterations in neuronal activity in the pathogenesis of polyglutamine repeat disorders.Insights from cerebellar transcriptomic analysis into the pathogenesis of ataxia.Macro- and microstructural changes in patients with spinocerebellar ataxia type 6: assessment of phylogenetic subdivisions of the cerebellum and the brain stem.Epidemiological, clinical, and molecular characterization of Cuban families with spinocerebellar ataxia type 3/Machado-Joseph disease.Modulation of error-sensitivity during a prism adaptation task in people with cerebellar degeneration Morphological Plasticity of Emerging Purkinje Cells in Response to Exogenous VEGF Depression and clinical progression in spinocerebellar ataxias.Altered Purkinje cell miRNA expression and SCA1 pathogenesis.Tissue plasminogen activator regulates Purkinje neuron development and survival.Early Cerebellar Network Shifting in Spinocerebellar Ataxia Type 6.Purkinje cell axonal anatomy: quantifying morphometric changes in essential tremor versus control brains.Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.Changes in CB(1) and CB(2) receptors in the post-mortem cerebellum of humans affected by spinocerebellar ataxias.How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia: can we learn from other noncoding repeat expansion disorders?Multiple system atrophy of the cerebellar type: clinical state of the art.Barcoding heat shock proteins to human diseases: looking beyond the heat shock response The expanding role for chromatin and transcription in polyglutamine disease.Redefining cerebellar ataxia in degenerative ataxias: lessons from recent research on cerebellar systems.Overexpression of cystathionine γ-lyase suppresses detrimental effects of spinocerebellar ataxia type 3.

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P2860

Brain pathology of spinocerebellar ataxias.

http://www.wikidata.org/entity/Q34298978

description

2012 nî lūn-bûn

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2012 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2012 թվականի հունիսին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

Brain pathology of spinocerebellar ataxias.

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Brain pathology of spinocerebellar ataxias.

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Brain pathology of spinocerebellar ataxias.

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type

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Brain pathology of spinocerebellar ataxias.

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Brain pathology of spinocerebellar ataxias.

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Brain pathology of spinocerebellar ataxias.

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Brain pathology of spinocerebellar ataxias.

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Brain pathology of spinocerebellar ataxias.

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Brain pathology of spinocerebellar ataxias.

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S00401-012-1000-X

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Acta Neuropathologica

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Brain pathology of spinocerebellar ataxias.

@en

P2093

Ewout R P Brunt

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

Kay Seidel

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Sonny Siswanto

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Udo Rüb

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Wilfred den Dunnen

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P2860

The SCA8 transcript is an antisense RNA to a brain-specific transcript encoding a novel actin-binding protein (KLHL1)

Ataxin-1 and Brother of ataxin-1 are components of the Notch signalling pathway

TTBK2 kinase substrate specificity and the impact of spinocerebellar-ataxia-causing mutations on expression, activity, localization and development

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures

Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation

Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.

A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected]

Glutamine-expanded ataxin-7 alters TFTC/STAGA recruitment and chromatin structure leading to photoreceptor dysfunction.

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s00401-012-1000-x

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1-21

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scholarly article

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10.1007/S00401-012-1000-X

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1

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124

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Horst-Werner Korf

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2012-06-09T00:00:00Z

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225287278

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1043887259

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22684686

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