(Q34100009)

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Neuronal nuclear alterations in dentatorubral-pallidoluysian atrophy: ultrastructural and morphometric studies of the cerebellar granule cells

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Europe PubMed Central

PubMed publication ID

31 July 2017

Neuronal nuclear alterations in dentatorubral-pallidoluysian atrophy: ultrastructural and morphometric studies of the cerebellar granule cells (English)

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Europe PubMed Central

PubMed publication ID

31 July 2017

dentatorubral-pallidoluysian atrophy

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Takahashi H

1

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Europe PubMed Central

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31 July 2017

Egawa S

2

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Europe PubMed Central

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31 July 2017

Piao YS

3

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Europe PubMed Central

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31 July 2017

Hayashi S

4

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Europe PubMed Central

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31 July 2017

Yamada M

5

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Europe PubMed Central

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31 July 2017

Shimohata T

6

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31 July 2017

Oyanagi K

7

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31 July 2017

Tsuji S

8

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31 July 2017

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publication date

1 November 2001

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31 July 2017

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31 July 2017

919

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31 July 2017

1

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31 July 2017

12-19

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Europe PubMed Central

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31 July 2017

Cell survival promoted by the Ras-MAPK signaling pathway by transcription-dependent and -independent mechanisms

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Neuropathological changes of the nucleus accumbens in Huntington's chorea

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Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice.

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Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

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From neuronal inclusions to neurodegeneration: neuropathological investigation of a transgenic mouse model of Huntington's disease

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Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain

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Hereditary dentatorubral-pallidoluysian atrophy: detection of widespread ubiquitinated neuronal and glial intranuclear inclusions in the brain

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Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions

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Cytoplasmic and nuclear polyglutamine aggregates in SCA6 Purkinje cells

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Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice

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Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy

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Interference by huntingtin and atrophin-1 with cbp-mediated transcription leading to cellular toxicity

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Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3.

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Evidence for apoptotic cell death in Huntington disease and excitotoxic animal models.

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Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA.

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Mediation by a CREB family transcription factor of NGF-dependent survival of sympathetic neurons

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Nuclear membrane indentations in Huntington's chorea

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When more is less: pathogenesis of glutamine repeat neurodegenerative diseases

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Intranuclear neuronal inclusions: a common pathogenic mechanism for glutamine-repeat neurodegenerative diseases?

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Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions.

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Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLA.

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Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription

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

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7 January 2021

Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathologic variants in a family

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DNA End Labeling (TUNEL) in Huntington's Disease and Other Neuropathological Conditions

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Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

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Unstable expansion of triplet repeats as a new disease mechanism for neurodegenerative diseases

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7 January 2021

Widespread occurrence of intranuclear atrophin-1 accumulation in the central nervous system neurons of patients with dentatorubral-pallidoluysian atrophy

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7 January 2021

Identifiers

10.1016/S0006-8993(01)02986-9

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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