(Q33633045)

28 July 2017

1 reference

title

Aggregates in neurodegenerative disease: crowds and power? (English)

1 reference

28 July 2017

1 reference

Tran PB

1

1 reference

PubMed ID

10322490

28 July 2017

Miller RJ

series ordinal

2

1 reference

28 July 2017

1 May 1999

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28 July 2017

Trends in Neurosciences

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28 July 2017

22

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28 July 2017

5

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28 July 2017

194-197

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Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

28 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Aggregation of mutant Cu/Zn superoxide dismutase proteins in a culture model of ALS

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Glutamate potentiates the toxicity of mutant Cu/Zn-superoxide dismutase in motor neurons by postsynaptic calcium-dependent mechanisms

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvement.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Formation of granular cytoplasmic aggregates in COS7 cells expressing mutant Cu/Zn superoxide dismutase associated with familial amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Thiol-dependent metal-catalyzed oxidation of copper, zinc superoxide dismutase

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Up-regulation of protein chaperones preserves viability of cells expressing toxic Cu/Zn-superoxide dismutase mutants associated with amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Decreased glutamate transport by the brain and spinal cord in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Huntingtin: a single bait hooks many species

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

The complex pathology of trinucleotide repeats

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

The fatal attraction of polyglutamine-containing proteins.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Polyglutamine-expanded human huntingtin transgenes induce degeneration of Drosophila photoreceptor neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Polyglutamine-mediated dysfunction and apoptotic death of a Caenorhabditis elegans sensory neuron

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Peptides containing glutamine repeats as substrates for transglutaminase-catalyzed cross-linking: relevance to diseases of the nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tract

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Mutant huntingtin expression in clonal striatal cells: dissociation of inclusion formation and neuronal survival by caspase inhibition.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Genetic dissection of familial Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Alpha synuclein in neurodegenerative disorders: murderer or accomplice?

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

The synucleins: a family of proteins involved in synaptic function, plasticity, neurodegeneration and disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

Alpha-synuclein in Lewy bodies

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

alpha-Synuclein in filamentous inclusions of Lewy bodies from Parkinson's disease and dementia with lewy bodies

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

The ubiquitin pathway in Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2899%2901409-5

7 January 2021

10.1016/S0166-2236(99)01409-5

Identifiers

DOI

1 reference

28 July 2017

1 reference

PubMed ID

10322490