(Q45296843)

11 December 2017

Protein precipitation: a common etiology in neurodegenerative disorders? (English)

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11 December 2017

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protein precipitation

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Kakizuka A

1

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11 December 2017

1 October 1998

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11 December 2017

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11 December 2017

14

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11 December 2017

396-402

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11 December 2017

10

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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

11 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Triplet repeat mutations in human disease

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

A CAG/CTG expansion in the normal population.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

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%2FS0168-9525%2898%2901559-5

7 January 2021

Cleavage, aggregation and toxicity of the expanded androgen receptor in spinal and bulbar muscular atrophy

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Aggregation of N-terminal huntingtin is dependent on the length of its glutamine repeats

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Truncated N-terminal fragments of huntingtin with expanded glutamine repeats form nuclear and cytoplasmic aggregates in cell culture.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Expanded polyglutamine protein forms nuclear inclusions and causes neural degeneration in Drosophila.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Alzheimer's disease: Initial report of the purification and characterization of a novel cerebrovascular amyloid protein

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

The precursor of Alzheimer's disease amyloid A4 protein resembles a cell-surface receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Candidate gene for the chromosome 1 familial Alzheimer's disease locus

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

New clues to Alzheimer's disease: unraveling the roles of amyloid and tau.

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Amyloid, the presenilins and Alzheimer's disease

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Tau protein mutations confirmed as neuron killers.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Seeding "one-dimensional crystallization" of amyloid: a pathogenic mechanism in Alzheimer's disease and scrapie?

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

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%2FS0168-9525%2898%2901559-5

7 January 2021

Molecular cloning of cDNA encoding an unrecognized component of amyloid in Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Alpha-synuclein in Lewy bodies

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Rad23 links DNA repair to the ubiquitin/proteasome pathway

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

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%2FS0168-9525%2898%2901559-5

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%2FS0168-9525%2898%2901559-5

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%2FS0168-9525%2898%2901559-5

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%2FS0168-9525%2898%2901559-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Glutamine repeats and inherited neurodegenerative diseases: molecular aspects

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

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%2FS0168-9525%2898%2901559-5

7 January 2021

Transglutaminase action imitates Huntington's disease: selective polymerization of Huntingtin containing expanded polyglutamine.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Oligomerization of expanded-polyglutamine domain fluorescent fusion proteins in cultured mammalian cells

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Huntington's disease gene product, huntingtin, associates with microtubules in vitro

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Polyglutamines, nuclear inclusions and neurodegeneration

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

The fatal attraction of polyglutamine-containing proteins.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

Nuclear inclusions of the androgen receptor protein in spinal and bulbar muscular atrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2898%2901559-5

7 January 2021

10.1016/S0168-9525(98)01559-5

Identifiers

DOI

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11 December 2017

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PubMed ID

9820028