Aggregation of expanded huntingtin in the brains of patients with Huntington disease. - Wikidata - wikimedia - TriplyDB

Aggregation of expanded huntingtin in the brains of patients with Huntington disease.

Aggregation of expanded huntingtin in the brains of patients with Huntington disease.

http://www.wikidata.org/entity/Q37079417

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Contrasting effects of nanoparticle-protein attraction on amyloid aggregation A selective inhibitor of histone deacetylase 3 prevents cognitive deficits and suppresses striatal CAG repeat expansions in Huntington's disease mice Caspase-6 activity in a BACHD mouse modulates steady-state levels of mutant huntingtin protein but is not necessary for production of a 586 amino acid proteolytic fragment.Single-chain fragment variable passive immunotherapies for neurodegenerative diseases.Huntington's Disease: An Immune Perspective.Transglutaminase 2 accelerates neuroinflammation in amyotrophic lateral sclerosis through interaction with misfolded superoxide dismutase 1.Prefibrillar huntingtin oligomers isolated from HD brain potently seed amyloid formation.NanoEHS beyond Toxicity - Focusing on Biocorona.Complete suppression of Htt fibrilization and disaggregation of Htt fibrils by a trimeric chaperone complex.Inositol 1,4,5-trisphosphate receptors and neurodegenerative disorders.

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Aggregation of expanded huntingtin in the brains of patients with Huntington disease.

http://www.wikidata.org/entity/Q37079417

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

@tr

scientific article published on January 2007

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Aggregation of expanded huntingtin in the brains of patients with Huntington disease.

@en

Aggregation of expanded huntingtin in the brains of patients with Huntington disease.

@nl

type

label

Aggregation of expanded huntingtin in the brains of patients with Huntington disease.

@en

Aggregation of expanded huntingtin in the brains of patients with Huntington disease.

@nl

prefLabel

Aggregation of expanded huntingtin in the brains of patients with Huntington disease.

@en

Aggregation of expanded huntingtin in the brains of patients with Huntington disease.

@nl

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Aggregation of expanded huntingtin in the brains of patients with Huntington disease

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Guylaine Hoffner

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Philippe Djian

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Sylvie Souès

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P2860

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

Differential expression of multiple transglutaminases in human brain. Increased expression and cross-linking by transglutaminases 1 and 2 in Alzheimer's disease

Huntingtin aggregation and toxicity in Huntington's disease

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

Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death

Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form

Tissue transglutaminase contributes to disease progression in the R6/2 Huntington's disease mouse model via aggregate-independent mechanisms

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

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

Amyloid fibers are water-filled nanotubes.

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26-31

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scholarly article

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10.4161/PRI.1.1.4056

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1

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2007-01-01T00:00:00Z

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23951252

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19172113

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Huntington disease

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2633704

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