Early autophagic response in a novel knock-in model of Huntington disease (Q34112214)

31 July 2017

title

Early autophagic response in a novel knock-in model of Huntington disease (English)

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31 July 2017

0 references

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Mary Y Heng

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31 July 2017

Duy K Duong

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31 July 2017

Roger L Albin

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31 July 2017

Sara J Tallaksen-Greene

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31 July 2017

Jesse M Hunter

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31 July 2017

Mathieu J Lesort

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31 July 2017

Alex Osmand

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31 July 2017

Henry L Paulson

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31 July 2017

Peter J Detloff

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31 July 2017

publication date

8 July 2010

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31 July 2017

published in

Human Molecular Genetics

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31 July 2017

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31 July 2017

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31 July 2017

page(s)

3702-3720

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describes a project that uses

31 July 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2935855/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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Mutant huntingtin causes context-dependent neurodegeneration in mice with Huntington's disease.

5 July 2018

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5 July 2018

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Aggregate-prone proteins with polyglutamine and polyalanine expansions are degraded by autophagy

5 July 2018

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Expanded CAG repeats in exon 1 of the Huntington's disease gene stimulate dopamine-mediated striatal neuron autophagy and degeneration

5 July 2018

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5 July 2018

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Neurological abnormalities in a knock-in mouse model of Huntington's disease

5 July 2018

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LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing

5 July 2018

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Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease

5 July 2018

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5 July 2018

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5 July 2018

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A Huntington's disease CAG expansion at the murine Hdh locus is unstable and associated with behavioural abnormalities in mice

5 July 2018

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Nuclear and neuropil aggregates in Huntington's disease: relationship to neuropathology.

5 July 2018

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Evidence for proteasome involvement in polyglutamine disease: localization to nuclear inclusions in SCA3/MJD and suppression of polyglutamine aggregation in vitro

5 July 2018

1 reference

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Distribution of inclusions in neuronal nuclei and dystrophic neurites in Huntington disease brain

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2935855

Huntingtin localization in brains of normal and Huntington's disease patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2935855

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

5 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2935855

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2935855

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2935855

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

5 July 2018

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Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice

21 January 2018

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Neuronal dysfunction in a polyglutamine disease model occurs in the absence of ubiquitin-proteasome system impairment and inversely correlates with the degree of nuclear inclusion formation

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ285

Acute polyglutamine expression in inducible mouse model unravels ubiquitin/proteasome system impairment and permanent recovery attributable to aggregate formation.

21 January 2018

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Trehalose, a novel mTOR-independent autophagy enhancer, accelerates the clearance of mutant huntingtin and alpha-synuclein.

21 January 2018

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Novel targets for Huntington's disease in an mTOR-independent autophagy pathway

21 January 2018

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Striatal D1 and D2 dopamine receptor loss in asymptomatic mutation carriers of Huntington's disease

21 January 2018

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Behavioral abnormalities precede neuropathological markers in rats transgenic for Huntington's disease.

21 January 2018

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A comparison of huntington disease and huntington disease-like 2 neuropathology

21 January 2018

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In search of an "autophagomometer".

21 January 2018

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RNAi suppresses polyglutamine-induced neurodegeneration in a model of spinocerebellar ataxia.

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ285

Chronology of behavioral symptoms and neuropathological sequela in R6/2 Huntington's disease transgenic mice

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ285

Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ285

Autophagy regulates the processing of amino terminal huntingtin fragments

21 January 2018

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Monitoring autophagic degradation of p62/SQSTM1.

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2FDDQ285

Paradoxical delay in the onset of disease caused by super-long CAG repeat expansions in R6/2 mice.

21 January 2018

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Sensitive biochemical aggregate detection reveals aggregation onset before symptom development in cellular and murine models of Huntington's disease

21 January 2018

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Mouse Huntington's disease homolog mRNA levels: variation and allele effects

28 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2935855

Huntingtin expression stimulates endosomal-lysosomal activity, endosome tubulation, and autophagy.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2935855

Purkinje cell expression of a mutant allele of SCA1 in transgenic mice leads to disparate effects on motor behaviors, followed by a progressive cerebellar dysfunction and histological alterations.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2935855

28 October 2018

Identifiers

DOI

10.1093/HMG/DDQ285

1 reference

31 July 2017

1 reference

31 July 2017

1 reference