(Q35092246)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12657365%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

review article

1 reference

title

Apoptosis in Huntington's disease (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12657365%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

0 references

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12657365%20AND%20SRC:MED&resulttype=core&format=json

Marie-Françoise Chesselet

1 November 2019

series ordinal

2

object named as

Marie Françoise Chesselet

1 reference

1 November 2019

publication date

1 April 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12657365%20AND%20SRC:MED&resulttype=core&format=json

Progress in Neuro-Psychopharmacology & Biological Psychiatry

1 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12657365%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

volume

27

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12657365%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

issue

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12657365%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

page(s)

255-265

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12657365%20AND%20SRC:MED&resulttype=core&format=json

Modulation of apoptotic regulatory proteins and early activation of cytochrome C following systemic 3-nitropropionic acid administration

1 November 2019

cites work

1 reference

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7 January 2021

Severe deficiencies in dopamine signaling in presymptomatic Huntington's disease mice

1 reference

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7 January 2021

Morphology and compartmental location of cells exhibiting DNA damage after quinolinic acid injections into rat striatum

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7 January 2021

Neuronal nuclear DNA fragmentation in the aged canine brain: apoptosis or nuclear DNA fragility?

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7 January 2021

Aberrant interactions of transcriptional repressor proteins with the Huntington's disease gene product, huntingtin

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7 January 2021

Replicating Huntington's disease phenotype in experimental animals

1 reference

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7 January 2021

Oxidative damage and metabolic dysfunction in Huntington's disease: selective vulnerability of the basal ganglia.

1 reference

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7 January 2021

Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH.

1 reference

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7 January 2021

Trinucleotide (CAG) repeat length is positively correlated with the degree of DNA fragmentation in Huntington's disease striatum

1 reference

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7 January 2021

Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation.

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7 January 2021

Transcriptional dysregulation in Huntington's disease

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7 January 2021

Altered brain neurotransmitter receptors in transgenic mice expressing a portion of an abnormal human huntington disease gene

1 reference

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7 January 2021

Altered neurotransmitter receptor expression in transgenic mouse models of Huntington's disease

1 reference

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7 January 2021

Increased huntingtin protein length reduces the number of polyglutamine-induced gene expression changes in mouse models of Huntington's disease

1 reference

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7 January 2021

Epidermal immunization by a needle-free powder delivery technology: Immunogenicity of influenza vaccine and protection in mice

1 reference

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7 January 2021

Striatal interneurons in Huntington's disease: selective increase in the density of calretinin-immunoreactive medium-sized neurons

1 reference

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7 January 2021

Glyceraldehyde 3-phosphate dehydrogenase abnormality in metabolically stressed Huntington disease fibroblasts.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

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%2FS0278-5846%2803%2900021-6

7 January 2021

Trinucleotide repeats: mechanisms and pathophysiology

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

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%2FS0278-5846%2803%2900021-6

7 January 2021

Survival of basal ganglia neuropeptide Y-somatostatin neurones in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Lentiviral-mediated delivery of mutant huntingtin in the striatum of rats induces a selective neuropathology modulated by polyglutamine repeat size, huntingtin expression levels, and protein length.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Premature aging in mice deficient in DNA repair and transcription

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Analysis of the subcellular localization of huntingtin with a set of rabbit polyclonal antibodies in cultured mammalian cells of neuronal origin: comparison with the distribution of huntingtin in Huntington's disease autopsy brain

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Sp1 and TAFII130 transcriptional activity disrupted in early Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Trinucleotide repeat length instability and age of onset in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Inactivation of the mouse Huntington's disease gene homolog Hdh

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Kennedy's disease: caspase cleavage of the androgen receptor is a crucial event in cytotoxicity

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

High level expression of expanded full-length ataxin-3 in vitro causes cell death and formation of intranuclear inclusions in neuronal cells

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Huntingtin interacts with a family of WW domain proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Possible organ and age-related epigenetic factors in Huntington's disease and colorectal carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Proliferative and degenerative changes in striatal spiny neurons in Huntington's disease: a combined study using the section-Golgi method and calbindin D28k immunocytochemistry

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Nuclear DNA fragmentation in Creutzfeldt-Jakob disease: does a mere positive in situ nuclear end-labeling indicate apoptosis?

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

N-myc and c-myc expression in Alzheimer disease, Huntington disease and Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Fas and Fas-L expression in Huntington's disease and Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Calpain activation in Huntington's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

The mitochondrial toxin 3-nitropropionic acid induces striatal neurodegeneration via a c-Jun N-terminal kinase/c-Jun module.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Evidence for degenerative and regenerative changes in neostriatal spiny neurons in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

p300/CBP/p53 interaction and regulation of the p53 response

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

The influence of huntingtin protein size on nuclear localization and cellular toxicity.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Huntingtin interacting protein 1 induces apoptosis via a novel caspase-dependent death effector domain

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

The Gln-Ala repeat transcriptional activator CA150 interacts with huntingtin: neuropathologic and genetic evidence for a role in Huntington's disease pathogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

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%2FS0278-5846%2803%2900021-6

7 January 2021

Early alterations in gene expression and cell morphology in a mouse model of Huntington's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Abundant expression and cytoplasmic aggregations of [alpha]1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

UVB irradiation-induced apoptosis increased in lymphocytes of Huntington's disease patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Altered proteasomal function due to the expression of polyglutamine-expanded truncated N-terminal huntingtin induces apoptosis by caspase activation through mitochondrial cytochrome c release

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

HIP1, a human homologue of S. cerevisiae Sla2p, interacts with membrane-associated huntingtin in the brain

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Tauroursodeoxycholic acid, a bile acid, is neuroprotective in a transgenic animal model of Huntington's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Huntingtin is present in the nucleus, interacts with the transcriptional corepressor C-terminal binding protein, and represses transcription

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Apoptosis: A Basic Biological Phenomenon with Wideranging Implications in Tissue Kinetics

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Oxidative stress and neuronal DNA fragmentation mediate age-dependent vulnerability to the mitochondrial toxin, 3-nitropropionic acid, in the mouse striatum

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

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%2FS0278-5846%2803%2900021-6

7 January 2021

Caspase 3-cleaved N-terminal fragments of wild-type and mutant huntingtin are present in normal and Huntington's disease brains, associate with membranes, and undergo calpain-dependent proteolysis.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Electrophysiological and morphological changes in striatal spiny neurons in R6/2 Huntington's disease transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Four deaths and a funeral: from caspases to alternative mechanisms.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Evidence of T-lymphocyte functional impairment in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Intranuclear huntingtin increases the expression of caspase-1 and induces apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Huntingtin aggregate-associated axonal degeneration is an early pathological event in Huntington's disease mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Interaction of Huntington disease protein with transcriptional activator Sp1

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Transgenic invertebrate models of age-associated neurodegenerative diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Selective discrimination learning impairments in mice expressing the human Huntington's disease mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Expression of polyglutamine-expanded Huntingtin activates the SEK1-JNK pathway and induces apoptosis in a hippocampal neuronal cell line

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Decreased expression of striatal signaling genes in a mouse model of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

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

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Disruption of CREB function in brain leads to neurodegeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Proteasomal-dependent aggregate reversal and absence of cell death in a conditional mouse model of Huntington's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Apoptosis in neurodegenerative disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Reduction of glyceraldehyde-3-phosphate dehydrogenase activity in Alzheimer's disease and in Huntington's disease fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Mouse models of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Decrease in striatal enkephalin mRNA in mouse models of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Early motor dysfunction and striosomal distribution of huntingtin microaggregates in Huntington's disease knock-in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Dentatorubral pallidoluysian atrophy (DRPLA) protein is cleaved by caspase-3 during apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Compartmental loss of NADPH diaphorase in the neuropil of the human striatum in Huntington's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Abnormal synaptic plasticity and impaired spatial cognition in mice transgenic for exon 1 of the human Huntington's disease mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Inhibition of caspase-1 slows disease progression in a mouse model of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

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%2FS0278-5846%2803%2900021-6

7 January 2021

CAG-polyglutamine-repeat mutations: independence from gene context

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Expanded polyglutamines in Caenorhabditis elegans cause axonal abnormalities and severe dysfunction of PLM mechanosensory neurons without cell death

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Mechanisms of apoptosis by c-Myc

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Mechanism of transcriptional activation by Sp1: evidence for coactivators

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Transgenic mice expressing mutated full-length HD cDNA: a paradigm for locomotor changes and selective neuronal loss in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Identification of the full-length huntingtin- interacting protein p231HBP/HYPB as a DNA-binding factor

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Differential loss of striatal projection neurons in Huntington disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Wild-type huntingtin protects from apoptosis upstream of caspase-3.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Neuronal distribution in the putamen in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Quantitative analysis of morphological features in Huntington's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Caspase-8 is required for cell death induced by expanded polyglutamine repeats.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Axonal transport of N-terminal huntingtin suggests early pathology of corticostriatal projections in Huntington disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Apoptosis and the nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

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%2FS0278-5846%2803%2900021-6

7 January 2021

Intraneuronal aggregate formation and cell death after viral expression of expanded polyglutamine tracts in the adult rat brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Reduction of Purkinje cell pathology in SCA1 transgenic mice by p53 deletion.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Neuronal death in cultured murine cortical cells is induced by inhibition of GAPDH and triosephosphate isomerase

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Huntington's disease intranuclear inclusions contain truncated, ubiquitinated huntingtin protein

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

The selective vulnerability of nerve cells in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Causes of death in patients with Huntington's disease and in unaffected first degree relatives

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

DNA end labeling (TUNEL) in Huntington's disease and other neuropathological conditions

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Nonapoptotic neurodegeneration in a transgenic mouse model of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

The mitochondrial toxin 3-nitropropionic acid induces differential expression patterns of apoptosis-related markers in rat striatum

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

1 reference

7 January 2021

Neuropathological classification of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Caspase activation during apoptotic cell death induced by expanded polyglutamine in N2a cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

HIP-I: a huntingtin interacting protein isolated by the yeast two-hybrid system

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

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%2FS0278-5846%2803%2900021-6

7 January 2021

Inhibiting caspase cleavage of huntingtin reduces toxicity and aggregate formation in neuronal and nonneuronal cells

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Caspase cleavage of mutant huntingtin precedes neurodegeneration in Huntington's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue

1 reference

https://api.crossref.org/works/10.1016%2FS0278-5846%2803%2900021-6

7 January 2021

10.1016/S0278-5846(03)00021-6

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12657365%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference