(Q44569570)

English

Hprt(CAG)146 mice: age of onset of behavioral abnormalities, time course of neuronal intranuclear inclusion accumulation, neurotransmitter marker alterations, mitochondrial function markers, and susceptibility to 1-methyl-4-phenyl-1,2,3,6-tetrahydro

scientific article published in October 2003

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7 November 2019

Hprt(CAG)146 mice: age of onset of behavioral abnormalities, time course of neuronal intranuclear inclusion accumulation, neurotransmitter marker alterations, mitochondrial function markers, and susceptibility to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (English)

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7 November 2019

neurotransmitter

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Walker S Jackson

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7 November 2019

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Sara J Tallaksen-Greene

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7 November 2019

Jared M Ordway

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7 November 2019

Andrew B Crouse

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7 November 2019

Peter J Detloff

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7 November 2019

Roger L Albin

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1 October 2003

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7 November 2019

The Journal of Comparative Neurology

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7 November 2019

465

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7 November 2019

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7 November 2019

205-219

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7 November 2019

Evidence for impairment of energy metabolism in vivo in Huntington's disease using localized 1H NMR spectroscopy

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

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Autosomal dominant cerebellar ataxia with retinal degeneration: clinical, neuropathologic, and genetic analysis of a large kindred

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https://api.crossref.org/works/10.1002%2FCNE.10855

21 January 2018

Does homozygosity advance the onset of dentatorubral-pallidoluysian atrophy?

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

21 January 2018

A clinical and pathologic study of a large Japanese family with Machado-Joseph disease tightly linked to the DNA markers on chromosome 14q

1 reference

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21 January 2018

Chronic administration of malonic acid produces selective neural degeneration and transient changes in calbindin immunoreactivity in rat striatum

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7 January 2021

based on heuristic

inferred from DOI database lookup

Age-dependent striatal excitotoxic lesions produced by the endogenous mitochondrial inhibitor malonate

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

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Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Increased vulnerability to 3-nitropropionic acid in an animal model of Huntington's disease.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

The role of protein composition in specifying nuclear inclusion formation in polyglutamine disease

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Live-cell imaging reveals divergent intracellular dynamics of polyglutamine disease proteins and supports a sequestration model of pathogenesis.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Inactivation of Hdh in the brain and testis results in progressive neurodegeneration and sterility in mice

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutant protein in Huntington disease is resistant to proteolysis in affected brain

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Therapeutic effects of coenzyme Q10 and remacemide in transgenic mouse models of Huntington's disease.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Brain-derived neurotrophic factor in Huntington disease

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterization of the excitotoxic potential of the reversible succinate dehydrogenase inhibitor malonate

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Early degenerative changes in transgenic mice expressing mutant huntingtin involve dendritic abnormalities but no impairment of mitochondrial energy production

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Transgenic mice expressing a Huntington's disease mutation are resistant to quinolinic acid-induced striatal excitotoxicity

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Partial resistance to malonate-induced striatal cell death in transgenic mouse models of Huntington's disease is dependent on age and CAG repeat length

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Resistance to NMDA toxicity correlates with appearance of nuclear inclusions, behavioural deficits and changes in calcium homeostasis in mice transgenic for exon 1 of the huntington gene

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

The role of dopamine in motor symptoms in the R6/2 transgenic mouse model of Huntington's disease

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

[3H]dihydrorotenone binding to NADH: ubiquinone reductase (complex I) of the electron transport chain: an autoradiographic study.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

A YAC mouse model for Huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegeneration.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Mice transgenic for an expanded CAG repeat in the Huntington's disease gene develop diabetes

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Testosterone reduction prevents phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Polyglutamine-expanded ataxin-7 antagonizes CRX function and induces cone-rod dystrophy in a mouse model of SCA7

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Amino-terminal fragments of mutant huntingtin show selective accumulation in striatal neurons and synaptic toxicity

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Polyglutamine expansion down-regulates specific neuronal genes before pathologic changes in SCA1.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

'Tissue' transglutaminase ablation reduces neuronal death and prolongs survival in a mouse model of Huntington's disease

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

CREB-binding protein sequestration by expanded polyglutamine

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Histone deacetylase inhibitors reduce polyglutamine toxicity

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

CAG-polyglutamine-repeat mutations: independence from gene context

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutamines.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Brain neurotransmitter deficits in mice transgenic for the Huntington's disease mutation

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Comparative distributions of dopamine D-1 and D-2 receptors in the cerebral cortex of rats, cats, and monkeys

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Polyglutamine pathogenesis: emergence of unifying mechanisms for Huntington's disease and related disorders

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Pivotal role of oligomerization in expanded polyglutamine neurodegenerative disorders.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Formation of polyglutamine inclusions in non-CNS tissue

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Transgenic mice harboring a full-length human mutant DRPLA gene exhibit age-dependent intergenerational and somatic instabilities of CAG repeats comparable with those in DRPLA patients.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Motoneuronal cell death is not correlated with aggregate formation of androgen receptors containing an elongated polyglutamine tract

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Nuclear inclusions in glutamine repeat disorders: are they pernicious, coincidental, or beneficial?

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Homozygosity for Machado-Joseph disease gene enhances phenotypic severity

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Vesicular neurotransmitter transporters in Huntington's disease: initial observations and comparison with traditional synaptic markers

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial dysfunction and free radical damage in the Huntington R6/2 transgenic mouse

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Androgen-dependent neurodegeneration by polyglutamine-expanded human androgen receptor in Drosophila.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Toxic proteins in neurodegenerative disease

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Studies on brain biopsies of patients with Huntington's chorea

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

"Fatal attractions" of proteins. A comprehensive hypothetical mechanism underlying Alzheimer's disease and other neurodegenerative disorders.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

[3H]methoxytetrabenazine: a high specific activity ligand for estimating monoaminergic neuronal integrity

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

The vesicular monoamine transporter is not regulated by dopaminergic drug treatments

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegeneration.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Homozygotes for Huntington's disease

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Morphological Purkinje cell changes in spinocerebellar ataxia type 6

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

SCA7 knockin mice model human SCA7 and reveal gradual accumulation of mutant ataxin-7 in neurons and abnormalities in short-term plasticity.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Increased sensitivity to N-methyl-D-aspartate receptor-mediated excitotoxicity in a mouse model of Huntington's disease

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Drosophila atrophin homolog functions as a transcriptional corepressor in multiple developmental processes

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Mouse and fly models of neurodegeneration

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

based on heuristic

inferred from DOI database lookup

Amphetamine-induced behavioral phenotype in a hypoxanthine-guanine phosphoribosyltransferase-deficient mouse model of Lesch-Nyhan syndrome

1 reference

https://api.crossref.org/works/10.1002%2FCNE.10855

7 January 2021

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inferred from DOI database lookup

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