(Q48291079)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

review article

1 reference

title

Pathogenesis of neurodegenerative diseases associated with expanded glutamine repeats: new answers, new questions (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

1 reference

C A Ross

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

R L Margolis

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

M W Becher

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

J D Wood

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

S Engelender

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

J K Cooper

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

A H Sharp

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

publication date

1 January 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

Progress in Brain Research

9 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

volume

117

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

page(s)

397-419

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

Androgen-specific gene activation via a consensus glucocorticoid response element is determined by interaction with nonreceptor factors

9 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Novel proteins that interact with the COOH-terminal cytosolic routing determinants of an integral membrane peptide-processing enzyme

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Kalirin, a cytosolic protein with spectrin-like and GDP/GTP exchange factor-like domains that interacts with peptidylglycine alpha-amidating monooxygenase, an integral membrane peptide-processing enzyme

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Alternative excitotoxic hypotheses

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Preferential loss of striato-external pallidal projection neurons in presymptomatic Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Rethinking genotype and phenotype correlations in polyglutamine expansion disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

CAG expansion affects the expression of mutant Huntingtin in the Huntington's disease brain

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Cloning and developmental expression analysis of the murine homolog of the spinocerebellar ataxia type 1 gene (Sca1).

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Mouse Huntington's disease gene homolog (Hdh).

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Expanded glutamines and neurodegeneration--a gain of insight

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Comparative sequence analysis of the human and pufferfish Huntington's disease genes

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Replication of the neurochemical characteristics of Huntington's disease by quinolinic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Does impairment of energy metabolism result in excitotoxic neuronal death in neurodegenerative illnesses?

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigrees

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Expression of normal and mutant huntingtin in the developing brain

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Fast transport and retrograde movement of huntingtin and HAP 1 in axons.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Characterization of an expanded glutamine repeat androgen receptor in a neuronal cell culture system

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

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%2FS0079-6123%2808%2964029-7

7 January 2021

Trinucleotide repeats in neurologic diseases: an hypothesis concerning the pathogenesis of Huntington's disease, Kennedy's disease, and spinocerebellar ataxia type I.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

The length and location of CAG trinucleotide repeats in the androgen receptor N-terminal domain affect transactivation function

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Huntingtin-associated protein 1 (HAP1) binds to a Trio-like polypeptide, with a rac1 guanine nucleotide exchange factor domain

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

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%2FS0079-6123%2808%2964029-7

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%2FS0079-6123%2808%2964029-7

7 January 2021

A novel neuronal messenger molecule in brain: the free radical, nitric oxide

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

The multidomain protein Trio binds the LAR transmembrane tyrosine phosphatase, contains a protein kinase domain, and has separate rac-specific and rho-specific guanine nucleotide exchange factor domains

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Subcellular localization of the Huntington's disease gene product in cell lines by immunofluorescence and biochemical subcellular fractionation

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neurons

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

GRIP: a synaptic PDZ domain-containing protein that interacts with AMPA receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

DNA sequences homologous to the Drosophila opa repeat are present in murine mRNAs that are differentially expressed in fetuses and adult tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Inactivation of the mouse Huntington's disease gene homolog Hdh

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Huntingtin-associated protein 1 (HAP1) interacts with the p150Glued subunit of dynactin

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Translational suppression by trinucleotide repeat expansion at FMR1.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Selective sparing of a class of striatal neurons in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Sparing of acetylcholinesterase-containing striatal neurons in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatum.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Relationship between trinucleotide repeats and neuropathological changes in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Transcriptional activation modulated by homopolymeric glutamine and proline stretches

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Absence of disease phenotype and intergenerational stability of the CAG repeat in transgenic mice expressing the human Huntington disease transcript

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

cDNA cloning and expression of rsca1, the rat counterpart of the human spinocerebellar ataxia type 1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

A Golgi study of the human neostriatum: neurons and afferent fibers.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Human genetic diseases due to codon reiteration: relationship to an evolutionary mechanism

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Codon reiteration and the evolution of proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Mitochondrial defect in Huntington's disease caudate nucleus

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Trinucleotide instability: a repeating theme in human inherited disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Identification and localization of huntingtin in brain and human lymphoblastoid cell lines with anti-fusion protein antibodies

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Neuronal loss in layers V and VI of cerebral cortex in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Characterization and localization of the Huntington disease gene product

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Gain of glutamines, gain of function?

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

A family of proteins structurally and functionally related to the E6-AP ubiquitin-protein ligase

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

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%2FS0079-6123%2808%2964029-7

7 January 2021

The gene for the TATA binding protein (TBP) that contains a highly polymorphic protein coding CAG repeat maps to 6q27.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Non-invasive neurochemical analysis of focal excitotoxic lesions in models of neurodegenerative illness using spectroscopic imaging

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Evidence from antibody studies that the CAG repeat in the Huntington disease gene is expressed in the protein

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Huntingtin is ubiquitinated and interacts with a specific ubiquitin-conjugating enzyme

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

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%2FS0079-6123%2808%2964029-7

7 January 2021

Trinucleotide repeats and long homopeptides in genes and proteins associated with nervous system disease and development

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Evidence for a repressive function of the long polyglutamine tract in the human androgen receptor: possible pathogenetic relevance for the (CAG)n-expanded neuronopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Expression and distribution of the dentatorubral-pallidoluysian atrophy gene product (atrophin-1/drplap) in neuronal and non-neuronal tissues.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Proteins with leucine-rich repeats

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Spinocerebellar ataxia type-1 and spinobulbar muscular atrophy gene products interact with glyceraldehyde-3-phosphate dehydrogenase

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Decreased apoptosis in the brain and premature lethality in CPP32-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Identification of a set of genes with developmentally down-regulated expression in the mouse brain

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

NMDA-dependent superoxide production and neurotoxicity

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Huntington's disease gene: regional and cellular expression in brain of normal and affected individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Trinucleotide repeat expansion in neurological disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Inherited neurodegenerative disorders caused by CAG/polyglutamine tract expansions: symposium introduction

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Huntington's disease gene (IT15) is widely expressed in human and rat tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

A huntingtin-associated protein enriched in brain with implications for pathology

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Huntingtin-associated protein (HAP1): discrete neuronal localizations in the brain resemble those of neuronal nitric oxide synthase

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Differential 3' polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expression

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Cloning and expression of the rat atrophin-I (DRPLA disease gene) homologue

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

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%2FS0079-6123%2808%2964029-7

7 January 2021

DRPLA gene (atrophin-1) sequence and mRNA expression in human brain

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

cDNAs with long CAG trinucleotide repeats from human brain

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

A nuclear factor containing the leucine-rich repeats expressed in murine cerebellar neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Iodoacetate produces striatal excitotoxic lesions.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Proton magnetic resonance spectroscopy on childhood-onset dentatorubral-pallidoluysian atrophy (DRPLA).

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA)

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Apoptosis by death factor

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Clinical aspects of CAG repeat diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

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%2FS0079-6123%2808%2964029-7

7 January 2021

Regional and cellular expression of the dentatorubral-pallidoluysian atrophy gene in brains of normal and affected individuals.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

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%2FS0079-6123%2808%2964029-7

7 January 2021

Molecular cloning of murine homologue dentatorubral-pallidoluysian atrophy (DRPLA) cDNA: strong conservation of a polymorphic CAG repeat in the murine gene

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Machado-Joseph disease gene product is a cytoplasmic protein widely expressed in brain

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Normal and expanded Huntington's disease gene alleles produce distinguishable proteins due to translation across the CAG repeat.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Huntington's disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Glutamine repeats and inherited neurodegenerative diseases: molecular aspects

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

The neuropathology of CAG repeat diseases: review and update of genetic and molecular features

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

The relevance of the structural co-factor (chemogenic lesion) in adverse and toxic reactions of neuropsychotropic agents

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Neurological sequelae of cyanide intoxication--the patterns of clinical, magnetic resonance imaging, and positron emission tomography findings.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

When more is less: pathogenesis of glutamine repeat neurodegenerative diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Huntington's disease and dentatorubral-pallidoluysian atrophy: proteins, pathogenesis and pathology

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Huntington disease and the related disorder, dentatorubral-pallidoluysian atrophy (DRPLA).

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Androgen concentration in motor neurons of cranial nerves and spinal cord

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

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%2FS0079-6123%2808%2964029-7

7 January 2021

Expression of the Huntington's disease (IT15) protein product in HD patients

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Predominant neuronal expression of the gene responsible for dentatorubral-pallidoluysian atrophy (DRPLA) in rat.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Involvement of free radicals in excitotoxicity in vivo.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Widespread expression of Huntington's disease gene (IT15) protein product

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Neurobiology of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Morphometric analysis of the prefrontal cortex in Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Evidence for neuronal degeneration and dendritic plasticity in cortical pyramidal neurons of Huntington's disease: a quantitative Golgi study.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Incorporation of glutamine repeats makes protein oligomerize: implications for neurodegenerative diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Mutational analysis of motor proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Yama/CPP32 beta, a mammalian homolog of CED-3, is a CrmA-inhibitable protease that cleaves the death substrate poly(ADP-ribose) polymerase

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Molecular genetics of triplet repeats: unstable expansion of triplet repeats as a new mechanism for neurodegenerative diseases.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

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%2FS0079-6123%2808%2964029-7

7 January 2021

Trinucleotide repeat expansions in neurological disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

The interaction between cytoplasmic dynein and dynactin is required for fast axonal transport

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Homozygotes for Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

opa: a novel family of transcribed repeats shared by the Notch locus and other developmentally regulated loci in D. melanogaster

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

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%2FS0079-6123%2808%2964029-7

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%2FS0079-6123%2808%2964029-7

7 January 2021

Atrophin-1, the DRPLA gene product, interacts with two families of WW domain-containing proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

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%2FS0079-6123%2808%2964029-7

7 January 2021

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Synthetic-lethal interactions identify two novel genes, SLA1 and SLA2, that control membrane cytoskeleton assembly in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Evidence that glyceraldehyde-3-phosphate dehydrogenase is involved in age-induced apoptosis in mature cerebellar neurons in culture.

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

Neuropathological classification of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0079-6123%2808%2964029-7

7 January 2021

10.1016/S0079-6123(08)64029-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9932422%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

1 reference