(Q34446570)

2 August 2017

1 reference

title

Are there CAG repeat expansion-related disorders outside the central nervous system? (English)

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2 August 2017

Ferro P

1

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2 August 2017

dell'Eva R

series ordinal

2

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2 August 2017

Pfeffer U

series ordinal

3

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2 August 2017

publication date

1 October 2001

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2 August 2017

published in

Brain Research Bulletin

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2 August 2017

volume

56

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2 August 2017

issue

3-4

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2 August 2017

page(s)

259-264

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Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy

2 August 2017

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Cleft hand/foot: clinical and developmental aspects

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

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7 January 2021

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome

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7 January 2021

Analysis of the role of heat shock protein (Hsp) molecular chaperones in polyglutamine disease

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7 January 2021

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

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7 January 2021

A one-hit model of cell death in inherited neuronal degenerations

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7 January 2021

Re: Prostate cancer and the androgen receptor

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7 January 2021

Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse

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7 January 2021

Cell death in polyglutamine diseases

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7 January 2021

The expression pattern of the Distal-less homeobox-containing gene Dlx-5 in the developing chick limb bud suggests its involvement in apical ectodermal ridge activity, pattern formation, and cartilage differentiation

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7 January 2021

Somatic alterations of the androgen receptor CAG repeat in human colon cancer delineate a novel mutation pathway independent of microsatellite instability

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7 January 2021

The CAG repeat within the androgen receptor gene and its relationship to prostate cancer

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7 January 2021

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

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7 January 2021

Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27.

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7 January 2021

Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch.

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7 January 2021

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

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7 January 2021

Polyglutamine length-dependent interaction of Hsp40 and Hsp70 family chaperones with truncated N-terminal huntingtin: their role in suppression of aggregation and cellular toxicity

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7 January 2021

Genetic suppression of polyglutamine toxicity in Drosophila

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7 January 2021

Dramatic mutation instability in HD mouse striatum: does polyglutamine load contribute to cell-specific vulnerability in Huntington's disease?

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7 January 2021

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

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7 January 2021

Chaperones Hsp70 and Hsp40 suppress aggregate formation and apoptosis in cultured neuronal cells expressing truncated androgen receptor protein with expanded polyglutamine tract

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7 January 2021

Caspase-3 cleaves the expanded androgen receptor protein of spinal and bulbar muscular atrophy in a polyglutamine repeat length-dependent manner

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7 January 2021

A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?

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7 January 2021

Aggregation of huntingtin in yeast varies with the length of the polyglutamine expansion and the expression of chaperone proteins

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7 January 2021

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

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7 January 2021

Nonneural nuclear inclusions of androgen receptor protein in spinal and bulbar muscular atrophy

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Reduced transcriptional regulatory competence of the androgen receptor in X-linked spinal and bulbar muscular atrophy

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7 January 2021

p63 is a p53 homologue required for limb and epidermal morphogenesis

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7 January 2021

Hsp70 and hsp40 chaperones can inhibit self-assembly of polyglutamine proteins into amyloid-like fibrils

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7 January 2021

De novo expansion of a (CAG)n repeat in sporadic Huntington's disease

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7 January 2021

Dentatorubral-pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate

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7 January 2021

CAG-polyglutamine-repeat mutations: independence from gene context

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7 January 2021

Toward an understanding of polyglutamine neurodegeneration

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7 January 2021

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

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7 January 2021

Modification of BRCA1-associated breast cancer risk by the polymorphic androgen-receptor CAG repeat

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Formation of polyglutamine inclusions in non-CNS tissue

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7 January 2021

Adenovirus-mediated expression of mutant DRPLA proteins with expanded polyglutamine stretches in neuronally differentiated PC12 cells. Preferential intranuclear aggregate formation and apoptosis

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7 January 2021

Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions.

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7 January 2021

The proximo-distal sequence of origin of the parts of the chick wing and the role of the ectoderm. 1948.

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7 January 2021

Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly

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7 January 2021

X-linked recessive bulbospinal neuronopathy: clinical phenotypes and CAG repeat size in androgen receptor gene

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7 January 2021

Molecular analysis of a de novo mutation for spinocerebellar ataxia type 6 and (CAG)n repeat units in normal elder controls

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7 January 2021

Cloning and characterization of two members of the vertebrate Dlx gene family

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7 January 2021

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

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7 January 2021

Drosophila retinal degeneration C (rdgC) encodes a novel serine/threonine protein phosphatase

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7 January 2021

Polyglutamine-expanded androgen receptors form aggregates that sequester heat shock proteins, proteasome components and SRC-1, and are suppressed by the HDJ-2 chaperone

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900663-3

7 January 2021

Tissue-specific somatic mosaicism in spinal and bulbar muscular atrophy is dependent on CAG-repeat length and androgen receptor--gene expression level.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900663-3

7 January 2021

Epithelial cell movements and interactions in limb, neural crest and vasculature

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https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900663-3

7 January 2021

Characterization and expression of a cDNA encoding the human androgen receptor

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https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900663-3

7 January 2021

Somatic mosaicism of CAG repeat in dentatorubral-pallidoluysian atrophy (DRPLA)

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https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900663-3

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900663-3

7 January 2021

Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900663-3

7 January 2021

De novo expansion of a CAG repeat in a Japanese patient with sporadic Huntington's disease

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https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900663-3

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900663-3

7 January 2021

p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900663-3

7 January 2021

Linkage disequilibrium between the expanded (CAG)n repeat and an allele of the adjacent (CCG)n repeat in Huntington's disease patients of Greek origin.

1 reference

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7 January 2021

Cell cycle arrest enhances the in vitro cellular toxicity of the truncated Machado-Joseph disease gene product with an expanded polyglutamine stretch

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7 January 2021

Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism

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7 January 2021

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

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7 January 2021

On the inheritance of the split hand/split foot malformation

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7 January 2021

CAG Repeats in SCA6: Anticipating new clues

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7 January 2021

10.1016/S0361-9230(01)00663-3

Identifiers

DOI

1 reference

2 August 2017

1 reference