Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions? (Q45295535)

11 December 2017

Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions? (English)

1 reference

11 December 2017

6

1 reference

11 December 2017

S W Davies

1

1 reference

11 December 2017

K Beardsall

2

1 reference

11 December 2017

M Turmaine

3

1 reference

11 December 2017

M DiFiglia

4

1 reference

11 December 2017

N Aronin

5

1 reference

11 December 2017

language of work or name

English

0 references

publication date

1 January 1998

1 reference

11 December 2017

1 reference

11 December 2017

351

1 reference

11 December 2017

9096

1 reference

11 December 2017

131-133

1 reference

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

11 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Identification and characterization of the gene causing type 1 spinocerebellar ataxia.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

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%2FS0140-6736%2897%2908360-8

7 January 2021

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

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%2FS0140-6736%2897%2908360-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Identification of an HD patient with a (CAG)180 repeat expansion and the propagation of highly expanded CAG repeats in lambda phage

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

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%2FS0140-6736%2897%2908360-8

7 January 2021

Transgenic models of Huntington's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

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%2FS0140-6736%2897%2908360-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

α-synuclein—a link between Parkinson and Alzheimer diseases?

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

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%2FS0140-6736%2897%2908360-8

7 January 2021

A light and electron microscopy study of an unusual widespread nuclear inclusion body disease. A possible residuum of an old herpesvirus infection

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Widespread intranuclear neuronal corpuscles (Marinesco bodies) associated with a familial spinal degeneration with cranial and peripheral nerve involvement

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Neuronal intranuclear hyaline inclusion disease presenting as Friedreich's ataxia.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Neuronal intranuclear hyaline inclusion disease with progressive cerebellar ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Light, fluorescence, and electron microscopic features of neuronal intranuclear hyaline inclusions associated with multisystem atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

An unusual degenerative disorder of neurons associated with a novel intranuclear hyaline inclusion (neuronal intranuclear hyaline inclusion disease). A clinicopathological study of a case

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Multiple system atrophy with neuronal intranuclear hyaline inclusions. Report of a case and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

Adult-onset neuronal intranuclear hyaline inclusion disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

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%2FS0140-6736%2897%2908360-8

7 January 2021

Direct detection of novel expanded trinucleotide repeats in the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

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%2FS0140-6736%2897%2908360-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2908360-8

7 January 2021

10.1016/S0140-6736(97)08360-8

Identifiers

DOI

1 reference

11 December 2017

1 reference