(Q42037871)

English

Somatic mosaicism of expanded CAG repeats in brains of patients with dentatorubral-pallidoluysian atrophy: cellular population-dependent dynamics of mitotic instability

scientific article published on June 1996

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scholarly article

1 reference

Europe PubMed Central

15 October 2017

Somatic mosaicism of expanded CAG repeats in brains of patients with dentatorubral-pallidoluysian atrophy: cellular population-dependent dynamics of mitotic instability (English)

1 reference

Europe PubMed Central

15 October 2017

dentatorubral-pallidoluysian atrophy

1 reference

based on heuristic

inferred from title

author name string

Takano H

1

1 reference

Europe PubMed Central

15 October 2017

Onodera O

2

1 reference

Europe PubMed Central

15 October 2017

Takahashi H

3

1 reference

Europe PubMed Central

15 October 2017

Igarashi S

4

1 reference

Europe PubMed Central

15 October 2017

Yamada M

5

1 reference

Europe PubMed Central

15 October 2017

Oyake M

6

1 reference

Europe PubMed Central

15 October 2017

Ikeuchi T

7

1 reference

Europe PubMed Central

15 October 2017

Koide R

8

1 reference

Europe PubMed Central

15 October 2017

Tanaka H

9

1 reference

Europe PubMed Central

15 October 2017

Iwabuchi K

10

1 reference

Europe PubMed Central

15 October 2017

Tsuji S

11

1 reference

Europe PubMed Central

15 October 2017

language of work or name

0 references

publication date

1 June 1996

1 reference

Europe PubMed Central

15 October 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

15 October 2017

58

1 reference

Europe PubMed Central

15 October 2017

6

1 reference

Europe PubMed Central

15 October 2017

1212-1222

1 reference

Europe PubMed Central

15 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

Transcriptional activation modulated by homopolymeric glutamine and proline stretches

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

Characterization and localization of the Huntington disease gene product

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

Molecular cloning of a full-length cDNA for dentatorubral-pallidoluysian atrophy and regional expressions of the expanded alleles in the CNS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

Study on two autopsied cases of degenerative type of myoclonus epilepsy with choreo-athetoid movement: Proposal of hereditary dentate and pallidal system atrophy (author's transl)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

Familial chorea and myoclonus epilepsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

17 August 2018

Expression of the mutant allele of IT-15 (the HD gene) in striatum and cortex of Huntington's disease patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

17 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915058

17 August 2018

Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathologic variants in a family

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dentatorubropallidoluysian atrophy (DRPLA): comparative pathological study on clinical groups classified into juvenile, early adult and late adult types

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

15 October 2017

1 reference

Europe PubMed Central

15 October 2017

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