(Q48524084)

English

Somatic mosaicism of the expanded CAG trinucleotide repeat in mRNAs for the responsible gene of Machado-Joseph disease (MJD), dentatorubral-pallidoluysian atrophy (DRPLA), and spinal and bulbar muscular atrophy (SBMA).

scientific article published in January 1998

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

Somatic mosaicism of the expanded CAG trinucleotide repeat in mRNAs for the responsible gene of Machado-Joseph disease (MJD), dentatorubral-pallidoluysian atrophy (DRPLA), and spinal and bulbar muscular atrophy (SBMA). (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

dentatorubral-pallidoluysian atrophy

1 reference

based on heuristic

inferred from title

Machado-Joseph disease

1 reference

based on heuristic

inferred from title

muscular atrophy

1 reference

based on heuristic

inferred from title

author name string

Y Ito

1

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

F Tanaka

2

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

M Yamamoto

3

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

M Doyu

4

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

M Nagamatsu

5

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

S Riku

6

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

T Mitsuma

7

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

G Sobue

8

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

publication date

1 January 1998

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

Neurochemical Research

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

23

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

1

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

25-32

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

https://scigraph.springernature.com/pub.10.1023/a:1022441101801

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential pattern in tissue-specific somatic mosaicism of expanded CAG trinucleotide repeats in dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and X-linked recessive spinal and bulbar muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

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/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification and characterization of the gene causing type 1 spinocerebellar ataxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked recessive bulbospinal neuronopathy. A clinicopathological study

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

When more is less: pathogenesis of glutamine repeat neurodegenerative diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Androgen receptor mRNA with increased size of tandem CAG repeat is widely expressed in the neural and nonneural tissues of X-linked recessive bulbospinal neuronopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unique features of the CAG repeats in Machado-Joseph disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severity of X-linked recessive bulbospinal neuronopathy correlates with size of the tandem CAG repeat in androgen receptor gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular features of the CAG repeats and clinical manifestation of Machado--Joseph disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and Machado-Joseph disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization and localization of the Huntington disease gene product

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1022441101801

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 February 2018

http://europepmc.org/abstract/MED/9482263

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q48524084&oldid=1528326353"