(Q48628376)

English

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.

scientific article published in October 1997

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6 November 2019

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 (English)

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6 November 2019

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6 November 2019

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H B Clark

1

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6 November 2019

E N Burright

2

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6 November 2019

W S Yunis

3

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6 November 2019

S Larson

4

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6 November 2019

C Wilcox

5

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6 November 2019

B Hartman

6

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6 November 2019

A Matilla

7

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6 November 2019

H T Orr

9

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6 November 2019

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1 October 1997

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6 November 2019

Journal of Neuroscience

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6 November 2019

17

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6 November 2019

19

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6 November 2019

7385-7395

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6 November 2019

Identification of a self-association region within the SCA1 gene product, ataxin-1

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

12 December 2020

based on heuristic

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purkinje cell degeneration, a new neurological mutation in the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

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/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

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/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/9295384

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/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Purkinje cell in olivopontocerebellar atrophy. A Golgi and immunocytochemical study

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

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/9295384

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/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disrupted cerebellar cortical development and progressive degeneration of Purkinje cells in SV40 T antigen transgenic mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic architecture of behavioural responses to novelty in mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dendritic spines: cellular specializations imparting both stability and flexibility to synaptic function

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Female transgenic mice carrying multiple copies of the human gene for S100 beta are hyperactive

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Behavioral responses to novelty and structural variation of the hippocampus in mice. I. Quantitative-genetic analysis of behavior in the open-field

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

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/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Purkinje cell and its afferents in human hereditary ataxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/9295384

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/9295384

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/9295384

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/9295384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1523/JNEUROSCI.17-19-07385.1997

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9295384%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9295384%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9295384%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

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