(Q28504521)

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Targeted deletion of a single Sca8 ataxia locus allele in mice causes abnormal gait, progressive loss of motor coordination, and Purkinje cell dendritic deficits

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scholarly article

1 reference

PubMed publication ID

24 January 2017

Targeted deletion of a single Sca8 ataxia locus allele in mice causes abnormal gait, progressive loss of motor coordination, and Purkinje cell dendritic deficits (English)

2 references

PubMed publication ID

24 January 2017

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

0 references

1 reference

GOA release 2020-03-11

4

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

author name string

Yungui He

1

2 references

PubMed publication ID

24 January 2017

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

Tao Zu

2

2 references

PubMed publication ID

24 January 2017

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

Kellie A Benzow

3

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

H Brent Clark

5

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

Michael D Koob

6

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

language of work or name

0 references

publication date

27 September 2006

1 reference

PubMed publication ID

24 January 2017

Journal of Neuroscience

2 references

PubMed publication ID

24 January 2017

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

26

2 references

PubMed publication ID

24 January 2017

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

39

2 references

PubMed publication ID

24 January 2017

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

9975-9982

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The SCA8 transcript is an antisense RNA to a brain-specific transcript encoding a novel actin-binding protein (KLHL1)

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monoclonal antibodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansion.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Signaling between the actin cytoskeleton and the postsynaptic density of dendritic spines

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clustering and anchoring mechanisms of molecular constituents of postsynaptic scaffolds in dendritic spines

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SCA8 repeat expansions in ataxia: a controversial association.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The KLHL1-antisense transcript ( KLHL1AS) is evolutionarily conserved

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular phylogeny of the kelch-repeat superfamily reveals an expansion of BTB/kelch proteins in animals

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The spinocerebellar ataxia 8 noncoding RNA causes neurodegeneration and associates with staufen in Drosophila.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haploinsufficiency for tumour suppressor genes: when you don't need to go all the way.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recovery from polyglutamine-induced neurodegeneration in conditional SCA1 transgenic mice.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential expression of T-type calcium channels in P/Q-type calcium channel mutant mice with ataxia and absence epilepsy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RNA and microRNAs in fragile X mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The occurrence of dominant spinocerebellar ataxias among 251 Finnish ataxia patients and the role of predisposing large normal alleles in a genetically isolated population

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Process elongation of oligodendrocytes is promoted by the Kelch-related actin-binding protein Mayven

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Giant SCA8 alleles in nine children whose mother has two moderately large ones

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gait analysis detects early changes in transgenic SOD1(G93A) mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular mechanisms of dendritic spine development and remodeling

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dendritic spine morphogenesis and plasticity

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A family with a novel frameshift mutation in the PMP22 gene (c.433_434insC) causing a phenotype of hereditary neuropathy with liability to pressure palsies.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interactions between CAP70 and actinfilin are important for integrity of actin cytoskeleton structures in neurons

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diseases of unstable repeat expansion: mechanisms and common principles

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of mammalian Staufen on mRNA traffic: a view from its nucleocytoplasmic shuttling function

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Decreases in the precision of Purkinje cell pacemaking cause cerebellar dysfunction and ataxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purkinje cell protein-2 regulatory regions and transgene expression in cerebellar compartments.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The POZ domain: a conserved protein-protein interaction motif

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The BTB/POZ domain: a new protein-protein interaction motif common to DNA- and actin-binding proteins.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Drosophila kelch is an oligomeric ring canal actin organizer

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Generalized lacZ expression with the ROSA26 Cre reporter strain

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable collagen disorders: from phenotype to genotype.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17005861

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1523/JNEUROSCI.2595-06.2006

2 references

PubMed publication ID

24 January 2017

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

PubMed publication ID

2 references

PubMed publication ID

24 January 2017

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6674467&resulttype=core&format=json

11 May 2020

ResearchGate publication ID

0 references

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