Candidate screening of the TRPC3 gene in cerebellar ataxia (Q35042571)

6 August 2017

Candidate screening of the TRPC3 gene in cerebellar ataxia (English)

1 reference

6 August 2017

7

Daniel H Geschwind

1 reference

6 August 2017

8

Kay E Davies

1 reference

6 August 2017

1

Esther B E Becker

1 reference

6 August 2017

6

Susan L Perlman

1 reference

6 August 2017

4

Anna Dulneva

1 reference

6 August 2017

Brent L Fogel

2

1 reference

PubMed ID

21321808

6 August 2017

Sanjeev Rajakulendran

series ordinal

3

1 reference

PubMed ID

21321808

6 August 2017

Michael G Hanna

series ordinal

5

1 reference

6 August 2017

1 June 2011

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6 August 2017

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6 August 2017

10

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6 August 2017

2

1 reference

6 August 2017

296-299

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https://scigraph.springernature.com/pub.10.1007/s12311-011-0253-6

6 August 2017

0 references

cites work

Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114078

Towards better mouse models: enhanced genotypes, systemic phenotyping and envirotype modelling

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114078

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114078

A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114078

TRPC3 channels are required for synaptic transmission and motor coordination

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114078

TRP channels: functions and involvement in neurologic disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114078

Primary episodic ataxias: diagnosis, pathogenesis and treatment

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114078

TRPC channels: integrators of multiple cellular signals

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114078

The wide spectrum of spinocerebellar ataxias (SCAs)

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114078

Predictive identification of exonic splicing enhancers in human genes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114078

Identification of common binding sites for calmodulin and inositol 1,4,5-trisphosphate receptors on the carboxyl termini of trp channels

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114078

Polyglutamine expansion down-regulates specific neuronal genes before pathologic changes in SCA1.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3114078

Enzymological analysis of mutant protein kinase Cgamma causing spinocerebellar ataxia type 14 and dysfunction in Ca2+ homeostasis.

8 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS12311-011-0253-6

An approach to the patient with late-onset cerebellar ataxia

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS12311-011-0253-6

TRPC channels promote cerebellar granule neuron survival.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS12311-011-0253-6

10.1007/S12311-011-0253-6

21 January 2018

Identifiers

DOI

1 reference

6 August 2017

1 reference

6 August 2017

1 reference

PubMed ID

21321808