The RNA-binding protein Rbfox1 regulates splicing required for skeletal muscle structure and function (Q35234123)

7 August 2017

title

The RNA-binding protein Rbfox1 regulates splicing required for skeletal muscle structure and function (English)

1 reference

7 August 2017

1 reference

Adan Dagnino-Acosta

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Simona Pedrotti

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Ravi K Singh

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Jimena Giudice

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Susan Hamilton

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Mark Knoblauch

1 reference

7 August 2017

Amy Hanna

1 reference

7 August 2017

Qianxing Mo

1 reference

7 August 2017

John Hicks

1 reference

7 August 2017

Thomas A Cooper

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7 August 2017

publication date

9 January 2015

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7 August 2017

published in

Human Molecular Genetics

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7 August 2017

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7 August 2017

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7 August 2017

page(s)

2360-2374

1 reference

describes a project that uses

7 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4380076/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

RBFOX1 cooperates with MBNL1 to control splicing in muscle, including events altered in myotonic dystrophy type 1

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Alternative splicing regulates vesicular trafficking genes in cardiomyocytes during postnatal heart development

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HITS-CLIP and integrative modeling define the Rbfox splicing-regulatory network linked to brain development and autism

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Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD)

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Rbfox-regulated alternative splicing is critical for zebrafish cardiac and skeletal muscle functions

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The splicing regulator Rbfox1 (A2BP1) controls neuronal excitation in the mammalian brain

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Global regulation of alternative splicing during myogenic differentiation

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Expansion of the eukaryotic proteome by alternative splicing

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

1 reference

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27 July 2018

1 reference

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Rbfox proteins regulate alternative mRNA splicing through evolutionarily conserved RNA bridges.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4380076

The splicing landscape is globally reprogrammed during male meiosis

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4380076

Four parameters increase the sensitivity and specificity of the exon array analysis and disclose 25 novel aberrantly spliced exons in myotonic dystrophy

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4380076

Sequential stages in the age-dependent gradual formation and accumulation of tubular aggregates in fast twitch muscle fibers: SERCA and calsequestrin involvement

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4380076

A tetracycline-inducible and skeletal muscle-specific Cre recombinase transgenic mouse

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4380076

Alternative isoform regulation in human tissue transcriptomes

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4380076

Strong association of de novo copy number mutations with sporadic schizophrenia

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4380076

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26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4380076

The origin of tubular aggregates in human myopathies

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4380076

The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4380076

Binding of an ankyrin-1 isoform to obscurin suggests a molecular link between the sarcoplasmic reticulum and myofibrils in striated muscles

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4380076

Evans Blue Dye as an in vivo marker of myofibre damage: optimising parameters for detecting initial myofibre membrane permeability

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4380076

Desmin-related neuromuscular disorders

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4380076

Tubular aggregates in skeletal muscle: Just a special type of protein aggregates?

26 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDV003

Rare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25575511

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDV003

1 reference

7 August 2017

1 reference

7 August 2017

1 reference