rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences. (Q55087601)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29789616%20AND%20SRC:MED&resulttype=core&format=json

27 March 2020

title

rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences (English)

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27 March 2020

1 reference

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27 March 2020

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27 March 2020

1 reference

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27 March 2020

Chantal Sellier

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27 March 2020

Estefanía Cerro-Herreros

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27 March 2020

Markus Blatter

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27 March 2020

Fernande Freyermuth

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27 March 2020

Angeline Gaucherot

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27 March 2020

Frank Ruffenach

1 reference

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27 March 2020

Partha Sarkar

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27 March 2020

Jack Puymirat

1 reference

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27 March 2020

Bjarne Udd

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27 March 2020

John W Day

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27 March 2020

Giovanni Meola

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27 March 2020

Guillaume Bassez

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27 March 2020

Harutoshi Fujimura

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27 March 2020

Masanori P Takahashi

1 reference

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27 March 2020

Benedikt Schoser

1 reference

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27 March 2020

Frédéric H T Allain

1 reference

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27 March 2020

Beatriz Llamusi

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27 March 2020

language of work or name

English

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publication date

22 May 2018

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27 March 2020

published in

Nature Communications

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27 March 2020

volume

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27 March 2020

issue

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27 March 2020

page(s)

2009

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Creative Commons Attribution 4.0 International

27 March 2020

start time

22 May 2018

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April 2022 Public Data File from Crossref

copyrighted

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19 June 2018

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Homologues of the Caenorhabditis elegans Fox-1 protein are neuronal splicing regulators in mammals

19 June 2018

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19 June 2018

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19 June 2018

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19 June 2018

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A vertebrate RNA-binding protein Fox-1 regulates tissue-specific splicing via the pentanucleotide GCAUG.

19 June 2018

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Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing

19 June 2018

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Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy

19 June 2018

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Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

19 June 2018

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Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy

19 June 2018

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Reduced mobility of the alternate splicing factor (ASF) through the nucleoplasm and steady state speckle compartments

19 June 2018

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High mobility of proteins in the mammalian cell nucleus

19 June 2018

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Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy

19 June 2018

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19 June 2018

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Myotonic dystrophy: candidate small molecule therapeutics

13 August 2018

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Disrupted prenatal RNA processing and myogenesis in congenital myotonic dystrophy.

13 August 2018

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13 August 2018

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Repression of the Central Splicing Regulator RBFox2 Is Functionally Linked to Pressure Overload-Induced Heart Failure

13 August 2018

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MBNL1 and RBFOX2 cooperate to establish a splicing programme involved in pluripotent stem cell differentiation

13 August 2018

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Ribonuclear inclusions and MBNL1 nuclear sequestration do not affect myoblast differentiation but alter gene splicing in myotonic dystrophy type 2.

13 August 2018

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Severity, type, and distribution of myotonic discharges are different in type 1 and type 2 myotonic dystrophy

13 August 2018

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

13 August 2018

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Myotonic dystrophy type 2 (DM2) and related disorders

13 August 2018

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Muscle pathology in 57 patients with myotonic dystrophy type 2

30 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5964235

Ribonuclear inclusions in skeletal muscle in myotonic dystrophy types 1 and 2

30 November 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41467-018-04370-X

7 January 2021

Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FS41467-018-04370-X

7 January 2021

Type 2 myotonic dystrophy can be predicted by the combination of type 2 muscle fiber central nucleation and scattered atrophy

1 reference

https://api.crossref.org/works/10.1038%2FS41467-018-04370-X

7 January 2021

Absence of a differentiation defect in muscle satellite cells from DM2 patients

1 reference

https://api.crossref.org/works/10.1038%2FS41467-018-04370-X

7 January 2021

Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat

1 reference

https://api.crossref.org/works/10.1038%2FS41467-018-04370-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FS41467-018-04370-X

7 January 2021

In vitro synthesis and cloning of long CAG repeats

1 reference

https://api.crossref.org/works/10.1038%2FS41467-018-04370-X

7 January 2021

10.1038/S41467-018-04370-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29789616%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

27 March 2020

ADS bibcode

2018NatCo...9.2009S

0 references

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29789616%20AND%20SRC:MED&resulttype=core&format=json

27 March 2020

PubMed publication ID

29789616

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29789616%20AND%20SRC:MED&resulttype=core&format=json