Transcriptional changes and developmental abnormalities in a zebrafish model of myotonic dystrophy type 1. (Q37438540)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24092878%20AND%20SRC:MED&resulttype=core&format=json

26 February 2020

title

Transcriptional changes and developmental abnormalities in a zebrafish model of myotonic dystrophy type 1 (English)

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26 February 2020

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3

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26 February 2020

author name string

Peter K Todd

1

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26 February 2020

Feras Y Ackall

2

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26 February 2020

Kush Sharma

4

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26 February 2020

Henry L Paulson

5

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26 February 2020

James J Dowling

6

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26 February 2020

publication date

2 October 2013

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Disease Models & Mechanisms

26 February 2020

published in

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26 February 2020

volume

7

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26 February 2020

issue

1

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26 February 2020

page(s)

143-155

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Creative Commons Attribution 3.0 Unported

26 February 2020

copyright license

start time

18 May 2021

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

ImageJ

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11 June 2022

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inferred from PubMed Central ID database lookup

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Affy package

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CZ Software Mentions: A large dataset of software mentions in the biomedical literature

cites work

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Muscleblind-like 2-mediated alternative splicing in the developing brain and dysregulation in myotonic dystrophy

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Zebrafish deficient for Muscleblind-like 2 exhibit features of myotonic dystrophy.

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Transcriptional and post-transcriptional impact of toxic RNA in myotonic dystrophy

23 August 2017

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Loss of myotubularin function results in T-tubule disorganization in zebrafish and human myotubular myopathy

23 August 2017

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Expanded CTG repeats within the DMPK 3' UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy

23 August 2017

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Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy

23 August 2017

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Defining early steps in mRNA transport: mutant mRNA in myotonic dystrophy type I is blocked at entry into SC-35 domains

23 August 2017

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23 August 2017

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Reversible model of RNA toxicity and cardiac conduction defects in myotonic dystrophy

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Myotonic dystrophy: emerging mechanisms for DM1 and DM2.

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Reversal of RNA missplicing and myotonia after muscleblind overexpression in a mouse poly(CUG) model for myotonic dystrophy

23 August 2017

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Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy

23 August 2017

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23 August 2017

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23 August 2017

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Changes in myotonic dystrophy protein kinase levels and muscle development in congenital myotonic dystrophy

23 August 2017

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23 August 2017

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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

23 August 2017

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Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2.

23 August 2017

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The myotonic dystrophy expanded CUG repeat tract is necessary but not sufficient to disrupt C2C12 myoblast differentiation

23 August 2017

1 reference

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

23 August 2017

1 reference

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

23 August 2017

1 reference

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Expanded CUG repeat RNAs form hairpins that activate the double-stranded RNA-dependent protein kinase PKR

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

The natural history of congenital myotonic dystrophy: mortality and long term clinical aspects

23 August 2017

1 reference

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Splice variants of the N-methyl-D-aspartate receptor NR1 identify domains involved in regulation by polyamines and protein kinase C.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

Congenital myotonic dystrophy in Britain. II. Genetic basis

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

Congenital myotonic dystrophy in Britain. I. Clinical aspects

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

Overexpression of 3'-untranslated region of the myotonic dystrophy kinase cDNA inhibits myoblast differentiation in vitro

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

Mutant human embryonic stem cells reveal neurite and synapse formation defects in type 1 myotonic dystrophy.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

Kindlin-2 is an essential component of intercalated discs and is required for vertebrate cardiac structure and function.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of myotonic dystrophy type 1.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

Antisense transcription and heterochromatin at the DM1 CTG repeats are constrained by CTCF.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

Molecular characterization and embryonic expression of the family of N-methyl-D-aspartate receptor subunit genes in the zebrafish

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

Altered mRNA splicing of the skeletal muscle ryanodine receptor and sarcoplasmic/endoplasmic reticulum Ca2+-ATPase in myotonic dystrophy type 1.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

Selective dendrite-targeting of mRNAs of NR1 splice variants without exon 5: identification of a cis-acting sequence and isolation of sequence-binding proteins

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3882056

Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat

2 September 2018

1 reference

12 December 2020

Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy

1 reference

12 December 2020

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member

1 reference

12 December 2020

Myotonic dystrophy type 1 is associated with nuclear foci of mutant RNA, sequestration of muscleblind proteins and deregulated alternative splicing in neurons

1 reference

12 December 2020

Identifiers

DOI

10.1242/DMM.012427

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24092878%20AND%20SRC:MED&resulttype=core&format=json

release_e6kbovh7j5e3rbke3557y62o3e

26 February 2020

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/e6kbovh7j5e3rbke3557y62o3e

24 November 2022

mapped directly with Wikidata item

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24092878%20AND%20SRC:MED&resulttype=core&format=json

26 February 2020

PubMed publication ID

24092878

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24092878%20AND%20SRC:MED&resulttype=core&format=json