(Q27028125)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23809187%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

title

Swimming into prominence: the zebrafish as a valuable tool for studying human myopathies and muscular dystrophies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23809187%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

0 references

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23809187%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

author name string

Elizabeth M Gibbs

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23809187%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

James J Dowling

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23809187%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

language of work or name

1 reference

25 July 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23809187%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23809187%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

volume

280

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23809187%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

issue

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23809187%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

page(s)

4187-4197

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23809187%20AND%20SRC:MED&resulttype=core&format=json

Efficient genome editing in zebrafish using a CRISPR-Cas system

4 March 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

RNA-guided human genome engineering via Cas9

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Multiplex genome engineering using CRISPR/Cas systems

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Dominant mutation of CCDC78 in a unique congenital myopathy with prominent internal nuclei and atypical cores

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

DHODH modulates transcriptional elongation in the neural crest and melanoma

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Zinc finger-based knockout punches for zebrafish genes

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

A splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafish

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

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

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

In vivo imaging of molecular interactions at damaged sarcolemma

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethality

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Animal models of human disease: zebrafish swim into view

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Genome editing with RNA-guided Cas9 nuclease in zebrafish embryos

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Zebrafish models flex their muscles to shed light on muscular dystrophies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

NAD+ biosynthesis ameliorates a zebrafish model of muscular 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=4017590

Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Hooked! Modeling human disease in zebrafish

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Sildenafil reduces respiratory muscle weakness and fibrosis in the mdx mouse model of Duchenne muscular 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=4017590

Muscle diseases in the zebrafish.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Neb: a zebrafish model of nemaline myopathy due to nebulin mutation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Connexin 39.9 protein is necessary for coordinated activation of slow-twitch muscle and normal behavior in zebrafish

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Drug screening in a zebrafish model of Duchenne muscular 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=4017590

Zebrafish Fukutin family proteins link the unfolded protein response with dystroglycanopathies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Sildenafil reverses cardiac dysfunction in the mdx mouse model of Duchenne muscular 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=4017590

Zebrafish models of collagen VI-related myopathies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Zebrafish models for human FKRP muscular dystrophies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Developmental defects in a zebrafish model for muscular dystrophies associated with the loss of fukutin-related protein (FKRP).

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Structure and function of skeletal muscle in zebrafish early larvae

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

The zebrafish ennui behavioral mutation disrupts acetylcholine receptor localization and motor axon stability.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

The dystrophin associated protein complex in zebrafish

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

In vivo genome editing using a high-efficiency TALEN system

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Basement membrane fragility underlies embryonic lethality in fukutin-null mice

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Zebrafish relatively relaxed mutants have a ryanodine receptor defect, show slow swimming and provide a model of multi-minicore disease.

31 May 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Targeted gene disruption in somatic zebrafish cells using engineered TALENs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Time course of the development of motor behaviors in the zebrafish embryo

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

accordion, a zebrafish behavioral mutant, has a muscle relaxation defect due to a mutation in the ATPase Ca2+ pump SERCA1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Quantification of birefringence readily measures the level of muscle damage in zebrafish.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Analysis of embryonic and larval zebrafish skeletal myofibers from dissociated preparations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Genes required for functional glycosylation of dystroglycan are conserved in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Protein O-mannosylation is necessary for normal embryonic development in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

A mutation in the human ryanodine receptor gene associated with central core disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

RYR1 mutations are a common cause of congenital myopathies with central nuclei

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

King–Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

A homozygous splicing mutation causing a depletion of skeletal muscle RYR1 is associated with multi-minicore disease congenital myopathy with ophthalmoplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Evaluation of exon-skipping strategies for Duchenne muscular dystrophy utilizing dystrophin-deficient zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Zebrafish integrin-linked kinase is required in skeletal muscles for strengthening the integrin-ECM adhesion complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

In-vivo characterization of human dilated cardiomyopathy genes in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Embryonic senescence and laminopathies in a progeroid zebrafish model

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Delta-sarcoglycan is required for early zebrafish muscle organization

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Delta-sarcoglycan is necessary for early heart and muscle development in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Depletion of zebrafish Tcap leads to muscular dystrophy via disrupting sarcomere-membrane interaction, not sarcomere assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Abnormal vascular development in zebrafish models for fukutin and FKRP deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Loss of selenoprotein N function causes disruption of muscle architecture in the zebrafish embryo.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Selenoprotein N is required for ryanodine receptor calcium release channel activity in human and zebrafish muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Knockdown of desmin in zebrafish larvae affects interfilament spacing and mechanical properties of skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Zebrafish as a model for caveolin-associated muscle disease; caveolin-3 is required for myofibril organization and muscle cell patterning.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FFEBS.12412

Removal of dystroglycan causes severe muscular dystrophy in zebrafish embryos.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Physiological properties of zebrafish embryonic red and white muscle fibers during early development

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

Genes controlling and mediating locomotion behavior of the zebrafish embryo and larva.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4017590

The molecular basis of muscular dystrophy in the mdx mouse: a point mutation

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23809187

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Centronuclear myopathy due to a de novo dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23809187

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/FEBS.12412

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23809187%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23809187%20AND%20SRC:MED&resulttype=core&format=json

4 March 2020

PubMed publication ID

23809187

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23809187%20AND%20SRC:MED&resulttype=core&format=json