[Potential of the zebrafish model to study congenital muscular dystrophies].

scientific article published on 19 October 2015

[Potential of the zebrafish model to study congenital muscular dystrophies]. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1051/MEDSCI/20153110018
P9108Erudit article ID20153110018
P698PubMed publication ID26481031

P2093author name stringLucile Ryckebüsch
P2860cites workMuscle diseases in the zebrafish.Q38014653
CRISPR/Cas9 and TALEN-mediated knock-in approaches in zebrafishQ38202388
The zebrafish runzel muscular dystrophy is linked to the titin geneQ39717199
Analysing regenerative potential in zebrafish models of congenital muscular dystrophy.Q41756663
The HDAC Inhibitor TSA Ameliorates a Zebrafish Model of Duchenne Muscular DystrophyQ41823347
Genes required for functional glycosylation of dystroglycan are conserved in zebrafishQ46480449
Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryoQ47073103
Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathologyQ47073756
Epistatic dissection of laminin-receptor interactions in dystrophic zebrafish muscle.Q47074022
Time course of the development of motor behaviors in the zebrafish embryoQ48325756
Out with the old, in with the new: reassessing morpholino knockdowns in light of genome editing technology.Q50643292
Characterization of the laminin gene family and evolution in zebrafish.Q51891008
[The revolution of the CRISPR is underway].Q52423327
Collagen VI deficiency induces early onset myopathy in the mouse: an animal model for Bethlem myopathy.Q52532612
Knockdown of col22a1 gene in zebrafish induces a muscular dystrophy by disruption of the myotendinous junction.Q52644388
Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycanQ24294992
Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycanQ24316123
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycanQ24321692
Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathiesQ24647603
The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophyQ24681141
Control of muscle fibre-type diversity during embryonic development: the zebrafish paradigmQ26823743
Swimming into prominence: the zebrafish as a valuable tool for studying human myopathies and muscular dystrophies.Q27028125
A splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafishQ27322025
Looking through zebrafish to study host-pathogen interactionsQ28086777
In vivo imaging of molecular interactions at damaged sarcolemmaQ28261975
Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethalityQ28512333
Animal models of human disease: zebrafish swim into viewQ29615723
The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathiesQ30499359
POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentationsQ30590282
NAD+ biosynthesis ameliorates a zebrafish model of muscular dystrophyQ31105806
The dystrophin associated protein complex in zebrafishQ31134324
Zebrafish models of collagen VI-related myopathiesQ33878282
Integrins in regulation of tissue development and function.Q35170439
Hooked! Modeling human disease in zebrafishQ36068284
Congenital muscular dystrophy: molecular and cellular aspects.Q36114687
Zebrafish models flex their muscles to shed light on muscular dystrophiesQ36359190
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndromeQ36439344
Molecular mechanisms of muscular dystrophies: old and new playersQ36593241
Structure and function of skeletal muscle in zebrafish early larvaeQ36593638
Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome.Q36731388
Genetic and pharmacologic inhibition of mitochondrial-dependent necrosis attenuates muscular dystrophyQ37127322
Dystroglycanopathies: coming into focusQ37852376
Muscular dystrophies due to glycosylation defects: diagnosis and therapeutic strategiesQ37913913
P433issue10
P407language of work or nameFrenchQ150
P921main subjectDanio rerioQ169444
P304page(s)912-919
P577publication date2015-10-19
P1433published inmédecine/sciencesQ3332441
P1476title[Potential of the zebrafish model to study congenital muscular dystrophies].
P478volume31