scholarly article | Q13442814 |
P356 | DOI | 10.1051/MEDSCI/20153110018 |
P9108 | Erudit article ID | 20153110018 |
P698 | PubMed publication ID | 26481031 |
P2093 | author name string | Lucile Ryckebüsch | |
P2860 | cites work | Muscle diseases in the zebrafish. | Q38014653 |
CRISPR/Cas9 and TALEN-mediated knock-in approaches in zebrafish | Q38202388 | ||
The zebrafish runzel muscular dystrophy is linked to the titin gene | Q39717199 | ||
Analysing regenerative potential in zebrafish models of congenital muscular dystrophy. | Q41756663 | ||
The HDAC Inhibitor TSA Ameliorates a Zebrafish Model of Duchenne Muscular Dystrophy | Q41823347 | ||
Genes required for functional glycosylation of dystroglycan are conserved in zebrafish | Q46480449 | ||
Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo | Q47073103 | ||
Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology | Q47073756 | ||
Epistatic dissection of laminin-receptor interactions in dystrophic zebrafish muscle. | Q47074022 | ||
Time course of the development of motor behaviors in the zebrafish embryo | Q48325756 | ||
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-dystroglycan | Q24294992 | ||
Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan | Q24316123 | ||
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan | Q24321692 | ||
Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies | Q24647603 | ||
The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy | Q24681141 | ||
Control of muscle fibre-type diversity during embryonic development: the zebrafish paradigm | Q26823743 | ||
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 zebrafish | Q27322025 | ||
Looking through zebrafish to study host-pathogen interactions | Q28086777 | ||
In vivo imaging of molecular interactions at damaged sarcolemma | Q28261975 | ||
Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethality | Q28512333 | ||
Animal models of human disease: zebrafish swim into view | Q29615723 | ||
The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies | Q30499359 | ||
POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations | Q30590282 | ||
NAD+ biosynthesis ameliorates a zebrafish model of muscular dystrophy | Q31105806 | ||
The dystrophin associated protein complex in zebrafish | Q31134324 | ||
Zebrafish models of collagen VI-related myopathies | Q33878282 | ||
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Hooked! Modeling human disease in zebrafish | Q36068284 | ||
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Zebrafish models flex their muscles to shed light on muscular dystrophies | Q36359190 | ||
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome | Q36439344 | ||
Molecular mechanisms of muscular dystrophies: old and new players | Q36593241 | ||
Structure and function of skeletal muscle in zebrafish early larvae | Q36593638 | ||
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 dystrophy | Q37127322 | ||
Dystroglycanopathies: coming into focus | Q37852376 | ||
Muscular dystrophies due to glycosylation defects: diagnosis and therapeutic strategies | Q37913913 | ||
P433 | issue | 10 | |
P407 | language of work or name | French | Q150 |
P921 | main subject | Danio rerio | Q169444 |
P304 | page(s) | 912-919 | |
P577 | publication date | 2015-10-19 | |
P1433 | published in | médecine/sciences | Q3332441 |
P1476 | title | [Potential of the zebrafish model to study congenital muscular dystrophies]. | |
P478 | volume | 31 |