Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo.
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Fam65b is important for formation of the HDAC6-dysferlin protein complex during myogenic cell differentiationMutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycanMutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycanA central function for perlecan in skeletal muscle and cardiovascular developmentThe zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy.Defects of the Glycinergic Synapse in Zebrafish.Tendon development and musculoskeletal assembly: emerging roles for the extracellular matrixSwimming into prominence: the zebrafish as a valuable tool for studying human myopathies and muscular dystrophies.Dasatinib as a treatment for Duchenne muscular dystrophyRemodeling of Mitochondrial Flashes in Muscular Development and Dystrophy in ZebrafishSpatio-Temporal Differences in Dystrophin Dynamics at mRNA and Protein Levels Revealed by a Novel FlipTrap LineThe caveolin-cavin system plays a conserved and critical role in mechanoprotection of skeletal muscle.A splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafishPOPDC1(S201F) causes muscular dystrophy and arrhythmia by affecting protein traffickingThe identification of zebrafish mutants showing alterations in senescence-associated biomarkersRecent advances using zebrafish animal models for muscle disease drug discoveryMuscular dystrophy begins early in embryonic development deriving from stem cell loss and disrupted skeletal muscle formationUsing Touch-evoked Response and Locomotion Assays to Assess Muscle Performance and Function in ZebrafishMultiscale models of skeletal muscle reveal the complex effects of muscular dystrophy on tissue mechanics and damage susceptibility.Defective glycinergic synaptic transmission in zebrafish motility mutants.Dynamic formation of microenvironments at the myotendinous junction correlates with muscle fiber morphogenesis in zebrafish.The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachmentDepletion of zebrafish Tcap leads to muscular dystrophy via disrupting sarcomere-membrane interaction, not sarcomere assemblyThe zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies.Macondo crude oil from the Deepwater Horizon oil spill disrupts specific developmental processes during zebrafish embryogenesis.Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophy.The dystrotelin, dystrophin and dystrobrevin superfamily: new paralogues and old isoforms.Zebrafish orthologs of human muscular dystrophy genesZebrafish models for human FKRP muscular dystrophiesTargeted deletion of the zebrafish obscurin A RhoGEF domain affects heart, skeletal muscle and brain developmentAnalysis of skeletal muscle defects in larval zebrafish by birefringence and touch-evoke escape response assaysThrombospondin-4 controls matrix assembly during development and repair of myotendinous junctions.Fluoxetine prevents dystrophic changes in a zebrafish model of Duchenne muscular dystrophy.The proteasomal inhibitor MG132 prevents muscular dystrophy in zebrafish.Flexible and general synthesis of functionalized phosphoisoprenoids for the study of prenylation in vivo and in vitro.Troponin T is essential for sarcomere assembly in zebrafish skeletal muscle.Zebrafish Fukutin family proteins link the unfolded protein response with dystroglycanopathiesHigh throughput screening in duchenne muscular dystrophy: from drug discovery to functional genomicsDystrophic muscle improvement in zebrafish via increased heme oxygenase signaling.Nanoscale imaging of caveolin-1 membrane domains in vivo.
P2860
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P2860
Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
Dystrophin is required for the ...... ments in the zebrafish embryo.
@en
Dystrophin is required for the ...... ments in the zebrafish embryo.
@nl
type
label
Dystrophin is required for the ...... ments in the zebrafish embryo.
@en
Dystrophin is required for the ...... ments in the zebrafish embryo.
@nl
prefLabel
Dystrophin is required for the ...... ments in the zebrafish embryo.
@en
Dystrophin is required for the ...... ments in the zebrafish embryo.
@nl
P2093
P50
P356
P1433
P1476
Dystrophin is required for the ...... ments in the zebrafish embryo.
@en
P2093
David F Daggett
David G Keenan
David I Bassett
P304
P356
10.1242/DEV.00799
P407
P577
2003-12-01T00:00:00Z