Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin. - Wikidata - wikimedia - TriplyDB

Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.

Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.

http://www.wikidata.org/entity/Q37102146

about

Defects of the Glycinergic Synapse in Zebrafish.Model organisms in the fight against muscular dystrophy: lessons from drosophila and Zebrafish Swimming into prominence: the zebrafish as a valuable tool for studying human myopathies and muscular dystrophies.Dasatinib as a treatment for Duchenne muscular dystrophy Spatio-Temporal Differences in Dystrophin Dynamics at mRNA and Protein Levels Revealed by a Novel FlipTrap Line Characterization of Zebrafish Models of Marinesco-Sjögren Syndrome Multiscale 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.Zebrafish models for human FKRP muscular dystrophies Functional effects of spinocerebellar ataxia type 13 mutations are conserved in zebrafish Kv3.3 channels Drug screening in a zebrafish model of Duchenne muscular dystrophy.Zebrafish models of collagen VI-related myopathies Zebrafish based small molecule screens for novel DMD drugs.Isolation and transcriptome analysis of adult zebrafish cells enriched for skeletal muscle progenitors.High throughput screening in duchenne muscular dystrophy: from drug discovery to functional genomics Dystrophic muscle improvement in zebrafish via increased heme oxygenase signaling.Evaluation of exon-skipping strategies for Duchenne muscular dystrophy utilizing dystrophin-deficient zebrafish.Porcine models of muscular dystrophy Zebrafish models flex their muscles to shed light on muscular dystrophies.Analysis of Zebrafish Larvae Skeletal Muscle Integrity with Evans Blue Dye.Recent developments in the treatment of Duchenne muscular dystrophy and spinal muscular atrophy.Vascular-targeted therapies for Duchenne muscular dystrophy MicroRNA-199a is induced in dystrophic muscle and affects WNT signaling, cell proliferation, and myogenic differentiation.Identification of novel MYO18A interaction partners required for myoblast adhesion and muscle integrity.Protein O-mannosylation in animal development and physiology: from human disorders to Drosophila phenotypes Zebrafish muscular disease models towards drug discovery.Neuromuscular disorders in zebrafish: state of the art and future perspectives.Lack of Apobec2-related proteins causes a dystrophic muscle phenotype in zebrafish embryos The psychoactive drug 25B-NBOMe recapitulates rhabdomyolysis in zebrafish larvae.Characterization of zebrafish dysferlin by morpholino knockdown.Application of complementary luminescent and fluorescent imaging techniques to visualize nuclear and cytoplasmic Ca²⁺ signalling during the in vivo differentiation of slow muscle cells in zebrafish embryos under normal and dystrophic conditions.Muscle dysfunction in a zebrafish model of Duchenne muscular dystrophy.

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Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.

http://www.wikidata.org/entity/Q37102146

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 28 October 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.

@en

Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.

@nl

type

label

Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.

@en

Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.

@nl

prefLabel

Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.

@en

Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.

@nl

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Human Molecular Genetics

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Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.

@en

P2093

Genri Kawahara

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Jeffrey R Guyon

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Julie Goswami

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Leta S Steffen

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Louis M Kunkel

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Marielle Thorne

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Melanie Howell

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Michal Galdzicki

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Susan J Jun

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Timothy Pusack

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P2860

Titin mutations as the molecular basis for dilated cardiomyopathy

The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12

The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin

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

T-Coffee: A novel method for fast and accurate multiple sequence alignment

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

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202-211

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scholarly article

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10.1093/HMG/DDN337

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1

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18

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2008-10-28T00:00:00Z

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18957474

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2644651

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