Zebrafish orthologs of human muscular dystrophy genes - Wikidata - wikimedia - TriplyDB

Zebrafish orthologs of human muscular dystrophy genes

Zebrafish orthologs of human muscular dystrophy genes

http://www.wikidata.org/entity/Q33279472

about

Automated drug screening with contractile muscle tissue engineered from dystrophic myoblasts Genetic Engineering of Dystroglycan in Animal Models of Muscular Dystrophy Dasatinib as a treatment for Duchenne muscular dystrophy Regulation of slow and fast muscle myofibrillogenesis by Wnt/beta-catenin and myostatin signaling Recent advances using zebrafish animal models for muscle disease drug discovery The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies.NAD+ biosynthesis ameliorates a zebrafish model of muscular dystrophy.Zebrafish models for human FKRP muscular dystrophies High-content drug screening with engineered musculoskeletal tissues Drug screening in a zebrafish model of Duchenne muscular dystrophy.Zebrafish models of collagen VI-related myopathies The proteasomal inhibitor MG132 prevents muscular dystrophy in zebrafish.Zebrafish based small molecule screens for novel DMD drugs.α-Actinin-2 deficiency results in sarcomeric defects in zebrafish that cannot be rescued by α-actinin-3 revealing functional differences between sarcomeric isoforms.Other model organisms for sarcomeric muscle diseases.Zebrafish models flex their muscles to shed light on muscular dystrophies.Chronic vitamin E deficiency promotes vitamin C deficiency in zebrafish leading to degenerative myopathy and impaired swimming behavior.Finfish and aquatic invertebrate pathology resources for now and the future.Therapeutic possibilities in the autosomal recessive limb-girdle muscular dystrophies.Protein O-mannosylation in animal development and physiology: from human disorders to Drosophila phenotypes The Zebrafish Heart as a Model of Mammalian Cardiac Function.Recent advancements in understanding mammalian O-mannosylation.Two novel COLVI long chains in zebrafish that are essential for muscle development.Characterization of zebrafish dysferlin by morpholino knockdown.Zebrafish ae2.2 encodes a second slc4a2 anion exchanger.

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Zebrafish orthologs of human muscular dystrophy genes

http://www.wikidata.org/entity/Q33279472

description

2007 nî lūn-bûn

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2007 թվականի մարտին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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name

Zebrafish orthologs of human muscular dystrophy genes

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Zebrafish orthologs of human muscular dystrophy genes

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Zebrafish orthologs of human muscular dystrophy genes.

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Zebrafish orthologs of human muscular dystrophy genes

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Zebrafish orthologs of human muscular dystrophy genes

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Zebrafish orthologs of human muscular dystrophy genes.

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Zebrafish orthologs of human muscular dystrophy genes

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Zebrafish orthologs of human muscular dystrophy genes

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Zebrafish orthologs of human muscular dystrophy genes.

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Zebrafish orthologs of human muscular dystrophy genes

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P2093

Emily D Vogel

http://www.w3.org/2001/XMLSchema#string

Jeffrey R Guyon

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Leonard I Zon

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Leta S Steffen

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Louis M Kunkel

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Rosanna Beltre

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Timothy J Pusack

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Yi Zhou

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P2860

Titins: giant proteins in charge of muscle ultrastructure and elasticity

Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)

Zebrafish hox clusters and vertebrate genome evolution

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

The dystrophin associated protein complex in zebrafish.

Facilitated forward chemical genetics using a tagged triazine library and zebrafish embryo screening.

Small molecules that delay S phase suppress a zebrafish bmyb mutant.

Zebrafish comparative genomics and the origins of vertebrate chromosomes.

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene.

Muscular dystrophies: genes to pathogenesis.

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10.1186/1471-2164-8-79

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