Identification of the Syrian hamster cardiomyopathy gene. - Wikidata - awgldk - TriplyDB

Identification of the Syrian hamster cardiomyopathy gene.

Identification of the Syrian hamster cardiomyopathy gene.

http://www.wikidata.org/entity/Q34421233

about

Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cells Many roads lead to a broken heart: the genetics of dilated cardiomyopathy.Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations Disease rescue and increased lifespan in a model of cardiomyopathy and muscular dystrophy by combined AAV treatments Expression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex Sarcoglycan isoforms in skeletal muscle rAAV vector-mediated sarcogylcan gene transfer in a hamster model for limb girdle muscular dystrophy A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease.Canine candidate genes for dilated cardiomyopathy: annotation of and polymorphic markers for 14 genes.A myocardium tropic adeno-associated virus (AAV) evolved by DNA shuffling and in vivo selection.Making sense of the limb-girdle muscular dystrophies.Full functional rescue of a complete muscle (TA) in dystrophic hamsters by adeno-associated virus vector-directed gene therapy.Sarcoglycans in muscular dystrophy.Rescue of hereditary form of dilated cardiomyopathy by rAAV-mediated somatic gene therapy: amelioration of morphological findings, sarcolemmal permeability, cardiac performances, and the prognosis of TO-2 hamsters.Translocation and cleavage of myocardial dystrophin as a common pathway to advanced heart failure: a scheme for the progression of cardiac dysfunction Worsening of cardiomyopathy using deflazacort in an animal model rescued by gene therapy.Animal models of cardiac disease: potential usefulness for studying health effects of inhaled particles.SERCA2a gene therapy can improve symptomatic heart failure in δ-sarcoglycan-deficient animals.The molecular neuropathology of the muscular dystrophies: a review and update.A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C.Does delta-sarcoglycan-associated autosomal-dominant cardiomyopathy exist?Sequencing, annotation and analysis of the Syrian hamster (Mesocricetus auratus) transcriptome.A novel locus for dilated cardiomyopathy maps to canine chromosome 8 Molecular mechanisms of inherited cardiomyopathies.Distinct pathophysiological mechanisms of cardiomyopathy in hearts lacking dystrophin or the sarcoglycan complex.Alpha-linolenic acid-enriched diet prevents myocardial damage and expands longevity in cardiomyopathic hamsters Ca2+/calmodulin-dependent kinase IIdelta causes heart failure by accumulation of p53 in dilated cardiomyopathy Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders: Thematic Review Series: Genetics of Human Lipid Diseases.Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamster The muscular dystrophies: from genes to therapies.Enhanced Na+/H+ exchange activity contributes to the pathogenesis of muscular dystrophy via involvement of P2 receptors.A delta-sarcoglycan gene polymorphism as a risk factor for hypertrophic cardiomyopathy.Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex.Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin.A novel mechanism of myocyte degeneration involving the Ca2+-permeable growth factor-regulated channel.Dilated cardiomyopathy: a tale of cytoskeletal proteins and beyond.Genetics of dilated cardiomyopathy.Dilated cardiomyopathy mutations in δ-sarcoglycan exert a dominant-negative effect on cardiac myocyte mechanical stability.

P2860

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P2860

Identification of the Syrian hamster cardiomyopathy gene.

http://www.wikidata.org/entity/Q34421233

description

1997 nî lūn-bûn

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1997 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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1997 թվականի ապրիլին հրատարակված գիտական հոդված

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1997年の論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年論文

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1997年论文

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Identification of the Syrian hamster cardiomyopathy gene.

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Identification of the Syrian hamster cardiomyopathy gene.

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Identification of the Syrian hamster cardiomyopathy gene.

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Identification of the Syrian hamster cardiomyopathy gene.

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Identification of the Syrian hamster cardiomyopathy gene.

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Identification of the Syrian hamster cardiomyopathy gene.

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Identification of the Syrian hamster cardiomyopathy gene.

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Identification of the Syrian hamster cardiomyopathy gene.

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Identification of the Syrian hamster cardiomyopathy gene.

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Identification of the Syrian hamster cardiomyopathy gene

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