Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy - Test2 - elhamkhani - TriplyDB

Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

http://www.wikidata.org/entity/Q24621454

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Oxidative Stress-Mediated Skeletal Muscle Degeneration: Molecules, Mechanisms, and Therapies Nanopatterned Human iPSC-Based Model of a Dystrophin-Null Cardiomyopathic Phenotype Characterization of dystrophin deficient rats: a new model for Duchenne muscular dystrophy Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy Telomere shortening and metabolic compromise underlie dystrophic cardiomyopathy CRISPR-Cpf1 correction of muscular dystrophy mutations in human cardiomyocytes and mice.Dystrophic Cardiomyopathy-Potential Role of Calcium in Pathogenesis, Treatment and Novel Therapies Telomere biology and translational research.Transient delivery of modified mRNA encoding TERT rapidly extends telomeres in human cells.Toward computational cumulative biology by combining models of biological datasets.Reversibility of Defective Hematopoiesis Caused by Telomere Shortening in Telomerase Knockout Mice.Cardiomyocyte Regeneration in the mdx Mouse Model of Nonischemic Cardiomyopathy Prospect of gene therapy for cardiomyopathy in hereditary muscular dystrophy.Comparative Genomics of X-linked Muscular Dystrophies: The Golden Retriever Model Self-renewal and differentiation of muscle satellite cells are regulated by the Fas-associated death domain.Current Translational Research and Murine Models For Duchenne Muscular Dystrophy.Calpain-mediated proteolysis of tropomodulin isoforms leads to thin filament elongation in dystrophic skeletal muscle.Treatment of dystrophin cardiomyopathies.Evaluation of telomere length in human cardiac tissues using cardiac quantitative FISH.Telomere dynamics in a lizard with morph-specific reproductive investment and self-maintenance.Cardiac telomere length in heart development, function, and disease.Understanding the process of fibrosis in Duchenne muscular dystrophy.Dystrophin: The dead calm of a dogma.From innate to adaptive immune response in muscular dystrophies and skeletal muscle regeneration: the role of lymphocytes Long telomeres protect against age-dependent cardiac disease caused by NOTCH1 haploinsufficiency.Cardiomyocyte-Specific Telomere Shortening is a Distinct Signature of Heart Failure in Humans.Single Stem Cell Imaging and Analysis Reveals Telomere Length Differences in Diseased Human and Mouse Skeletal Muscles.Cardiac Aging - Benefits of Exercise, Nrf2 Activation and Antioxidant Signaling.Nicorandil, a Nitric Oxide Donor and ATP-Sensitive Potassium Channel Opener, Protects Against Dystrophin-Deficient Cardiomyopathy.Dystrophic Cardiomyopathy: Complex Pathobiological Processes to Generate Clinical Phenotype.Profile of Helen M. Blau.Short telomeres - A hallmark of heritable cardiomyopathies.Toward modeling the human nervous system in a dish: recent progress and outstanding challenges.Variants in TERT influencing telomere length are associated with paranoid schizophrenia risk.Humanizing the mdx mouse model of DMD: the long and the short of it.Mesenchymal stem cells confer resistance to doxorubicin-induced cardiac senescence by inhibiting microRNA-34a.Telomere shortening is a hallmark of genetic cardiomyopathies

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Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

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2013 nî lūn-bûn

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2013 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2013 թվականի օգոստոսին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

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Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

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Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

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Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

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Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

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Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

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Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

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Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

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Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

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Nature Cell Biology

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Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy

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Alan K Meeker

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Alexei Protopopov

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Daniel Bernstein

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Foteini Mourkioti

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Helen M Blau

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Jackie Kustan

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John W Day

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Maria Kost-Alimova

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Ming-Ming Zhao

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Peggy Kraft

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P2860

Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy

Wild-derived inbred mouse strains have short telomeres.

Evidence for cardiomyocyte renewal in humans

Short telomeres and stem cell exhaustion model Duchenne muscular dystrophy in mdx/mTR mice

Population frequencies of inherited neuromuscular diseases--a world survey

X chromosome-linked muscular dystrophy (mdx) in the mouse

Urinary 8-hydroxy-2'-deoxyguanosine as a biological marker of in vivo oxidative DNA damage

Telomere shortening and tumor formation by mouse cells lacking telomerase RNA

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

Essential role of mouse telomerase in highly proliferative organs

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10.1038/NCB2790

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