Pages that link to "Q24621454"
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The following pages link to Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy (Q24621454):
Displaying 50 items.
- Oxidative Stress-Mediated Skeletal Muscle Degeneration: Molecules, Mechanisms, and Therapies (Q26769962) (← links)
- Nanopatterned Human iPSC-Based Model of a Dystrophin-Null Cardiomyopathic Phenotype (Q26779454) (← links)
- Characterization of dystrophin deficient rats: a new model for Duchenne muscular dystrophy (Q27335054) (← links)
- Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy (Q28084979) (← links)
- Telomere shortening and metabolic compromise underlie dystrophic cardiomyopathy (Q28315028) (← links)
- CRISPR-Cpf1 correction of muscular dystrophy mutations in human cardiomyocytes and mice. (Q33558467) (← links)
- Dystrophic Cardiomyopathy-Potential Role of Calcium in Pathogenesis, Treatment and Novel Therapies (Q33608478) (← links)
- Telomere biology and translational research. (Q33613946) (← links)
- Transient delivery of modified mRNA encoding TERT rapidly extends telomeres in human cells (Q34459333) (← links)
- Human telomere biology: A contributory and interactive factor in aging, disease risks, and protection (Q34509804) (← links)
- Toward computational cumulative biology by combining models of biological datasets (Q35452191) (← links)
- Reversibility of Defective Hematopoiesis Caused by Telomere Shortening in Telomerase Knockout Mice (Q35680392) (← links)
- Cardiomyocyte Regeneration in the mdx Mouse Model of Nonischemic Cardiomyopathy (Q35844422) (← links)
- Prospect of gene therapy for cardiomyopathy in hereditary muscular dystrophy (Q37021623) (← links)
- Comparative Genomics of X-linked Muscular Dystrophies: The Golden Retriever Model (Q37148808) (← links)
- Self-renewal and differentiation of muscle satellite cells are regulated by the Fas-associated death domain (Q37596364) (← links)
- Current Translational Research and Murine Models For Duchenne Muscular Dystrophy. (Q37610505) (← links)
- Calpain-mediated proteolysis of tropomodulin isoforms leads to thin filament elongation in dystrophic skeletal muscle (Q37635343) (← links)
- Treatment of dystrophin cardiomyopathies (Q38178061) (← links)
- Evaluation of telomere length in human cardiac tissues using cardiac quantitative FISH. (Q38372293) (← links)
- Telomere dynamics in a lizard with morph-specific reproductive investment and self-maintenance (Q38399415) (← links)
- Cardiac telomere length in heart development, function, and disease (Q38678302) (← links)
- Understanding the process of fibrosis in Duchenne muscular dystrophy. (Q39699112) (← links)
- Dystrophin: The dead calm of a dogma (Q40401861) (← links)
- From innate to adaptive immune response in muscular dystrophies and skeletal muscle regeneration: the role of lymphocytes (Q42071747) (← links)
- Long telomeres protect against age-dependent cardiac disease caused by NOTCH1 haploinsufficiency (Q42175550) (← links)
- Cardiomyocyte-Specific Telomere Shortening is a Distinct Signature of Heart Failure in Humans. (Q42373663) (← links)
- Single Stem Cell Imaging and Analysis Reveals Telomere Length Differences in Diseased Human and Mouse Skeletal Muscles. (Q42376231) (← links)
- Cardiac Aging - Benefits of Exercise, Nrf2 Activation and Antioxidant Signaling (Q46288550) (← links)
- Nicorandil, a Nitric Oxide Donor and ATP-Sensitive Potassium Channel Opener, Protects Against Dystrophin-Deficient Cardiomyopathy (Q46585617) (← links)
- Dystrophic Cardiomyopathy: Complex Pathobiological Processes to Generate Clinical Phenotype (Q49428049) (← links)
- Profile of Helen M. Blau (Q50097717) (← links)
- Low dystrophin levels in heart can delay heart failure in mdx mice. (Q51164233) (← links)
- Short telomeres - A hallmark of heritable cardiomyopathies (Q51767161) (← links)
- Toward modeling the human nervous system in a dish: recent progress and outstanding challenges. (Q52795421) (← links)
- Variants in TERT influencing telomere length are associated with paranoid schizophrenia risk. (Q53301331) (← links)
- Humanizing the mdx mouse model of DMD: the long and the short of it. (Q55010648) (← links)
- Mesenchymal stem cells confer resistance to doxorubicin-induced cardiac senescence by inhibiting microRNA-34a. (Q55312032) (← links)
- Cardiac ageing: extrinsic and intrinsic factors in cellular renewal and senescence (Q57165494) (← links)
- CRISPR Correction of Duchenne Muscular Dystrophy (Q58086427) (← links)
- Telomere shortening is a hallmark of genetic cardiomyopathies (Q58700280) (← links)
- Engineered DNA plasmid reduces immunity to dystrophin while improving muscle force in a model of gene therapy of Duchenne dystrophy (Q59353297) (← links)
- hnRNPA2 mediated acetylation reduces telomere length in response to mitochondrial dysfunction (Q59807501) (← links)
- Length-independent telomere damage drives post-mitotic cardiomyocyte senescence (Q64233922) (← links)
- Myoediting: Toward Prevention of Muscular Dystrophy by Therapeutic Genome Editing (Q88540277) (← links)
- PRDX1 and MTH1 cooperate to prevent ROS-mediated inhibition of telomerase (Q88720757) (← links)
- Targeting Age-Related Pathways in Heart Failure (Q89801635) (← links)
- Targeting cardiac fibrosis with engineered T cells (Q90069573) (← links)
- Pim1 Maintains Telomere Length in Mouse Cardiomyocytes by Inhibiting TGFβ Signaling (Q90353758) (← links)
- Mouse models for muscular dystrophies: an overview (Q90733720) (← links)