Short telomeres and stem cell exhaustion model Duchenne muscular dystrophy in mdx/mTR mice - Test2 - elhamkhani - TriplyDB

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

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

http://www.wikidata.org/entity/Q24633931

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Increased muscle stress-sensitivity induced by selenoprotein N inactivation in mouse: a mammalian model for SEPN1-related myopathy Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy The telomere syndromes Muscle Satellite Cells: Exploring the Basic Biology to Rule Them Oxidative Stress-Mediated Skeletal Muscle Degeneration: Molecules, Mechanisms, and Therapies Decoding the stem cell quiescence cycle--lessons from yeast for regenerative biology A muscle stem cell for every muscle: variability of satellite cell biology among different muscle groups Tissue-specific stem cells: lessons from the skeletal muscle satellite cell A comparative study of N-glycolylneuraminic acid (Neu5Gc) and cytotoxic T cell (CT) carbohydrate expression in normal and dystrophin-deficient dog and human skeletal muscle Characterization of dystrophin deficient rats: a new model for Duchenne muscular dystrophy Adult stem cell and mesenchymal progenitor theories of aging.Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy Loss of a single allele for Ku80 leads to progenitor dysfunction and accelerated aging in skeletal muscle Lin28: primal regulator of growth and metabolism in stem cells Telomere shortening and metabolic compromise underlie dystrophic cardiomyopathy Donor satellite cell engraftment is significantly augmented when the host niche is preserved and endogenous satellite cells are incapacitated A mouse model for dominant collagen VI disorders: heterozygous deletion of Col6a3 Exon 16 Combinations of Kinase Inhibitors Protecting Myoblasts against Hypoxia P2RX7 purinoceptor: a therapeutic target for ameliorating the symptoms of duchenne muscular dystrophy The mdx mouse model as a surrogate for Duchenne muscular dystrophy Gastrocnemius medialis muscle architecture and physiological cross sectional area in adult males with Duchenne muscular dystrophy.CD34 promotes satellite cell motility and entry into proliferation to facilitate efficient skeletal muscle regeneration.Reduced IGF signaling prevents muscle cell death in a Caenorhabditis elegans model of muscular dystrophy Biomimetic engineered muscle with capacity for vascular integration and functional maturation in vivo Biochemical and Functional Comparisons of mdx and Sgcg(-/-) Muscular Dystrophy Mouse Models.DNA damage, somatic aneuploidy, and malignant sarcoma susceptibility in muscular dystrophies.Notch signaling deficiency underlies age-dependent depletion of satellite cells in muscular dystrophy.Rapid depletion of muscle progenitor cells in dystrophic mdx/utrophin-/- mice.Pharmacologic management of Duchenne muscular dystrophy: target identification and preclinical trials Stem cell aging: mechanisms, regulators and therapeutic opportunities.PKC theta ablation improves healing in a mouse model of muscular dystrophy.BAF60 A, B, and Cs of muscle determination and renewal.Highlights of mechanistic and therapeutic cachexia and sarcopenia research 2010 to 2012 and their relevance for cardiology.Skeletal muscle satellite cells: mediators of muscle growth during development and implications for developmental disorders.Rejuvenation of the muscle stem cell population restores strength to injured aged muscles.Transient delivery of modified mRNA encoding TERT rapidly extends telomeres in human cells.Grafting of a single donor myofibre promotes hypertrophy in dystrophic mouse muscle Gene replacement therapies for duchenne muscular dystrophy using adeno-associated viral vectors.Physical activity and telomere biology: exploring the link with aging-related disease prevention.Coaxing stem cells for skeletal muscle repair

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

http://www.wikidata.org/entity/Q24633931

description

2010 nî lūn-bûn

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2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Short telomeres and stem cell ...... ular dystrophy in mdx/mTR mice

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Short telomeres and stem cell ...... ular dystrophy in mdx/mTR mice

@en

Short telomeres and stem cell ...... ular dystrophy in mdx/mTR mice

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type

label

Short telomeres and stem cell ...... ular dystrophy in mdx/mTR mice

@ast

Short telomeres and stem cell ...... ular dystrophy in mdx/mTR mice

@en

Short telomeres and stem cell ...... ular dystrophy in mdx/mTR mice

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prefLabel

Short telomeres and stem cell ...... ular dystrophy in mdx/mTR mice

@ast

Short telomeres and stem cell ...... ular dystrophy in mdx/mTR mice

@en

Short telomeres and stem cell ...... ular dystrophy in mdx/mTR mice

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J.CELL.2010.11.039

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Short telomeres and stem cell ...... ular dystrophy in mdx/mTR mice

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P2860

Identification of a specific telomere terminal transferase activity in Tetrahymena extracts

Essential role of limiting telomeres in the pathogenesis of Werner syndrome

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

Rejuvenation of aged progenitor cells by exposure to a young systemic environment

Telomere shortening and tumor formation by mouse cells lacking telomerase RNA

How shelterin protects mammalian telomeres

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

Increased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis

Essential role of mouse telomerase in highly proliferative organs

Asymmetric self-renewal and commitment of satellite stem cells in muscle.

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