Runx1 prevents wasting, myofibrillar disorganization, and autophagy of skeletal muscle. - Wikidata - awgldk - TriplyDB

Runx1 prevents wasting, myofibrillar disorganization, and autophagy of skeletal muscle.

Runx1 prevents wasting, myofibrillar disorganization, and autophagy of skeletal muscle.

http://www.wikidata.org/entity/Q42921219

about

The beneficial role of proteolysis in skeletal muscle growth and stress adaptation The effect of mild traumatic brain injury on peripheral nervous system pathology in wild-type mice and the G93A mutant mouse model of motor neuron disease Novel approach to meta-analysis of microarray datasets reveals muscle remodeling-related drug targets and biomarkers in Duchenne muscular dystrophy RUNX1 and its understudied role in breast cancer Systems analysis of transcriptional data provides insights into muscle's biological response to botulinum toxin.Runx family genes in a cartilaginous fish, the elephant shark (Callorhinchus milii).categoryCompare, an analytical tool based on feature annotations.Runx1 directly promotes proliferation of hair follicle stem cells and epithelial tumor formation in mouse skin.RNA expression analysis of passive transfer myasthenia supports extraocular muscle as a unique immunological environment.Dexamethasone-induced autophagy mediates muscle atrophy through mitochondrial clearance.Genome-wide mapping of Sox6 binding sites in skeletal muscle reveals both direct and indirect regulation of muscle terminal differentiation by Sox6.Genetic architecture of gene expression in ovine skeletal muscle Skeletal muscle atrophy and the E3 ubiquitin ligases MuRF1 and MAFbx/atrogin-1 The order of exercise during concurrent training for rehabilitation does not alter acute genetic expression, mitochondrial enzyme activity or improvements in muscle function Autophagy as a stress-response and quality-control mechanism: implications for cell injury and human disease Myotubularin family phosphatase ceMTM3 is required for muscle maintenance by preventing excessive autophagy in Caenorhabditis elegans.The Sick and the Weak: Neuropathies/Myopathies in the Critically Ill.Identification of genes that elicit disuse muscle atrophy via the transcription factors p50 and Bcl-3.Neurofibromin (Nf1) is required for skeletal muscle development AML1/RUNX1 phosphorylation by cyclin-dependent kinases regulates the degradation of AML1/RUNX1 by the anaphase-promoting complex Muscle-derived extracellular signal-regulated kinases 1 and 2 are required for the maintenance of adult myofibers and their neuromuscular junctions.RUNX transcription factors: association with pediatric asthma and modulated by maternal smoking.A transcriptional map of the impact of endurance exercise training on skeletal muscle phenotype Runx1 Transcription Factor Is Required for Myoblasts Proliferation during Muscle Regeneration Dual roles of autophagy in the survival of Caenorhabditis elegans during starvation.Rel A/p65 is required for cytokine-induced myotube atrophy.Stress-induced skeletal muscle Gadd45a expression reprograms myonuclei and causes muscle atrophy.Genomic-wide transcriptional profiling in primary myoblasts reveals Runx1-regulated genes in muscle regeneration.Gene profiling of embryonic skeletal muscle lacking type I ryanodine receptor Ca(2+) release channel.Failed reinnervation in aging skeletal muscle.Neuron specific reduction in CuZnSOD is not sufficient to initiate a full sarcopenia phenotype.The role of autophagy in sensitizing malignant glioma cells to radiation therapy.Defective Acetylcholine Receptor Subunit Switch Precedes Atrophy of Slow-Twitch Skeletal Muscle Fibers Lacking ERK1/2 Kinases in Soleus Muscle.Voluntary resistance wheel exercise from mid-life prevents sarcopenia and increases markers of mitochondrial function and autophagy in muscles of old male and female C57BL/6J mice.Transcriptional activation of TFEB/ZKSCAN3 target genes underlies enhanced autophagy in spinobulbar muscular atrophy.Autophagy in health and disease. 3. Involvement of autophagy in muscle atrophy.Mitochondrial pathways in sarcopenia of aging and disuse muscle atrophy.Transcriptional networks regulating the costamere, sarcomere, and other cytoskeletal structures in striated muscle.Deconvoluting the ontogeny of hematopoietic stem cells.Mechanisms of muscle growth and atrophy in mammals and Drosophila.

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Runx1 prevents wasting, myofibrillar disorganization, and autophagy of skeletal muscle.

http://www.wikidata.org/entity/Q42921219

description

2005 nî lūn-bûn

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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2005年论文

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2005年论文

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name

Runx1 prevents wasting, myofibrillar disorganization, and autophagy of skeletal muscle.

@en

Runx1 prevents wasting, myofibrillar disorganization, and autophagy of skeletal muscle.

@nl

type

label

Runx1 prevents wasting, myofibrillar disorganization, and autophagy of skeletal muscle.

@en

Runx1 prevents wasting, myofibrillar disorganization, and autophagy of skeletal muscle.

@nl

prefLabel

Runx1 prevents wasting, myofibrillar disorganization, and autophagy of skeletal muscle.

@en

Runx1 prevents wasting, myofibrillar disorganization, and autophagy of skeletal muscle.

@nl

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Genes & Development

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Runx1 prevents wasting, myofibrillar disorganization, and autophagy of skeletal muscle.

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P2093

Chris Blagden

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

Dan R Littman

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Ichiro Taniuchi

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Jihua Fan

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Scott J Nowak

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Steven J Burden

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Xiaoxia Wang

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P2860

A missense mutation in the alphaB-crystallin chaperone gene causes a desmin-related myopathy

A dysfunctional desmin mutation in a patient with severe generalized myopathy

Missense mutations in desmin associated with familial cardiac and skeletal myopathy

Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis

Signalling pathways that mediate skeletal muscle hypertrophy and atrophy

Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation

Mutations in myotilin cause myofibrillar myopathy

Core-binding factors in hematopoiesis and immune function

AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis

Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients

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10.1101/GAD.1318305

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14

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19

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16024660

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