Megf10 regulates the progression of the satellite cell myogenic program
about
Muscle satellite cell heterogeneity and self-renewalMutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)Cysteine mutations cause defective tyrosine phosphorylation in MEGF10 myopathyPathophysiological concepts in the congenital myopathies: blurring the boundaries, sharpening the focusMegf10 Is a Receptor for C1Q That Mediates Clearance of Apoptotic Cells by AstrocytesConsequences of MEGF10 deficiency on myoblast function and Notch1 interactions.Nap1-mediated actin remodeling is essential for mammalian myoblast fusion.p38-{gamma}-dependent gene silencing restricts entry into the myogenic differentiation program.Discovery and characterization of nutritionally regulated genes associated with muscle growth in Atlantic salmon.Satellite cells and the muscle stem cell nicheA defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome.Syndecan-3 and Notch cooperate in regulating adult myogenesisTNF/p38α/polycomb signaling to Pax7 locus in satellite cells links inflammation to the epigenetic control of muscle regeneration.Satellite cell heterogeneity with respect to expression of MyoD, myogenin, Dlk1 and c-Met in human skeletal muscle: application to a cohort of power lifters and sedentary men.Wnt/β-catenin controls follistatin signalling to regulate satellite cell myogenic potential.Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicoresCanonical and non-canonical Notch ligands.Transcriptional networks that regulate muscle stem cell function.The origin and fate of muscle satellite cells.Runx2 promotes both osteoblastogenesis and novel osteoclastogenic signals in ST2 mesenchymal progenitor cells.The role of Delta-like 1 shedding in muscle cell self-renewal and differentiation.Codependent activators direct myoblast-specific MyoD transcription.Protein hairy enhancer of split-1 expression during differentiation of muscle-derived stem cells into neuron-like cells.Silencing of drpr leads to muscle and brain degeneration in adult Drosophila.Molecular evolutionary analysis of the duck MYOD gene family and its differential expression pattern in breast muscle development.MyoD and Myf6 gene expression patterns in skeletal muscle during embryonic and posthatch development in the domestic duck (Anas platyrhynchos domestica).Adult-onset respiratory insufficiency, scoliosis, and distal joint hyperlaxity in patients with multiminicore disease due to novel Megf10 mutations.
P2860
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P2860
Megf10 regulates the progression of the satellite cell myogenic program
description
2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2007
@ast
im Dezember 2007 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
@en
vedecký článok (publikovaný 2007/12/03)
@sk
vědecký článek publikovaný v roce 2007
@cs
wetenschappelijk artikel (gepubliceerd op 2007/12/03)
@nl
наукова стаття, опублікована в грудні 2007
@uk
مقالة علمية (نشرت في 3-12-2007)
@ar
name
Megf10 regulates the progression of the satellite cell myogenic program
@ast
Megf10 regulates the progression of the satellite cell myogenic program
@en
Megf10 regulates the progression of the satellite cell myogenic program
@nl
type
label
Megf10 regulates the progression of the satellite cell myogenic program
@ast
Megf10 regulates the progression of the satellite cell myogenic program
@en
Megf10 regulates the progression of the satellite cell myogenic program
@nl
prefLabel
Megf10 regulates the progression of the satellite cell myogenic program
@ast
Megf10 regulates the progression of the satellite cell myogenic program
@en
Megf10 regulates the progression of the satellite cell myogenic program
@nl
P2093
P2860
P356
P1476
Megf10 regulates the progression of the satellite cell myogenic program
@en
P2093
Chet E. Holterman
Fabien Le Grand
Michael A. Rudnicki
Patrick Seale
Shihuan Kuang
P2860
P304
P356
10.1083/JCB.200709083
P407
P577
2007-12-03T00:00:00Z