Pages that link to "Q28511899"

The following pages link to Megf10 regulates the progression of the satellite cell myogenic program (Q28511899):

Displaying 33 items.

• Muscle satellite cell heterogeneity and self-renewal (Q21131319) (← links)
• Multiple EGF-like-domains 10 (Q21985116) (← links)
• Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD) (Q24298002) (← links)
• Cysteine mutations cause defective tyrosine phosphorylation in MEGF10 myopathy (Q24318323) (← links)
• Pathophysiological concepts in the congenital myopathies: blurring the boundaries, sharpening the focus (Q28087567) (← links)
• Megf10 Is a Receptor for C1Q That Mediates Clearance of Apoptotic Cells by Astrocytes (Q28115888) (← links)
• Consequences of MEGF10 deficiency on myoblast function and Notch1 interactions. (Q30274553) (← links)
• Nap1-mediated actin remodeling is essential for mammalian myoblast fusion (Q30489945) (← links)
• p38-{gamma}-dependent gene silencing restricts entry into the myogenic differentiation program (Q33589771) (← links)
• Discovery and characterization of nutritionally regulated genes associated with muscle growth in Atlantic salmon (Q33642610) (← links)
• Satellite cells and the muscle stem cell niche (Q33816665) (← links)
• A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome. (Q33891096) (← links)
• Syndecan-3 and Notch cooperate in regulating adult myogenesis (Q34070002) (← links)
• TNF/p38α/polycomb signaling to Pax7 locus in satellite cells links inflammation to the epigenetic control of muscle regeneration. (Q34181742) (← links)
• 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. (Q34195544) (← links)
• Wnt/β-catenin controls follistatin signalling to regulate satellite cell myogenic potential. (Q35575301) (← links)
• Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores (Q35904556) (← links)
• Canonical and non-canonical Notch ligands (Q37785194) (← links)
• Transcriptional networks that regulate muscle stem cell function. (Q37787939) (← links)
• The origin and fate of muscle satellite cells. (Q37978773) (← links)
• Runx2 promotes both osteoblastogenesis and novel osteoclastogenic signals in ST2 mesenchymal progenitor cells. (Q38332288) (← links)
• The role of Delta-like 1 shedding in muscle cell self-renewal and differentiation. (Q39924099) (← links)
• Codependent activators direct myoblast-specific MyoD transcription (Q39929531) (← links)
• Protein hairy enhancer of split-1 expression during differentiation of muscle-derived stem cells into neuron-like cells (Q41773425) (← links)
• Silencing of drpr leads to muscle and brain degeneration in adult Drosophila (Q41852412) (← links)
• Identification of satellite cells from anole lizard skeletal muscle and demonstration of expanded musculoskeletal potential (Q47226233) (← links)
• Molecular evolutionary analysis of the duck MYOD gene family and its differential expression pattern in breast muscle development (Q48055858) (← links)
• MyoD and Myf6 gene expression patterns in skeletal muscle during embryonic and posthatch development in the domestic duck (Anas platyrhynchos domestica). (Q50712252) (← links)
• Adult-onset respiratory insufficiency, scoliosis, and distal joint hyperlaxity in patients with multiminicore disease due to novel Megf10 mutations (Q51553063) (← links)
• Platelet endothelial aggregation receptor-1 (PEAR1) is involved in C2C12 myoblast differentiation (Q52431020) (← links)
• Pax3 cooperates with Ldb1 to direct local chromosome architecture during myogenic lineage specification (Q64283883) (← links)
• The impact of Megf10/Drpr gain-of-function on muscle development in Drosophila (Q91894815) (← links)
• Genomic inbreeding trends, influential sire lines and selection in the global Thoroughbred horse population (Q92712258) (← links)