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Showing 1 to 9 of 9 for “"Myocardin"”.

  1. Roles of Myocardin-Related Transcription Factors in Muscle and Brain

    … between Serum response Factor (SRF) and its Myocardin Related Transcription Factor (MRTF) coactivators during development. I present here my studies on the functions of MRTFs during brain and muscle development. First, I show that MRTF-A and -B redundantly control neuronal migration and …

    utswmed Repository record for Roles of Myocardin-Related Transcription Factors in Muscle and Brain (opens in a new tab)

  2. Investigating the Impact of K+ Channel Expression on Mechanosurveillance of Disseminated Cancer Cells

    … regulators of cellular stiffness downstream of myocardin related transcription factor A (MRTFA). In primary pericytes, KCNMB1 knockdown increased cellular stiffness, which is consistent with the role of potassium efflux in promoting relaxation during excitation-contraction coupling. In a …

    uic

  3. Identification of RBPMS as a smooth muscle master splicing regulator via association of its gene with super-enhancers

    … as well as the key SMC transcription factor Myocardin. Structure-function analyses revealed that the two major RBPMS isoforms (RBPMS-A and B) have differential activity, and that dimerization and RBPMS C- terminus are essential to RBPMS splicing activity. Yet, RBPMS RRM was insufficient for …

    cambridge Repository record for Identification of RBPMS as a smooth muscle master splicing regulator via association of its gene with super-enhancers (opens in a new tab)

  4. Serum response factor-dependent regulation of smooth muscle gene transcription

    … I found that SRF transcription cofactor myocardin acts together with SRF to regulate expression of microRNAs-143 and 145 but not microRNAs-133a and 133b. SRF can, thus, further modulate gene expression through post-transcriptional mechanisms via changes in microRNA levels. Overall my …

    iupui Repository record for Serum response factor-dependent regulation of smooth muscle gene transcription (opens in a new tab)

  5. TARGETING FIBROBLAST-MATRIX INTERACTIONS TO TREAT VOCAL FOLD SCARRING

    … VF myofibroblasts to fibroblasts to identify the myocardin related transcription factor A (MRTF-A)/serum response factor (SRF) signaling axis as required for VF myofibroblast activation. We demonstrate the therapeutic potential of MRTF-A/SRF inhibition across in vitro and in vivo models of VF …

    penn Repository record for TARGETING FIBROBLAST-MATRIX INTERACTIONS TO TREAT VOCAL FOLD SCARRING (opens in a new tab)

  6. The Effect of Microenvironmental Cues on Adipocyte Cytoskeletal Remodeling

    … actin stress fiber formation facilitated by myocardin-related transcription factor A (MRTF-A/MKL1) nuclear translocation. The second aim explores the effects of mechanical unloading (simulated microgravity) on key adipocyte functions and actin cytoskeletal remodeling. This study demonstrated …

    temple Repository record for The Effect of Microenvironmental Cues on Adipocyte Cytoskeletal Remodeling (opens in a new tab)

  7. Effects of The Acta2 R258C Mutation On Vascular Smooth Muscle Cell Phenotype and Properties

    … to wildtype SMCs and have predominantly nuclear Myocardin-Related Transcription Factor A (MRTF-A) localization. However, ultracentrifugation assays showed large unpolymerized actin fractions, suggesting that the filaments are brittle. In contrast, <em>Acta2<sup>+/- R258C TG</sup></em> SMCs are …

    uthsc Repository record for Effects of The Acta2 R258C Mutation On Vascular Smooth Muscle Cell Phenotype and Properties (opens in a new tab)

  8. Characterizing PIAS1 Function During Embryogenesis and Lung Cancer Progression

    … cooperate with the cardiac transcription factors Myocardin and GATA-4 in promoting cardiac differentiation. Because Pias1 loss primarily affects erythrogenesis and vascular development of the YS, we also tested how conditional Pias1 deletion in endothelial cells of the YS would affect …

    utswmed Repository record for Characterizing PIAS1 Function During Embryogenesis and Lung Cancer Progression (opens in a new tab)

  9. Investigating the Mechanisms Underlying the Heterogeneous VSMC Contribution to Vascular Disease

    In healthy blood vessels, vascular smooth muscle cells (VSMCs) exist in a contractile, quiescent state but upon vascular insult can switch phenotype to activate proliferation, migration and remodelling of the extracellular matrix. Phenotypically switched VSMCs contribute most cells within …

    cambridge Repository record for Investigating the Mechanisms Underlying the Heterogeneous VSMC Contribution to Vascular Disease (opens in a new tab)