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抗Mouse (Murine) 抗体:
抗Rat (Rattus) 抗体:
myocardin is an essential component of the regulatory pathway for myocardial differentiation
several transcription factors, that is SRF, myocardin, and GATA6, that induce the expression of SM-MHC in animal cap cells
YAP (显示 YAP1 抗体) negatively regulates differentiation of Vascular smooth muscle cells (VSMCs) derived from cardiovascular progenitor cell (CVPC) by decreasing transcription of myocardin in a NKX2.5 (显示 NKX2-5 抗体)-dependent manner.
Myocardin inhibits estrogen receptor alpha (显示 ESR1 抗体)-mediated proliferation of human breast cancer cells via regulating MicroRNA expression.
Key role for miR (显示 MLXIP 抗体)-214 in modulation of MEF2C (显示 MEF2C 抗体)-MYOCD-LMOD1 (显示 LMOD1 抗体) signaling.
Study demonstrates that myocardin indirectly down-regulates Cx43 (显示 GJA1 抗体) through its repressive action on miR (显示 MLXIP 抗体)-206 to regulate vascular smooth muscle cell phenotypic switch.
These results have revealed the roles for atrogin-1 (显示 FBXO32 抗体) in the regulation of smooth muscle contractility through enhancement of myocardin ubiquitylation/degradation and its transcriptional activity.
our study reveals that Ang II (显示 AGT 抗体) downregulates miR (显示 MLXIP 抗体)-145 to regulate Klf4 (显示 KLF4 抗体) and myocardin expression in HCASMCs under high glucose conditions. Ang II (显示 AGT 抗体) plays a critical role in the regulation of miR (显示 MLXIP 抗体)-145 under hyperglycemic conditions
Human expression data disclosed correlations of MYOCD with CAV1 in a majority of human tissues and in the heart, correlation with MKL2 (MRTF-B) was observed.
inhibition of GSK-3beta reduces myocardin transcriptional activity, suggesting a role for GSK-3beta in myocardin transcriptional activity and smooth muscle differentiation
STAT3 protein regulates vascular smooth muscle cell phenotypic switch by interaction with myocardin and SRF.
TMEM16A (显示 ANO1 抗体) and myocardin form a positive feedback loop that is disrupted by KLF5 (显示 KLF5 抗体) during Ang II (显示 AGT 抗体)-induced vascular remodeling.
Long noncoding RNAs cardiac autophagy inhibitory factor (lncRNA CAIF) regulates autophagy through controlling p53 (显示 TP53 抗体) and myocardin.
TAZ (显示 TAZ 抗体) and MyoC856 physically interact. SynergyTAZ and Myocardin (MyoC856), in regulating smooth muscle gene activation was observed in primary aortic vascular smooth muscle cells.
two MEF2 (显示 MEF2C 抗体) sites in the enhancer function cooperatively due to bridging of the MEF2C (显示 MEF2C 抗体)-bound sites by the SAP (显示 APCS 抗体) domain-containing co-activator protein myocardin
c-Myb (显示 MYB 抗体) regulates proliferation/differentiation of adventitial Sca1 (显示 ATXN1 抗体)+ vascular smooth muscle progenitor cells by transcriptional activation of myocardin.
Knock down of the serum response factor (SRF), which mediates many of the effects of myocardin, decreased cavin-1 but increased caveolin-1 and -2 mRNAs.
Cholesterol loading of vascular smooth muscle cells converts them to a macrophage-appearing state by downregulating the miR (显示 MLXIP 抗体)-143/145-myocardin axis.
Our data illustrate a novel mechanism that connects MRTF-A (显示 MKL1 抗体) dependent histone H3K4 methylation to HSC (显示 FUT1 抗体) activation.
DKK3 (显示 DKK3 抗体) induces stem cell differentiation into smooth muscle lineage via ATF6 (显示 ATF6 抗体) signaling and myocardin expression.
a moderate inhibition (e.g., normalization) of the activated MYOCD signaling in the diseased heart may be promising from a therapeutic point of view
MYOCD DeltaExon 11 may participate in modulating smooth muscle cell phenotype, potentially acting as a dominant-negative repressor of contraction-related genes.
Data show that forced myocd-A expression in the LVFW caused abnormal ECG.
Thrombin (显示 F2 抗体) stimulates swine smooth muscle cell differentiation from peripheral blood mononuclear cells via protease-activated receptor-1 (显示 F2R 抗体), RhoA (显示 RHOA 抗体), and myocardin.
This gene encodes a nuclear protein, which is expressed in heart, aorta, and in smooth muscle cell-containing tissues. It functions as a transcriptional co-activator of serum response factor (SRF) and modulates expression of cardiac and smooth muscle-specific SRF-target genes, and thus may play a crucial role in cardiogenesis and differentiation of the smooth muscle cell lineage. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
, SRF co-factor protein (cardiac and smooth muscle)
, SRF cofactor protein
, basic SAP coiled-coil transcription activator 2
, transcription factor myocardin