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SRF and its cofactor MYOCD (显示 MYOCD ELISA试剂盒) likely contribute to the hypertrophy of peripheral airway smooth muscle observed in equine asthmatic airways, while the remodeling of the central airways is more static or involves different transcription factors.
Equine primary fibroblasts were transformed by lentiviral transduction of equine myogenic differentiation 1 into fusion-competent myoblasts.
The results strongly suggest that the combination of MYCL plus MYOD1 may promote direct conversion of human fibroblasts into functional myoblasts that could potentially be used for regenerative therapy for muscle diseases and congenital muscle defects.
Analysis of the chromatin status of Cdkn1c (显示 CDKN1C ELISA试剂盒) promoter and KvDMR1 in unresponsive compared to responsive cell types showed that their differential responsiveness to the MyoD-dependent induction of the gene does not involve just their methylation status but, rather, the differential H3 lysine 9 dimethylation at KvDMR1.
Data show that MeCP2 promotes gastric cancer (GC) cell proliferation via FOXF1 (显示 FOXF1 ELISA试剂盒)-mediated Wnt5a (显示 WNT5A ELISA试剂盒)/beta-Catenin (显示 CTNNB1 ELISA试剂盒) signaling pathway, and suppresses GC cell apoptosis through MYOD1-mediated Caspase-3 (显示 CASP3 ELISA试剂盒) signaling pathway.
Our results on Pax7 and MyoD protein expression suggest that proliferation and differentiation of skeletal muscle stem cells are affected in ALS patients, and the myogenic processes cannot overcome the denervation-induced wasting.
The molecular pathogenesis of radiotherapy-induced muscle fibrosis involves the TGF-beta1 (显示 TGFB1 ELISA试剂盒) pathway and its repression of MyoD expression. Our results suggest a correlation between traditional swallow therapy /neuromuscular electrical stimulation combined therapy and the restoration of TGF-beta1 (显示 TGFB1 ELISA试剂盒)/MyoD homeostasis in cervical muscles.
Unmethylated MYOD1 gene is associated with chemoradiation resistance in Invasive Cervical Carcinoma.
We provide the first description of a human phenotype that appears to result from MYOD1 mutation. The presentation with Lethal fetal akinesia deformation sequence is consistent with a large body of data demonstrating that in the mouse, MyoD is a major controller of precursor cell commitment to the myogenic differentiation programme
these results suggest that sarcoma metastasis can be partially controlled through Pax7 (显示 PAX7 ELISA试剂盒)/MyoD-dependent activation of miR (显示 MLXIP ELISA试剂盒)-182 and provide insight into the role that myogenic transcription factors have in sarcoma progression
These observations demonstrated the first time that Wnt3a (显示 WNT3A ELISA试剂盒) can directly activate MyoD expression through targeting cis (显示 CISH ELISA试剂盒)-elements in the DE and the L fragment.
Studies indicate that MyoD occupies multiple promoters that induce the transcription of genes vital for establishing the myogenic fate and is also implicated as a mediator of many chromatin modifying enzymes for their recruitment to myogenic enhancers.
MyoD regulates the oxidative metabolic capacity of adult skeletal muscle;ChIP-seq analysis identified MyoD binding on the PGC (显示 PGC ELISA试剂盒)-1b, but not PGC (显示 PGC ELISA试剂盒)-1a, gene locus;MyoD cooperates with alternative NF-kappaB (显示 NFKB1 ELISA试剂盒) to regulate PGC (显示 PGC ELISA试剂盒)-1b transcription; MyoD and RelB (显示 RELB ELISA试剂盒) co-occupy many other genes involved in aerobic respiration
LSD1 (显示 KDM1A ELISA试剂盒) is required for the timely expression of MyoD in limb buds.
bn1 (显示 CCR6 ELISA试剂盒) expression is induced during myoblast differentiation, in a p38 MAP kinase (显示 MAPK14 ELISA试剂盒)- and MyoD- dependent manner. RNAi-mediated depletion of drebrin (显示 DBN1 ELISA试剂盒), or treatment with a chemical drebrin (显示 DBN1 ELISA试剂盒) inhibitor, resulted in a similar phenotype in myoblasts: defective differentiation, with low levels of early and late differentiation markers and inefficient production of myofibers.
Data show that MyoD and myogenin (显示 MYOG ELISA试剂盒) associate with distinct chromatin states.
lf5 ChIP-seq revealed that Klf5 (显示 KLF5 ELISA试剂盒) binding overlaps that of MyoD and Mef2 (显示 MEF2C ELISA试剂盒), and Klf5 (显示 KLF5 ELISA试剂盒) physically associates with both MyoD and Mef2 (显示 MEF2C ELISA试剂盒). In addition, MyoD recruitment was greatly reduced in the absence of Klf5 (显示 KLF5 ELISA试剂盒). These results indicate that Klf5 (显示 KLF5 ELISA试剂盒) is an essential regulator of skeletal muscle differentiation, acting in concert with myogenic transcription factors such as MyoD and Mef2 (显示 MEF2C ELISA试剂盒).
Results indicate the importance of integrating histone modifications and MyoD chromatin binding for coordinated gene activation and repression during myogenic differentiation.
Data suggest Tle3 plays role in regulation of MyoD1 function during myogenesis; up-regulation of Tle3 expression suppresses myogenesis; conversely, down-regulation of Tle3 expression promotes myogenesis/cell proliferation; Tle3 interferes with MyoD1 by disrupting association of basic helix-loop-helix domain of MyoD with E proteins. (Tle3 = transducin (显示 GNAT1 ELISA试剂盒)-like enhancer of split 3; MyoD1 = myogenic differentiation protein 1)
significant co-localization of binding sites for MyoD and Six proteins on over a thousand mouse genomic DNA regions, were found.
Through mutational analysis, we derive an optimally active phospho-mutant form of MyoD that has a dramatically enhanced ability to drive myogenic reprogramming in vivo. Mechanistically, this is achieved through increased protein stability and enhanced chromatin association. Therefore, multi-site phospho-regulation of class II bHLH proteins is conserved across cell lineages and germ layers, and manipulation of phosphorylat
results suggest that the miR (显示 MLXIP ELISA试剂盒)-29a-Tet1 pathway upregulates MyoD expression and conversely downregulates Cdk6 (显示 CDK6 ELISA试剂盒) expression
an Enhancer box and a binding site for a cooperative co-activator of MyoD are present in the promoter region of porcine PPARgamma (显示 PPARG ELISA试剂盒).
Of the eight adult pig tissue types that were tested, the expression of Myf5 (显示 MYF5 ELISA试剂盒) and MyoD1 was highest in the muscle tissue.
Single nucleotide polymorphisms in the MYOD1 and GDF8 (显示 MSTN ELISA试剂盒) genes are associated with genetic transcription during myogenesis in pigs.
Therefore, this study demonstrated that the different regulatory adipogenic roles of MSTN (显示 MSTN ELISA试剂盒) in ADSCs and MSCs act by differentially regulating PPARgamma (显示 PPARG ELISA试剂盒) and MyoD expression.
Therefore, the g.489C>T and g.1264C>A SNPs in MYOD1 may be meaningful DNA markers that can be used for improving important porcine economic traits.
The total expression profile of MyoD and Pax7 (显示 PAX7 ELISA试剂盒) genes suggests that higher muscularity in Pietrain pigs is associated with the presence of a greater number of active satellite stem cells compared to other breeds.
Exons and promoters are amplified and sequenced in the 5'UTR (显示 UTS2R ELISA试剂盒) region of this gene.
Relative MYOD1 expression was not different, but MYOG (显示 MYOG ELISA试剂盒) expression was higher in the (ligated-tube)crowded group embryos.
MYOD1 intron 1 DdeI polymorphism was not significantly associated with any meat quality traits tested
Transcript abundance for the muscle regulatory gene MYOD1 was lower in animals with more tender beef.
Bos taurus MYF5 (显示 MYF5 ELISA试剂盒) activates MYF5 (显示 MYF5 ELISA试剂盒) and MYOD1 expression in cultured fibroblasts.
results suggest that MyoD and Myf5 influence the MyHC isoform expression, although the effects are not decisive in specifying the phenotypes of adult muscles
n conclusion, hypoxia stimulates the proliferation of satellite cells and promotes their myogenic differentiation with MyoD playing an important role
Irxl1/Mkx (显示 MKX ELISA试剂盒) can repress myoD expression through direct binding to its promoter and may thus play a negative regulatory role in muscle differentiation.
Myod in turn up-regulates cdkn1c (显示 CDKN1C ELISA试剂盒), thereby providing a positive feedback loop that switches myogenic cells to terminal differentiation
Myf5 (显示 MYF5 ELISA试剂盒) and Myod function independently during cranial myogenesis.
This gene encodes a nuclear protein that belongs to the basic helix-loop-helix family of transcription factors and the myogenic factors subfamily. It regulates muscle cell differentiation by inducing cell cycle arrest, a prerequisite for myogenic initiation. The protein is also involved in muscle regeneration. It activates its own transcription which may stabilize commitment to myogenesis.
myogenic factor 3
, myogenic differentiation 1
, myoblast determination protein 1
, MYOD protein
, myogenic factor MyoD1
, MYOD1 homolog
, myoblast determination protein 1 homolog
, myogenic factor 1
, class C basic helix-loop-helix protein 1
, myogenic regulatory factor
, myogenic differenciation 1, transcription activator
, myogenic differenciation 1
, myoblast determination 1