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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

Myogenic factor 5

Top mentioned proteins: MyoD, Myogenin, MRF4, CAN, Actin
Papers using Myf5 antibodies
The del22q11.2 candidate gene Tbx1 controls regional outflow tract identity and coronary artery patterning.
Sham Mai Har, In PLoS ONE, 2007
... A17-Myf5-nlacZ-T55 (T55) and Mlc1v-nlacZ-24 transgenic mice have been previously ...
Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation
Brunelli Silvia et al., In The Journal of Cell Biology, 2003
... 3-phosphate dehydrogenase (GAPDH) mAb from Biogenesis; anti-MyoD mAb from DakoCytomation; anti-PCNA mAb, anti-MyoD, anti-Mef2A, and anti-Myf5 pAbs from Santa Cruz Biotechnology, Inc.; antisarcomeric myosin MF20, ...
Papers on Myf5
Increased Expression of Beige/Brown Adipose Markers from Host and Breast Cancer Cells Influence Xenograft Formation in Mice.
Pervin et al., Los Angeles, United States. In Mol Cancer Res, Jan 2016
In addition to uncoupling protein-1 (UCP1) that is exclusively expressed in beige/brown adipocytes, gene expression for classical brown (MYF5, EVA1, and OPLAH) as well as beige (CD137/TNFRSF9 and TBX1) adipocyte markers was also elevated in the xenografts.
Generation and Characterization of a MYF5 Reporter Human iPS Cell Line Using CRISPR/Cas9 Mediated Homologous Recombination.
Darabi et al., Houston, United States. In Sci Rep, Dec 2015
Therefore, this study was aimed to generate a knock-in reporter human iPS cell line for MYF5, as an early myogenic specification gene, to allow prospective identification and purification of myogenic progenitors from human iPS cells.
Early myogenic responses to acute exercise before and after resistance training in young men.
Cameron-Smith et al., Melbourne, Australia. In Physiol Rep, Sep 2015
Increased mRNA expression of PAX7 (threefold), NCAM (threefold), MYF5 (threefold), MYOD (threefold) and MYOGENIN (twofold) was observed 3 h after the acute resistance exercise test, both pre and posttraining.
A population of Pax7-expressing muscle progenitor cells show differential responses to muscle injury dependent on developmental stage and injury extent.
Knight et al., London, United Kingdom. In Front Aging Neurosci, 2014
We found that both small focal injuries, and large injuries affecting the entire myotome, lead to expression of myf5 and myogenin, which was prolonged in older larvae, indicating a slower process of regeneration.
Comparative analysis of microRNA expression in mouse and human brown adipose tissue.
Russell et al., Australia. In Bmc Genomics, 2014
Of these 25 miRNAs, miR-20a was predicted to target MYF5 and PPARγ, two important genes involved in brown adipogenesis, as well as BMP2 and BMPR2, genes involved in white adipogenesis.
PTEN loss in the Myf5 lineage redistributes body fat and reveals subsets of white adipocytes that arise from Myf5 precursors.
Guertin et al., Worcester, United States. In Cell Metab, 2012
By lineage tracing and gene expression analysis in mice, we provide evidence that mesenchymal precursors expressing Myf5--which are thought to give rise only to brown adipocytes and skeletal muscle--also give rise to a subset of white adipocytes.
Beige adipocytes are a distinct type of thermogenic fat cell in mouse and human.
Spiegelman et al., Boston, United States. In Cell, 2012
Recent data suggest that there are two distinct types of brown fat: classical brown fat derived from a myf-5 cellular lineage and UCP1-positive cells that emerge in white fat from a non-myf-5 lineage.
Muscle satellite cells are primed for myogenesis but maintain quiescence with sequestration of Myf5 mRNA targeted by microRNA-31 in mRNP granules.
Buckingham et al., Paris, France. In Cell Stem Cell, 2012
Myf5 mRNA, together with microRNA-31, which regulates its translation.
Musculin and TCF21 coordinate the maintenance of myogenic regulatory factor expression levels during mouse craniofacial development.
Carvajal et al., London, United Kingdom. In Development, 2012
Data show that correct levels of expression of Myf5 and MyoD during mouse craniofacial development result from activation by musculin and TCF21 through direct binding to specific enhancers.
Leucine limitation regulates myf5 and myoD expression and inhibits myoblast differentiation.
Dardevet et al., Clermont-Ferrand, France. In Exp Cell Res, 2012
Upregulation of myf5 mRNA and a decrease of myoD protein level during leucine starvation.
Efficient in vitro myogenic reprogramming of human primary mesenchymal stem cells and endothelial cells by Myf5.
Vigon et al., Paris, France. In Biol Cell, 2011
results are the first demonstration of a myogenic conversion of human mesenchymal and endothelial cells by Myf5
Follistatin improves skeletal muscle healing after injury and disease through an interaction with muscle regeneration, angiogenesis, and fibrosis.
Huard et al., Pittsburgh, United States. In Am J Pathol, 2011
follistatin stimulated myoblasts to express MyoD, Myf5, and myogenin, which are myogenic transcription factors that promote myogenic differentiation
Many routes to the same destination: lessons from skeletal muscle development.
Sweetman et al., Loughborough, United Kingdom. In Reproduction, 2011
Recent findings show that a core transcriptional network, initiated by the myogenic regulatory factors (MRFs; MYF5, MYOD, myogenin and MRF4), is activated by separate populations of cells in embryos in response to various signalling pathways.
Adaptive processes in skeletal muscle: molecular regulators and genetic influences.
Rittweger et al., United Kingdom. In J Musculoskelet Neuronal Interact, 2006
Among others, the insulin-like growth factors, calcineurin, desmin, myf5, mrf4, MyoD and myogenin have been identified as positive regulators of muscle size, while TNF-alpha, myostatin and components of the ubiquitin pathway have been recognized as regulators of muscle wasting.
Limb muscle development.
Brand-Saberi et al., Freiburg, Germany. In Int J Dev Biol, 2001
This is achieved by the expression of the transcription factors Pax3, Pax7 and myf5.
Regulation and functions of myogenic regulatory factors in lower vertebrates.
Rescan, Rennes, France. In Comp Biochem Physiol B Biochem Mol Biol, 2001
Four members, MyoD, myogenin, myf5 and MRF4/herculin/myf6, have been identified in higher vertebrates and have been shown to exhibit distinct but overlapping functions.
Genetic and epigenetic control of muscle development in vertebrates.
Christ et al., Freiburg, Germany. In Cell Tissue Res, 1999
Markers of myogenic specification are myf5, myoD, mrf4 and myogenin, which encode transcription factors of the basic helix-loop-helix family.
Muscle progenitor cells failing to respond to positional cues adopt non-myogenic fates in myf-5 null mice.
Buckingham et al., Paris, France. In Nature, 1996
Mice that have mutations in both myogenic transcription factors Myf-5 and MyoD totally lack skeletal muscle fibres and their precursor myoblasts, whereas with either mutation alone, muscle is present.
Growth hormone and the insulin-like growth factor system in myogenesis.
Coolican et al., Syracuse, United States. In Endocr Rev, 1996
As levels of myogenin mRNA rise, those of myf-5 mRNA (the only other member of the MyoD family expressed significantly in L6 myoblasts) fall dramatically, although myf-5 expression is required for the initial elevation of myogenin.
Transcriptional activation domain of the muscle-specific gene-regulatory protein myf5.
Arnold et al., Hamburg, Germany. In Nature, 1990
The human muscle determination factor myf5, like MyoD and other members of the family of skeletal muscle-specific regulatory proteins, contains a highly conserved putative helix-loop-helix domain.
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