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

Myeloid-associated differentiation marker

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Top mentioned proteins: CAN, ACID, HAD, OUT, fibrillin-1
Papers on MUG
Highly specific and rapid immuno-fluorescent visualization and detection of E. coli O104:H4 with protein-A coated magnetic beads based LST-MUG assay.
Dweik et al., Jefferson City, United States. In J Microbiol Methods, Aug 2015
The magnetic bead complex was added to the LST-MUG (lauryl sulfate tryptose-4-methylumbelliferyl-β-D-glucuronide), a signaling reporter.
A red fluorescent protein (DsRED) from Discosoma sp. as a reporter for gene expression in walnut somatic embryos.
Leslie et al., Davis, United States. In Plant Cell Rep, May 2015
This method is more reliable than GFP and provides more efficient embryo selection than β-glucuronidase assays (GUS, MUG).
A meta-analysis of gene expression signatures of blood pressure and hypertension.
Levy et al., Bethesda, United States. In Plos Genet, Mar 2015
Of note, rs3184504 in SH2B3, which was also reported in GWAS to be associated with BP, was found to be a trans regulator of the expression of 6 of the transcripts we found to be associated with BP (FOS, MYADM, PP1R15A, TAGAP, S100A10, and FGBP2).
A structural determinant in the uracil DNA glycosylase superfamily for the removal of uracil from adenine/uracil base pairs.
Cao et al., United States. In Nucleic Acids Res, 2015
Family 2 mismatch-specific uracil DNA glycosylase (MUG) from Escherichia coli is known to exhibit glycosylase activity on three mismatched base pairs, T/U, G/U and C/U.
Facile high-throughput forward chemical genetic screening by in situ monitoring of glucuronidase-based reporter gene expression in Arabidopsis thaliana.
Kombrink et al., Köln, Germany. In Front Plant Sci, 2014
Here, we describe a facile forward chemical screening methodology for intact Arabidopsis seedlings harboring the β-glucuronidase (GUS) reporter by directly quantifying GUS activity in situ with 4-methylumbelliferyl-β-D-glucuronide (4-MUG) as substrate.
Isolation of aerobic cultivable cellulolytic bacteria from different regions of the gastrointestinal tract of giant land snail Achatina fulica.
Frasés et al., Rio de Janeiro, Brazil. In Front Microbiol, 2014
The overall enzymatic repertoire of the isolated strains was investigated by enzymatic plate assays, containing the following substrates: powdered sugarcane bagasse, carboxymethylcellulose (CMC), p-nitrophenyl-β-D-glucopyranoside (pNPG), p-nitrophenyl-β-D-cellobioside (pNPC), 4-methylumbelliferyl-β-D-glucopyranoside (MUG), 4-methylumbelliferyl-β-D-cellobioside (MUC), and 4-methylumbelliferyl-β-D-xylopyranoside (MUX).
Different Proportions of Huangqi (Radix Astragali Mongolici) and Honghua (Flos Carthami) Injection on α-Glucosidase and α-Amylase Activities.
Banbury et al., Taiyuan, China. In Evid Based Complement Alternat Med, 2014
The assay for potential α-glucosidase inhibitors was based on the hydrolysis of 4-methylumbelliferyl-α-D-glucopyranoside (4-MUG).
Coelomocyte-derived fluorescence and DNA markers of composting earthworm species.
Plytycz et al., Częstochowa, Poland. In J Exp Zool A Ecol Genet Physiol, 2014
Coelomic fluid of E. andrei exhibits a very distinct spectra of MUG fluorophore which are absent in D. veneta and in the majority of E. fetida, while some E. fetida possess MUG-like fluorophore.
Histone deacetylase inhibitors as potential therapeutic approaches for chordoma: an immunohistochemical and functional analysis.
Liegl et al., Graz, Austria. In J Orthop Res, 2013
Pan-HDAC-inhibitors Vorinostat (SAHA), Panobinostat (LBH-589), and Belinostat (PXD101) were tested for their efficacy in the chordoma cell line MUG-Chor1 via Western blot, cell cycle analysis, caspase 3/7 activity (MUG-Chor1, UCh-1), cleaved caspase-3, and PARP cleavage.
Resolving tumor heterogeneity: genes involved in chordoma cell development identified by low-template analysis of morphologically distinct cells.
Rinner et al., Graz, Austria. In Plos One, 2013
UCHL3, coding for an ubiquitin hydrolase, was found to be over-expressed in the large physaliferous cell phenotype of MUG-Chor1 (18.7-fold) and U-CH1 (3.7-fold) cells.
Development of a calcium phosphate nanocomposite for fast fluorogenic detection of bacteria.
Cortés et al., Bejucal, Cuba. In Molecules, 2013
The composite was obtained by combining calcium phosphate nanoparticles (Ca:P ratio, 1.33:1) with a nutritive mixture of protein hydrolysates and carbon sources, which promote fast bacterial multiplication, and the fluorogenic substrate 4-methylumbellipheryl-β-D-glucuronide (MUG).
A divergent Artiodactyl MYADM-like repeat is associated with erythrocyte traits and weight of lamb weaned in domestic sheep.
White et al., Pullman, United States. In Plos One, 2012
We observed a large (>50 kb) variant haplotype sequence containing a full-length divergent artiodactyl MYADM-like repeat in strong linkage disequilibrium with the associated SNP.
The novel myxofibrosarcoma cell line MUG-Myx1 expresses a tumourigenic stem-like cell population with high aldehyde dehydrogenase 1 activity.
Rinner et al., Graz, Austria. In Bmc Cancer, 2012
METHODS: After the establishment of the novel myxofibrosarcoma cell lines MUG-Myx1, cells were characterized using short tandem repeat (STR), copy number variation (CNV), and genotype/loss-of-heterozygosity (LOH) analyses.
MYADM regulates Rac1 targeting to ordered membranes required for cell spreading and migration.
Alonso et al., Madrid, Spain. In Mol Biol Cell, 2011
Myeloid-associated differentiation marker (MYADM) regulates Rac1 targeting to ordered membranes required for cell spreading and migration.
The enigmatic thymine DNA glycosylase.
Schär et al., Basel, Switzerland. In Dna Repair (amst), 2007
TDG turned out to be the founding member of a newly emerging family of mismatch-directed uracil-DNA glycosylases, the MUG proteins, that act on a comparably broad spectrum of base lesion including G.U as the common, most efficiently processed substrate.
Characterization of the mouse myeloid-associated differentiation marker (MYADM) gene: promoter analysis and protein localization.
Jönsson et al., Malmö, Sweden. In Mol Biol Rep, 2005
Functional analysis of the promotor region of the MYADM gene.
Cloning of human myeloid-associated differentiation marker (MYADM) gene whose expression was up-regulated in NB4 cells induced by all-trans retinoic acid.
Zhao et al., Shanghai, China. In Mol Biol Rep, 2000
Cloning and characterization of human MYADM gene whose expression was up-regulated in NB4 cells induced by all-trans retinoic acid.
Microprojectile-DNA delivery in conifer species: factors affecting assessment of transient gene expression using the β-glucuronidase reporter gene.
Tsang et al., Canada. In Plant Cell Rep, 1993
The fluorescent MUG assay was more sensitive than the histochemical X-GLU assay to detect the activity of the β-glucuronidase gene.
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