Search results for "microarray."

showing 10 items of 384 documents

The Role of Immunohistochemistry in Rhabdomyosarcoma Diagnosis Using Tissue Microarray Technology and a Xenograft Model

2015

Rhabdomyosarcomas (RMS) may resemble other non-myogenic sarcomas and malignant rhabdoid tumor (MRT). Alveolar rhabdomyosarcoma (ARMS) often harbors a typical translocation, but embryonal rhabdomyosarcoma (ERMS) lacks any specific rearrangement. Histopathology is not always sufficient for an unequivocal diagnosis, necessitating ancillary studies, including immunohistochemistry (IHC). Sixteen genetically tested RMS and two MRT were xenografted and followed in successive passages. Tissue microarrays were constructed including samples from original and xenograft tumors. Desmin, myogenin, CK, EMA, INI1, LSD1, AP2 beta, fibrillin-2, HMGA2, nestin, and SIRT1 were tested using immunohistochemical s…

Malemusculoskeletal diseasesmedicine.medical_specialtyPathologygenetic structuresMice NudeBiologyPathology and Forensic MedicineDiagnosis DifferentialMiceRhabdomyosarcomaBiomarkers TumormedicineAnimalsHumansRhabdomyosarcomaRhabdoid TumorTissue microarraytissue microarraysGeneral MedicineNestinmedicine.diseasemusculoskeletal systemImmunohistochemistryDisease Models AnimalxenograftsTissue Array AnalysisPediatrics Perinatology and Child HealthimmunohistochemistryAlveolar rhabdomyosarcomaCancer researchHeterograftsImmunohistochemistryHistopathologyDesminEmbryonal rhabdomyosarcomarhabdomyosarcoma
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Imbibition of Femtoliter-Scale DNA-Rich Aqueous Droplets into Porous Nylon Substrates by Molecular Printing

2019

This work presents the first reported imbibition mechanism of femtoliter (fL)-scale droplets produced by microchannel cantilever spotting (μCS) of DNA molecular inks into porous substrates (hydrophilic nylon). Differently from macroscopic or picoliter droplets, the downscaling to the fL-size leads to an imbibition process controlled by the subtle interplay of evaporation, spreading, viscosity, and capillarity, with gravitational forces being quasi-negligible. In particular, the minimization of droplet evaporation, surface tension, and viscosity allows for a reproducible droplet imbibition process. The dwell time on the nylon surface permits further tuning of the droplet lateral size, in acc…

Materials scienceDiffusionSettore CHIM/05 - Scienza e Tecnologia dei Materiali PolimericiEvaporation02 engineering and technology010402 general chemistry01 natural sciencesSurface tensionMolecular ImprintingViscosityElectrochemistrySurface TensionGeneral Materials Sciencedroplets imbibition molecular printing nylon substrates biosensors microarraysPorositySpectroscopyMicrochannelFemtoliterNucleic Acid HybridizationWaterSurfaces and InterfacesDNA021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesNylonsChemical engineeringSettore CHIM/03 - Chimica Generale E InorganicaImbibition0210 nano-technologyHydrophobic and Hydrophilic InteractionsPorosity
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Evaluation of T7 and lambda phage display systems for survey of autoantibody profiles in cancer patients.

2008

In the current study we attempted to evaluate the suitability of T7 Select 10-3b and lambdaKM8 phage display systems for the identification of antigens eliciting B cell responses in cancer patients and the production of phage-displayed antigen microarrays that could be exploited for the monitoring of autoantibody profiles. Members of 15 tumour-associated antigen (TAA) families were cloned into both phage display vectors and the TAA mini-libraries were immunoscreened with 22 melanoma patients' sera resulting in the detection of reactivity against members of 5 antigen families in both systems, yet with variable sensitivity. T7 phage display system showed greater sensitivity for the detection …

Melanoma-associated antigenPhage displayMicroarrayT7 phageAntibodies NeoplasmImmunologyAutoantibodyProtein Array AnalysisBiologybiology.organism_classificationVirologyMolecular biologyBacteriophage lambdaBacteriophageAntigenAntigens NeoplasmPeptide LibraryBacteriophage T7Immunology and AllergyHumansGenomic libraryCloning MolecularMelanomaAutoantibodiesGene LibraryJournal of immunological methods
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Identification of novel peroxisome proliferator-activated receptor alpha (PPARalpha) target genes in mouse liver using cDNA microarray analysis.

2001

Peroxisome proliferators, which function as peroxisome proliferator-activated receptor-alpha (PPARalpha) agonists, are a group of structurally diverse nongenotoxic hepatocarcinogens including the fibrate class of hypolipidemic drugs that induce peroxisome proliferation in liver parenchymal cells. Sustained activation of PPARalpha by these agents leads to the development of liver tumors in rats and mice. To understand the molecular mechanisms responsible for the pleiotropic effects of these agents, we have utilized the cDNA microarray to generate a molecular portrait of gene expression in the liver of mice treated for 2 weeks with Wy-14,643, a potent peroxisome proliferator. PPARalpha activa…

Mice KnockoutPeroxisome proliferator-activated receptor gammaDNA ComplementaryChemistryMicroarray analysis techniquesGene Expression ProfilingPeroxisome ProliferationReceptors Cytoplasmic and NuclearPeroxisomeArticleCell biologyGene expression profilingMice Inbred C57BLMicePyrimidinesLiverGene expressionGeneticsAnimalsPeroxisome proliferator-activated receptor deltaPeroxisome proliferator-activated receptor alphaMolecular BiologyOligonucleotide Array Sequence AnalysisTranscription FactorsGene expression
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Medical Imaging Applications: Three Case Studies

2006

Microarray Image Analysis Three Dimensional segmentation of Computer Tomography data Breast Shape Analysis
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A Tutorial on Computational Cluster Analysis with Applications to Pattern Discovery in Microarray Data

2008

Background Inferring cluster structure in microarray datasets is a fundamental task for the so-called -omic sciences. It is also a fundamental question in Statistics, Data Analysis and Classification, in particular with regard to the prediction of the number of clusters in a dataset, usually established via internal validation measures. Despite the wealth of internal measures available in the literature, new ones have been recently proposed, some of them specifically for microarray data. Results We consider five such measures: Clest, Consensus (Consensus Clustering), FOM (Figure of Merit), Gap (Gap Statistics) and ME (Model Explorer), in addition to the classic WCSS (Within Cluster Sum-of-S…

Microarray analysis techniquesComputer scienceApplied Mathematicscomputer.software_genreDisease clusterClusteringComputational MathematicsComputingMethodologies_PATTERNRECOGNITIONComputational Theory and MathematicsGene chip analysisMicroarray databasesData miningDNA microarrayCluster analysiscomputerMathematics in Computer Science
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Bayesian network based pathway analysis of microarray data

2011

Microarray analysis techniquesComputer scienceBiomedical EngineeringMicroarray databasesBayesian networkBioengineeringComputational biologyPathway analysisBiotechnologyCurrent Opinion in Biotechnology
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MGFM

2017

The package is designed to detect marker genes from Microarray gene expression data sets.

Microarray experimentGene expression
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C-DNA Microarray Analysis

2008

Microarray DNA
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Prediction of the gene expression measure by means of a GLMM

2007

Microarrays permit to scientists the screening of thousands of genes simultaneously to determine, for example, whether those genes are active, hyperactive or silent in normal or cancerous tissues. A primary task in microarray analysis is to obtain a good measure of the gene expression that can be used for a so called higher level analysis. Different methods have been proposed for high density oligonucleotide arrays (see Cope et al. (2004) for a review). Aim of this paper is to obtain a new gene expression measure based on the background correction model proposed by Mineo et al. (2006). The proposed method is validated by means of a free available data-set called Spike-In133 experiment, wher…

Microarray background correction gene expression measure GLMM.
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