Search results for "LOCUS"

showing 10 items of 632 documents

Contour/Outline/Silhouette

2020

The contour is the locus at which the parts of opaque solid objects appear to form an edge because it corresponds for the viewer to the projection of the rim, namely the curve that divides the surfaces into visible and invisible parts. The rim between the visible front and the invisible rear side is projected onto the contour that is the envelope of all the curves of equal depth. Although the rim and the contour run into depth, they are distinct concepts that regard the object-centred and the viewer-centred description. The outline is the boundary of the surface delimited by the contour, which fills a spatial region. Rubin (1921) discovered the property that allows the contour and the outli…

Surface (mathematics)Settore M-PSI/01 - Psicologia GeneraleOpacityProjection (mathematics)Settore M-FIL/04 - EsteticaGeometryObserver (special relativity)Edge (geometry)Locus (mathematics)perception picture vision geometryObject (philosophy)GeologySilhouette
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Genome-based analyses reveal a synonymy among Halorubrum distributum Zvyagintseva and Tarasov 1989; Oren and Ventosa 1996, Halorubrum terrestre Vento…

2020

A comparative taxonomic study of Halorubrum distributum , Halorubrum terrestre , Halorubrum arcis and Halorubrum litoreum was carried out using different approaches, 16S rRNA gene sequence analysis, multilocus sequence analysis (MLSA), phylogenomic analysis based on the comparison of the core genome, orthologous average nucleotide identity (OrthoANI), Genome-to-Genome Distance Calculator (GGDC), synteny plots and polar lipid profile (PLP). The MLSA study, using the five concatenated housekeeping genes atpB, EF-2, glnA, ppsA and rpoB′, and the phylogenomic analysis based on 1347 core translated gene sequences obtained from their genomes showed that Halorubrum distributum JCM 9100T, Halorubru…

SynonymNew TaxaSequence analysisSynonymHalorubrum distributumMicrobiologyGenomeGenes ArchaealEmended description03 medical and health sciencestaxonomyTaxonomic NoteRNA Ribosomal 16SHalorubrum distributumHalorubrumEcology Evolution Behavior and SystematicsPhylogeny030304 developmental biologySyntenyTaxonomyGenetics0303 health sciencesbiology030306 microbiologysynonymGeneral MedicineSequence Analysis DNA16S ribosomal RNAbiology.organism_classificationrpoBArchaeaLipidsDNA Archaealemended descriptionHalorubrumMultilocus Sequence Typing
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Characterization of the bulk flow properties of industrial powders from shear tests

2020

Bulk flow properties from shear analysis of compacted powders can be evaluated following different approaches. Experimental values of shear stresses obtained by conventional shear cells are traditionally used to build yield loci, from which the most relevant flow properties could be found. Such flow properties play an important role in determining their performance under fluidization conditions. In this work, a useful app, named cYield, was developed by using the new Matlab&rsquo

TPMaterials scienceBest fittingBioengineeringflowability02 engineering and technologylcsh:Chemical technologypowder characterizationlcsh:Chemistry020401 chemical engineeringMatlab AppUltimate tensile strengthChemical Engineering (miscellaneous)lcsh:TP1-1185Fluidization0204 chemical engineeringMATLABcomputer.programming_languagepowder characterization; flowability; Matlab App; yield locus; tensile strengthT1Process Chemistry and Technology021001 nanoscience & nanotechnologyShear (geology)tensile strengthlcsh:QD1-9990210 nano-technologyBiological systemFlow propertiescomputeryield locus
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Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

2013

Journal article TERT-locus SNPs and leukocyte telomere measures are reportedly associated with risks of multiple cancers. Using the Illumina custom genotyping array iCOGs, we analyzed ~480 SNPs at the TERT locus in breast (n = 103,991), ovarian (n = 39,774) and BRCA1 mutation carrier (n = 11,705) cancer cases and controls. Leukocyte telomere measurements were also available for 53,724 participants. Most associations cluster into three independent peaks. The minor allele at the peak 1 SNP rs2736108 associates with longer telomeres (P = 5.8 × 10!-7), lower risks for estrogen receptor (ER)-negative (P = 1.0 × 10!-8) and BRCA1 mutation carrier (P = 1.1 × 10!-5) breast cancers and altered promot…

TelomeraseMessengerCàncer d'ovariEstrogen receptorAetiology screening and detection [ONCOL 5]0302 clinical medicineBreast cancerRisk FactorsAlternative Splicing; Biomarkers Tumor; Breast Neoplasms; Case-Control Studies; Chromatin; DNA Methylation; Female; Gene Expression Profiling; Genetic Loci; Genetic Predisposition to Disease; Genome-Wide Association Study; Genotype; Humans; Luciferases; Oligonucleotide Array Sequence Analysis; Ovarian Neoplasms; Polymorphism Single Nucleotide; RNA Messenger; Real-Time Polymerase Chain Reaction; Reverse Transcriptase Polymerase Chain Reaction; Risk Factors; Telomerase; Telomere; GeneticsGenotypeBUCCAL CELLSLuciferasesTelomeraseOligonucleotide Array Sequence AnalysisOvarian Neoplasms0303 health sciencesTumorTelòmerReverse Transcriptase Polymerase Chain ReactionGENETIC-VARIATIONCOMMON VARIANTSSingle Nucleotidetert-clptm1l locus; genome-wide association; genetic-variation; susceptibility loci; buccal cells; fibroblasts; common variants; carcinoma; reverse-transcriptase htert; metaanalysisTelomereAetiology screening and detection Immune Regulation [ONCOL 5]Chromatin3. Good healthTumor Markers Biological030220 oncology & carcinogenesisFemaleFIBROBLASTSGenotypeSUSCEPTIBILITY LOCICARCINOMASingle-nucleotide polymorphismBreast NeoplasmsBiologyReal-Time Polymerase Chain ReactionPolymorphism Single NucleotideArticleCàncer de mama03 medical and health sciencesBreast cancerSDG 3 - Good Health and Well-beingTranslational research [ONCOL 3]Ovarian cancermedicineGeneticsBiomarkers TumorHumansGenetic Predisposition to DiseaseRNA MessengerPolymorphismAlleleGENOME-WIDE ASSOCIATIONMETAANALYSIS030304 developmental biologyMolecular epidemiology Aetiology screening and detection [NCEBP 1]Breast cancer susceptibilityHereditary cancer and cancer-related syndromes [ONCOL 1]Translational research Genomic disorders and inherited multi-system disorders [ONCOL 3]Gene Expression ProfilingDNA Methylationmedicine.diseaseMolecular biologyTERT-CLPTM1L LOCUSTelomereMinor allele frequencyAlternative SplicingGenetic LociCase-Control StudiesRNABiomarkersREVERSE-TRANSCRIPTASE HTERTGenome-Wide Association StudyNature genetics
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Cognitive behavior therapy for functional gastrointestinal disorders: is group treatment effective?

2003

Objective:The intention of this study was to evaluate therapy outcome of a cognitive-behavioral group treatment program for functional gastrointestinal disorders. As a particular characteristic, gastrointestinal symptoms were investigated independently from diagnostic categories on a dimensional basis, considering the persistence of symptoms as well as the aspect of severity.Methods:A total of 64 subjects participated in the 10-week treatment program, and 49 completed the study. Subjects underwent four assessments (baseline, pre-, post-treatment, 12-month follow-up), each comprising several self-rated questionnaires on gastrointestinal, somatoform, depressive, hypochondriacal and anxious sy…

Therapy OutcomeComorbid psychopathologymedicine.medical_specialtybusiness.industryTreatment outcomeDiagnostic interviewCognitionmedicine.diseaseGroup treatmentPsychiatry and Mental healthLocus of controlInternal medicinePhysical therapyMedicinebusinessBiological PsychiatryIrritable bowel syndromeActa Neuropsychiatrica
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Role of tir and intimin in the virulence of rabbit enteropathogenic Escherichia coli serotype O103:H2.

2000

ABSTRACT Attaching and effacing (A/E) rabbit enteropathogenic Escherichia coli (REPEC) strains belonging to serogroup O103 are an important cause of diarrhea in weaned rabbits. Like human EPEC strains, they possess the locus of enterocyte effacement clustering the genes involved in the formation of the A/E lesions. In addition, pathogenic REPEC O103 strains produce an Esp-dependent but Eae (intimin)-independent alteration of the host cell cytoskeleton characterized by the formation of focal adhesion complexes and the reorganization of the actin cytoskeleton into bundles of stress fibers. To investigate the role of intimin and its translocated coreceptor (Tir) in the pathogenicity of REPEC, …

Time Factors[SDV]Life Sciences [q-bio]MutantAdministration OralPATHOGENICITEmedicine.disease_causeBacterial AdhesionMICROSCOPIE ELECTRONIQUE A TRANSMISSIONFecesCytoskeleton0303 health sciencesVirulenceEscherichia coli ProteinsEnterobacteriaceae3. Good health[SDV] Life Sciences [q-bio]IntestinesInfectious DiseasesMolecular and Cellular PathogenesisRabbitsLocus of enterocyte effacementBacterial Outer Membrane ProteinsImmunologyMolecular Sequence DataVirulenceReceptors Cell SurfaceBiologyMicrobiologydigestive systemMicrobiologyCell Line03 medical and health sciencesBacterial ProteinsIleummedicineEscherichia coliAnimalsHumansEnteropathogenic Escherichia coliAdhesins BacterialEscherichia coli030304 developmental biologyIntiminModels Genetic030306 microbiologyGenetic Complementation TestEpithelial Cellsbiochemical phenomena metabolism and nutritionbiology.organism_classificationActin cytoskeleton[SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/BacteriologyActinsKineticsMicroscopy ElectronMicroscopy FluorescenceMutagenesisParasitologyCarrier ProteinsHeLa CellsInfection and immunity
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Mutational synergy coordinately remodels chromatin accessibility, enhancer landscape and 3-Dimensional DNA topology to alter gene expression during l…

2020

AbstractAltered transcription is a cardinal feature of acute myeloid leukemia (AML), however, exactly how mutations synergize to remodel the epigenetic landscape and rewire 3-Dimensional (3-D) DNA topology is unknown. Here we apply an integrated genomic approach to a murine allelic series that models the two most common mutations in AML, Flt3-ITD and Npm1c. We then deconvolute the contribution of each mutation to alterations of the epigenetic landscape and genome organization, and infer how mutations synergize in the induction of AML. These analyses allow the identification of long-range cis-regulatory circuits, including a novel super-enhancer of the Hoxa locus, as well as larger and more …

Transcription (biology)hemic and lymphatic diseasesMyeloid leukemiaLocus (genetics)EpigeneticsAlleleBiologyEnhancerTopologyChromatinGenomic organization
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Detection, validation, and downstream analysis of allelic variation in gene expression.

2009

AbstractCommon sequence variants within a gene often generate important differences in expression of corresponding mRNAs. This high level of local (allelic) control—or cis modulation—rivals that produced by gene targeting, but expression is titrated finely over a range of levels. We are interested in exploiting this allelic variation to study gene function and downstream consequences of differences in expression dosage. We have used several bioinformatics and molecular approaches to estimate error rates in the discovery of cis modulation and to analyze some of the biological and technical confounds that contribute to the variation in gene expression profiling. Our analysis of SNPs and alter…

Transcription GeneticQuantitative Trait LociGene ExpressionQuantitative trait locusBiologyInvestigationsPolymerase Chain ReactionPolymorphism Single NucleotideMiceGene mappingGene expressionDatabases GeneticGeneticsAnimalsHumansRNA MessengerGene3' Untranslated RegionsAllelesOligonucleotide Array Sequence AnalysisGeneticsGene Expression ProfilingAlternative splicingGene targetingComputational BiologyReproducibility of ResultsSequence Analysis DNAGene expression profilingAlternative SplicingExpression quantitative trait lociGenetics
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A new glucose-repressible gene identified from the analysis of chromatin structure in deletion mutants of yeast SUC2 locus.

1991

We have previously shown that some changes occur in the chromatin structure of the 3' flank of the yeast SUC2 gene in going from a repressed to an active state. In an attempt to find out the causes of these changes, we have carried out experiments in which mutant copies of SUC2 locus lacking either 5' or 3' flanks have been analysed for their transcriptional activity and chromatin structure. These experiments allowed us to discard any relationship between SUC2 transcription and chromatin changes within its 3'flank. Sequencing of this flank and mRNA analysis, however, resulted in the location of a putative peroxisomal 3-oxoacyl-CoA thiolase gene (POT1), which is repressible by glucose. The d…

Transcription GeneticSaccharomyces cerevisiaeMutantGenes FungalMolecular Sequence DataBioengineeringLocus (genetics)Saccharomyces cerevisiaeApplied Microbiology and BiotechnologyBiochemistryOpen Reading FramesGene Expression Regulation FungalGeneticsAmino Acid SequenceDNA FungalGeneChIA-PETRegulation of gene expressionGeneticsbiologyBase SequenceNucleic acid sequencebiology.organism_classificationAcetyl-CoA C-AcyltransferaseBlotting NorthernChromatinChromatinGlucoseMutagenesisBiotechnologyPlasmidsYeast (Chichester, England)
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Expression of Histocompatibility Antigens during the Growth Cycle of Cultured Lymphoid Cells

1974

Histocompatibility antigens are genetically determined markers which are located on plasma membranes of tissue cells of each member of a species. HL-A antigens are the gene products of the major histocompatibility locus in man and represent the human counterparts of the H-2, Ag-B, ChL-A and DL-A systems in mice, rats, chimpanzees and dogs, respectively (Palm, 1964; Snell and Stimpfling, 1966; Rapaport et al., 1970; Balner et al., 1971; Klein and Shreffler, 1971). The great interest in the serologic, genetic, chemical and immunological characterization of histocompatibility antigens is attributable to the fact they provide cell surface markers useful in selecting transplant donors and recipi…

Transplantationmedicine.anatomical_structureCluster of differentiationAntigenImmunologyCellmedicineLocus (genetics)BiologyPan-T antigensGeneHistocompatibility
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