Search results for " Library"

showing 10 items of 734 documents

A fixed point theorem for G-monotone multivalued mapping with application to nonlinear integral equations

2017

We extend notion and theorem of [21] to the case of a multivalued mapping defined on a metric space endowed with a finite number of graphs. We also construct an example to show the generality of our result over existing results. Finally, we give an application to nonlinear integral equations

GeneralityGeneral Mathematics010102 general mathematicsFixed-point theoremFixed pointConstruct (python library)Nonlinear integral equation01 natural sciencesGraph010101 applied mathematicsAlgebraMetric spaceMonotone polygonSettore MAT/05 - Analisi Matematica0101 mathematicsG-monotone multivalued mappingFinite setMathematicsFilomat
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Human type I cytokeratin genes are a compact cluster

1997

A YAC clone (211F11) containing approximately 0.5 Mb of human DNA was isolated from a human genomic library by PCR-based screening with cytokeratin (KRT) 13-specific primers. The YAC clone was mapped by FISH to the long arm of chromosome 17 (17q12→q21), a region to which several other type I KRT genes had been mapped previously. We now show by Southern blot hybridization and PFGE analyses that KRT13, 14, 15, and 16 are all contained within YAC clone 211F11. Long-range restriction mapping analysis of clone 211F11 and of two smaller YAC clones that were also isolated with KRT13-specific primers, suggests that KRT13, 14, 15, 16 and their linked type I genes KRT17 and 19, are contained in less …

Genetic LinkageLocus (genetics)BiologyPolymerase Chain ReactionRestriction mapGene mappingGene clusterGeneticsHumansGenomic libraryCloning MolecularChromosomes Artificial YeastMolecular BiologyIn Situ Hybridization FluorescenceGenetics (clinical)Southern blotGeneticsBase SequenceChromosome MappingMolecular biologyChromosome 17 (human)genomic DNAMultigene FamilyKeratinsDNA ProbesChromosomes Human Pair 17
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Sequence and evolution of the gene for the monomeric globin I and its linkage to genes coding for dimeric globins in the insect Chironomus thummi.

1995

We isolated genomic clones containing sequences encoding globins I and IA from a Chironomus thummi thummi genomic library. Three clones contain globin IA (ctt-1A) genes, while one contains a globin I (ctt-1) gene. The coding regions of the four genes are identical except for the single base substitution accounting for the globin I/IA polymorphism. The noncoding DNA flanking the coding region is more than 98% similar, confirming a previous hypothesis that the globin ctt-1 and ctt-1A genes are alleles. Hemoglobins I and IA are monomeric in the insect hemolymph. Earlier in situ hybridization studies suggested that monomeric and dimeric globin genes are clustered at different chromosomal loci. …

Genetic LinkageMolecular Sequence DataGenes InsectBiologyChironomidaechemistry.chemical_compoundMolecular evolutionhemic and lymphatic diseasesGeneticsCoding regionAnimalsGenomic libraryGlobinAmino Acid SequenceMolecular BiologyGeneEcology Evolution Behavior and SystematicsIn Situ HybridizationGeneticsPolytene chromosomeBase SequenceSequence Homology Amino AcidChromosome MappingMolecular biologyNoncoding DNABiological EvolutionGlobinschemistrySequence AlignmentDNAJournal of molecular evolution
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Baculoviral display of functional scFv and synthetic IgG-binding domains.

2000

Viral vectors displaying specific ligand binding moities such as scFv fragments or intact antibodies hold promise for the development of targeted gene therapy vectors. In this report we describe baculoviral vectors displaying either functional scFv fragments or the synthetic Z/ZZ IgG binding domain derived from protein A. Display on the baculovirus surface was achieved via fusion of the scFv fragment or Z/ZZ domain to the N-terminus of gp64, the major envelope protein of the Autographa californica nuclear polyhedrosis virus, AcNPV. As examples of scFv fragments we have used a murine scFv specific for the hapten 2-phenyloxazolone and a human scFv specific for carcinoembryonic antigen. In pri…

Genetic enhancementvirusesRecombinant Fusion ProteinsBlotting WesternBiophysicschemical and pharmacologic phenomenaEnzyme-Linked Immunosorbent AssayVectors in gene therapySpodopteraBiochemistryViral vector03 medical and health sciencesMice0302 clinical medicineAntibody SpecificityPeptide LibraryAnimalsHumansMolecular BiologyImmunoglobulin FragmentsCells Cultured030304 developmental biology0303 health sciencesbiologyOxazoloneNuclear Polyhedrosis VirusCell Biologyrespiratory systembiology.organism_classificationMolecular biology3. Good healthCarcinoembryonic AntigenAutographa californicaIgG binding030220 oncology & carcinogenesisImmunoglobulin Gbiology.proteinBinding Sites AntibodyAntibodyHaptenBaculoviridaeHaptensViral Fusion ProteinsBiochemical and biophysical research communications
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Distributed and Lumped Parameter Models for the Characterization of High Throughput Bioreactors

2016

Next generation bioreactors are being developed to generate multiple human cell-based tissue analogs within the same fluidic system, to better recapitulate the complexity and interconnection of human physiology. The effective development of these devices requires a solid understanding of their interconnected fluidics, to predict the transport of nutrients and waste through the constructs and improve the design accordingly. In this work, we focus on a specific model of bioreactor, with multiple input/outputs, aimed at gen- erating osteochondral constructs, i.e., a biphasic construct in which one side is cartilagi- nous in nature, while the other is osseous. We next develop a general computat…

Genetics and Molecular Biology (all)0301 basic medicineComputer scienceDistributed computinglcsh:Medicine02 engineering and technologyMedicine (all); Biochemistry Genetics and Molecular Biology (all); Agricultural and Biological Sciences (all)BiochemistryOxygenPLLA bioreactor computational modelMedicine and Health SciencesFluid dynamicslcsh:ScienceThroughput (business)Flow RateMultidisciplinaryPhysicsSimulation and ModelingMedicine (all)Classical MechanicsVolumetric flow rateChemistryConnective TissuePhysical SciencesAnatomyResearch ArticleChemical ElementsCell Physiology0206 medical engineeringMicrofluidicschemistry.chemical_elementFluid MechanicsResearch and Analysis MethodsContinuum Mechanics03 medical and health sciencesBioreactorFluidicsFluid Flowlcsh:RBiology and Life SciencesBiological TransportFluid DynamicsCell BiologyConstruct (python library)020601 biomedical engineeringCell MetabolismOxygenMetabolismBiological TissueCartilage030104 developmental biologyAgricultural and Biological Sciences (all)chemistryFlow (mathematics)lcsh:QPorous mediumPLOS ONE
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Minisatellite DNA Probe MZ 1.3: Application in Paternity Testing and Estimate of the Number of Genetic Loci

1990

The use of hypervariable DNA minisatellite probes recognizing repetitive genomic DNA sequences has become a valuable and powerful tool in paternity testing as well as in forensic stain analysis (Jeffreys et al. 1985, 1987; Werrett et al. 1988). It has been shown that bacteriophage Ml3 DNA can also be used to obtain hypervariable DNA restriction fragment patterns in humans and other species (Vassart et al. 1987). To obtain more informative and specific fragment patterns for the DNA ‘fingerprint’ analysis in man, we have used Ml3 DNA as a probe to screen a human genomic library. Thus, we have isolated the minisatellite DNA probe MZ 1.3 (Schacker et al., in press). MZ 1.3 is a 1.9 kb fragment …

GeneticsBacteriophagegenomic DNAchemistry.chemical_compoundMinisatellitebiologychemistryProtein IIIGenomic librarybiology.organism_classificationGeneHomology (biology)DNA
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The mouseClq genes are clustered on chromosome 4 and show conservation of gene organization

1996

Mouse complement component C1q is a serum glycoprotein which consists of six A chains, six B chains and six C chains. The three polypeptides are 223, 228, and 217 residues long, respectively, and are encoded by three genes. DNA probes for mouse C1q A, B, and C chains were hybridized to Southern blots of DNA obtained from various inbred mouse strains. On the basis of fragment length polymorphisms, two different alleles of each of the genes could be identified. The distribution of these alleles was determined in the BXD and LXPL recombinant inbred strain series. Comparison with previously reported strain distribution patterns shows that the genes encoding mouseClq map to the same locus on dis…

GeneticsChromosome 4Complementary DNAImmunologyGene clusterGeneticsGenomic libraryRecombinant inbred strainLocus (genetics)BiologyGeneMolecular biologySouthern blotImmunogenetics
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Expression profiling of human fetal growth plate cartilage by EST sequencing.

2005

The differentiation of mesenchymal stem cells into hypertrophic chondrocytes is an integral and multistep process important in pattern formation, endochondral ossification, and postnatal growth of the skeleton. In recent years, novel genes involved in these processes have been identified, but still only little is known about the large-scale gene expression profile during skeletal development. We initiated an expressed sequence tag (EST) project aiming at the identification of genes and pathways involved in this complex process. Candidate genes are expected to be of value for diagnosis and treatment of monogenic and multigenic heritable disorders of the skeleton. Here, we describe the sequen…

GeneticsExpressed Sequence TagsCandidate geneExpressed sequence tagExtracellular Matrix ProteinscDNA libraryIn silicoGene Expression ProfilingGene Expression Regulation DevelopmentalBiologyGene expression profilingFetusGene expressionHumansProteoglycansGrowth PlateMolecular BiologyEndochondral ossificationGeneMatrix biology : journal of the International Society for Matrix Biology
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A simple sequence repeat-based linkage map of barley.

2000

Abstract A total of 568 new simple sequence repeat (SSR)-based markers for barley have been developed from a combination of database sequences and small insert genomic libraries enriched for a range of short simple sequence repeats. Analysis of the SSRs on 16 barley cultivars revealed variable levels of informativeness but no obvious correlation was found with SSR repeat length, motif type, or map position. Of the 568 SSRs developed, 242 were genetically mapped, 216 with 37 previously published SSRs in a single doubled-haploid population derived from the F1 of an interspecific cross between the cultivar Lina and Hordeum spontaneum Canada Park and 26 SSRs in two other mapping populations. A …

GeneticsGenetic Markerseducation.field_of_studyDNA PlantGenetic LinkagePopulationfood and beveragesChromosome MappingHordeumBiologyGenes Plantgenomic DNAGene mappingGenetic markerGenetic linkageGeneticsMicrosatelliteGenomic libraryRestriction fragment length polymorphismeducationCrosses GeneticGenome PlantResearch ArticleRepetitive Sequences Nucleic Acid
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Subrepeats result from regional DNA sequence conservation in tandem repeats in Chironomus telomeres

1990

Repeat units, widespread in eukaryotic genomes, are often partially or entirely built up of subrepeats. Homogenization between whole repeat units arranged in tandem usually can best be understood as a result of unequal crossing over. Such a mechanism is less plausible for maintaining similarities between subrepeats within a repeat unit when present in a regular array. In Chironomus telomeres, large blocks of tandemly repeated approximately 350 base-pair units contain two or three pairs of subrepeats with high mutual identities, embedded in linker DNA, non-repetitive within the repeat unit. Measurements of evolutionary base changes in two closely related species, Chironomus tentans and Chiro…

GeneticsGenomic LibraryUnequal crossing overBase SequencebiologyMolecular Sequence DataGene AmplificationDNAbiology.organism_classificationBiological EvolutionGenomeLinker DNAChironomidaeDNA sequencingSpecies SpecificityTandem repeatStructural BiologyMolecular evolutionSequence Homology Nucleic AcidAnimalsChironomusMolecular BiologyRepetitive Sequences Nucleic AcidRepeat unitJournal of Molecular Biology
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