Search results for "PRINTING"

showing 10 items of 532 documents

Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families.

1999

Previously reported linkage of bipolar affective disorder to DNA markers on chromosome 18 was reexamined in a large sample of German bipolar families. Twenty-three short tandem repeat markers were investigated in 57 families containing 103 individuals with bipolar I disorder (BPI), 26 with bipolar II disorder (BPII), nine with schizoaffective disorder of the bipolar type (SA/BP), and 38 individuals with recurrent unipolar depression (UPR). Evidence for linkage was tested with parametric and non-parametric methods under two definitions of the affected phenotype. Analysis of all 57 families revealed no robust evidence for linkage. Following previous reports we performed separate analyses afte…

Genetic MarkersMaleBipolar I disorderBipolar DisorderGenetic LinkageSchizoaffective disorderGenes RecessiveGenetic determinismNuclear FamilyCellular and Molecular NeuroscienceBipolar II disorderGenomic ImprintingChromosome 18GermanymedicineHumansFamilyBipolar disorderMolecular BiologyGenes DominantLinkage (software)GeneticsRecombination GeneticSex CharacteristicsModels GeneticChromosome Mappingmedicine.diseasePsychiatry and Mental healthChromosomal regionFemaleLod ScorePsychologyChromosomes Human Pair 18Molecular psychiatry
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Isolation By Distance (IBD) signals in the deep-water rose shrimp Parapenaeus longirostris (Lucas, 1846) (Decapoda, Panaeidae) in the Mediterranean S…

2013

Abstract The identification of boundaries of genetic demes is one of the major goals for fishery management, and few Mediterranean commercial species have not been studied from a genetic point of view yet. The deep-water rose shrimp Parapenaeus longirostris (Lucas, 1846) is one of the most important components of commercial landings in Mediterranean, its fishery aspects have received much attention, regrettably without any concern for the genetic architecture of its populations. The population structure in the central and eastern Mediterranean Sea (captures from six Italian and two Greek landings) has been analysed on the basis of surveys carried out with mitochondrial and AFLP markers. Dat…

Genetic MarkersMediterranean climateSettore BIO/05 - ZoologiaAquatic ScienceOceanographyDNA MitochondrialPolymerase Chain ReactionRose shrimpMediterranean BasinMediterranean seaPenaeidaeMediterranean SeaAnimalsAmplified Fragment Length Polymorphism AnalysisPhylogenyIsolation by distancebiologyDecapodaEcologyGenetic VariationSequence Analysis DNAGeneral Medicinebiology.organism_classificationDNA FingerprintingPollutionFisheryParapenaeus longirostrisFisheries managementParapenaeus longirostris Isolation By Distance AFLP mtDNAMarine Environmental Research
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Data for nine autosomal STRs markers from Valencia (East Mediterranean coast of the Iberian Peninsula)

2000

Nine STRs loci have been typed in a sample from Valencia, a population from the East Mediterranean coast of the Iberian Peninsula.

Genetic MarkersQuality ControlPopulationPolymerase Chain ReactionLinkage DisequilibriumWhite PeoplePathology and Forensic MedicineGene FrequencyPeninsulaHumansEast mediterraneaneducationValenciaInterneteducation.field_of_studygeographygeography.geographical_feature_categorybiologyMediterranean Regionbiology.organism_classificationDNA FingerprintingArchaeologySpainTandem Repeat SequencesPopulation dataLawSoftwareForensic Science International
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Geosphere-biosphere interactions in bio-activity volcanic lakes: Evidences from Hule and Rìo Cuarto (Costa Rica)

2014

Hule and R ́ıo Cuarto are maar lakes located 11 and 18 km N of Poa ́s volcano along a 27 km long fracture zone, in the Central Volcanic Range of Costa Rica. Both lakes are characterized by a stable thermic and chemical stratification and recently they were affected by fish killing events likely related to the uprising of deep anoxic waters to the surface caused by rollover phenomena. The vertical profiles of temperature, pH, redox potential, chemical and isotopic compositions of water and dissolved gases, as well as prokaryotic diversity estimated by DNA fingerprinting and massive 16S rRNA pyrosequencing along the water column of the two lakes, have highlighted that different bio-geochemica…

Genetics and Molecular Biology (all)Aerobic bacterialcsh:MedicineMarine and Aquatic Sciencestrace elementsSettore BIO/19 - Microbiologia GeneraleBiochemistryWater columnBiochemistry Genetics and Molecular Biology (all); Agricultural and Biological Sciences (all)RNA Ribosomal 16SLimnologylcsh:SciencePhylogenyTotal organic carbonMultidisciplinarygeography.geographical_feature_categoryEcologyBiosphereBiogeochemistryHydrogen-Ion ConcentrationAnoxic watersMaarChemistryOceanographyPhysical SciencesMethaneOxidation-ReductionResearch ArticleFreshwater EnvironmentsCosta RicaSettore BIO/07 - EcologiaVolcanic EruptionsCarbon CycleHydrothermal VentsEnvironmental ChemistryMolecular Biology TechniquesSequencing TechniquesMolecular BiologygeographyVolcanic lakeBacterialcsh:RHigh Throughput SequencingEcology and Environmental SciencesOrganismsChemical CompoundsBiology and Life SciencesAquatic EnvironmentsCarbon DioxideArchaeaDNA FingerprintingOxygenLakesGeochemistryVolcanoAgricultural and Biological Sciences (all)Settore GEO/08 - Geochimica e VulcanologiaEarth SciencesEnvironmental sciencelcsh:QSurface water
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2015

AbstractReprogramming of mouse somatic cells into induced pluripotent stem cells (iPSCs) often generates partially reprogrammed iPSCs (pre-iPSCs), low-grade chimera forming iPSCs (lg-iPSCs) and fully reprogrammed, high-grade chimera production competent iPSCs (hg-iPSCs). Lg-iPSC transcriptome analysis revealed misregulated Dlk1-Dio3 cluster gene expression and subsequently the imprinting defect at the Dlk1-Dio3 locus. Here, we show that germ-cell marker Dppa3 is present only in lg-iPSCs and hg-iPSCs, and that induction with exogenous Dppa3 enhances reprogramming kinetics, generating all hg-iPSCs, similar to vitamin C (Vc). Conversely, Dppa3-null fibroblasts show reprogramming block at pre-i…

Genetics0303 health sciencesMultidisciplinarySomatic cellGeneral Physics and AstronomyGeneral ChemistryBiologyGeneral Biochemistry Genetics and Molecular BiologyCell biology03 medical and health sciences0302 clinical medicineDLK1Imprinting (psychology)Induced pluripotent stem cellReprogramming030217 neurology & neurosurgery030304 developmental biologyNature Communications
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Chicken orthologues of mammalian imprinted genes are clustered on macrochromosomes and replicate asynchronously.

2005

In the chicken genome, most orthologues of mouse imprinted genes are clustered on macrochromosomes. Only a few orthologues are located in the microchromosome complement. Macrochromosomal and, to a lesser extent, microchromosomal regions containing imprinted gene orthologues exhibit asynchronous DNA replication. We conclude that highly conserved arrays of imprinted gene orthologues were selected during vertebrate evolution, long before these genes were recruited for parent-specific gene expression by genomic imprinting mechanisms. Evidently, the macrochromosome complement provides a better chromatin environment for the establishment of asynchronous DNA replication and imprinted gene expressi…

GeneticsDNA ReplicationChromosomes Artificial BacterialGenomeDNA replicationBiologyGenomeChromosomesChromatinEvolution MolecularGenomic ImprintingMiceGene expressionGene clusterGeneticsMicrochromosomeAnimalsHumansGenomic imprintingGeneChickensTrends in genetics : TIG
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rRNA gene restriction patterns and biotypes of Shigella sonnei.

1993

SUMMARYShigella sonneiis a major agent of diarrhoeal disease in developed as well as in developing countries. Several phenotypic methods to define strain differences have been applied to this species ofShigellaincluding, more recently, analysis of extrachromosomal and chromosomal DNA.In this study, 432 endemic and epidemic strains isolated between 1975 and 1991 in Italy, France and Switzerland were submitted to rRNA gene restriction pattern analysis, after digestion of whole-cell DNA byHincII, and to concomitant biotyping.Thirteen ribotypes, HI to H13, and five biotypes, a, d, e, f, g, were detected. Xinety-five percent of the sporadic strains were assigned to ribotypes HI to H4, which coul…

GeneticsDNA BacterialEpidemiologyShigella sonneiDNA Restriction EnzymesRibosomal RNABiologymedicine.disease_causeDNA FingerprintingDNA RibosomalSubtypingMicrobiologyBacterial Typing TechniquesRibotypingRNA BacterialInfectious DiseasesRestriction mapDNA profilingRNA RibosomalmedicineShigellaShigella sonneiRibosomal DNAResearch Article
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340 EPIGENETIC ANALYSIS OF DEVELOPMENTALLY IMPORTANT GENES IN BOVINE OOCYTES OF DIFFERENT ORIGINS

2010

A critical step in assisted reproductive technologies (ART) is the IVM of oocytes. The quality of the oocyte is crucial for successful fertilization and subsequent embryo development. Studies in bovine ART, and epidemiological studies in children from ART, reveal a degree of abnormal development thought to be primarily caused by aberrant DNA methylation patterns in imprinted and non-imprinted genes. Due to the inherent similarities in bovine and human preimplantation embryonic development, bovine oocyte and embryo development is increasingly being used as a model for human development. The goal of this project is to investigate the effects of specific IVM conditions on the DNA methylation …

GeneticsEmbryoReproductive technologyBiologyOocyteOogenesisOxygen tensionAndrologyEndocrinologyDifferentially methylated regionsmedicine.anatomical_structureReproductive MedicineDNA methylationGeneticsmedicineAnimal Science and ZoologyGenomic imprintingMolecular BiologyDevelopmental BiologyBiotechnologyReproduction, Fertility and Development
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Forensic validation of the SNPforID 52-plex assay.

2007

The advantages of single nucleotide polymorphism (SNP) typing in forensic genetics are well known and include a wider choice of high-throughput typing platforms, lower mutation rates, and improved analysis of degraded samples. However, if SNPs are to become a realistic supplement to current short tandem repeat (STR) typing methods, they must be shown to successfully and reliably analyse the challenging samples commonly encountered in casework situations. The European SNPforID consortium, supported by the EU GROWTH programme, has developed a multiplex of 52 SNPs for forensic analysis, with the amplification of all 52 loci in a single reaction followed by two single base extension (SBE) react…

GeneticsForensic GeneticsAnalysis of VarianceGenotypeDNABiologySingle-base extensionDNA FingerprintingPolymorphism Single NucleotideSensitivity and SpecificityPathology and Forensic MedicineEuropeDNA profilingSTR analysisGeneticsMicrosatelliteHumansMultiplexTypingCooperative BehaviorLow copy numberLaboratoriesAllelesSNP arrayMicrosatellite RepeatsForensic science international. Genetics
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Forensic typing of autosomal SNPs with a 29 SNP-multiplex--results of a collaborative EDNAP exercise.

2008

We report the results of an inter-laboratory exercise on typing of autosomal single nucleotide polymorphisms (SNP) for forensic genetic investigations in crime cases. The European DNA Profiling Group (EDNAP), a working group under the International Society for Forensic Genetics (ISFG), organised the exercise. A total of 11 European and one US forensic genetic laboratories tested a subset of a 52 SNP-multiplex PCR kit developed by the SNPforID consortium. The 52 SNP-multiplex kit amplifies 52 DNA fragments with 52 autosomal SNP loci in one multiplex PCR. The 52 SNPs are detected in two separate single base extension (SBE) multiplex reactions with 29 and 23 SNPs, respectively, using SNaPshot …

GeneticsForensic GeneticsGenotypeElectrophoresis CapillarySingle-nucleotide polymorphismBiologySingle-base extensionDNA FingerprintingPolymerase Chain ReactionPolymorphism Single NucleotideUnited StatesPathology and Forensic MedicineSNP genotypingEuropeDNA profilingBlood StainsMultiplex polymerase chain reactionGeneticsSNPHumansMultiplexTypingLaboratoriesAllelesRepetitive Sequences Nucleic AcidForensic science international. Genetics
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