Search results for "types"

showing 10 items of 956 documents

Recent speciation and secondary contact in endemic ants

2014

Gene flow is the main force opposing divergent selection, and its effects are greater in populations in close proximity. Thus, complete reproductive isolation between parapatric populations is not expected, particularly in the absence of ecological adaptation and sharp environmental differences. Here, we explore the biogeographical patterns of an endemic ant species, Cataglyphis floricola, for which two colour morphs (black and bicolour) coexist in parapatry throughout continuous sandy habitat in southern Spain. Discriminant analyses of six biometric measurements of male genitalia and 27 cuticular hydrocarbons reveal high differentiation between morphs. Furthermore, the low number of shared…

Gene FlowMaleanimal structuresgenetic structuresGenetic SpeciationPopulation geneticsSpeciationMolecular Sequence DataPopulation geneticsParapatric speciationBiologyDNA MitochondrialBehaviour/social evolutionGene flowGeneticsVicarianceAnimalsEcology Evolution Behavior and SystematicsPhylogenyreproductive and urinary physiologyPhylogenetic treeAntsfungiBayes TheoremReproductive isolationSequence Analysis DNAInsects[SDV.BA.ZI]Life Sciences [q-bio]/Animal biology/Invertebrate ZoologyPhylogeographyPhylogeographyGenetics PopulationHaplotypesEvolutionary biologySpainta1181AdaptationMicrosatellite RepeatsMolecular Ecology
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A study on Pomatoschistus tortonesei Miller 1968 (Perciformes, Gobiidae) reveals the Siculo-Tunisian Strait (STS) as a breakpoint to gene flow in the…

2009

The current genetic structure of P. tortonesei, exclusively inhabiting lagoons, may reflect a Plio-Pleistocene colonisation of an ancestor line which has undergone phases of population decline and expansion, following alternate cooling phases. Regarding the calculation of divergence time, it has been estimated that P. tortonesei seems to be the most recent species within the Pomatoschistus genus. It appears also that the discrepancy of P. tortonesei into two distinct phyletic lineages occurred 0.1 Mya. Recurring shifts in sea level and sea surface temperatures of Mediterranean Sea caused the desiccation of shallower lagoons and the consequent bottleneck phenomena of the brackish populations…

Gene FlowSettore BIO/05 - ZoologiaDNA MitochondrialMediterranean BasinPerciformesGene flowEvolution MolecularRNA Ribosomal 16SMediterranean SeaGeneticsAnimalsMolecular BiologyPhylogenyEcology Evolution Behavior and SystematicsGeographybiologyEcologyPomatoschistus tortoneseiBreakpointSequence Analysis DNAbiology.organism_classificationPerciformesFisheryGenetics PopulationHaplotypesmtDNA Pomatoschistus tortonesei Siculo-Tunisian Strait (STS)
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Genetic structure and demographic inference of the regular sea urchin Sterechinus neumayeri (Meissner, 1900) in the Southern Ocean: the role of the l…

2018

22 pages; International audience; One of the most relevant characteristics of the extant Southern Ocean fauna is its resiliency to survive glacial processes of the Quaternary. These climatic events produced catastrophic habitat reductions and forced some marine benthic species to move, adapt or go extinct. The marine benthic species inhabiting the Antarctic upper continental shelf faced the Quaternary glaciations with different strategies that drastically modified population sizes and thus affected the amount and distribution of intraspecific genetic variation. Here we present new genetic information for the most conspicuous regular sea urchin of the Antarctic continental shelf, Sterechinus…

Gene FlowTopographyHeredityEcological MetricsPopulation geneticsOceans and SeasGenetic locilcsh:MedicineDNA MitochondrialGeographical LocationsBodies of waterOceansGeneticsAnimalslcsh:ScienceEcosystemSpecies diversityPopulation DensityIslandsEvolutionary BiologyLandforms[SDV.GEN.GPO]Life Sciences [q-bio]/Genetics/Populations and Evolution [q-bio.PE]Population BiologyGeographyEcologylcsh:REcology and Environmental SciencesBiology and Life SciencesGeomorphologyBayes TheoremMarine and aquatic sciencesGenetic MappingPhylogeographyAntarctic OceanGenetics PopulationBiogeographyHaplotypesSea UrchinsPeople and PlacesEarth SciencesAntarcticalcsh:QResearch Article
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Gene expression of neuregulin-1 isoforms in different brain regions of elderly schizophrenia patients

2010

One important risk gene in schizophrenia is neuregulin-1 (NRG1), which is expressed in different isoforms in the brain. To determine if alterations of NRG1 are present in schizophrenia, we measured gene expression of NRG1 and its main isoforms as well as the impact of genetic variation of NRG1 in an exploratory study examining three brain regions instead of only one as published so far. In all, we examined post-mortem samples from 11 schizophrenia patients and eight normal subjects. We investigated gene expression of total NRG1 and isoforms I, II and III by real-time PCR in the prefrontal cortex (Brodmann areas 9 and 10) and right hippocampal tissue. For the genetic study, we genotyped the …

Gene isoformMalemedicine.medical_specialtyGenotypeNeuregulin-1HippocampusGene ExpressionPrefrontal CortexHippocampal formationHippocampusPolymorphism Single Nucleotide03 medical and health sciences0302 clinical medicineInternal medicinemental disordersGenetic variationGene expressionmedicineHumansProtein IsoformsNeuregulin 1Prefrontal cortexAllelesBiological Psychiatry030304 developmental biologyAged0303 health sciencesbiologyReverse Transcriptase Polymerase Chain ReactionBrainmedicine.disease030227 psychiatryPsychiatry and Mental healthEndocrinologyHaplotypesSchizophreniabiology.proteinSchizophreniaFemalePsychologyNeuroscience030217 neurology & neurosurgeryWorld Journal of Biological Psychiatry
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Allelic age of the USH2A c.2299delG mutation

2010

24 p., figuras y bibliografía

Gene isoformUsher syndromePopulationc.2299delGSingle-nucleotide polymorphismBiologyPolymorphism Single NucleotideArticleLinkage DisequilibriumWhite PeopleExonUSH2Aotorhinolaryngologic diseasesGeneticsmedicineHaplotypeHumansAlleleeducationGeneAllelesPhylogenyGenetics (clinical)GeneticsExtracellular Matrix Proteinseducation.field_of_studyHaplotypemedicine.diseaseHaplotypesMutationDatingUsher Syndromes
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Introducing ARTMO's Machine-Learning Classification Algorithms Toolbox: Application to Plant-Type Detection in a Semi-Steppe Iranian Landscape.

2022

Accurate plant-type (PT) detection forms an important basis for sustainable land management maintaining biodiversity and ecosystem services. In this sense, Sentinel-2 satellite images of the Copernicus program offer spatial, spectral, temporal, and radiometric characteristics with great potential for mapping and monitoring PTs. In addition, the selection of a best-performing algorithm needs to be considered for obtaining PT classification as accurate as possible . To date, no freely downloadable toolbox exists that brings the diversity of the latest supervised machine-learning classification algorithms (MLCAs) together into a single intuitive user-friendly graphical user interface (GUI). To…

General Earth and Planetary SciencesAutomated Radiative Transfer Models Operator; machine-learning classification toolbox; Gaussian process classifier; plant types; Sentinel-2Remote sensing
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Mondiale ma non troppo

2020

La Storia mondiale dell’Italia costituisce un’interessante sperimentazione di scrittura in chiave non piu nazionale della storia (o delle storie) della penisola. Priva, volutamente, di una logica narrativa, si pone l’obiettivo di reperire, nel passato lontano, o lontanissimo, e recente, quanti piu spunti possibili di costruzione dell’Italia come oggetto culturale fino all’emergere recente dell’idioma nazionale, e dell’Italiano come tipologia o carattere. Si nota che lo spazio entro cui si attivano questi meccanismi, una volta gettato lo sguardo fuori dalla penisola, e si il mondo, ma e molto di piu l’Europa.

General MedicineCultural stereotypes Europe National tradition
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Polymerase chain reaction analysis of the Xba I polymorphism of the human complement C4 genes provides evidence for strong haplotype conservation.

1995

The genes coding for the two isotypes of the fourth component of human complement, C4A and C4B, are located between the HLA-B and -DR loci of the MHC. We studied the linkage relationship of the previously described XbaI RFLP to obtain further insight into the evolution of the tandemly arranged C4 genes. Using exon-specific PCR amplification followed by restriction analysis and direct DNA sequencing, the polymorphic site could be located in exon 40 of the C4 gene (cDNA position 5095). The polymorphism does not change an amino acid residue. Using nested PCR amplification with isotype-specific primers to amplify either C4A or C4B alleles the haplotype arrangement of the XbaI sites in both isot…

Genetic LinkageImmunologyMolecular Sequence DataBiologyPolymerase Chain Reactionlaw.inventionExonlawComplementary DNAImmunology and AllergyHumansDeoxyribonucleases Type II Site-SpecificGenePolymerase chain reactionGeneticsPolymorphism GeneticBase SequenceHaplotypeIntronChromosome MappingComplement C4General MedicineMolecular biologyRestriction siteHaplotypesRestriction fragment length polymorphismPolymorphism Restriction Fragment LengthHuman immunology
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Replication of linkage of familial hypobetalipoproteinemia to chromosome 3p in six kindreds

2002

Familial hypobetalipoproteinemia (FHBL) is a genetically heterogeneous condition characterized by very low apolipoprotein B (apoB) concentrations in plasma and/or low levels of LDL-cholesterol (LDL-C) with a propensity to developing fatty liver. In a minority of cases, truncation-specifying mutations of the apoB gene (APOB) are etiologic, but the genetic basis of most cases is unknown. We previously reported linkage of FHBL to a 10 cM region on 3p21.1-22 in one kindred. The objectives of the current study were to identify other FHBL families with linkage to 3p and to narrow the FHBL susceptibility region on 3p. Six additional FHBL kindreds unlinked to the APOB region on chromosome 2 were ge…

Genetic MarkersAdultMaleMeiosiSettore MED/09 - Medicina InternaApolipoprotein BGenotypeGenetic LinkageQD415-436BiologyBiochemistryChromosomal crossoverHypobetalipoproteinemiasEndocrinologyQuantitative Trait HeritableGenetic linkageGenetic MarkerHaplotypeHumanslinkage analysisCrossing Over GeneticChildAgedAdult; Aged; Aged 80 and over; Child; Chromosome Mapping; Chromosomes Human Pair 3; Crossing Over Genetic; Female; Genetic Linkage; Genetic Markers; Genotype; Haplotypes; Humans; Hypobetalipoproteinemias; Male; Meiosis; Middle Aged; Pedigree; Quantitative Trait HeritableGeneticsAged 80 and overGenetic heterogeneityHaplotypeChromosomeChromosome MappingCell BiologyoligogenicMiddle AgedPedigreeMeiosisMarkov chain Monte CarloChromosome 3HaplotypesGenetic markerbiology.proteinvariance componentslipids (amino acids peptides and proteins)FemaleChromosomes Human Pair 3geneticHypobetalipoproteinemiaHuman
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HLA antigens in Sicilian patients affected by chronic myelogenous leukaemia.

1987

SUMMARY HLA antigens were investigated in Sicilian patients with chronic myelogenous leukaemia (CML) and in Sicilian healthy controls. The frequency of the HLA-DRw6 antigen was significantly decreased in the group of patients. These results suggest that DRw6 may be a marker for decreased susceptibility to the etiological or pathogenic mechanism(s) which produce CMLs.

Genetic MarkersGenetic LinkageImmunologyHLA-DR6 AntigenHuman leukocyte antigenImmunogeneticsHLA-DR AntigensBiologylanguage.human_languageAntigenGene FrequencyHaplotypesItalyHLA Antigenshemic and lymphatic diseasesLeukemia Myelogenous Chronic BCR-ABL PositiveImmunologyGeneticsEtiologylanguageHumansRisk factorChronic myelogenous leukaemiaSicilianJournal of immunogenetics
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