Search results for "Trait"

showing 10 items of 1361 documents

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.

2003

Developmental dyslexia, or reading disability, is a multigenic complex disease for which at least five loci, i.e. DYX1-3 and DYX5-6, have been clearly identified from the human genome. To date, DYX1C1 is the only dyslexia candidate gene cloned. We have previously reported linkage to 2p11 and 7q32 in 11 Finnish pedigrees. Here, we report the fine mapping of the approximately 40-cM linked region from chromosome 2 as we increased marker density to one per 1.8 cM. Linkage was supported with the highest NPL score of 3.0 (P=0.001) for marker D2S2216. Association analysis using the six pedigrees showing linkage pointed to marker D2S286/rs3220265 (P value0.001) in the near vicinity of D2S2216. We w…

Genetic MarkersCandidate geneLocus (genetics)Quantitative trait locusBiologyPolymorphism Single NucleotideDyslexia03 medical and health sciences0302 clinical medicineGene mappingGenetic linkageGeneticsmedicineHumansGenetics (clinical)FinlandReceptors Tachykinin030304 developmental biologyGenetics0303 health sciencesGene Expression ProfilingHaplotypeDyslexiaChromosome Mappingmedicine.diseaseBlotting NorthernPedigreeGenetic markerChromosomes Human Pair 2030217 neurology & neurosurgeryMicrosatellite RepeatsHuman genetics
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Identification of a genetic contamination in a commercial mouse strain using two panels of polymorphic markers

2007

Rapid detection of genetic contamination is critical in mouse studies involving inbred strains. During a Quantitative Trait Locus (QTL) study using simple sequence length polymorphism (SSLP) markers, we noticed heterozygosity at some loci of a commercially available inbred C57BL/6N mouse strain, suggesting a contamination by another mouse strain. A panel of 100 single-nucleotide polymorphism (SNP) markers was used to confirm and specify the genetic contamination suspected. Retrospective analyses demonstrated that the contamination took place as early as autumn 2003 and has persisted ever since at a fairly constant level. Contaminating alleles most probably originated from a DBA strain. Our…

Genetic MarkersGenotypeMice Inbred StrainsBiologyQuantitative trait locusMice03 medical and health sciences0302 clinical medicineInbred strainGenotypeAnimalsGenetic TestingAlleleSimple sequence length polymorphism030304 developmental biologyGeneticsMice Inbred BALB C0303 health sciencesPolymorphism GeneticBase SequenceGeneral VeterinaryGenetic Carrier ScreeningStrain (biology)Mice Inbred C57BLGenetic marker030220 oncology & carcinogenesisAnimal Science and ZoologyGenetic monitoringLaboratory Animals
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Evaluation of intra-cultivar variability in Olea europaea L. cv. Leccino using morphological, biochemical and molecular markers

2020

The phenotypic and genotypic variability of olive tree cv. Leccino (Olea europaea L.), an ancient cultivar from North-Central Italy, was investigated using 44 quantitative and qualitative agro-morphological traits, SDS-PAGE of seed proteins (storage proteins and tegument proteins) and molecular markers such as RAPDs (30 primers) and SSRs (8 primers). Fifteen accessions of Olea europaea catalogued as "Leccino" and one certified tree of "Leccino" (LESt) were examined. The plants were clonally propagated and the measuring of all morphological characteristics was conducted over a period of seven years. The ANOVA analysis showed that all accessions were homogenous for many traits while very few …

Genetic diversityOlea europaea L.molecular markersfood and beveragesOlea europaea LLeccino cultivarPlant ScienceBiologybiology.organism_classificationOlea europaea L. Leccino cultivar intra-cultivar variability morphological traits molecular markers seed proteins.intra-cultivar variabilityGenetic markerPlant morphologyOleamorphological traitsBotanyGenetic variationShootMicrosatelliteseed proteinsCultivarAgronomy and Crop ScienceApril 2020
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Local old olive landrace varieties in Israel—Valuable plant genetic resources in olive cultivation

2008

It is assumed that the cultivation of olive trees started in the East Mediterranean in the third millennia BCE. Throughout history and until recently, successful olive clones were maintained vegetatively and were grafted either on seedlings or on spheroblasts removed from the base of the trunk. It therefore can be hypothesized that local old olive trees, older than 500 years might represent an ancient gene pool. Modern terminology categorizes local genotypes into four main variety groups. However, in traditional terminology these were further differentiated into 27 cultivars according to their phenotypic traits. This genetic diversity, along with the fact that olive trees have been cultivat…

Genetic diversityRange (biology)Plant SciencePhenotypic traitBiologyOlive treesAgronomyBotanyCultivarGene poolRootstockAgronomy and Crop ScienceEcology Evolution Behavior and SystematicsSelection (genetic algorithm)Israel Journal of Plant Sciences
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Genome-Wide Patterns of Homozygosity Reveal the Conservation Status in Five Italian Goat Populations.

2021

The application of genomic technologies has facilitated the assessment of genomic inbreeding based on single nucleotide polymorphisms (SNPs). In this study, we computed several runs of homozygosity (ROH) parameters to investigate the patterns of homozygosity using Illumina Goat SNP50 in five Italian local populations: Argentata dell’Etna (N = 48), Derivata di Siria (N = 32), Girgentana (N = 59), Maltese (N = 16) and Messinese (N = 22). The ROH results showed well-defined differences among the populations. A total of 3687 ROH segments &gt

Genetic diversityruns of homozygosityGeneral Veterinarygenomic regions.Veterinary medicinePopulation sizeinbreedingSingle-nucleotide polymorphismPhenotypic traitBiologyRuns of Homozygositylocal goat populationBreedArticleGene flowQL1-991Evolutionary biologylocal goat populationsSF600-1100Animal Science and Zoologygenomic regionsZoologyInbreedingGenomic regions; Inbreeding; Local goat populations; Runs of homozygosityAnimals : an open access journal from MDPI
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Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics stud…

2008

Contains fulltext : 71374.pdf (Publisher’s version ) (Closed access) Attention-deficit/hyperactivity disorder (ADHD) is typically characterized by inattention, excessive motor activity, impulsivity, and distractibility. Individuals with ADHD have significant impairment in family and peer relations, academic functioning, and show high co-morbidity with a wide range of psychiatric disorders including oppositional defiant disorder (ODD), conduct disorder (CD), anxiety disorder, depression, substance abuse, and pervasive developmental disorder (PDD). Family studies suggest that ADHD + CD represents a specific subtype of the ADHD disorder with familial risk factors only partly overlapping with t…

Genetics and epigenetic pathways of disease [NCMLS 6]2804 Cellular and Molecular NeuroscienceMedizinPoison controlComorbidityNeuroinformatics [DCN 3]Linkage DisequilibriumCohort Studies2738 Psychiatry and Mental Health0302 clinical medicinePerception and Action [DCN 1]Genetics(clinical)ChildGenetics (clinical)Oligonucleotide Array Sequence Analysis0303 health sciencesAntisocial Personality Disorder10058 Department of Child and Adolescent Psychiatry3. Good healthPedigreeEuropePsychiatry and Mental healthConduct disorderAttention Deficit and Disruptive Behavior DisordersADHD -- conduct disorder -- genome wide association study -- genetic association information networkmedicine.symptomPsychologyFunctional Neurogenomics [DCN 2]Anxiety disorderAlgorithmsClinical psychologyConduct DisorderGenetic Markers2716 Genetics (clinical)Quantitative Trait LociContext (language use)610 Medicine & healthChild Behavior DisordersImpulsivityPolymorphism Single NucleotideMental health [NCEBP 9]behavioral disciplines and activitiesGenomic disorders and inherited multi-system disorders [IGMD 3]03 medical and health sciencesCellular and Molecular NeuroscienceCognitive neurosciences [UMCN 3.2]mental disordersmedicinePervasive developmental disorderHumansddc:610Medizinische Fakultät » Universitätsklinikum Essen » LVR-Klinikum Essen » Klinik für Psychiatrie Psychosomatik und Psychotherapie des Kindes- und Jugendalters030304 developmental biologyPsychiatric Status Rating ScalesGenome HumanAntisocial personality disordermedicine.diseaseComorbidityGenetic defects of metabolism [UMCN 5.1]Attention Deficit Disorder with Hyperactivity030217 neurology & neurosurgeryGenome-Wide Association Study
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Analysis of HLA-DQA, HLA-DQB frequencies in a group of Sardinian centenarians

2006

Human leukocyte antigen (HLA) alleles, regulating type and intensity of the immune response, might influence life expectancy. In previous case-control studies the authors have demonstrated that both HLA-DR and -DQ alleles are not associated with longevity in the Sardinian population. On the other hand, association studies are subjected (as part of the homogeneity of the population in terms of geographic origin) to a number of possible confounding factors. Therefore, the authors typed the HLA-DQA1 and HLA-DQB1 alleles in 24 sibs (age range 85 to 97) of 17 centenarians by PCR-SSP. Sib pair analysis showed non-significant differences between the observed and expected percentage of DQA* or DQB1…

GeneticsAged 80 and overAgingeducation.field_of_studymedia_common.quotation_subjectPopulationConfoundingLongevityLongevityAnalysis of HLA-DQA HLA-DQBHuman leukocyte antigenBiologyHLA-DQ alpha-ChainsHLA-DQ AntigensTraitHLA-DQ beta-ChainsHumansGeriatrics and GerontologyAlleleAllele sharingeducationAllelesmedia_commonGenetic association
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The Genetics of Evolutionary Change in Senecio vulgaris L.: A QTL Mapping Approach

2001

: The cosmopolitan weed Senecio vulgaris var. vulgaris is likely to have originated from the non-weedy S. vulgaris ssp. denticulatus from which it differs by showing no seed dormancy, by completing its life cycle from germination to seed formation much faster and by lacking ray florets. An F2 generation of 120 individuals obtained through selfing of one hybrid individual between var. vulgaris and ssp. denticulatus was used to construct a linkage map based on RAPD polymorphisms and the presence or absence of ray florets. This linkage map was used for a QTL analysis of 12 characters distinguishing the two taxa. For seven of these 12 characters, three significant QTLs could be found. One of th…

GeneticsBractfungiSeed dormancySenecio vulgarisfood and beveragesSelfingLocus (genetics)Plant ScienceGeneral MedicineBiologyQuantitative trait locusbiology.organism_classificationRAPDGerminationBotanyEcology Evolution Behavior and SystematicsPlant Biology
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Analysis of the melanocortin receptor 1 (MC1R) gene in Sicilian goat breeds

2010

AbstractMammalian coat colour is mainly determined by the distribution of two different types of melanins: pheomelanin (red/yellow pigments) and eumelanin (black pigments). Their synthesis is regulated by the melanocortin 1 receptor (MC1R/Extension locus) that binds the α-melanocyte-stimulating hormone (α-MSH) and the agouti signalling protein (ASIP, coded by the Agouti locus). In mammals, several studies have reported that loss-of-function mutations in MC1R lead to red/yellow pigmentation, while gain-of-function mutations lead to black/dark colours. Mutations at the Agouti locus exert, in general, epistatic interactions on the Extension locus. In goats, classical genetic studies have indic…

GeneticsCoatintegumentary systemMUTATIONSdigestive oral and skin physiologygoatLocus (genetics)Phenotypic traitCOAT COLOUR GENESBiologySettore AGR/17 - Zootecnica Generale E Miglioramento GeneticoBREEDSMC1RMelanocortin Receptor 1EpistasisAnimal Science and Zoologylcsh:Animal cultureMc1r genelcsh:SF1-1100Melanocortin 1 receptor
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Amplified fragment length polymorphism (AFLP) and biochemical typing of Photobacterium damselae subsp. damselae.

2002

Aims: The aim of the present study was to characterize subspecifically Photobacterium damselae subsp. damselae strains isolated from cultured Sparus aurata and Dicentrarchus labrax by means of phenotypic and molecular typing techniques (amplified fragment length polymorphism, AFLP). Methods and Results: Seventy-one strains of P. damselae subsp. damselae were isolated from 38 cultured fishes at different fish farms located on the Mediterranean coast near Valencia, Spain. Most fish studied were asymptomatic and some were recovered during infectious outbreaks. Phenotypic characterization revealed a considerable degree of variability within the subspecies, including some characters, such as pro…

GeneticsDNA BacterialPhotobacteriumDendrogramUPGMAGeneral MedicinePhenotypic traitAquacultureBiologySubspeciesPhotobacteriumbiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyBacterial Typing TechniquesPerciformesFish DiseasesPhotobacterium damselaePhenotypeAnimalsAmplified fragment length polymorphismTypingGram-Negative Bacterial InfectionsPolymorphism Restriction Fragment LengthBiotechnologyJournal of applied microbiology
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