Search results for "prion"

showing 10 items of 53 documents

Genetic Basis of Body Color and Spotting Pattern in Redheaded Pine Sawfly Larvae (Neodiprion lecontei)

2018

Abstract Pigmentation has emerged as a premier model for understanding the genetic basis of phenotypic evolution, and a growing catalog of color loci is starting to reveal biases in the mutations, genes, and genetic architectures underlying color variation in the wild. However, existing studies have sampled a limited subset of taxa, color traits, and developmental stages. To expand the existing sample of color loci, we performed QTL mapping analyses on two types of larval pigmentation traits that vary among populations of the redheaded pine sawfly (Neodiprion lecontei): carotenoid-based yellow body color and melanin-based spotting pattern. For both traits, our QTL models explained a substan…

0106 biological sciences0301 basic medicineCandidate geneGenetic LinkageGenome InsectQuantitative Trait LociQuantitative trait locusBiologyInvestigationsevolutionary genetics010603 evolutionary biology01 natural sciencestoukat03 medical and health sciencesQuantitative Trait HeritableGenetic linkageGeneticsGene familyAnimalssahapistiäisetconvergent evolutionDomesticationGeneGenetic Association Studies030304 developmental biologyGenetics0303 health sciencesHuman evolutionary geneticsPigmentationta1184väri (ominaisuudet)carotenoidsChromosome Mappingbiology.organism_classificationgeneettinen muuntelugenetic architectureHymenopteraGenetic architecturekarotenoiditmelaninSawflyNeodiprion lecontei030104 developmental biologyPhenotypeEvolutionary biologyLarvata1181Femalepigmentti (biologia)
researchProduct

Ecological conditions alter cooperative behaviour and its costs in a chemically defended sawfly

2018

The evolution of cooperation and social behaviour is often studied in isolation from the ecology of organisms. Yet, the selective environment under which individuals evolve is much more complex in nature, consisting of ecological and abiotic interactions in addition to social ones. Here, we measured the life-history costs of cooperative chemical defence in a gregarious social herbivore, Diprion pini pine sawfly larvae, and how these costs vary under different ecological conditions. We ran a rearing experiment where we manipulated diet (resin content) and attack intensity by repeatedly harassing larvae to produce a chemical defence. We show that forcing individuals to allocate more to coope…

0106 biological sciences0301 basic medicineMaleautomimicrygenetic structures[SDV]Life Sciences [q-bio]Social behaviourTrade-offlife-history costs01 natural sciencesantipredator defencesocial behavioursahapistiäisetCooperative BehaviorComputingMilieux_MISCELLANEOUSGeneral Environmental ScienceAbiotic componentbiologyBehavior AnimalEcology[SDV.BA]Life Sciences [q-bio]/Animal biologyPinus sylvestrisGeneral MedicineSawflyLarvaFemaleGeneral Agricultural and Biological SciencesDiprion piniAdaptive valueCheatingeläinten käyttäytyminen010603 evolutionary biologyGeneral Biochemistry Genetics and Molecular Biology03 medical and health sciencesAnimalsBehaviourpuolustusmekanismit (biologia)Social BehaviorHerbivoreGeneral Immunology and Microbiologymimikryfungibiology.organism_classificationHymenopteraImmunity InnateDiet030104 developmental biologyPredatory Behaviorta1181Resins Plant
researchProduct

Assessing multiple sources of data to detect illegal fishing, trade and mislabelling of elasmobranchs in Greek markets

2020

Abstract Elasmobranchs, extremely charismatic and threatened animals, still are an important economic source for fishers in many parts of the world, providing significant income through trade. Even though Greek seas host at least 67 elasmobranch species, our knowledge about their biology and ecology is to a large extent unknown. In the present study the integration of conventional (legislation, official data from fisheries landings and fish market value and import/export data) and unconventional (social media) sources of data, accompanied with the use of genetics, aim at outlining the elasmobranch fisheries and trade in Greece and identifying “weak spots” that sabotage their conservation. R…

0106 biological sciencesEconomics and EconometricsEastern MediterraneanSettore BIO/05 - ZoologiaLegislationContext (language use)Management Monitoring Policy and LawAquatic Science01 natural sciencesseafood fraudsharkdata qualitymedia_common.cataloged_instanceEuropean unionGeneral Environmental Sciencemedia_commonbiologyrayskate010604 marine biology & hydrobiologyPrionace glaucaLegislature04 agricultural and veterinary sciencesbiology.organism_classificationIllegal fishingFisherytraceabilityThreatened species040102 fisheries0401 agriculture forestry and fisheriesFisheries managementLawMarine Policy
researchProduct

Deadly impalement of a blue shark Prionace glauca by a swordfish Xiphias gladius

2017

In September, 2016, an adult female blue shark (Prionace glauca) 247 cm long stranded alive on the coast of Valencia (Spain, Western Mediterranean) but died shortly afterwards. The necropsy revealed ongoing pregnancy, with 65 embryos in early stage of development, and a healthy condition with no signs of starvation. Two fishing hooks surrounded by scarred tissue were detected in the mandible, indicating past interaction with fisheries. In addition, a fragment of the tip of a swordfish (Xiphias gladius) rostrum (length: 18 cm long, width: 0.5 cm (distal) and 3 cm (proximal)) was removed from the animal. The fragment had pierced the head producing an incision of 3.5 cm close to the left eye, …

0106 biological sciencesEnvironmental EngineeringAquatic ScienceOceanography010603 evolutionary biology01 natural sciencesmedicineJuvenileGladiusEcology Evolution Behavior and SystematicsXiphias gladiusbiology010604 marine biology & hydrobiologySwordfishRostrumPrionace glaucaMandibleWestern Mediterranean.Pelagic zoneAnatomyPrionace glaucabiology.organism_classificationstrandingSkullmedicine.anatomical_structuredeadly interactionimpalementMediterranean Marine Science
researchProduct

Aggressive interactions between juvenile swordfishes and blue sharks in the Western Mediterranean: a widespread phenomenon?

2019

There are numerous reports of billfishes spearing objects, marine organisms, and even humans. Whether or not this behaviour is intentional and, if so, what is its functional meaning, are open questions. In 2016, an adult blue shark (Prionace glauca) was found to be killed by a juvenile swordfish (Xiphias gladius) in the western Mediterranean. Here we report on three more recent cases involving both species in the same area. In February 2017, an adult male blue shark was found stranded in Garrucha (Spain) with a fragment of a juvenile swordfish’s rostrum (18cm long x 2cm wide at proximal end) inserted in its cranium. In March 2017, an adult pregnant female blue shark was stranded alive on th…

0106 biological sciencesMediterranean climateXiphias gladiusEnvironmental EngineeringAdult femalelethal interaction010604 marine biology & hydrobiologySwordfishRostrumPrionace glaucaZoologyPrionace glaucaAquatic ScienceBiologyPregnant femaleOceanographybiology.organism_classification010603 evolutionary biology01 natural sciencesstrandingJuvenileimpalementGladiuswestern MediterraneanEcology Evolution Behavior and SystematicsMediterranean Marine Science
researchProduct

Temporal dynamics of hippocampal neurogenesis in chronic neurodegeneration.

2014

Increased neurogenesis has been reported in neurodegenerative disease, but its significance is unclear. In a mouse model of prion disease, Gomez-Nicola et al. detect increased neurogenesis in the dentate gyrus that partially counteracts neuronal loss. Targeting neurogenesis may have therapeutic potential.

AdultMaleAntimetabolites AntineoplasticPatch-Clamp TechniquesTime FactorsPrionsNeurogenesisGenetic VectorsHippocampusTissue BanksBiologyHippocampal formationHippocampusCreutzfeldt-Jakob SyndromePrion DiseasesMiceYoung AdultNeural Stem CellsAlzheimer Diseasevariant CJDNeural PathwaysmedicineAnimalsHumansAgedCell ProliferationDentate gyrusNeurogenesisNeurodegenerationCytarabineNeurodegenerative DiseasesOriginal ArticlesMiddle Agedmedicine.diseaseNeural stem cellMice Inbred C57BLNeuroanatomical Tract-Tracing Techniquesadult neurogenesisDisease Models AnimalChronic DiseaseDentate GyrusMossy Fibers HippocampalDisease ProgressionFemaleNeurology (clinical)Alzheimer's diseaseNeuroscienceNeural developmentAlzheimer’s diseaseBrain : a journal of neurology
researchProduct

The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion disease.

2005

Objective: To assess cognitive function in variant Creutzfeldt-Jakob disease (vCJD). We describe the neuropsychological profiles of 10 cases and compare these data with cross sectional data obtained from patients with histologically confirmed sporadic CJD and cases with inherited prion disease with confirmed mutations in the prion protein gene. Methods: Patients referred to the Specialist Cognitive Disorders Clinic at the National Hospital for Neurology and Neurosurgery and the National Prion Clinic at St Mary's Hospital, London for further investigation of suspected CJD were recruited into the study. The neuropsychological test battery evaluated general intelligence, visual and verbal memo…

AdultMalePaperPediatricsmedicine.medical_specialtyPrionsanimal diseasesDNA Mutational AnalysisNeuropsychological TestsCreutzfeldt-Jakob SyndromePrion DiseasesNational Prion Clinicmental disordersmedicineDementiaHumansCognitive declinePsychiatrymedicine.diagnostic_testSettore M-PSI/02 - Psicobiologia E Psicologia Fisiologicabusiness.industryNeuropsychologyNeuropsychological testCreutzfeldt-Jakob SyndromeMiddle Agedmedicine.diseasenervous system diseasesPsychiatry and Mental healthCross-Sectional StudiesAdult Cognition Disorders/etiology Creutzfeldt-Jakob Syndrome/complications Creutzfeldt-Jakob Syndrome/genetics Creutzfeldt-Jakob Syndrome/psychology Cross-Sectional Studies DNA Mutational Analysis Disease Progression Female Humans Male Middle Aged Neuropsychological Tests Prion Diseases/genetics Prion Diseases/psychology Prions/genetics Visual PerceptionDisease ProgressionVisual PerceptionSurgeryFemaleNeurology (clinical)Verbal memorybusinessCognition DisordersExecutive dysfunctionJournal of neurology, neurosurgery, and psychiatry
researchProduct

Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation

2012

Background The human prion diseases are a group of universally fatal neurodegenerative disorders associated with the auto-catalytic misfolding of the normal cell surface prion protein (PrP). Mutations causative of inherited human prion disease (IPD) include an insertion of six additional octapeptide repeats (6-OPRI) and a missense mutation (P102L) with large families segregating for each mutation residing in southern England. Here we report for the first time the neuropsychological and clinical assessments in these two groups. Method The cognitive profiles addressing all major domains were obtained for 26 patients (18 6-OPRI, 8 P102L) and the cortical thickness determined using 1.5T MRI in …

AdultMalePathologymedicine.medical_specialtyPrionsprion diseaseNeuroimagingDiseaseNeuropsychological Testsmedicine.disease_causePrion DiseasesExecutive FunctionYoung AdultHumansMedicineDementiaMissense mutationStrokeMemory DisordersMutationSettore M-PSI/02 - Psicobiologia E Psicologia Fisiologicabusiness.industryGenetic heterogeneityNeuropsychologyBrainMiddle Agedmedicine.diseaseMagnetic Resonance ImagingUnited KingdomMutagenesis InsertionalPsychiatry and Mental healthFemaleSurgeryNeurology (clinical)Cognition DisordersbusinessExecutive dysfunctionJournal of Neurology, Neurosurgery and Psychiatry
researchProduct

No Association Between Genetic Polymorphism at Codon 129 of the Prion Protein Gene and Primary Progressive Multiple Sclerosis

2011

AdultMalePrionsChromosomes Human Pair 20Primary Progressive Multiple SclerosisPolymorphism Single Nucleotide03 medical and health sciences0302 clinical medicineArts and Humanities (miscellaneous)HumansMedicineGenetic Predisposition to DiseasePrion proteinCodonGene030304 developmental biologyGenetics0303 health sciencesbusiness.industryMiddle AgedMultiple Sclerosis Chronic ProgressivePrnp geneFemaleNeurology (clinical)business030217 neurology & neurosurgeryArchives of Neurology
researchProduct

Association study of a SNP coding for a M129V substitution in the prion protein in schizophrenia.

2003

AdultPsychosisAmyloidAdolescentGenotypePrionsSchizophrenia (object-oriented programming)610 Medicine & healthBiologymedicine.disease_causeGenetic determinismPrion Proteins2738 Psychiatry and Mental HealthOpen Reading FramesPolymorphism (computer science)medicineSNPHumansPoint MutationGenetic Predisposition to DiseaseProtein PrecursorsCodonBiological PsychiatryAgedGeneticsMutationSubstitution (logic)Case-control study11359 Institute for Regenerative Medicine (IREM)Middle Agedmedicine.diseasePsychiatry and Mental healthAmino Acid SubstitutionCase-Control StudiesSchizophrenia2803 Biological PsychiatrySchizophrenia research
researchProduct