Search results for "Terminal"

showing 10 items of 364 documents

Efferent connections of the "olfactostriatum": a specialized vomeronasal structure within the basal ganglia of snakes.

2005

Abstract The olfactostriatum is a portion of the basal ganglia of snakes that receives substantial vomeronasal afferents through projections from the nucleus sphericus. In a preceding article, the olfactostriatum of garter snakes (Thamnophis sirtalis) was characterized on the basis of chemoarchitecture (distribution of serotonin, neuropeptide Y and tyrosine hydroxylase) and pattern of afferent connections [Martinez-Marcos, A., Ubeda-Banon, I., Lanuza, E., Halpern, M., 2005. Chemoarchitecture and afferent connections of the “olfactostriatum”: a specialized vomeronasal structure within the basal ganglia of snakes. J. Chem. Neuroanat. 29, 49–69]. In the present study, its efferent connections …

MaleHypoglossal nucleusHypothalamus PosteriorBiotinBiologyNucleus accumbensAmygdalaEfferent PathwaysBasal GangliaNucleus AccumbensVentral pallidumCellular and Molecular NeuroscienceBasal gangliamedicineAnimalsRhodaminesColubridaeDextransAnatomyOlfactory PathwaysAmygdalaVentral tegmental areaSmellStria terminalismedicine.anatomical_structureFemaleFluoresceinVomeronasal OrganRaphe nucleiNeuroscienceJournal of chemical neuroanatomy
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Revision of the Shore-fly Genera Parahyadina Tonnoir and Malloch and New Zealand Hyadina Haliday (Diptera: Ephydridae).

2019

Two genera of the shore-fly tribe Hyadinini, Hyadina Haliday and Parahyadina Tonnoir & Malloch, are revised, and all species treated, save P. lacustris Tonnoir & Malloch, are described for the first time. The phylogenetic position of both genera within Hyadinini is presented along with confirming, morphological evidence. The New Zealand fauna of Hyadina is now limited to the single new species H. breva, and Parahyadina is expanded from being a monotypic genus based on P. lacustris to also include the following 9 endemic new species: P. angusta, P. atra, P. bifurcata, P. bulla, P. debilis, P. edmistoni, P. hennigi, P. irwini, and P. latistylis. For both genera, emphasis is given to s…

MaleInsectaArthropodaFaunaZoologyEphydridaeTribe (biology)HyadinaEphydridaekeyGenusAnimaliaAnimalsEcology Evolution Behavior and SystematicsBulla (gastropod)PhylogenyTaxonomynew speciesPhylogenetic treebiologyDipteraTerminaliaBiodiversityParahyadinabiology.organism_classificationKey (lock)Animal Science and ZoologyAnimal DistributionNew ZealandZootaxa
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New taxonomic twists in shore flies as revealed in discovery of Neozealides, a new genus from New Zealand (Diptera: Ephydridae)

2019

We describe Neozealides to accommodate two endemic species from New Zealand that were previously placed in the shore-fly genus Hyadina Haliday. Although similar to Hyadina, both species are more closely related to the Hyadina and Philygria groups of genera (Zatwarnicki & Ryczko 2014) than they are to species within Hyadina. To document these discoveries, we revise both species, placing them in Neozealides. Emphasis is given to structures of the male terminalia, which are fully illustrated. Detailed locality data and distribution maps for both species are provided. For perspective and to facilitate recognition of genera, the tribe Hyadinini is diagnosed and a key to genera from New Zeala…

MaleInsectaArthropodaZoologyEphydridaeBiologyTribe (biology)EphydridaekeyGenusAnimalsAnimaliaEndemismEcology Evolution Behavior and SystematicsTaxonomyShoregeographygeography.geographical_feature_categoryDipteraTerminaliaBiodiversitybiology.organism_classificationNeozealidesKey (lock)Animal Science and ZoologyAnimal DistributionNew Zealand
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PBX1 acts as terminal selector for olfactory bulb dopaminergic neurons

2020

15 páginas, 8 figuras. Supplementary information available online at http://dev.biologists.org/lookup/doi/10.1242/dev.186841.supplemental

MaleInterneuronCell SurvivalNeurogenesisRNA SplicingNeuron differentiationMitosisBiologyAdult neurogenesis03 medical and health sciencesOlfactory bulb0302 clinical medicineNeuroblastInterneuronsmedicineAnimalsProtein IsoformsCell LineageProgenitor cellTerminal selector10. No inequalityMolecular BiologyTranscription factorBody Patterning030304 developmental biologyMice KnockoutDopaminergic neuron0303 health sciencesDopaminergic NeuronsPre-B-Cell Leukemia Transcription Factor 1fungiNeurogenesisDopaminergicCell DifferentiationExonsEmbryo Mammalian3. Good healthOlfactory bulbmedicine.anatomical_structureMutationNeuron differentiationNeuroscience030217 neurology & neurosurgeryTranscription FactorsAlternative splicingDevelopmental BiologyDevelopment
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Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15.

2019

Abstract N-alpha-acetylation is one of the most common co-translational protein modifications in humans and is essential for normal cell function. NAA10 encodes for the enzyme NAA10, which is the catalytic subunit in the N-terminal acetyltransferase A (NatA) complex. The auxiliary and regulatory subunits of the NatA complex are NAA15 and Huntington-interacting protein (HYPK), respectively. Through a genotype-first approach with exome sequencing, we identified and phenotypically characterized 30 individuals from 30 unrelated families with 17 different de novo or inherited, dominantly acting missense variants in NAA10 or NAA15. Clinical features of affected individuals include variable levels…

MaleModels Molecular0301 basic medicineProtein ConformationMicrophthalmia0302 clinical medicineEnzyme StabilityMissense mutationN-Terminal Acetyltransferase EChildN-Terminal Acetyltransferase AExome sequencingGenetics (clinical)GeneticsbiologyGeneral MedicinePhenotypeRecombinant ProteinsChemistryPhenotypeChild PreschoolHMG-CoA reductaseCohortFemaleGeneral ArticleCorrigendumAdultNatA complexmedicine.medical_specialtyAdolescentGenotypeFrameshift mutationStructure-Activity RelationshipYoung Adult03 medical and health sciencesMolecular geneticsGeneticsmedicineHumansGenetic Predisposition to DiseaseGenetic TestingAlleleBiologyMolecular BiologyAllelesGenetic Association StudiesComputational BiologyFaciesGenetic VariationInfantmedicine.diseaseEnzyme ActivationLenz microphthalmia syndrome030104 developmental biologyGenetic LociMutationbiology.proteinHuman medicineBiomarkers030217 neurology & neurosurgeryNAA15Human molecular genetics
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Brain processing of the mammary pheromone in newborn rabbits.

2011

International audience; Chemosignals strongly contribute to social interactions in mammals, including mother-young relationships. In the European rabbit, a volatile compound emitted by lactating females in milk, the 2-methylbut-2-enal, has been isolated. Carrying the properties of a pheromone, in particular the spontaneous ability to release critical sucking-related movements in newborns, it has been called the mammary pheromone (MP). Lesion of the vomeronasal organ and preliminary 2-deoxyglucose data suggested that the MP could be processed by the main olfactory system. However, the neuronal substrate that sustains the MP-induced response of neonates remained unknown. Here, we evaluated Fo…

MaleOlfactory systemVomeronasal organ[ SDV.AEN ] Life Sciences [q-bio]/Food and NutritionMESH: NeuronsMESH: RabbitsPheromonesMESH : PheromonesMESH: Animals NewbornThirstMESH: Vomeronasal OrganBehavioral Neuroscience0302 clinical medicinePiriform cortexMESH : HabenulaMESH : FemaleMESH: AnimalsMESH : Olfactory BulbNeurons0303 health sciencesMESH: PheromonesLamina terminalisMESH: Proto-Oncogene Proteins c-fosMESH : Animals NewbornOlfactory PathwaysOlfactory BulbHabenulamedicine.anatomical_structureMESH: HabenulaPheromoneFemaleRabbitsVomeronasal Organmedicine.symptomProto-Oncogene Proteins c-fosMESH: Olfactory Bulbmedicine.medical_specialtyMESH : HypothalamusMESH : Vomeronasal OrganMESH : MaleHypothalamusBiologyMESH : Neurons03 medical and health sciencesInternal medicinemedicineAnimalsMESH : Rabbits030304 developmental biologyHabenulaMESH : Olfactory PathwaysNewbornMESH: HypothalamusMESH: MaleOlfactory bulbEndocrinologyMESH : Proto-Oncogene Proteins c-fosAnimals NewbornMESH : AnimalsMESH: Female[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition030217 neurology & neurosurgeryMESH: Olfactory Pathways
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Heterozygous nonsense SCN5A mutation W822X explains a simultaneous sudden infant death syndrome.

2008

The sudden, unexpected, and unexplained death of both members of a set of healthy twins (simultaneous sudden infant death syndrome (SSIDS)) is defined as a case in which both infants meet the definition of sudden infant death syndrome individually. A search of the world medical literature resulted in only 42 reported cases of SSIDS. We report the case of a pair of identical, male, monozygotic twins, 138 days old, who suddenly died, meeting the full criteria of SSIDS and where a genetic screen was performed, resulting in a heterozygous nonsense SCN5A mutation (W822X) in both twins. Immunohistochemistry was performed on cardiac tissue samples utilizing polyclonal antibodies anti-Na+ CP type V…

MalePathologymedicine.medical_specialtyNav1.5 protein functionv1.5 protein functionmedia_common.quotation_subject2734Nonsense mutationNonsenseNa+ channel functionMuscle ProteinsSocio-culturaleBiology+Nav1.5 protein function; Na+ channel function; SCN5A gene mutation; Simultaneous sudden infant death syndrome; W822X mutation; Codon Nonsense; Diseases in Twins; Humans; Infant; Male; Muscle Proteins; NAV1.5 Voltage-Gated Sodium Channel; Sodium Channels; Sudden Infant Death; 2734Sudden deathSodium ChannelsNAV1.5 Voltage-Gated Sodium ChannelPathology and Forensic MedicinePathogenesisSCN5A gene mutationDiseases in TwinsmedicineHumansSimultaneous sudden infant death syndromeSCN5A gene mutationW822X mutationNa+ channel functionNav1.5 protein functionNaSimultaneous sudden infant death syndrome SCN5A gene mutation W822X mutation Na+ channel function Nav1.5 protein function CodonMolecular BiologyCellular localizationmedia_commonSimultaneous sudden infant death syndromeSettore BIO/16 - Anatomia UmanaSimultaneous sudden infant death syndrome SCN5A gene mutation W822X mutation Na+ channel function Nav1.5 protein functionW822X mutationInfantCell BiologyGeneral MedicineSudden infant death syndromeNonsenseTerminal deoxynucleotidyl transferaseCodon NonsenseImmunohistochemistryNa; v; 1.5 protein function; Na; +; channel function; SCN5A gene mutation; Simultaneous sudden infant death syndrome; W822X mutationchannel functionSudden Infant Death
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Synaptic vesicle alterations in rod photoreceptors of synaptophysin-deficient mice.

2001

Abstract The abundance of the integral membrane protein synaptophysin in synaptic vesicles and its multiple possible functional contributions to transmitter exocytosis and synaptic vesicle formation stand in sharp contrast to the observed lack of defects in synaptophysin knockout mice. Assuming that deficiencies are compensated by the often coexpressed synaptophysin isoform synaptoporin, we now show that retinal rod photoreceptors, which do not synthesize synaptoporin either in wild-type or in knockout mice, are affected by the loss of synaptophysin. Multiple pale-appearing photoreceptors, as seen by electron microscopy, possess reduced cytoplasmic electron density, swollen mitochondria, an…

MalePresynaptic TerminalsSynaptophysinAction PotentialsFluorescent Antibody TechniqueDark AdaptationBiologyRibbon synapseSynaptic vesicleSynaptic TransmissionExocytosisExocytosisMiceRetinal Rod Photoreceptor CellsElectroretinographySynaptic vesicle recyclingAnimalsMice KnockoutSex CharacteristicsGeneral NeuroscienceVesicleMembrane ProteinsClathrin-Coated VesiclesSynaptoporinCell biologyMice Inbred C57BLMicroscopy ElectronProtein TransportKnockout mouseSynaptophysinbiology.proteinFemaleSynaptic VesiclesNeurosciencePhotic StimulationNeuroscience
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Natural and engineered carboxy-terminal variants: decreased secretion and gain-of-function result in asymptomatic coagulation factor VII deficiency.

2012

We report 2 asymptomatic homozygotes for the nonsense p.R462X mutation affecting the carboxy-terminus of coagulation factor VII (FVII, 466 aminoacids). FVII levels of 3-5% and 2.7 ± 0.4% were found in prothrombin time-based and activated factor X (FXa) generation assays with human thromboplastins. Noticeably, FVII antigen levels were barely detectable (0.7 ± 0.2%) which suggested a gain-of-function effect. This effect was more pronounced with bovine thromboplastin (4.8 ± 0.9%) and disappeared with rabbit thromboplastin (0.7 ± 0.2%). This suggests that the mutation influences tissue factor/FVII interactions. Whereas the recombinant rFVII-462X variant confirmed an increase in specific activit…

MaleProteasesHeterozygoteFactor VII DeficiencyEnzyme-Linked Immunosorbent AssayFVIIBiologymedicine.disease_causeThromboplastinTissue factorchemistry.chemical_compoundCarboxy-terminalhemic and lymphatic diseasesmedicineFACTOR VII DEFICIENCY MOLECULAR VARIANTSThromboplastinMissense mutationAnimalsHumanscardiovascular diseasesChildBlood CoagulationProthrombin timeMutationmedicine.diagnostic_testFactor VIIHomozygoteHematologyFactor VIIMiddle AgedMolecular biologyAsymptomatic; Carboxy-terminal; FVII; Mutation;AsymptomaticchemistryCoagulationCodon NonsenseMutationMutagenesis Site-DirectedProthrombin TimeCattleFemaleRabbitsOriginal Articles and Brief Reports
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Assessing quality of care for the dying from the bereaved relatives' perspective: Using pre-testing survey methods across seven countries to develop …

2019

Background: The provision of care for dying cancer patients varies on a global basis. In order to improve care, we need to be able to evaluate the current level of care. One method of assessment is to use the views from the bereaved relatives. Aim: The aim of this study is to translate and pre-test the ‘Care Of the Dying Evaluation’ (CODETM) questionnaire across seven participating countries prior to conducting an evaluation of current quality of care. Design: The three stages were as follows: (1) translation of CODE in keeping with standardised international principles; (2) pre-testing using patient and public involvement and cognitive interviews with bereaved relatives; and (3) utilising …

MaleQuality Assurance Health Careproxycognitive interviewingProxy (climate)Survey methodology0302 clinical medicineGermanySurveys and QuestionnairesOutcome Assessment Health CareTerminal careMedicineNorwayPalliative CarePre testingOutcome measuresGeneral MedicineMiddle Aged3. Good healthPeer reviewquality of healthcareCaregiverssurvey and questionnaire030220 oncology & carcinogenesisFemalequality of care for the dying0305 other medical scienceBrazilAdultmedicine.medical_specialtyArgentina03 medical and health sciences030502 gerontologyHumansTerminally IllFamilyQuality of careCognitive interviewAgedbusiness.industryOriginal ArticlesUnited KingdomCross-Sectional StudiesAnesthesiology and Pain MedicineFamily medicineUruguayPolandLevel of carebusinessBereavement
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