Search results for "Motor"

showing 10 items of 3137 documents

Effects of GABA-transporter (GAT) inhibitors on rat behaviour in open-field and elevated plus-maze.

1999

The behavioural consequences of inhibition of gamma-aminobutyric acid (GABA) uptake were studied. Two GABA uptake inhibitors, tiagabine and SKF 89976-A, were administered to rats, and behaviour was analysed 30 min later in a standard open field, an enriched open field, and an elevated plus-maze. Eight groups of animals received either saline (0.9%), tiagabine, or SKF 89976-A. At a dose of 18.5 mg/kg, tiagabine, an established antiseizure drug, impaired motor coordination, enhanced exploratory activity and reduced anxiety related behaviour. SKF 89976-A exhibited minimal effects over the dose range tested. These results indicate that inhibition of GABA uptake might be a pharmacological strate…

GABA Plasma Membrane Transport ProteinsMaleElevated plus mazeGABA Plasma Membrane Transport ProteinsTiagabineGABA AgentsNipecotic AcidsOrganic Anion TransportersPharmacologyAnxietyEnvironmentMotor Activitygamma-Aminobutyric acidOpen fieldmedicineGABA transporterAnimalsTiagabineGABA Agonistsgamma-Aminobutyric AcidPharmacologybiologyBehavior AnimalDose-Response Relationship DrugChemistryMembrane ProteinsMembrane Transport ProteinsRatsPsychiatry and Mental healthGABA Agentsnervous systembiology.proteinExploratory BehaviorGABA Uptake InhibitorsAnticonvulsantsCarrier Proteinsmedicine.drugBehavioural pharmacology
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Problematiche energetiche e sviluppi connessi alla combustione double fuel

2014

Gas naturale GPL motore numero di ottano sovralimentazione HCCISettore ING-IND/10 - Fisica Tecnica Industriale
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Field Reconstruction for Modeling Multiple Faults in Permanent Magnet Synchronous Motors in Transient States

2021

Conventional field reconstruction model (FRM) for electrical machines has proved its main strength in efficient computations of magnetic fields and forces in healthy permanent magnet synchronous machines (PMSM) or faulty machines in steady states. This study aims to develop a magnet library of different magnet defects and include inter-turn short-circuit (ITSC) in the FRM for PMSM. The developed FRM can model a combination fault between ITSC, and magnet defect in a PMSM in transient states. Within the framework, an 8-turn ITSC was modelled in both finite element analysis (FEA) and FRM, and then identified by the extended Park’s vector approach. The air-gap magnetic field reproduced b…

General Computer ScienceRotor (electric)Computer scienceStatorMathematics::General Mathematicsinter-turn short circuitfield reconstructionGeneral EngineeringFault (power engineering)Finite element methodlaw.inventionMagnetic fieldTK1-9971VDP::Teknologi: 500DemagnetisationlawControl theoryElectromagnetic coilMagnetpermanent magnet synchronous motorGeneral Materials ScienceTransient (oscillation)Electrical engineering. Electronics. Nuclear engineeringIEEE Access
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Effect of claustrum stimulation on neurons of the contralateral medial oculomotor area, in the cat

1990

In chloralose-anaesthetized cats, the extracellular spontaneous unitary activity was recorded from 157 neurons, located in the medial oculomotor area. 98 units were identified as projecting onto the superior colliculus. Electrical stimulations of the contralateral claustrum provoked, on 13 of these cells, an excitatory effect, lasting 10-35 ms and appearing with a latency of 20-50 ms. Full length section of the corpus callosum totally abolished the contralateral claustrum effect. The results suggest that in the cat, the claustrum may have a role in the bilateral control of the visuo-motor performance.

General NeuroscienceSuperior colliculusCentral nervous systemAnatomyBiologyCorpus callosumClaustrumBasal GangliaElectric StimulationFunctional LateralityFrontal LobeOculomotor nucleusElectrophysiologyElectrophysiologymedicine.anatomical_structureBasal gangliaCatsExcitatory postsynaptic potentialmedicineAnimalsNeuroscienceNeuroscience Letters
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Response of abducens internuclear neurons to axotomy in the adult cat

2000

The highly specific projection of abducens internuclear neurons on the medial rectus motoneurons of the oculomotor nucleus constitutes an optimal model for investigating the effects of axotomy in the central nervous system. We have analyzed the morphological changes induced by this lesion on both the cell bodies and the transected axons of abducens internuclear neurons in the adult cat. Axotomy was performed by the transection of the medial longitudinal fascicle. Cell counts of Nissl-stained material and calretinin-immunostained abducens internuclear neurons revealed no cell death by 3 months postaxotomy. Ultrastructural examination of these cells at 6, 14, 24, and 90 days postaxotomy showe…

General Neurosciencemedicine.medical_treatmentAnatomyBiologyOculomotor nucleusLesionchemistry.chemical_compoundmedicine.anatomical_structurenervous systemchemistryGliosisBiocytinmedicineCalretininmedicine.symptomAxotomyAbducens nerveReinnervationThe Journal of Comparative Neurology
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Homozygous SMN1 exons 1-6 deletion: pitfalls in genetic counseling and general recommendations for spinal muscular atrophy molecular diagnosis.

2012

We report on a rare homozygous intragenic deletion encompassing exons 1-6 of the SMN1 gene in a patient with spinal muscular atrophy (SMA) born into a consanguineous family. This exceptional configuration induced misinterpretation of the molecular defect involved in this patient, who was first reported as having a classic SMN1 exon 7 deletion. This case points out the possible pitfalls in molecular diagnosis of SMA in affected patients and their relatives: exploration of the SMN1 exon 7 (c.840C/T alleles) may be disturbed by several non-pathological or pathological variants around the SMN1 exon 7. In order to accurately describe the molecular defect in an SMA-affected patient, we propose to…

Genetic counselingGenetic CounselingSMN1BiologyMuscular Atrophy SpinalExonGeneticsmedicineHumansAlleleGeneGenetics (clinical)AllelesGeneticsHomozygoteChromosome MappingInfantSpinal muscular atrophyExonsmedicine.diseaseSMA*Survival of Motor Neuron 1 Proteinnervous system diseasesPedigreeHuman genomeFemaleGene DeletionAmerican journal of medical genetics. Part A
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Motor and linguistic linking of space and time in the cerebellum

2009

Background: Recent literature documented the presence of spatial-temporal interactions in the human brain. The aim of the present study was to verify whether representation of past and future is also mapped onto spatial representations and whether the cerebellum may be a neural substrate for linking space and time in the linguistic domain. We asked whether processing of the tense of a verb is influenced by the space where response takes place and by the semantics of the verb. Principal Findings: Responses to past tense were facilitated in the left space while responses to future tense were facilitated in the right space. Repetitive transcranial magnetic stimulation (rTMS) of the right cereb…

Genetics and Molecular Biology (all)Time FactorsNeural substratelcsh:MedicinePoison controlSpace (commercial competition)LinguisticBiochemistryVocabularyPsycholinguisticsAdult; Brain Mapping; Cerebellum; Humans; Language; Motor Skills; Psycholinguistics; Reaction Time; Reproducibility of Results; Semantics; Time Factors; Transcranial Magnetic Stimulation; Verbal Behavior; Vocabulary; Linguistics; Biochemistry Genetics and Molecular Biology (all); Agricultural and Biological Sciences (all)Cerebellumlcsh:ScienceMotor skilltimeLanguageMotor SkillBrain MappingMultidisciplinaryNeuroscience/Behavioral NeurosciencePsycholinguisticsMedicine (all)PsycholinguisticTranscranial Magnetic StimulationLinguisticsNeuroscience/Experimental PsychologySemanticsNeuroscience/PsychologyMotor Skillsspace; time; past; future; cerebellumPsycholinguistics; Verbal Behavior; Reproducibility of Results; Humans; Cerebellum; Vocabulary; Motor Skills; Semantics; Brain Mapping; Adult; Language; Linguistics; Time Factors; Transcranial Magnetic Stimulation; Reaction TimeSettore MED/26 - NeurologiaResearch ArticleHumanfutureAdultTime FactorReproducibility of ResultVerbBiologySemanticsNONeurolinguisticsReaction TimeHumanspastNeuroscience/Cognitive NeuroscienceBiochemistry Genetics and Molecular Biology (all)Settore M-PSI/02 - Psicobiologia E Psicologia FisiologicaVerbal Behaviorlcsh:RReproducibility of ResultsLinguisticsspacecerebellum language spaceAgricultural and Biological Sciences (all)lcsh:QSemantic
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Dejerine-Sottas neuropathy associated with De Novo S79P mutation of the peripheral myelin protein 22 (PMP22) gene

1998

GeneticsFamily HealthMaleDNA Mutational AnalysisDNABiologyDEJERINE-SOTTAS NEUROPATHYPedigreeAmino Acid SubstitutionPeripheral myelin protein 22Child PreschoolMutation (genetic algorithm)MutationGeneticsHumansPoint MutationFemaleChildHereditary Sensory and Motor NeuropathyPmp22 geneGenetics (clinical)Myelin ProteinsPolymorphism Single-Stranded Conformational
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Genetics of the Charcot-Marie-Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy-Russe in depth

2012

Four private mutations responsible for three forms demyelinating of Charcot-Marie-Tooth (CMT) or hereditary motor and sensory neuropathy (HMSN) have been associated with the Gypsy population: the NDRG1 p.R148X in CMT type 4D (CMT4D/HMSN-Lom); p.C737_P738delinsX and p.R1109X mutations in the SH3TC2 gene (CMT4C); and a G>C change in a novel alternative untranslated exon in the HK1 gene causative of CMT4G (CMT4G/HMSN-Russe). Here we address the findings of a genetic study of 29 Gypsy Spanish families with autosomal recessive demyelinating CMT. The most frequent form is CMT4C (57.14%), followed by HMSN-Russe (25%) and HMSN-Lom (17.86%). The relevant frequency of HMSN-Russe has allowed us to inv…

GeneticsProbandcongenital hereditary and neonatal diseases and abnormalitiesWeaknesseducation.field_of_studyHaplotypePopulationBiologymedicine.diseaseTooth diseaseDistal sensory lossGeneticsmedicinemedicine.symptomeducationHereditary motor and sensory neuropathyFounder mutationGenetics (clinical)Clinical Genetics
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Prosocial and Aggressive Behavior Occurrence in Young Athletes: Field Research Results in Six European Countries

2020

Aggression and violence among youth are researched as social phenomena in sport. This paper was designed to determine the occurrence of these behaviors as well as prosocial behaviors among young athletes. The current paper is a research report aiming to detect the frequency of aggressive behavior, social exclusion, prosocial behavior and cohesion in the youth environment, the frequency of personal experience of peer violence or social exclusion, and to evaluate cross-national differences in terms of occurrence of these phenomena.The field research was conducted in six European countries (Austria, Bosnia and Herzegovina, Croatia, Italy, Lithuania, and Serbia) on a sample of 482 children aged…

Geography Planning and DevelopmentSocialinės problemos / Social problemsSocialinis mokslas / Social scienceRenewable energy sourcesDevelopmental psychology0302 clinical medicineLietuva (Lithuania)GE1-350media_commonyouthbiologyEnvironmental effects of industries and plantsAustrija (Austria)05 social sciencesaggressionsocial exclusionaggression ; social exclusion ; motivation ; youth ; sportItalija (Italy)Prosocial behaviorFeelingScale (social sciences)Clubmedicine.symptomPsychologyAggression Motivation Social exclusion Sport YouthSettore M-EDF/01 - Metodi E Didattiche Delle Attivita' Motorie050104 developmental & child psychologySerbija (Serbia)media_common.quotation_subjectTJ807-830Management Monitoring Policy and LawTD194-195Jaunimas / Youth03 medical and health sciencesmotivationBosnija ir Hercegovina (Bosna i Hercegovina. Босна и Херцеговина)aggression; social exclusion; motivation; youth; sportmedicineField research0501 psychology and cognitive sciencesRenewable Energy Sustainability and the EnvironmentAggressionAthletesSportas / Sport030229 sport sciencesKroatija (Croatia)biology.organism_classificationEnvironmental sciencesSocial exclusionsportSustainability; Volume 12; Issue 12; Pages: 5085
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