Search results for "Map"

showing 10 items of 3484 documents

Functional relevant loss of long association fibre tracts integrity in early Alzheimer's disease.

2007

Abstract The aim of our study was to quantify the structural integrity of the long association fibre tracts in early Alzheimer's disease (AD) and to correlate the findings with the cognitive performance of the patients. We conducted region-of-interest-based analyses of color-coded diffusion-tensor imaging in 12 patients with early AD (age 69.8 ± 8.0 years; MMSE 25.3 ± 1.8) and 16 age- and education-matched healthy controls. Early AD patients showed significantly decreased fractional anisotropy (FA) of the cingulate bundles and the inferior fronto-occipital fascicles bilaterally, whereas FA values of the superior longitudinal fascicles (second division) did not differ significantly between p…

Malemedicine.medical_specialtyCognitive NeuroscienceExperimental and Cognitive PsychologyDiseaseAudiologyNeuropsychological TestsFunctional LateralityStatistics NonparametricBehavioral NeuroscienceAlzheimer DiseaseMemoryFractional anisotropyNeural PathwaysmedicineHumansEffects of sleep deprivation on cognitive performanceEpisodic memoryAgedBrain MappingNeuropsychologyStructural integrityBrainAssociation fibreMiddle AgedBoston Naming TestDiffusion Magnetic Resonance ImagingAnisotropyFemalePsychologyCognition DisordersNeuroscienceNeuropsychologia
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The left occipitotemporal system in reading: disruption of focal fMRI connectivity to left inferior frontal and inferior parietal language areas in c…

2011

Developmental dyslexia is a severe reading disorder, which is characterized by dysfluent reading and impaired automaticity of visual word processing. Adults with dyslexia show functional deficits in several brain regions including the so-called "Visual Word Form Area" (VWFA), which is implicated in visual word processing and located within the larger left occipitotemporal VWF-System. The present study examines functional connections of the left occipitotemporal VWF-System with other major language areas in children with dyslexia. Functional connectivity MRI was used to assess connectivity of the VWF-System in 18 children with dyslexia and 24 age-matched controls (age 9.7-12.5 years) using f…

Malemedicine.medical_specialtyCognitive Neurosciencemedia_common.quotation_subjectWord processingAutomaticityAudiologyNeuropsychological TestsBrain mappingFunctional LateralityDyslexiaReading (process)mental disordersNeural PathwaysmedicineImage Processing Computer-AssistedReaction TimeHumansFunctional disconnectionVisual word form areaVisual WordChildmedia_commonLanguageBrain MappingDyslexiamedicine.diseaseMagnetic Resonance ImagingTemporal LobeNeurologyReadingData Interpretation StatisticalFemaleOccipital LobePsychologyPhotic StimulationPsychomotor PerformanceCognitive psychologyNeuroImage
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Disruption of TCBA1 associated with a de novo t(1;6)(q32.2;q22.3) presenting in a child with developmental delay and recurrent infections

2005

A boy with developmental delay, particularly of speech, a distinct face, antineutrophil cytoplasmic antibodies, and recurrent infections was found to have an apparently balanced de novo t(1;6)(q32.3;q22.3) translocation. Fluorescent in situ hybridisation with BAC/PAC clones and long range polymerase chain reaction products assessed in the human genome sequence localised the chromosome 1 breakpoint to a 9.8 kb segment within a hypothetical gene, LOC388735, and the chromosome 6 breakpoint to a 12.8 kb segment in intron 4 of the T-cell lymphoma breakpoint-associated target 1 (TCBA1) gene. Disruption and/or formation of TCBA1 fusion genes in T cell lymphoma and leukaemia cell lines suggests a r…

Malemedicine.medical_specialtyDevelopmental DisabilitiesMolecular Sequence DataShort ReportBiologyInfectionsTranslocation GeneticFusion geneExonMiceMolecular geneticsGeneticsmedicineAnimalsHumansAmino Acid SequenceChildGeneGenetics (clinical)GeneticsGenome HumanGene Expression ProfilingBreakpointChromosome MappingMembrane ProteinsChromosome BreakageExonsNull alleleMolecular biologyGene expression profilingChromosomes Human Pair 1Child PreschoolCytogenetic AnalysisChromosomes Human Pair 6Chromosome breakage
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Enhancement of Gamma Oscillations Indicates Preferential Processing of Native over Foreign Phonemic Contrasts in Infants

2013

Young infants discriminate phonetically relevant speech contrasts in a universal manner, that is, similarly across languages. This ability fades by 12 months of age as the brain builds language-specific phonemic maps and increasingly responds preferentially to the infant's native language. However, the neural mechanisms that underlie the development of infant preference for native over non-native phonemes remain unclear. Since gamma-band power is known to signal infants' preference for native language rhythm, we hypothesized that it might also indicate preference for native phonemes. Using high-density electroencephalogram/event-related potential (EEG/ERP) recordings and source-localization…

Malemedicine.medical_specialtyFirst languageElectroencephalography Phase SynchronizationElectroencephalographyAudiologyLanguage DevelopmentBrain mappingPhoneticsImage Processing Computer-AssistedmedicineHumansTheta RhythmLanguageAnalysis of VarianceBrain MappingCommunicationmedicine.diagnostic_testbusiness.industryGeneral NeuroscienceInfant NewbornBrainInfantElectroencephalographyPhoneticsArticlesLanguage acquisitionMagnetic Resonance ImagingElectroencephalography Phase SynchronizationLanguage developmentEnglandData Interpretation StatisticalEvoked Potentials AuditorySpeech PerceptionFemaleSyllablePsychologybusinessThe Journal of Neuroscience
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Corpus Callosum Morphology in Attention Deficit-Hyperactivity Disorder: Morphometric Analysis of MRI

1991

Although behavioral evidence provides support for the notion that attention deficit-hyperactivity disorder (ADHD) is related to central nervous system dysfunction, there is little direct evidence to reveal which neurometabolic systems or brain structures are involved. Recent magnetic resonance imaging (MRI) studies suggest that, compared to nondisabled controls, ADHD children may have a smaller right frontal region. Morphometric analysis of MRI scans was used in this exploratory study to determine whether correlated regional variation might exist in the corpus callosum of children with ADHD. While all MRI scans were judged to be clinically normal, morphometric analysis revealed that, compa…

Malemedicine.medical_specialtyHealth (social science)Neurologymedia_common.quotation_subjectCentral nervous systemSpleniumCorpus callosumCorpus CallosumEducation03 medical and health sciences0302 clinical medicinemental disordersmedicineHumansAttention deficit hyperactivity disorder030212 general & internal medicineChildDominance Cerebralmedia_commonBrain Mappingmedicine.diagnostic_testMagnetic resonance imagingAnatomymedicine.diseaseMagnetic Resonance Imaging030227 psychiatryDevelopmental disordermedicine.anatomical_structureAttention Deficit Disorder with HyperactivityGeneral Health ProfessionsFemalePsychologyNeuroscienceVigilance (psychology)Journal of Learning Disabilities
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Effects of cerivastatin on adrenergic pathways, hypertrophic growth and TGFbeta expression in adult ventricular cardiomyocytes.

2010

Abstract The effects of statin treatment in the setting of heart failure have already been shown. Nevertheless, there is little knowledge about its influence on adrenergic pathways in cardiomyocytes. Therefore, this study investigated the impact of cerivastatin on adrenoceptor-mediated signalling pathways in isolated adult ventricular cardiomyocytes. It focused on two endpoints: hypertrophic growth and TGFbeta expression. Cultured cardiomyocytes were used to study rac activation (analysed by its translocation into the membrane fraction), ROS formation (H 2 DCF fluorescence) and hypertrophic growth ( 14 C-phenylalanine incorporation). Alpha- and beta-adrenoceptor stimulation showed significa…

Malemedicine.medical_specialtyHistologyAdrenergic receptorMAP Kinase Signaling SystemPyridinesp38 mitogen-activated protein kinasesHeart VentriclesAdrenergicAlpha (ethology)StimulationPharmacologyp38 Mitogen-Activated Protein KinasesPathology and Forensic MedicineTransforming Growth Factor betaInternal medicineReceptors Adrenergic betamedicineAnimalsMyocytes CardiacRats WistarCells CulturedHeart FailurebiologyCerivastatinCell BiologyGeneral MedicineReceptors Adrenergic alphaRatsEnzyme ActivationEndocrinologyGene Expression RegulationNAD(P)H oxidaseMitogen-activated protein kinasebiology.proteinHydroxymethylglutaryl-CoA Reductase InhibitorsReactive Oxygen SpeciesProto-Oncogene Proteins c-aktmedicine.drugEuropean journal of cell biology
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Responses to histamine and selective H2-receptor agonists in lung parenchymal strips from normal and sensitized guinea-pigs.

1989

Histamine produces concentration-dependent contractions of lung parenchyma strips obtained from normal and sensitized guinea-pigs. The responsiveness of the sensitized lung strips to histamine was significantly increased compared to normal tissues. Clemizole (0.1 microM) was equally effective as an H1-antagonist in normal (dose-ratio 9.12) and sensitized (dose-ratio 9.77) tissues. The concentration-response curves to histamine were displaced to the left by cimetidine (0.1 microM to 0.1 mM) with similar dose-ratios in normal and sensitized tissues. Cimetidine enhanced maximal responses to histamine only in normal lung strips. The effects of submaximal equieffective concentrations of histamin…

Malemedicine.medical_specialtyImmunologyGuinea PigsToxicologyGuanidineschemistry.chemical_compoundImpromidineHistamine H2 receptorDimapritInternal medicineParenchymamedicineAnimalsPharmacology (medical)Receptors Histamine H2CimetidineLungPharmacologyLungDose-Response Relationship Drugbusiness.industryMethylhistaminesImidazolesIsoproterenolThioureaMuscle SmoothImpromidineDimapritClemizolemedicine.anatomical_structureEndocrinologychemistryBenzimidazolesbusinessCimetidineHistaminemedicine.drugHistamineMuscle ContractionAgents and actions
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Children’s Single-Leg Landing Movement Capability Analysis According to the Type of Sport Practiced

2020

(1) Background: Understanding children&rsquo

Malemedicine.medical_specialtyKnee JointHealth Toxicology and MutagenesisMovementlcsh:MedicineKnee Jointmedicine.disease_causeStatistical parametric mappingStandard deviationArticleBarefoot03 medical and health sciences0302 clinical medicineJumpingPhysical medicine and rehabilitationstatistical parametric mappingdrop jump landingmedicinemotor controlHumansmotor developmentChildMotor skillchildhoodLeglcsh:RPublic Health Environmental and Occupational HealthMotor control030229 sport sciencesBiomechanical Phenomenamedicine.anatomical_structureMotor SkillsFemaleAnklePsychologyhuman activities030217 neurology & neurosurgeryInternational Journal of Environmental Research and Public Health
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Altered REDD1, myostatin, and Akt/mTOR/FoxO/MAPK signaling in streptozotocin-induced diabetic muscle atrophy

2011

Type 1 diabetes, if poorly controlled, leads to skeletal muscle atrophy, decreasing the quality of life. We aimed to search highly responsive genes in diabetic muscle atrophy in a common diabetes model and to further characterize associated signaling pathways. Mice were killed 1, 3, or 5 wk after streptozotocin or control. Gene expression of calf muscles was analyzed using microarray and protein signaling with Western blotting. We identified translational repressor protein REDD1 (regulated in development and DNA damage responses) that increased seven- to eightfold and was associated with muscle atrophy in diabetes. The diabetes-induced increase in REDD1 was confirmed at the protein level. …

Malemedicine.medical_specialtyMAP Kinase Signaling SystemPhysiologyEndocrinology Diabetes and MetabolismFOXO1P70-S6 Kinase 1MyostatinBiologyMiceRandom Allocation03 medical and health sciences0302 clinical medicinePhysiology (medical)Internal medicinemedicineAnimalsRNA MessengerPhosphorylationMuscle SkeletalProtein kinase BPI3K/AKT/mTOR pathwayOligonucleotide Array Sequence Analysis030304 developmental biology0303 health sciencesForkhead Box Protein O1Gene Expression ProfilingTOR Serine-Threonine KinasesUbiquitinationForkhead Transcription FactorsOrgan SizeMyostatinProtein ubiquitinationMuscle atrophyMuscular AtrophyDNA Repair EnzymesDiabetes Mellitus Type 1EndocrinologyGene Expression Regulationbiology.proteinPhosphorylationmedicine.symptomProto-Oncogene Proteins c-akt030217 neurology & neurosurgeryTranscription FactorsAmerican Journal of Physiology-Endocrinology and Metabolism
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Chest Surgery for Transgender and Gender Nonconforming Individuals

2018

Chest surgery can greatly facilitate the experience of living in a gender role. For transfeminine chest surgery, most surgeons recommend a 12-month period of feminizing hormone therapy prior to breast augmentation. For those who already have some breast volume due to hormone treatment, lipofilling can be a good option. Transmasculine chest surgery includes mastectomy and creation of a male chest. Preoperative parameters to be evaluated include breast volume, degree of excess skin, nipple-areola complex size and position, and skin elasticity. The algorithm the authors developed and modified can help choose from 5 techniques, resulting in an aesthetically pleasing male chest.

Malemedicine.medical_specialtyMammaplastymedicine.medical_treatmentSubcutaneous mastectomy030230 surgeryTransgender Persons03 medical and health sciencesChest surgery0302 clinical medicineTransgenderHumansMedicineThoracoplastyChest surgeryBreast augmentationSubcutaneous MastectomyMastectomybusiness.industryBreast augmentationmedicine.diseaseSurgeryGynecomastia030220 oncology & carcinogenesisMammaplastyTransgenderFemaleSurgeryHormone therapybusinessTranssexualismMastectomyHumanClinics in Plastic Surgery
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