Search results for "REGIONS"

showing 10 items of 1521 documents

Diagnostic efficacy of the ELISA test for the detection of deamidated anti-gliadin peptide antibodies in the diagnosis and monitoring of celiac disea…

2009

Background and Aim: We evaluated the diagnostic performance of an ELISA test for anti-gliadin IgA and IgG antibodies, which uses synthetic deamidated gliadin peptides (anti-gliadin antibodies, AGAs) as coating; the results were compared with a test that uses extracted gliadin (AGAe). Methods: The study was conducted on the sera of 144 patients suffering from celiac disease (CD), including 20 patients with IgA deficiency and 9 who were following a gluten-free diet (GFD), and 129 controls. Results: In the 115 CD patients (without IgA deficiency), the sensitivity of AGAe IgA and IgG was 32.2 and 60.9%, whereas that of AGAs IgA and IgG was 59.1 and 72.2%. The specificity for AGAe IgA and IgG, a…

MaleSettore MED/09 - Medicina InternaTissue transglutaminaseClinical BiochemistryGliadinSerologyImmunology and AllergyMedicinedeamidated anti-gliadin peptide antibodieChildFalse Negative Reactionsreproductive and urinary physiologybiologyHematologyMiddle Agedfemale genital diseases and pregnancy complicationsMedical Laboratory TechnologyChild PreschoolAnti-transglutaminase antibodiesAnti-gliadin antibodiesELISAFemaleAntibodyMicrobiology (medical)AdultAdolescenteducationEnzyme-Linked Immunosorbent AssaySensitivity and SpecificityAntibodiesYoung AdultAntigenELISA; deamidated anti-gliadin peptide antibodies; celiac diseaseHumansFalse Positive ReactionsSerologic TestsAgedAutoantibodiesTransglutaminasesbusiness.industryBiochemistry (medical)Public Health Environmental and Occupational HealthAutoantibodyOriginal ArticlesImmunoglobulin Abody regionsCeliac DiseaseROC CurveCase-Control StudiesImmunoglobulin GImmunologybiology.proteinbusinessGliadinPeptides
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Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia

2010

Mutations in the SPG4 gene are the most common causes of hereditary spastic paraplegia (HSP) accounting for up to 40% of autosomal dominant (AD) forms and 12-18% of sporadic cases. The phenotype associated with HSP due to mutations in the SPG4 gene tends to be pure. There is increasing evidence, however, of patients with complicated forms of spastic paraplegia in which SPG4 mutations were identified. A cohort of 38 unrelated Italian patients with spastic paraplegia, of which 24 had a clear dominant inheritance and 14 were apparently sporadic, were screened for mutations in the SPG4 gene.We identified 11 different mutations, six of which were novel (p.Glu143GlyfsX8, p.Tyr415X, p.Asp548Asn, c…

MaleSpastinDNA Mutational AnalysisHereditary spastic paraplegiaEXON DELETIONSGene mutationmedicine.disease_causeSpastinFAMILIESCohort StudiesExonGenotypeSpasticMutation frequencyChild3' Untranslated RegionsChromatography High Pressure LiquidAdenosine TriphosphatasesGeneticsMutationHereditary spastic paraplegia SPG4Reverse Transcriptase Polymerase Chain ReactionMutation analysiExonsMiddle AgedMLPAPhenotypeMutation analysisItalyNeurologySettore MED/26 - NeurologiaFemaleAdultAdolescentGenotypeHereditary spastic paraplegia3 ' UTR3′ UTRMutation MissenseFREQUENTSPG4CLASSIFICATIONYoung AdultmedicineHumansAgedParaplegiaSPECTRUMbusiness.industrymedicine.diseaseNeurology (clinical)businessCOLLECTIONEXPRESSION ANALYSISGene Deletion
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Large-scale brain networks emerge from dynamic processing of musical timbre, key and rhythm

2012

We investigated the neural underpinnings of timbral, tonal, and rhythmic features of a naturalistic musical stimulus. Participants were scanned with functional Magnetic Resonance Imaging (fMRI) while listening to a stimulus with a rich musical structure, a modern tango. We correlated temporal evolutions of timbral, tonal, and rhythmic features of the stimulus, extracted using acoustic feature extraction procedures, with the fMRI time series. Results corroborate those obtained with controlled stimuli in previous studies and highlight additional areas recruited during musical feature processing. While timbral feature processing was associated with activations in cognitive areas of the cerebel…

MaleSpeech recognition0302 clinical medicineBASAL GANGLIAPREMOTORDefault mode networkMusical formBrain MappingTemporal evolutionmedicine.diagnostic_test05 social sciencesfMRIBrainREGIONSMagnetic Resonance ImaginghumanitiesNeurologyta6131SYNCHRONIZATIONAuditory PerceptionFemalePsychologypsychological phenomena and processesCognitive psychologyAuditory perceptionComputational feature extractionCognitive NeuroscienceFeature extractionMusic processingTOPOGRAPHYStimulus (physiology)ta3112behavioral disciplines and activities050105 experimental psychology03 medical and health sciencesYoung Adultotorhinolaryngologic diseasesmedicineEMOTIONHumans0501 psychology and cognitive sciencesTonalityMETAANALYSISPERCEPTIONNaturalistic stimulusNerve NetFunctional magnetic resonance imagingTimbre030217 neurology & neurosurgeryMusicAUDITORY-CORTEXNEUROIMAGE
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Cognitive vs. affective listening modes and judgments of music - An ERP study

2010

The neural correlates of processing deviations from Western music rules are relatively well known. Less is known of the neural dynamics of top-down listening modes and affective liking judgments in relation with judgments of tonal correctness. In this study, subjects determined if tonal chord sequences sounded correct or incorrect, or if they liked them or not, while their electroencephalogram (EEG) was measured. The last chord of the sequences could be congruous with the previous context, ambiguous (unusual but still enjoyable) or harmonically inappropriate. The cognitive vs. affective listening modes were differentiated in the event-related potential (ERP) responses already before the end…

MaleStatistics as TopicEXPECTANCYNeuropsychological TestsElectroencephalographyEvent-related potential (ERP)CognitionProfessional Competence0302 clinical medicineBRAIN-REGIONSJudgment processesmedia_commonBrain Mappingmedicine.diagnostic_testLate positive potential (LPP)General Neuroscience05 social sciencesElectroencephalographyCognitionhumanitiesContingent negative variationNeuropsychology and Physiological PsychologyEMOTIONSAuditory PerceptionEvoked Potentials AuditoryFemaleMusic perceptionPsychologypsychological phenomena and processesSENSORY CONSONANCECognitive psychologyAdultAdolescentmedia_common.quotation_subjectEarly right anterior negativity (ERAN)AestheticsEVENT-RELATED POTENTIALSbehavioral disciplines and activities050105 experimental psychologyBIOELECTRICAL ECHOESJudgmentYoung Adult03 medical and health sciencesEvent-related potentialPerceptionReaction TimemedicineHumans0501 psychology and cognitive sciencesActive listeningCONTINGENT NEGATIVE-VARIATIONAnalysis of VarianceNeural correlates of consciousnessPERCEPTIONMusical preferenceAffectAcoustic StimulationChord (music)LikingMusic030217 neurology & neurosurgeryAUDITORY-CORTEXRESPONSES
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Distribution of origin of nitric oxide synthase-immunoreactive nerve fibers in the rat epididymis.

1996

Abstract Distribution of neuronal nitric oxide synthase-immunoreactive (nNOS-IR) nerve fibers and somata in the rat epididymis and major pelvic ganglia was studied by immunohistochemical methods. In the epididymis, the supply of nNOS-IR fibers was highest in the cauda and became progressively fewer toward the caput. In the cauda and corpus, nNOS-IR fibers were distributed throughout the subepithelial tissues and around the epithelium. The pattern of distribution of vasoactive intestinal polypeptide (VIP)- and tyrosine hydroxylase (TH)-immunoreactive fibers in the epididymis was similar but the latter was generally more numerous in a given region as compared to that of nNOS-IR fibers. A popu…

MaleStilbamidinesTyrosine 3-MonooxygenaseVasoactive intestinal peptidePopulationBiologyRats Sprague-DawleyNerve FibersDorsal root ganglionGanglia SpinalmedicineAnimalseducationMolecular Biologyreproductive and urinary physiologyFluorescent DyesEpididymisNeuronseducation.field_of_studyNeurotransmitter AgentsHypogastric PlexusGeneral NeuroscienceVas deferensSmooth muscle contractionAnatomyEpididymisCholine acetyltransferaseImmunohistochemistryEpitheliumRatsbody regionsmedicine.anatomical_structurePhenotypenervous systemNeurology (clinical)Nitric Oxide SynthaseDevelopmental BiologyVasoactive Intestinal PeptideBrain research
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Algorithm for clinical evaluation and surgical treatment of gynaecomastia.

2006

Algorithm for clinical evaluation and surgical treatment of gynaecomastia. Cordova A, Moschella F. Source Dipartimento di Discipline Chirurgiche ed Oncologiche, Cattedra di Chirurgia Plastica e Ricostruttiva, Università degli Studi di Palermo, Palermo, Italy. adriana.cordova@excite.com Abstract BACKGROUND: Gynaecomastia can be classified on the basis of the main characterising factors, i.e. pathogenesis, histopathology and morphology. The morphological classifications of gynaecomastia currently made often use subjective parameters and qualifying adjectives. In this paper the authors propose a scheme for morphological classification of gynaecomastia which can serve as a guide for choosing th…

MaleThoraxmedicine.medical_specialtyMammaplastymedicine.medical_treatmentDecision MakingSettore MED/19 - Chirurgia PlasticaScarsSeverity of Illness IndexPeriareolarLipectomyPtosisHumansMedicineInframammary foldReduction (orthopedic surgery)Retrospective Studiesbusiness.industryRetrospective cohort studymedicine.diseaseSurgerybody regionsGynecomastiaGynecomastiaSurgerymedicine.symptombusinessAlgorithmsgynecomastia.
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Thyroid hormone induction of the adrenoleukodystrophy-related gene (ABCD2).

2003

X-linked adrenoleukodystrophy (X-ALD) is a demyelinating disorder associated with impaired very-long-chain fatty-acid (VLCFA) beta-oxidation caused by mutations in the ABCD1 (ALD) gene that encodes a peroxisomal membrane ABC transporter. ABCD2 (ALDR) displays partial functional redundancy because when overexpressed, it is able to correct the X-ALD biochemical phenotype. The ABCD2 promoter contains a putative thyroid hormone-response element conserved in rodents and humans. In this report, we demonstrate that the element is capable of binding retinoid X receptor and 3,5,3'-tri-iodothyronine (T3) receptor (TRbeta) as a heterodimer and mediating T3 responsiveness of ABCD2 in its promoter conte…

MaleThyroid HormonesReceptors Retinoic AcidGene ExpressionATP-binding cassette transporterRetinoid X receptorRats Sprague-DawleyMiceABCD3Gene expressionABCD2medicineAnimalsHumansReceptorAdrenoleukodystrophyPromoter Regions GeneticGeneCells CulturedRepetitive Sequences Nucleic AcidPharmacologyChemokine CCL22Mice KnockoutReceptors Thyroid Hormonebiologymedicine.diseaseCell biologyRatsUp-RegulationOligodendrogliaRetinoid X ReceptorsLiverAstrocytesChemokines CCbiology.proteinCancer researchMolecular MedicineTriiodothyronineAdrenoleukodystrophyChemokine CCL17Transcription FactorsMolecular pharmacology
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Mouse photoreceptor synaptic ribbons lose and regain material in response to illumination changes

2004

Abstract Chemical synapses equipped with ribbons are tonically active, high-output synapses. The ribbons may play a role in the trafficking of synaptic vesicles. Recent findings in retinal rod cells of BALB/c mice indicate that ribbons are large and smooth in the dark phase, and, due to the formation and release of protrusions, small during the light phase. As a consequence of these changes, ribbons may traffick fewer vesicles in the light than in the dark phases. The aim of the present study was to find out whether the above ribbon changes in this mouse strain are strictly illumination-dependent and which signalling processes may be involved. Here, we show that ribbons form protrusions and…

MaleTime FactorsLightRibbon diagramDark AdaptationBiologyRibbon synapseModels BiologicalSynaptic vesicleRetinaPhotoreceptor cellCalcium ChlorideMiceOrgan Culture TechniquesmedicineAnimalsDrug InteractionsPhotoreceptor CellsCyclic GMPEgtazic AcidCalcimycinLightingChelating AgentsMelatoninSynaptic ribbonMice Inbred BALB CRetinaIonophoresGeneral NeurosciencefungiDarknessThionucleotidesCircadian Rhythmbody regionsMicroscopy Electronmedicine.anatomical_structurenervous systemSynapsesSynaptic plasticityBiophysicssense organsNeurosciencePhotic StimulationVisual phototransductionEuropean Journal of Neuroscience
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Ipsilateral corticomotor responses are confined to the homologous muscle following cross-education of muscular strength

2017

Cross-education of strength occurs when strength-training 1 limb increases the strength of the untrained limb and is restricted to the untrained homologous muscle. Cortical circuits located ipsilateral to the trained limb might be involved. We used transcranial magnetic stimulation (TMS) to determine the corticomotor responses from the untrained homologous (biceps brachii) and nonhomologous (flexor carpi radialis) muscle following strength-training of the right elbow flexors. Motor evoked potentials were recorded from the untrained left biceps brachii and flexor carpi radialis during a submaximal contraction from 20 individuals (10 women, 10 men; aged 18–35 years; training group, n = 10; c…

MaleTime FactorsPhysiologyEndocrinology Diabetes and MetabolismCross-activationPhysical strengthRandom Allocation0302 clinical medicineCross activationMedicineInhibitionMotor NeuronsNutrition and DieteticsMotor CortexGeneral MedicineAnatomymusculoskeletal systemTranscranial Magnetic StimulationestotTreatment OutcomeFemalelihaskuntoMuscle ContractionAdultAgonistmedicine.medical_specialtyAdolescentmedicine.drug_classAgonistCross educationYoung Adult03 medical and health sciencesPhysical medicine and rehabilitationPhysiology (medical)Homologous chromosomeHumansMuscle StrengthMuscle SkeletalSynergistCortical circuitsExcitabilityElectromyographybusiness.industryNeural InhibitionResistance Training030229 sport sciencesEvoked Potentials MotorC600raajatbody regionsbusiness030217 neurology & neurosurgerylihasvoimaApplied Physiology, Nutrition, and Metabolism
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Fibrate induction of the adrenoleukodystrophy-related gene (ABCD2)

2001

X-linked adrenoleukodystrophy (X-ALD) is a neurodegenerative disease due to a defect in the ABCD1 (ALD) gene. ABCD1, and the two close homologues ABCD2 (ALDR) and ABCD3 (PMP70), are genes encoding ATP-binding cassette half-transporters of the peroxisomal membrane. As overexpression of the ABCD2 or ABCD3 gene can reverse the biochemical phenotype of X-ALD (reduced beta-oxidation of very-long-chain fatty acids), pharmacological induction of these partially redundant genes may represent a therapeutic approach to X-ALD. We previously reported that the ABCD2 and ABCD3 genes could be strongly induced by fibrates, which are hypolipidaemic drugs and peroxisome-proliferators in rodents. We provide e…

MaleTranscription GeneticMolecular Sequence DataResponse elementReceptors Cytoplasmic and NuclearATP-binding cassette transporterATP Binding Cassette Transporter Subfamily DBiochemistryMiceFenofibrateABCD3Sequence Homology Nucleic AcidABCD2medicineAnimalsHumansRats WistarAdrenoleukodystrophyPromoter Regions GeneticGeneHypolipidemic AgentsMice KnockoutBase SequencebiologyDNATransfectionPeroxisomemedicine.diseaseMolecular biologyRatsGene Expression Regulationbiology.proteinATP-Binding Cassette TransportersAdrenoleukodystrophyTranscription FactorsEuropean Journal of Biochemistry
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