Search results for " Localization"

showing 10 items of 319 documents

Immunocytochemistry of M-cadherin in mature and regenerating rat muscle

1994

Background: Cadherins are transmembrane proteins mediating calcium-dependent cell–cell adhesion in a cell type-specific manner by means of homophilic binding. M(muscle)-cadherin is a recently detected member of the cadherin family. Methods: We have investigated the localization of M-cadherin innormal and aneurally regenerating skeletal muscle of rat by means of pre-embedding immunocytochemistry. The antibody was directed against the extra-cellular domain of M-cadherin. Results: Myoblasts and myotubes in regenerating muscles tended to be arranged in clusters enclosed by a common basal lamina. Satellite cells of mature muscle fibers were attached to the underlying fiber without separating bas…

MaleImmunocytochemistryBiologyMuscle DevelopmentReference ValuesExtracellularmedicineAnimalsRegenerationMyocyteTissue DistributionRats WistarCellular localizationMyogenesisCadherinMusclesSkeletal muscleCadherinsImmunohistochemistryAgricultural and Biological Sciences (miscellaneous)Molecular biologyRatsCell biologyMicroscopy Electronmedicine.anatomical_structureBasal laminaAnatomyThe Anatomical Record
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Hsp10 nuclear localization and changes in lung cells response to cigarette smoke suggest novel roles for this chaperonin

2014

Heat-shock protein (Hsp)10 is the co-chaperone for Hsp60 inside mitochondria, but it also resides outside the organelle. Variations in its levels and intracellular distribution have been documented in pathological conditions, e.g. cancer and chronic obstructive pulmonary disease (COPD). Here, we show that Hsp10 in COPD undergoes changes at the molecular and subcellular levels in bronchial cells from human specimens and derived cell lines, intact or subjected to stress induced by cigarette smoke extract (CSE). Noteworthy findings are: (i) Hsp10 occurred in nuclei of epithelial and lamina propria cells of bronchial mucosa from non-smokers and smokers; (ii) human bronchial epithelial (16HBE) a…

MaleMitochondrionChaperoninPulmonary Disease Chronic ObstructiveCytosolSmokeSettore BIO/10 - Biochimicabronchial epithelial cellChaperonin 10nuclear localizationlcsh:QH301-705.5LungCOPD; Hsp10; bronchial epithelial cells; lung fibroblasts; nuclear localizationbronchial epithelial cellsGeneral NeuroscienceSmokingTobacco ProductsMiddle Aged33ImmunohistochemistryNucleosomesRespiratory Function TestsCell biologymedicine.anatomical_structureFemaleHSP60IntracellularResearch Article1001Hsp10ImmunologyBronchiBiologyGeneral Biochemistry Genetics and Molecular BiologyMitochondrial ProteinsOrganellemedicineHumansCOPDComputer SimulationIsoelectric PointAgedCell NucleusSettore BIO/16 - Anatomia UmanaResearchlung fibroblastsEpithelial CellsChaperonin 60DNAFibroblastsrespiratory tract diseasesMolecular WeightCell nucleusCytosollcsh:Biology (General)Immunologylung fibroblastNuclear localization sequenceOpen Biology
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Detection of AA-type amyloid protein in labial salivary glands

2010

Objectives: Among the diverse forms of amyloidosis, secondary type is the most frequent one. Diagnosis of amyloid deposition is based on the identification of the fibrillary protein amyloid by means of Congo Red (CR) or crystal violet (CV) stains, but these techniques do not differentiate between the different types of amyloid fibrils. The aim of this study was to identify by immunofluorescence (IF) AA amyloid a pathological fibrillar low-molecularweight protein formed by cleavage of serum amyloid A (SAA) protein in labial salivary gland (LSG) biopsies from patients with secondary amyloidosis. Study design: 98 LSG were studied, 65 were from patients with secondary amyloidosis and 33 from su…

MalePathologychronic inflammationImmunofluorescenceH&E stainFluorescent Antibody Techniquechemistry.chemical_compoundprotein cleavageAged 80 and overmedicine.diagnostic_testAmyloidosisAmyloidosisMiddle Aged:CIENCIAS MÉDICAS [UNESCO]Congo redeosinUNESCO::CIENCIAS MÉDICASFemaleamyloid A proteinAdultmedicine.medical_specialtyAmyloidAmyloidAdolescentSalivary Gland Diseasesprotein localizationSalivary glandsImmunofluorescenceSalivary Glands MinorSensitivity and SpecificityYoung AdultBiopsymedicineHumansSerum amyloid AGeneral DentistryPathologicalAgedamyloidosisSerum Amyloid A Proteinbusiness.industryhematoxylinmolecular weightmedicine.diseasemajor clinical study//purl.org/pe-repo/ocde/ford#3.02.14 [https]human tissueLipOtorhinolaryngologychemistryprotein analysisSurgerybusiness
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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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Auditory event-related potentials show altered hemispheric responses in dyslexia

2011

Dyslexia is characterized by deficits in phonological processing abilities. However, it is unclear what the underlying factors for poor phonological abilities or speech sound representations are. One hypothesis suggests that individuals with dyslexia have problems in basic acoustic perception which in turn can also cause problems in speech perception. Here basic auditory processing was assessed by auditory event-related potentials recorded for paired tones presented in an oddball paradigm in 9-year-old children with dyslexia and a familial background of dyslexia, typically reading children at familial risk for dyslexia and control children without risk for dyslexia. The tone pairs elicited …

MaleReading disabilityTime FactorsSpeech perceptionSource LocalizationAuditory eventmedia_common.quotation_subjectDevelopmental Dyslexiabehavioral disciplines and activitiesDyslexiaTone (musical instrument)Reading-DisabilityReading (process)Perceptionmental disordersDiscriminationmedicineHumansAuditory ProcessingChildDominance CerebralPatternsOddball paradigmChildrenta515media_commonAuditory CortexGeneral NeuroscienceDyslexiaAsymmetryElectroencephalographyFamilial RiskFrequencymedicine.diseaseAudiometry Evoked Responsenervous system diseasesReadingInter-Stimulus IntervalEvoked Potentials AuditorySpeech PerceptionEvoked-PotentialsFemalePsychologyInfantspsychological phenomena and processesCognitive psychologyIndraStra Global
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Inactivation of electrophilic metabolites by glutathione S-transferases and limitation of the system due to subcellular localization

1977

Benzo(a)pyrene was activated to metabolites mutagenic for Salmonella typhimurium TA 98 by liver microsomes from control and phenobarbital treated mice. Under these conditions benzo(a)pyrene 4,5-oxide accounts for most of the mutagenicity. We have therefore investigated (1) the conjugation of benzo(a)pyrene 4,5-oxide with glutathione and (2) the effect of glutathione on the mutagenicity of benzo(a)pyrene.

MaleSalmonella typhimuriumendocrine systemHealth Toxicology and MutagenesisMutagenToxicologymedicine.disease_causeMicechemistry.chemical_compoundCytosolBiotransformationpolycyclic compoundsmedicineAnimalsBenzopyrenesBiotransformationGlutathione Transferasebiologyfungifood and beveragesGeneral MedicineGlutathioneSubcellular localizationGlutathioneCytosolGlutathione S-transferaseBenzo(a)pyrenechemistryBiochemistryMicrosomes Liverbiology.proteinPyreneMutagensArchives of Toxicology
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Time-dependent contribution of non neuronal cells to BDNF production after ischemic stroke in rats.

2010

International audience; Although brain-derived neurotrophic factor (BDNF) plays a central role in recovery after cerebral ischemia, little is known about cells involved in BDNF production after stroke. The present study testes the hypothesis that neurons are not the unique source of neosynthesized BDNF after stroke and that non neuronal-BDNF producing cells differ according to the delay after stroke induction. For this purpose, cellular localization of BDNF and BDNF content of each hemisphere were analysed in parallel before and after (4h, 24h and 8d) ischemic stroke in rats. Stroke of different severities was induced by embolization of the brain with variable number of calibrated microsphe…

MaleTime Factorsmedicine.medical_treatmentCentral nervous systemIschemiaBDNF productionFunctional LateralityBrain IschemiaBrain ischemia03 medical and health sciencesCellular and Molecular Neuroscience0302 clinical medicineNeurotrophic factorsGlial Fibrillary Acidic ProteinmedicineAnimalsRats WistarStrokeCellular localization030304 developmental biologyBrain-derived neurotrophic factorBrain ChemistryNeurons0303 health sciencesbusiness.industryBDNF localization[SCCO.NEUR]Cognitive science/NeuroscienceBrain-Derived Neurotrophic Factor[SCCO.NEUR] Cognitive science/NeuroscienceBrainCell BiologyCerebral Infarctionmedicine.diseaseRatsStrokemedicine.anatomical_structurenervous systemIntracranial Embolism[ SCCO.NEUR ] Cognitive science/NeurosciencebusinessStroke recoveryNeuroscience030217 neurology & neurosurgeryNeurochemistry international
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Assembly of the ribonucleoprotein complex containing the mRNA of the β-subunit of the mitochondrial H+-ATP synthase requires the participation of two…

2002

The mRNA encoding the beta-subunit of the mitochondrial H(+)-ATP synthase (beta-F1-ATPase) is localized in an approx. 150 nm structure of the hepatocyte of mammals. In the present study, we have investigated the cis- and trans-acting factors involved in the generation of the ribonucleoprotein complex containing beta-F1-ATPase mRNA. Two cis-acting elements (beta1.2 and 3'beta) have been identified. The beta1.2 element is placed in the open reading frame, downstream of the region encoding the mitochondrial pre-sequence of the protein. The 3'beta element is the 3' non-translated region of the mRNA. Complex sets of proteins from the soluble and non-soluble fractions of the liver interact with t…

MaleTranslationBlotting WesternMitochondria LiverRNA-binding proteinBiochemistryReticulocytePregnancyPolysomeP-bodiesmedicineAnimalsOxidative phosphorylationRNA MessengerRats Wistar3' Untranslated RegionsMolecular BiologyIn Situ HybridizationMessenger RNAATP synthasebiologyThree prime untranslated regionRNA-Binding ProteinsRNACell BiologyImmunohistochemistryRatsProton-Translocating ATPasesmedicine.anatomical_structureBiochemistrybiology.proteinmRNA localizationFemaleResearch ArticleBiochemical Journal
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Children show hemispheric differences in the basic auditory response properties

2019

Auditory cortex in each hemisphere shows preference to sounds from the opposite hemifield in the auditory space. Besides this contralateral dominance, the auditory cortex shows functional and structural lateralization, presumably influencing the features of subsequent auditory processing. Children have been shown to differ from adults in the hemispheric balance of activation in higher-order auditory based tasks. We studied, first, whether the contralateral dominance can be detected in 7- to 8-year-old children and, second, whether the response properties of auditory cortex in children differ between hemispheres. Magnetoencephalography (MEG) responses to simple tones revealed adult-like cont…

Malecortical maturationMIDDLE-LATENCYAuditory responseLanguage functionLANGUAGEINFANTSAudiology3124 Neurology and psychiatryFunctional LateralityN100m0302 clinical medicineChild DevelopmentEVOKED-POTENTIALS10. No inequalityChildta515Research Articleselectromagnetic brain imagingMEGRadiological and Ultrasound Technologymedicine.diagnostic_test05 social sciencesAge FactorsMagnetoencephalographySPEECHkuuloNeurologyAuditory PerceptionEvoked Potentials AuditoryFemaleAnatomyPsychologyAdultmedicine.medical_specialtyEVENT-RELATED POTENTIALSlapset (ikäryhmät)Auditory cortexta3112MATURATION050105 experimental psychologyLateralization of brain function03 medical and health sciencesYoung AdultEvent-related potentialmedicineHumans0501 psychology and cognitive sciencesRadiology Nuclear Medicine and imagingSOURCE LOCALIZATIONdevelopmentAuditory Cortex3112 NeurosciencesMagnetoencephalographyNeurophysiology3126 Surgery anesthesiology intensive care radiologyaivokuoriN250mChild populationDEVELOPMENTAL-CHANGESNeurology (clinical)030217 neurology & neurosurgery
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Time course of ERP generators to syllables in infants: A source localization study using age-appropriate brain templates

2011

article i nfo Event-related potentials (ERPs) have become an important tool in the quest to understand how infants pro- cess perceptual information. Identification of the activation loci of the ERP generators is a technique that pro- vides an opportunity to explore the neural substrates that underlie auditory processing. Nevertheless, as infant brain templates from healthy, non-clinical samples have not been available, the majority of source localization studies in infants have used non-realistic head models, or brain templates derived from older children or adults. Given the dramatic structural changes seen across infancy, all of which profoundly affect the electrical fields measured with …

Malemedicine.medical_specialtyTime FactorsCognitive NeuroscienceSpeech recognitionElectroencephalographyAudiologyAuditory cortexPhoneticsEvent-related potentialSource localizationmedicineHumansEvoked PotentialsOddball paradigmta515Anterior cingulate cortexCerebral CortexTemporal cortexBrain Mappingmedicine.diagnostic_testVoice-onset timeAge FactorsInfantMagnetic Resonance Imagingmedicine.anatomical_structureNeurologyFemalePsychologyNeuroImage
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