Search results for "mitosi"

showing 10 items of 158 documents

Neuron regeneration reverses 3-acetylpyridine-induced cell loss in the cerebral cortex of adult lizards

1991

Systemic administration of the neurotoxin 3-acetylpyridine to adult lizards results in extensive loss of neurons in the medial cerebral cortex, other brain areas remaining largely unaffected. After the neurotoxic trauma, new cells are produced by mitotic division of cells in the ventricular wall. The new cells migrate along radial glial fibers and replace lost neurons in the medial cortex. Electron microscopic examination of cells labeled with [3H]thymidine confirms that the newly generated cells are neurons. Thus, neuron regeneration can occur in the cerebral cortex of adult lizards.

MaleTime FactorsPyridinesMedial cortexCentral nervous systemHippocampusBiologyCell MovementmedicineAnimalsNeurotoxinMolecular BiologyMitosisCerebral CortexNeuronsCell DeathStaining and LabelingGeneral NeuroscienceNeurogenesisLizardsNerve Regenerationmedicine.anatomical_structurenervous systemCerebral cortexNerve DegenerationFemaleNeurology (clinical)NeuronNeuroscienceCell DivisionDevelopmental BiologyBrain Research
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Apoptosis of male germ-line stem cells after laser ablation of their niche.

2007

AbstractMale germ-line stem cells (GSCs) and their niche-the apical cells or hub cells-display a unique feature at the apices of insect testicular follicles. In the locust, Locusta migratoria, the niche consists of only one large apical cell surrounded by about 60 GSCs. The apical cell can be readily identified in the intact follicle. Using laser ablation it is feasible to destroy the apical cell exclusively without injuring neighboring GSCs or any other cells. The most immediate effect on GSCs is the loss of their structural polarity. Beginning about 3 h after laser treatment chromatin starts to clump and condense in individual GSCs, and some show the first signs of cellular breakdown. The…

Maleendocrine systemLocusta migratoriaMitosisApoptosisApical cellBiologyGermlineFollicleAnimalsStem Cell NicheMitosisMedicine(all)TUNEL assayStem CellsfungiCell PolarityGeneral MedicineAnatomyCell BiologyChromatinCell biologyGerm CellsApoptosisLaser TherapyStem cellDevelopmental BiologyStem cell research
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24-hour-variation of pineal gland volume, pinealocyte nuclear volume and mitotic activity in male Sprague-Dawley rats

1983

In two experiments carried out on two alternate days, the 24-h-rhythmicity of pineal gland volume, pinealocyte nuclear size in cortex and medulla and mitotic activity were studied in male Sprague-Dawley rats, to assess to what extent morphological parameters reflect the pronounced day/night differences in pineal melatonin formation. Pineal volume exhibited statistically significant changes in the second experiment only, with a distinct trough at 6 p.m. Karyometry revealed highly variable patterns. In the first experiment, pinealocyte nuclear changes lacked parallelism in cortex and medulla. The cortex exhibited a bimodal curve with peaks at noon of the first day and at 6 a.m. of the second …

Maleendocrine systemmedicine.medical_specialtyMitosisCell CountBiologyPineal GlandPinealocyteKaryometryPineal glandCortex (anatomy)Internal medicinemedicineAnimalsCircadian rhythmMitosisBiological PsychiatryMedullaCell NucleusNeuronsRats Inbred StrainsOrgan SizeCircadian RhythmRatsPsychiatry and Mental healthmedicine.anatomical_structureEndocrinologyNeurologyMitotic FigureNeurology (clinical)Journal of Neural Transmission
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Spermatocyte chromosome analysis of Helicella virgata (Pulmonata: Helicidae): silver-stained and C-banded chromosomes.

1991

Chromosome numbers of the snail Helicella virgata from the fields of Castellammare del Golfo (Sicily) are n = 26 and 2n = 52. Silver-staining analyses of testicular cells suggest that both mitotic and meiotic chromosomes are involved in nucleolus organization. A within-individual variability in NOR-banding pattern is present in each of the 20 specimens analyzed.

Malemedicine.medical_specialtySnailsMitosisChromosomesHelicidaeMeiosisSpermatocytesOxazinesGeneticsmedicineAnimalsSpermatogenesisMolecular BiologyGenetics (clinical)GeneticsbiologyStaining and LabelingCytogeneticsChromosomeKaryotypeNucleolus organizationbiology.organism_classificationMolecular biologyChromosome BandingMeiosisKaryotypingHelicellaNucleolus organizer regionBiotechnologyThe Journal of heredity
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1 GHz low-thermal microwaves effect on mitotic division of vegetal tissues

2014

Materials scienceOpticsbusiness.industryDivision (mathematics)businessMitosisMicrowave2014 International Conference and Exposition on Electrical and Power Engineering (EPE)
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Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors

2014

SummaryExome sequencing analysis of over 2,000 children with complex malformations of cortical development identified five independent (four homozygous and one compound heterozygous) deleterious mutations in KATNB1, encoding the regulatory subunit of the microtubule-severing enzyme Katanin. Mitotic spindle formation is defective in patient-derived fibroblasts, a consequence of disrupted interactions of mutant KATNB1 with KATNA1, the catalytic subunit of Katanin, and other microtubule-associated proteins. Loss of KATNB1 orthologs in zebrafish (katnb1) and flies (kat80) results in microcephaly, recapitulating the human phenotype. In the developing Drosophila optic lobe, kat80 loss specificall…

Microtubule-associated proteinNeurogenesisNeuroscience(all)Cell CountKataninSpindle ApparatusBiologymedicine.disease_causeArticleMice03 medical and health sciences0302 clinical medicineNeural Stem CellsNeuroblastmedicineAnimalsDrosophila ProteinsHumansProgenitor cellZebrafishMitosisZebrafishAdenosine TriphosphatasesMutationGeneral NeuroscienceOptic Lobe NonmammalianBrainDendritesbiology.organism_classificationSpindle apparatusmedicine.anatomical_structureCentrosome030220 oncology & carcinogenesisCerebral malformationsMutationMicrocephalybiology.proteinDrosophilaNeuronKataninMicrotubule-Associated ProteinsNeuroscienceCell Division030217 neurology & neurosurgery
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Mitotic Recombination and Genetic Changes in Saccharomyces cerevisiae during Wine Fermentation

2000

Natural strains of Saccharomyces cerevisiae are prototrophic homothallic yeasts that sporulate poorly, are often heterozygous, and may be aneuploid. This genomic constitution may confer selective advantages in some environments. Different mechanisms of recombination, such as meiosis or mitotic rearrangement of chromosomes, have been proposed for wine strains. We studied the stability of the URA3 locus of a URA3/ura3 wine yeast in consecutive grape must fermentations. ura3/ura3 homozygotes were detected at a rate of 1 x 10(-5) to 3 x 10(-5) per generation, and mitotic rearrangements for chromosomes VIII and XII appeared after 30 mitotic divisions. We used the karyotype as a meiotic marker an…

Mitotic crossoverSaccharomyces cerevisiaeMitosisGenetics and Molecular BiologyWineSaccharomyces cerevisiaeApplied Microbiology and BiotechnologyGenetic recombinationFungal ProteinsMeiosisFermentacióDNA FungalMitosisGeneticsFermentation in winemakingRecombination GeneticEcologybiologyHomozygotefood and beveragesvinificationSpores Fungalbiology.organism_classificationElectrophoresis Gel Pulsed-FieldYeast in winemakingMeiosiswine fermentationKaryotypingFermentationMitotic recombinationChromosomes FungalHomologous recombinationFood ScienceBiotechnology
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Isoindolo[2,1-a]quinoxaline derivatives, novel potent antitumor agents with dual inhibition of tubulin polymerization and topoisomerase I.

2008

Isoindoloquinoxalines 4 and 5 were obtained by refluxing 2-(2'-aminoaryl)-1-cyanoisoindoles 3a- e in acetic or formic acid. All derivatives were screened by the National Cancer Institute (Bethesda, MD) for the in vitro one dose primary anticancer assay against a 3-cell line panel. Compounds 4a- e, screened against a panel of about 60 human tumor cell lines, showed remarkable antineoplastic activity; they had GI 50 values in the low micromolar or submicromolar range and reached, in the case of 4c, nanomolar concentrations on 88% of the 59 tested cell lines. Flow cytometric analysis of cell cycle after treatment with 4c demonstrated an arrest of the cell cycle in G2/M phase. This effect was a…

Mitotic indexMagnetic Resonance SpectroscopySpectrophotometry InfraredPolymersFLUORESCENT-PROBELIGAND-DNA SYSTEMSMitosisCELL-LINESAntineoplastic AgentsACRIDINE-ORANGETopoisomerase-I InhibitorMITOCHONDRIATubulinCell Line TumorQuinoxalinesDrug DiscoveryHumansCytotoxicitybiologyChemistryTopoisomeraseB-DNACell CycleCell cycleAPOPTOSISCDEnzyme ActivationMICROTUBULESBiochemistryMicroscopy FluorescenceCell cultureApoptosisEnzyme inhibitorLINEAR DICHROISM SPECTROSCOPYCaspasesbiology.proteinMolecular MedicineDrug Screening Assays AntitumorTopoisomerase I InhibitorsReactive Oxygen SpeciesJournal of medicinal chemistry
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Assessment in vitro of cytogenetic and genotoxic effects of propolis on human lymphocytes

2012

We evaluated the genetic damage by ethanolic extract of propolis (EEP) induced to human lymphocytes which were exposed to increasing concentrations (0–2000 μg ml−1). The results indicated that EEP reduced significantly the mitotic index (MI) and proliferation index (PI) when high concentrations of EEP were used. Sister chromatid exchange (SCE) rates indicated that EEP could have genotoxic effects at high concentrations. Exposure of the cells to the amount of ethanol used as solvent did not alter either the MI and cell proliferation kinetics (CPK), or the rate of SCE. The results showed: (a) statistical increase in the percentage the cells with CAs and in the frequency of SCE at the highest …

Mitotic indexProliferation indexCytotoxicityMitosisSister chromatid exchangeBiologyToxicologymedicine.disease_causeINGENIERIA NUCLEARPropolisToxicologyAndrologyIn vitroHuman lymphocytesmedicineHumansEthanolic extract of propolisLymphocytesCytotoxicityCells CulturedCell ProliferationCell growthMutagenicity TestsGeneral MedicinePropolisIn vitroGenotoxicitySister Chromatid ExchangeGenotoxicityFood Science
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Restitutionserscheinungen an pflanzlichen Meristemen nach Röntgenbestrahlung

1964

Young undifferentiated embryos ofEranthis hiemalis were treated with x-rays (1000–4000 r) and their further development was observed. In most of the 4000 r-group the division-activity is completely and irreversibly arrested, but the cell image remains unchanged. The embryos treated with doses between 1000 and 2000 r are also severely damaged, this time undergoing radical disorganization of the tissue, due to degeneration and necrosis. In these embryos small cell groups or even single cells are able to regain their mitotic potency. Meristematic centers (“embryoids”) arise and develop into normal or sometimes misformed viable adventive embryos. This restitution takes place only in x-rayed emb…

NecrosisSomatic cellCellTotipotentEmbryoPlant ScienceAnatomyDegeneration (medical)BiologyMeristemAndrologymedicine.anatomical_structureembryonic structuresGeneticsmedicinemedicine.symptomMitosisPlanta
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