Search results for "structures"

showing 10 items of 4815 documents

Development of the wing discs of Zophobas atratus under natural and experimental conditions: occurrence of a gradual larval-pupal commitment in the e…

1999

Using light and electron microscopy, we studied the development of the wing discs in the large beetle Zophobas atratus, under natural and experimental conditions. A reversible differentiation of the wing discs is usually observed during supernumerary instars of crowded larvae. Juvenile hormone analog (JHA) application during the wandering period or compelled experimental crowding during the larval-pupal switchover – or commitment – inhibits the onset of metamorphosis. Isolation, followed by recrowding, also induces the disc cells to secrete unusual cuticular material. Recrowding is able to trigger the reversal of metamorphosis during the 4-day period when larval-pupal commitment is taking p…

animal structuresHistologyEmbryo Nonmammalianmedia_common.quotation_subjectZoologyBiologyPathology and Forensic MedicineReversible differentiationMorphogenesisAnimalsWings AnimalMetamorphosismedia_commonLarvaWingfungiCell DifferentiationCell BiologyAnatomyPupaColeopteraMicroscopy ElectronEcdysisInsect HormonesJuvenile hormoneInstarEpidermisCell and tissue research
researchProduct

Blue-green algalike cells associated with the tunic of Ciona intestinalis L.

1980

Certain organisms resembling blue-green algae embedded in the tunic of the solitary ascidian Ciona intestinalis L. are described. Their probable symbiotic role as related to the peculiar habitat of this ascidian is suggested.

animal structuresHistologybiologyfungiZoologyCell Biologybiology.organism_classificationCyanobacteriaPathology and Forensic MedicineCiona intestinalisAlgaeembryonic structuresAnimalsCiona intestinalisUrochordataSymbiosisCell and tissue research
researchProduct

Improved method to retain cytosolic reporter protein fluorescence while staining for nuclear proteins

2014

Staining of transcription factors (TFs) together with retention of fluorescent reporter proteins is hindered by loss of fluorescence using current available methods. In this study, it is shown that current TF staining protocols do not destroy fluorescent proteins (FPs) but rather that fixation is not sufficient to retain FPs in the cytosol of the permeabilized cells. In this article, a simple and reliable protocol is elaborated, which allows efficient TF and cytokine staining while retaining FPs inside fixed cells.

animal structuresHistologymedicine.diagnostic_testmedicine.medical_treatmentCell BiologyBiologyFluorescencePathology and Forensic MedicineCell biologyFlow cytometryGreen fluorescent proteinStainingCytosolCytokineBiochemistryembryonic structuresmedicineNuclear proteinTranscription factorCytometry Part A
researchProduct

Electron microscopy of a double helical tubular filament in keyhole limpet (Megathura crenulata) hemolymph.

1992

A approximately 25 nm hollow double helical filament has been detected ultrastructurally in the cell-free supernatant from hemolymph of the keyhole limpet Megathura crenulata (Gastropoda: Prosobranchia: Fissurellidae). Subsequently, much higher concentrations of this material were found in the cell pellet from hemolymph. Both negative staining and thin sectioning have been performed in an attempt to obtain a preliminary structural characterization of this new filament. It is proposed that the filaments are released or secreted from blood hemocytes in response to bleeding, but it has not been possible to define absolutely an intracellular organelle containing this material. It is shown that …

animal structuresHistologymedicine.medical_treatmentchemical and pharmacologic phenomenamacromolecular substancesMegathura crenulataMicrotubulesPathology and Forensic MedicineProtein filamentIntracellular organelleHemolymphHemolymphmedicineAnimalsFissurellidaebiologyCell-Free SystemLimpetHemocyaninCell BiologyAnatomybiology.organism_classificationActin CytoskeletonMicroscopy ElectronMolluscaHemocyaninsbiology.proteinBiophysicsCollagenKeyhole limpet hemocyaninCell and tissue research
researchProduct

Sea urchin deciliation induces thermoresistance and activates the p38 mitogen-activated protein kinase pathway.

2003

In this study, we demonstrate by a variety of approaches (ie, morphological analysis, Western blots, immunolocalization, and the use of specific antibodies) that hyperosmotic deciliation stress of sea urchin embryos induces a thermotolerant response. Deciliation is also able to activate a phosphorylation signaling cascade the effector of which might be the p38 stress-activated protein kinase because we found that the administration of the p38 inhibitor SB203580 to sea urchin deciliated gastrula embryos makes the hyperosmotic deciliation stress lethal.

animal structuresHot TemperaturePyridinesp38 mitogen-activated protein kinasesSEA URCHIN DECILIATION p38MAP KINASEBiochemistryp38 Mitogen-Activated Protein KinasesEnzyme activatorStress Physiologicalbiology.animalAnimalsCiliaSettore BIO/06 - Anatomia Comparata E CitologiaPhosphorylationProtein kinase ASea urchinbiologyEffectorImidazolesAntibodies MonoclonalCell BiologyGastrulaOriginal ArticlesMolecular biologyBlotEnzyme ActivationSea Urchinsembryonic structuresPhosphorylationElectrophoresis Polyacrylamide GelSignal transductionMitogen-Activated Protein KinasesSignal TransductionCell stresschaperones
researchProduct

Achievement of thermotolerance through hsps phosphorylation in sea urchin embryos.

1995

TPA treatment of sea urchin embryos is able to induce thermotolerance. Evidence is provided that TPA treatment induces phosphorylation of a constitutive stress protein of 38 KDa.

animal structuresHot Temperatureintegumentary systemTrough (geology)Cell BiologyGeneral MedicineSea urchin embryoBiologyCell biologySea Urchinsembryonic structuresBotanyPhosphorylationAnimalsTetradecanoylphorbol AcetateElectrophoresis Gel Two-DimensionalFemalePhosphorylationHeat-Shock ProteinsBody Temperature RegulationCell biology international
researchProduct

Vibriosis in aquaculture. 16th EAFP Conference, Tampere, Finland, 4th September 2013

2014

Aquaculture in brackish and marine water is growing worldwide (FAO, 2014), including new cultured species. Various Vibrio infections occur, and cause significant problems, in fish, crustacean and shellfish (Austin & Austin, 2007. Vibrio anguillarum, V. salmonicida, V. ordalii and V. vulnificus are among the pathogens that lead to the biggest losses in aquaculture all over the world (Toranzo et al. 2005, Sandlund et al., 2010; Sitjà-Bobadilla et al. 2014).

animal structuresIDENTIFICATIONVULNIFICUS BIOTYPE 2STRAINSfungiAqüiculturaPeixos/dk/atira/pure/sustainabledevelopmentgoals/life_below_waterANGUILLA-ANGUILLABacteris patògensINFECTIONEEL FARMPATHOGENSEROVAR-ESDG 14 - Life Below WaterFISHERIESMARINEOUTBREAKSCRASSOSTREA-GIGAS
researchProduct

Territorial localization of heat shock mRNA production in sea urchin gastrulae.

1985

In situ hybridization experiments with a labeled DNA probe indicate that the ability to respond to heat shock with the production of the mRNA for the 70 kd heat shock protein is segregated into the ectodermal cells already at the gastrula stage or earlier during the embryonic development of Paracentrotus lividus.

animal structuresIn situ hybridizationParacentrotus lividusbiology.animalEctodermmedicineAnimalsRNA MessengerSea urchinHeat-Shock ProteinsMessenger RNAbiologyHybridization probeEmbryogenesisNucleic Acid HybridizationCell BiologyAnatomyGastrulabiology.organism_classificationCell biologyGastrulationMolecular WeightShock (circulatory)Sea Urchinsembryonic structuresAutoradiographymedicine.symptomCell biology international reports
researchProduct

Sterol oxidation in ready-to-eat infant foods during storage.

2008

The effect of storage on sterol oxidation of ready-to-eat infant foods was evaluated. Two different flavor (honey -LH- or fruits-LF-) liquid infant foods, prepared with milk and cereals, were stored for 0, 2, 4, 7 and 9 months, at 25ºC. Sterol oxidation products (SOP) were extracted by cold saponification, purified by silica solid-phase and analyzed by gas chromatography (GC) and GC-mass spectrometry. -sitosterol was the most representative sterol, followed by cholesterol and campesterol. No significant differences in the total and single SOP content (0.8-1 mg/kg of product) were observed with respect to storage time and type of sample; the main SOP found was 7-ketositosterol (< …

animal structuresInfants AlimentacióCampesterolRaw materialMILK CEREALSchemistry.chemical_compoundFood PreservationFood scienceINFANT FOODSStigmasterolChromatographyPhytosterolFatty AcidsFood preservationPhytosterolsGeneral ChemistrySitosterolsSterolPHYTOSTEROL OXIDATION PRODUCTSSterolsCholesterolchemistrylipids (amino acids peptides and proteins)Infant FoodGas chromatographyGeneral Agricultural and Biological SciencesOxidation-ReductionSaponificationSTEROL OXIDATION PRODUCTSSTORAGEJournal of agricultural and food chemistry
researchProduct

Neurobiological Models of the Central Complex and the Mushroom Bodies

2013

This study reviews the actual knowledge on functions of the central complex (CX) and the mushroom bodies (MBs) in a genetic model insect, the fly Drosophila melanogaster. Ongoing research of UNIMAINZ and respective data are included. Reference is made to other insects, where respective functions are not yet studied in Drosophila. Neuroanatomical information is reported with regard to the general flow of information in these central brain neuropils. Particular projection systems and circuits are taken into account where this can be linked to functions. Models are developed.

animal structuresKenyon cellbiologyfungibiology.organism_classificationmedicine.anatomical_structureMushroom bodiesGenetic modelmedicineAntennal lobeDrosophila melanogasterProjection (set theory)DrosophilaNeuroscience
researchProduct