Search results for "Integument"

showing 10 items of 754 documents

The MC3 receptor binding affinity of melanocortins correlates with the nitric oxide production inhibition in mice brain inflammation model

2006

Melanocortins possess strong anti-inflammatory effects acting in the central nervous system via inhibition of the production of nitric oxide (NO) during brain inflammation. To shed more light into the role of melanocortin (MC) receptor subtypes involved we synthesized and evaluated some novel peptides, modified in the melanocyte-stimulating hormone (MSH) core structure, natural MCs and known MC receptor selective peptides - MS05, MS06. Since the study included both selective, high affinity binders and the novel peptides, it was possible to do the correlation analysis of binding activities and the NO induction-related anti-inflammatory effect of the peptides. beta-MSH, gamma1-MSH, gamma2-MSH…

Central Nervous SystemLipopolysaccharidesMalemedicine.medical_specialtyInsectaLipopolysaccharidePhysiologyAnti-Inflammatory AgentsInflammationBiologyNitric OxideBiochemistryNitric oxideMiceCellular and Molecular Neurosciencechemistry.chemical_compoundEndocrinologyMelanocortin receptorInternal medicinemedicineAnimalsReceptorMelanocortinsInflammationMice Inbred ICRintegumentary systemReceptors MelanocortinElectron Spin Resonance SpectroscopyCell biologyEndocrinologychemistryForebrainmedicine.symptomMelanocortinPeptideshormones hormone substitutes and hormone antagonistsProtein BindingReceptor Melanocortin Type 3Peptides
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RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosmin

2005

The ORF15 isoform of RPGR (RPGR(ORF15)) and RPGR interacting protein 1 (RPGRIP1) are mutated in a variety of retinal dystrophies but their functions are poorly understood. Here, we show that in cultured mammalian cells both RPGR(ORF15) and RPGRIP1 localize to centrioles. These localizations are resistant to the microtubule destabilizing drug nocodazole and persist throughout the cell cycle. RPGR and RPGRIP1 also co-localize at basal bodies in cells with primary cilia. The C-terminal (C2) domain of RPGR(ORF15) (ORF15(C2)) is highly conserved across 13 mammalian species, suggesting that it is a functionally important domain. Using matrix-assisted laser desorption ionization time-of-flight mas…

CentrioleFluorescent Antibody TechniqueMicechemistry.chemical_compoundChlorocebus aethiopsGuanine Nucleotide Exchange FactorsProtein IsoformsBasal bodyConserved SequenceGenetics (clinical)CentriolesGlutathione Transferaseintegumentary systemNuclear ProteinsExonsGeneral MedicineRetinitis pigmentosa GTPase regulatorImmunohistochemistryNocodazoleCOS CellsNucleophosminCell NucleolusRecombinant Fusion ProteinsMolecular Sequence DataBiologyOpen Reading FramesMicrotubuleTwo-Hybrid System TechniquesGeneticsAnimalsHumansAmino Acid SequenceEye ProteinsMolecular BiologyNucleophosminSequence Homology Amino AcidProteinsPrecipitin TestsMolecular biologyeye diseasesProtein Structure TertiaryMice Inbred C57BLCytoskeletal ProteinschemistryCentrosomeCytoplasmSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationMutationCattleHeLa CellsHuman Molecular Genetics
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Dimethylsulfoxide as carrier in enzyme cytochemistry.

1971

Addition of dimethylsulfoxide (DMSO) to the incubation medium of succinate dehydrogenase in a concentration of 10% enhances the staining reaction in the hyphae of the fungus Cercosporella herpotrichoides after an incubation period of 15 min. Controls without DMSO remain unstained. DMSO causes a rapid penetration of the components of the medium through the mucilage that covers the hyphae.

CercosporellaHistologyintegumentary systembiologyHyphaStaining and LabelingHistocytochemistryorganic chemicalsSuccinate dehydrogenasefungiCell BiologyStainingIncubation periodMedical Laboratory TechnologyBiochemistryMucilagebiology.proteinCytochemistryDimethyl SulfoxideMitosporic FungiMolecular BiologyIncubationHistochemie. Histochemistry. Histochimie
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Vascular Patterns in Dermoscopy

2012

Under the right conditions, dermoscopy allows us to observe the vascular features of many different types of skin lesions. The visualization and identification of vessels with a characteristic morphology can be the key to diagnosis, especially in hypopigmented lesions in which the typical pigmented structures are not visible. Some of the more characteristic associations are the presence of crown vessels in sebaceous hyperplasia, arborizing telangiectasias in basal cell carcinoma, comma-shaped vessels in intra- dermal and compound nevi, dotted vessels in Spitz nevi and melanoma, and hairpin vessels in seborrheic keratoses. The recognition of distinctive vascular features can be of great help…

Characteristic morphologymedicine.medical_specialtyPathologyHistologyintegumentary systemSeborrheic keratosesbusiness.industryMelanomaSebaceous hyperplasiaDermatologymedicine.diseaseDermatologyPathology and Forensic MedicinemedicineBasal cell carcinomaSkin lesionbusinessActas Dermo-Sifiliográficas (English Edition)
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Compartmentalized Production of CCL17 In Vivo

2003

Dendritic cells (DCs)**Abbreviations used in this paper: BM, bone marrow; CHS, contact hypersensitivity; cLN, cutaneous lymph node; CRP, C-reactive protein; DC, dendritic cell; DNFB, dinitrofluorobenzene; EGFP, enhanced green fluorescent protein; LC, Langerhans cell; LP, lamina propria; MACS, magnetic-activated cell sorting; mLN, mesenteric lymph node; ODN, oligodeoxynucleotide; PFA, paraformaldehyde; PP, Peyer's patch; TLR, Toll-like receptor; TRITC, tetramethylrhodamine-5-(and-6-)-isothiocyanate. fulfill an important regulatory function at the interface of the innate and adaptive immune system. The thymus and activation-regulated chemokine (TARC/CCL17) is produced by DCs and facilitates t…

Chemokineintegumentary systemImmunologySpleenStimulationBiologyAcquired immune systemCell biologymedicine.anatomical_structureLymphatic systemAntigenImmunologymedicinebiology.proteinImmunology and AllergyCCL17CD8Journal of Experimental Medicine
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Chlorophyll a Fluorescence Emission, Xanthophyll Cycle Activity, and Net Photosynthetic Rate Responses to Ozone in Some Foliose and Fruticose Lichen …

2000

The lichens Parmelia quercina, Parmelia sulcata, Evernia prunastri, Hypogymnia physodes, and Anaptychia ciliaris were exposed to ozone (O3) in controlled environment cuvettes designed to maintain the lichens at optimal physiological activity during exposure. Measurements of gas exchange, modulated chlorophyll (Chl) fluorescence, and pigment analysis were conducted before and after exposure to 300 mm3 (O3) m−3, 4 h per d for 14 d. No changes in the efficiency of photosystem 2 (PS2) photochemistry, the reduction state of QA, or the electron flow through PS2, measured by Chl fluorescence, were detected in any of the five lichen species studied. Additionally, neither photosynthetic CO2 assimila…

Chlorophyll aParmeliaintegumentary systembiologyPhysiologyAntheraxanthinPlant SciencePhotosynthetic pigmentbiology.organism_classificationEverniachemistry.chemical_compoundchemistryChlorophyllParmelia sulcataBotanyskin and connective tissue diseasesFruticose lichenPhotosynthetica
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Evaluation of molecular mass and tacticity of polyvinyl alcohol by non-equilibrium capillary electrophoresis of equilibrium mixtures of a polymer and…

2011

Non-equilibrium capillary electrophoresis of equilibrium mixtures (NECEEM) has been used to characterize polyvinyl alcohol (PVA). Commercial PVA samples with different molecular masses, from M(w)=15 up to 205 kDa, were used. According to the (13)C NMR spectra, the samples also differed in tacticity (stereoregularity). Mixtures of PVA and the anionic azo-dye Congo Red (CR) were injected in the presence of a borate buffer. The electropherograms gave a band and a peak due to the residual PVA-CR complex and the excess dye, respectively, plus a superimposed exponential decay due to the partial dissociation of the complex during migration. The stoichiometry of the PVA-CR complex, q=[monomer]/[dye…

Chromatographyintegumentary systemOrganic ChemistryElectrophoresis CapillaryCongo RedGeneral MedicineBiochemistryPolyvinyl alcoholDissociation (chemistry)Analytical ChemistryMolecular Weightchemistry.chemical_compoundElectrophoresisMonomerCapillary electrophoresischemistryStability constants of complexesPolyvinyl AlcoholTacticityBoratesSpectrophotometry UltravioletAzo CompoundsStoichiometryJournal of Chromatography A
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Influence of sodium lauryl sulphate on the in vitro percutaneous absorption of compounds with different lipophilicity

1997

Abstract The effects of sodium lauryl sulphate (SLS) at different concentrations on the “in vitro” percutaneous absorption of a number of compounds (5-fluorouracil, antipyrine, pentoxifylline, salicylamide, 4-ethylaniline, 4-n-butylaniline and indomethacin) with a wide range of lipophilicity values (log POCT from −0.95 to 4.42) through rat skin were analysed. After pretreatment of the skin with SLS (1% and 5%, w/w) the permeability coefficients increased only for compounds having a log POCT

Chromatographyintegumentary systemPermeability (electromagnetism)ChemistrySodium lauryl sulphateLipophilicityPercutaneous absorptionmedicinePharmaceutical ScienceSalicylamideIn vitroPentoxifyllinemedicine.drugEuropean Journal of Pharmaceutical Sciences
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Genotoxicity characteristics of reverse diol-epoxides of chrysene.

2017

Trans-3,4-dihydroxy-3,4-dihydrochrysene (chrysene-3,4-diol), a major metabolite of chrysene, is further metabolized by rat liver enzymes to products which effectively revert the his- Salmonella typhimurium strain TA98 to histidine prototrophy, but are only weakly mutagenic in strain TA100 and in Chinese hamster V79 cells (acquisition of resistance to 6-thioguanine). The liver enzyme mediated mutagenicity of chrysene-3,4-diol is substantially enhanced in the presence of 1,1,1-trichloropropene 2,3-oxide, an inhibitor of microsomal epoxide hydrolase. The predominant metabolites of chrysene-3,4-diol, namely the anti- and syn-isomers of its 1,2-oxide (termed reverse diol-epoxides), proved to be …

ChryseneMaleSalmonella typhimuriumCancer ResearchMetaboliteMutagenGene mutationmedicine.disease_causeChrysenesRats Sprague-Dawleychemistry.chemical_compoundMiceCricetulusCricetinaemedicinepolycyclic compoundsAnimalsheterocyclic compoundsEpoxide hydrolaseSOS Response GeneticsBiotransformationCells CulturedTrichloroepoxypropaneEpoxide HydrolasesMice Inbred C3Hintegumentary systemChemistryorganic chemicalsGeneral MedicineDNARatsCell Transformation NeoplasticBiochemistryMicrosomal epoxide hydrolaseEpoxide HydrolasesCarcinogensMicrosomes LiverGenotoxicityhormones hormone substitutes and hormone antagonistsMutagensCarcinogenesis
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Relationship between mutagenicity and DNA adduct formation in mammalian cells for fjord- and bay-region diol-epoxides of polycyclic aromatic hydrocar…

1991

Abstract Chinese hamster V79 cells were treated with the anti- and syn-diastereomers of the bay- or fjord-region diol-epoxides of four polycyclic aromatic hydrocarbons, namely benzo[a]pyrene (BP), benzo[c]chrysene (BcC), benzo[g]chrysene (BgC) and benzo[c]phenanthrene (BcPh). The frequency of induction of 6-thioguanine-resistant mutations was determined, and the extent of formation of DNA adducts was measured by 32P-postlabelling. When expressed as mutation frequency per nanomoles compound per millilitre incubation medium, this group of chemicals expressed a 160-fold range in potency. In agreement with previous experimental studies, the anti-diol-epoxide of BcC was highly mutagenic, inducin…

ChryseneStereochemistryCell SurvivalBenzo(c)phenanthreneToxicologyAdductchemistry.chemical_compoundCricetulusIsomerismCricetinaepolycyclic compoundsBenzo(a)pyreneAnimalsheterocyclic compoundsPolycyclic CompoundsMutation frequencyCells Culturedintegumentary systemorganic chemicalsfungiGeneral MedicineDNAPhenanthrenechemistryBenzo(a)pyreneMutationPyreneDNAMutagensChemico-biological interactions
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