Search results for "M2"

showing 10 items of 256 documents

A plant-wide energy model for wastewater treatment plants: application to anaerobic membrane bioreactor technology

2016

[EN] The aim of this study is to propose a detailed and comprehensive plant-wide model for assessing the energy demand of different wastewater treatment systems (beyond the traditional activated sludge) in both steady- and unsteady-state conditions. The proposed model makes it possible to calculate power and heat requirements (W and Q, respectively), and to recover both power and heat from methane and hydrogen capture. In order to account for the effect of biological processes on heat requirements, the model has been coupled to the extended version of the BNRM2 plant-wide mathematical model, which is implemented in DESSAS simulation software. Two case studies have been evaluated to assess t…

INGENIERIA HIDRAULICAEngineeringPlant-wide energy modelAnaerobic MBR020209 energyPortable water purificationWastewater treatment02 engineering and technologyWastewatercomputer.software_genreWaste Disposal FluidMethaneWater Purificationchemistry.chemical_compoundBioreactorsBNRM20202 electrical engineering electronic engineering information engineeringBioreactorEnvironmental ChemistryAnaerobiosisProcess engineeringWaste Management and DisposalTECNOLOGIA DEL MEDIO AMBIENTEWater Science and Technologybusiness.industryTemperatureEnvironmental engineeringMembranes ArtificialGeneral MedicineDESASSModels TheoreticalPower (physics)Simulation softwareActivated sludgeWastewaterchemistrySewage treatmentbusinessMethanecomputerEnvironmental Technology
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Molecular modeling approaches in the discovery of new drugs for anti-cancer therapy: the investigation of p53-MDM2 interaction and its inhibition by …

2010

The mdm2 oncogene product, MDM2, is an ubiquitin protein ligase that inhibits the transcriptional activity of the tumor suppressor p53 and promotes its degradation. About 50% of all human cancers present mutations or deletions in the TP53 gene. In the remaining half of all human neoplasias that express the wild-type protein, aberrations of p53 regula- tors, such as MDM2, account for p53 inhibition. For this reason, designing small-molecule inhibitors of the p53-MDM2 protein-protein interaction is a promising strategy for the treatment of cancers retaining wild-type p53. The development of inhibitors has been challenging. Although many small-molecule MDM2 inhibitors have shown potent in vitr…

IndolesTumor suppressor geneAntineoplastic AgentsMolecular Dynamics SimulationBioinformaticsBiochemistryGene productNeoplasmsDrug DiscoverymedicineHumansImidazolinesMolecular Modeling New Drugs for Anti-Cancer Therapy p53-MDM2 InteractionPharmacologyBenzodiazepinonesbiologyOncogeneOrganic ChemistryCancerProto-Oncogene Proteins c-mdm2medicine.diseaseSettore CHIM/08 - Chimica FarmaceuticaSmall moleculeUbiquitin ligaseOxindolesProtein Structure TertiaryDrug Designbiology.proteinCancer researchMolecular MedicineMdm2PharmacophoreTumor Suppressor Protein p53Current medicinal chemistry
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FRI0152 Inflammasomes activation occurs in the inflamed tissues of as patients and drives il-23 expression

2018

Background A growing body of evidences indicate that the aberrant activation of innate immune systems, occurring in genetically predisposed patients, drives inflammatory processes in Ankylosing Spondylitis (AS).1 Objectives Aim of this study was to evaluate the activation and the functional relevance of inflammasome pathways in patients with AS. Methods Intestinal, synovial and bone marrow expression of inflammasome pathways, pyroptosis and IL-1b and IL-18 was evaluated in AS patients. Organic acid extraction was performed on ileal samples as previously described on.2 The expression of the metabolite-sensing receptors GPR43 and GPR109A involved in the regulation of the intestinal inflammaso…

Innate immune systembusiness.industryMonocytePyroptosisInflammasomemedicine.diseaseAIM2medicine.anatomical_structureNLRC4ImmunologymedicineGlucose homeostasisbusinessDysbiosismedicine.drugFRIDAY, 15 JUNE 2018
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Rationally integrable vector fields and rational additive group actions

2016

International audience; We characterize rational actions of the additive group on algebraic varieties defined over a field of characteristic zero in terms of a suitable integrability property of their associated velocity vector fields. This extends the classical correspondence between regular actions of the additive group on affine algebraic varieties and the so-called locally nilpotent derivations of their coordinate rings. Our results lead in particular to a complete characterization of regular additive group actions on semi-affine varieties in terms of their associated vector fields. Among other applications, we review properties of the rational counterpart of the Makar-Limanov invariant…

Integrable systemRationally integrable derivationsGeneral Mathematics010102 general mathematics05 social sciencesLocally nilpotentAlgebraic variety01 natural sciencesLocally nilpotent derivations[ MATH.MATH-AG ] Mathematics [math]/Algebraic Geometry [math.AG]AlgebraHomogeneousRational additive group actions0502 economics and businessVector fieldAffine transformation[MATH.MATH-AG]Mathematics [math]/Algebraic Geometry [math.AG]050207 economics0101 mathematicsInvariant (mathematics)MSC: 14E07 14L30 14M25 14R20Additive groupMathematics
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Novel isatin-derived molecules activate p53 via interference with Mdm2 to promote apoptosis

2018

International audience; The p53 protein is a key tumor suppressor in mammals. In response to various forms of genotoxic stress p53 stimulates expression of genes whose products induce cell cycle arrest and/or apoptosis. An E3-ubiquitin ligase, Mdm2 (mouse-double-minute 2) and its human ortholog Hdm2, physically interact with the amino-terminus of p53 to mediate its ubiquitin-mediated degradation via the proteasome. Thus, pharmacological inhibition of the p53-Mdm2 interaction leads to overall stabilization of p53 and stimulation of its anti-tumorigenic activity. In this study we characterize the biological effects of a novel class of non-genotoxic isatin Schiff and Mannich base derivatives (…

Isatin0301 basic medicineProgrammed cell deathCell cycle checkpointAntineoplastic AgentsApoptosis[SDV.BC]Life Sciences [q-bio]/Cellular BiologyBiologyPiperazinesHistonesMice03 medical and health scienceschemistry.chemical_compound0302 clinical medicineNutlinCell Line TumorProto-Oncogene ProteinsAnimalsHumansMolecular Biologychemistry.chemical_classificationDNA ligaseIsatinImidazolesISMBDsProto-Oncogene Proteins c-mdm2Cell BiologyNutlinp53-activating moleculesCell biology030104 developmental biologychemistryProteasomeApoptosis030220 oncology & carcinogenesisbiology.proteinMdm2PumaTumor Suppressor Protein p53Apoptosis Regulatory Proteinsautomated microscopy system OperettaResearch PaperDevelopmental BiologyCell Cycle
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Eléments d'économie managériale

1989

JEL : M - Business Administration and Business Economics • Marketing • Accounting • Personnel Economics/M.M1 - Business Administration/M.M1.M10 - GeneralJEL: M - Business Administration and Business Economics • Marketing • Accounting • Personnel Economics/M.M1 - Business Administration/M.M1.M10 - General[ SHS.ECO ] Humanities and Social Sciences/Economies and financesJEL : M - Business Administration and Business Economics • Marketing • Accounting • Personnel Economics/M.M2 - Business Economics/M.M2.M21 - Business EconomicsJEL: M - Business Administration and Business Economics • Marketing • Accounting • Personnel Economics/M.M2 - Business Economics/M.M2.M21 - Business Economics[SHS.ECO] Humanities and Social Sciences/Economics and Finance[SHS.ECO]Humanities and Social Sciences/Economics and Finance
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Khovanov homology for signed divides

2009

The purpose of this paper is to interpret polynomial invariants of strongly invertible links in terms of Khovanov homology theory. To a divide, that is a proper generic immersion of a finite number of copies of the unit interval and circles in a [math] –disc, one can associate a strongly invertible link in the [math] –sphere. This can be generalized to signed divides: divides with [math] or [math] sign assignment to each crossing point. Conversely, to any link [math] that is strongly invertible for an involution [math] , one can associate a signed divide. Two strongly invertible links that are isotopic through an isotopy respecting the involution are called strongly equivalent. Such isotopi…

Khovanov homologyPure mathematicsDivides[ MATH.MATH-AT ] Mathematics [math]/Algebraic Topology [math.AT]Homology (mathematics)01 natural scienceslaw.inventionMorse signed dividessymbols.namesakelawEuler characteristic0103 physical sciencesFOS: MathematicsAlgebraic Topology (math.AT)Mathematics - Algebraic Topology0101 mathematicsInvariant (mathematics)Finite setMathematicsKhovanov homology010102 general mathematics16. Peace & justiceInvertible matrix57M27[MATH.MATH-AT]Mathematics [math]/Algebraic Topology [math.AT]IsotopysymbolsStrongly invertible links010307 mathematical physicsGeometry and TopologyVector space
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Targeted Repolarization of Tumor‐Associated Macrophages via Imidazoquinoline‐Linked Nanobodies

2021

Abstract Tumor‐associated macrophages (TAMs) promote the immune suppressive microenvironment inside tumors and are, therefore, considered as a promising target for the next generation of cancer immunotherapies. To repolarize their phenotype into a tumoricidal state, the Toll‐like receptor 7/8 agonist imidazoquinoline IMDQ is site‐specifically and quantitatively coupled to single chain antibody fragments, so‐called nanobodies, targeting the macrophage mannose receptor (MMR) on TAMs. Intravenous injection of these conjugates result in a tumor‐ and cell‐specific delivery of IMDQ into MMRhigh TAMs, causing a significant decline in tumor growth. This is accompanied by a repolarization of TAMs to…

Lung NeoplasmsGeneral Chemical Engineeringmedicine.medical_treatmentGeneral Physics and AstronomyMedicine (miscellaneous)TLR 7/8 agonist02 engineering and technology01 natural scienceschemistry.chemical_compoundCancer immunotherapyTumor-Associated MacrophagesTumor MicroenvironmentMacrophageM2 macrophagesGeneral Materials ScienceReceptorResearch ArticlesMice KnockoutMembrane GlycoproteinsChemistrytumor associated macrophagesQGeneral EngineeringImidazoles021001 nanoscience & nanotechnologynanobodiesmedicine.anatomical_structureDrug deliveryQuinolines0210 nano-technologyMannose ReceptorResearch ArticleT cellScience010402 general chemistryBiochemistry Genetics and Molecular Biology (miscellaneous)Immune systemmedicineAnimalsrepolarizationcancer immunotherapyCancerSingle-Domain Antibodiesmedicine.disease0104 chemical sciencesImidazoquinolineMice Inbred C57BLDisease Models AnimalToll-Like Receptor 6Toll-Like Receptor 7drug deliveryCancer research
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Mikrokokoistetut leviämisvastus- ja nelipisteanturimittaukset puolijohderakenteen varauksenkuljettajien syvyysjakaumien määrittämisessä

2013

Entistä pienemmät puolijohderakenteet vaativat analyysityökaluilta erittäin hyvää herkkyyttä, jonka on myös kehityttävä rakenteiden vaatimusten mukaisesti -- muussa tapauksessa kehitys voi hidastua hyvin paljon ilman kunnollista tietoa valmistusmenetelmien tuloksista. Yksi oleellinen osa rakenteiden analysoimisessa on tieto seostusatomien ja varauksenkuljettajien pitoisuuksista rakenteen syvyyssuunnassa, eli syvyysjakauma. Vuosikymmeniä syvyysjakauman mittaukseen on käytetty leviämisvastusmittausta (SRP, engl. Spreading Resistance Profiling), ja nelipisteanturimittausta (4PP, engl. Four Point Probe) on käytetty kuvaamaan koko syvyysjakauman vaikutusta sähköisessä kontaktissa. Molempien tekn…

M4PPmittausfour point probeSRPsyvyysjakaumaleviämisvastusmittaus4PPmittausmenetelmätleviämisvastuspuolijohteetneliövastusM2PPspreading resistance profilingnelipisteanturimittausvarauksenkuljettajien syvyysjakauma
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MONOCYTES MACROPHAGES EXPRESSION OF Ml OR M2 PHENOTYPES IN LATENT TUBERCULOSIS, ACTIVE DISEASES AND UNINFECTED MIGRANTS AND SICILIAN PATIENTS

2016

The high grade ofphenotype plasticity of monocytes macrophages, is resumed in two different cell subsets named M1 or M2. Several studies of microbial infections in vitro and in vivo, showed that, during the early stage of infection, macrophages are polarized toward Ml phenotype that should be protective against pathogen, while during the chronic phase of infection/disease macrophages polarize toward M2 phenotype to avoid damages from a prolonged Ml type activation.Obiettivo: In order to investigate if Mycobacterium tuberculosis infection can drive circulating monocytes toward the expression of Ml or M2 phenotypes, we have analyzed by flow cytometry monocytes obtained from patients with acti…

MONOCYTES Ml OR M2 PHENOTYPES TUBERCULOSIS
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