Search results for "fox"

showing 10 items of 607 documents

Effects of adjuvants of the cholera toxin family on CD4 + T cell responses in a murine model of intrarectal immunization with rotavirus-like particles

2011

Mucosal immunization is an important goal of vaccine development to protect against pathogens that use mucosa as portals of entry. However, the use of non-replicating antigens requires the addition of adjuvants.Cholera-like enterotoxins, cholera toxin (CT) from Vibrio cholerae and the heat-labile enterotoxin (LT) from toxinogenic strains of E. coli, as well as the mutant LR-192G and their B subunits (CTB and LTB) have been shown to increase immune responses against unrelated co-administered antigens by mucosal routes. However, their mechanism of action is very complex and not completely understood and differences exist between holotoxins and B subunits and within molecules, differences exis…

[SDV.SA] Life Sciences [q-bio]/Agricultural sciences[SDV.MHEP] Life Sciences [q-bio]/Human health and pathologyIL-2Cholera toxinLT-R192GVaccination muqueuseMucosal immunizationCD4 T lymphocyteE. coli heat-labile enterotoxinB subunitFoxp3[ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathologyLymphocyte T CD4Lymphocyte T régulateurSous-unité BEntérotoxine thermolabile d’E. coliRegulatory T cell[ SDV.SA ] Life Sciences [q-bio]/Agricultural sciencesAdjuvantToxine du choléra
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Aspects fonctionnels et pronostiques des cellules myéloïdes suppressives et de Foxp3 dans le cancer

2011

Evasion of immune surveillance by certain tumour cells seems to be a basic requirement for tumour development in preclinical models and in humans. The mechanisms by which the tumour mediates its immune evasion are manifold, and involve the majority of immune system cells. Among these, immunoregulatory cells such as myeloid-derived suppressor cells (MDSCs) or regulatory T lymphocytes (T-regs, which express the transcription factor Foxp3) appear to play a predominant role. The results presented in this work aim to improve our understanding of the functional and prognostic roles of myeloid suppressor cells and T-regs in cancer, focussing particularly on how these cells are modulated by chemoth…

[SDV.SA]Life Sciences [q-bio]/Agricultural sciences[SDV.SA] Life Sciences [q-bio]/Agricultural sciencesLymphocytes T régulateurs[SDV.MHEP] Life Sciences [q-bio]/Human health and pathologyRegulatory T-LymphocytesMyeloid-derived suppressor cells[ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathologyFoxp3[ SDV.SA ] Life Sciences [q-bio]/Agricultural sciencesCellules myéloides suppressives[SDV.MHEP]Life Sciences [q-bio]/Human health and pathologyCancer
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Semiconductor-photocatalyzed sulfoxidation of alkanes.

2008

alkanebusiness.industryGeneral ChemistryPhotochemistryCatalysissulfoxidationchemistry.chemical_compoundphotocatalysiSemiconductorchemistryPhotocatalysisOrganic chemistrysulfur dioxidebusinessC-H activationSulfur dioxideAngewandte Chemie (International ed. in English)
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Osmotic and cryoprotective effects of a mixture of DMSO and ethylene glycol on rabbit morulae.

1993

Abstract Comparisons were made of the osmotic and cryoprotective effects on rabbit embryos preserved by vitrification with 2 solutions and by conventional freezing. Embryos obtained from rabbits killed 70 to 72 h after mating were used in the study (n = 948). Initially, toxicity of the 3 cryoprotectants was studied in fresh (unfrozen) embryos (n = 135). Subsequently, embryos placed in ethylene glycol (EG, 40% v/v; n = 88) and ethylene glycol with dimethyl sulfoxide (EG+DMSO, 20% v/v each, respectively; n = 344) were loaded into straws and plunged directly into liquid nitrogen. Embryos placed in 1.5 M DMSO and 20% heat inactivated rabbit serum were subjected to conventional freezing in a pro…

animal structuresCryoprotectantEquineDimethyl sulfoxideLiquid nitrogenBiologyCryopreservationAndrologychemistry.chemical_compoundmedicine.anatomical_structureFood AnimalsBiochemistrychemistryEmbryo cryopreservationembryonic structuresmedicineAnimal Science and ZoologyVitrificationBlastocystSmall AnimalsEthylene glycolTheriogenology
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Direct transfer of vitrified rabbit embryos.

1994

In this study we looked at the feasibility of transferring vitrified rabbit embryos directly into recipient does. Compacted morulae were vitrified in a solution of 20% ethylene glycol and 20% dimethyl sulfoxide. After thawing, and without step-wise diluted solution, the vitrified embryos were transferred into the recipient's uterine horns. Survival rate at birth differed from fresh rabbit embryos (40% vs 55%, P0.05). However, the percentage of does that delivered (94%) and the survival rate suggested this method is suitable for both storage and simple transfer of rabbit morulae.

animal structuresEquineChemistryDimethyl sulfoxideUterine hornsEmbryoRabbit (nuclear engineering)AnatomyDirect transferAndrologychemistry.chemical_compoundFood Animalsembryonic structuresAnimal Science and ZoologyVitrificationSmall AnimalsEthylene glycolTheriogenology
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Type 1 Diabetes and Autoimmune Thyroid Disease—The Genetic Link

2021

Type 1 diabetes (T1D) and autoimmune thyroid disease (AITD) are the most frequent chronic autoimmune diseases worldwide. Several autoimmune endocrine and non-endocrine disorders tend to occur together. T1D and AITD often cluster in individuals and families, seen in the formation of autoimmune polyendocrinopathy (AP). The close relationship between these two diseases is largely explained by sharing a common genetic background. The HLA antigens DQ2 (DQA1*0501-DQB1*0201) and DQ8 (DQA1*0301-DQB1*0302), tightly linked with DR3 and DR4, are the major common genetic predisposition. Moreover, functional single nucleotide polymorphisms (or rare variants) of various genes, such as the cytotoxic T-lym…

autoimmune polyendocrinopathyendocrine system diseasestype 1 diabetesEndocrinology Diabetes and MetabolismSingle-nucleotide polymorphismGenome-wide association studyCLEC16AHuman leukocyte antigenReviewBiologyPolymorphism Single Nucleotidelcsh:Diseases of the endocrine glands. Clinical endocrinologyPTPN22single nucleotide polymorphismsEndocrinologyimmune system diseasesGenetic predispositionHumansGenetic Predisposition to Diseasesusceptibility genesHLA antigensgenetic linkGeneticslcsh:RC648-665Thyroiditis AutoimmuneFOXP3nutritional and metabolic diseasesAutoimmune polyendocrinopathyDiabetes Mellitus Type 1autoimmune thyroid diseaseFrontiers in Endocrinology
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[3+2]‐Cycloadditions of N ‐Cyano Sulfoximines with 1,3‐Dipoles

2020

Involving the cyano group of N‐cyano sulfoximines in [3+2]‐cycloaddition reactions with 1,3‐dipoles provides practical routes for the construction of 5‐membered heterocycles bearing sulfoximinoyl moieties. An ytterbium‐catalyzed cycloaddition utilizing hydrazonoyl chlorides was developed, as well as a reaction involving imidoyl chlorides proceeding without the aid of a catalyst. Following these protocols, a range of sulfoximines with N‐1,2,4‐triazolyl and N‐1,2,4‐oxadiazolyl substituents was prepared. peerReviewed

betaiinisulfoximinebioaktiiviset yhdisteetOrganic ChemistryTriazoleOxadiazoleCycloadditiontriazolechemistry.chemical_compoundDipolechemistryPolymer chemistrybetaine13-dipolePhysical and Theoretical Chemistry13-dipolecycloadditionoxadiazoleorgaaniset yhdisteetEuropean Journal of Organic Chemistry
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Tumoricidal Activity of Endothelial Cells

2001

The mechanism of NO- and H(2)O(2)-induced tumor cytotoxicity was examined during B16 melanoma (B16M) adhesion to the hepatic sinusoidal endothelium (HSE) in vitro. We used endothelial nitric-oxide synthetase gene disruption and N(G)-nitro-l-arginine methyl ester-induced inhibition of nitric-oxide synthetase activity to study the effect of HSE-derived NO on B16M cell viability. Extracellular H(2)O(2) was removed by exogenous catalase. H(2)O(2) was not cytotoxic in the absence of NO. However, NO-induced tumor cytotoxicity was increased by H(2)O(2) due to the formation of potent oxidants, likely ( small middle dot)OH and (-)OONO radicals, via a trace metal-dependent process. B16M cells culture…

biologyEndotheliumChemistryEbselenCell BiologyGlutathioneBiochemistryMolecular biologychemistry.chemical_compoundmedicine.anatomical_structureBiochemistryCatalasebiology.proteinmedicineCytotoxic T cellButhionine sulfoximineViability assayCytotoxicityMolecular BiologyJournal of Biological Chemistry
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CCDC 652238: Experimental Crystal Structure Determination

2007

Related Article: M.Ruiz, R.Ortiz, L.Perello, J.Latorre, J.Server-Carrio|1997|J.Inorg.Biochem.|65|87|doi:10.1016/S0162-0134(96)00092-X

bis(Cinoxacinato)-bis(dimethylsulfoxide)-nickel(ii) tetrahydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1876681: Experimental Crystal Structure Determination

2020

Related Article: Fernando Machado dos Santos, Meiry Edivirges Alvarenga, Ana Karoline Silva Mendanha Valdo, Renato Rabelo, Danielle Cangussu de Castro Gomes, Ângelo de Fátima, Thiago Vinicius Costa Lara, Cleiton Moreira da Silva, Thiago Teixeira Tasso, João Honorato Araujo Neto, Alzir Azevedo Batista, Alejandro Pedro Ayala, Javier Alcides Ellena, Vinicius Ferraz Guimarães, Cecília Maria Alves Oliveira, Lidya Cardozo da Silva, Boniek Gontijo Vaz, Felipe Terra Martins|2020|Chem.Commun.|56|15024|doi:10.1039/D0CC07043B

bis(mu-252627-tris((carboxymethyl)oxy)-28-((carboxylatomethyl)oxy)calix(4)arene)-dichloro-copper(ii)-di-sodium dimethyl sulfoxide solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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