Search results for "QD415"

showing 10 items of 87 documents

FABP4 plasma levels are increased in familial combined hyperlipidemia

2010

The lipid profile of familial combined hyperlipidemia (FCHL) shares some characteristics with atherogenic dyslipidemia seen in diabetes, metabolic syndrome, and obesity. Adipocyte fatty acid-binding protein 4 (FABP4) appears to be a determinant of atherogenic dyslipidemia. We examined relationships between FABP4 plasma concentrations, dyslipidemia, and metabolic variables in patients with FCHL. We studied 273 unrelated FCHL patients and 118 control subjects. FABP4 was higher in FCHL than controls, with mean levels of 21.8 (10.1) microg/l and 19.2 (9.2) microg/l, respectively (adjusted P= 0.012). In FCHL, FABP4 correlated to body mass index (BMI), waist circumference, insulin levels, and hom…

Maleobesitymedicine.medical_specialtyMagnetic Resonance Spectroscopymedicine.medical_treatmentHyperlipidemia Familial CombinedQD415-436Fatty Acid-Binding ProteinsBiochemistryCohort StudiesInsulin resistanceEndocrinologyinsulin resistanceInternal medicineDiabetes mellitusmedicineHumansmedicine.diagnostic_testbusiness.industryInsulindyslipidemiaHypertriglyceridemiaCell BiologyMiddle AgedLipid Metabolismmedicine.diseaseEndocrinologyFCHLFemaleMetabolic syndromePatient-Oriented and Epidemiological ResearchLipid profilebusinessBody mass indexDyslipidemiaJournal of Lipid Research
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Defect induced room temperature ferromagnetism in high quality Co-doped ZnO bulk samples

2021

The nature of the often reported room temperature ferromagnetism in transition metal doped oxides is still a matter of huge debate. Herein we report on room temperature ferromagnetism in high quality Co-doped ZnO (Zn1-xCoxO) bulk samples synthesized via standard solid-state reaction route. Reference paramagnetic Co-doped ZnO samples with low level of structural defects are subjected to heat treatments in a reductive atmosphere in order to introduce defects in the samples in a controlled way. A detailed structural analysis is carried out in order to characterize the induced defects and their concentration. The magnetometry revealed the coexistence of a paramagnetic and a ferromagnetic phase …

Materials scienceMagnetometerFOS: Physical sciences02 engineering and technologyQ1010402 general chemistryPolaron01 natural sciencesDefect engineeringlaw.inventionCondensed Matter::Materials ScienceParamagnetismTransition metallawPhase (matter)Materials ChemistryDoped oxidesQDCondensed Matter - Materials ScienceCondensed matter physicsSpintronicsMechanical EngineeringDopingMetals and AlloysMaterials Science (cond-mat.mtrl-sci)Spintronics021001 nanoscience & nanotechnology0104 chemical sciencesSPINTRÔNICAFerromagnetismMechanics of MaterialsFerromagnetismCondensed Matter::Strongly Correlated Electrons0210 nano-technologyhuman activitiesQD415
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PANI-Based Wearable Electrochemical Sensor for pH Sweat Monitoring

2021

Nowadays, we are assisting in the exceptional growth in research relating to the development of wearable devices for sweat analysis. Sweat is a biofluid that contains useful health information and allows a non-invasive, continuous and comfortable collection. For this reason, it is an excellent biofluid for the detection of different analytes. In this work, electrochemical sensors based on polyaniline thin films deposited on the flexible substrate polyethylene terephthalate coated with indium tin oxide were studied. Polyaniline thin films were abstained by the potentiostatic deposition technique, applying a potential of +2 V vs. SCE for 90 s. To improve the sensor performance, the electronic…

Materials scienceelectrochemical sensor02 engineering and technologySubstrate (electronics)QD415-436wearable sensor010402 general chemistry01 natural sciencespH meterBiochemistryreduced graphene oxidepolyanilineAnalytical ChemistryContact anglechemistry.chemical_compoundPolyanilineSettore ING-IND/17 - Impianti Industriali MeccanicipH sensorPhysical and Theoretical ChemistryThin filmSettore ING-IND/34 - Bioingegneria Industriale021001 nanoscience & nanotechnology0104 chemical sciencesElectrochemical gas sensorIndium tin oxidesweatSettore ING-IND/23 - Chimica Fisica ApplicataChemical engineeringchemistryElectrode0210 nano-technologyChemosensors
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Plasmonic Biosensors for the Detection of Lung Cancer Biomarkers: A Review

2021

Lung cancer is the most common and deadliest cancer type globally. Its early diagnosis can guarantee a five-year survival rate. Unfortunately, application of the available diagnosis methods such as computed tomography, chest radiograph, magnetic resonance imaging (MRI), ultrasound, low-dose CT scan, bone scans, positron emission tomography (PET), and biopsy is hindered due to one or more problems, such as phenotypic properties of tumours that prevent early detection, invasiveness, expensiveness, and time consumption. Detection of lung cancer biomarkers using a biosensor is reported to solve the problems. Among biosensors, optical biosensors attract greater attention due to being ultra-sensi…

Materials sciencemedicine.diagnostic_testChip fabricationtechnology industry and agriculturebiomarkersNanotechnologyQD415-436plasmonic biosensorsmedicine.diseaselocalised surface plasmon resonanceBiochemistryAnalytical Chemistrylung cancerMolecular levelPositron emission tomographysurface enhanced Raman scatteringWide dynamic rangemedicinePhysical and Theoretical ChemistrySurface plasmon resonanceLung cancerBiosensorsurface plasmon resonancePlasmonChemosensors
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Co-administration of human MSC overexpressing HIF-1α increases human CD34+ cell engraftment in vivo

2021

Abstract Background Poor graft function or graft failure after allogeneic stem cell transplantation is an unmet medical need, in which mesenchymal stromal cells (MSC) constitute an attractive potential therapeutic approach. Hypoxia-inducible factor-1α (HIF-1α) overexpression in MSC (HIF-MSC) potentiates the angiogenic and immunomodulatory properties of these cells, so we hypothesized that co-transplantation of MSC-HIF with CD34+ human cord blood cells would also enhance hematopoietic stem cell engraftment and function both in vitro and in vivo. Methods Human MSC were obtained from dental pulp. Lentiviral overexpression of HIF-1α was performed transducing cells with pWPI-green fluorescent pr…

Medicine (General)Mesenchymal stromal cellsMedicine (miscellaneous)HIF-1αAntigens CD34Trasplantació d'òrgans teixits etc.Mice SCIDQD415-436Biochemistry Genetics and Molecular Biology (miscellaneous)BiochemistryMiceR5-920Mice Inbred NODPoor graft functionAnimalsHumansResearchHematopoietic Stem Cell TransplantationStem cell transplantationEngraftmentMesenchymal Stem CellsCell BiologyFetal BloodHypoxia-Inducible Factor 1 alpha SubunitMolecular MedicineGraft failureCèl·lules mareHematopoietic stem cellsStem Cell Research & Therapy
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From High-Throughput Microarray-Based Screening to Clinical Application: The Development of a Second Generation Multigene Test for Breast Cancer Prog…

2013

Several multigene tests have been developed for breast cancer patients to predict the individual risk of recurrence. Most of the first generation tests rely on proliferation-associated genes and are commonly carried out in central reference laboratories. Here, we describe the development of a second generation multigene assay, the EndoPredict test, a prognostic multigene expression test for estrogen receptor (ER) positive, human epidermal growth factor receptor (HER2) negative (ER+/HER2−) breast cancer patients. The EndoPredict gene signature was initially established in a large high-throughput microarray-based screening study. The key steps for biomarker identification are discussed in det…

Microarrayendocrine therapyBiomedical EngineeringBioengineeringReviewComputational biologyBiologyGene signaturemedicine.diseaseBioinformaticsIndividual riskBiochemistryFirst generationlcsh:BiochemistryMultigene expressionbreast cancerBreast cancerReal-time polymerase chain reactionmedicineProficiency testinglcsh:QD415-436multigene testEndoPredictBiotechnologyMicroarrays
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Molecular cloning, gene structure and expression profile of two mouse peroxisomal 3-ketoacyl-CoA thiolase genes

2004

Abstract Background In rats, two peroxisomal 3-ketoacyl-CoA thiolase genes (A and B) have been cloned, whereas only one thiolase gene is found in humans. The aim of this study was thus to clone the different mouse thiolase genes in order to study both their tissue expression and their associated enzymatic activity. Results In this study, we cloned and characterized two mouse peroxisomal 3-ketoacyl-CoA thiolase genes (termed thiolase A and B). Both thiolase A and B genes contain 12 exons and 11 introns. Using RNA extracted from mouse liver, we cloned the two corresponding cDNAs. Thiolase A and B cDNAs possess an open reading frame of 1272 nucleotides encoding a protein of 424 amino acids. In…

Molecular Sequence Datalcsh:Animal biochemistryGene Expressionexpérimentation animalesourislcsh:BiochemistryMiceFenofibratePeroxisomesAnimals[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyTissue Distributionlcsh:QD415-436Amino Acid SequenceRNA MessengerCloning Molecularlcsh:QP501-801adn complémentaireBase Sequencegèneactivité enzymatiquemammifèreBIOLOGIE MOLECULAIREAcetyl-CoA C-AcyltransferasefoieGene Componentsprotéinegénie génétiqueclonageResearch Articleexpression des gènesBMC Biochemistry
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Argan oil prevents down-regulation induced by endotoxin on liver fatty acid oxidation and gluconeogenesis and on peroxisome proliferator-activated re…

2015

In patients with sepsis, liver metabolism and its capacity to provide other organs with energetic substrates are impaired. This and many other pathophysiological changes seen in human patients are reproduced in mice injected with purified endotoxin (lipopolysaccharide, LPS). In the present study, down-regulation of genes involved in hepatic fatty acid oxidation (FAOx) and gluconeogenesis in mice exposed to LPS was challenged by nutritional intervention with Argan oil. Mice given a standard chow supplemented or not with either 6% (w/w) Argan oil (AO) or 6% (w/w) olive oil (OO) prior to exposure to LPS were explored for liver gene expressions assessed by mRNA transcript levels and/or enzyme a…

Peroxisome proliferator-activated receptor gammamedicine.medical_specialtyOO olive oilResearch paper[SDV]Life Sciences [q-bio]Peroxisome proliferator-activated receptorBiologyBiochemistryNuclear receptor 30lcsh:BiochemistryEstrogen-related receptorEstrogen-related receptor alphaInternal medicineACADS acyl CoA dehydrogenase short-chainACADL acyl CoA dehydrogenase long-chainmedicinePGC-1α peroxisome proliferator-activated receptor γ coactivator-1αlcsh:QD415-436ReceptorBeta oxidationHNF-4α hepatic nuclear factor-4αchemistry.chemical_classificationACADM acyl CoA dehydrogenase medium-chainPPARα peroxisome proliferator-activated receptor αERRα estrogen related receptor α[ SDV ] Life Sciences [q-bio]PEPCK phospoenolpyruvate carboxykinaseGluconeogenesisBeta-oxidationGlut4 glucose transporter 4[SDV] Life Sciences [q-bio]G6PH glucose-6-phosphataseEndocrinologyGlut2 glucose transporter 2chemistryNuclear receptorArgan oilAO Argan oilNuclear receptorACOX1 acyl-CoA oxidase 1CoactivatorLPS lipopolysaccharidePeroxisome proliferator-activated receptor alpha
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Dephosphorylation of Centrins by Protein Phosphatase 2C α and β.

2009

In the present study, we identified protein phosphatases dephosphorylating centrins previously phosphorylated by protein kinase CK2. The following phosphatases known to be present in the retina were tested: PP1, PP2A, PP2B, PP2C, PP5, and alkaline phosphatase. PP2C 𝛼 and 𝛽 were capable of dephosphorylating P-Thr138-centrin1 most efficiently. PP2C𝛿 was inactive and the other retinal phosphatases also had much less or no effect. Similar results were observed for centrins 2 and 4. Centrin3 was not a substrate for CK2. The results suggest PP2C 𝛼 and 𝛽 to play a significant role in regulating the phosphorylation status of centrins in vivo.

PhosphatasePyruvate dehydrogenase phosphataseBioinformaticsDephosphorylationlcsh:Chemistrylcsh:QD241-441lcsh:Biochemistrychemistry.chemical_compoundlcsh:Organic chemistryIn vivoResearch LetterMedicinelcsh:QD415-436lcsh:Sciencelcsh:QH301-705.5Earth-Surface Processesbusiness.industryRetinalProtein phosphatase 2Biochemistrychemistrylcsh:Biology (General)lcsh:QD1-999embryonic structuresAlkaline phosphatasePhosphorylationlcsh:QbusinessResearch letters in biochemistry
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n-3 PUFAs modulate T-cell activation via protein kinase C-α and -ε and the NF-κB signaling pathway

2005

We elucidated the mechanisms of action of two n-3 PUFAs, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), in Jurkat T-cells. Both DHA and EPA were principally incorporated into phospholipids in the following order: phosphatidylcholine < phosphatidylethanolamine < phosphatidylinositol/phosphatidylserine. Furthermore, two isoforms of phospholipase A(2) (i.e., calcium-dependent and calcium-independent) were implicated in the release of DHA and EPA, respectively, during activation of these cells. The two fatty acids inhibited the phorbol 12-myristate 13-acetate (PMA)-induced plasma membrane translocation of protein kinase C (PKC)-alpha and -epsilon. The two n-3 PUFAs also inhibited t…

PhosphatidylethanolaminePhospholipase Amitogen-activated protein kinaseProtein Kinase C-epsilonQD415-436Cell BiologyPhosphatidylserineBiologyfatty acidsBiochemistryJurkat cellsCell biologychemistry.chemical_compoundEndocrinologychemistryBiochemistryDocosahexaenoic acidlipids (amino acids peptides and proteins)Phosphatidylinositolnuclear factor κBProtein kinase Cpolyunsaturated fatty acidsJournal of Lipid Research
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