Search results for "44"

showing 10 items of 1507 documents

Durability of Biodegradable Polymer Nanocomposites

2021

Biodegradable polymers (BP) are often regarded as the materials of the future, which address the rising environmental concerns. The advancement of biorefineries and sustainable technologies has yielded various BP with excellent properties comparable to commodity plastics. Water resistance, high dimensional stability, processability and excellent physicochemical properties limit the reviewed materials to biodegradable polyesters and modified compositions of starch and cellulose, both known for their abundance and relatively low price. The addition of different nanofillers and preparation of polymer nanocomposites can effectively improve BP with controlled functional properties and change the…

Absorption of waterNanocompositeMaterials sciencePolymers and PlasticsPolymer nanocompositeOrganic chemistryGeneral ChemistryReviewBiodegradationBiodegradable polymerDurabilitybiodegradationcreepPolyestermodellingCommodity plasticsQD241-441biodegradable polymersenvironmental ageingnanocompositesdurabilityComposite materialPolymers
researchProduct

Estudio bibliométrico de producción y consumo de la revista Farmacia Hospitalaria (2004-2012)

2014

Objetivo: Analizar la actividad científica y la producción de información de la revista Farmacia Hospitalaria como publicación científica española de referencia en el área de la farmacia. Método: Estudio descriptivo transversal de los resultados obtenidos del análisis bibliométrico de los artículos publicados en la revista, obteniéndose los datos de la consulta directa y acceso, vía Internet, a la literatura científica recogida en la versión electrónica de la revista en el periodo 2004 a 2012. Resultados: Durante el periodo estudiado se publicaron 756 artículos. El número de originales fue de 258 (34,13%), siendo el índice de productividad de 2,40. Se identificaron 246 instituciones con tra…

Acceso a la informaciónBibliometric Indicatorslcsh:Rlcsh:Medicinelcsh:RS1-441; Medical Subject Headings; Journal ArticleIndicadores bibliométricosArtículo de revistaAccess to Informationlcsh:Pharmacy and materia medicaMedical Subject HeadingsBibliometricsBibliometríaJournal ArticleFarmacia Hospitalaria
researchProduct

Potential involvement of IL-22 and IL-22-producing cells in the inflamed salivary glands of patients with Sjogren's syndrome.

2012

OBJECTIVES: In chronic inflammatory disorders, interleukin (IL)-22 may act either as a protective or as a pro-inflammatory cytokine. At mucosal sites, IL-22 is mainly produced by CD4(+) T cells and by a subset of mucosal natural killer (NK) cells expressing the receptor NKp44 (NKp44(+) NK cells). The aim of this study was to investigate the IL-22 expression in the salivary glands of patients with primary Sjögren's syndrome (pSS). METHODS: Minor salivary gland biopsies were obtained from 19 patients with pSS and 16 with non-specific chronic sialoadenitis. Quantitative gene expression analysis by TaqMan real-time PCR and immunohistochemistry for IL-17, IL-22, IL-23 and STAT3 (signal transduce…

AdultCD4-Positive T-LymphocytesMaleSTAT3 Transcription FactorAnkylosing Spondylitis IL-22 NKp44NK cells intestinal inflammationmedicine.medical_treatmentImmunologySalivary Glands MinorInterleukin-23General Biochemistry Genetics and Molecular BiologySialadenitisInterleukin 22PathogenesisRheumatologyintestinal inflammationIL-22Immunology and AllergyMedicineHumansRNA MessengerSTAT3ReceptorAgedAnkylosing SpondylitibiologySalivary glandNatural Cytotoxicity Triggering Receptor 2business.industryReverse Transcriptase Polymerase Chain ReactionInterleukinsInterleukin-17InterleukinMiddle AgedNKp44NK cellKiller Cells NaturalSettore MED/16 - ReumatologiaCytokinemedicine.anatomical_structureSjogren's SyndromeCase-Control StudiesImmunologybiology.proteinImmunohistochemistryFemalebusinessAnnals of the rheumatic diseases
researchProduct

Diagnostic genetic screening for assisted reproductive technologies patients with macrozoospermia

2017

International audience; Macrozoospermia is characterized by a high proportion of abnormal spermatozoa with enlarged heads. So far, it has been associated with mutations only in the Aurora Kinase C gene (AURKC) in some cases. Although many publications have reported failure to conceive in couples with macrozoospermia, a few others have described successful pregnancies, thus raising questions as to whether ICSI and AURKC genetic screening should be recommended in all patients with macrozoospermia. First, we report on two monozygotic twins presenting macrozoospermia for whom the genetic status was explored (Aurora Kinase C sequencing) and whole semen and gradient-selected spermatozoa were anal…

AdultMale0301 basic medicineReproductive Techniques Assistedpregnancy outcomesUrologyEndocrinology Diabetes and MetabolismTwinsmenSemenReproductive technologyBiologymedicine.disease_causeAndrologyTeratozoospermia03 medical and health sciences0302 clinical medicineEndocrinologyPolyploidc c.144delc mutationmedicineHumansAurora Kinase CGenetic TestingAurora Kinase C Gene[SDV.GEN]Life Sciences [q-bio]/Geneticsaurora kinase C geneMutationassisted reproductive technologies030219 obstetrics & reproductive medicineurogenital systemtailed spermatozoaGenetic StatusheadSperm3. Good healthmacrozoospermiahuman sperm030104 developmental biologyReproductive Medicinemale-infertilitySperm HeadAurora Kinase Caneuploidy rateflow-cytometry[ SDV.GEN ] Life Sciences [q-bio]/Geneticspolyploid spermatozoaAndrology
researchProduct

Expression of CD44 variant proteins in adenocarcinoma of Barrett's esophagus and its relation to prognosis

1998

BACKGROUND None of the commonly used staging criteria accurately determine the prognosis of a patient with adenocarcinoma of Barrett's esophagus. The authors therefore assessed the expression pattern and prognostic impact of CD44 standard and CD44 isoforms CD44v4, v5,v6,v7, and v10 in adenocarcinoma of Barrett's esophagus. METHODS Specimens from 41 patients with adenocarcinoma of Barrett's esophagus who underwent esophageal resection were embedded in paraffin and studied immunohistochemically to determine the expression of CD44 splice variants. Histomorphologic parameters and survival time were not known at the time of the investigation. RESULTS Correlations between favorable clinical or hi…

AdultMaleCancer Researchmedicine.medical_specialtyEsophageal NeoplasmsAdenocarcinomaGastroenterologyBarrett EsophagusAntigens NeoplasmInternal medicineBiopsymedicineHumansEsophagusAgedGlycoproteinsAnalysis of Variancebiologymedicine.diagnostic_testbusiness.industryEsophageal diseaseCD44CancerMiddle Agedmedicine.diseasedigestive system diseasesHyaluronan Receptorsmedicine.anatomical_structureOncologyBarrett's esophagusbiology.proteinAdenocarcinomaFemaleComplicationbusinessCancer
researchProduct

Analysis of seroprevalence against Coxiella burnetii in a sample of farm workers in Western Sicily

2016

Introduction and objective. Little is known about the development of chronic Q fever caused by Coxiella burnetii in occupational risk groups and in the general population in Italy, as well as in many countries in the world. The aim of this study was to highlight the presence of the infection in a sample of workers operating outdoors (but not directly in contact with animals), in three provinces of western Sicily, in order to detect the human seroprevalence and compare the obtained data with those found in animals raised in the same territory. Materials and methods. The study included 126 generic seasonal agricultural workers (labourers), 84 male and 42 female; none of whom were aware of any…

AdultMaleFarmersSheepSettore MED/44 - Medicina Del LavoroCattle DiseasesSheep DiseasesMiddle AgedYoung AdultCoxiella burnetiiSeroepidemiologic StudiesPrevalenceQ fever environmental exposure Coxiella burnetiiAnimalsHumansCattleFemaleFluorescent Antibody Technique IndirectQ FeverSicily
researchProduct

Neural dynamics of learning sound-action associations.

2008

A motor component is pre-requisite to any communicative act as one must inherently move to communicate. To learn to make a communicative act, the brain must be able to dynamically associate arbitrary percepts to the neural substrate underlying the pre-requisite motor activity. We aimed to investigate whether brain regions involved in complex gestures (ventral pre-motor cortex, Brodmann Area 44) were involved in mediating association between novel abstract auditory stimuli and novel gestural movements. In a functional resonance imaging (fMRI) study we asked participants to learn associations between previously unrelated novel sounds and meaningless gestures inside the scanner. We use functio…

AdultMaleNeural substratelcsh:MedicineBiologyBrain mapping050105 experimental psychologyAssociation03 medical and health sciences0302 clinical medicineMental ProcessesNeuroscience/Motor SystemsHumansLearningSpeech0501 psychology and cognitive sciencesAssociation (psychology)lcsh:ScienceNeuroscience/Cognitive NeuroscienceBrain MappingMultidisciplinaryBlood-oxygen-level dependentGesturesWorking memory05 social scienceslcsh:RPsychophysiological InteractionBrodmann area 44BrainMagnetic Resonance ImagingNeuroscience/Experimental PsychologySoundAcoustic StimulationFemalelcsh:Q030217 neurology & neurosurgeryPsychomotor PerformanceCognitive psychologyGestureResearch ArticlePLoS ONE
researchProduct

The long-term effect of job mobility on workers' mental health: a propensity score analysis

2022

Abstract Objectives The main purpose of this longitudinal study was to elucidate the impact of external job mobility, due to a change of employer, on mental health. Methods A cohort of Belgian employees from the IDEWE occupational medicine registry was followed-up for twenty-seven years, from 1993 to 2019. The use of drugs for neuropsychological diseases was considered as an objective indicator of mental health. The covariates were related to demographic, physical, behavioural characteristics, occupational and work-related risks. Propensity scores were calculated with a Cox regression model with time-varying covariates. The PS matching was used to eliminate the systematic differences in sub…

AdultMaleOccupational MedicineDepressive disorder Epidemiology Job mobility Longitudinal study Mental health Neuropsychological treatment Adult Female Humans Longitudinal Studies Male Mental Health Propensity Score Occupational Health Occupational MedicineScience & TechnologyDepressive disorderEpidemiologyILLSettore MED/44 - Medicina Del LavoroPublic Health Environmental and Occupational HealthSettore MED/01 - Statistica MedicaMental HealthHumansNeuropsychological treatmentFemaleMental healthLongitudinal StudiesLongitudinal studyPropensity ScoreLife Sciences & BiomedicineJob mobilityOccupational HealthPublic Environmental & Occupational Health
researchProduct

The aging heart, myocardial fibrosis, and its relationship to circulating C-type natriuretic Peptide.

2011

Myocardial aging is characterized by left ventricular (LV) fibrosis leading to diastolic and systolic dysfunction. Studies have established the potent antifibrotic and antiproliferative properties of C-type natriuretic peptide (CNP); however, the relationship between circulating CNP, LV fibrosis, and associated changes in LV function with natural aging are undefined. Accordingly, we characterized the relationship of plasma CNP with LV fibrosis and function in 2-, 11-, and 20-month–old male Fischer rats. Further in vitro, we established the antiproliferative actions of CNP and the participation of the clearance receptor using adult human cardiac fibroblasts. Here we establish for the first t…

AdultMaleSenescenceAgingmedicine.medical_specialtyTime Factorsmedicine.drug_classDiastoleBlood PressureArticleFibrosisInternal medicineMyocardial fibrosisNatriuretic Peptide BrainInternal MedicinemedicineNatriuretic peptideAnimalsHumansReceptorCells CulturedCell Proliferationbusiness.industryMyocardiumHeartNatriuretic Peptide C-TypeFibroblastsmedicine.diseaseFibrosisSettore MED/11 - Malattie Dell'Apparato CardiovascolareRats Inbred F344In vitroRatsMicroscopy ElectronEndocrinologyBlood pressureMyocardial fibrosisbusiness
researchProduct

Analysis of thiamine transporter genes in sporadic beriberi

2014

Abstract Objective Thiamine or vitamin B 1 deficiency diminishes thiamine-dependent enzymatic activity, alters mitochondrial function, impairs oxidative metabolism, and causes selective neuronal death. We analyzed for the first time, the role of all known mutations within three specific thiamine carrier genes, SLC19 A2, SLC19 A3 , and SLC25 A19 , in a patient with atrophic beriberi, a multiorgan nutritional disease caused by thiamine deficiency. Methods A 44-year-old male alcoholic patient from Morocco developed massive bilateral leg edema, a subacute sensorimotor neuropathy, and incontinence. Despite normal vitamin B 1 serum levels, his clinical picture was rapidly reverted by high-dose in…

AdultMalemedicine.medical_specialtySLC19 A- SLC25 A19SLC19 AEndocrinology Diabetes and MetabolismGene mutationBeriberimedicine.disease_causeMitochondrial Membrane Transport Proteinslaw.inventionBeriberilawInternal medicineGenotypemedicineThiamine transporterObjective: Thiamine or vitamin B1 deficiency diminishes thiamine-dependent enzymatic activity alters mitochondrial function impairs oxidative metabolism and causes selective neuronal death. We analyzed for the first time the role of all known mutations within three specific thiamine carrier genes SLC19 A2 SLC19 A3 and SLC25 A19 in a patient with atrophic beriberi a multiorgan nutritional disease caused by thiamine deficiency. Methods: A 44-year-old male alcoholic patient from Morocco developed massive bilateral leg edema a subacute sensorimotor neuropathy and incontinence. Despite normal vitamin B1 serum levels his clinical picture was rapidly reverted by high-dose intramuscular thiamine treatment suggesting a possible genetic resistance. We used polymerase chain reaction followed by amplicon sequencing to study all the known thiamine-related gene mutations identified within the Human Gene Mutation Database. Results: Thirty-seven mutations were tested: 29 in SLC19 A2 6 in SLC19 A3 and 2 in SLC25 A19. Mutational analyses showed a wild-type genotype for all sequences investigated. Conclusion: This is the first genetic study in beriberi disease. We did not detect any known mutation in any of the three genes in a sporadic dry beriberi patient. We cannot exclude a role for other known or unknown mutations in the same genes or in other thiamine-associated genes in the occurrence of this nutritional neuropathy.HumansThiamineGenePolymerase chain reactionGeneticsMutationNutrition and DieteticsbiologyMembrane Transport ProteinsThiamine Deficiencymedicine.diseaseAlcoholismEndocrinologyMutationbiology.proteinThiamineMutations
researchProduct