Search results for "570"

showing 10 items of 1074 documents

Case Report: Primary Peritonitis as the Onset of Pediatric Ménétriers Disease

2021

Introduction: Primary peritonitis (PP) and Ménétrier's Disease (MD) are both rare conditions among pediatric population. Although about 150 MD cases have been described in the scientific literature to date, its onset with a PP is an unusual condition.Case Presentation: We present a case of an 11-year-old boy who was admitted to our unit because of abdominal pain and distension. Complementary tests showed ascites, bilateral pleural effusion, leukocytosis, increased acute phase reactants and hypoproteinemia with hypoalbuminemia. Laparoscopy ruled out appendicitis or visceral perforations and exposed purulent peritoneal fluid, compatible with PP. Biochemical stool analysis showed increased cle…

Abdominal painmedicine.medical_specialtyPediatricsGastroenterology03 medical and health sciencesHypoproteinemia0302 clinical medicine030225 pediatricsInternal medicineMénétrier's diseaseAscitesmedicinecase reportEnteropathyHypoalbuminemiaprotein-losing enteropathybusiness.industryProtein losing enteropathylcsh:RJ1-570lcsh:Pediatricsmedicine.diseaseAppendicitisMénétrier's diseasehypertrophic gastropathyPediatrics Perinatology and Child Health030211 gastroenterology & hepatologymedicine.symptombusinessprimary peritonitisFrontiers in Pediatrics
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Lung on a Chip Development from Off-Stoichiometry Thiol–Ene Polymer

2021

Institute of Solid-State Physics, University of Latvia as the Center of Excellence has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART2. Finally, we would like to thank Biol. Kaspars Tars from Latvian Biomedical research and study center for giving us the opportunity to participate in this consortium and contribute to Latvian scientists’ effort in response to the COVID-19 pandemic.

Absorption (pharmacology)Materials scienceNanotechnology02 engineering and technologyOrgan-on-a-chipArticlelung on a chip03 medical and health scienceschemistry.chemical_compoundPDMS:NATURAL SCIENCES:Physics [Research Subject Categories]TJ1-1570Mechanical engineering and machineryElectrical and Electronic Engineering030304 developmental biologychemistry.chemical_classification0303 health sciencesPolydimethylsiloxaneMechanical Engineeringoff-stoichiometry thiol–enefungitechnology industry and agricultureorgan on a chipPolymer021001 nanoscience & nanotechnologyFluorescenceSmall moleculeMembranechemistryControl and Systems EngineeringThiol0210 nano-technologyMicromachines
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[Spanish funded paediatric research: Contribution of Anales de Pediatría to its dissemination].

2017

Objective: To identify Spanish funded paediatric research published in general paediatric journals included in the Web of Science (WoS) from 2010 to 2014 and those published in Anales de Pediatría. To examine the relationship between funding and the prestige of the journals. To describe the journal conditions to meet the open access criteria. Material and method: Spanish funded paediatric articles (FA) were identified by using the WoS Funding Agency field, and by reviewing the original documents for Anales de Pediatria (AP). For the FA published in AP the number and kind of funding agencies were identified. The possible differences in citations between FA and non-funded was assessed for art…

Acceso abiertoPediatricsmedicine.medical_specialtyFinanciaciónBiomedical ResearchInformation DisseminationLibrary sciencePediatricsRJ1-57003 medical and health sciences0302 clinical medicine030225 pediatricsManagement of Technology and InnovationOpen-access mandatemedicineFunding AgencyPublishingbusiness.industryInformation Dissemination05 social sciencesAnales de PediatríaImpacto científicoPublishingSpainInvestigación pediátrica0509 other social sciencesPeriodicals as Topic050904 information & library sciencesbusinessAnales de pediatria (Barcelona, Spain : 2003)
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The role of parasitism in adaptive radiations – when might parasites promote and when might they constrain ecological speciation?

2012

Research on speciation and adaptive radiation has flourished during the past decades, yet factors underlying initiation of reproductive isolation often remain unknown. Parasites represent important selective agents and have received renewed attention in speciation research. We review the literature on parasite-mediated divergent selection in context of ecological speciation and present empirical evidence for three nonexclusive mechanisms by which parasites might facilitate speciation: reduced viability or fecundity of immigrants and hybrids, assortative mating as a pleiotropic by-product of host adaptation, and ecologically-based sexual selection. We emphasise the lack of research on specia…

Adaptive radiationlcsh:QH1-199.5EcologyEcologyAssortative matingReproductive isolationlcsh:General. Including nature conservation geographical distributionBiologyIncipient speciationEcological speciationAdaptiivinen radiaatioDivergent evolutionEvolutionary biologylcsh:QH540-549.5Sexual selectionAdaptive radiationGenetic algorithm570 Life sciences; biologylcsh:EcologyEcology Evolution Behavior and Systematics
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The reverse transcription signature of N-1-methyladenosine in RNA-Seq is sequence dependent

2015

The combination of Reverse Transcription (RT) and high-throughput sequencing has emerged as a powerful combination to detect modified nucleotides in RNA via analysis of either abortive RT-products or of the incorporation of mismatched dNTPs into cDNA. Here we simultaneously analyze both parameters in detail with respect to the occurrence of N-1-methyladenosine (m1A) in the template RNA. This naturally occurring modification is associated with structural effects, but it is also known as a mediator of antibiotic resistance in ribosomal RNA. In structural probing experiments with dimethylsulfate, m1A is routinely detected by RT-arrest. A specifically developed RNA-Seq protocol was tailored to …

AdenosineSequence Analysis RNAHigh-Throughput Nucleotide SequencingReverse TranscriptionL1Sciences bio-médicales et agricoles13570 Life sciencesMachine LearningMiceSequence Homology Nucleic AcidRNAAnimalsHumans[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology570 Biowissenschaften
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Prevalencia del trastorno por atracón en una muestra clínica de obesos

2012

Resumen: Introducción: El trastorno por atracón se caracteriza por presencia de episodios de sobreingesta recurrentes en un periodo corto, acompañados de pérdida de control. Este trastorno es el más frecuente de entre todos los trastornos de la conducta alimentaria en población obesa, tanto en adultos como en niños. Objetivo: El objetivo de este estudio fue obtener datos prevalencia del trastorno por atracón en una muestra de niños y adolescentes obesos, usuarios de una unidad de pediatría especializada en el tratamiento de la obesidad infantil. Material y métodos: Se contó con una muestra 70 niños y adolescentes con edades comprendidas entre los 9 y los 16 años, con una edad media de 12 añ…

AdolescentPsychopathologybusiness.industryEating DisordersPediatricsRJ1-570Feeding behaviorPediatrics Perinatology and Child HealthEating disordersPrevalenceMedicineObesitybusinessChildrenHumanitiesAnales de Pediatría
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Induction of B-cell development in adult mice reveals the ability of bone marrow to produce B-1a cells

2009

AbstractTo study B-cell development from bone marrow (BM), we generated recombination-activating gene 1 (Rag1)–targeted mice lacking mature lymphocytes. B-cell development can be induced in such mice by B cell–specific restoration of a functional Rag1 transcription unit. Follicular and marginal zone B cells populated the spleen when Rag1 expression was permitted. Notably, the peritoneal cavity was dominated by bona fide B-1a cells, as judged by surface markers and functional properties. These BM-derived B-1a cells exhibited a polyclonal VDJ repertoire with substantial N nucleotide insertions. Nevertheless, physiologic frequencies of phosphatidylcholine-specific B cells were detected. Import…

Adoptive cell transfer1303 BiochemistryGenes RAG-1Immunology2720 HematologyB-Lymphocyte SubsetsSpleenBone Marrow CellsEnzyme-Linked Immunosorbent AssayMice Transgenic610 Medicine & healthBiology10263 Institute of Experimental ImmunologyBiochemistryPolymerase Chain ReactionRecombination-activating gene1307 Cell BiologyPeritoneal cavityMicemedicineAnimalsB cellB-Lymphocytes2403 ImmunologyStem CellsCell DifferentiationCell BiologyHematologyMarginal zoneFlow CytometryMolecular biologyAdoptive Transfermedicine.anatomical_structureImmunoglobulin MImmunologybiology.protein570 Life sciences; biologyBone marrow
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Chemical Properties of Element 105 in Aqueous Solution: Halide Complex Formation and Anion Exchange into Triisoctyl Amine

2017

Studies of the halide complexation of element 105 in aqueous solution were performed on 34-s 262Ha produced in the 249Bk(18-O,5n) reaction. The 262Ha was detected by measuring the fission and alpha activities associated with its decay and the alpha decays of its daughter, 4.3-s 258Lr. Time-correlated pairs of parent and daughter alpha particles provided a unique identification of the presence of 262Ha. About 1600 anion exchange separations of 262Ha from HCl and mixed HC1/HF solutions were performed on a one-minute time scale. Reversed-phase micro-chromatographic columns incorporating triisooctyl amine (TIOA) on an inert support were used in the computer-controlled liquid chromatography appa…

AdsorptionAqueous solutionIon exchangeStripping (chemistry)ChemistryOxohalide540 ChemistryInorganic chemistry570 Life sciences; biologyHalideAmine gas treatingAlpha particlePhysical and Theoretical Chemistryract
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Epigenetic dysregulation in the developing Down syndrome cortex

2016

Using Illumina 450K arrays, 1.85% of all analyzed CpG sites were significantly hypermethylated and 0.31% hypomethylated in fetal Down syndrome (DS) cortex throughout the genome. The methylation changes on chromosome 21 appeared to be balanced between hypo- and hyper-methylation, whereas, consistent with prior reports, all other chromosomes showed 3–11 times more hyper- than hypo-methylated sites. Reduced NRSF/REST expression due to upregulation of DYRK1A (on chromosome 21q22.13) and methylation of REST binding sites during early developmental stages may contribute to this genome-wide excess of hypermethylated sites. Upregulation of DNMT3L (on chromosome 21q22.4) could lead to de novo methyl…

Adult0301 basic medicineCancer ResearchDown syndromeDown syndromeNeuronal OutgrowthDNMT3BProtein Serine-Threonine KinasesBiologyDNA Methyltransferase 3AEpigenesis Genetic03 medical and health sciencesfetal brain developmentddc:570medicineHumansDNA (Cytosine-5-)-MethyltransferasesEpigeneticsddc:610Molecular BiologyCerebral CortexGeneticsDNA methylationfrontal cortexGene Expression Regulation DevelopmentalChromosomeMethylationProtein-Tyrosine KinasesCadherinsmedicine.diseaseMolecular biologyprotocadherin gamma cluster030104 developmental biologyCpG siteDNA methylationChromosome 21Research Paper
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Glutathione S-transferase T1 and M1 gene defects in ovarian carcinoma

1998

Glutathione S-transferases (GSTs) M1 and T1 are known to be polymorphic in humans. Both polymorphisms are due to gene deletions, which are responsible for the existence of null genotypes. The gene defect of GSTT1 has been reported to be associated with an increased risk of myelodysplastic syndromes, astrocytoma and meningioma. A lack of GSTM1 was associated with tobacco smoke-induced lung and bladder cancer. In this study we examined whether the GSTT1 and/or GSTM1 homozygous null genotypes were associated with an increased risk of ovarian cancer using a multiplex polymerase chain reaction protocol. The GSTT1 null genotype was observed in 14% of the control subjects that had never suffered f…

AdultGenetic MarkersCancer Researchmedicine.medical_specialty10050 Institute of Pharmacology and Toxicology610 Medicine & healthGastroenterologyInternal medicineOvarian carcinomaGenotypemedicineCarcinomaHumans1306 Cancer ResearchFamily historyneoplasmsAgedGlutathione TransferaseAged 80 and overOvarian NeoplasmsPolymorphism GeneticBladder cancerbiologyAge FactorsAstrocytomaMiddle Agedmedicine.diseaseNeoplasm ProteinsGlutathione S-transferaseEndocrinologyOncologybiology.protein570 Life sciences; biologyFemale2730 OncologyOvarian cancerCancer Letters
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