Search results for "BN"

showing 10 items of 1136 documents

NT-pro-BNP nozīme agrīnā HSM diagnostikā 2. tipa cukura diabēta pacientiem

2020

Ievads. Pacientiem ar otrā tipa cukura diabētu ir ievērojami lielāks risks attīstīties kardiovaskulārai slimībai. Lielai daļai pacientu ar otrā tipa diabētu var attīstīties kardiovaksulāra saslimšana bez tipiskas klīniskās ainas, kā rezultātā kardiovaskulāru slimību diagnosticē novēloti, kad tā jau ir progresējusi. Līdz ar to būtu svarīgi šiem pacientiem veikt skrīningu, lai priekšlaicīgi diagnosticētu vai novērstu kardiovaskulāru slimību attīstību – noteikt NT-pro-BNP. Pētījuma mērķis. Pētīt NT-pro-BNP izmaiņas otrā tipa cukura diabēta pacientiem, kuriem slimības vēsturē nav kardiovaskulāru saslimšanu, un vai NT-pro-BNP līmenim asinīs ir saistība pacienta dzimumu, vecumu un slimošanas ar o…

Cukura diabētsSirds mazspējaKardiovaskulārsMedicīnaNT-pro-BNP
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Nuclear Translocation of Mismatch Repair Proteins MSH2 and MSH6 as a Response of Cells to Alkylating Agents

2000

Mammalian mismatch repair has been implicated in mismatch correction, the prevention of mutagenesis and cancer, and the induction of genotoxicity and apoptosis. Here, we show that treatment of cells specifically with agents inducing O(6)-methylguanine in DNA, such as N-methyl-N'-nitro-N-nitrosoguanidine and N-methyl-N-nitrosourea, elevates the level of MSH2 and MSH6 and increases GT mismatch binding activity in the nucleus. This inducible response occurs immediately after alkylation, is long-lasting and dose-dependent, and results from translocation of the preformed MutSalpha complex (composed of MSH2 and MSH6) from the cytoplasm into the nucleus. It is not caused by an increase in MSH2 gen…

CytoplasmDNA RepairBase Pair MismatchRNA StabilityChromosomal translocationmedicine.disease_causeBiochemistrychemistry.chemical_compoundMismatch Repair Endonuclease PMS2Adenosine TriphosphatasesNuclear ProteinsMethylnitrosoureaNeoplasm ProteinsDNA-Binding ProteinsMutS Homolog 2 ProteinDNA mismatch repairMutL Protein Homolog 1Protein BindingAlkylating AgentsMethylnitronitrosoguanidinecongenital hereditary and neonatal diseases and abnormalitiesGuanineActive Transport Cell NucleusBiologyCell LineO(6)-Methylguanine-DNA MethyltransferaseProto-Oncogene ProteinsDNA Repair ProteinmedicineHumansRNA MessengerneoplasmsMolecular BiologyAdaptor Proteins Signal TransducingCell NucleusMutagenesisnutritional and metabolic diseasesDNACell BiologyDNA MethylationMolecular biologydigestive system diseasesMSH6DNA Repair EnzymesGene Expression RegulationchemistryMSH2Carrier ProteinsGenotoxicityDNADNA DamageHeLa CellsJournal of Biological Chemistry
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Użycie słowa „czas” w Księdze Syracydesa

2020

Artykuł ma na celu przedstawienie użycia słowa „czas” w Księdze Syracydesa. W tym celu autor syntetycznie ukazał najpierw pole semantyczne terminu „czas” w języku hebrajskim i greckim. Następnie, na podstawie wskazanych rozróżnień, zostały przedstawione fragmenty, w których pojawia się omawiany termin, z uwzględnieniem kontekstu całej księgi, jak i pozostałych ksiąg biblijnych. Dla mędrca z Jerozolimy czas nie jest jedynie pojęciem wyznaczającym chronologię, ale rzeczywistością, którą codziennie człowiek odkrywa jako sposobność do czynienia dobra i przestrzeń działania Boga jako Stwórcy i Pana całego stworzonego świata. Różnorodność sytuacji życiowych, które przedstawia Ben Syrach w swej ks…

Czaswłaściwa porathe right timeKsięga Syracydesaokazjathe Book of Ben Sirachthe right momentchwila sposobnaThe timeopportunityVerbum Vitae
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Motores de búsqueda y derechos de autor: infracción y responsabilidad

2015

Los motores de búsqueda se configuran como herramientas indispensables para localizar fácilmente cualquier tipo de información entre las más de tres billones de páginas web existentes en la red. Estos buscadores se presentan, de facto, como instrumentos básicos para que todo usuario pueda tener acceso a la información, cultura y educación, de manera que están convirtiéndose en unas herramientas indispensables para el libre desarrollo de las personas. Sin embargo, a pesar de estas ventajas, en ocasiones, los buscadores vuelcan contenidos protegidos en la página de resultados sin autorización de su titular, de forma que de no mediar algún límite o excepción tasado en la ley, pueden estar vuln…

DMCAcopyrightthumbnails:CIENCIAS JURÍDICAS Y DERECHO [UNESCO]googleresponsabilidadbuscadorsafe harbourUNESCO::CIENCIAS JURÍDICAS Y DERECHOsnippetsinfraccióncachetakedownderecho de autorpuerto segurofair use doctrine
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Metabolic and Functional Genomic Studies Identify Deoxythymidylate Kinase as a target in LKB1 Mutant Lung Cancer

2013

Abstract The LKB1/STK11 tumor suppressor encodes a serine/threonine kinase, which coordinates cell growth, polarity, motility, and metabolism. In non–small cell lung carcinoma, LKB1 is somatically inactivated in 25% to 30% of cases, often concurrently with activating KRAS mutations. Here, we used an integrative approach to define novel therapeutic targets in KRAS-driven LKB1-mutant lung cancers. High-throughput RNA interference screens in lung cancer cell lines from genetically engineered mouse models driven by activated KRAS with or without coincident Lkb1 deletion led to the identification of Dtymk, encoding deoxythymidylate kinase (DTYMK), which catalyzes dTTP biosynthesis, as synthetica…

DNA Replicationcongenital hereditary and neonatal diseases and abnormalitiesLung NeoplasmsMutantSTK11BiologyAMP-Activated Protein KinasesProtein Serine-Threonine Kinasesmedicine.disease_causeArticleProto-Oncogene Proteins p21(ras)MiceDeoxythymidylate kinaseAMP-Activated Protein Kinase KinasesRNA interferenceCell Line TumorCarcinoma Non-Small-Cell LungmedicineMetabolomicsThymine NucleotidesAnimalsHumansMolecular Targeted TherapyLung cancerskin and connective tissue diseasesCell DeathModels GeneticKinaseCell growthGenomicsmedicine.diseaseMolecular biologyHigh-Throughput Screening AssaysOncologyGene Knockdown TechniquesCancer researchRNA InterferenceKRASNucleoside-Phosphate KinaseDNA Damage
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Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus

2012

Coats plus is a highly pleiotropic disorder particularly affecting the eye, brain, bone and gastrointestinal tract. Here, we show that Coats plus results from mutations in CTC1, encoding conserved telomere maintenance component 1, a member of the mammalian homolog of the yeast heterotrimeric CST telomeric capping complex. Consistent with the observation of shortened telomeres in an Arabidopsis CTC1 mutant and the phenotypic overlap of Coats plus with the telomeric maintenance disorders comprising dyskeratosis congenita, we observed shortened telomeres in three individuals with Coats plus and an increase in spontaneous γ 3H2AX-positive cells in cell lines derived from two affected individual…

DNA polymeraseMolecular Sequence DataTelomere-Binding ProteinsHistones/metabolismHDE GENHDE NEU PEDCST complexCEREBRORETINAL MICROANGIOPATHY FAMILIAL SYNDROME CALCIFICATIONS CYSTS PROTEIN DNA LEUKOENCEPHALOPATHY EVOLUTION DEFECTSHistoneschemistry.chemical_compoundAbnormalities Multiple/geneticsGeneticsmedicineAbnormalities MultipleGenetic Predisposition to DiseaseGeneticsTelomere-binding proteinTelomere/pathologyddc:618biologyBase SequenceGenetic Predisposition to Disease/geneticsDNA replicationSequence Analysis DNATelomeremedicine.diseaseFlow CytometryTelomereCell biologyRetinal Telangiectasis/genetics/pathologychemistrySequence Analysis DNA/methodsbiology.proteinRetinal TelangiectasisPrimaseTelomere-Binding Proteins/geneticsDNADyskeratosis congenitaNature Genetics
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Search for Technicolor Particles Produced in Association with a W Boson at CDF

2010

7 páginas, 3 figuras, 1 tabla.-- PACS numbers: 14.80.Tt, 12.60.Nz, 13.85.Rm.-- CDF Collaboration: et al.

DYNAMICSParticle physicsHadronTevatronGeneral Physics and AstronomyFOS: Physical sciencesElementary particleddc:500.27. Clean energy01 natural sciences114 Physical sciencesStandard ModelHigh Energy Physics - ExperimentNuclear physicsSYMMETRY-BREAKINGHigh Energy Physics - Experiment (hep-ex)13.85.Rm 14.80.Bn0103 physical sciences[PHYS.HEXP]Physics [physics]/High Energy Physics - Experiment [hep-ex]Invariant mass010306 general physicsPhysicsMuon010308 nuclear & particles physicsPhysicsHigh Energy Physics::PhenomenologySYMMETRY-BREAKING; DYNAMICSHigh Energy Physics::ExperimentEnergy (signal processing)Lepton
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Limit on the production of a light vector gauge boson in $\phi $ mesondecays with the KLOE detector

2012

We present a new limit on the production of a light dark-force mediator with the KLOE detector at DAPHNE. This boson, called U, has been searched for in the decay phi --> eta U, U --> e+ e-, analyzing the decay eta --> pi0 pi0 pi0 in a data sample of 1.7 fb-1. No structures are observed in the e+e- invariant mass distribution over the background. This search is combined with a previous result obtained from the decay eta --> pi+ pi- pi0, increasing the sensitivity. We set an upper limit at 90% C.L. on the ratio between the U boson coupling constant and the fine structure constant of alpha'/alpha < 1.7x10^-5 for 30<M_U<400 MeV and alpha'/alpha < 8x10^-6 for the sub-region 50<M_U<210 MeV. This…

Dark forcesNuclear and High Energy PhysicsParticle physicsElectron–positron annihilationFOS: Physical sciences01 natural sciencesSettore FIS/04 - Fisica Nucleare e Subnuclearee(+)e(-) Collisions Dark forces Gauge vector bosonHigh Energy Physics - ExperimentNuclear physicsHigh Energy Physics - Experiment (hep-ex)e(+)e(-) Collisions0103 physical sciencesgauge vector bosonInvariant massNuclear Experiment010306 general physicsBosonPhysicsCoupling constantGauge boson$e^{+}e^{-}$ collisions010308 nuclear & particles physicsSettore FIS/01 - Fisica SperimentaleForm factor (quantum field theory)Vector meson dominancePhi mesondark forcesHigh Energy Physics::ExperimentGauge vector boson
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Parameter Rating by Diffusion Gradient

2014

Anomaly detection is a central task in high-dimensional data analysis. It can be performed by using dimensionality reduction methods to obtain a low-dimensional representation of the data, which reveals the geometry and the patterns that exist and govern it. Usually, anomaly detection methods classify high-dimensional vectors that represent data points as either normal or abnormal. Revealing the parameters (i.e., features) that cause detected abnormal behaviors is critical in many applications. However, this problem is not addressed by recent anomaly-detection methods and, specifically, by nonparametric methods, which are based on feature-free analysis of the data. In this chapter, we provi…

Data pointbusiness.industryComputer scienceDimensionality reductionNonparametric statisticsDiffusion mapAnomaly detectionFeature selectionPattern recognitionArtificial intelligenceAbnormalityRepresentation (mathematics)business
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Fragile X-syndrome: literature review and report of two cases

2009

Fragile X-syndrome is caused by a mutation in chromosome X. It is one of the most frequent causes of learning disability. The most frequent manifestations of fragile X-syndrome are learning disability, different orofacial morphological alterations and an increase in testicle size. The disease is associated with cardiac malformations, joint hyperextension and behavioural alterations. We present two male patients aged 17 and 10 years, treated in our Service due to severe gingivitis. Both showed the typical facial and dental characteristics of the syndrome. In addition, we detected the presence of root anomalies such as taurodontism and root bifurcation, which had not been associated with frag…

Deficiència mentalAnomalies cromosòmiquesMental deficiencyDental abnormalitiesChromosome abnormalitiesMalalties hereditàriesMalformacions dentalsUNESCO:CIENCIAS MÉDICASGenetic diseases
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