Search results for "Loin"

showing 10 items of 294 documents

Improved Frequentist Prediction Intervals for Autoregressive Models by Simulation

2015

It is well known that the so called plug-in prediction intervals for autoregressive processes, with Gaussian disturbances, are too narrow, i.e. the coverage probabilities fall below the nominal ones. However, simulation experiments show that the formulas borrowed from the ordinary linear regression theory yield one-step prediction intervals, which have coverage probabilities very close to what is claimed. From a Bayesian point of view the resulting intervals are posterior predictive intervals when uniform priors are assumed for both autoregressive coefficients and logarithm of the disturbance variance. This finding opens the path how to treat multi-step prediction intervals which are obtain…

GaussianPrediction intervalsymbols.namesakeautoregressive modelsAutoregressive modelFrequentist inferenceprediction intervalsStatisticsCredible intervalEconometricssymbolssimulointiSTAR modelMathematics
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A ceRNA approach may unveil unexpected contributors to deletion syndromes, the model of 5q- syndrome.

2015

In genomic deletions, gene haploinsufficiency might directly configure a specific disease phenotype. Nevertheless, in some cases no functional association can be identified between haploinsufficient genes and the deletion-associated phenotype. Transcripts can act as microRNA sponges. The reduction of transcripts from the hemizygous region may increase the availability of specific microRNAs, which in turn may exert in-trans regulation of target genes outside the deleted region, eventually contributing to the phenotype. Here we prospect a competing endogenous RNA (ceRNA) approach for the identification of candidate genes target of epigenetic regulation in deletion syndromes. As a model, we an…

GeneticsCancer ResearchCandidate gene5q- syndromeCompeting endogenous RNAgenomic deletionsSettore BIO/11 - Biologia MolecolareBiologySettore MED/08 - Anatomia PatologicaPhenotypemyelodysplastic syndromeTranscriptomecompeting endogenous RNAsOncologymicroRNAResearch PerspectiveCeRNAcompeting endogenous RNAEpigeneticsgenomic deletion5q- syndrome; CeRNA; competing endogenous RNAs; genomic deletions; myelodysplastic syndromeHaploinsufficiencyGeneOncoscience
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Putative Breast Cancer Driver Mutations in TBX3 Cause Impaired Transcriptional Repression

2015

The closely related T-box transcription factors TBX2 and TBX3 are frequently overexpressed in melanoma and various types of human cancers, in particular, breast cancer. The overexpression of TBX2 and TBX3 can have several cellular effects, among them suppression of senescence, promotion of epithelial–mesenchymal transition, and invasive cell motility. In contrast, loss of function of TBX3 and most other human T-box genes causes developmental haploinsufficiency syndromes. Stephens and colleagues (1), by exome sequencing of breast tumor samples, identified five different mutations in TBX3, all affecting the DNA-binding T-domain. One in-frame deletion of a single amino acid, p.N212delN, was ob…

GeneticsCancer Researchp21frameshift mutationin-frame deletionMelanomadriver mutationTBX3Biologylcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogensmedicine.diseaselcsh:RC254-282Frameshift mutationbreast cancerBreast cancerOncologymedicinesomatic mutationsHaploinsufficiencyGeneTranscription factorLoss functionExome sequencingOriginal ResearchFrontiers in Oncology
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4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterization

2014

Abstract Background Microscopically chromosome rearrangements of the short arm of chromosome 4 include the two known clinical entities: partial trisomy 4p and deletions of the Wolf-Hirschhorn critical regions 1 and 2 (WHSCR-1 and WHSCR-2, respectively), which cause cranio-facial anomalies, congenital malformations and developmental delay/intellectual disability. Methods/results We report on clinical findings detected in a Chinese patient with a de novo 4p16.1-p15.32 duplication in association with a subtle 4p terminal deletion of 6 Mb in size. This unusual chromosome imbalance resulted in WHS classical phenotype, while clinical manifestations of 4p trisomy were practically absent. Conclusio…

GenotypeArray-CGHDevelopmental DisabilitiesTrisomy 4pChromosome DisordersTrisomyAsian PeopleChinese childrenGene duplicationmedicineHumansWolf–Hirschhorn syndromeOligonucleotide Array Sequence AnalysisGeneticsWolf-Hirschhorn syndromeGenome Humanbusiness.industryChromosomeGeneral Medicinemedicine.diseasePhenotypePenetranceDuplication/deletion 4pPhenotypeChromosome 4Child PreschoolPediatrics Perinatology and Child HealthFemaleNeurology (clinical)Chromosome DeletionChromosomes Human Pair 4HaploinsufficiencybusinessTrisomyEuropean Journal of Paediatric Neurology
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Valvontakapitalismin ensimmäiset vuosikymmenet

2021

Arvio teoksesta: Zuboff, Shoshana. 2019. The Age of Surveillance Capitalism: The Fight for the Future at the New Frontier of Power. Lontoo: Profile Books, 704 s.

H1-99profilointikapitalismiCommunication. Mass mediateknologinen kehitysP87-96Journalism. The periodical press etc.PN4699-5650Social sciences (General)kirja-arvosteluthenkilötiedotyksityisyysasiakastiedotKirja-arviotsuuryrityksetdigitalisaatiovalvontaMedia & viestintä
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A heuristic model-based approach for compensating wind effects in ski jumping.

2021

Wind influences the jump length in ski jumping, which raises questions about the fairness. To counteract the wind problem, the International Ski Federation has introduced a wind compensation system in 2009: time-averaged wind velocity components tangential to the landing slope are obtained from several sites along the landing slope, and these data are used in a linear statistical model for estimating the jump length effect of wind. This is considered in the total score of the ski jump. However, it has been shown that the jump length effect estimates can be inaccurate and misleading. The present manuscript introduces an alternative mathematical wind compensation approach that is based on an …

Heuristic (computer science)Biomedical EngineeringBiophysicsKinematicsWindwind compensation systemWind speedInverse dynamicsSkiingcomputer simulationaerodynamiikkaHeuristicsOrthopedics and Sports MedicinesimulointiComputer Simulationmathematical modellingPhysics::Atmospheric and Oceanic PhysicsMathematicsObservational errorRehabilitationStatistical modelAerodynamicsMechanicstuuliBiomechanical PhenomenamäkihyppyJumpmatemaattiset mallitJournal of biomechanics
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Pythia 8 as hadronic interaction model in air shower simulations

2023

Hadronic interaction models are a core ingredient of simulations of extensive air showers and pose the major source of uncertainties of predictions of air shower observables. Recently, Pythia~8, a hadronic interaction model popular in accelerator-based high-energy physics, became usable in air shower simulations as well. We have integrated Pythia~8 with its new capabilities into the air shower simulation framework CORSIKA~8. First results show significantly shallower shower development, which we attribute to higher cross-section predictions by the new simplified nuclear model of Pythia.

High Energy Astrophysical Phenomena (astro-ph.HE)High Energy Physics - PhenomenologyHigh Energy Physics - Phenomenology (hep-ph)FOS: Physical sciencessimulointihiukkasfysiikkaAstrophysics - High Energy Astrophysical Phenomena
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Täpläravun (Pacifastacus leniusculus) vaikutus ahventen (Perca fluviatilis) loisyhteisöihin Päijänteellä

2010

Täplärapu (Pacifastacus leniusculus) on tulokaslaji Suomen vesistöissä. Sen on käyttäytymisellään ja ravinnonkäytöllään todettu vähentävän elinalueidensa eliöyhteisöjen monimuotoisuutta. Esimerkiksi Päijänteellä on havaittu joidenkin pohjaeläinten kuten kotiloiden tiheyksien olevan alhaisempia ravun elinalueilla kuin ravuttomilla alueilla. Pohjaselkärangattomat ovat välttämättömiä väli-isäntiä monelle kalan loiselle. Tässä tutkimuksessa selvitettiin, millaisia muutoksia täplärapu voi välillisesti aiheuttaa kalojen loisyhteisöissä muuttamalla pohjaeläinten runsautta. Päijänteeltä valittiin viisi toisistaan riippumatonta ravullista ja ravutonta aluetta. Jokaiselta alueelta pyydettiin mahdolli…

Ichthyocotylurus pileatusvesistötAcanthocephalus luciiloisetvälillinen vaikutusPäijänneahventäplärapuloinenväli-isäntäisäntälajitepäsuora elämänkierto
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Virtual Enterprise Simulation Game as an Environment for Collaborative Creativity and Learning

2021

AbstractWhen employees become accustomed to everyday working habits it can prevent them from generating creative ideas. This familiarity takes the forms of mainly collaborating with familiar colleagues, playing roles that develop over years, and solving encountered problems with proven strategies. This chapter considers how a virtual enterprise simulation game (RealGame) can potentially foster digital creativity and collaborative learning. The game simulates a situation where team members take responsibility for managing a virtual manufacturing company and its supply chain. Theoretically, we consider RealGame a facilitating environment for people to collaborate by offering a safe environmen…

Knowledge managementComputer scienceTheory of Formsmedia_common.quotation_subjectSupply chainenterpriseManufacturingluovuussimulation gamesimulointiyhteisöllinen oppiminenbusinessEmpirical evidencecreativitymedia_commonEncountered problemslearningbusiness.industryEnterprise simulationCollaborative learningsimulationyrittäjyysCreativitycollaborationoppimispelithyötypelitliiketoimintagameongelmanratkaisubusiness
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New Insights into Potocki-Shaffer Syndrome: Report of Two Novel Cases and Literature Review

2020

Potocki-Shaffer syndrome (PSS) is a rare non-recurrent contiguous gene deletion syndrome involving chromosome 11p11.2. Current literature implies a minimal region with haploinsufficiency of three genes, ALX4 (parietal foramina), EXT2 (multiple exostoses), and PHF21A (craniofacial anomalies, and intellectual disability). The rest of the PSS phenotype is still not associated with a specific gene. We report a systematic review of the literature and included two novel cases. Because deletions are highly variable in size, we defined three groups of patients considering the PSS-genes involved. We found 23 full PSS cases (ALX4, EXT2, and PHF21A), 14 cases with EXT2-ALX4, and three with PHF21A only…

LSD-CoRESTPotocki–Shaffer syndromeReviewBioinformaticsSCNAlcsh:RC321-57103 medical and health sciences0302 clinical medicineEpileptic encephalopathy; Infantile spasms; Intellectual disability; LSD-CoREST; PHF21A; Potocki-Shaffer; SCNA; West syndromePotocki-ShafferIntellectual disabilityMedicineCraniofaciallcsh:Neurosciences. Biological psychiatry. Neuropsychiatry030304 developmental biology0303 health sciencesbusiness.industryGeneral NeuroscienceWest Syndromewest syndromemedicine.diseasePhenotypePHF21Astomatognathic diseasesEpileptic spasmsepileptic encephalopathySCNAintellectual disability<i>PHF21A</i>businessHaploinsufficiency030217 neurology & neurosurgeryinfantile spasmsBrain Sciences
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