Search results for "P11"

showing 10 items of 42 documents

Työkulttuurien jännitteitä koulutusyhteisöissä

2019

Tarkastelemme artikkelissa jännitteitä koulutusyhteisöjen työkulttuureissa. Lähestymme aihetta opettajankoulutuksen kehittämiseen orientoituneesta koulutusmallista valmistuneiden opettajien kokemusten avulla. Tutkimuksen empiirisenä aineistona on 13 puolistrukturoitua yksilöhaastattelua, jotka kerättiin koulutusmalliin osallistuneilta opettajilta. Teoriasidonnaisessa sisällönanalyysissa keskityttiin yhteisön työkulttuuriin etsien myös sen vaikeammin havaittavia elementtejä, Scheinin (2017) sanoin perusolettamuksia.
 Tarkastelemme, miten yhteisöllisen ja kriittistä ammatillisuutta tukevan koulutusmallin anti on koettu ja miten sen vaikutukset ovat näyttäytyneet työelämässä. Tutkimuksemm…

työkulttuuri [http://www.yso.fi/onto/yso/p11260]Tiedeartikkelikoulutusyhteisötyöyhteisöt [http://www.yso.fi/onto/yso/p8543]professionalismi [http://www.yso.fi/onto/yso/p10140]General MedicineGeneral Chemistrykouluyhteisö [http://www.yso.fi/onto/yso/p8558]perusolettamuksetopettajankoulutustyökulttuuriopettajankoulutus [http://www.yso.fi/onto/yso/p10746]perusoletuksetAikuiskasvatus
researchProduct

What determines the likelihood of structural reforms?

2015

We use data for a panel of 60 countries over the period 1980–2005 to investigate the main drivers of the likelihood of structural reforms. We find that: (i) external debt crises are the main trigger of financial and banking reforms; (ii) inflation and banking crises are the key drivers of external capital account reforms; (iii) banking crises also hasten financial reforms; and (iv) economic recessions play an important role in promoting the necessary consensus for financial, capital, banking and trade reforms, especially in the group of OECD-countries. Additionally, we also observe that the degree of globalisation is relevant for financial reforms, in particular in the group of non-OECD cou…

MacroeconomicsG28Economics and EconometricEconomics and EconometricsCrisis episodemedia_common.quotation_subjectCrisis episodesRecessionPolitical setupSocial SciencesFinancial systemGlobalisationRecessionPoliticsGlobalization0502 economics and business050602 political science & public administrationEconomics050207 economicsStructural reformmedia_commonP1105 social sciences1. No povertyRecessionsSettore SECS-P/02 Politica EconomicaP16External debtCapital account0506 political scienceStructural reforms8. Economic growthPolitical Science and International Relations
researchProduct

Miten käsitteellistää ammatillista toimijuutta työssä?

2014

Artikkelissa tarkastellaan, miten toimijuus on ymmärretty monitieteisessä keskustelussa. Lisäksi pohditaan, miten ammatillista toimijuutta työssä tulisi käsitteellistää. peerReviewed

monitieteisyys [http://www.yso.fi/onto/yso/p11916]sosiokulttuuriset tekijät [http://www.yso.fi/onto/yso/p21870]monitieteisyyskäsitteenmuodostustyöelämä [http://www.yso.fi/onto/yso/p16262]General MedicineGeneral Chemistryammatillinen toimijuustoimijuuskäsityksettoimijuus [http://www.yso.fi/onto/yso/p2335]työ [http://www.yso.fi/onto/yso/p1810]käsitteellistäminenArtikkelittyöelämäontologia (filosofia) [http://www.yso.fi/onto/yso/p1055]
researchProduct

Role of THAP11 in the transcriptional regulation and chromatin structure of the human MYC locus

C-MYC è uno dei geni più frequentemente deregolati nei tumori umani. Una comprensione dettagliata della regolazione trascrizionale di questo gene è essenziale per comprendere meglio gli aspetti molecolari delle sue diverse funzioni. Usando diversi tipi di analisi (EMSA, 2D-IPG e analisi MALDI), nei nostri laboratori abbiamo caratterizzato un elemento con funzione di enhancer blocker (HB2.8) situato 32Kb valle del gene c-MYC . Saggi di trasfezione transiente e stabile hanno dimostrato che l'attività dell’elemento enhancer-blocker può essere attribuita esclusivamente ad un sub-regione di DNA di circa 400 bp chiamato AA0.4. Ulteriori test per valutare l'attività enhancer blocker di questa sequ…

C-MYC THAP11 Chromosome Conformation Capture
researchProduct

Onko osaamisella sukupuoli?

2001

Työn sukupuolen mukainen jako vallitsee kaikkien Euroopan maiden työ- ja koulutusmarkkinoita. Ammatillista osaamista ja sukupuolta koskevat käytännölliset ja tieteelliset keskustelut kohtaavat kuitenkin harvoin. Artikkeli kuvaa kansainvälistä tutkimusta, jossa selvitetään osaamisen sukupuolittumista ja sen ylittämisen mahdollisuuksia työpaikkojen ja oppilaitosten kasvatuskäytännöissä. Suomalaisten tutkimushaastattelujen alustavassa luennassa niin miehet kuin naiset pitävät osaamisia sukupuolettomina. Syvempi tulkinta edellyttää osaamis- ja gender-diskurssien kriittistä hyödyntämistä.

ammatillinen koulutus [http://www.yso.fi/onto/yso/p9700]osaaminenammattitaito [http://www.yso.fi/onto/yso/p9365]kasvatusosaaminen [http://www.yso.fi/onto/yso/p8343]General MedicineGeneral ChemistrySociologyArtikkelitsukupuoli [http://www.yso.fi/onto/yso/p5291]ammatit [http://www.yso.fi/onto/yso/p1179]sukupuolierot [http://www.yso.fi/onto/yso/p5290]sukupuoliAikuiskasvatus
researchProduct

HSP110 : role in colorectal cancer development and immunogenicity

2015

Our team studies HSPs, including HSP110. HSPs are chaperones involved in the folding of newly synthesized and denatured proteins. HSPs are overexpressed under stress conditions and are involved in cell survival thanks to their anti-apoptotic and anti-aggregation functions. HSP110 is overexpressed in colorectal cancer and is associated with a poor prognosis. The expression of a mutant HSP110, named HSP110DE9, has been shown in MSI colorectal cancer. This one was shown to act there as a dominant negative, by binding HSP110 and inhibiting its functions. Its expression sensitizes cancer cells to chemotherapy and is associated with a better prognosis for patients.I was first interested in HSP110…

STAT3Cancer colorectal[SDV.MHEP] Life Sciences [q-bio]/Human health and pathologyMacrophage polarizationHSP110DE9Colorectal cancerHSP110
researchProduct

HSPH1 inhibition downregulates Bcl-6 and c-Myc and hampers the growth of human aggressive B-cell non-Hodgkin lymphoma

2015

We have shown that human B-cell non-Hodgkin lymphomas (B-NHLs) express heat shock protein (HSP)H1/105 in function of their aggressiveness. Here, we now clarify its role as a functional B-NHL target by testing the hypothesis that it promotes the stabilization of key lymphoma oncoproteins. HSPH1 silencing in 4 models of aggressive B-NHLs was paralleled by Bcl-6 and c-Myc downregulation. In vitro and in vivo analysis of HSPH1-silenced Namalwa cells showed that this effect was associated with a significant growth delay and the loss of tumorigenicity when 10(4) cells were injected into mice. Interestingly, we found that HSPH1 physically interacts with c-Myc and Bcl-6 in both Namalwa cells and pr…

Lymphoma B-CellXenograft Model Antitumor AssayDNA-Binding ProteinImmunologyDown-RegulationMice SCIDSettore MED/08 - Anatomia PatologicaBiologyBiochemistryHSP110 Heat-Shock ProteinProto-Oncogene Proteins c-mycMiceDownregulation and upregulationimmune system diseasesCell Line Tumorhemic and lymphatic diseasesHeat shock proteinGene Knockdown TechniquesmedicineAnimalsHumansGene silencingHSP110 Heat-Shock ProteinsAnimals; Cell Line Tumor; DNA-Binding Proteins; Down-Regulation; Gene Knockdown Techniques; HSP110 Heat-Shock Proteins; Humans; Lymphoma B-Cell; Mice; Mice SCID; Proto-Oncogene Proteins c-myc; Xenograft Model Antitumor Assays; Biochemistry; Immunology; Medicine (all); Hematology; Cell BiologyAnimalMedicine (all)Cell BiologyHematologymedicine.diseaseXenograft Model Antitumor AssaysIn vitroLymphomaDNA-Binding ProteinsCell cultureGene Knockdown TechniquesGene Knockdown TechniqueImmunologyProto-Oncogene Proteins c-bcl-6Cancer researchB-Cell Non-Hodgkin LymphomaHumanBlood
researchProduct

Sisäistyneet ristiriidat, tunnetyö ja tietotyöläissubjektiviteetin rakentuminen

2015

Yliopistotyö on esimerkki uuden työn muodoista, joissa työ kiinnittyy aiempaa vahvemmin yksilöön. Samalla vastuu työelämän vaatimuksiin yltämisestä siirtyy työntekijälle itselleen. Työyhteisön ristiriitatilanteissa organisaation ongelmat sisäistyvät työntekijän yksityisiksi ja tunne-elämän ongelmiksi.

työntekijät [http://www.yso.fi/onto/yso/p1075]tunne-elämä [http://www.yso.fi/onto/yso/p8353]subjektiviteettiGeneral MedicineGeneral Chemistryristiriidatyliopistot [http://www.yso.fi/onto/yso/p10895]tunnetyöpersoona [http://www.yso.fi/onto/yso/p7199]subjektiivisuus [http://www.yso.fi/onto/yso/p4242]kokemukset [http://www.yso.fi/onto/yso/p3209]työ [http://www.yso.fi/onto/yso/p1810]tietotyö [http://www.yso.fi/onto/yso/p12926]tietotyösubjektiussubjekti (filosofia) [http://www.yso.fi/onto/yso/p25021]Aikuiskasvatuksen vuoden tiedeartikkelitArtikkelitsopeutuminen [http://www.yso.fi/onto/yso/p6137]yliopistotristiriidat [http://www.yso.fi/onto/yso/p2187]affektiivisuus [http://www.yso.fi/onto/yso/p11268]Aikuiskasvatus
researchProduct

In the literature: February 2020.

2020

The phosphatidylinositol-3-kinase (PI3K)/Akt and the mammalian target of rapamycin (mTOR) signaling pathways is one of the most frequently deregulated pathways in human cancers. This pathway controls multiple cellular processes, including metabolism, motility, proliferation, growth and survival. It can be aberrantly activated through multiple mechanisms, including diverse genomic alterations involving oncogenes and tumour suppressor genes.1 These alterations offer opportunities for therapeutic targeting of the pathway. PI3Kα protein complex is composed of regulatory (p85α) and catalytic (p110α) subunits. Pik3ca codes for p110α, which is the most frequently mutated oncogene across different …

Cancer ResearchOncogeneFulvestrantKinaseBiologyP110αmedicine.diseaseBreast cancerEditorialOncologymedicineCancer research1506Signal transductionProtein kinase BPI3K/AKT/mTOR pathwaymedicine.drugESMO open
researchProduct

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants

2019

Purpose: To assess the contribution of rare variants in the genetic background toward variability of neurodevelopmental phenotypes in individuals with rare copy-number variants (CNVs) and gene-disruptive variants. Methods: We analyzed quantitative clinical information, exome sequencing, and microarray data from 757 probands and 233 parents and siblings who carry disease-associated variants. Results: The number of rare likely deleterious variants in functionally intolerant genes (“other hits”) correlated with expression of neurodevelopmental phenotypes in probands with 16p12.1 deletion (n=23, p=0.004) and in autism probands carrying gene-disruptive variants (n=184, p=0.03) compared with thei…

MaleParents0301 basic medicineProbandNeuronalGenetic Carrier Screening16p11.2 deletion030105 genetics & heredityCognitionFamily historyNeural Cell Adhesion MoleculesGenetics (clinical)Exome sequencingSequence DeletionGeneticsGenetic Carrier ScreeningPhenotypePenetrancePedigreePhenotypeAutistic Disorder/genetics; Autistic Disorder/physiopathology; Cell Adhesion Molecules Neuronal/genetics; Chromosomes Human Pair 16/genetics; Cognition/physiology; DNA Copy Number Variations/genetics; Female; Gene Expression Regulation/genetics; Genetic Background; Genetic Carrier Screening; Humans; Male; Methyltransferases/genetics; Nerve Tissue Proteins/genetics; Parents; Pedigree; Phenotype; Proteins/genetics; Sequence Deletion/genetics; Siblings; 16p11.2 deletion; CNV; autism; modifier; phenotypic variabilityFemaleGenetic BackgroundHumanDNA Copy Number VariationsCell Adhesion Molecules NeuronalCNVautismNerve Tissue ProteinsBiologyChromosomesArticle03 medical and health sciencesmental disordersmedicineHumansAutistic DisorderBiologyGenemodifierPair 16SiblingsCalcium-Binding ProteinsProteinsMethyltransferasesmedicine.disease16p11.2 deletion; autism; CNV; modifier; phenotypic variability; Genetics (clinical)Cytoskeletal Proteins030104 developmental biologyGene Expression Regulation[SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human geneticsAutismphenotypic variabilityHuman medicine16p11.2 deletion; autism; CNV; modifier; phenotypic variability; Autistic Disorder; Cell Adhesion Molecules Neuronal; Chromosomes Human Pair 16; Cognition; DNA Copy Number Variations; Female; Gene Expression Regulation; Genetic Background; Humans; Male; Methyltransferases; Nerve Tissue Proteins; Parents; Pedigree; Phenotype; Proteins; Sequence Deletion; Siblings; Genetic Carrier ScreeningCell Adhesion MoleculesChromosomes Human Pair 16Transcription FactorsGenetics in Medicine
researchProduct