Search results for "Asian"

showing 10 items of 494 documents

Valmistuvien fysioterapeuttiopiskelijoiden käsityksiä neurologisesta fysioterapiasta

2014

TIIVISTELMÄ Anne Ryhänen (2014). Valmistuvien fysioterapeuttiopiskelijoiden käsityksiä neurologisesta fysioterapiasta. Terveystieteiden laitos, Jyväskylän yliopisto, (fysioterapia) pro gradu -tutkielma. 49 s., 9 liitettä. Tutkimuksen tarkoituksena oli ymmärtää valmistuvien fysioterapeuttien käsityksiä neurologisesta fysioterapiasta ja sen oppimisesta. Ymmärtämällä opiskelijoiden käsityksiä tutkittavasta ilmiöstä voidaan kehittää opetussuunnitelmaa opiskelijalähtöisesti. Neurologiset potilaat ovat olleet vuosikymmenien ajan yksi keskeisimmistä fysioterapiaa saaneista asiakasryhmistä ja väestön ikääntyessä neurologisia sairauksia sairastavien määrä lisääntyy edelleen. Neurologisen fysioterapi…

Fenomenografiaoppiminenopiskelijatosaaminenkäsityksetneurologinen fysioterapiafysioterapiaasiantuntijuus
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The Monte San Nicola section (Sicily) revisited: A potential unit-stratotype of the Gelasian Stage

2022

The Monte San Nicola area (Southern Sicily) offers a spectacular exposure of open-marine sediments that were employed in 1998 for defining the Global Stratotype Section and Point (GSSP) of the Gelasian Stage (Upper Pliocene). After the lowering of the Pliocene/Pleistocene boundary to ca. 2.6 Ma in 2010, the Gelasian GSSP has been redefined as the base of both the Pleistocene Series and the Quaternary Period, which increased its importance and visibility within the scientific community. However, documentation on the Monte San Nicola reference section is still sparse. In the light of its renewed status, we decided to undertake a complete revision of the Gelasian Stage in its type area, in ord…

GSSPArcheologyGlobal and Planetary ChangeSettore GEO/02 - Geologia Stratigrafica E SedimentologicaStratigraphyPliocene-Pleistocene boundarymarine sedimentGeologySettore GEO/01 - Paleontologia E PaleoecologiaGelasianQuaternaryCalabrianmagnetostratigraphyEcology Evolution Behavior and Systematics
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Civic Participation and Gender Beliefs: An Analysis of 46 Countries

2016

Gender equality has progressed a great deal in recent decades in response to modernisation, industrialisation, and the generally rising level of education. A transformation in gender beliefs has accompanied the progress on gender equality and beliefs about gender roles have mainly changed in countries in North America and Europe, while in Muslim and Asian countries they have remained the same. The analysis in this article focuses on civic participation and investigates its relation to equalitarian gender beliefs. Multi-level regression models and data from World Values Survey (WVS) collected from 46 countries in 2005 allow depicting the relationships. The findings show that membership in ci…

Gender equality050402 sociologySociology and Political Science05 social sciencesInstrumental variableSign (semiotics)Gender studiesSocial value orientationsModernization theoryhumanities0506 political scienceIndustrialisation0504 sociology050602 political science & public administrationAsian countryWorld Values SurveySociologySocial psychologyCzech Sociological Review
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Ancestry and demography and descendants of Iron Age nomads of the Eurasian Steppe

2017

During the 1st millennium before the Common Era (BCE), nomadic tribes associated with the Iron Age Scythian culture spread over the Eurasian Steppe, covering a territory of more than 3,500 km in breadth. To understand the demographic processes behind the spread of the Scythian culture, we analysed genomic data from eight individuals and a mitochondrial dataset of 96 individuals originating in eastern and western parts of the Eurasian Steppe. Genomic inference reveals that Scythians in the east and the west of the steppe zone can best be described as a mixture of Yamnaya-related ancestry and an East Asian component. Demographic modelling suggests independent origins for eastern and western g…

Gene FlowMale0301 basic medicineSteppePopulation geneticsHuman MigrationGenomic dataBiological anthropologyScience[SHS.ANTHRO-BIO]Humanities and Social Sciences/Biological anthropologyDatasets as TopicGeneral Physics and AstronomyDNA MitochondrialWhite PeopleArticleGeneral Biochemistry Genetics and Molecular BiologyRussia03 medical and health sciencesAsian Peopleddc:590HumansEast AsiaHistory AncientTransients and MigrantsModels StatisticalMultidisciplinarygeography.geographical_feature_categoryHuman migrationbusiness.industryQGenetic VariationGeneral ChemistryGrasslandKazakhstan030104 developmental biologyGeographyIron AgeEthnologybusiness
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Hemocyanin subunit organization of the gastropod Rapana thomasiana

1999

Abstract RtH1 and RtH2, the two hemocyanin isoforms of the prosobranch gastropod Rapana thomasiana, have been purified by anion-exchange chromatography and studied by SDS–PAGE and immunoelectrophoresis. Both subunit types are built up of eight functional units (FUs). Under reducing conditions subunit RtH2 splits into two fragments, RtH2- a – f and RtH2- gh, suggesting the presence of a disulfide bridge between FU2- f and FU2- g. By proteolytic cleavage of the subunits into three-, two-, and single-FU fragments, purification of fragments by HPLC, N-terminal sequencing of the peptides, and crossed-line immunoelectrophoresis, FUs- a – h of RtH2 and FU- a, FU- d, FU- e, and FU- f of RtH1 were i…

Gene isoformSubunitProtein subunitmedicine.medical_treatmentMolecular Sequence DataBiophysicsImmunoelectrophoresisBiologyMegathura crenulataCleavage (embryo)BiochemistryHigh-performance liquid chromatographyHemocyaninRapana thomasianamedicineAnimalsProtein IsoformsAmino Acid SequenceProtein Structure QuaternaryMolecular BiologyGasteropodsmedicine.diagnostic_testPancreatic ElastaseImmunochemistryStructureHemocyaninbiology.organism_classificationMolecular biologyPeptide FragmentsMolluscaHemocyanin; Gasteropods; Structure; SubunitHemocyaninsImmunoelectrophoresis Two-Dimensional
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Työelämän asiantuntijuus ja korkeakoulupedagogiikka

2008

”Korkeakouluopetuksen yksi ydinkysymys on se, millaista on asiantuntijuus, jota korkeasti koulutetuilta yhteiskunnan jäseniltä odotetaan. Tämän päivän asiantuntijatyölle on ominaista, että siinä yhdistyvät perinteiset akateemiset hyveet, kuten tieteellinen ajattelu, ja nykypäivän yhteiskunnan toiminnassa keskeisiksi nousevat verkostoitumis- ja sosiaaliset taidot. Keskeinen kysymys korkeakouluopetuksen kehittämisessä onkin se, miten voimme kehittää sellaista pedagogiikkaa, joka samanaikaisesti edesauttaa tieteellistä ajattelua ja yleisiä työelämän taitoja”, kirjoittaa professori Päivi Tynjälä. – Päivi Tynjälän virkaanastujaispuhe Jyväskylän yliopistossa 7.5.2008.

General MedicineGeneral Chemistrykorkeakoulupedagogiikkaasiantuntijuus
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Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis.

2012

Familial idiopathic basal ganglia calcification (IBGC) is a genetic condition with a wide spectrum of neuropsychiatric symptoms, including parkinsonism and dementia. Here, we identified mutations in SLC20A2, encoding the type III sodium-dependent phosphate transporter 2 (PiT2), in IBGC-affected families of varied ancestry, and we observed significantly impaired phosphate transport activity for all assayed PiT2 mutants in Xenopus laevis oocytes. Our results implicate altered phosphate homeostasis in the etiology of IBGC.

Genetic Markersmedicine.medical_specialtyGenetic LinkageMolecular Sequence DataMutation MissenseXenopusBasal ganglia calcification610 Medicine & healthPhosphates10052 Institute of PhysiologyXenopus laevis03 medical and health scienceschemistry.chemical_compound0302 clinical medicineAsian PeopleBasal Ganglia Diseases1311 GeneticsCalcinosisGenetic linkageInternal medicineGeneticsmedicineAnimalsHomeostasisHumansBasal ganglia disease030304 developmental biology0303 health sciencesBase SequencebiologySodium-Phosphate Cotransporter Proteins Type IIIParkinsonismCalcinosisSequence Analysis DNAmedicine.diseasePhosphatebiology.organism_classificationPedigreeEndocrinologychemistry10076 Center for Integrative Human PhysiologyOocytes570 Life sciences; biologyLod Score030217 neurology & neurosurgeryHomeostasisChromosomes Human Pair 8Nature genetics
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Genetic polymorphism of human complement factor I (C3b inactivator) in the Chinese Han population.

1999

The human complement factor I (IF) polymorphism has been analysed by polyacrylamide gel isoelectric focusing electrophoresis of neuraminidase-treated EDTA plasma samples followed by immunoblotting and enzymatic detection. In a population study among 121 random individuals from Chengdu, PR China, three different common phenotypes were observed. The results show that IF is polymorphic in the Chinese population. The allele frequencies were as follows: FI*A = 0.153, FI*B = 0.847. The distribution of observed phenotypes was in accordance with the Hardy-Weinberg equilibrium. In comparison to other Asian population studies, the frequency of the IF*A allele was the highest in the Chinese population…

GeneticsChinaPolymorphism GeneticGenotypeIsoelectric focusingImmunologyComplement factor IBiologyMolecular biologyEdta plasmaChinese han populationAsian PeopleComplement Factor IC3b inactivatorGeneticsHumansPolyacrylamide gel electrophoresisGenetics (clinical)AllelesExperimental and clinical immunogenetics
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The TaqIB and −629C>A polymorphisms at the cholesteryl ester transfer protein locus: associations with lipid levels in a multiethnic population. T…

2002

The Singapore population comprises Chinese, Malays and Asian Indians. Within this population, Asian Indians have the highest rates of coronary heart disease, whereas Chinese have the lowest. Conversely, Indians have the lowest high-density lipoprotein cholesterol (HDL-C) concentrations, followed by Malays and Chinese. We studied the TaqIB and -629C>A polymorphisms at the CETP locus in 1300 Chinese, 364 Malay and 282 Asian Indian men, and in 1558 Chinese, 397 Malay and 306 Asian Indian women, to determine whether these polymorphisms are responsible for the ethnic difference in HDL-C concentration. The frequency of the B2 allele in Chinese, Malays and Indians was 0.384, 0.339 and 0.449 in men…

GeneticsLinkage disequilibriumeducation.field_of_studybiologyAsian IndianPopulationLocus (genetics)language.human_languageGenotypeCholesterylester transfer proteinGeneticsbiology.proteinlanguagelipids (amino acids peptides and proteins)AlleleeducationGenetics (clinical)DemographyMalayClinical Genetics
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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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