8 research outputs found
Közép- és kelet-európai nyelvek korpuszalapú többnyelvű terminológiai adatbázisai = Central- and East-European corpus-based multilingual terminological databases
A projekt három tĂ©maköre: - terminolĂłgia Ă©s nyelvpolitika, - kontrasztĂv nyelvĂ©szet, - finnugor nyelvi korpuszok összeállĂtása. Mindhárom terĂĽleten folyt - kutatás Ă©s/vagy - tudományszervezĹ‘ tevĂ©kenysĂ©g: konferenciák, tudományos publikáciĂłk közreadása. Az eredeti elkĂ©pzelĂ©seknek megfelelĹ‘en a közĂ©p-eurĂłpai tĂ©rsĂ©g nyelveinek Ă©s az oroszországi finnugor nyelvek terminolĂłgia-alkotására összpontosĂtottunk. A projekt keretĂ©ben, az UNESCO magyarországi titkárságával egyĂĽttműködve lĂ©trehoztuk a Magyar Nyelv TerminolĂłgiai Tanácsát (MaTT), illetve megalapĂtottuk a TerminolĂłgiai InnováciĂłs Központot (TermIK). Konferenciákat szervezĂĽnk kifejezetten e nyelvekre vonatkozĂł nyelvpolitikai Ă©s terminolĂłgiai kĂ©rdĂ©sekrĹ‘l, továbbá a kontrasztĂv nyelvĂ©szet terĂĽletĂ©n (magyar-finn Ă©s magyar-Ă©szt vonatkozásban) Ă©s e konferenciák anyagát, valamint az oroszországi finnugor köztársaságokban megalkotott terminolĂłgiai jegyzĂ©keket kiadjuk. PrimĂ©r kutatást folytatunk az igekötĹ‘-rendszerek összehasonlĂtásával (magyar-Ă©szt), illetve igekötĹ‘s Ă©s igekötĹ‘vel nem rendelkezĹ‘ nyelv összevetĂ©sĂ©vel (magyar-cseremisz) - e kutatások anyaga kĂ©t monográfia formájában 2008-ban megjelenik. CseremiszbĹ‘l Ă©s udmurtbĂłl nyelvi korpusz kĂ©szĂĽlt. A projekt folytatásának lehetĹ‘sĂ©ge: A 2008-ban megalakulĂł Collegium Fenno-Ugricum intĂ©zet egyik profilja az oroszországi finnugor nĂ©pek nyelvfejlesztĂ©si tevĂ©kenysĂ©gĂ©nek támogatása az oktatás Ă©s a terminolĂłgia-alkotás terĂ©n. | The project covered three areas: - terminology and language policy, - contrastive linguistics, - compilation of Finno-Ugric corpora. Work in each of the three areas involved: - research and/or - academic work: conferences, publication of scientific papers. The project has focussed on the development of terminology for the languages of the Central-European region and the Finno-Ugric languages of Russia. Within the framework of the project the Council of Hungarian Terminology (Magyar Nyelv TerminolĂłgiai Tanácsa - MaTT) has been established in cooperation with the Hungarian National Commission for UNESCO, and the Terminology Innovation Centre (TerminolĂłgiai InnováciĂłs Központ - TermIK) has been founded. Conferences have been organized on language policy and terminological issues specific to these languages, and on contrastive linguistics (Hungarian-Finnish; Hungarian-Estonian). The proceedings of these conferences and the terminologies worked out in the Finno-Ugric republics of Russia are being published. Primary research was carried out in respect of the comparison of verbal prefix systems (Hungarian-Estonian), and the comparison of languages whith and without verbal prefixes (Hungarian-Cheremis) - the results of these researches will be published as monographies in 2008. A corpus of Cheremis and of Udmurtian has been compiled. Follow-up to the project: One profile of the Collegium Fenno-Ugricum to be founded in 2008 is the support of language development activities in the field of education and terminology creation for the Finno-Ugric peoples of Russia
Erfolgsmodell Tandemkurs
Not Reviewe
Chronic infections and genetic factors in the development of ischemic stroke
The aim of this study was to examine whether chronic infections and genetic factors of the host play roles in the pathophysiology of acute noncardioembolic ischemic stroke. Blood samples from 59 subjects with ischemic stroke and 52 control patients were investigated by nested PCR for the presence of C. pneumoniae DNA, HCMV DNA and enterovirus RNA, by ELISA for the levels of antibodies to C. pneumoniae, HCMV, HSV, HHV-6, EBV and the inflammatory chemokine IL-8, and by PCR for promoter polymorphism of the IL-8 and CD14 host genes. Associations of stroke with the HCMV IgG and HSV-1 IgA antibody levels were observed. No association of stroke was detected with the presence of C. pneumoniae, HCMV or enterovirus nucleic acids in the peripheral blood, C. pneumoniae IgM, IgG and IgA, the HSV IgG, the EBV IgG, or HHV-6 IgG antibody levels, the pathogen burden, the IL-8 or CD 14 promoter polymorphisms, or with the serum levels of IL-8 in the overall study population. These results are consistent with the hypothesis that certain pathogens are involved in the development of ischemic stroke
Endotoxins do not influence transplacental transmission of lymphotropic human herpesviruses and human papillomaviruses into amniotic fluid taken from healthy mothers before parturition in Hungary
Pregnant women were examined following healthy pregnancies at term. Amniotic fluids were sampled before arteficial rupture of membranes using closed vacutainer system. Blood samples were also taken from the pregnants simultaneously. Endotoxin concentrations of amniotic fluids were tested by the semiquantitative Limulus amebocyte lysate. Both amniotic fluids and blood samples were tested for the presence of DNA of lymphotropic human herpesviruses. The DNA of human papillomaviruses were tested only in the amniotic fluid samples. One-third of the amniotic fluids tested were found to contain measurable amounts of endotoxin. Lymphotropic herpesvirus DNA was deteced in every fourth amniotic fluid sample and in every 8th blood sample. The prevalence of papillomaviruses was 7 of 96 samples. No significant correlation was found between the presence of endotoxin and viruses in the amniotic fluids. Epstein-Barr virus, human cytomegalovirus and human herpesvirus type 7 were found more frequently in the amniotic fluids than in blood samples (7 to 1). The prevalence of human herpesvirus 6 and 8 was higher in the blood samples than that in the amniotic fluids. The mean weight of the neonates were not impaired significantly by the presence of either viruses or endotoxin. Possible post partum consequences, i.e. partial immunotolerance to viruses is discussed
Herkunftssprache als Zielsprache. Erfahrungen aus der Wiener Hungarologie
Kein Abstract verfĂĽgbarAbstract not availabl