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Träfflista för sökning "WFRF:(Svalastog Anna Lydia 1966 ) "

Sökning: WFRF:(Svalastog Anna Lydia 1966 )

  • Resultat 11-20 av 23
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  • Svalastog, Anna Lydia, 1966- (författare)
  • Gene myths in public perception
  • 2012
  • Ingår i: Public Understanding of Science. - 0963-6625 .- 1361-6609. ; 21:4, s. 478-494
  • Tidskriftsartikel (refereegranskat)abstract
    • <p>In this article I examine myths in the gene science debate, and their use as a tool in analysis of popular perceptions and public opinion of genetic science and gene technology. In daily language myth means something untrue, though theories of myth present them as carriers of knowledge and truth. I understand myth as a narrative, a cultural construct that aims to describe the world, its origin, and its constituent elements. I compare scholars’ usage of myths, considering their implications. I conclude that i) As an analytical tool the concept of myth is too loosely defined, or understood through theories which leave out context, social relations and interaction. This provides limited insight about myths and myth-making in present day society. ii) An updated understanding of myths, including location/context and interaction/process would enrich analysis.</p>
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13.
  • Svalastog, Anna Lydia, 1966- (författare)
  • Making it Transparent. On Naming, Framing and Administrating Biobank Research on Native People in Sweden
  • 2013
  • Ingår i: New genetics and society (Print). - Taylor & Francis Group. - 1463-6778 .- 1469-9915. ; 32:3, s. 209-242
  • Tidskriftsartikel (refereegranskat)abstract
    • <p>Despite more than 50 years of genetic research on Sámi people in Sweden, there has been very little engagement with the ethical issues related to this research. My aim is to investigate the ethical challenges in biobank research on Sámi people, to identify ethical challenges that have been overlooked and to find ethical solutions. In my historical research inquiry of published material and interviews with people that have participated in this research, my research questions have been: How are blood samples from Sámi people collected, codified, governed and analyzed? What ethical strategies have been utilized? My main findings are: Sweden acquired biobank collections from Sámi people that are not registered or cannot be traced through the biobank register at the Swedish National Board of Health and Welfare. These collections entail ethical challenges concerning how the donors are identified, how the material is categorized, the regional ethical committees, governance and Sámi representation. My suggestions focus on transparency and traceability, competence and native peoples' rights and representation in biobank-related activities.</p>
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  • Resultat 11-20 av 23
  • Föregående 1[2]3Nästa
 
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