The moral, social, and commercial imperatives of genetic testing and screening : the Australian case
| 000 | 01029namuu2200253 a 4500 | |
| 001 | 000045286752 | |
| 005 | 20060816110002 | |
| 008 | 060814s2006 ne 001 0 eng d | |
| 020 | ▼a 1402046189 | |
| 040 | ▼a 211009 ▼c 211009 ▼d 211009 | |
| 082 | 0 4 | ▼a 362.196042 ▼2 22 |
| 090 | ▼a 362.196042 ▼b M828 | |
| 245 | 0 4 | ▼a The moral, social, and commercial imperatives of genetic testing and screening : ▼b the Australian case / ▼c edited by Michaela Betta. |
| 260 | ▼a Dordrecht : ▼b Springer , ▼c 2006. | |
| 300 | ▼a xv, 268 p. ; ▼c 25 cm. | |
| 440 | 0 | ▼a International library of ethics, law, and the new medicine ; ▼v v. 30 |
| 500 | ▼a Includes index. | |
| 650 | 0 | ▼a Genetic screening ▼x Moral and ethical aspects ▼z Australia. |
| 650 | 0 | ▼a Genetic screening ▼x Social aspects ▼z Australia. |
| 650 | 0 | ▼a Genetic screening ▼x Economic aspects ▼z Australia. |
| 650 | 0 | ▼a Human chromosome abnormalities ▼x Diagnosis ▼x Social aspects ▼z Australia. |
| 700 | 1 | ▼a Betta, Michela ▼d 1960- |
| 945 | ▼a KINS |
소장정보
| No. | 소장처 | 청구기호 | 등록번호 | 도서상태 | 반납예정일 | 예약 | 서비스 |
|---|---|---|---|---|---|---|---|
| No. 1 | 소장처 중앙도서관/서고6층/ | 청구기호 362.196042 M828 | 등록번호 111374532 | 도서상태 대출가능 | 반납예정일 | 예약 | 서비스 |
컨텐츠정보
책소개
In the past people were classified as being healthy or sick. With genetic testing and screening, adults might be healthy, predisposed to an illness, probably at risk, at risk, or carriers of certain risks. Genetic testing and screening hits another dramatic note when cells and embryos are tested and subsequently altered to hit targets of perfection. This insightful book combines theory and social practice, drawing on a range of disciplines and presenting contrasting viewpoints.
New feature
This is a dynamic book that successfully combines global and local thinking with regard to an emerging technology that will contribute to the expansion of proteomics and pharmacogenomics, the science of tailored healthcare and treatments. Genetic testing and screening will change the way people understand health, diagnostic knowledge, illness but also crime, databases and private information, paternity, and self-knowledge. In addition to giving individuals the opportunity to think differently about their well-being, it installs a new taxonomy in terms of illness, because its probabilistic effects will introduce a new narrative in the health discourse of 21st century society. While in the past people could be classified as being healthy or sick, now, through genetic testing and screening, adults can be classified as being healthy, predisposed to an illness, probably at risk, at risk, or carriers of certain risks. The effects of this taxonomy do not remain confined to the individual who is tested but extends to an entire family, as genetic knowledge is family knowledge. But the technology of genetic testing and screening installs a second dramatic register in the prenatal phase when cells and embryos are tested and subsequently altered in order to hit targets of perfection. However, this technology can also be seen as a strategy for the acquisition of new knowledge about oneself, as it instigates a different attitude towards ourselves in a scenario in which the notion of life as a singular noun is seriously questioned by cultural practices that make it necessary to speak of forms of life. The complexity of the Self resulting from this epistemological shift evoke the ancient Greco-roman practices of the care of the self leading to self-knowledge. Genetic testing and screening could therefore be understood as a form of self-quest, and attempt to discover what we are beyond our wishes and desires - beyond what we would like to be.
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목차
Contributors. About This Book. Part I: POSITIONING. 1. From Freedom to Destiny? On Human Nature and Liberal Eugenics in the Age of Genetic Manipulation; M. Betta. 2. Diagnostic Knowledge in the Genetic Economy and Commerce; M. Betta. Part II: THE AUSTRALIAN CASE. 3. Body Talk: Genetic Screening as a Device of Crime Regulation; R. Hil, R. Hindmarsh. 4. Genetic Testing and Human Genetic Databases; A.H. Gesche. 5. The Imperative of the 'New Genetics': Challenge for Ethics, Law and Social Policy; D. Weisbrot. 6. Insurance and Genetics: Regulating a Private Market in the Public Interest; D. Weisbrot, B. Opeskin. 7. The Social Imperative for Community Genetic Screening: An Australian Perspective; M.A. Aitken, S. Metcalfe. 8. Genetically Transformed Healthcare: Healthy Children and Parents; E. Palombo, M. Bhave. 9. The Australian Unions and the Inquiry into Genetic Testing in the Workplace; S. Pennicuik. 10. Genetic Information and the Australian Labour Movement; S. Jamieson. 11. Protecting the Vulnerable: Genetic Testing and Screening for Parentage, Immigration and Aboriginality; A.H. Gesche. 12. Essentially Whose? Genetic Testing and the Ownership of Genetic Information; L. Turney. Part III: FUTURE PERSPECTIVE. 13. Self-Knowledge and Self-Care in the Age of Genetic Manipulation; M. Betta. Part IV: CONCLUSION. Index.
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