These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 17050056)

  • 1. Tackling community concerns about commercialisation and genetic research: a modest interdisciplinary proposal.
    Haddow G; Laurie G; Cunningham-Burley S; Hunter KG
    Soc Sci Med; 2007 Jan; 64(2):272-82. PubMed ID: 17050056
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Data storage and DNA banking for biomedical research: informed consent, confidentiality, quality issues, ownership, return of benefits. A professional perspective.
    Godard B; Schmidtke J; Cassiman JJ; Aymé S
    Eur J Hum Genet; 2003 Dec; 11 Suppl 2():S88-122. PubMed ID: 14718939
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sharing the benefits of genetic resources: from biodiversity to human genetics.
    Schroeder D; Lasén-Díaz C
    Dev World Bioeth; 2006 Dec; 6(3):135-43. PubMed ID: 17038005
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Procedures and methods of benefit assessments for medicines in Germany.
    Bekkering GE; Kleijnen J
    Eur J Health Econ; 2008 Nov; 9 Suppl 1():5-29. PubMed ID: 18987905
    [TBL] [Abstract][Full Text] [Related]  

  • 5. North-South benefit sharing arrangements in bioprospecting and genetic research: a critical ethical and legal analysis.
    Schüklenk U; Kleinsmidt A
    Dev World Bioeth; 2006 Dec; 6(3):122-34. PubMed ID: 17038004
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Community engagement in genetic research: results of the first public consultation for the Quebec CARTaGENE project.
    Godard B; Marshall J; Laberge C
    Community Genet; 2007; 10(3):147-58. PubMed ID: 17575459
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Consent, commercialisation and benefit-sharing.
    Nicol D; Otlowski M; Chalmers D
    J Law Med; 2001 Aug; 9(1):80-94. PubMed ID: 12116675
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The governance of human genetic research databases in mental health research.
    Mc Fleming J
    Int J Law Psychiatry; 2007; 30(3):182-90. PubMed ID: 17449098
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Population genetic studies: is there an emerging legal obligation to share benefits?
    Sheremeta L
    Health Law Rev; 2003; 12(1):36-8. PubMed ID: 15742495
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ethical, legal, and social implications of biobanks for genetics research.
    Haga SB; Beskow LM
    Adv Genet; 2008; 60():505-44. PubMed ID: 18358331
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Procedures and methods of benefit assessments for medicines in Germany].
    Bekkering GE; Kleijnen J
    Dtsch Med Wochenschr; 2008 Dec; 133 Suppl 7():S225-46. PubMed ID: 19034813
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ethical issues raised by incorporation of genetics into the National Birth Defects Prevention Study.
    Jenkins MM; Rasmussen SA; Moore CA; Honein MA
    Am J Med Genet C Semin Med Genet; 2008 Feb; 148C(1):40-6. PubMed ID: 18189287
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Big pharma and health care: unsolvable conflict of interests between private enterprise and public health.
    Brezis M
    Isr J Psychiatry Relat Sci; 2008; 45(2):83-9; discussion 90-4. PubMed ID: 18982834
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Views of female breast cancer patients who donated biologic samples regarding storage and use of samples for genetic research.
    Kaphingst KA; Janoff JM; Harris LN; Emmons KM
    Clin Genet; 2006 May; 69(5):393-8. PubMed ID: 16650074
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ethical implications of including children in a large biobank for genetic-epidemiologic research: a qualitative study of public opinion.
    Kaufman D; Geller G; Leroy L; Murphy J; Scott J; Hudson K
    Am J Med Genet C Semin Med Genet; 2008 Feb; 148C(1):31-9. PubMed ID: 18189289
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The "GeneTrustee": a universal identification system that ensures privacy and confidentiality for human genetic databases.
    Burnett L; Barlow-Stewart K; Proos AL; Aizenberg H
    J Law Med; 2003 May; 10(4):506-13. PubMed ID: 12852322
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Public attitudes to the storage of blood left over from routine general practice tests and its use in research.
    Treweek S; Doney A; Leiman D
    J Health Serv Res Policy; 2009 Jan; 14(1):13-9. PubMed ID: 19103912
    [TBL] [Abstract][Full Text] [Related]  

  • 18. After the smoke has cleared--reflections on Scotland's tobacco control legislation.
    Donnelly P; Whittle P
    Public Health; 2008 Aug; 122(8):762-6. PubMed ID: 18485428
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic research into Alzheimer's disease: a European focus group study on ethical issues.
    van der Vorm A; Rikkert MO; Vernooij-Dassen M; Dekkers W;
    Int J Geriatr Psychiatry; 2008 Jan; 23(1):11-5. PubMed ID: 17477450
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Naturally occurring asbestos: a recurring public policy challenge.
    Lee RJ; Strohmeier BR; Bunker KL; Van Orden DR
    J Hazard Mater; 2008 May; 153(1-2):1-21. PubMed ID: 18180100
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.