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 *

152 related articles for article (PubMed ID: 15119332)

  • 1. A critical appraisal of protections for aboriginal communities in biomedical research.
    Weijer C; Anderson JA
    Jurimetrics; 2002; 42(2):187-98. PubMed ID: 15119332
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Protecting communities in research: current guidelines and limits of extrapolation.
    Weijer C; Goldsand G; Emanuel EJ
    Nat Genet; 1999 Nov; 23(3):275-80. PubMed ID: 10545946
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An analysis of research guidelines on the collection and use of human biological materials from American Indian and Alaskan Native communities.
    Sharp RR; Foster MW
    Jurimetrics; 2002; 42(2):165-86. PubMed ID: 15119331
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Building a new culture of ethics in research involving humans in Brazil.
    Pessini L
    Not Polit; 2002; 18(67):101-12. PubMed ID: 15282926
    [No Abstract]   [Full Text] [Related]  

  • 5. Native American recommendations for genetic research to be culturally respectful.
    Burhansstipanov L; Bemis LT; Dignan M
    Jurimetrics; 2002; 42(2):149-57. PubMed ID: 15119329
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The role and responsibilities of witnesses in the informed consent process.
    Angeles-Llerenas AR; Wirtz V; Lara-Alvarez CF
    Dev World Bioeth; 2009 Apr; 9(1):18-25. PubMed ID: 18370932
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Applied research ethics with Aboriginal people: a Canadian dilemma.
    McPherson DH; Nelson CH; Rabb JD
    NCEHR Commun; 2004; 12(2):6-11. PubMed ID: 15460562
    [No Abstract]   [Full Text] [Related]  

  • 8. Ethical genetic research on human subjects.
    Harris J
    Jurimetrics; 1999; 40():77-91. PubMed ID: 16285118
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Research involving persons with mental disorders that may affect decisionmaking capacity.
    National Bioethics Advisory Commission (United States)
    J Int Bioethique; 2002; 13(3-4):173-9. PubMed ID: 12747354
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Protecting human subjects.
    Kaufman D
    NCEHR Commun; 2000; 10(2):15-8. PubMed ID: 15468468
    [No Abstract]   [Full Text] [Related]  

  • 11. Informing study participants of research results: an ethical imperative.
    Fernandez CV; Kodish E; Weijer C
    IRB; 2003; 25(3):12-9. PubMed ID: 14569989
    [No Abstract]   [Full Text] [Related]  

  • 12. Beyond informed consent.
    Bhutta ZA
    Bull World Health Organ; 2004 Oct; 82(10):771-7. PubMed ID: 15643799
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Beginning anew: same principles, different direction for research ethics.
    Simmerling M; Schwegler B
    Am J Bioeth; 2005; 5(1):44-6; author reply W15-8. PubMed ID: 16036659
    [No Abstract]   [Full Text] [Related]  

  • 14. Rethinking research ethics.
    Rhodes R
    Am J Bioeth; 2005; 5(1):7-28. PubMed ID: 16036651
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Grappling with groups: protecting collective interests in biomedical research.
    Sharp RR; Foster MW
    J Med Philos; 2007; 32(4):321-37. PubMed ID: 17712706
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Informed consent in clinical research: policies and practices in Singapore.
    Ramachandran AJ
    J Biolaw Bus; 2003; 6(1):65-75. PubMed ID: 15239181
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ethics in population-based genetic research.
    DeCamp M; Sugarman J
    Account Res; 2004; 11(1):1-26. PubMed ID: 15341044
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Children as research subjects: a proposal to revise the current federal regulations using a moral framework.
    Ross LF
    Stanford Law Pol Rev; 1997; 8(1):159-76. PubMed ID: 16528858
    [No Abstract]   [Full Text] [Related]  

  • 19. Communal discourse as a supplement to informed consent for genetic research.
    Foster MW; Eisenbraun AJ; Carter TH
    Nat Genet; 1997 Nov; 17(3):277-9. PubMed ID: 9354789
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Vulnerability in human subject research: existential state, not category designation.
    Finder SG
    Am J Bioeth; 2004; 4(3):68-70; discussion W32. PubMed ID: 16192149
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.