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.
91 related articles for article (PubMed ID: 23520913)
41. [International regulation of ethics committees on biomedical research as protection mechanisms for people: analysis of the Additional Protocol to the Convention on Human Rights and Biomedicine, concerning Biomedical Research of the Council of Europe]. de Lecuona I Rev Derecho Genoma Hum; 2013; (38):71-123. PubMed ID: 24340828 [TBL] [Abstract][Full Text] [Related]
42. National population-based biobanks for genetic research. Swede H; Stone CL; Norwood AR Genet Med; 2007 Mar; 9(3):141-9. PubMed ID: 17413418 [TBL] [Abstract][Full Text] [Related]
43. Collaborative international research: ethical and regulatory issues pertaining to human biological materials at a South African institutional research ethics committee. Sathar A; Dhai A; van der Linde S Dev World Bioeth; 2014 Dec; 14(3):150-7. PubMed ID: 23724945 [TBL] [Abstract][Full Text] [Related]
50. Whose cell line is it anyway? Intellectual property implications of New Jersey's policy on stem cell research. Tulp GR Seton Hall Law Rev; 2008; 38(3):1167-96. PubMed ID: 18623905 [No Abstract] [Full Text] [Related]
51. 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]
52. Currents in contemporary bioethics. Open access as benefit sharing? The example of publicly funded large-scale genomic databases. Joly Y; Allen C; Knoppers BM J Law Med Ethics; 2012; 40(1):143-6. PubMed ID: 22458469 [No Abstract] [Full Text] [Related]
53. Human genetic research databases and biobanks: towards uniform terminology and Australian best practice. Chalmers D; Nicol D J Law Med; 2008 Feb; 15(4):538-55. PubMed ID: 18365521 [TBL] [Abstract][Full Text] [Related]
55. 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]
56. Lessons from European population genetic databases: comparing the law in Estonia, Iceland, Sweden and the United Kingdom. Gibbons SM; Helgason HH; Kaye J; Nõmper A; Wendel L Eur J Health Law; 2005 Jun; 12(2):103-33. PubMed ID: 16144230 [TBL] [Abstract][Full Text] [Related]
57. [Accessing medical records for research purposes]. Alcalde Bezhold G; Alfonso Farnós I Rev Derecho Genoma Hum; 2013; (39):137-72. PubMed ID: 24868961 [TBL] [Abstract][Full Text] [Related]
58. Disclosure of individual genetic data to research participants: the debate reconsidered. Bredenoord AL; Kroes HY; Cuppen E; Parker M; van Delden JJ Trends Genet; 2011 Feb; 27(2):41-7. PubMed ID: 21190750 [TBL] [Abstract][Full Text] [Related]
59. Patenting of human genes, cells and parts of the body? -- the ethical dimensions of patent law. Moufang R IIC Int Rev Ind Prop Copyr Law; 1994; 25(4):487-515. PubMed ID: 11660161 [No Abstract] [Full Text] [Related]
60. Genetics. Genomic research and human subject privacy. Lin Z; Owen AB; Altman RB Science; 2004 Jul; 305(5681):183. PubMed ID: 15247459 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]