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Volumn 308, Issue 5729, 2005, Pages 1777-1783

Developmental Biology: Patient-specific embryonic stem cells derived from human SCNT blastocysts

Author keywords

[No Author keywords available]

Indexed keywords

BIOMEDICAL ENGINEERING; DISEASES; DNA; IMMUNOLOGY; TRANSPLANTATION (SURGICAL);

EID: 20544451854     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.1112286     Document Type: Article
Times cited : (408)

References (32)
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    • note
    • Before beginning any experiments, we obtained approval for this study from the IRB for Human Subjects Research and Ethics Committee at Hanyang University Hospital, Seoul, Korea, which was required by existing regulations that were in place up to 31 December 2004. IRB approvals are included in (9). Oocyte and/or somatic cell donors were counseled by two IRB members to ensure that they were fully aware of the scope of the investigation, and each donor signed informed consent forms. Both of the parents of children under 18 years old donating somatic cells were similarly counseled, and each signed informed consent forms on behalf of their child. On 1 January 2005, the Republic of Korea's new regulation entitled Bioethics and Biosafety Act-Act No. 7150, requiring governmental licensing of SCNT using human oocytes and subsequent derivation of NT-hESCs (Therapeutic Cloning), became effective. On 12 January 2005, we received governmental approval in accordance with this new stem cell law. This law also required IRB approval from the College of Veterinary Medicine, Seoul National University, which was granted on 25 January 2005. When our previous report on NT-hESCs appeared online on 12 February 2004 (6), we imposed a voluntary moratorium on new NT-hESC derivations. in September 2004, we announced that we were again performing SCNT and deriving NT-hESCs, under the auspices and oversight of the Hanyang University IRB for Human Subjects Research and Ethics Committee. All IRB documents are included in (9).
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    • note
    • Materials, methods, and IRB documents are available as supporting material on Science Online.
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  • 32
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    • note
    • We thank foremost all donors. We also thank K. H. Man, J. H. Choi, J. T. Kang, S. G. Hong, and O. S. Kwon (Seoul National University); M. H. Kim, H. J. Jeong, E. K. Chun, and Y. J. Kim (MizMedi Hospital); and M. K. Koong and I. S. Kang (Samsung Cheil Hospital and Women's Healthcare Center) for assistance on NT-hESC culture; D. H. Chung (Seoul National University Hospital) for teratoma histopathology; J. Y. Kim and M. H. Park (Seoul National University Hospital) for HLA typing; and S. S. Yoo (Harvard Medical School) and the anonymous reviewers for their constructive critiques. All experiments were performed in Korea by Korean scientists, and all results were obtained in Korea using Korean equipment and Korean sponsorship. G.S and J.-H.P are grateful for the private philanthropy of the Magee-Womens Foundation, which supported their advisory roles in the analysis and for the interpretation and preparation for publication of these results obtained in Korea. No U.S. federal or Commonwealth of Pennsylvania funds were used in any aspect of this report. The authors are grateful for a graduate fellowship provided by the Ministry of Education, through BK21 program. This study was supported by grants from the Biodiscovery program of the Korean Ministry of Science and Technology to W.S.H. Until the formal establishment by the Republic of Korea of its National Center for Stem Cell Research, in which the previous NT-hESC line (-1) (6) and these new ones (-2 to -12) will be deposited and available for distribution, requests for cells and/or other materials should be addressed to W.S.H.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.