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Kazuto Kato

Showing results (11-20 of 66) with videos related to

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Frontiers in Genetics|June 19, 2018
Authentication of Patients and Participants in Health Information Exchange and Consent for Medical Research: A Key Step for Privacy Protection, Respect for Autonomy, and TrustworthinessAtsushi Kogetsu, Soichi Ogishima, Kazuto Kato
Cell Stem Cell|May 11, 2010
Regulatory impacts on stem cell research in JapanMasahiro Kawakami, Douglas Sipp, Kazuto Kato
Life Sciences, Society and Policy|June 19, 2015
Ethical considerations of research policy for personal genome analysis: the approach of the Genome Science Project in JapanJusaku Minari, Tetsuya Shirai, Kazuto Kato
Asian Bioethics Review|March 15, 2021
Ethical Perspectives of Japanese Engineers on Ambient Assisted Living Technologies: Semi-structured InterviewJungen Koimizu, Minori Kokado, Kazuto Kato
Plos One|March 18, 2022
Why does it take so long for rare disease patients to get an accurate diagnosis?-A qualitative investigation of patient experiences of hereditary angioedemaMoeko Isono, Minori Kokado, Kazuto Kato
Frontiers in Genetics|February 12, 2024
Access, autonomy, and affordability: ethical and human rights issues surrounding multigene panel testing for cancer in Japan and SwitzerlandKate Nakasato, Carlotta Manz, Kazuto Kato
Frontiers in Digital Health|February 27, 2026
Perspectives on the use of artificial intelligence in Japan: a focus group interview study of healthcare providersAtsushi Kogetsu, Kazuto Kato, Beverley Anne Yamamoto
Human Genomics|May 18, 2022
Evaluating standards for 'serious' disease for preimplantation genetic testing: a multi-case study on regulatory frameworks in Japan, the UK, and Western AustraliaKate Nakasato, Beverley Anne Yamamoto, Kazuto Kato
Journal of Human Genetics|December 25, 2019
A proposal on the first Japanese practical guidance for the return of individual genomic results in research settingsYayoi Aizawa, Fuji Nagami, Noriko Ohashi, et al.
Frontiers in Public Health|August 5, 2022
Patient involvement in priority-setting for medical research: A mini review of initiatives in the rare disease fieldAmelia Katirai, Atsushi Kogetsu, Kazuto Kato, et al.
Pageof 7

Showing results (11-20 of 66) with videos related to

Sort By:
Pageof 7
Frontiers in Genetics|June 19, 2018
Authentication of Patients and Participants in Health Information Exchange and Consent for Medical Research: A Key Step for Privacy Protection, Respect for Autonomy, and TrustworthinessAtsushi Kogetsu, Soichi Ogishima, Kazuto Kato
Cell Stem Cell|May 11, 2010
Regulatory impacts on stem cell research in JapanMasahiro Kawakami, Douglas Sipp, Kazuto Kato
Life Sciences, Society and Policy|June 19, 2015
Ethical considerations of research policy for personal genome analysis: the approach of the Genome Science Project in JapanJusaku Minari, Tetsuya Shirai, Kazuto Kato
Asian Bioethics Review|March 15, 2021
Ethical Perspectives of Japanese Engineers on Ambient Assisted Living Technologies: Semi-structured InterviewJungen Koimizu, Minori Kokado, Kazuto Kato
Plos One|March 18, 2022
Why does it take so long for rare disease patients to get an accurate diagnosis?-A qualitative investigation of patient experiences of hereditary angioedemaMoeko Isono, Minori Kokado, Kazuto Kato
Frontiers in Genetics|February 12, 2024
Access, autonomy, and affordability: ethical and human rights issues surrounding multigene panel testing for cancer in Japan and SwitzerlandKate Nakasato, Carlotta Manz, Kazuto Kato
Frontiers in Digital Health|February 27, 2026
Perspectives on the use of artificial intelligence in Japan: a focus group interview study of healthcare providersAtsushi Kogetsu, Kazuto Kato, Beverley Anne Yamamoto
Human Genomics|May 18, 2022
Evaluating standards for 'serious' disease for preimplantation genetic testing: a multi-case study on regulatory frameworks in Japan, the UK, and Western AustraliaKate Nakasato, Beverley Anne Yamamoto, Kazuto Kato
Journal of Human Genetics|December 25, 2019
A proposal on the first Japanese practical guidance for the return of individual genomic results in research settingsYayoi Aizawa, Fuji Nagami, Noriko Ohashi, et al.
Frontiers in Public Health|August 5, 2022
Patient involvement in priority-setting for medical research: A mini review of initiatives in the rare disease fieldAmelia Katirai, Atsushi Kogetsu, Kazuto Kato, et al.
Pageof 7