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dc.contributor.authorInoue, Hen
dc.contributor.authorYamanaka, Sen
dc.contributor.alternative井上, 治久ja
dc.contributor.alternative山中, 伸弥ja
dc.date.accessioned2012-10-17T07:11:30Z-
dc.date.available2012-10-17T07:11:30Z-
dc.date.issued2011-05-
dc.identifier.issn0009-9236-
dc.identifier.urihttp://hdl.handle.net/2433/160140-
dc.description.abstractInduced pluripotent stem cell (iPSC) technology is revolutionizing medical science, allowing the exploration of disease mechanisms and novel therapeutic molecular targets, and offering opportunities for drug discovery and proof-of-concept studies in drug development. This review focuses on the recent advancements in iPSC technology including disease modeling and control setting in its analytical paradigm. We describe how iPSC technology is integrated into existing paradigms of drug development and discuss the potential of iPSC technology in personalized medicine.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherNature Publishing Groupen
dc.rights© 2012 American Society for Clinical Pharmacology and Therapeuticsen
dc.rightsThis is not the published version. Please cite only the published version.en
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.subjectiPS cellen
dc.subjectdrug developmenten
dc.subjectdisease modelingen
dc.subjectcontrol definitionen
dc.subjectanimal modelen
dc.subjectpersonalized medicineen
dc.subject.meshAnimalsen
dc.subject.meshCell Differentiation/physiologyen
dc.subject.meshDrug Discovery/methodsen
dc.subject.meshDrug Discovery/trendsen
dc.subject.meshDrug Evaluation, Preclinical/methodsen
dc.subject.meshDrug Evaluation, Preclinical/trendsen
dc.subject.meshHumansen
dc.subject.meshInduced Pluripotent Stem Cells/cytologyen
dc.subject.meshInduced Pluripotent Stem Cells/transplantationen
dc.subject.meshNuclear Reprogramming/physiologyen
dc.titleThe use of induced pluripotent stem cells in drug development.en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA00607986-
dc.identifier.jtitleClinical pharmacology and therapeuticsen
dc.identifier.volume89-
dc.identifier.issue5-
dc.identifier.spage655-
dc.identifier.epage661-
dc.relation.doi10.1038/clpt.2011.38-
dc.textversionauthor-
dc.identifier.pmid21430656-
dcterms.accessRightsopen access-
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