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Induced Pluripotency for Translational Research

The advent of induced pluripotent stem cells (iPSCs) has revolutionized the concept of cellular reprogramming and potentially will solve the immunological compatibility issues that have so far hindered the application of human pluripotent stem cells in regenerative medicine. Recent findings showed t...

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Detalles Bibliográficos
Autores principales: Wu, Menghua, Chen, Guilai, Hu, Baoyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357792/
https://www.ncbi.nlm.nih.gov/pubmed/24056061
http://dx.doi.org/10.1016/j.gpb.2013.08.001
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author Wu, Menghua
Chen, Guilai
Hu, Baoyang
author_facet Wu, Menghua
Chen, Guilai
Hu, Baoyang
author_sort Wu, Menghua
collection PubMed
description The advent of induced pluripotent stem cells (iPSCs) has revolutionized the concept of cellular reprogramming and potentially will solve the immunological compatibility issues that have so far hindered the application of human pluripotent stem cells in regenerative medicine. Recent findings showed that pluripotency is defined by a state of balanced lineage potency, which can be artificially instated through various procedures, including the conventional Yamanaka strategy. As a type of pluripotent stem cell, iPSCs are subject to the usual concerns over purity of differentiated derivatives and risks of tumor formation when used for cell-based therapy, though they provide certain advantages in translational research, especially in the areas of personalized medicine, disease modeling and drug screening. iPSC-based technology, human embryonic stem cells (hESCs) and direct lineage conversion each will play distinct roles in specific aspects of translational medicine, and continue yielding surprises for scientists and the public.
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spelling pubmed-43577922015-05-06 Induced Pluripotency for Translational Research Wu, Menghua Chen, Guilai Hu, Baoyang Genomics Proteomics Bioinformatics Review The advent of induced pluripotent stem cells (iPSCs) has revolutionized the concept of cellular reprogramming and potentially will solve the immunological compatibility issues that have so far hindered the application of human pluripotent stem cells in regenerative medicine. Recent findings showed that pluripotency is defined by a state of balanced lineage potency, which can be artificially instated through various procedures, including the conventional Yamanaka strategy. As a type of pluripotent stem cell, iPSCs are subject to the usual concerns over purity of differentiated derivatives and risks of tumor formation when used for cell-based therapy, though they provide certain advantages in translational research, especially in the areas of personalized medicine, disease modeling and drug screening. iPSC-based technology, human embryonic stem cells (hESCs) and direct lineage conversion each will play distinct roles in specific aspects of translational medicine, and continue yielding surprises for scientists and the public. Elsevier 2013-10 2013-09-19 /pmc/articles/PMC4357792/ /pubmed/24056061 http://dx.doi.org/10.1016/j.gpb.2013.08.001 Text en © 2013 Beijing Institute of Genomics, Chinese Academy of Sciences and Genetics Society of China. Production and hosting by Elsevier B.V. All rights reserved. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open access article under the CC BY-NC-SA license (http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Review
Wu, Menghua
Chen, Guilai
Hu, Baoyang
Induced Pluripotency for Translational Research
title Induced Pluripotency for Translational Research
title_full Induced Pluripotency for Translational Research
title_fullStr Induced Pluripotency for Translational Research
title_full_unstemmed Induced Pluripotency for Translational Research
title_short Induced Pluripotency for Translational Research
title_sort induced pluripotency for translational research
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357792/
https://www.ncbi.nlm.nih.gov/pubmed/24056061
http://dx.doi.org/10.1016/j.gpb.2013.08.001
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