Neurodegenerative diseases in a dish: the promise of iPSC technology in disease modeling and therapeutic discovery

The study of stem-cell biology has been a flourishing research area because of its multi-differentiation potential. The emergence of induced pluripotent stem cells (iPSCs) open up the possibility of addressing obstructs, such as the limited cell source, inherent complexity of the human brain, and et...

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Main Authors: Xie, Y. Z., Zhang, R. X.
Format: Online
Language:English
Published: Springer Milan 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282683/
id pubmed-4282683
recordtype oai_dc
spelling pubmed-42826832015-01-08 Neurodegenerative diseases in a dish: the promise of iPSC technology in disease modeling and therapeutic discovery Xie, Y. Z. Zhang, R. X. Review Article The study of stem-cell biology has been a flourishing research area because of its multi-differentiation potential. The emergence of induced pluripotent stem cells (iPSCs) open up the possibility of addressing obstructs, such as the limited cell source, inherent complexity of the human brain, and ethical constrains. Though still at its infancy phase, reprogramming of somatic cells has been demonstrating the ability to enhance in vitro study of neurodegenerative diseases and potential treatment. However, iPSCs would not thoroughly translate to the clinic before limitations are addressed. In this review, by summarizing the recent development of iPSC-based models, we will discuss the feasibility of iPSC technology on relevant diseases depth and illustrate how this new tool applies to drug screening and celluar therapy. Springer Milan 2014-10-30 2015 /pmc/articles/PMC4282683/ /pubmed/25354658 http://dx.doi.org/10.1007/s10072-014-1989-9 Text en © The Author(s) 2014 Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Xie, Y. Z.
Zhang, R. X.
spellingShingle Xie, Y. Z.
Zhang, R. X.
Neurodegenerative diseases in a dish: the promise of iPSC technology in disease modeling and therapeutic discovery
author_facet Xie, Y. Z.
Zhang, R. X.
author_sort Xie, Y. Z.
title Neurodegenerative diseases in a dish: the promise of iPSC technology in disease modeling and therapeutic discovery
title_short Neurodegenerative diseases in a dish: the promise of iPSC technology in disease modeling and therapeutic discovery
title_full Neurodegenerative diseases in a dish: the promise of iPSC technology in disease modeling and therapeutic discovery
title_fullStr Neurodegenerative diseases in a dish: the promise of iPSC technology in disease modeling and therapeutic discovery
title_full_unstemmed Neurodegenerative diseases in a dish: the promise of iPSC technology in disease modeling and therapeutic discovery
title_sort neurodegenerative diseases in a dish: the promise of ipsc technology in disease modeling and therapeutic discovery
description The study of stem-cell biology has been a flourishing research area because of its multi-differentiation potential. The emergence of induced pluripotent stem cells (iPSCs) open up the possibility of addressing obstructs, such as the limited cell source, inherent complexity of the human brain, and ethical constrains. Though still at its infancy phase, reprogramming of somatic cells has been demonstrating the ability to enhance in vitro study of neurodegenerative diseases and potential treatment. However, iPSCs would not thoroughly translate to the clinic before limitations are addressed. In this review, by summarizing the recent development of iPSC-based models, we will discuss the feasibility of iPSC technology on relevant diseases depth and illustrate how this new tool applies to drug screening and celluar therapy.
publisher Springer Milan
publishDate 2014
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282683/
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