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Description
  • Human pluripotent stem cells represent an accessible cell source for novel cell-based clinical research and therapies. With the realization of induced pluripotent stem cells (iPSCs), it is possible to produce almost any desired cell type from any patient's cells. Current developments in gene modification methods have opened the possibility for creating genetically corrected human iPSCs for certain genetic diseases that could be used later in autologous transplantation. Promising preclinical studies have demonstrated correction of disease-causing mutations in a number of hematological, neuronal, and muscular disorders. This review aims to summarize these recent advances with a focus on iPSC generation techniques, as well as gene modification methods. We will then further discuss some of the main obstacles remaining to be overcome before successful application of human pluripotent stem cell-based therapy arrives in the clinic and what the future of stem cell research may look like.
  • Human pluripotent stem cells represent an accessible cell source for novel cell-based clinical research and therapies. With the realization of induced pluripotent stem cells (iPSCs), it is possible to produce almost any desired cell type from any patient's cells. Current developments in gene modification methods have opened the possibility for creating genetically corrected human iPSCs for certain genetic diseases that could be used later in autologous transplantation. Promising preclinical studies have demonstrated correction of disease-causing mutations in a number of hematological, neuronal, and muscular disorders. This review aims to summarize these recent advances with a focus on iPSC generation techniques, as well as gene modification methods. We will then further discuss some of the main obstacles remaining to be overcome before successful application of human pluripotent stem cell-based therapy arrives in the clinic and what the future of stem cell research may look like. (en)
Title
  • Pluripotent stem cells and gene therapy
  • Pluripotent stem cells and gene therapy (en)
skos:prefLabel
  • Pluripotent stem cells and gene therapy
  • Pluripotent stem cells and gene therapy (en)
skos:notation
  • RIV/00216224:14330/13:00068030!RIV14-MSM-14330___
http://linked.open...avai/riv/aktivita
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  • P(ED1.100/02/0123), Z(MSM0021622430)
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  • 96517
http://linked.open...ai/riv/idVysledku
  • RIV/00216224:14330/13:00068030
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  • pluripotent stem cells; gene therapy (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [A04AAB214681]
http://linked.open...i/riv/nazevZdroje
  • Translational Research
http://linked.open...in/vavai/riv/obor
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http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 161
http://linked.open...iv/tvurceVysledku
  • Šimara, Pavel
  • Kaufman, Dan
  • Motl, Jason
http://linked.open...ain/vavai/riv/wos
  • 000316837400008
http://linked.open...n/vavai/riv/zamer
issn
  • 1931-5244
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.trsl.2013.01.001
http://localhost/t...ganizacniJednotka
  • 14330
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