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Single stem cell gene therapy for genetic skin disease
Stem cell gene therapy followed by transplantation into damaged regions of the skin has been successfully used to treat genetic skin blistering disorder. Usually, many stem cells are virally transduced to obtain a sufficient number of genetically corrected cells required for successful transplantati...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403039/ https://www.ncbi.nlm.nih.gov/pubmed/25724199 http://dx.doi.org/10.15252/emmm.201404859 |
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author | Larsimont, Jean-Christophe Blanpain, Cédric |
author_facet | Larsimont, Jean-Christophe Blanpain, Cédric |
author_sort | Larsimont, Jean-Christophe |
collection | PubMed |
description | Stem cell gene therapy followed by transplantation into damaged regions of the skin has been successfully used to treat genetic skin blistering disorder. Usually, many stem cells are virally transduced to obtain a sufficient number of genetically corrected cells required for successful transplantation, as genetic insertion in every stem cell cannot be precisely defined. In this issue of EMBO Molecular Medicine, Droz-Georget Lathion et al developed a new strategy for ex vivo single cell gene therapy that allows extensive genomic and functional characterization of the genetically repaired individual cells before they can be used in clinical settings. |
format | Online Article Text |
id | pubmed-4403039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44030392015-04-23 Single stem cell gene therapy for genetic skin disease Larsimont, Jean-Christophe Blanpain, Cédric EMBO Mol Med Closeup Stem cell gene therapy followed by transplantation into damaged regions of the skin has been successfully used to treat genetic skin blistering disorder. Usually, many stem cells are virally transduced to obtain a sufficient number of genetically corrected cells required for successful transplantation, as genetic insertion in every stem cell cannot be precisely defined. In this issue of EMBO Molecular Medicine, Droz-Georget Lathion et al developed a new strategy for ex vivo single cell gene therapy that allows extensive genomic and functional characterization of the genetically repaired individual cells before they can be used in clinical settings. BlackWell Publishing Ltd 2015-04 2015-02-27 /pmc/articles/PMC4403039/ /pubmed/25724199 http://dx.doi.org/10.15252/emmm.201404859 Text en © 2015 The Authors. Published under the terms of the CC BY 4.0 license http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Closeup Larsimont, Jean-Christophe Blanpain, Cédric Single stem cell gene therapy for genetic skin disease |
title | Single stem cell gene therapy for genetic skin disease |
title_full | Single stem cell gene therapy for genetic skin disease |
title_fullStr | Single stem cell gene therapy for genetic skin disease |
title_full_unstemmed | Single stem cell gene therapy for genetic skin disease |
title_short | Single stem cell gene therapy for genetic skin disease |
title_sort | single stem cell gene therapy for genetic skin disease |
topic | Closeup |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403039/ https://www.ncbi.nlm.nih.gov/pubmed/25724199 http://dx.doi.org/10.15252/emmm.201404859 |
work_keys_str_mv | AT larsimontjeanchristophe singlestemcellgenetherapyforgeneticskindisease AT blanpaincedric singlestemcellgenetherapyforgeneticskindisease |