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Review: R28 retinal precursor cells: The first 20 years
The R28 retinal precursor cell line was established 20 years ago, originating from a postnatal day 6 rat retinal culture immortalized with the 12S E1A (NP-040507) gene of the adenovirus in a replication-incompetent viral vector. Since that time, R28 cells have been characterized and used for a varie...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Molecular Vision
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955414/ https://www.ncbi.nlm.nih.gov/pubmed/24644404 |
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author | Seigel, Gail M. |
author_facet | Seigel, Gail M. |
author_sort | Seigel, Gail M. |
collection | PubMed |
description | The R28 retinal precursor cell line was established 20 years ago, originating from a postnatal day 6 rat retinal culture immortalized with the 12S E1A (NP-040507) gene of the adenovirus in a replication-incompetent viral vector. Since that time, R28 cells have been characterized and used for a variety of in vitro and in vivo studies of retinal cell behavior, including differentiation, neuroprotection, cytotoxicity, and light stimulation, as well as retinal gene expression and neuronal function. While no cell culture is equivalent to the intact eye, R28 cells continue to provide an important experimental system for the study of many retinal processes. |
format | Online Article Text |
id | pubmed-3955414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Molecular Vision |
record_format | MEDLINE/PubMed |
spelling | pubmed-39554142014-03-18 Review: R28 retinal precursor cells: The first 20 years Seigel, Gail M. Mol Vis Review The R28 retinal precursor cell line was established 20 years ago, originating from a postnatal day 6 rat retinal culture immortalized with the 12S E1A (NP-040507) gene of the adenovirus in a replication-incompetent viral vector. Since that time, R28 cells have been characterized and used for a variety of in vitro and in vivo studies of retinal cell behavior, including differentiation, neuroprotection, cytotoxicity, and light stimulation, as well as retinal gene expression and neuronal function. While no cell culture is equivalent to the intact eye, R28 cells continue to provide an important experimental system for the study of many retinal processes. Molecular Vision 2014-03-14 /pmc/articles/PMC3955414/ /pubmed/24644404 Text en Copyright © 2014 Molecular Vision. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited, used for non-commercial purposes, and is not altered or transformed. |
spellingShingle | Review Seigel, Gail M. Review: R28 retinal precursor cells: The first 20 years |
title | Review: R28 retinal precursor cells: The first 20 years |
title_full | Review: R28 retinal precursor cells: The first 20 years |
title_fullStr | Review: R28 retinal precursor cells: The first 20 years |
title_full_unstemmed | Review: R28 retinal precursor cells: The first 20 years |
title_short | Review: R28 retinal precursor cells: The first 20 years |
title_sort | review: r28 retinal precursor cells: the first 20 years |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955414/ https://www.ncbi.nlm.nih.gov/pubmed/24644404 |
work_keys_str_mv | AT seigelgailm reviewr28retinalprecursorcellsthefirst20years |