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Gene editing in dermatology: Harnessing CRISPR for the treatment of cutaneous disease

The discovery of the Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) system has revolutionized gene editing research. Through the repurposing of programmable RNA-guided CRISPR-associated (Cas) nucleases, CRISPR-based genome editing systems allow for the precise modification of spe...

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Detalles Bibliográficos
Autores principales: Baker, Catherine, Hayden, Matthew S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265575/
https://www.ncbi.nlm.nih.gov/pubmed/32528662
http://dx.doi.org/10.12688/f1000research.23185.2
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author Baker, Catherine
Hayden, Matthew S.
author_facet Baker, Catherine
Hayden, Matthew S.
author_sort Baker, Catherine
collection PubMed
description The discovery of the Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) system has revolutionized gene editing research. Through the repurposing of programmable RNA-guided CRISPR-associated (Cas) nucleases, CRISPR-based genome editing systems allow for the precise modification of specific sites in the human genome and inspire novel approaches for the study and treatment of inherited and acquired human diseases. Here, we review how CRISPR technologies have stimulated key advances in dermatologic research.  We discuss the role of CRISPR in genome editing for cutaneous disease and highlight studies on the use of CRISPR-Cas technologies for genodermatoses, cutaneous viruses and bacteria, and melanoma. Additionally, we examine key limitations of current CRISPR technologies, including the challenges these limitations pose for the widespread therapeutic application of CRISPR-based therapeutics.
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spelling pubmed-72655752020-06-10 Gene editing in dermatology: Harnessing CRISPR for the treatment of cutaneous disease Baker, Catherine Hayden, Matthew S. F1000Res Review The discovery of the Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) system has revolutionized gene editing research. Through the repurposing of programmable RNA-guided CRISPR-associated (Cas) nucleases, CRISPR-based genome editing systems allow for the precise modification of specific sites in the human genome and inspire novel approaches for the study and treatment of inherited and acquired human diseases. Here, we review how CRISPR technologies have stimulated key advances in dermatologic research.  We discuss the role of CRISPR in genome editing for cutaneous disease and highlight studies on the use of CRISPR-Cas technologies for genodermatoses, cutaneous viruses and bacteria, and melanoma. Additionally, we examine key limitations of current CRISPR technologies, including the challenges these limitations pose for the widespread therapeutic application of CRISPR-based therapeutics. F1000 Research Limited 2020-10-07 /pmc/articles/PMC7265575/ /pubmed/32528662 http://dx.doi.org/10.12688/f1000research.23185.2 Text en Copyright: © 2020 Baker C and Hayden MS http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Baker, Catherine
Hayden, Matthew S.
Gene editing in dermatology: Harnessing CRISPR for the treatment of cutaneous disease
title Gene editing in dermatology: Harnessing CRISPR for the treatment of cutaneous disease
title_full Gene editing in dermatology: Harnessing CRISPR for the treatment of cutaneous disease
title_fullStr Gene editing in dermatology: Harnessing CRISPR for the treatment of cutaneous disease
title_full_unstemmed Gene editing in dermatology: Harnessing CRISPR for the treatment of cutaneous disease
title_short Gene editing in dermatology: Harnessing CRISPR for the treatment of cutaneous disease
title_sort gene editing in dermatology: harnessing crispr for the treatment of cutaneous disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265575/
https://www.ncbi.nlm.nih.gov/pubmed/32528662
http://dx.doi.org/10.12688/f1000research.23185.2
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