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Small molecule screening in zebrafish: an in vivo approach to identifying new chemical tools and drug leads

In the past two decades, zebrafish genetic screens have identified a wealth of mutations that have been essential to the understanding of development and disease biology. More recently, chemical screens in zebrafish have identified small molecules that can modulate specific developmental and behavio...

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Detalles Bibliográficos
Autores principales: Taylor, Kerrie L, Grant, Nicola J, Temperley, Nicholas D, Patton, E Elizabeth
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2912314/
https://www.ncbi.nlm.nih.gov/pubmed/20540792
http://dx.doi.org/10.1186/1478-811X-8-11
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author Taylor, Kerrie L
Grant, Nicola J
Temperley, Nicholas D
Patton, E Elizabeth
author_facet Taylor, Kerrie L
Grant, Nicola J
Temperley, Nicholas D
Patton, E Elizabeth
author_sort Taylor, Kerrie L
collection PubMed
description In the past two decades, zebrafish genetic screens have identified a wealth of mutations that have been essential to the understanding of development and disease biology. More recently, chemical screens in zebrafish have identified small molecules that can modulate specific developmental and behavioural processes. Zebrafish are a unique vertebrate system in which to study chemical genetic systems, identify drug leads, and explore new applications for known drugs. Here, we discuss some of the advantages of using zebrafish in chemical biology, and describe some important and creative examples of small molecule screening, drug discovery and target identification.
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spelling pubmed-29123142010-07-30 Small molecule screening in zebrafish: an in vivo approach to identifying new chemical tools and drug leads Taylor, Kerrie L Grant, Nicola J Temperley, Nicholas D Patton, E Elizabeth Cell Commun Signal Review In the past two decades, zebrafish genetic screens have identified a wealth of mutations that have been essential to the understanding of development and disease biology. More recently, chemical screens in zebrafish have identified small molecules that can modulate specific developmental and behavioural processes. Zebrafish are a unique vertebrate system in which to study chemical genetic systems, identify drug leads, and explore new applications for known drugs. Here, we discuss some of the advantages of using zebrafish in chemical biology, and describe some important and creative examples of small molecule screening, drug discovery and target identification. BioMed Central 2010-06-12 /pmc/articles/PMC2912314/ /pubmed/20540792 http://dx.doi.org/10.1186/1478-811X-8-11 Text en Copyright ©2010 Taylor et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Taylor, Kerrie L
Grant, Nicola J
Temperley, Nicholas D
Patton, E Elizabeth
Small molecule screening in zebrafish: an in vivo approach to identifying new chemical tools and drug leads
title Small molecule screening in zebrafish: an in vivo approach to identifying new chemical tools and drug leads
title_full Small molecule screening in zebrafish: an in vivo approach to identifying new chemical tools and drug leads
title_fullStr Small molecule screening in zebrafish: an in vivo approach to identifying new chemical tools and drug leads
title_full_unstemmed Small molecule screening in zebrafish: an in vivo approach to identifying new chemical tools and drug leads
title_short Small molecule screening in zebrafish: an in vivo approach to identifying new chemical tools and drug leads
title_sort small molecule screening in zebrafish: an in vivo approach to identifying new chemical tools and drug leads
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2912314/
https://www.ncbi.nlm.nih.gov/pubmed/20540792
http://dx.doi.org/10.1186/1478-811X-8-11
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