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Review
. 2014 Jul;7(7):739-43.
doi: 10.1242/dmm.015545.

Zebrafish models in translational research: tipping the scales toward advancements in human health

Affiliations
Review

Zebrafish models in translational research: tipping the scales toward advancements in human health

Jennifer B Phillips et al. Dis Model Mech. 2014 Jul.

Abstract

Advances in genomics and next-generation sequencing have provided clinical researchers with unprecedented opportunities to understand the molecular basis of human genetic disorders. This abundance of information places new requirements on traditional disease models, which have the potential to be used to confirm newly identified pathogenic mutations and test the efficacy of emerging therapies. The unique attributes of zebrafish are being increasingly leveraged to create functional disease models, facilitate drug discovery, and provide critical scientific bases for the development of new clinical tools for the diagnosis and treatment of human disease. In this short review and the accompanying poster, we highlight a few illustrative examples of the applications of the zebrafish model to the study of human health and disease.

Keywords: Cancer; Individualized medicine; Muscular dystrophy; Tuberculosis; Usher syndrome.

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References

    1. Ablain J., Zon L. I. (2013). Of fish and men: using zebrafish to fight human diseases. Trends Cell Biol. 23, 584–586 - PMC - PubMed
    1. Austin-Tse C., Halbritter J., Zariwala M. A., Gilberti R. M., Gee H. Y., Hellman N., Pathak N., Liu Y., Panizzi J. R., Patel-King R. S., et al. (2013). Zebrafish ciliopathy screen plus human mutational analysis identifies C21orf59 and CCDC65 defects as causing primary ciliary dyskinesia. Am. J. Hum. Genet. 93, 672–686 - PMC - PubMed
    1. Baraban S. C., Dinday M. T., Hortopan G. A. (2013). Drug screening in Scn1a zebrafish mutant identifies clemizole as a potential Dravet syndrome treatment. Nat. Commun. 4, 2410. - PMC - PubMed
    1. Baxendale S., Holdsworth C. J., Meza Santoscoy P. L., Harrison M. R., Fox J., Parkin C. A., Ingham P. W., Cunliffe V. T. (2012). Identification of compounds with anti-convulsant properties in a zebrafish model of epileptic seizures. Dis. Model. Mech. 5, 773–784 - PMC - PubMed
    1. Bedell V. M., Westcot S. E., Ekker S. C. (2011). Lessons from morpholino-based screening in zebrafish. Brief. Funct. Genomics 10, 181–188 - PMC - PubMed

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