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Please use this identifier to cite or link to this item: http://dspace.bsu.edu.ru/handle/123456789/49567
Title: Genetically modified animal models of hereditary diseases for testing of gene-directed therapy
Authors: Polikarpova, A. V.
Egorova, T. V.
Bardina, M. V.
Keywords: medicine
pharmacology
animal models of human diseases
gene therapy
antisense oligonucleotides
hereditary diseases
adeno-associated virus
transgenesis
Issue Date: 2022
Citation: Polikarpova, A.V. Genetically modified animal models of hereditary diseases for testing of gene-directed therapy / A.V. Polikarpova, T.V. Egorova, M.V. Bardina // Research Results in Pharmacology. - 2022. - Vol.8, №2.-P. 11-26. - Doi: 10.3897/rrpharmacology.8.82618. - Refer.: p. 22-26.
Abstract: Given the specific gene therapy approach, appropriate animal models can be generated using a variety of technologies ranging from transgenesis to precise genome editing. In this review, we discuss technologies used to generate small and large animal models of the most common muscular and neurological genetic disorders. We specifically focus on animal models that were used to test gene therapies based on adeno-associated vectors and antisense nucleotides
URI: http://dspace.bsu.edu.ru/handle/123456789/49567
Appears in Collections:Vol. 8, № 2

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