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Please use this identifier to cite or link to this item: http://dspace.bsu.edu.ru/handle/123456789/49567
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dc.contributor.authorPolikarpova, A. V.-
dc.contributor.authorEgorova, T. V.-
dc.contributor.authorBardina, M. V.-
dc.date.accessioned2022-11-14T08:22:28Z-
dc.date.available2022-11-14T08:22:28Z-
dc.date.issued2022-
dc.identifier.citationPolikarpova, 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.ru
dc.identifier.urihttp://dspace.bsu.edu.ru/handle/123456789/49567-
dc.description.abstractGiven 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 nucleotidesru
dc.language.isoenru
dc.subjectmedicineru
dc.subjectpharmacologyru
dc.subjectanimal models of human diseasesru
dc.subjectgene therapyru
dc.subjectantisense oligonucleotidesru
dc.subjecthereditary diseasesru
dc.subjectadeno-associated virusru
dc.subjecttransgenesisru
dc.titleGenetically modified animal models of hereditary diseases for testing of gene-directed therapyru
dc.typeArticleru
Appears in Collections:Vol. 8, № 2

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