| DC Field | Value | Language |
|---|
| dc.contributor.author | Kalmykov., V. A. | - |
| dc.contributor.author | Kusov, P. A. | - |
| dc.contributor.author | Yablonskaia, M. I. | - |
| dc.contributor.author | Korshunov, E. N. | - |
| dc.contributor.author | Korshunova, D. S. | - |
| dc.date.accessioned | 2022-04-22T10:35:37Z | - |
| dc.date.available | 2022-04-22T10:35:37Z | - |
| dc.date.issued | 2018 | - |
| dc.identifier.citation | New personalized genetic mouse model of Lesch-Nyhan syndrome for pharmacology and gene therapy / V.A. Kalmykov [et al.] // Research Results in Pharmacology. - 2018. - Vol. 4, № 4.- P. 115-122. - Doi: 10.3897/rrpharmacology.4.32209. - Refer.: p. 121-122. | ru |
| dc.identifier.uri | http://dspace.bsu.edu.ru/handle/123456789/46292 | - |
| dc.description.abstract | In the current study, we present the results of the generation of a genetically modified mouse strain carrying a deletion in the HPRT1 gene. These mice can be effectively used for the preclinical testing of new drugs aimed at the treatment of Lesch-Nyhan syndrome | ru |
| dc.language.iso | en | ru |
| dc.subject | medicine | ru |
| dc.subject | pharmacology | ru |
| dc.subject | transgenic mice | ru |
| dc.subject | Lesch-Nyhan syndrome | ru |
| dc.subject | personalized medicine | ru |
| dc.subject | orphane deases | ru |
| dc.title | New personalized genetic mouse model of Lesch-Nyhan syndrome for pharmacology and gene therapy | ru |
| dc.type | Article | ru |
| Appears in Collections: | Vol. 4, № 4
|
