Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Yuliya Y. Silaeva"'
Autor:
Anna V. Polikarpova, Tatiana V. Egorova, Evgenii A. Lunev, Alexandra A. Tsitrina, Svetlana G. Vassilieva, Irina M. Savchenko, Yuliya Y. Silaeva, Alexey V. Deykin, Maryana V. Bardina
Publikováno v:
Frontiers in Genome Editing, Vol 5 (2023)
The development of personalized medicine for genetic diseases requires preclinical testing in the appropriate animal models. GNAO1 encephalopathy is a severe neurodevelopmental disorder caused by heterozygous de novo mutations in the GNAO1 gene. GNAO
Externí odkaz:
https://doaj.org/article/23346d150ced45478ada50824f70075c
Autor:
Zamkova M; 'N. N. Blokhin National Medical Research Centre of Oncology' of the Health Ministry of Russia, Moscow, Russia., Kalinina A; 'N. N. Blokhin National Medical Research Centre of Oncology' of the Health Ministry of Russia, Moscow, Russia., Silaeva Y; Institute of Gene Biology, Russian Academy of Sciences, Moscow, Russia., Persiyantseva N; 'N. N. Blokhin National Medical Research Centre of Oncology' of the Health Ministry of Russia, Moscow, Russia., Bruter A; Russian Academy of Sciences, Engelhardt Institute of Molecular Biology, Moscow, Russia., Deikin A; Institute of Gene Biology, Russian Academy of Sciences, Moscow, Russia., Khromykh L; 'N. N. Blokhin National Medical Research Centre of Oncology' of the Health Ministry of Russia, Moscow, Russia., Kazansky D; 'N. N. Blokhin National Medical Research Centre of Oncology' of the Health Ministry of Russia, Moscow, Russia.
Publikováno v:
Oncotarget [Oncotarget] 2019 Aug 06; Vol. 10 (47), pp. 4808-4821. Date of Electronic Publication: 2019 Aug 06 (Print Publication: 2019).