0561877 - ÚMG 2023 RIV CH eng J - Journal Article
Syding, Linn Amanda - Kubik-Zahorodna, Agnieszka - Nickl, Petr - Novosadová, Vendula - Kopkanová, Jana - Kašpárek, Petr - Procházka, Jan - Sedláček, Radislav
Generation and Characterization of a Novel Angelman Syndrome Mouse Model with a Full Deletion of the Ube3a Gene.
Cells. Roč. 11, č. 18 (2022), č. článku 2815. E-ISSN 2073-4409
R&D Projects: GA MŠMT(CZ) LM2018126; GA MŠMT EF16_013/0001789; GA MŠMT EF18_046/0015861; GA MŠMT ED2.1.00/19.0395
Institutional support: RVO:68378050
Keywords : Angelman syndrome * ube3a * mouse model * neurodevelopmental disease * autism spectrum disorder
OECD category: Cell biology
Impact factor: 6, year: 2022
Method of publishing: Open access
https://www.mdpi.com/2073-4409/11/18/2815
Permanent Link: https://hdl.handle.net/11104/0338398
Syding, Linn Amanda - Kubik-Zahorodna, Agnieszka - Nickl, Petr - Novosadová, Vendula - Kopkanová, Jana - Kašpárek, Petr - Procházka, Jan - Sedláček, Radislav
Generation and Characterization of a Novel Angelman Syndrome Mouse Model with a Full Deletion of the Ube3a Gene.
Cells. Roč. 11, č. 18 (2022), č. článku 2815. E-ISSN 2073-4409
R&D Projects: GA MŠMT(CZ) LM2018126; GA MŠMT EF16_013/0001789; GA MŠMT EF18_046/0015861; GA MŠMT ED2.1.00/19.0395
Institutional support: RVO:68378050
Keywords : Angelman syndrome * ube3a * mouse model * neurodevelopmental disease * autism spectrum disorder
OECD category: Cell biology
Impact factor: 6, year: 2022
Method of publishing: Open access
https://www.mdpi.com/2073-4409/11/18/2815
Permanent Link: https://hdl.handle.net/11104/0338398