Search results
- 1.0570587 - ÚMG 2024 RIV CH eng J - Journal Article
Syding, Linn Amanda - Kubik-Zahorodna, Agnieszka - Reguera, David Pajuelo - Nickl, Petr - Hrušková, Bohdana - Králíková, Michaela - Kopkanová, Jana - Novosadová, Vendula - Kašpárek, Petr - Procházka, Jan - Rozman, Jan - Tureček, Rostislav - Sedláček, Radislav
Ablation of Gabra5 Influences Corticosterone Levels and Anxiety-like Behavior in Mice.
Genes. Roč. 14, č. 2 (2023), č. článku 285. E-ISSN 2073-4425
R&D Projects: GA MŠMT(CZ) LM2018126; GA MŠMT EF16_013/0001789; GA MŠMT EF18_046/0015861; GA MŠMT ED2.1.00/19.0395; GA ČR(CZ) GA19-09283S
EU Projects: European Commission(XE) 765269 - EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions
Grant - others:AV ČR(CZ) StrategieAV21/29
Program: StrategieAV
Institutional support: RVO:68378041 ; RVO:68378050
Keywords : corticosterone * GABA receptor * anxiety * behavior * mouse model
OECD category: Technologies involving identifying the functioning of DNA, proteins and enzymes and how they influence the onset of disease and maintenance of well-being (gene-based diagnostics and therapeutic interventions (pharmacogenomics, gene-based therapeutics); Neurosciences (including psychophysiology (UEM-P)
Impact factor: 3.5, year: 2022
Method of publishing: Open access
https://www.mdpi.com/2073-4425/14/2/285
Permanent Link: https://hdl.handle.net/11104/0341891 - 2.0561877 - 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 - 3.0531015 - ÚMG 2021 RIV CH eng J - Journal Article
Syding, Linn Amanda - Nickl, Petr - Kašpárek, Petr - Sedláček, Radislav
CRISPR/Cas9 Epigenome Editing Potential for Rare Imprinting Diseases: A Review.
Cells. Roč. 9, č. 4 (2020), č. článku 993. E-ISSN 2073-4409
R&D Projects: GA MŠMT(CZ) LM2015040; GA MŠMT(CZ) LM2018126; GA MŠMT(CZ) ED1.1.00/02.0109
Institutional support: RVO:68378050
Keywords : rare disease * crispr * Cas9 * epigenome editing * transcriptome editing * genomic imprinting * Angelman syndrome * Prader-Willi syndrome * transient neonatal diabetes mellitus * Silver-Russell syndrome
OECD category: Genetics and heredity (medical genetics to be 3)
Impact factor: 6.600, year: 2020
Method of publishing: Open access
https://www.mdpi.com/2073-4409/9/4/993
Permanent Link: http://hdl.handle.net/11104/0309782