0521524 - ÚMG 2020 RIV GB eng J - Journal Article
Szczerkowska, Katarzyna - Petrezselyova, Silvia - Lindovský, Jiří - Pálková, Marcela - Dvořák, Jan - Makovický, Peter - Fang, M. - Jiang, C. - Chen, L. - Shi, M. - Liu, W. - Zhang, J. - Kubik-Zahorodna, Agnieszka - Schuster, Bjorn - Beck, Inken - Novosadová, Vendula - Procházka, Jan - Sedláček, Radislav
Myopia disease mouse models: a missense point mutation (S673G) and a protein-truncating mutation of the Zfp644 mimic human disease phenotype.
Cell and Bioscience. Roč. 9, February (2019), č. článku 21. E-ISSN 2045-3701
R&D Projects: GA MŠMT(CZ) LH14276; GA MŠMT(CZ) LM2015040; GA MŠMT(CZ) ED1.1.00/02.0109; GA MŠMT(CZ) LQ1604; GA ČR GA19-21696S; GA MŠMT ED2.1.00/19.0395
Institutional support: RVO:68378050
Keywords : Myopia * Mouse model * Genetics * Zinc finger 644 * Vision * Eye
OECD category: Genetics and heredity (medical genetics to be 3)
Impact factor: 5.026, year: 2019 ; AIS: 1.092, rok: 2019
Method of publishing: Open access
Result website:
https://cellandbioscience.biomedcentral.com/articles/10.1186/s13578-019-0280-4DOI: https://doi.org/10.1186/s13578-019-0280-4
Permanent Link: http://hdl.handle.net/11104/0306124