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0579890 - ÚMG 2024 RIV CH eng J - Journal Article
Freke, G. M. - Martins, T. - Davies, R. J. - Beyer, T. - Seda, M. - Peskett, E. - Haq, N. - Prasai, Avishek - Otto, G. - Srikaran, J. J. - Hernandez, V. - Diwan, G. D. - Russell, R. B. - Ueffing, M. - Huranová, Martina - Boldt, K. - Beales, P. L. - Jenkins, D.
De-Suppression of Mesenchymal Cell Identities and Variable Phenotypic Outcomes Associated with Knockout of iBbs1/i.
Cells. Roč. 12, č. 22 (2023), č. článku 2662. E-ISSN 2073-4409
R&D Projects: GA ČR GA21-21612S; GA MŠMT(CZ) LM2015062; GA MŠMT(CZ) EF16_013/0001775; GA MŠMT LO1419
EU Projects: European Commission(CZ) CZ.2.16/3.1.00/21547
Institutional support: RVO:68378050
Keywords : bardet-biedl-syndrome * syndrome proteins * enrichment analysis * neural crest * disease * bbsome * Bardet-Biedl syndrome * primary cilia * epithelial-to-mesenchymal transition * kidney * collecting duct cells * Wnt signalling * fibrosis
OECD category: Cell biology
Impact factor: 6, year: 2022
Method of publishing: Open access
https://www.mdpi.com/2073-4409/12/22/2662
Permanent Link: https://hdl.handle.net/11104/0348675