Search results
- 1.0575029 - ÚŽFG 2024 RIV US eng J - Journal Article
Celiker, C. - Weissová, Kamila - Černá, K. A. - Oppelt, J. - Dorgau, B. - Gambin, F. M. - Šebestíková, J. - Lako, M. - Sernagor, E. - Lisková, P. - Bárta, T.
Light-responsive microRNA molecules in human retinal organoids are differentially regulated by distinct wavelengths of light.
iScience. Roč. 26, č. 7 (2023), č. článku 107237. E-ISSN 2589-0042
R&D Projects: GA MZd NU22-07-00380
Institutional support: RVO:67985904
Keywords : human retina * wavelenghts of light
OECD category: Cell biology
Impact factor: 5.8, year: 2022
Method of publishing: Open access
https://www.sciencedirect.com/science/article/pii/S2589004223013147?via%3Dihub
Permanent Link: https://hdl.handle.net/11104/0345014 - 2.0472714 - ÚMG 2017 RIV US eng J - Journal Article
Davidson, A.E. - Lisková, P. - Evans, C.J. - Dudakova, L. - Nosková, L. - Pontikos, N. - Hartmannová, H. - Hodanová, K. - Stránecký, V. - Kozmik, Zbyněk - Levis, H.J. - Idigo, N. - Sasai, N. - Maher, G.J. - Bellingham, J. - Veli, N. - Ebenezer, N.D. - Cheetham, M.E. - Daniels, J.T. - Thaung, C.M.H. - Jirsová, K. - Plagnol, V. - Filipec, M. - Kmoch, S. - Tuft, S.J. - Hardcastle, A.J.
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2.
American Journal of Human Genetics. Roč. 98, č. 1 (2016), s. 75-89. ISSN 0002-9297. E-ISSN 1537-6605
R&D Projects: GA MŠMT(CZ) ED1.1.00/02.0109; GA MZd(CZ) NT13116; GA MZd(CZ) NV15-28208A; GA MŠMT(CZ) 7F14156
Institutional support: RVO:68378050
Keywords : gene * cells * chromosome-20 * linkage * differentiation * identification * expression * management * membrane * adhesion
Subject RIV: EB - Genetics ; Molecular Biology
Impact factor: 9.025, year: 2016
Permanent Link: http://hdl.handle.net/11104/0269945 - 3.0425276 - ÚMG 2014 RIV DK eng J - Journal Article
Lisková, P. - Ulmanová, O. - Těšina, Petr - Melsová, H. - Diblik, P. - Hansíková, H. - Tesařová, M. - Votruba, M.
Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder.
Acta Ophthalmologica. Roč. 91, č. 3 (2013), e225-e231. ISSN 1755-375X. E-ISSN 1755-3768
Institutional research plan: CEZ:AV0Z50520514
Keywords : ataxia * autosomal dominant * deafness * encephalomyopathy
Subject RIV: EB - Genetics ; Molecular Biology
Impact factor: 2.512, year: 2013
Permanent Link: http://hdl.handle.net/11104/0231199 - 4.0392766 - ÚOCHB 2014 RIV DK eng J - Journal Article
Lisková, P. - Ulmanová, O. - Těšina, Petr - Melsová, H. - Diblik, P. - Hansíková, H. - Tesařová, M. - Votruba, M.
Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder.
Acta Ophthalmologica. Roč. 91, č. 3 (2013), E225-E231. ISSN 1755-375X. E-ISSN 1755-3768
Grant - others:GA MZd(CZ) NT11190
Institutional research plan: CEZ:AV0Z40550506
Keywords : ataxia * autosomal dominant * deafness * encephalomyopathy
Subject RIV: FF - HEENT, Dentistry
Impact factor: 2.512, year: 2013
Permanent Link: http://hdl.handle.net/11104/0221562 - 5.0345733 - ÚEM 2011 RIV GB eng J - Journal Article
Brejchová, K. - Lisková, P. - Čejková, Jitka - Jirsová, K.
Role of matrix metalloproteinases in recurrent corneal melting.
Experimental Eye Research. Roč. 90, č. 5 (2010), s. 583-590. ISSN 0014-4835. E-ISSN 1096-0007
Institutional research plan: CEZ:AV0Z50390512
Keywords : corneal melting * extracellular matrix degradation * matrix metalloproteinases
Subject RIV: FF - HEENT, Dentistry
Impact factor: 2.817, year: 2010
http://arl-repository.lib.cas.cz/uloziste_av/UEM-P/cav_un_epca-0345733_01.pdf
Permanent Link: http://hdl.handle.net/11104/0186936