Search results
- 1.0538918 - ÚEM 2023 RIV US eng J - Journal Article
Rodriguez-Jiménez, F.J. - Vilches, A. - Perez-Arago, M.A. - Clemente, E. - Roman, R. - Leal, J. - Castro, A.A. - Fustero, S. - Moreno-Manzano, V. - Jendelová, Pavla - Stojkovic, M. - Erceg, Slaven
Activation of Neurogenesis in Multipotent Stem Cells CulturedIn Vitroand in the Spinal Cord Tissue After Severe Injury by Inhibition of Glycogen Synthase Kinase-3.
Neurotherapeutics. Roč. 18, č. 1 (2021), s. 515-533. ISSN 1933-7213. E-ISSN 1878-7479
R&D Projects: GA MŠMT(CZ) EF15_003/0000419; GA MŠMT(CZ) LTAUSA17120
Institutional support: RVO:68378041
Keywords : spinal cord injury * stem cells * neurogenesis
OECD category: Neurosciences (including psychophysiology
Impact factor: 6.088, year: 2021
Method of publishing: Open access
https://link.springer.com/article/10.1007/s13311-020-00928-0
Permanent Link: http://hdl.handle.net/11104/0328086 - 2.0517479 - ÚEM 2021 RIV NL eng J - Journal Article
Machuca, C. - Vilches, A. - Clemente, E. - Pascual-Pascual, S.I. - Bolinches-Amorós, A. - Castro, A.A. - Espinos, C. - León, M. - Jendelová, Pavla - Erceg, Slaven
Generation of human induced pluripotent stem cell (iPSC) line from an unaffected female carrier of mutation in SACSIN gene.
Stem Cell Research. Roč. 33, dec. (2018), s. 166-170. ISSN 1873-5061. E-ISSN 1876-7753
R&D Projects: GA ČR(CZ) GBP304/12/G069; GA MŠMT(CZ) EF15_003/0000419
Institutional support: RVO:68378041
Keywords : ARSACs patient * induced pluripotent stem cells * reprogramming * non-integrative Sendai virus
OECD category: Human genetics
Impact factor: 3.929, year: 2018
Method of publishing: Open access
https://www.sciencedirect.com/science/article/pii/S1873506118302617?via%3Dihub
Permanent Link: http://hdl.handle.net/11104/0302788 - 3.0494382 - ÚEM 2019 RIV NL eng J - Journal Article
Arellano, C.M. - Vilches, A. - Clemente, E. - Pascual-Pascual, S.I. - Bolinches-Amorós, A. - Castro, A.A. - Espinos, C. - Rodriguez, M.L. - Jendelová, Pavla - Erceg, Slaven
Generation of a human iPSC line from a patient with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) caused by mutation in SACSIN gene.
Stem Cell Research. Roč. 31, aug (2018), s. 249-252. ISSN 1873-5061. E-ISSN 1876-7753
R&D Projects: GA ČR(CZ) GBP304/12/G069; GA MŠMT(CZ) EF15_003/0000419
Institutional support: RVO:68378041
Keywords : induced pluripotent stem cells * gene mutation * SACSIN * ARSACS * non-integrative reprogramming technology
OECD category: Cell biology
Impact factor: 3.929, year: 2018
Permanent Link: http://hdl.handle.net/11104/0294018 - 4.0478710 - ÚEM 2018 RIV US eng J - Journal Article
Lukovic, D. - Moreno-Manzano, V. - Rodriquez - Jimenez, F.J. - Vilches, A. - Syková, Eva - Jendelová, Pavla - Stojkovic, M. - Erceg, Slaven
hiPSC Disease Modeling of Rare Hereditary Cerebellar Ataxias: Opportunities and Future Challenges.
Neuroscientist. Roč. 23, č. 5 (2017), s. 554-566. ISSN 1073-8584. E-ISSN 1089-4098
R&D Projects: GA ČR(CZ) GBP304/12/G069; GA MŠMT(CZ) LO1309; GA MŠMT(CZ) ED1.1.00/02.0109
Institutional support: RVO:68378041
Keywords : 3D organoids * ataxia * disease modelling
OECD category: Developmental biology
Impact factor: 7.461, year: 2017
Permanent Link: http://hdl.handle.net/11104/0275496