Zobrazeno 1 - 10
of 126
pro vyhledávání: '"Slaven Erceg"'
Publikováno v:
Journal of Advanced Research, Vol 54, Iss , Pp 105-118 (2023)
Background: Synaptic dysfunction is a major contributor to Alzheimeŕs disease (AD) pathogenesis in addition to the formation of neuritic β-amyloid plaques and neurofibrillary tangles of hyperphosphorylated Tau protein. However, how these features
Externí odkaz:
https://doaj.org/article/c8db61961ddf4949b9acbca33d3b4387
Publikováno v:
Stem Cell Research & Therapy, Vol 14, Iss 1, Pp 1-11 (2023)
Abstract Ependymal cells, a dormant population of ciliated progenitors found within the central canal of the spinal cord, undergo significant alterations after spinal cord injury (SCI). Understanding the molecular events that induce ependymal cell ac
Externí odkaz:
https://doaj.org/article/9abfd59a86524c5abe4a002a5cdec608
Autor:
Santosh Gupta, Lyubomyr Lytvynchuk, Taras Ardan, Hana Studenovska, Georgina Faura, Lars Eide, Ljubo Znaor, Slaven Erceg, Knut Stieger, Jan Motlik, Kapil Bharti, Goran Petrovski
Publikováno v:
Biomedicines, Vol 11, Iss 2, p 310 (2023)
The retinal pigment epithelium (RPE) forms an important cellular monolayer, which contributes to the normal physiology of the eye. Damage to the RPE leads to the development of degenerative diseases, such as age-related macular degeneration (AMD). Ap
Externí odkaz:
https://doaj.org/article/6d2f10bd906d4f7d9307110dfc09a9a3
Autor:
Dunja Lukovic, Ana Artero Castro, Marian León, Verónica del Buey Furió, Marta Cortón, Carmen Ayuso, Slaven Erceg
Publikováno v:
Stem Cell Research, Vol 33, Iss , Pp 151-155 (2018)
The human induced pluripotent stem cell (hiPSC) line, derived from dermal fibroblasts from Leber congenital amaurosis patient with homozygous mutation c.265 T > C, p.Cys89Arg in aryl hydrocarbon receptor-interacting protein-like 1 (AIPL1) was generat
Externí odkaz:
https://doaj.org/article/8639abdda911492687cdfb7f7d911aee
Autor:
Candela Machuca, Angel Vilches, Eleonora Clemente, Samuel Ignacio Pascual-Pascual, Arantxa Bolinches-Amorós, Ana Artero Castro, Carmen Espinos, Marian Leon, Pavla Jendelova, Slaven Erceg
Publikováno v:
Stem Cell Research, Vol 33, Iss , Pp 166-170 (2018)
The human iPSC cell line, CARS-FiPS4F1 (ESi064-A), derived from dermal fibroblast from the apparently healthy carrier of the mutation of the gene SACSIN, was generated by non-integrative reprogramming technology using OCT3/4, SOX2, CMYC and KLF4 repr
Externí odkaz:
https://doaj.org/article/6099d90be0f440dab9874731f3220b0f
Autor:
Candela Machuca, Marta Correa-Vela, Deyanira García-Navas, Alejandra Darling, Irene Villalón-García, José Antonio Sánchez-Alcázar, Belén Pérez-Dueñas, Slaven Erceg, Carmen Espinós
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102338- (2021)
The human iPSC cell lines, PLANFiPS1-Sv4F-1 (RCPFi004-A), PLANFiPS2-Sv4F-1 (RCPFi005-A), PLANFiPS3-Sv4F-1 RCPFi006-A), derived from dermal fibroblast from three patients suffering PLAN (PLA2G6-associated neurodegeneration; MIM 256600) caused by mutat
Externí odkaz:
https://doaj.org/article/1a353abcb7a84e1589a0d39f34e813f1
Autor:
Ángeles Arzalluz-Luque, Jose Luis Cabrera, Heli Skottman, Alberto Benguria, Arantxa Bolinches-Amorós, Nicolás Cuenca, Vincenzo Lupo, Ana Dopazo, Sonia Tarazona, Bárbara Delás, Miguel Carballo, Beatriz Pascual, Imma Hernan, Slaven Erceg, Dunja Lukovic
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Retinitis pigmentosa (RP) is a rare, progressive disease that affects photoreceptors and retinal pigment epithelial (RPE) cells with blindness as a final outcome. Despite high medical and social impact, there is currently no therapeutic options to sl
Externí odkaz:
https://doaj.org/article/347373adf3fd4a898beb0087c33bbc18
Autor:
Lyubomyr Lytvynchuk, Annabelle Ebbert, Hana Studenovska, Richárd Nagymihály, Natasha Josifovska, David Rais, Štěpán Popelka, Lucie Tichotová, Yaroslav Nemesh, Jana Čížková, Jana Juhásová, Štefan Juhás, Pavla Jendelová, Janka Franeková, Igor Kozak, Slaven Erceg, Zbynek Straňák, Brigitte Müller, Zdenka Ellederová, Jan Motlík, Knut Stieger, Taras Ardan, Goran Petrovski
Publikováno v:
Biomedicines, Vol 10, Iss 3, p 669 (2022)
Purpose: The development of primary human retinal pigmented epithelium (hRPE) for clinical transplantation purposes on biodegradable scaffolds is indispensable. We hereby report the results of the subretinal implantation of hRPE cells on nanofibrous
Externí odkaz:
https://doaj.org/article/5d73f0ae7dea408d92490324821988b6
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 7 (2019)
The neurogenic niche of the subventricular zone (SVZ) in adult brain tissue takes the form of a pinwheel-like cytoarchitectural structure, with mono-ciliated astrocytes displaying neural stem cell (NSC) characteristics present in the core surrounded
Externí odkaz:
https://doaj.org/article/559f55ced1d04805854ba8c22b9019af
Autor:
Candela Machuca Arellano, Angel Vilches, Eleonora Clemente, Samuel Ignacio Pascual-Pascual, Arantxa Bolinches-Amorós, Ana Artero Castro, Carmen Espinos, Marian Leon Rodriguez, Pavla Jendelova, Slaven Erceg
Publikováno v:
Stem Cell Research, Vol 31, Iss , Pp 249-252 (2018)
The human iPSC cell line, ARS-FiPS4F1 (ESi063-A), derived from dermal fibroblast from the patient autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) caused by mutations on the gene SACSIN, was generated by non-integrative reprogrammin
Externí odkaz:
https://doaj.org/article/0e4c7322f2a443f193c4de107a9fca4b