Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Ana Artero Castro"'
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 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
Autor:
Arantxa Bolinches-Amorós, Dunja Lukovic, Ana Artero Castro, Marian León, Kunka Kamenarova, Radka Kaneva, Pavla Jendelova, Fiona Blanco-Kelly, Carmen Ayuso, Marta Cortón, Slaven Erceg
Publikováno v:
Stem Cell Research, Vol 28, Iss , Pp 96-99 (2018)
The human iPSC cell line, GLC-FiPS4F1 (ESi047-A), derived from dermal fibroblast from the patient with congenital glaucoma caused by the mutation of the gene CYP1B1, was generated by non-integrative reprogramming technology using OCT3/4, SOX2, CMYC a
Externí odkaz:
https://doaj.org/article/01f270337c324567810fb2c2a6dca75a
Publikováno v:
Stem Cell Research, Vol 28, Iss , Pp 157-160 (2018)
The human iPSC cell line, derived from foreskin fibroblasts was generated by non-integrative, non-viral reprogramming technology using OCT4, SOX2, KLF4, LIN28, c-MYC mRNAs.
Externí odkaz:
https://doaj.org/article/b5724c9ae6ce46f39735cedf9ded037d
Autor:
Ana Artero Castro, Kathleen Long, Andrew Bassett, Candela Machuca, Marian León, Almudena Ávila-Fernandez, Marta Cortón, Toni Vidal-Puig, Carmen Ayuso, Dunja Lukovic, Slaven Erceg
Publikováno v:
Stem Cell Research, Vol 34, Iss , Pp - (2019)
The human induced pluripotent stem cell (hiPSC) line RP1-FiPS4F1 generated from the patient with autosomal recessive retinitis pigmentosa (arRP) caused by homozygous Ser331Cysfs*5 mutation in Mer tyrosine kinase receptor (MERTK) was genetically corre
Externí odkaz:
https://doaj.org/article/77eb224cd7874491953401fb390c2b30
Autor:
Dunja Lukovic, Aranzazu Bolinches Amoros, Ana Artero Castro, Beatriz Pascual, Miguel Carballo, Imma Hernán, Slaven Erceg
Publikováno v:
Stem Cell Research, Vol 21, Iss C, Pp 23-25 (2017)
The human iPSC cell line, RP2-FiPS4F1 (RCPFi001-A), derived from dermal fibroblasts from the patient with retinitis pigmentosa caused by the mutation of the gene PRPF8, was generated by non-integrative reprogramming technology using OCT3/4, SOX2, CMY
Externí odkaz:
https://doaj.org/article/741dccf33a7f438280644209b59f08a7
Autor:
Ana Artero-Castro, Kathleen Long, Andrew Bassett, Almudena Ávila-Fernandez, Marta Cortón, Antonio Vidal-Puig, Pavla Jendelova, Francisco Javier Rodriguez-Jimenez, Eleonora Clemente, Carmen Ayuso, Slaven Erceg
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 4, p 2092 (2021)
Hereditary retinal dystrophies (HRD) represent a significant cause of blindness, affecting mostly retinal pigment epithelium (RPE) and photoreceptors (PRs), and currently suffer from a lack of effective treatments. Highly specialized RPE and PR cells
Externí odkaz:
https://doaj.org/article/e451dc4c6e53475f8e2dc5999d6e62de
Autor:
Taras Ardan, Slaven Erceg, Ana Artero‐Castro, Hana Studenovská, Brigitte Mueller, Knut Stieger, Štěpan Popelka, Lyubomyr Lytvynchuk, Zbyněk Straňák, Lucie Tichotová, Zdeňka Ellederová, Jana Čížková, Jana Juhásová, Jan Motlík, Goran Petrovski
Publikováno v:
Acta Ophthalmologica. 100
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ba0e9477244ba3dab02158075a39c13
https://doi.org/10.1111/j.1755-3768.2022.0105
https://doi.org/10.1111/j.1755-3768.2022.0105
Autor:
T. Ardan, Anna Brymová, Saskia Drutovič, Lucie Tichotová, Pavla Jendelova, Miroslava Sedláčková, Ana Artero-Castro, Zdeňka Ellederová, Jan Motlik, Goran Petrovski, Lyubomyr Lytvynchuk, Štěpán Popelka, S. S. Rohiwal, Zbyněk Straňák, Yaroslav Nemesh, Slaven Erceg, Hana Studenovská
Publikováno v:
Acta Ophthalmologica. 100
Purpose Dysfunction of the retinal pigment epithelium (RPE) causes numerous forms of retinal degeneration. RPE replacement is a modern option to save vision. We aimed to test the results of transplanting cultured RPEs on biocompatible membranes. Meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff9a873eb12fd0be3148f73c5b8174b8
https://doi.org/10.1111/aos.15034
https://doi.org/10.1111/aos.15034