-
Autor
Erceg, Slaven 2 Machuca, Candela 2 Artero Castro, Ana 1 Bolinches-Amorós, Arantxa 1 Clemente, Eleonora 1 Correa-Vela, Marta 1 Darling, Alejandra 1 Espinos, Carmen 1 Espinós, Carmen 1 García-Navas, Deyanira 1 Jendelova, Pavla 1 Leon, Marian 1 Pascual-Pascual, Samuel Ignacio 1 Pérez-Dueñas, Belén 1 Sánchez-Alcázar, José Antonio 1 Vilches, Angel 1 Villalón-García, Irene 1
-
Pracoviště
Centro Andaluz de Biología del Desarr... 1 Centro de Investigación Biomédica en ... 1 Department of Genetics Universitat de... 1 Department of Pediatric Neurology Hos... 1 Department of Pediatric Neurology Hos... 1 Institute of Experimental Medicine De... 1 Institute of Experimental Medicine De... 1 National Stem Cell Bank Valencia Node... 1 National Stem Cell Bank Valencian Nod... 1 Rare Diseases Joint Units CIPF IIS La... 1 Servicio de Neuropediatría Hospital U... 1 Stem Cells Therapies in Neurodegenera... 1 Stem Cells Therapies in Neurodegenera... 1 Unit of Genetics and Genomics of Neur... 1 Unit of Pediatric Movement Disorders ... 1 Unit of Rare Neurodegenerative Diseas... 1 Universitat Autònoma de Barcelona Bar... 1
- Formát
- Publikační typ
- Check Tag
- Kategorie
- Jazyk
- Země
- Časopis/zdroj
- Dostupnost
- Vlastník
-
Autor
Erceg, Slaven 2 Machuca, Candela 2 Artero Castro, Ana 1 Bolinches-Amorós, Arantxa 1 Clemente, Eleonora 1 Correa-Vela, Marta 1 Darling, Alejandra 1 Espinos, Carmen 1 Espinós, Carmen 1 García-Navas, Deyanira 1 Jendelova, Pavla 1 Leon, Marian 1 Pascual-Pascual, Samuel Ignacio 1 Pérez-Dueñas, Belén 1 Sánchez-Alcázar, José Antonio 1 Vilches, Angel 1 Villalón-García, Irene 1
-
Pracoviště
Centro Andaluz de Biología del Desarr... 1 Centro de Investigación Biomédica en ... 1 Department of Genetics Universitat de... 1 Department of Pediatric Neurology Hos... 1 Department of Pediatric Neurology Hos... 1 Institute of Experimental Medicine De... 1 Institute of Experimental Medicine De... 1 National Stem Cell Bank Valencia Node... 1 National Stem Cell Bank Valencian Nod... 1 Rare Diseases Joint Units CIPF IIS La... 1 Servicio de Neuropediatría Hospital U... 1 Stem Cells Therapies in Neurodegenera... 1 Stem Cells Therapies in Neurodegenera... 1 Unit of Genetics and Genomics of Neur... 1 Unit of Pediatric Movement Disorders ... 1 Unit of Rare Neurodegenerative Diseas... 1 Universitat Autònoma de Barcelona Bar... 1
- Formát
- Publikační typ
- Check Tag
- Kategorie
- Jazyk
- Země
- Časopis/zdroj
- Dostupnost
- Vlastník
-
Machuca, Candela
Autor Machuca, Candela Unit of Rare Neurodegenerative Diseases, Centro de Investigación Príncipe Felipe (CIPF), Valencia, Spain Rare Diseases Joint Units, CIPF-IIS La Fe & INCLIVA, Valencia, Spain Stem Cells Therapies in Neurodegenerative Diseases Lab, Centro de Investigación Príncipe Felipe (CIPF), Valencia, Spain
- Correa-Vela, Marta
- García-Navas, Deyanira
- Darling, Alejandra
- Villalón-García, Irene
- Sánchez-Alcázar, José Antonio
- Pérez-Dueñas, Belén
-
Erceg, Slaven
Autor Erceg, Slaven Rare Diseases Joint Units, CIPF-IIS La Fe & INCLIVA, Valencia, Spain Stem Cells Therapies in Neurodegenerative Diseases Lab, Centro de Investigación Príncipe Felipe (CIPF), Valencia, Spain National Stem Cell Bank-Valencia Node, Biomolecular and Bioinformatics Resources Platform PRB2, ISCIII, Centro de Investigación Príncipe Felipe (CIPF), Valencia, Spain Institute of Experimental Medicine, Department of Tissue Cultures and Stem Cells, Czech Academy of Sciences, Prague, Czech Republic
- Espinós, Carmen
NLK
Directory of Open Access Journals
od 2014
Open Access Digital Library
od 2007-10-01
Open Access Digital Library
od 2014-01-01
Elsevier Open Access Journals
od 2007-10-01
ROAD: Directory of Open Access Scholarly Resources
od 2007
PubMed
34087982
DOI
10.1016/j.scr.2021.102338
Knihovny.cz E-zdroje
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 mutations in the PLA2G6 gene, was generated by non-integrative reprogramming technology using OCT3/4, SOX2, CMYC and KLF4 reprogramming factors. The pluripotency was assessed by immunocytochemistry and RT-PCR. Differentiation capacity was verified in vitro. This iPSC line can be further differentiated toward affected cells to better understand molecular mechanisms of disease and pathophysiology.
-
Machuca, Candela
Autor Machuca, Candela Stem Cells Therapies in Neurodegenerative Diseases Lab, Centro de Investigacion Principe Felipe (CIPF), Valencia, Spain Unit of Genetics and Genomics of Neuromuscular and Neurodegenerative Disorders and Service of Genomics and Translational Genetics, Centro de Investigación Príncipe Felipe (CIPF), Valencia, Spain
- Vilches, Angel
- Clemente, Eleonora
- Pascual-Pascual, Samuel Ignacio
- Bolinches-Amorós, Arantxa
- Artero Castro, Ana
- Espinos, Carmen
- Leon, Marian
- Jendelova, Pavla
-
Erceg, Slaven
Autor Erceg, Slaven Stem Cells Therapies in Neurodegenerative Diseases Lab, Centro de Investigacion Principe Felipe (CIPF), Valencia, Spain National Stem Cell Bank-Valencian Node, Platform for Proteomics, Genotyping and Cell Lines PRB3, Research Centre Principe Felipe, c/Eduardo Primo Yufera 3, 46012, Valencia, Spain Institute of Experimental Medicine, Department of Tissue Cultures and Stem Cells, Academy of Science of the Czech Republic, Prague, Czech Republic. Electronic address: serceg@cipf.es
NLK
Directory of Open Access Journals
od 2014
Open Access Digital Library
od 2007-10-01
Open Access Digital Library
od 2014-01-01
Elsevier Open Access Journals
od 2007-10-01
ROAD: Directory of Open Access Scholarly Resources
od 2007
PubMed
30384130
DOI
10.1016/j.scr.2018.10.016
Knihovny.cz E-zdroje
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 reprogramming factors. The pluripotency was assessed by immunocytochemistry and RT-PCR. This iPSC line can be used as control for Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) disease.
Sdílet
Název dokumentu
Po ukončení testovacího provozu bude odkaz přesměrován adresu produkční verze portálu Medvik.