Portal de investigación
Estudio preclínico de terapia celular con progenitores neurales derivados de hESC e ihPSC combinado con modulación de astroglia en tratamiento de lesiones medulares
Datos básicos
- Código Financiador:
- Año inicial:
- 2015
- Año final:
- 2018
Documentos
- No hay documentos
Participantes
Grupos de Investigación
Financiadores
Resultados del Proyecto
3D Retinal Cups from Human iPS Cells Display Differentiated Subtypes of Amacrine Cells and Immature Synaptic Contacts
Lukovic, D; (...); Erceg, S
Meeting Abstract. 2017
Concise Review: Human Induced Pluripotent Stem Cell Models of Retinitis Pigmentosa
Castro, AA; (...); Erceg, S
Review. 10.1002/stem.2783. 2018
Connexin 50 Expression in Ependymal Stem Progenitor Cells after Spinal Cord Injury Activation
Rodriguez-Jimenez, FJ; (...); Moreno-Manzano, V
Article. 10.3390/ijms161125981. 2015
Connexin 50 modulates Sox2 expression in spinal-cord-derived ependymal stem/progenitor cells
Rodriguez-Jimenez, F; (...); Moreno-Manzano, V
Article. 10.1007/s00441-016-2421-y. 2016
Current developments in cell- and biomaterial-based approaches for stroke repair
Jendelova, P; (...); Sykova, E
Review. 10.1517/14712598.2016.1094457. 2016
FM19G11 and Ependymal Progenitor/Stem Cell Combinatory Treatment Enhances Neuronal Preservation and Oligodendrogenesis after Severe Spinal Cord Injury
Alastrue-Agudo, A; (...); Moreno-Manzano, V
Article. 10.3390/ijms19010200. 2018
Generation of a human iPSC line by mRNA reprogramming
Castro, AA; (...); Lukovic, D
Editorial Material. 10.1016/j.scr.2018.02.011. 2018
Generation of a human iPSC line by mRNA reprogramming (vol 28, pg 157, 218)
Castro, AA; (...); Lukovic, D
Correction. 10.1016/j.scr.2018.06.012. 2018
Generation of a human iPSC line from a patient with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) caused by mutation in SACSIN gene
MACHUCA, C.; (...); ERCEG, S.
Editorial Material. 10.1016/j.scr.2018.07.012. 2018
Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 gene
Bolinches-Amoros, A; (...); Erceg, S
Editorial Material. 10.1016/j.scr.2018.01.004. 2018
Generation of a human iPSC line from a patient with Leber congenital amaurosis caused by mutation in AIPL1
Lukovic, D; (...); Erceg, S
Editorial Material. 10.1016/j.scr.2018.10.012. 2018
Generation of a human iPSC line froma patient with retinitis pigmentosa caused by mutation in PRPF8 gene
DUNJA LUKOVIC; (...); SLAVEN ERCEG VUKICEVIC
Editorial Material. 10.1016/j.scr.2017.03.007. 2017
Generation of gene-corrected human induced pluripotent stem cell lines derived from retinitis pigmentosa patient with Ser331Cysfs*5 mutation in MERTK
Artero Castro A; (...); Erceg S
Editorial Material. 10.1016/j.scr.2018.11.003. 2019
Generation of human induced pluripotent stem cell (iPSC) line from an unaffected female carrier of mutation in SACSIN gene
Machuca, C; (...); Erceg, S
Editorial Material. 10.1016/j.scr.2018.10.016. 2018
Highly Efficient Neural Conversion of Human Pluripotent Stem Cells in Adherent and Animal-Free Conditions
Lukovic, D; (...); Erceg, S
Article. 10.1002/sctm.16-0371. 2017
hiPSC Disease Modeling of Rare Hereditary Cerebellar Ataxias: Opportunities and Future Challenges
Lukovic, D; (...); Erceg, S
Article. 10.1177/1073858416672652. 2017
IN VITRO MODULATION OF GSK3 PATHWAY IN MOUSE EPENDYMAL AND HUMAN PLURIPOTENT STEM CELLS AS A STRATEGY FOR DEVELOPMENT OF NEW CELL TREATMENTS FOR SPINAL CORD INJURY
Erceg, S; (...); Lukovic, D
Meeting Abstract. 2016
Neural Stem Cells Derived from Human-Induced Pluripotent Stem Cells and Their Use in Models of CNS Injury
Jendelova P, Sykova E, Erceg S
Article. 10.1007/978-3-319-93485-3_3. 2018
Stem Cell-Based Therapy in Transplantation and Immune-Mediated Diseases
Volarevic, V; (...); Stojkovic, M
Editorial Material. 10.1155/2017/7379136. 2017
Stem Cells and Labeling for Spinal Cord Injury
Gazdic, M; (...); Stojkovic, M
Review. 10.3390/ijms18010006. 2017