Portal de investigación
3D retinas derivadas de células iPS como herramienta para encontrar terapias eficaces para enfermedades hereditarias de la retina
Datos básicos
- Código Financiador:
- Año inicial:
- 2017
- Año final:
- 2020
Documentos
- No hay documentos
Participantes
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
Deciphering retinal diseases through the generation of three dimensional stem cell-derived organoids: Concise Review.
Artero Castro A; (...); Erceg S
Article. 10.1002/stem.3089. 2019
Gene-edited mouse models and human retinal organoids to study the function of CERKL, NR2E3 and ATXN3 genes in inherited retinal dystrophies
Marfany, G; (...); Gonzalez-Duarte, R
Meeting Abstract. 2019
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 an iPSC line from a retinitis pigmentosa patient carrying a homozygous mutation in CERKL and a healthy sibling
Bolinches-Amorós A; (...); Lukovic D
Editorial Material. 10.1016/j.scr.2019.101455. 2019
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
Short Review: Investigating ARSACS: models for understanding cerebellar degeneration
Artero Castro A; (...); Erceg S
Review. 10.1111/nan.12540. 2019
The identification of small molecules that stimulate retinal pigment epithelial cells: potential novel therapeutic options for treating retinopathies
Artero-Castro, A; (...); Erceg, S
Review. 10.1080/17460441.2019.1559148. 2019
Transcriptome-based molecular staging of human stem cell-derived retinal organoids uncovers accelerated photoreceptor differentiation by 9-cis retinal
Kaya, KD; (...); Swaroop, A
Article. 2019