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Slaven Erceg

Showing results (51-60 of 80) with videos related to

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Stem Cell Research|November 2, 2018
Generation of human induced pluripotent stem cell (iPSC) line from an unaffected female carrier of mutation in SACSIN geneCandela Machuca, Angel Vilches, Eleonora Clemente, et al.
Neurochemistry International|August 18, 2004
Alterations in soluble guanylate cyclase content and modulation by nitric oxide in liver diseaseRegina Rodrigo, Carmina Montoliu, Nicolas Chatauret, et al.
Toxins|April 13, 2019
Assessment of Toxic Effects of Ochratoxin A in Human Embryonic Stem CellsSlaven Erceg, Eva María Mateo, Iván Zipancic, et al.
Stem Cell Research|June 5, 2021
Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patientsCandela Machuca, Marta Correa-Vela, Deyanira García-Navas, et al.
Biomedicines|February 25, 2023
Retinal Pigment Epithelium Cell Development: Extrapolating Basic Biology to Stem Cell ResearchSantosh Gupta, Lyubomyr Lytvynchuk, Taras Ardan, et al.
Stem Cells (Dayton, Ohio)|January 31, 2013
Hypoxia increases the yield of photoreceptors differentiating from mouse embryonic stem cells and improves the modeling of retinogenesis in vitroMarcela Garita-Hernández, Francisco Diaz-Corrales, Dunja Lukovic, et al.
Stem Cell Research|January 7, 2019
Generation of gene-corrected human induced pluripotent stem cell lines derived from retinitis pigmentosa patient with Ser331Cysfs*5 mutation in MERTKAna Artero Castro, Kathleen Long, Andrew Bassett, et al.
Journal of Tissue Engineering and Regenerative Medicine|March 28, 2013
Methacrylate-endcapped caprolactone and FM19G11 provide a proper niche for spinal cord-derived neural cellsTeresa Valdes-Sánchez, Francisco Javier Rodriguez-Jimenez, Dunia M García-Cruz, et al.
Stem Cell Research|February 18, 2018
Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 geneArantxa Bolinches-Amorós, Dunja Lukovic, Ana Artero Castro, et al.
Stem Cell Research|August 26, 2018
Generation of a human iPSC line from a patient with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) caused by mutation in SACSIN geneCandela Machuca Arellano, Angel Vilches, Eleonora Clemente, et al.
Pageof 8

Showing results (51-60 of 80) with videos related to

Sort By:
Pageof 8
Stem Cell Research|November 2, 2018
Generation of human induced pluripotent stem cell (iPSC) line from an unaffected female carrier of mutation in SACSIN geneCandela Machuca, Angel Vilches, Eleonora Clemente, et al.
Neurochemistry International|August 18, 2004
Alterations in soluble guanylate cyclase content and modulation by nitric oxide in liver diseaseRegina Rodrigo, Carmina Montoliu, Nicolas Chatauret, et al.
Toxins|April 13, 2019
Assessment of Toxic Effects of Ochratoxin A in Human Embryonic Stem CellsSlaven Erceg, Eva María Mateo, Iván Zipancic, et al.
Stem Cell Research|June 5, 2021
Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patientsCandela Machuca, Marta Correa-Vela, Deyanira García-Navas, et al.
Biomedicines|February 25, 2023
Retinal Pigment Epithelium Cell Development: Extrapolating Basic Biology to Stem Cell ResearchSantosh Gupta, Lyubomyr Lytvynchuk, Taras Ardan, et al.
Stem Cells (Dayton, Ohio)|January 31, 2013
Hypoxia increases the yield of photoreceptors differentiating from mouse embryonic stem cells and improves the modeling of retinogenesis in vitroMarcela Garita-Hernández, Francisco Diaz-Corrales, Dunja Lukovic, et al.
Stem Cell Research|January 7, 2019
Generation of gene-corrected human induced pluripotent stem cell lines derived from retinitis pigmentosa patient with Ser331Cysfs*5 mutation in MERTKAna Artero Castro, Kathleen Long, Andrew Bassett, et al.
Journal of Tissue Engineering and Regenerative Medicine|March 28, 2013
Methacrylate-endcapped caprolactone and FM19G11 provide a proper niche for spinal cord-derived neural cellsTeresa Valdes-Sánchez, Francisco Javier Rodriguez-Jimenez, Dunia M García-Cruz, et al.
Stem Cell Research|February 18, 2018
Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 geneArantxa Bolinches-Amorós, Dunja Lukovic, Ana Artero Castro, et al.
Stem Cell Research|August 26, 2018
Generation of a human iPSC line from a patient with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) caused by mutation in SACSIN geneCandela Machuca Arellano, Angel Vilches, Eleonora Clemente, et al.
Pageof 8