Celine Nanteau

Paris, 75012, France

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 13 publications

Bankable human iPSC-derived retinal progenitors represent a valuable source of multipotent cells.

Bankable human iPSC-derived retinal progenitors represent a valuable source of multipotent cells.

Journal: Communications biology

Published: February 21, 2022

Modeling PRPF31 retinitis pigmentosa using retinal pigment epithelium and organoids combined with gene augmentation rescue.

Modeling PRPF31 retinitis pigmentosa using retinal pigment epithelium and organoids combined with gene augmentation rescue.

Journal: NPJ Regenerative medicine

Published: December 08, 2021

Dynamic full-field optical coherence tomography allows live imaging of retinal pigment epithelium stress model.

Dynamic full-field optical coherence tomography allows live imaging of retinal pigment epithelium stress model.

Journal: Communications biology

Published: July 22, 2021

Reproducing diabetic retinopathy features using newly developed human induced-pluripotent stem cell-derived retinal Müller glial cells.

Reproducing diabetic retinopathy features using newly developed human induced-pluripotent stem cell-derived retinal Müller glial cells.

Journal: Glia

Published: August 28, 2020

Generation of a Transplantable Population of Human iPSC-Derived Retinal Ganglion Cells.

Generation of a Transplantable Population of Human iPSC-Derived Retinal Ganglion Cells.

Journal: Frontiers in cell and developmental biology

Published: July 21, 2020

Reprogramming of Adult Retinal Müller Glial Cells into Human-Induced Pluripotent Stem Cells as an Efficient Source of Retinal Cells.

Reprogramming of Adult Retinal Müller Glial Cells into Human-Induced Pluripotent Stem Cells as an Efficient Source of Retinal Cells.

Journal: Stem cells international

Published: April 04, 2019

Defined Xeno-free and Feeder-free Culture Conditions for the Generation of Human iPSC-derived Retinal Cell Models.

Defined Xeno-free and Feeder-free Culture Conditions for the Generation of Human iPSC-derived Retinal Cell Models.

Journal: Journal of visualized experiments : JoVE

Published: September 25, 2018

Characterization and Transplantation of CD73-Positive Photoreceptors Isolated from Human iPSC-Derived Retinal Organoids.

Characterization and Transplantation of CD73-Positive Photoreceptors Isolated from Human iPSC-Derived Retinal Organoids.

Journal: Stem cell reports

Published: March 07, 2018

Establishment of an induced pluripotent stem (iPS) cell line from dermal fibroblasts of an asymptomatic patient with dominant PRPF31 mutation.

Establishment of an induced pluripotent stem (iPS) cell line from dermal fibroblasts of an asymptomatic patient with dominant PRPF31 mutation.

Journal: Stem cell research

Published: September 25, 2017

Generation of an induced pluripotent stem cell (iPSC) line from a patient with autosomal dominant retinitis pigmentosa due to a mutation in the NR2E3 gene.

Generation of an induced pluripotent stem cell (iPSC) line from a patient with autosomal dominant retinitis pigmentosa due to a mutation in the NR2E3 gene.

Journal: Stem cell research

Published: February 03, 2017

Generation of Storable Retinal Organoids and Retinal Pigmented Epithelium from Adherent Human iPS Cells in Xeno-Free and Feeder-Free Conditions.

Generation of Storable Retinal Organoids and Retinal Pigmented Epithelium from Adherent Human iPS Cells in Xeno-Free and Feeder-Free Conditions.

Journal: Stem cells (Dayton, Ohio)

Published: August 09, 2016

From confluent human iPS cells to self-forming neural retina and retinal pigmented epithelium.

From confluent human iPS cells to self-forming neural retina and retinal pigmented epithelium.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: June 10, 2014

Showing 1-12 of 13

Last Updated: 09/26/2026