Blanca Gonzalez-Arango

Elfriede Aulhorn Str. 7
Tuebingen, BW 72076, Germany

Last Updated: 09/26/2026

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Found 38 publications

Organotypic retinal cultures as an ex vivo screening platform for PLGA-based neuroprotective microspheres.

Organotypic retinal cultures as an ex vivo screening platform for PLGA-based neuroprotective microspheres.

Journal: European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences

Published: February 20, 2026

Safety and neuroprotective efficacy of the VCP inhibitor ML240 in large-animal and human retinal explants: a preclinical ex vivo study.

Safety and neuroprotective efficacy of the VCP inhibitor ML240 in large-animal and human retinal explants: a preclinical ex vivo study.

Journal: BMC medicine

Published: August 22, 2025

Ocular delivery of different valosin-containing protein (VCP) inhibitory formulations prevents retinal degeneration in rho∆I255 mice.

Ocular delivery of different valosin-containing protein (VCP) inhibitory formulations prevents retinal degeneration in rho∆I255 mice.

Journal: Journal of controlled release : official journal of the Controlled Release Society

Published: July 08, 2025

Signaling Pathways in Retinal Pigment Epithelium (RPE) Cells in Response to Stress Conditions of Age-Related Macular Degeneration (AMD).

Signaling Pathways in Retinal Pigment Epithelium (RPE) Cells in Response to Stress Conditions of Age-Related Macular Degeneration (AMD).

Journal: Advances in experimental medicine and biology

Published: February 10, 2025

The AMD-associated genetic polymorphism CFH Y402H confers vulnerability to Hydroquinone-induced stress in iPSC-RPE cells.

The AMD-associated genetic polymorphism CFH Y402H confers vulnerability to Hydroquinone-induced stress in iPSC-RPE cells.

Journal: Frontiers in immunology

Published: November 12, 2024

Mutant dominant-negative rhodopsin∆I256 causes protein aggregates degraded via ERAD and prevents normal rhodopsin from proper membrane trafficking.

Mutant dominant-negative rhodopsin∆I256 causes protein aggregates degraded via ERAD and prevents normal rhodopsin from proper membrane trafficking.

Journal: Frontiers in molecular biosciences

Published: January 11, 2024

Method for siRNA delivery in retina explants.

Method for siRNA delivery in retina explants.

Journal: Methods in cell biology

Published: May 10, 2023

Pathomechanisms of Inherited Retinal Degeneration and Perspectives for Neuroprotection.

Pathomechanisms of Inherited Retinal Degeneration and Perspectives for Neuroprotection.

Journal: Cold Spring Harbor perspectives in medicine

Published: September 19, 2022

Tailoring surface properties of liposomes for dexamethasone intraocular administration.

Tailoring surface properties of liposomes for dexamethasone intraocular administration.

Journal: Journal of controlled release : official journal of the Controlled Release Society

Published: September 12, 2022

In vitro Model Systems for Studies Into Retinal Neuroprotection.

In vitro Model Systems for Studies Into Retinal Neuroprotection.

Journal: Frontiers in neuroscience

Published: May 06, 2022

Pharmacokinetics of Pullulan-Dexamethasone Conjugates in Retinal Drug Delivery.

Pharmacokinetics of Pullulan-Dexamethasone Conjugates in Retinal Drug Delivery.

Journal: Pharmaceutics

Published: November 22, 2021

Complement Factor H Loss in RPE Cells Causes Retinal Degeneration in a Human RPE-Porcine Retinal Explant Co-Culture Model.

Complement Factor H Loss in RPE Cells Causes Retinal Degeneration in a Human RPE-Porcine Retinal Explant Co-Culture Model.

Journal: Biomolecules

Published: September 30, 2021

Showing 1-12 of 38

Last Updated: 09/26/2026