Dimitra Athanasiou

11-43 Bath Street
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 16 publications

Single-cell analysis reveals impaired Müller glia-mediated intercellular communication and photoreceptor pathology in USH1C retinal organoids.

Single-cell analysis reveals impaired Müller glia-mediated intercellular communication and photoreceptor pathology in USH1C retinal organoids.

Journal: Cellular and molecular life sciences : CMLS
Published: June 05, 2025

Correction: Small molecule treatment alleviates photoreceptor cilia defects in LCA5-deficient human retinal organoids.

Correction: Small molecule treatment alleviates photoreceptor cilia defects in LCA5-deficient human retinal organoids.

Journal: Acta neuropathologica communications
Published: May 19, 2025

Preventing light-induced toxicity in a new mouse model of sector retinitis pigmentosa caused by Rhodopsin M39R variant.

Preventing light-induced toxicity in a new mouse model of sector retinitis pigmentosa caused by Rhodopsin M39R variant.

Journal: Cell death discovery
Published: May 12, 2025

Small molecule treatment alleviates photoreceptor cilia defects in LCA5-deficient human retinal organoids.

Small molecule treatment alleviates photoreceptor cilia defects in LCA5-deficient human retinal organoids.

Journal: Acta neuropathologica communications
Published: October 07, 2024

Eupatilin Improves Cilia Defects in Human CEP290 Ciliopathy Models.

Eupatilin Improves Cilia Defects in Human CEP290 Ciliopathy Models.

Journal: Cells
Published: April 06, 2023

CRISPR-Cas9 correction of a nonsense mutation in LCA5 rescues lebercilin expression and localization in human retinal organoids.

CRISPR-Cas9 correction of a nonsense mutation in LCA5 rescues lebercilin expression and localization in human retinal organoids.

Journal: Molecular therapy. Methods & clinical development
Published: October 11, 2022

Corrigendum to: The co-chaperone and reductase ERdj5 facilitates rod opsin biogenesis and quality control.

Corrigendum to: The co-chaperone and reductase ERdj5 facilitates rod opsin biogenesis and quality control.

Journal: Human molecular genetics
Published: January 09, 2020

AAV-mediated ERdj5 overexpression protects against P23H rhodopsin toxicity.

AAV-mediated ERdj5 overexpression protects against P23H rhodopsin toxicity.

Journal: Human molecular genetics
Published: December 04, 2019

Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4.

Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4.

Journal: American journal of human genetics
Published: December 15, 2017

The role of the ER stress-response protein PERK in rhodopsin retinitis pigmentosa.

The role of the ER stress-response protein PERK in rhodopsin retinitis pigmentosa.

Journal: Human molecular genetics
Published: August 24, 2017

The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy.

The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy.

Journal: Progress in retinal and eye research
Published: July 31, 2017

Rescue of mutant rhodopsin traffic by metformin-induced AMPK activation accelerates photoreceptor degeneration.

Rescue of mutant rhodopsin traffic by metformin-induced AMPK activation accelerates photoreceptor degeneration.

Journal: Human molecular genetics
Published: August 12, 2016
Showing 1-12 of 16

Last Updated: 09/26/2026