Davide Piccolo

University College London

United Kingdom

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Articles (5)

Year:

2024

Year:

2024

Year:

2023

Year:

2022

Year:

2020

Collaborators (8)

Enrico Maria Surace

PROFESSORE ASSOCIATO

Università degli Studi di Napoli Federico II

ITALY

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Jorge García Piqueras

Assistant Professor

Universidad Autónoma de Madrid

SPAIN

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Simona Brillante

Telethon Institute of Genetics and Medicine

ITALY

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Kalliopi Ziaka

University College London

UNITED KINGDOM

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Alex Garanto

Assistant Professor & Junior Principal Investigator

Radboudumc

NETHERLANDS

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Alessia Indrieri

Telethon Institute of Genetics and Medicine

ITALY

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Michael Cheetham

University College London

UNITED KINGDOM

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David Parfitt

NETHERLANDS

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Davide Piccolo

Research Interests

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Articles (5)

Proof-of-concept for multiple AON delivery by a single U7snRNA vector to restore splicing defects in ABCA4

A Proximity Complementation Assay to Identify Small Molecules That Enhance the Traffic of ABCA4 Misfolding Variants

Antisense oligonucleotide therapy corrects splicing in the common Stargardt disease type 1-causing variant ABCA4 c.5461-10T>C

miR ‐181a/b downregulation: a mutation‐independent therapeutic approach for inherited retinal diseases

Detailed Phenotyping and Therapeutic Strategies for Intronic ABCA4 Variants in Stargardt Disease.

Collaborators (8)

Enrico Maria Surace

Jorge García Piqueras

Simona Brillante

Kalliopi Ziaka

Alex Garanto

Alessia Indrieri

Michael Cheetham

David Parfitt

Make your next move.

Davide Piccolo

Research Interests

Explore related searches

Contact this professor

Articles (5)

Proof-of-concept for multiple AON delivery by a single U7snRNA vector to restore splicing defects in ABCA4

A Proximity Complementation Assay to Identify Small Molecules That Enhance the Traffic of ABCA4 Misfolding Variants

Antisense oligonucleotide therapy corrects splicing in the common Stargardt disease type 1-causing variant ABCA4 c.5461-10T&gt;C

miR ‐181a/b downregulation: a mutation‐independent therapeutic approach for inherited retinal diseases

Detailed Phenotyping and Therapeutic Strategies for Intronic ABCA4 Variants in Stargardt Disease.

Collaborators (8)

Enrico Maria Surace

Jorge García Piqueras

Simona Brillante

Kalliopi Ziaka

Alex Garanto

Alessia Indrieri

Michael Cheetham

David Parfitt

Make your next move.

Antisense oligonucleotide therapy corrects splicing in the common Stargardt disease type 1-causing variant ABCA4 c.5461-10T>C