Leszek Lisowski

Associate Professor

Military Institute of Medicine

Poland

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Leszek Lisowski is an Associate Professor at the Military Institute of Medicine in Poland. His research focuses on gene therapy, adeno-associated virus (AAV) vectors, and their applications in liver and neurological disorders. Recent publications include studies on functional transduction of murine hepatocytes, AAV vector engineering, and mechanisms in colorectal carcinogenesis. His work contributes significantly to advancements in targeted gene therapies and disease intervention strategies.

Articles (10)

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2021

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2021

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2021

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2020

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2020

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2020

Collaborators (8)

Gareth Davies

Sitryx Therapeutics

UNITED KINGDOM

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Peter L. Carlen

University Health Network

CANADA

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Grant J. Logan

University of Sydney

AUSTRALIA

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Alastair Burt

Professor of Precision and Molecular Pathology

Newcastle University

UNITED KINGDOM

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Anais Amaya

Lander University

UNITED STATES

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Hsin-Hui Shen

MONASH UNIVERSITY

AUSTRALIA

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Maddison Knight

Children's Medical Research Institute

AUSTRALIA

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Shane Grey

Head of School

University of New South Wales - Randwick Campus

AUSTRALIA

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Leszek Lisowski

Research Interests

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About

Articles (10)

A drug-tunable Flt23k gene therapy for controlled intervention in retinal neovascularization

Single amino acid insertion allows functional transduction of murine hepatocytes with human liver tropic AAV capsids.

Neurological Disorders Associated with WWOX Germline Mutations—A Comprehensive Overview

Selection of a novel AAV2/TNFAIP3 vector for local suppression of islet xenograft inflammation.

The Balance of Stromal BMP Signaling Mediated by GREM1 and ISLR Drives Colorectal Carcinogenesis.

Engineering domain-inlaid SaCas9 adenine base editors with reduced RNA off-targets and increased on-target DNA editing.

Restoring the natural tropism of AAV2 vectors for human liver.

Attenuation of Heparan Sulfate Proteoglycan Binding Enhances In Vivo Transduction of Human Primary Hepatocytes with AAV2.

High-Throughput In Vitro, Ex Vivo, and In Vivo Screen of Adeno-Associated Virus Vectors Based on Physical and Functional Transduction.

Systemic AAV8-mediated delivery of a functional copy of muscle glycogen phosphorylase (Pygm) ameliorates disease in a murine model of McArdle disease.

Collaborators (8)

Gareth Davies

Peter L. Carlen

Grant J. Logan

Alastair Burt

Anais Amaya

Hsin-Hui Shen

Maddison Knight

Shane Grey

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