Rami I. Aqeilan

Jerusalem, JM, Israel

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 94 publications

Neuron-specific WWOX gene therapy produces dose-dependent, durable rescue in a model of WWOX-related epileptic encephalopathy.

Neuron-specific WWOX gene therapy produces dose-dependent, durable rescue in a model of WWOX-related epileptic encephalopathy.

Journal: Molecular therapy. Advances

Published: April 17, 2026

WWOX maintains epidermal identity and suppresses EMT to prevent aggressive cutaneous squamous cell carcinoma.

WWOX maintains epidermal identity and suppresses EMT to prevent aggressive cutaneous squamous cell carcinoma.

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

Published: April 15, 2026

WWOX in brain development and disease: Molecular mechanisms and therapeutic opportunities.

WWOX in brain development and disease: Molecular mechanisms and therapeutic opportunities.

Journal: Neurobiology of disease

Published: March 16, 2026

Superenhancers shape the landscape and repair dynamics of transcription-associated DNA breaks in cancer.

Superenhancers shape the landscape and repair dynamics of transcription-associated DNA breaks in cancer.

Journal: Science advances

Published: January 21, 2026

Disrupted WWOX-MYC interplay impairs neurogenesis in human brain organoids.

Disrupted WWOX-MYC interplay impairs neurogenesis in human brain organoids.

Journal: Brain : a journal of neurology

Published: December 17, 2025

Endogenous Processes Underlying Clock-Like Mutational Signatures.

Endogenous Processes Underlying Clock-Like Mutational Signatures.

Journal: Genes, chromosomes & cancer

Published: November 20, 2025

Breaking the script: transcriptional addiction as a driver of genome instability in cancer.

Breaking the script: transcriptional addiction as a driver of genome instability in cancer.

Journal: Trends in genetics : TIG

Published: September 16, 2025

The breakome of BRCA1 and BRCA2 pathway mutation carriers reveals early processes in breast oncogenesis.

The breakome of BRCA1 and BRCA2 pathway mutation carriers reveals early processes in breast oncogenesis.

Journal: Cell death & disease

Published: June 30, 2025

Precise Mapping of Physiological DSBs Using In-Suspension Break Labeling In Situ and Sequencing (sBLISS).

Precise Mapping of Physiological DSBs Using In-Suspension Break Labeling In Situ and Sequencing (sBLISS).

Journal: Methods in molecular biology (Clifton, N.J.)

Published: March 14, 2025

Causes and consequences of T cell DNA damage.

Causes and consequences of T cell DNA damage.

Journal: Trends in immunology

Published: January 21, 2025

Generation of human induced pluripotent stem cell lines HUJIi004 and HUJIi005 from two individuals carrying autosomal-dominant mutations in the CTNBB1 gene resulting in CTNNB1 neurodevelopmental disorder.

Generation of human induced pluripotent stem cell lines HUJIi004 and HUJIi005 from two individuals carrying autosomal-dominant mutations in the CTNBB1 gene resulting in CTNNB1 neurodevelopmental disorder.

Journal: Stem cell research

Published: April 27, 2024

Protocol for mapping physiological DSBs using in-suspension break labeling in situ and sequencing.

Protocol for mapping physiological DSBs using in-suspension break labeling in situ and sequencing.

Journal: STAR protocols

Published: March 02, 2024

Showing 1-12 of 94

Last Updated: 09/26/2026