NATHAN HARMSTON

Lecturer

Cardiff University

United Kingdom

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Nathan Harmston is a Lecturer at Cardiff University, located in the UK. His research focuses on oncogenic mechanisms in multiple myeloma, epigenetic reprogramming, and the interactions of Wnt signaling pathways. His recent publications explore topics such as stem cell rejuvenation, RNA translation, and the implications of regulatory domains in genomic analyses.

Articles (12)

Year:

2025

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2024

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2024

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2024

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2022

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2022

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2022

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2022

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2022

Year:

2022

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2021

Year:

2020

Collaborators (6)

Jean-Michel Carter

University of Bath

UNITED KINGDOM

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Kris Wood

Assistant Professor

Duke University

UNITED STATES

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David M Virshup

Professor, Program Director

Duke-NUS Medical School

SINGAPORE

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Nicholas Tolwinski

Associate Professor

Duke-NUS Medical School

SINGAPORE

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Babita Madan

Asst. Professor

Duke-NUS Medical School

SINGAPORE

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Yinghui Li

Assistant Professor

Nanyang Technological University (NTU)

SINGAPORE

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NATHAN HARMSTON

Research Interests

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About

Articles (12)

ATF4:p52 complex activates oncogenic enhancers in multiple myeloma via p300/CBP recruitment to regulate BACH1

Aberrant non-canonical NF-κB signalling reprograms the epigenome landscape to drive oncogenic transcriptomes in multiple myeloma

The cholesterol biosynthesis enzyme FAXDC2 couples Wnt/β-catenin to RTK/MAPK signaling

The Wnt Co-Receptor PTK7/Otk and Its Homolog Otk-2 in Neurogenesis and Patterning

A p300/GATA6 axis determines differentiation and Wnt dependency in pancreatic cancer models

Wnt Signaling Rescues Amyloid Beta-Induced Gut Stem Cell Loss

A high-resolution map of human RNA translation.

The importance of considering regulatory domains in genome-wide analyses – the nearest gene is often wrong!

Combining stem cell rejuvenation and senescence targeting to synergistically extend lifespan.

A non-canonical Raf function is required for dorsal-ventral patterning during Drosophila embryogenesis.

Widespread Repression of Gene Expression in Cancer by a Wnt/β-Catenin/MAPK Pathway

The Functional Landscape of Patient-Derived RNF43 Mutations Predicts Sensitivity to Wnt Inhibition

Collaborators (6)

Jean-Michel Carter

Kris Wood

David M Virshup

Nicholas Tolwinski

Babita Madan

Yinghui Li

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