Colin A. Johnson

University of Leeds

United Kingdom

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Articles (12)

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2024

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2024

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2024

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2024

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2023

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2023

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2022

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2022

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2022

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2022

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2021

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2021

Collaborators (19)

John Ladbury

Professor and Director of Leeds Centre for Disease Models

University of Leeds

UNITED KINGDOM

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Robin Ali

King's College London

UNITED KINGDOM

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Christopher Inglehearn

University of Leeds

UNITED KINGDOM

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Adnan Halim

University of Copenhagen

DENMARK

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Kathryn Hentges

Reader

The University of Manchester

UNITED KINGDOM

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Mahetab Amer

The University of Manchester

UNITED KINGDOM

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Tom Fowler

Queen Mary University of London

UNITED KINGDOM

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John Hintze

Københavns Universitet

DENMARK

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James A. Poulter

University of Leeds

UNITED KINGDOM

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Marzena Kurzawa-Akanbi

Lecturer in Regenerative Medicine

Newcastle University

UNITED KINGDOM

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Weihua Tian

Technical University of Denmark

DENMARK

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Thomas Hughes

Professor of Biosciences

York St John University

UNITED KINGDOM

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Anke Brüning-Richardson

University of Huddersfield

UNITED KINGDOM

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Natalia Riobo-Del Galdo

Associate Professor

University of Leeds

UNITED KINGDOM

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Jamie Ellingford

The University of Manchester

UNITED KINGDOM

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David Westhead

Prof

University of Leeds

UNITED KINGDOM

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Hiren Joshi

Københavns Universitet

DENMARK

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Lucy Stead

Associate Professor

University of Leeds Leeds Institute of Health Sciences

UNITED KINGDOM

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Tim @timjph Hubbard

King’s College London

UNITED KINGDOM

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Colin A. Johnson

Research Interests

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Articles (12)

IDHwt glioblastomas can be stratified by their transcriptional response to standard treatment, with implications for targeted therapy

Glycogen myophosphorylase loss causes increased dependence on glucose in iPSC-derived retinal pigment epithelium

PRPF8-mediated dysregulation of hBrr2 helicase disrupts human spliceosome kinetics and 5´-splice-site selection causing tissue-specific defects

Cilia function and dysfunction

The SHDRA syndrome-associated gene <i>TMEM260</i> encodes a protein-specific O-mannosyltransferase.

Towards modular engineering of cell signalling: Topographically-textured microparticles induce osteogenesis via activation of canonical hedgehog signalling

From mesenchymal niches to engineered in vitro model systems: Exploring and exploiting biomechanical regulation of vertebrate hedgehog signalling

Unlocking the potential of the <scp>UK</scp> 100,000 Genomes Project—lessons learned from analysis of the “Congenital Malformations caused by Ciliopathies” cohort

Uncovering the burden of hidden ciliopathies in the 100 000 Genomes Project: a reverse phenotyping approach.

RNA-Seq analysis of a Pax3-expressing myoblast clone in-vitro and effect of culture surface stiffness on differentiation

Molecular diagnoses in the congenital malformations caused by ciliopathies cohort of the 100,000 Genomes Project

Novel loss-of-function mutation in HERC2 is associated with severe developmental delay and paediatric lethality

Collaborators (19)

John Ladbury

Robin Ali

Christopher Inglehearn

Adnan Halim

Kathryn Hentges

Mahetab Amer

Tom Fowler

John Hintze

James A. Poulter

Marzena Kurzawa-Akanbi

Weihua Tian

Thomas Hughes

Anke Brüning-Richardson

Natalia Riobo-Del Galdo

Jamie Ellingford

David Westhead

Hiren Joshi

Lucy Stead

Tim @timjph Hubbard

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