Linking structure, function and genomics at single cell resolution: an integrative approach to understanding inherited heart disease

Project Code

CMD27Ca Fowler

Project Type

Wet lab

Research Theme

Cardiometabolic Disease

Project Summary Download

Summary

This project aims to address a research priority for patients with the inherited heart condition, hypertrophic cardiomyopathy (HCM), by investigating how the same mutation can result in widely different phenotypes. Increased variability can manifest between different individuals, regions of the heart, and from one cell to the next. To address this, you will develop a unique process for capturing structural (confocal microscopy), functional (electrophysiology and Ca2+ imaging), and transcriptomic data all from the same cell. Integrating function and genomics will provide unprecedented power to identify possible causal factors responsible for pathology, and opportunities for intervention.

Can the project be completed part time?

No

Lead Supervisor

Dr Ewan Fowler

Lead Supervisor Email

FowlerED@Cardiff.ac.uk

University Affiliation

Cardiff University

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