C. Hooper

发表

Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion

H. Watkins, A. Goel, B. Davies, 2018, Journal of molecular and cellular cardiology.

Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction

A. Pagnamenta, S. Knight, H. Watkins, 2016, Circulation. Cardiovascular genetics.

MLP and CARP are linked to chronic PKCα signalling in dilated cardiomyopathy

Stephan Lange, Ju Chen, M. Bang, 2016, Nature Communications.

Changes in the cardiac metabolome caused by perhexiline treatment in a mouse model of hypertrophic cardiomyopathy.

J. W. Allwood, W. Dunn, L. Carrier, 2015, Molecular bioSystems.

Insights into the Role of a Cardiomyopathy-Causing Genetic Variant in ACTN2

G. Douglas, H. Watkins, M. Gautel, 2023, Cells.

Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variant

H. Watkins, B. Davies, E. Ehler, 2021, Basic Research in Cardiology.

Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction

A. Pagnamenta, S. Knight, H. Watkins, 2016, Circulation. Cardiovascular genetics.

Combination of whole genome sequencing, linkage, and functional studies implicates a missense mutation in titin as a cause of autosomal dominant cardiomyopathy with features of left ventricular noncompaction

A. Pagnamenta, S. Knight, H. Watkins, 2016 .

Combination of whole genome sequencing, linkage, and functional studies implicates a missense mutation in titin as a cause of autosomal dominant cardiomyopathy with features of left ventricular noncompaction

A. Pagnamenta, S. Knight, H. Watkins, 2016 .