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Cardiovascular Research|June 2, 2022
PHACTR1 modulates vascular compliance but not endothelial function: a translational studyAlice Wood, Alexios Antonopoulos, Surawee Chuaiphichai, et al.Journal of Molecular and Cellular Cardiology|May 1, 2023
Comparing the effects of chemical Ca2+ dyes and R-GECO on contractility and Ca2+ transients in adult and human iPSC cardiomyocytesPaul Robinson, Alexander J Sparrow, Yiangos Psaras, et al.Atherosclerosis|October 18, 2017
Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisationRona J Strawbridge, Angela Silveira, Marcel den Hoed, et al.Hypertension (Dallas, Tex. : 1979)|November 1, 2006
Polymorphic variation in the 11beta-hydroxylase gene associates with reduced 11-hydroxylase efficiencyMarianne Barr, Scott M MacKenzie, Elaine C Friel, et al.Proceedings of the National Academy of Sciences of the United States of America|June 16, 2016
Mutation of Fnip1 is associated with B-cell deficiency, cardiomyopathy, and elevated AMPK activityOwen M Siggs, Alexander Stockenhuber, Mukta Deobagkar-Lele, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 20, 2024
Metabolic profiling of aortic stenosis and hypertrophic cardiomyopathy identifies mechanistic contrasts in substrate utilizationNikhil Pal, Animesh Acharjee, Zsuzsanna Ament, et al.Basic Research in Cardiology|February 27, 2021
Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variantHe Jiang, Charlotte Hooper, Matthew Kelly, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 28, 2012
Nprl3 is required for normal development of the cardiovascular systemMonika S Kowalczyk, Jim R Hughes, Christian Babbs, et al.Heart (British Cardiac Society)|May 28, 2026
COVID-19 outcomes and persistent symptoms in patients with hypertrophic cardiomyopathy: association with pre-existing cardiovascular magnetic resonance phenotypeArchit Singhal, Ellen Appleby, Owen Agnel, et al.Proceedings of the National Academy of Sciences of the United States of America|February 19, 2015
iASPP, a previously unidentified regulator of desmosomes, prevents arrhythmogenic right ventricular cardiomyopathy (ARVC)-induced sudden deathMario Notari, Ying Hu, Gopinath Sutendra, et al.Pageof 43