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You searched for: Author/Creator Cook, Stuart A

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1. 171 The genetic signature in ischaemic heart disease with myocardial infarction (MI) and significant left ventricular (LV) dysfunction. (6th June 2015)

3. 209 Whole Exome Sequencing Identifies Genetic Cause of Histiocytoid Cardiomyopathy. (3rd June 2016)

4. 5 Defining the effects of genetic variation using machine learning analysis of CMRS: a study in hypertrophic cardiomyopathy and in a healthy population. (May 2018)

5. 95 Identification Of Likely Pathogenic Variants In Patients With Bicuspid Aortic Valve: Correlation Of Complex Genotype With A More Severe Aortic Phenotype. (31st May 2014)

7. Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23. (3rd March 2021)

8. IL11 is elevated in systemic sclerosis and IL11-dependent ERK signalling underlies TGFβ-mediated activation of dermal fibroblasts. (16th February 2021)

10. Loss of Yap/Taz in cardiac fibroblasts attenuates adverse remodelling and improves cardiac function. Issue 7 (16th June 2021)