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Current Atherosclerosis Reports
|
April 14, 2011
Genetic mechanisms mediating atherosclerosis susceptibility at the chromosome 9p21 locus
Michael S Cunnington, Bernard Keavney
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions
|
January 13, 2016
Microvascular dysfunction in the immediate aftermath of chronic total coronary occlusion recanalization
Andrew Ladwiniec, Michael S Cunnington, Jennifer Rossington, et al.
Plos Genetics
|
April 14, 2010
Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression
Michael S Cunnington, Mauro Santibanez Koref, Bongani M Mayosi, et al.
JACC. Case Reports
|
July 22, 2021
Untreatable Severe Structural Degeneration of a Transcatheter Aortic Heart Valve
Noman Ali, Christopher J Malkin, Michael S Cunnington, et al.
The British Journal of Cardiology
|
February 7, 2025
Artificial intelligence in heart valve disease: diagnosis, innovation and treatment. A state-of-the-art review
Paul Bamford, Amr Abdelrahman, Christopher J Malkin, et al.
Coronary Artery Disease
|
February 25, 2016
Biomarkers of coronary endothelial health: correlation with invasive measures of collateral function, flow and resistance in chronically occluded coronary arteries and the effect of recanalization
Andrew Ladwiniec, Camille Ettelaie, Michael S Cunnington, et al.
BMC Medical Genetics
|
December 17, 2009
STK39 polymorphisms and blood pressure: an association study in British Caucasians and assessment of cis-acting influences on gene expression
Michael S Cunnington, Chris Kay, Peter J Avery, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)
|
September 17, 2020
A cohort study examining urgent and emergency treatment for decompensated severe aortic stenosis
Noman Ali, Peysh Patel, Ali Wahab, et al.
BMC Genetics
|
December 26, 2014
Chromosome 16q22 variants in a region associated with cardiovascular phenotypes correlate with ZFHX3 expression in a transcript-specific manner
Ruairidh I R Martin, W Andrew Owens, Michael S Cunnington, et al.
Annals of Human Genetics
|
September 24, 2010
MLH1 Differential allelic expression in mutation carriers and controls
Mauro Santibanez Koref, Valerie Wilson, Nicola Cartwright, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
Current Atherosclerosis Reports
|
April 14, 2011
Genetic mechanisms mediating atherosclerosis susceptibility at the chromosome 9p21 locus
Michael S Cunnington, Bernard Keavney
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions
|
January 13, 2016
Microvascular dysfunction in the immediate aftermath of chronic total coronary occlusion recanalization
Andrew Ladwiniec, Michael S Cunnington, Jennifer Rossington, et al.
Plos Genetics
|
April 14, 2010
Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression
Michael S Cunnington, Mauro Santibanez Koref, Bongani M Mayosi, et al.
JACC. Case Reports
|
July 22, 2021
Untreatable Severe Structural Degeneration of a Transcatheter Aortic Heart Valve
Noman Ali, Christopher J Malkin, Michael S Cunnington, et al.
The British Journal of Cardiology
|
February 7, 2025
Artificial intelligence in heart valve disease: diagnosis, innovation and treatment. A state-of-the-art review
Paul Bamford, Amr Abdelrahman, Christopher J Malkin, et al.
Coronary Artery Disease
|
February 25, 2016
Biomarkers of coronary endothelial health: correlation with invasive measures of collateral function, flow and resistance in chronically occluded coronary arteries and the effect of recanalization
Andrew Ladwiniec, Camille Ettelaie, Michael S Cunnington, et al.
BMC Medical Genetics
|
December 17, 2009
STK39 polymorphisms and blood pressure: an association study in British Caucasians and assessment of cis-acting influences on gene expression
Michael S Cunnington, Chris Kay, Peter J Avery, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)
|
September 17, 2020
A cohort study examining urgent and emergency treatment for decompensated severe aortic stenosis
Noman Ali, Peysh Patel, Ali Wahab, et al.
BMC Genetics
|
December 26, 2014
Chromosome 16q22 variants in a region associated with cardiovascular phenotypes correlate with ZFHX3 expression in a transcript-specific manner
Ruairidh I R Martin, W Andrew Owens, Michael S Cunnington, et al.
Annals of Human Genetics
|
September 24, 2010
MLH1 Differential allelic expression in mutation carriers and controls
Mauro Santibanez Koref, Valerie Wilson, Nicola Cartwright, et al.
Page
of 3