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European Heart Journal|June 7, 2019
Genetically modulated educational attainment and coronary disease riskLingyao Zeng, Ioanna Ntalla, Thorsten Kessler, et al.
The Journal of Biological Chemistry|March 16, 2007
The effect of mutations in alpha-tropomyosin (E40K and E54K) that cause familial dilated cardiomyopathy on the regulatory mechanism of cardiac muscle thin filamentsMahmooda Mirza, Paul Robinson, Elena Kremneva, et al.
American Journal of Physiology. Heart and Circulatory Physiology|July 4, 2020
Dilated cardiomyopathy mutations in thin-filament regulatory proteins reduce contractility, suppress systolic Ca2+, and activate NFAT and Akt signalingPaul Robinson, Alexander J Sparrow, Suketu Patel, et al.
Plos One|January 17, 2009
Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patientsLisa E Creary, Pinar Ulug, Stephan Menzel, et al.
The Journal of Trauma and Acute Care Surgery|February 8, 2012
Geriatric trauma service: a one-year experienceAlicia J Mangram, Christopher D Mitchell, Vanessa K Shifflette, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
Insights from early experience of a Rare Disease Genomic Medicine Multidisciplinary Team: a qualitative studyElizabeth Ormondroyd, Michael P Mackley, Edward Blair, et al.
Circulation. Cardiovascular Genetics|March 16, 2011
Common variation at the 11-β hydroxysteroid dehydrogenase type 1 gene is associated with left ventricular massThahira J Rahman, Bongani M Mayosi, Darroch Hall, et al.
Circulation Research|February 28, 2002
Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathyEdward Blair, Charles Redwood, Marisa de Jesus Oliveira, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|March 16, 2019
Measuring inorganic phosphate and intracellular pH in the healthy and hypertrophic cardiomyopathy hearts by in vivo 7T 31P-cardiovascular magnetic resonance spectroscopyLadislav Valkovič, William T Clarke, Albrecht I Schmid, et al.
Atherosclerosis|December 9, 2004
A novel common single nucleotide polymorphism in the promoter region of the C-reactive protein gene associated with the plasma concentration of C-reactive proteinAlexander Kovacs, Fiona Green, Lars-Olof Hansson, et al.
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