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Circulation Research|November 12, 2014
Myocardial ischemia and reperfusion leads to transient CD8 immune deficiency and accelerated immunosenescence in CMV-seropositive patientsJedrzej Hoffmann, Evgeniya V Shmeleva, Stephen E Boag, et al.
Journal of Medical Genetics|February 26, 2015
Positional mapping of PRKD1, NRP1 and PRDM1 as novel candidate disease genes in truncus arteriosusRanad Shaheen, Amal Al Hashem, Mohammed H Alghamdi, et al.
Nanoscale|July 17, 2012
Strongly exchange coupled inverse ferrimagnetic soft/hard, Mn(x)Fe(3-x)O4/Fe(x)Mn(3-x)O4, core/shell heterostructured nanoparticlesA López-Ortega, M Estrader, G Salazar-Alvarez, et al.
Nature Communications|November 14, 2018
Author Correction: Promoter interactome of human embryonic stem cell-derived cardiomyocytes connects GWAS regions to cardiac gene networksMun-Kit Choy, Biola M Javierre, Simon G Williams, et al.
Nature Communications|June 30, 2018
Promoter interactome of human embryonic stem cell-derived cardiomyocytes connects GWAS regions to cardiac gene networksMun-Kit Choy, Biola M Javierre, Simon G Williams, et al.
Disease Models & Mechanisms|November 22, 2024
Beyond genomic studies of congenital heart defects through systematic modelling and phenotypingDeborah J Henderson, Ahlam Alqahtani, Bill Chaudhry, et al.
BMC Genetics|June 21, 2013
Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of FallotJulian Palomino Doza, Ana Topf, Jamie Bentham, et al.
Bioinformatics (Oxford, England)|December 3, 2019
The use of missing values in proteomic data-independent acquisition mass spectrometry to enable disease activity discriminationKathryn A McGurk, Arianna Dagliati, Davide Chiasserini, et al.
Congenital Heart Disease|April 12, 2014
Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart DevelopmentThor Thorsson, William W Russell, Nour El-Kashlan, et al.
European Heart Journal. Cardiovascular Imaging|November 7, 2012
Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriersMatthew G D Bates, Kieren G Hollingsworth, Jane H Newman, et al.
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