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Geroscience|April 22, 2023
Activation of telomerase by TA-65 enhances immunity and reduces inflammation post myocardial infarctionBilal Bawamia, Luke Spray, Vincent K Wangsaputra, et al.
Genes|September 5, 2019
Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions: Neuroblastoma and Congenital Heart DiseaseAlessandro Testori, Vito A Lasorsa, Flora Cimmino, et al.
Heart (British Cardiac Society)|October 13, 2010
Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variantsHelen R Griffin, Ana Töpf, Elise Glen, et al.
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.
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.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|November 20, 2014
Impact of age on the prognostic value of left ventricular function in relation to procedural outcomes following percutaneous coronary intervention: insights from the British Cardiovascular Intervention SocietyChun Shing Kwok, Simon G Anderson, Katherine S L McAllister, 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.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 18, 2010
Coronary artery disease-related genetic variant on chromosome 10q11 is associated with carotid intima-media thickness and atherosclerosisStefan Kiechl, Ross C Laxton, Qingzhong Xiao, et al.
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