about
Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation studyGenetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathyATP-binding cassette transporter A7 (ABCA7) binds apolipoprotein A-I and mediates cellular phospholipid but not cholesterol effluxGenome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.ATP-binding cassette transporter A7 enhances phagocytosis of apoptotic cells and associated ERK signaling in macrophagesPotential role of ABCA7 in cellular lipid efflux to apoA-IGenetic causes of myocardial infarction: new insights from genome-wide association studies.Genetic regulation of serum phytosterol levels and risk of coronary artery disease.HDL as a target in the treatment of atherosclerotic cardiovascular disease.Macrophage cholesterol efflux correlates with lipoprotein subclass distribution and risk of obstructive coronary artery disease in patients undergoing coronary angiography.Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery diseaseNew susceptibility locus for coronary artery disease on chromosome 3q22.3.Sorting out cholesterol and coronary artery disease.Association of the single nucleotide polymorphism rs599839 in the vicinity of the sortilin 1 gene with LDL and triglyceride metabolism, coronary heart disease and myocardial infarction. The Ludwigshafen Risk and Cardiovascular Health Study.Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease.Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.Association between degenerative aortic valve disease and long-term exposure to cardiovascular risk factors: results of the longitudinal population-based KORA/MONICA survey.The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol.Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German population.Physicians' perception of guideline-recommended low-density lipoprotein target values: characteristics of misclassified patients.Lack of association between a common polymorphism near the INSIG2 gene and BMI, myocardial infarction, and cardiovascular risk factors.Chromosome 9p21 and coronary risk--the mystery continues.Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarctionGenome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23Lack of Association Between the MEF2A Gene and Myocardial InfarctionGenetic basis of myocardial infarction: Novel insights from genome-wide association studiesAn Alternative Splice Variant inAbcc6, the Gene Causing Dystrophic Calcification, Leads to Protein Deficiency in C3H/He MiceDie Herzinsuffizienz als komplexe genetische ErkrankungAssociation of a functional polymorphism in the CYP4A11 gene with systolic blood pressure in survivors of myocardial infarction
P50
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P50
description
onderzoeker
@nl
name
Patrick Linsel-Nitschke
@en
Patrick Linsel-Nitschke
@es
Patrick Linsel-Nitschke
@sl
type
label
Patrick Linsel-Nitschke
@en
Patrick Linsel-Nitschke
@es
Patrick Linsel-Nitschke
@sl
prefLabel
Patrick Linsel-Nitschke
@en
Patrick Linsel-Nitschke
@es
Patrick Linsel-Nitschke
@sl