[HTML][HTML] Genetics of coronary artery disease and myocardial infarction
X Dai, S Wiernek, JP Evans… - World journal of …, 2016 - ncbi.nlm.nih.gov
Atherosclerotic coronary artery disease (CAD) comprises a broad spectrum of clinical
entities that include asymptomatic subclinical atherosclerosis and its clinical complications …
entities that include asymptomatic subclinical atherosclerosis and its clinical complications …
Genetic determinants of inherited susceptibility to hypercholesterolemia–a comprehensive literature review
CS Paththinige, ND Sirisena… - Lipids in health and …, 2017 - Springer
Hypercholesterolemia is a strong determinant of mortality and morbidity associated with
cardiovascular diseases and a major contributor to the global disease burden. Mutations in …
cardiovascular diseases and a major contributor to the global disease burden. Mutations in …
Sorting through the extensive and confusing roles of sortilin in metabolic disease
Sortilin is a post-Golgi trafficking receptor homologous to the yeast vacuolar protein sorting
receptor 10 (VPS10). The VPS10 motif on sortilin is a 10-bladed β-propeller structure …
receptor 10 (VPS10). The VPS10 motif on sortilin is a 10-bladed β-propeller structure …
Sortilin and its multiple roles in cardiovascular and metabolic diseases
Cardiovascular disease is a leading cause of morbidity and mortality in the Western world.
Studies of sortilin's influence on cardiovascular and metabolic diseases goes far beyond the …
Studies of sortilin's influence on cardiovascular and metabolic diseases goes far beyond the …
Deficiency of PSRC1 accelerates atherosclerosis by increasing TMAO production via manipulating gut microbiota and flavin monooxygenase 3
T Luo, Z Guo, D Liu, Z Guo, Q Wu, Q Li, R Lin… - Gut …, 2022 - Taylor & Francis
Maladaptive inflammatory and immune responses are responsible for intestinal barrier
integrity and function dysregulation. Proline/serine-rich coiled-coil protein 1 (PSRC1) …
integrity and function dysregulation. Proline/serine-rich coiled-coil protein 1 (PSRC1) …
Transcriptome-wide association study of coronary artery disease identifies novel susceptibility genes
L Li, Z Chen, M von Scheidt, S Li, A Steiner… - Basic research in …, 2022 - Springer
The majority of risk loci identified by genome-wide association studies (GWAS) are in non-
coding regions, hampering their functional interpretation. Instead, transcriptome-wide …
coding regions, hampering their functional interpretation. Instead, transcriptome-wide …
Trafficking in Alzheimer's disease: modulation of APP transport and processing by the transmembrane proteins LRP1, SorLA, SorCS1c, sortilin, and calsyntenin
The amyloid precursor protein (APP), one key player in Alzheimer's disease (AD), is
extensively processed by different proteases. This leads to the generation of diverging …
extensively processed by different proteases. This leads to the generation of diverging …
Sortilin, encoded by the cardiovascular risk gene SORT1, and its suggested functions in cardiovascular disease
M Kjolby, MS Nielsen, CM Petersen - Current atherosclerosis reports, 2015 - Springer
Several genome-wide association studies have linked novel loci to a wide range of
cardiovascular phenotypes including low-density lipoprotein (LDL)-cholesterol, early onset …
cardiovascular phenotypes including low-density lipoprotein (LDL)-cholesterol, early onset …
Sortilin as a biomarker for cardiovascular disease revisited
Genetic variants in the genomic region containing SORT1 (encoding the protein sortilin) are
strongly associated with cholesterol levels and the risk of coronary artery disease (CAD) …
strongly associated with cholesterol levels and the risk of coronary artery disease (CAD) …
Powerful and robust inference of complex phenotypes' causal genes with dependent expression quantitative loci by a median-based Mendelian randomization
Isolating the causal genes from numerous genetic association signals in genome-wide
association studies (GWASs) of complex phenotypes remains an open and challenging …
association studies (GWASs) of complex phenotypes remains an open and challenging …