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Identification of Drug-Induced Myocardial Infarction-Related Protein Targets through the Prediction of Drug–Target Interactions and Analysis of Biological Processes

https://doi.org/10.1021/tx500147d
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The Structures of the Human Calcium Channel α1 Subunit (CACNL1A2) and β Subunit (CACNLB3) Genes
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Fatty Acids and Atherosclerotic Risk
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Expression of fatty-acid-handling proteins in human adipose tissue in relation to obesity and insulin resistance
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Insulin Resistance, Hyperglycemia, and Atherosclerosis
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GPEC: A Cytoscape plug-in for random walk-based gene prioritization and biomedical evidence collection
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Is testosterone or estrogen more important for male patients with coronary artery disease?
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Sumatriptan provokes coronary artery spasm in patients with variant angina: Possible involvement of serotonin 1B receptor
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AHA/ACC Guidelines for Secondary Prevention for Patients With Coronary and Other Atherosclerotic Vascular Disease: 2006 Update
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Fatty acids in cardiovascular health and disease: A comprehensive update
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The GGN and CAG repeat polymorphisms in the exon-1 of the androgen receptor gene are, respectively, associated with insulin resistance in men and with dyslipidemia in women
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Nociceptin/orphanin FQ stimulates human monocyte chemotaxis via NOP receptor activation
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Cytochrome P450 Epoxygenase CYP2J2 and the Risk of Coronary Artery Disease
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The GPIIIa (β3 integrin) PlA polymorphism in the early development of coronary atherosclerosis
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Changes in gene expression in atherosclerotic plaques analyzed using DNA array
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Beyond blood pressure: the endothelium and atherosclerosis progression*
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Keynote review: In vitro safety pharmacology profiling: an essential tool for successful drug development
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Human 25-Hydroxyvitamin D3-24-Hydroxylase, a Multicatalytic Enzyme
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PPAR-α and PPAR-γ activators induce cholesterol removal from human macrophage foam cells through stimulation of the ABCA1 pathway
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Histone H3K9 methyltransferase G9a represses PPARγ expression and adipogenesis
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P2X receptor characterization and IL‐1/IL‐1Ra release from human endothelial cells
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Probabilistic Approaches in Activity Prediction
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4,4′-Di-isothiocyanatostilbene-2,2′-disulphonic acid (‘DIDS’) activates protein kinase C and Na+/H+ exchange in human platelets via α2A-adrenergic receptors
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Role of apoptosis in atherosclerosis and its therapeutic implications
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The androgen receptor gene CAG polymorphism is associated with the severity of coronary artery disease in men
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Indomethacin decreases insulin secretion in patients with type 2 diabetes mellitus
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Class of Antiretroviral Drugs and the Risk of Myocardial Infarction
inferredcites →https://doi.org/10.1073/pnas.0811834106openalex-snapshot
Prostaglandin F 2α elevates blood pressure and promotes atherosclerosis
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ABCG1 (ABC8), the human homolog of the Drosophila white gene, is a regulator of macrophage cholesterol and phospholipid transport
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Human Geranylgeranyl Diphosphate Synthase
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Estrogen Signals to the Preservation of Endothelial Cell Form and Function
inferredcites →https://doi.org/10.1074/jbc.m111.298463openalex-snapshot
A Distinct Mechanism for Coactivator versus Corepressor Function by Histone Methyltransferase G9a in Transcriptional Regulation
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Cathepsin V, a Novel and Potent Elastolytic Activity Expressed in Activated Macrophages
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Histone H3 Lysine 9 Methyltransferase G9a Is a Transcriptional Coactivator for Nuclear Receptors
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Activation of αVβ3 on Vascular Cells Controls Recognition of Prothrombin
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Matrix Metalloproteinases (MMPs) Regulate Fibrin-invasive Activity via MT1-MMP–dependent and –independent Processes
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NSAID use and the risk of hospitalization for first myocardial infarction in the general population: a nationwide case-control study from Finland
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Intraplaque haemorrhages as the trigger of plaque vulnerability
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World Health Organization definition of myocardial infarction: 2008-09 revision
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Coronary Vasospasm and Myocardial Infarction Induced by Oral Sumatriptan
inferredcites →https://doi.org/10.1097/mol.0b013e3281338558openalex-snapshot
Fatty acid transport proteins
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Lipid lowering with thyroid hormone and thyromimetics
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Non steroidal anti‐inflammatory drug use and levels of oestrogens and androgens in men
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Role of Endothelin‐1 in Atherosclerosisa
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Leukocyte Behavior in Atherosclerosis, Myocardial Infarction, and Heart Failure
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Inhibition of malonyl-CoA decarboxylase reduces the inflammatory response associated with insulin resistance
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Oxytocin attenuates NADPH-dependent superoxide activity and IL-6 secretion in macrophages and vascular cells
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Association Between Prostaglandin E Receptor Subtype EP4 Overexpression and Unstable Phenotype in Atherosclerotic Plaques in Human
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Topographical Association Between the Cyclin-Dependent Kinases Inhibitor P21, p53 Accumulation, and Cellular Proliferation in Human Atherosclerotic Tissue
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Protective Function of Transcription Factor TR3 Orphan Receptor in Atherogenesis
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Expression of α2-Adrenergic Receptors in Normal and Atherosclerotic Rabbit Aorta
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Angiotensin II and Aldosterone Regulate Gene Transcription Via Functional Mineralocortocoid Receptors in Human Coronary Artery Smooth Muscle Cells
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Laminar Shear Stress Regulates Endothelial Kinin B1 Receptor Expression and Function
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Induction of Transglutaminase 2 by a Liver X Receptor/Retinoic Acid Receptor α Pathway Increases the Clearance of Apoptotic Cells by Human Macrophages
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Bile salt–dependent lipase interacts with platelet CXCR4 and modulates thrombus formation in mice and humans
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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.12334-0openalex-snapshot
Systems Chemical Biology: Integrating Medicinal Chemistry and Systems Biology for Drug Discovery
inferred← citeshttps://doi.org/10.1016/b978-0-443-29808-0.00025-xopenalex-snapshot
Systems chemical biology: Integrating medicinal chemistry and systems biology for drug discovery
inferred← citeshttps://doi.org/10.1016/j.drudis.2015.07.018openalex-snapshot
In silico assessment of adverse drug reactions and associated mechanisms
inferred← citeshttps://doi.org/10.1039/c6mb00052eopenalex-snapshot
Illuminating drug action by network integration of disease genes: a case study of myocardial infarction
inferred← citeshttps://doi.org/10.1080/1062936x.2015.1078407openalex-snapshot
PASS Targets: Ligand-based multi-target computational system based on a public data and naïve Bayes approach
inferred← citeshttps://doi.org/10.1093/toxsci/kfv054openalex-snapshot
Identification of Drug Targets Related to the Induction of Ventricular Tachyarrhythmia Through a Systems Chemical Biology Approach
inferred← citeshttps://doi.org/10.1134/s1990750820030117openalex-snapshot
Computer-Aided Drug Design: from Discovery of Novel Pharmaceutical Agents to Systems Pharmacology
inferred← citeshttps://doi.org/10.18097/pbmc20206601030openalex-snapshot
Computer-aided drug design: from discovery of novel pharmaceutical agents to systems pharmacology
inferred← citeshttps://doi.org/10.30895/2312-7821-2023-11-4-372-389openalex-snapshot
In Silico Estimation of the Safety of Pharmacologically Active Substances Using Machine Learning Methods: A Review
inferred← citeshttps://doi.org/10.7287/peerj.7325v0.1/reviews/1openalex-snapshot
Peer Review #1 of "In silico analyses of CD14 molecule reveal significant evolutionary diversity, potentially associated with speciation and variable immune response in mammals (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7325v0.1/reviews/2openalex-snapshot
Peer Review #2 of "In silico analyses of CD14 molecule reveal significant evolutionary diversity, potentially associated with speciation and variable immune response in mammals (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7325v0.1/reviews/3openalex-snapshot
Peer Review #3 of "In silico analyses of CD14 molecule reveal significant evolutionary diversity, potentially associated with speciation and variable immune response in mammals (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.7325openalex-snapshot
In silico analyses of CD14 molecule reveal significant evolutionary diversity, potentially associated with speciation and variable immune response in mammals
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.