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The UPR in atherosclerosis

https://doi.org/10.1007/s00281-013-0372-x
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1 of the 91 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-21): 10.2337/db09-1637 (notice 2026-07-20).

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/biof.17openalex-snapshot
Contributions of hyperhomocysteinemia to atherosclerosis: Causal relationship and potential mechanisms
inferredcites →https://doi.org/10.1002/eji.201141717openalex-snapshot
Regulatory macrophages: Setting the Threshold for Therapy
inferredcites →https://doi.org/10.1016/0092-8674(93)90521-qopenalex-snapshot
A transmembrane protein with a cdc2+CDC28-related kinase activity is required for signaling from the ER to the nucleus
inferredcites →https://doi.org/10.1016/0092-8674(93)90648-aopenalex-snapshot
Transcriptional induction of genes encoding endoplasmic reticulum resident proteins requires a transmembrane protein kinase
inferredcites →https://doi.org/10.1016/j.atherosclerosis.2009.04.019openalex-snapshot
Free cholesterol overloading induced smooth muscle cells death and activated both ER- and mitochondrial-dependent death pathway
inferredcites →https://doi.org/10.1016/j.bcp.2005.03.017openalex-snapshot
Quercetin, but not rutin and quercitrin, prevention of H2O2-induced apoptosis via anti-oxidant activity and heme oxygenase 1 gene expression in macrophages
inferredcites →https://doi.org/10.1016/j.cell.2007.04.027openalex-snapshot
ER Stress Triggers Apoptosis by Activating BH3-Only Protein Bim
inferredcites →https://doi.org/10.1016/j.cell.2009.07.017openalex-snapshot
IRE1α Kinase Activation Modes Control Alternate Endoribonuclease Outputs to Determine Divergent Cell Fates
inferredcites →https://doi.org/10.1016/j.cell.2010.02.034openalex-snapshot
Endoplasmic Reticulum Stress and the Inflammatory Basis of Metabolic Disease
inferredcites →https://doi.org/10.1016/j.cmet.2009.03.003openalex-snapshot
Reduced Apoptosis and Plaque Necrosis in Advanced Atherosclerotic Lesions of Apoe−/− and Ldlr−/− Mice Lacking CHOP
inferredcites →https://doi.org/10.1016/j.cmet.2010.09.010openalex-snapshot
Atherogenic Lipids and Lipoproteins Trigger CD36-TLR2-Dependent Apoptosis in Macrophages Undergoing Endoplasmic Reticulum Stress
inferredcites →https://doi.org/10.1016/j.cmet.2012.07.007openalex-snapshot
IRE1α Induces Thioredoxin-Interacting Protein to Activate the NLRP3 Inflammasome and Promote Programmed Cell Death under Irremediable ER Stress
inferredcites →https://doi.org/10.1016/j.mam.2010.09.002openalex-snapshot
Flavonols and cardiovascular disease
inferredcites →https://doi.org/10.1016/j.mcn.2008.01.014openalex-snapshot
Loss of c/EBP-β activity promotes the adaptive to apoptotic switch in hypoxic cortical neurons
inferredcites →https://doi.org/10.1016/j.molcel.2010.04.001openalex-snapshot
Flavonol Activation Defines an Unanticipated Ligand-Binding Site in the Kinase-RNase Domain of IRE1
inferredcites →https://doi.org/10.1016/j.numecd.2004.04.002openalex-snapshot
Is homocysteine important as risk factor for coronary heart disease?
inferredcites →https://doi.org/10.1016/s0008-6363(98)00212-0openalex-snapshot
Apoptosis of vascular smooth muscle cells in vascular remodelling and atherosclerotic plaque rupture
inferredcites →https://doi.org/10.1016/s0022-2275(20)32363-4openalex-snapshot
Oxidized LDL induces the expression of ALBP/aP2 mRNA and protein in human THP-1 macrophages
inferredcites →https://doi.org/10.1016/s0140-6736(96)07495-8openalex-snapshot
Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study
inferredcites →https://doi.org/10.1021/jf803390mopenalex-snapshot
Blockade of Oxidized LDL-Triggered Endothelial Apoptosis by Quercetin and Rutin through Differential Signaling Pathways Involving JAK2
inferredcites →https://doi.org/10.1038/89076openalex-snapshot
Lack of macrophage fatty-acid–binding protein aP2 protects mice deficient in apolipoprotein E against atherosclerosis
inferredcites →https://doi.org/10.1038/cddis.2011.132openalex-snapshot
ER stress activates the NLRP3 inflammasome via an UPR-independent pathway
inferredcites →https://doi.org/10.1038/nature04399openalex-snapshot
Role of cholesterol and lipid organization in disease
inferredcites →https://doi.org/10.1038/nature06796openalex-snapshot
Translating molecular discoveries into new therapies for atherosclerosis
inferredcites →https://doi.org/10.1038/nature07203openalex-snapshot
From endoplasmic-reticulum stress to the inflammatory response
inferredcites →https://doi.org/10.1038/ncb0311-184openalex-snapshot
Integrating the mechanisms of apoptosis induced by endoplasmic reticulum stress
inferredcites →https://doi.org/10.1038/ncb1035openalex-snapshot
The endoplasmic reticulum is the site of cholesterol-induced cytotoxicity in macrophages
inferredcites →https://doi.org/10.1038/nm.2067openalex-snapshot
Reducing endoplasmic reticulum stress through a macrophage lipid chaperone alleviates atherosclerosis
inferredcites →https://doi.org/10.1038/nrm2199openalex-snapshot
Signal integration in the endoplasmic reticulum unfolded protein response
inferredcites →https://doi.org/10.1038/nrm3270openalex-snapshot
The unfolded protein response: controlling cell fate decisions under ER stress and beyond
inferredcites →https://doi.org/10.1038/sj.embor.7400779openalex-snapshot
Mediators of endoplasmic reticulum stress‐induced apoptosis
inferredcites →https://doi.org/10.1056/nejmra043430openalex-snapshot
Inflammation, Atherosclerosis, and Coronary Artery Disease
inferredcites →https://doi.org/10.1073/pnas.0438011100openalex-snapshot
JNK phosphorylation of Bim-related members of the Bcl2 family induces Bax-dependent apoptosis
inferredcites →https://doi.org/10.1073/pnas.0509487102openalex-snapshot
On the mechanism of sensing unfolded protein in the endoplasmic reticulum
inferredcites →https://doi.org/10.1073/pnas.0605457103openalex-snapshot
Identification of inflammatory gene modules based on variations of human endothelial cell responses to oxidized lipids
inferredcites →https://doi.org/10.1073/pnas.0609671104openalex-snapshot
Combinatorial pattern recognition receptor signaling alters the balance of life and death in macrophages
inferredcites →https://doi.org/10.1073/pnas.0903197106openalex-snapshot
Sustained activation of XBP1 splicing leads to endothelial apoptosis and atherosclerosis development in response to disturbed flow
inferredcites →https://doi.org/10.1074/jbc.m100747200openalex-snapshot
Homocysteine Induces Programmed Cell Death in Human Vascular Endothelial Cells through Activation of the Unfolded Protein Response
inferredcites →https://doi.org/10.1074/jbc.m111.338673openalex-snapshot
Endoplasmic Reticulum Stress Controls M2 Macrophage Differentiation and Foam Cell Formation
inferredcites →https://doi.org/10.1074/jbc.m212897200openalex-snapshot
TDAG51 Is Induced by Homocysteine, Promotes Detachment-mediated Programmed Cell Death, and Contributes to the Development of Atherosclerosis in Hyperhomocysteinemia
inferredcites →https://doi.org/10.1074/jbc.m405195200openalex-snapshot
Enrichment of Endoplasmic Reticulum with Cholesterol Inhibits Sarcoplasmic-Endoplasmic Reticulum Calcium ATPase-2b Activity in Parallel with Increased Order of Membrane Lipids
inferredcites →https://doi.org/10.1074/jbc.m501759200openalex-snapshot
Free Cholesterol-loaded Macrophages Are an Abundant Source of Tumor Necrosis Factor-α and Interleukin-6
inferredcites →https://doi.org/10.1083/jcb.153.5.1011openalex-snapshot
Feedback Inhibition of the Unfolded Protein Response by GADD34-Mediated Dephosphorylation of eIF2α
inferredcites →https://doi.org/10.1083/jcb.200904060openalex-snapshot
Role of ERO1-α–mediated stimulation of inositol 1,4,5-triphosphate receptor activity in endoplasmic reticulum stress–induced apoptosis
inferredcites →https://doi.org/10.1083/jcb.201003138openalex-snapshot
Regulation of basal cellular physiology by the homeostatic unfolded protein response
inferredcites →https://doi.org/10.1091/mbc.e05-12-1107openalex-snapshot
Caspase-2–induced Apoptosis Requires Bid Cleavage: A Physiological Role for Bid in Heat Shock–induced Death
inferredcites →https://doi.org/10.1096/fj.07-105353openalex-snapshot
Hyperhomocysteinemia induced by methionine supplementation does not independently cause atherosclerosis in C57BL/6J mice
inferredcites →https://doi.org/10.1096/fj.10-159319openalex-snapshot
Induction of the unfolded protein response after monocyte to macrophage differentiation augments cell survival in early atherosclerotic lesions
inferredcites →https://doi.org/10.1096/fj.11-182931openalex-snapshot
Peptides derived from the bifunctional kinase/RNase enzyme IRE1α modulate IRE1α activity and protect cells from endoplasmic reticulum stress
inferredcites →https://doi.org/10.1097/00041433-199810000-00012openalex-snapshot
The response‐to‐retention hypothesis of atherogenesis reinforced
inferredcites →https://doi.org/10.1101/gad.1250704openalex-snapshot
CHOP induces death by promoting protein synthesis and oxidation in the stressed endoplasmic reticulum
inferredcites →https://doi.org/10.1111/j.1365-2249.2005.02934.xopenalex-snapshot
Macrophage activation switching: an asset for the resolution of inflammation
inferredcites →https://doi.org/10.1111/j.1463-1326.2010.01282.xopenalex-snapshot
Restoring endoplasmic reticulum function by chemical chaperones: an emerging therapeutic approach for metabolic diseases
inferredcites →https://doi.org/10.1126/science.1090031openalex-snapshot
Bypassing a Kinase Activity with an ATP-Competitive Drug
inferredcites →https://doi.org/10.1126/science.1101902openalex-snapshot
A Selective Inhibitor of eIF2α Dephosphorylation Protects Cells from ER Stress
inferredcites →https://doi.org/10.1126/science.1128294openalex-snapshot
Chemical Chaperones Reduce ER Stress and Restore Glucose Homeostasis in a Mouse Model of Type 2 Diabetes
inferredcites →https://doi.org/10.1126/science.1201396openalex-snapshot
Selective Inhibition of a Regulatory Subunit of Protein Phosphatase 1 Restores Proteostasis
inferredcites →https://doi.org/10.1126/science.1226191openalex-snapshot
IRE1α Cleaves Select microRNAs During ER Stress to Derepress Translation of Proapoptotic Caspase-2
inferredcites →https://doi.org/10.1126/science.287.5453.664openalex-snapshot
Coupling of Stress in the ER to Activation of JNK Protein Kinases by Transmembrane Protein Kinase IRE1
inferredcites →https://doi.org/10.1128/mcb.01507-09openalex-snapshot
Molecular Symbiosis of CHOP and C/EBPβ Isoform LIP Contributes to Endoplasmic Reticulum Stress-Induced Apoptosis
inferredcites →https://doi.org/10.1128/mcb.19.12.8469openalex-snapshot
BCL-2 Is Phosphorylated and Inactivated by an ASK1/Jun N-Terminal Protein Kinase Pathway Normally Activated at G2/M
inferredcites →https://doi.org/10.1128/mcb.21.4.1249-1259.2001openalex-snapshot
Gadd153 Sensitizes Cells to Endoplasmic Reticulum Stress by Down-Regulating Bcl2 and Perturbing the Cellular Redox State
inferredcites →https://doi.org/10.1128/mcb.24.24.10703-10717.2004openalex-snapshot
NAD(P)H Oxidase Nox-4 Mediates 7-Ketocholesterol-Induced Endoplasmic Reticulum Stress and Apoptosis in Human Aortic Smooth Muscle Cells
inferredcites →https://doi.org/10.1155/2012/356487openalex-snapshot
Amelioration of Glucolipotoxicity-Induced Endoplasmic Reticulum Stress by a “Chemical Chaperone” in Human THP-1 Monocytes
inferredcites →https://doi.org/10.1161/01.atv.0000184783.04864.9fopenalex-snapshot
Consequences and Therapeutic Implications of Macrophage Apoptosis in Atherosclerosis
inferredcites →https://doi.org/10.1161/01.atv.0000242903.41158.a1openalex-snapshot
The Unfolded Protein Response Is an Important Regulator of Inflammatory Genes in Endothelial Cells
inferredcites →https://doi.org/10.1161/01.cir.0000134487.51510.97openalex-snapshot
Association of Multiple Cellular Stress Pathways With Accelerated Atherosclerosis in Hyperhomocysteinemic Apolipoprotein E-Deficient Mice
inferredcites →https://doi.org/10.1161/01.cir.0000160864.31351.c1openalex-snapshot
Activation of the Unfolded Protein Response Occurs at All Stages of Atherosclerotic Lesion Development in Apolipoprotein E–Deficient Mice
inferredcites →https://doi.org/10.1161/01.cir.90.4.2126openalex-snapshot
Lewis A. Conner Memorial Lecture. Mechanisms leading to myocardial infarction: insights from studies of vascular biology.
inferredcites →https://doi.org/10.1161/atvbaha.107.159327openalex-snapshot
Role of Smooth Muscle Cells in the Initiation and Early Progression of Atherosclerosis
inferredcites →https://doi.org/10.1161/atvbaha.110.206094openalex-snapshot
The Endoplasmic Reticulum Stress-C/EBP Homologous Protein Pathway-Mediated Apoptosis in Macrophages Contributes to the Instability of Atherosclerotic Plaques
inferredcites →https://doi.org/10.1161/atvbaha.111.232827openalex-snapshot
Paraoxonase-2 Modulates Stress Response of Endothelial Cells to Oxidized Phospholipids and a Bacterial Quorum–Sensing Molecule
inferredcites →https://doi.org/10.1161/circgenetics.110.958926openalex-snapshot
Coronary Artery Endothelial Transcriptome In Vivo
inferredcites →https://doi.org/10.1161/circresaha.108.182568openalex-snapshot
Free Cholesterol Accumulation in Macrophage Membranes Activates Toll-Like Receptors and p38 Mitogen-Activated Protein Kinase and Induces Cathepsin K
inferredcites →https://doi.org/10.1161/circresaha.109.203711openalex-snapshot
Chronic Endoplasmic Reticulum Stress Activates Unfolded Protein Response in Arterial Endothelium in Regions of Susceptibility to Atherosclerosis
inferredcites →https://doi.org/10.1161/circresaha.110.224766openalex-snapshot
The Role of Endoplasmic Reticulum Stress in the Progression of Atherosclerosis
inferredcites →https://doi.org/10.1161/circresaha.110.227819openalex-snapshot
Endoplasmic Reticulum Stress As a Therapeutic Target in Cardiovascular Disease
inferredcites →https://doi.org/10.1161/circulationaha.106.676890openalex-snapshot
Subendothelial Lipoprotein Retention as the Initiating Process in Atherosclerosis
inferredcites →https://doi.org/10.1161/circulationaha.106.682054openalex-snapshot
Increased Endoplasmic Reticulum Stress in Atherosclerotic Plaques Associated With Acute Coronary Syndrome
inferredcites →https://doi.org/10.1161/circulationaha.109.900928openalex-snapshot
Reduction of AMP-Activated Protein Kinase α2 Increases Endoplasmic Reticulum Stress and Atherosclerosis In Vivo
inferredcites →https://doi.org/10.1161/circulationaha.110.014050openalex-snapshot
Involvement of Endoplasmic Stress Protein C/EBP Homologous Protein in Arteriosclerosis Acceleration With Augmented Biological Stress Responses
inferredcites →https://doi.org/10.1161/hypertensionaha.109.129924openalex-snapshot
High Dietary Taurine Reduces Apoptosis and Atherosclerosis in the Left Main Coronary Artery
inferredcites →https://doi.org/10.1172/jci37262openalex-snapshot
Macrophage deficiency of p38α MAPK promotes apoptosis and plaque necrosis in advanced atherosclerotic lesions in mice
inferredcites →https://doi.org/10.1172/jci38857openalex-snapshot
Calcium/calmodulin-dependent protein kinase II links ER stress with Fas and mitochondrial apoptosis pathways
inferredcites →https://doi.org/10.1186/1476-511x-10-229openalex-snapshot
M2 macrophages exhibit higher sensitivity to oxLDL-induced lipotoxicity than other monocyte/macrophage subtypes
inferredcites →https://doi.org/10.1258/ebm.2012.012027openalex-snapshot
Quercetin protects macrophages from oxidized low-density lipoprotein-induced apoptosis by inhibiting the endoplasmic reticulum stress-C/EBP homologous protein pathway
inferredcites →https://doi.org/10.1371/journal.pone.0008852openalex-snapshot
Macrophage Plasticity in Experimental Atherosclerosis
inferredcites →https://doi.org/10.1371/journal.pone.0039586openalex-snapshot
CHOP Potentially Co-Operates with FOXO3a in Neuronal Cells to Regulate PUMA and BIM Expression in Response to ER Stress
inferredcites →https://doi.org/10.2337/db09-1637openalex-snapshot
Activation of AMP-Activated Protein Kinase Inhibits Oxidized LDL-Triggered Endoplasmic Reticulum Stress In Vivo
inferredcites →https://doi.org/10.3410/f.717959717.793462943openalex-snapshot
Faculty Opinions recommendation of IRE1α cleaves select microRNAs during ER stress to derepress translation of proapoptotic Caspase-2.
inferredcites →https://doi.org/10.7326/0003-4819-131-5-199909070-00008openalex-snapshot
Homocyst(e)ine and Cardiovascular Disease: A Critical Review of the Epidemiologic Evidence

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4152835openalex-extracted
XBP1: An Adaptor in the Pathogenesis of Atherosclerosis
inferred← citeshttps://doi.org/10.2139/ssrn.4639349openalex-extracted
Protein-Rich Foods, Sea Foods, and Gut Microbiota Amplify Immune Responses in Chronic Diseases and Cancers – Targeting Perk as a Novel Therapeutic Strategy for Cancer
inferred← citeshttps://doi.org/10.1002/biof.1635openalex-snapshot
High‐throughput profiling reveals perturbation of endoplasmic reticulum stress‐related genes in atherosclerosis induced by high‐cholesterol diet and the protective role of vitamin E
inferred← citeshttps://doi.org/10.1002/jbt.70881openalex-snapshot
Inflammation and Stress: The Resemblance and Variance Between Atherosclerosis and Carcinogenesis—A Pilot Study
inferred← citeshttps://doi.org/10.1002/jcp.28446openalex-snapshot
Scutellarin exerts protective effects against atherosclerosis in rats by regulating the Hippo–FOXO3A and PI3K/AKT signaling pathways
inferred← citeshttps://doi.org/10.1002/mnfr.201500750openalex-snapshot
Dietary compound α‐asarone alleviates ER stress‐mediated apoptosis in 7β‐hydroxycholesterol‐challenged macrophages
inferred← citeshttps://doi.org/10.1007/82_2017_1openalex-snapshot
The Unfolded Protein Response in the Immune Cell Development: Putting the Caretaker in the Driving Seat
inferred← citeshttps://doi.org/10.1007/82_2017_41openalex-snapshot
Coordinating Organismal Metabolism During Protein Misfolding in the ER Through the Unfolded Protein Response
inferred← citeshttps://doi.org/10.1007/82_2017_54openalex-snapshot
ER Protein Quality Control and the Unfolded Protein Response in the Heart
inferred← citeshttps://doi.org/10.1007/978-3-030-53868-2_10openalex-snapshot
Atherosclerosis
inferred← citeshttps://doi.org/10.1007/s00018-025-05602-2openalex-snapshot
NR4A1 deficiency promotes carotid plaque vulnerability by activating integrated stress response via targeting Bcat1
inferred← citeshttps://doi.org/10.1007/s00380-014-0557-9openalex-snapshot
Possible role of fibroblast growth factor 21 on atherosclerosis via amelioration of endoplasmic reticulum stress-mediated apoptosis in apoE−/− mice
inferred← citeshttps://doi.org/10.1007/s10495-014-0986-zopenalex-snapshot
Overexpression of CREB protein protects from tunicamycin-induced apoptosis in various rat cell types
inferred← citeshttps://doi.org/10.1007/s10753-018-0873-9openalex-snapshot
Catalpol Inhibits Homocysteine-induced Oxidation and Inflammation via Inhibiting Nox4/NF-κB and GRP78/PERK Pathways in Human Aorta Endothelial Cells
inferred← citeshttps://doi.org/10.1007/s11010-014-2073-8openalex-snapshot
Endoplasmic reticulum stress-induced hepatic stellate cell apoptosis through calcium-mediated JNK/P38 MAPK and Calpain/Caspase-12 pathways
inferred← citeshttps://doi.org/10.1007/s11010-018-3362-4openalex-snapshot
Apocynin protects endothelial cells from endoplasmic reticulum stress-induced apoptosis via IRE1α engagement
inferred← citeshttps://doi.org/10.1007/s11010-023-04780-6openalex-snapshot
IRE1α: from the function to the potential therapeutic target in atherosclerosis
inferred← citeshttps://doi.org/10.1007/s11655-019-3052-4openalex-snapshot
Pollen Typhae Total Flavone Inhibits Endoplasmic Reticulum Stress-Induced Apoptosis in Human Aortic-Vascular Smooth Muscle Cells through Down-Regulating PERK-eIF2α-ATF4-CHOP Pathway
inferred← citeshttps://doi.org/10.1007/s11756-021-00769-yopenalex-snapshot
Endoplasmic reticulum Metallo protease 1, a triggering factor for unfolded protein response and promising target in colorectal cancer
inferred← citeshttps://doi.org/10.1007/s11883-015-0503-zopenalex-snapshot
AIP1-Mediated Stress Signaling in Atherosclerosis and Arteriosclerosis
inferred← citeshttps://doi.org/10.1007/s12975-021-00968-4openalex-snapshot
Contribution of Endoplasmic Reticulum Stress to the Clinical Instability of Carotid Plaques in Human Carotid Stenosis
inferred← citeshttps://doi.org/10.1016/b978-0-323-63600-1.00003-xopenalex-snapshot
10.1016/b978-0-323-63600-1.00003-x
inferred← citeshttps://doi.org/10.1016/b978-0-443-41553-1.00002-5openalex-snapshot
Role of endoplasmic reticulum stress in angiogenesis
inferred← citeshttps://doi.org/10.1016/j.arr.2017.07.005openalex-snapshot
Protein aggregation, cardiovascular diseases, and exercise training: Where do we stand?
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2014.09.001openalex-snapshot
Vascular oxidative stress, nitric oxide and atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2021.08.033openalex-snapshot
Promoting athero-protective immunity by vaccination with low density lipoprotein-derived antigens
inferred← citeshttps://doi.org/10.1016/j.bbrep.2015.08.009openalex-snapshot
Micro-RNAs and macrophage diversity in atherosclerosis: New players, new challenges…new opportunities for therapeutic intervention?
inferred← citeshttps://doi.org/10.1016/j.cellsig.2020.109699openalex-snapshot
Unfolded protein response in cardiovascular disease
inferred← citeshttps://doi.org/10.1016/j.cjca.2016.12.010openalex-snapshot
Macrophage Apoptosis and Necrotic Core Development in Atherosclerosis: A Rapidly Advancing Field with Clinical Relevance to Imaging and Therapy
inferred← citeshttps://doi.org/10.1016/j.cmet.2015.07.010openalex-snapshot
ER Stress and Angiogenesis
inferred← citeshttps://doi.org/10.1016/j.csbj.2020.02.005openalex-snapshot
Catestatin improves insulin sensitivity by attenuating endoplasmic reticulum stress: In vivo and in silico validation
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.04.023openalex-snapshot
The UPR Activator ATF6 Responds to Proteotoxic and Lipotoxic Stress by Distinct Mechanisms
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.116030openalex-snapshot
Small molecules as modulators of the proteostasis machinery: Implication in cardiovascular diseases
inferred← citeshttps://doi.org/10.1016/j.ejphar.2022.174912openalex-snapshot
Astragaloside IV protects against C/EBP homologous protein-mediated apoptosis in oxidized low-density lipoprotein-treated macrophages by promoting autophagy
inferred← citeshttps://doi.org/10.1016/j.febslet.2014.09.046openalex-snapshot
Hypoxia triggers endothelial endoplasmic reticulum stress and apoptosis via induction of VLDL receptor
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2014.09.031openalex-snapshot
Basic mechanisms in endoplasmic reticulum stress and relation to cardiovascular diseases
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.113209openalex-snapshot
Trimethylamine N-oxide promotes PERK-mediated endothelial-mesenchymal transition and apoptosis thereby aggravates atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.jacc.2018.12.055openalex-snapshot
Intercepting the Lipid-Induced Integrated Stress Response Reduces Atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.jacc.2019.01.015openalex-snapshot
Integrated Stress Response Inhibition in Atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.jrras.2026.102184openalex-snapshot
Identification and regulatory mechanisms of biomarkers related to endoplasmic reticulum stress in coronary artery disease
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2016.10.022openalex-snapshot
PPARβ/δ activation protects against corticosterone-induced ER stress in astrocytes by inhibiting the CpG hypermethylation of microRNA-181a
inferred← citeshttps://doi.org/10.1016/j.pathophys.2019.05.005openalex-snapshot
Cholesterol enriched diet suppresses ATF6 and PERK and upregulates the IRE1 pathways of the unfolded protein response in spontaneously hypertensive rats: Relevance to pathophysiology of atherosclerosis in the setting of hypertension
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2024.108604openalex-snapshot
Protein-rich foods, sea foods, and gut microbiota amplify immune responses in chronic diseases and cancers – Targeting PERK as a novel therapeutic strategy for chronic inflammatory diseases, neurodegenerative disorders, and cancer
inferred← citeshttps://doi.org/10.1016/j.phrs.2018.04.013openalex-snapshot
Natural products targeting ER stress pathway for the treatment of cardiovascular diseases
inferred← citeshttps://doi.org/10.1016/j.redox.2017.02.025openalex-snapshot
Impact of high cholesterol and endoplasmic reticulum stress on metabolic diseases: An updated mini-review
inferred← citeshttps://doi.org/10.1016/j.redox.2019.101274openalex-snapshot
8-Chloroadenosine induces apoptosis in human coronary artery endothelial cells through the activation of the unfolded protein response
inferred← citeshttps://doi.org/10.1016/j.tox.2025.154305openalex-snapshot
Polycyclic aromatic hydrocarbons-enriched diesel exhaust particles induced hypertrophy in rat primary neonatal cardiomyocytes and apoptotic cell death in H9c2 cardiomyocytes
inferred← citeshttps://doi.org/10.1016/j.vph.2015.07.011openalex-snapshot
Pharmacological evidence for a role of the transient receptor potential canonical 3 (TRPC3) channel in endoplasmic reticulum stress-induced apoptosis of human coronary artery endothelial cells
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2018.02.011openalex-snapshot
Activation of the unfolded protein response downregulates cardiac ion channels in human induced pluripotent stem cell-derived cardiomyocytes
inferred← citeshttps://doi.org/10.1038/aps.2017.81openalex-snapshot
Activation of aldehyde dehydrogenase 2 slows down the progression of atherosclerosis via attenuation of ER stress and apoptosis in smooth muscle cells
inferred← citeshttps://doi.org/10.1038/cddis.2017.277openalex-snapshot
Dickkopf1 destabilizes atherosclerotic plaques and promotes plaque formation by inducing apoptosis of endothelial cells through activation of ER stress
inferred← citeshttps://doi.org/10.1038/nrrheum.2016.192openalex-snapshot
Causes and consequences of endoplasmic reticulum stress in rheumatic disease
inferred← citeshttps://doi.org/10.1038/s41580-024-00794-0openalex-snapshot
Homeostasis control in health and disease by the unfolded protein response
inferred← citeshttps://doi.org/10.1073/pnas.1621188114openalex-snapshot
Targeting IRE1 with small molecules counteracts progression of atherosclerosis
inferred← citeshttps://doi.org/10.1074/jbc.m113.524512openalex-snapshot
Endoplasmic Reticulum Stress Promotes Macrophage-derived Foam Cell Formation by Up-regulating Cluster of Differentiation 36 (CD36) Expression
inferred← citeshttps://doi.org/10.1074/jbc.m115.641415openalex-snapshot
Dickkopf Homolog 3 Induces Stem Cell Differentiation into Smooth Muscle Lineage via ATF6 Signalling
inferred← citeshttps://doi.org/10.1080/10799893.2021.1918167openalex-snapshot
Methylglyoxal stimulates endoplasmic reticulum stress in vascular smooth muscle cells
inferred← citeshttps://doi.org/10.1080/15376516.2016.1273429openalex-snapshot
The effects of endoplasmic reticulum stress inducer thapsigargin on the toxicity of ZnO or TiO 2 nanoparticles to human endothelial cells
inferred← citeshttps://doi.org/10.1089/ars.2016.6697openalex-snapshot
Protein Thiol Redox Signaling in Monocytes and Macrophages
inferred← citeshttps://doi.org/10.1093/toxsci/kfu233openalex-snapshot
Molecular Mechanisms of Acrolein Toxicity: Relevance to Human Disease
inferred← citeshttps://doi.org/10.1097/xce.0000000000000068openalex-snapshot
The role of lipoxins in cardiometabolic physiology and disease
inferred← citeshttps://doi.org/10.1101/615997openalex-snapshot
Catestatin improves insulin sensitivity in diet-induced obese mice: in vivo and in silico validation
inferred← citeshttps://doi.org/10.1101/cshperspect.a041400openalex-snapshot
Endoplasmic Reticulum Membrane Homeostasis and the Unfolded Protein Response
inferred← citeshttps://doi.org/10.1111/joim.12562openalex-snapshot
Calcium signalling and ER stress in insulin resistance and atherosclerosis
inferred← citeshttps://doi.org/10.1126/science.aau6499openalex-snapshot
IRE1α–XBP1 signaling in leukocytes controls prostaglandin biosynthesis and pain
inferred← citeshttps://doi.org/10.1126/scitranslmed.aaf9087openalex-snapshot
Prevention of atherosclerosis by bioactive palmitoleate through suppression of organelle stress and inflammasome activation
inferred← citeshttps://doi.org/10.1155/2017/2049217openalex-snapshot
The Role of Endoplasmic Reticulum Stress in Cardiovascular Disease and Exercise
inferred← citeshttps://doi.org/10.1155/2019/3462530openalex-snapshot
ER Stress Activates the NLRP3 Inflammasome: A Novel Mechanism of Atherosclerosis
inferred← citeshttps://doi.org/10.1155/2023/7006749openalex-snapshot
RNA Sequencing Reveals the Differentially Expressed circRNAs between Stable and Unstable Carotid Atherosclerotic Plaques
inferred← citeshttps://doi.org/10.1159/000363008openalex-snapshot
The Impact of Intermittent and Repetitive Cold Stress Exposure on Endoplasmic Reticulum Stress and Instability of Atherosclerotic Plaques
inferred← citeshttps://doi.org/10.1161/hypertensionaha.115.05377openalex-snapshot
Brain Endoplasmic Reticulum Stress Mechanistically Distinguishes the Saline-Intake and Hypertensive Response to Deoxycorticosterone Acetate–Salt
inferred← citeshttps://doi.org/10.1161/jaha.114.000949openalex-snapshot
Endoplasmic Reticulum Stress Effector CCAAT/Enhancer‐binding Protein Homologous Protein (CHOP) Regulates Chronic Kidney Disease–Induced Vascular Calcification
inferred← citeshttps://doi.org/10.1161/jaha.120.020441openalex-snapshot
Aging and Hypercholesterolemia Differentially Affect the Unfolded Protein Response in the Vasculature of ApoE −/− Mice
inferred← citeshttps://doi.org/10.1186/s11658-016-0017-xopenalex-snapshot
Posttranscriptional and transcriptional regulation of endothelial nitric-oxide synthase during hypoxia: the role of microRNAs
inferred← citeshttps://doi.org/10.1186/s12859-023-05545-0openalex-snapshot
Ab initio protein structure prediction: the necessary presence of external force field as it is delivered by Hsp40 chaperone
inferred← citeshttps://doi.org/10.1186/s12906-015-0759-4openalex-snapshot
Ethanol extract of propolis protects macrophages from oxidized low density lipoprotein-induced apoptosis by inhibiting CD36 expression and endoplasmic reticulum stress-C/EBP homologous protein pathway
inferred← citeshttps://doi.org/10.1186/s12944-025-02554-1openalex-snapshot
High-fat stimulation induces atrial structural remodeling via the TPM1/P53/SHISA5 Axis
inferred← citeshttps://doi.org/10.1186/s12967-018-1481-zopenalex-snapshot
Endoplasmic reticulum stress in perivascular adipose tissue promotes destabilization of atherosclerotic plaque by regulating GM-CSF paracrine
inferred← citeshttps://doi.org/10.1186/s12967-025-07402-5openalex-snapshot
Foam cells: tracing the diverse cellular origins and their linked signaling pathways
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011014openalex-snapshot
Genome-wide census of ATF4 binding sites and functional profiling of trait-associated genetic variants overlapping ATF4 binding motifs
inferred← citeshttps://doi.org/10.1371/journal.pone.0075249openalex-snapshot
A Deficiency of Herp, an Endoplasmic Reticulum Stress Protein, Suppresses Atherosclerosis in ApoE Knockout Mice by Attenuating Inflammatory Responses
inferred← citeshttps://doi.org/10.1371/journal.pone.0087787openalex-snapshot
The Modulation of Endoplasmic Reticulum Stress by Chemical Chaperone Upregulates Immune Negative Cytokine IL-35 in Apolipoprotein E-Deficient Mice
inferred← citeshttps://doi.org/10.1371/journal.pone.0110581openalex-snapshot
Purple Perilla Extracts Allay ER Stress in Lipid-Laden Macrophages
inferred← citeshttps://doi.org/10.14336/ad.2022.0824openalex-snapshot
X-box Binding Protein 1: An Adaptor in the Pathogenesis of Atherosclerosis
inferred← citeshttps://doi.org/10.1515/labmed-2017-0138openalex-snapshot
ATF3 and EGR2 gene expression levels in sdLDL-treated macrophages of patients with coronary artery stenosis
inferred← citeshttps://doi.org/10.15252/emmm.202115344openalex-snapshot
Intercepting IRE1 kinase‐FMRP signaling prevents atherosclerosis progression
inferred← citeshttps://doi.org/10.15407/fz64.02.054openalex-snapshot
The study of the initial stages of atherogenesis against high-fat diet
inferred← citeshttps://doi.org/10.1615/critrevimmunol.2014010267openalex-snapshot
Scavenger Receptor-A (CD204): A Two-Edged Sword in Health and Disease
inferred← citeshttps://doi.org/10.17802/2306-1278-2024-13-3s-191-207openalex-snapshot
CURRENT APPROACHES TO THE IDENTIFICATION OF CELLULAR MARKERS OF ENDOTHELIAL DYSFUNCTION
inferred← citeshttps://doi.org/10.18295/2075-0528.1676openalex-snapshot
The Role of Damage-Associated Molecular Patterns (DAMPs) in Human Diseases : Part II: DAMPs as diagnostics, prognostics and therapeutics in clinical medicine
inferred← citeshttps://doi.org/10.18632/oncotarget.10025openalex-snapshot
Methamphetamine-mediated endoplasmic reticulum (ER) stress induces type-1 programmed cell death in astrocytes via ATF6, IRE1α and PERK pathways
inferred← citeshttps://doi.org/10.18632/oncotarget.19849openalex-snapshot
Unfolded protein response signaling impacts macrophage polarity to modulate breast cancer cell clearance and melanoma immune checkpoint therapy responsiveness
inferred← citeshttps://doi.org/10.18632/oncotarget.20431openalex-snapshot
Salubrinal attenuated retinal neovascularization by inhibiting CHOP-HIF1α-VEGF pathways
inferred← citeshttps://doi.org/10.2147/dddt.s512752openalex-snapshot
Oleanolic Acid@SPIONs Alleviates Lipid-Oxidative Stress Injury of Zebrafish Blood Vessels via Regulating the Expression of JNK and MAPK Signaling Pathways in Vascular Endothelial Cells
inferred← citeshttps://doi.org/10.2174/2666796703666220602155421openalex-snapshot
In Silico Modeling of COVID-19 Pandemic Course Differentiation Using the FOD Model
inferred← citeshttps://doi.org/10.22074/cellj.2021.7849openalex-snapshot
Toll-Like Receptor 4: A Macrophage Cell Surface Receptor Is Activated By Trimethylamine-N-Oxide.
inferred← citeshttps://doi.org/10.3345/kjp.2018.06856openalex-snapshot
Changes of Bax, Bcl-2, CCR-2, MCP-1, and TGF-β1 genes in the left ventricle of spontaneously hypertensive rat after losartan treatment
inferred← citeshttps://doi.org/10.3389/fcell.2021.674103openalex-snapshot
Pathological Crosstalk Between Oxidized LDL and ER Stress in Human Diseases: A Comprehensive Review
inferred← citeshttps://doi.org/10.3389/fcvm.2022.988266openalex-snapshot
NF-κB and its crosstalk with endoplasmic reticulum stress in atherosclerosis
inferred← citeshttps://doi.org/10.3389/fgene.2014.00242openalex-snapshot
Endoplasmic reticulum stress in hepatic steatosis and inflammatory bowel diseases
inferred← citeshttps://doi.org/10.3389/fncel.2014.00213openalex-snapshot
A Molecular Web: Endoplasmic Reticulum Stress, Inflammation, and Oxidative Stress
inferred← citeshttps://doi.org/10.3389/fphar.2018.00565openalex-snapshot
Berberine Attenuates Macrophages Infiltration in Intracranial Aneurysms Potentially Through FAK/Grp78/UPR Axis
inferred← citeshttps://doi.org/10.3389/fphys.2024.1347888openalex-snapshot
Developmental endothelial locus 1: the present and future of an endogenous factor in vessels
inferred← citeshttps://doi.org/10.3390/antiox13020232openalex-snapshot
Reactive Carbonyl Species and Protein Lipoxidation in Atherogenesis
inferred← citeshttps://doi.org/10.3390/biom12050622openalex-snapshot
How Similar Are Proteins and Origami?
inferred← citeshttps://doi.org/10.3390/ijms18122721openalex-snapshot
Sphingosine-1-Phosphate Receptor 1, Expressed in Myeloid Cells, Slows Diet-Induced Atherosclerosis and Protects against Macrophage Apoptosis in Ldlr KO Mice
inferred← citeshttps://doi.org/10.3390/ijms21010169openalex-snapshot
Endoplasmic Reticulum Stress Pathway, the Unfolded Protein Response, Modulates Immune Function in the Tumor Microenvironment to Impact Tumor Progression and Therapeutic Response
inferred← citeshttps://doi.org/10.3390/ijms23052504openalex-snapshot
Atherosclerosis in HIV Patients: What Do We Know so Far?
inferred← citeshttps://doi.org/10.3390/ijms23137373openalex-snapshot
GANAB and N-Glycans Substrates Are Relevant in Human Physiology, Polycystic Pathology and Multiple Sclerosis: A Review
inferred← citeshttps://doi.org/10.3390/jcdd13020085openalex-snapshot
Atherosclerosis: A Pathologist’s Perspective
inferred← citeshttps://doi.org/10.3390/jcdd13090435openalex-snapshot
Atherosclerotic Cell Fates: A Single-Cell View of ER Stress
inferred← citeshttps://doi.org/10.3390/jcm8122047openalex-snapshot
Ca2+ Flux: Searching for a Role in Efferocytosis of Apoptotic Cells in Atherosclerosis
inferred← citeshttps://doi.org/10.3390/life13020496openalex-snapshot
The Joint Link of the rs1051730 and rs1902341 Polymorphisms and Cigarette Smoking to Peripheral Artery Disease and Atherosclerotic Lesions of Different Arterial Beds
inferred← citeshttps://doi.org/10.3892/etm.2020.8733openalex-snapshot
Rosuvastatin protects against endothelial cell apoptosis in vitro and alleviates atherosclerosis in ApoE‑/‑ mice by suppressing endoplasmic reticulum stress
inferred← citeshttps://doi.org/10.3892/mmr.2016.4975openalex-snapshot
Atorvastatin attenuates atherosclerotic plaque destabilization by inhibiting endoplasmic reticulum stress in hyperhomocysteinemic mice
inferred← citeshttps://doi.org/10.70675/9406b143zf2d7z40b8zbdc2z2c90188b8eb1openalex-snapshot
Implication des phagocytes mononuclées dans l'évolution de la plaque d'athérosclérose et relation avec l'homéostasie du cholestérol et des lipoprotéines
inferred← citeshttps://doi.org/10.70675/be4af298z55cbz4f73z8215zc8e08ac3608eopenalex-snapshot
Régulations intrinsèques et extrinsèques du métabolisme de la glutamine sur les fonctions effectrices des macrophages et conséquences sur le développement des plaques d'athéromes
inferred← citeshttps://doi.org/10.71548/15747openalex-snapshot
The Functional Domains of PHLDA1: Modulation of Intracellular Localization Impacts Apoptotic Cell Death
inferred← citeshttps://doi.org/10.7554/elife.20390openalex-snapshot
Experimental reconstitution of chronic ER stress in the liver reveals feedback suppression of BiP mRNA expression
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