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Visualizing the Role of ER Stress in Diabetic Cardiomyopathy: A Bibliometric Analysis

https://doi.org/10.2139/ssrn.4641193
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1 of the 123 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.1677/joe-07-0230 (notice 2010-10-01).

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Diabetic Cardiomyopathy: A Brief Summary on Lipid Toxicity
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Cardioprotection by Ischemic Preconditioning Preserves Mitochondrial Function and Functional Coupling Between Adenine Nucleotide Translocase and Creatine Kinase
inferredcites →https://doi.org/10.1007/s00125-014-3171-6openalex-extracted
Molecular mechanisms of diabetic cardiomyopathy
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Epidemiology of diabetes and diabetic complications in China
inferredcites →https://doi.org/10.1007/s10495-008-0302-xopenalex-extracted
Role of apoptosis in cardiovascular disease
inferredcites →https://doi.org/10.1007/s10741-021-10200-yopenalex-extracted
Mechanisms of cardiac dysfunction in diabetic cardiomyopathy: molecular abnormalities and phenotypical variants
inferredcites →https://doi.org/10.1007/s11154-010-9131-7openalex-extracted
Diabetic cardiomyopathy, causes and effects
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New type of cardiomyopathy associated with diabetic glomerulosclerosis
inferredcites →https://doi.org/10.1016/j.bbadis.2014.05.006openalex-extracted
Endoplasmic reticulum stress and protein quality control in diabetic cardiomyopathy
inferredcites →https://doi.org/10.1016/j.biocel.2012.09.017openalex-extracted
The hyperglycemia stimulated myocardial endoplasmic reticulum (ER) stress contributes to diabetic cardiomyopathy in the transgenic non-obese type 2 diabetic rats: A differential role of unfolded protein response (UPR) signaling proteins
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Current status on the therapeutic strategies for heart failure and diabetic cardiomyopathy
inferredcites →https://doi.org/10.1016/j.biopha.2023.115669openalex-extracted
Targeting mitochondrial quality control for diabetic cardiomyopathy: Therapeutic potential of hypoglycemic drugs
inferredcites →https://doi.org/10.1016/j.cbi.2021.109755openalex-extracted
In vitro and in vivo studies reveal the beneficial effects of chlorogenic acid against ER stress mediated ER-phagy and associated apoptosis in the heart of diabetic rat
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Protein kinase RNA-like endoplasmic reticulum kinase (PERK)/calcineurin signaling is a novel pathway regulating intracellular calcium accumulation which might be involved in ventricular arrhythmias in diabetic cardiomyopathy
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A Conserved Role for Phosphatidylinositol 3-Kinase but Not Akt Signaling in Mitochondrial Adaptations that Accompany Physiological Cardiac Hypertrophy
inferredcites →https://doi.org/10.1016/j.cpcardiol.2023.102052openalex-extracted
Diabetic Cardiomyopathy: 2023 Update by the International Multidisciplinary Board of Experts
inferredcites →https://doi.org/10.1016/j.diabres.2018.02.023openalex-extracted
IDF Diabetes Atlas: Global estimates of diabetes prevalence for 2017 and projections for 2045
inferredcites →https://doi.org/10.1016/j.ejphar.2020.173749openalex-extracted
Crosstalk between endoplasmic reticulum stress and oxidative stress: Focus on protein disulfide isomerase and endoplasmic reticulum oxidase 1
inferredcites →https://doi.org/10.1016/j.ejps.2011.02.005openalex-extracted
Valsartan protects against ER stress-induced myocardial apoptosis via CHOP/Puma signaling pathway in streptozotocin-induced diabetic rats
inferredcites →https://doi.org/10.1016/j.ijcard.2014.03.176openalex-extracted
PPARβ/δ attenuates palmitate-induced endoplasmic reticulum stress and induces autophagic markers in human cardiac cells
inferredcites →https://doi.org/10.1016/j.ijcard.2015.04.245openalex-extracted
SIRT1 suppresses cardiomyocyte apoptosis in diabetic cardiomyopathy: An insight into endoplasmic reticulum stress response mechanism
inferredcites →https://doi.org/10.1016/j.jep.2019.111857openalex-extracted
Astragalus polysaccharides inhibits cardiomyocyte apoptosis during diabetic cardiomyopathy via the endoplasmic reticulum stress pathway
inferredcites →https://doi.org/10.1016/j.joi.2017.08.007openalex-extracted
bibliometrix : An R-tool for comprehensive science mapping analysis
inferredcites →https://doi.org/10.1016/j.joi.2018.03.005openalex-extracted
Examining the usage, citation, and diffusion patterns of bibliometric mapping software: A comparative study of three tools
inferredcites →https://doi.org/10.1016/j.mam.2018.03.002openalex-extracted
ROS signaling and ER stress in cardiovascular disease
inferredcites →https://doi.org/10.1016/j.pharmthera.2014.01.003openalex-extracted
Diabetic cardiomyopathy: Mechanisms and new treatment strategies targeting antioxidant signaling pathways
inferredcites →https://doi.org/10.1016/j.semcancer.2019.11.007openalex-extracted
Regulation of autophagy by canonical and non-canonical ER stress responses
inferredcites →https://doi.org/10.1016/j.taap.2020.115378openalex-extracted
Astaxanthin attenuates alcoholic cardiomyopathy via inhibition of endoplasmic reticulum stress-mediated cardiac apoptosis
inferredcites →https://doi.org/10.1016/j.toxlet.2013.04.025openalex-extracted
Metallothionein prevention of arsenic trioxide-induced cardiac cell death is associated with its inhibition of mitogen-activated protein kinases activation in vitro and in vivo
inferredcites →https://doi.org/10.1016/j.toxlet.2014.03.011openalex-extracted
Metallothionein prevents intermittent hypoxia-induced cardiac endoplasmic reticulum stress and cell death likely via activation of Akt signaling pathway in mice
inferredcites →https://doi.org/10.1016/j.toxlet.2015.01.010openalex-extracted
Zinc treatment prevents type 1 diabetes-induced hepatic oxidative damage, endoplasmic reticulum stress, and cell death, and even prevents possible steatohepatitis in the OVE26 mouse model: Important role of metallothionein
inferredcites →https://doi.org/10.1016/j.yexcr.2017.03.032openalex-extracted
Palmitate mediated diacylglycerol accumulation causes endoplasmic reticulum stress, Plin2 degradation, and cell death in H9C2 cardiomyoblasts
inferredcites →https://doi.org/10.1016/s0140-6736(22)01655-5openalex-extracted
Type 2 diabetes
inferredcites →https://doi.org/10.1023/b:mcbi.0000009866.75225.e2openalex-extracted
Alterations of the bioenergetics systems of the cell in acute and chronic myocardial ischemia
inferredcites →https://doi.org/10.1038/emboj.2010.177openalex-extracted
An intimate liaison: spatial organization of the endoplasmic reticulum–mitochondria relationship
inferredcites →https://doi.org/10.1038/nrendo.2015.216openalex-extracted
Insulin resistance and hyperinsulinaemia in diabetic cardiomyopathy
inferredcites →https://doi.org/10.1038/s41420-023-01553-4openalex-extracted
Diabetic cardiomyopathy: Early diagnostic biomarkers, pathogenetic mechanisms, and therapeutic interventions
inferredcites →https://doi.org/10.1038/s41569-020-0339-2openalex-extracted
Mechanisms of diabetic cardiomyopathy and potential therapeutic strategies: preclinical and clinical evidence
inferredcites →https://doi.org/10.1042/cs20160168openalex-extracted
Myocardial redox status, mitophagy and cardioprotection: a potential way to amend diabetic heart?
inferredcites →https://doi.org/10.1056/nejmoa1608664openalex-extracted
Mortality and Cardiovascular Disease in Type 1 and Type 2 Diabetes
inferredcites →https://doi.org/10.1073/pnas.0705407104openalex-extracted
PAS kinase is required for normal cellular energy balance
inferredcites →https://doi.org/10.1073/pnas.1716439115openalex-extracted
Transmembrane E3 ligase RNF183 mediates ER stress-induced apoptosis by degrading Bcl-xL
inferredcites →https://doi.org/10.1074/jbc.m112.412783openalex-extracted
XBP1 mRNA Splicing Triggers an Autophagic Response in Endothelial Cells through BECLIN-1 Transcriptional Activation
inferredcites →https://doi.org/10.1074/jbc.m405195200openalex-extracted
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/10.1080/1061186x.2022.2064479openalex-extracted
Empagliflozin alleviates myocardial I/R injury and cardiomyocyte apoptosis via inhibiting ER stress-induced autophagy and the PERK/ATF4/Beclin1 pathway
inferredcites →https://doi.org/10.1080/13510002.2023.2246720openalex-extracted
Oxidative stress signaling in the pathogenesis of diabetic cardiomyopathy and the potential therapeutic role of antioxidant naringenin
inferredcites →https://doi.org/10.1080/21645515.2023.2207441openalex-extracted
Trends in research related to vaccine and cancer prevention from 1992 to 2022: A 30-years bibliometric analysis
inferredcites →https://doi.org/10.1089/ars.2009.2898openalex-extracted
Hydrogen Sulfide Attenuates Hyperhomocysteinemia-Induced Cardiomyocytic Endoplasmic Reticulum Stress in Rats
inferredcites →https://doi.org/10.1093/cvr/cvq102openalex-extracted
Hyperglycaemia-induced cardiomyocyte death is mediated via MCP-1 production and induction of a novel zinc-finger protein MCPIP
inferredcites →https://doi.org/10.1093/nar/gkt563openalex-extracted
The eIF2α/ATF4 pathway is essential for stress-induced autophagy gene expression
inferredcites →https://doi.org/10.1101/gad.1250704openalex-extracted
CHOP induces death by promoting protein synthesis and oxidation in the stressed endoplasmic reticulum
inferredcites →https://doi.org/10.1111/ejn.13160openalex-extracted
Endoplasmic reticulum stress‐mediated upregulation of miR‐29a enhances sensitivity to neuronal apoptosis
inferredcites →https://doi.org/10.1111/febs.13369openalex-extracted
ATF 4 mediates necrosis induced by glucose deprivation and apoptosis induced by 2‐deoxyglucose in the same cells
inferredcites →https://doi.org/10.1111/j.1582-4934.2009.00833.xopenalex-extracted
Diabetes‐ and angiotensin II‐induced cardiac endoplasmic reticulum stress and cell death: metallothionein protection
inferredcites →https://doi.org/10.1126/science.1096645openalex-extracted
Regulation of an ATG7 - beclin 1 Program of Autophagic Cell Death by Caspase-8
inferredcites →https://doi.org/10.1126/science.1128294openalex-extracted
Chemical Chaperones Reduce ER Stress and Restore Glucose Homeostasis in a Mouse Model of Type 2 Diabetes
inferredcites →https://doi.org/10.1126/science.1218099openalex-extracted
A Mitochondrial Pyruvate Carrier Required for Pyruvate Uptake in Yeast, Drosophila , and Humans
inferredcites →https://doi.org/10.1128/mcb.01453-06openalex-extracted
Autophagy Is Activated for Cell Survival after Endoplasmic ReticulumStress
inferredcites →https://doi.org/10.1128/mcb.26.8.3071-3084.2006openalex-extracted
Autocrine Tumor Necrosis Factor Alpha Links Endoplasmic Reticulum Stress to the Membrane Death Receptor Pathway through IRE1α-Mediated NF-κB Activation and Down-Regulation of TRAF2 Expression
inferredcites →https://doi.org/10.1152/ajpcell.00248.2012openalex-extracted
Exendin-4 attenuates high glucose-induced cardiomyocyte apoptosis via inhibition of endoplasmic reticulum stress and activation of SERCA2a
inferredcites →https://doi.org/10.1152/ajpendo.00629.2013openalex-extracted
Inhibition of JNK by novel curcumin analog C66 prevents diabetic cardiomyopathy with a preservation of cardiac metallothionein expression
inferredcites →https://doi.org/10.1152/ajpheart.00471.2001openalex-extracted
Alteration of mitochondrial function in a model of chronic ischemia in vivo in rat heart
inferredcites →https://doi.org/10.1152/physiol.00008.2006openalex-extracted
Mitochondrial Uncoupling: A Key Contributor to Reduced Cardiac Efficiency in Diabetes
inferredcites →https://doi.org/10.1155/2012/827971openalex-extracted
Endoplasmic Reticulum Stress and Diabetic Cardiomyopathy
inferredcites →https://doi.org/10.1155/2013/630537openalex-extracted
Glucagon-Like Peptide-1 Analog Liraglutide Protects against Diabetic Cardiomyopathy by the Inhibition of the Endoplasmic Reticulum Stress Pathway
inferredcites →https://doi.org/10.1155/2013/753150openalex-extracted
Trends in Prevalence, Awareness, Treatment, and Control of Diabetes Mellitus in Mainland China from 1979 to 2012
inferredcites →https://doi.org/10.1159/000320548openalex-extracted
Partial Inactivation of Cardiac 14-3-3 Protein in vivo Elicits Endoplasmic Reticulum Stress (ERS) and Activates ERS-initiated Apoptosis in ERS-induced Mice
inferredcites →https://doi.org/10.1161/01.atv.0000242903.41158.a1openalex-extracted
The Unfolded Protein Response Is an Important Regulator of Inflammatory Genes in Endothelial Cells
inferredcites →https://doi.org/10.1161/01.cir.0000049742.68848.99openalex-extracted
Association Between Plasma Levels of Monocyte Chemoattractant Protein-1 and Long-Term Clinical Outcomes in Patients With Acute Coronary Syndromes
inferredcites →https://doi.org/10.1161/circresaha.110.227819openalex-extracted
Endoplasmic Reticulum Stress As a Therapeutic Target in Cardiovascular Disease
inferredcites →https://doi.org/10.1161/circresaha.117.311586openalex-extracted
Diabetic Cardiomyopathy
inferredcites →https://doi.org/10.1161/circresaha.118.314665openalex-extracted
Diabetic Cardiomyopathy
inferredcites →https://doi.org/10.1161/circresaha.121.318241openalex-extracted
Cardiac Energy Metabolism in Heart Failure
inferredcites →https://doi.org/10.1161/circulationaha.105.537894openalex-extracted
Cardiac Metallothionein Induction Plays the Major Role in the Prevention of Diabetic Cardiomyopathy by Zinc Supplementation
inferredcites →https://doi.org/10.1161/circulationaha.105.554360openalex-extracted
Reduced Mitochondrial Oxidative Capacity and Increased Mitochondrial Uncoupling Impair Myocardial Energetics in Obesity
inferredcites →https://doi.org/10.1161/circulationaha.106.679597openalex-extracted
Diabetic Cardiomyopathy Revisited
inferredcites →https://doi.org/10.1161/circulationaha.113.008476openalex-extracted
Myocardial Contractile Dysfunction Is Associated With Impaired Mitochondrial Function and Dynamics in Type 2 Diabetic but Not in Obese Patients
inferredcites →https://doi.org/10.1161/circulationaha.119.040551openalex-extracted
Unlocking the Secrets of Mitochondria in the Cardiovascular System
inferredcites →https://doi.org/10.1162/qss_a_00018openalex-extracted
Web of Science as a data source for research on scientific and scholarly activity
inferredcites →https://doi.org/10.1172/jci26373openalex-extracted
Endoplasmic reticulum stress: cell life and death decisions
inferredcites →https://doi.org/10.1172/jci40027openalex-extracted
The unfolded protein response protects human tumor cells during hypoxia through regulation of the autophagy genes MAP1LC3B and ATG5
inferredcites →https://doi.org/10.1186/1475-2840-12-158openalex-extracted
Protein kinase RNA- like endoplasmic reticulum kinase (PERK) signaling pathway plays a major role in reactive oxygen species (ROS)- mediated endoplasmic reticulum stress- induced apoptosis in diabetic cardiomyopathy
inferredcites →https://doi.org/10.1186/s12967-019-1810-xopenalex-extracted
Emerging trends and research foci in gastrointestinal microbiome
inferredcites →https://doi.org/10.1186/s40001-023-01175-7openalex-extracted
Bibliometric and visual analysis of diabetes mellitus and pyroptosis from 2011 to 2022
inferredcites →https://doi.org/10.1254/jphs.10047fpopenalex-extracted
14-3-3 Protein Protects Against Cardiac Endoplasmic Reticulum Stress (ERS) and ERS-Initiated Apoptosis in Experimental Diabetes
inferredcites →https://doi.org/10.1371/journal.pbio.0030101openalex-extracted
PGC-1α Deficiency Causes Multi-System Energy Metabolic Derangements: Muscle Dysfunction, Abnormal Weight Control and Hepatic Steatosis
inferredcites →https://doi.org/10.1371/journal.pone.0118365openalex-extracted
Awareness, Treatment, and Control of Diabetes in Bangladesh: A Nationwide Population-Based Study
inferredcites →https://doi.org/10.1385/ct:3:3:219openalex-extracted
Cell Death and Diabetic Cardiomyopathy
inferredcites →https://doi.org/10.1515/jdis-2017-0006openalex-extracted
Science Mapping: A Systematic Review of the Literature
inferredcites →https://doi.org/10.1523/jneurosci.2760-08.2009openalex-extracted
Saturated Fatty Acids Produce an Inflammatory Response Predominantly through the Activation of TLR4 Signaling in Hypothalamus: Implications for the Pathogenesis of Obesity
inferredcites →https://doi.org/10.1677/joe-07-0230openalex-extracted
Endoplasmic reticulum stress is involved in myocardial apoptosis of streptozocin-induced diabetic rats
inferredcites →https://doi.org/10.2119/2007-00114.jouihanopenalex-extracted
Iron-Mediated Inhibition of Mitochondrial Manganese Uptake Mediates Mitochondrial Dysfunction in a Mouse Model of Hemochromatosis
inferredcites →https://doi.org/10.21203/rs.3.rs-1461727/v1openalex-extracted
Prevalence, awareness and control of type 2 diabetes mellitus and risk factors in Chinese elderly population
inferredcites →https://doi.org/10.2337/db07-0481openalex-extracted
Mitochondrial Energetics in the Heart in Obesity-Related Diabetes
inferredcites →https://doi.org/10.2337/db09-0158openalex-extracted
Endoplasmic Reticulum Stress in Diabetic Hearts Abolishes Erythropoietin-Induced Myocardial Protection by Impairment of Phospho–Glycogen Synthase Kinase-3β–Mediated Suppression of Mitochondrial Permeability Transition
inferredcites →https://doi.org/10.2337/db09-1800openalex-extracted
Deficiency of Rac1 Blocks NADPH Oxidase Activation, Inhibits Endoplasmic Reticulum Stress, and Reduces Myocardial Remodeling in a Mouse Model of Type 1 Diabetes
inferredcites →https://doi.org/10.2337/db12-1233openalex-extracted
A Novel Mechanism by Which SDF-1β Protects Cardiac Cells From Palmitate-Induced Endoplasmic Reticulum Stress and Apoptosis via CXCR7 and AMPK/p38 MAPK-Mediated Interleukin-6 Generation
inferredcites →https://doi.org/10.2337/diabetes.51.6.1938openalex-extracted
Hyperglycemia-Induced Apoptosis in Mouse Myocardium
inferredcites →https://doi.org/10.3164/jcbn.2007008openalex-extracted
Involvement of Endoplasmic Reticulum Stress in Myocardial Apoptosis of Streptozocin-Induced Diabetic Rats
inferredcites →https://doi.org/10.3389/fcvm.2022.1006213openalex-extracted
Bibliometric analysis of the inflammation in diabetic cardiomyopathy
inferredcites →https://doi.org/10.3389/fcvm.2022.1018841openalex-extracted
Research status and trends of the diabetic cardiomyopathy in the past 10 years (2012–2021): A bibliometric analysis
inferredcites →https://doi.org/10.3389/fcvm.2022.891428openalex-extracted
Knowledge domain and emerging trends in diabetic cardiomyopathy: A scientometric review based on CiteSpace analysis
inferredcites →https://doi.org/10.3389/fendo.2019.00451openalex-extracted
Type 2 Diabetes: How Much of an Autoimmune Disease?
inferredcites →https://doi.org/10.3389/fimmu.2022.815575openalex-extracted
Knowledge Mapping of Immunotherapy for Hepatocellular Carcinoma: A Bibliometric Study
inferredcites →https://doi.org/10.3389/fimmu.2022.939433openalex-extracted
Knowledge Mapping of Exosomes in Autoimmune Diseases: A Bibliometric Analysis (2002–2021)
inferredcites →https://doi.org/10.3389/fimmu.2023.1142512openalex-extracted
The role of circadian clock-controlled mitochondrial dynamics in diabetic cardiomyopathy
inferredcites →https://doi.org/10.3389/fmed.2021.787228openalex-extracted
Mapping Knowledge Structure and Themes Trends of Osteoporosis in Rheumatoid Arthritis: A Bibliometric Analysis
inferredcites →https://doi.org/10.3389/fphar.2022.1009025openalex-extracted
Bibliometric and visualized analysis of sodium–Glucose cotransporter 2 inhibitors
inferredcites →https://doi.org/10.3390/foods9020166openalex-extracted
Knowledge Domain and Emerging Trends in Vinegar Research: A Bibliometric Review of the Literature from WoSCC
inferredcites →https://doi.org/10.3390/ijerph17072449openalex-extracted
The Innovative and Sustainable Use of Dental Panoramic Radiographs for the Detection of Osteoporosis
inferredcites →https://doi.org/10.3390/ijerph19052508openalex-extracted
A Bibliometric Analysis of the Literature on Norovirus Disease from 1991–2021
inferredcites →https://doi.org/10.3390/ijms17030327openalex-extracted
Endoplasmic Reticulum Stress and Associated ROS
inferredcites →https://doi.org/10.3390/metabo12070635openalex-extracted
Exercise Augments the Effect of SGLT2 Inhibitor Dapagliflozin on Experimentally Induced Diabetic Cardiomyopathy, Possible Underlying Mechanisms
inferredcites →https://doi.org/10.3892/mmr.2014.1956openalex-extracted
Liraglutide alleviates diabetic cardiomyopathy by blocking CHOP-triggered apoptosis via the inhibition of the IRE-α pathway
inferredcites →https://doi.org/10.3892/ol.2015.3508openalex-extracted
Interplay between unfolded protein response and autophagy promotes tumor drug resistance
inferredcites →https://doi.org/10.4061/2011/259462openalex-extracted
Endoplasmic Reticulum Stress-Related Inflammation and Cardiovascular Diseases
inferredcites →https://doi.org/10.4103/wjtcm.wjtcm_27_21openalex-extracted
Acupuncture for Hot Flashes
inferredcites →https://doi.org/10.4172/2327-4638.1000105openalex-extracted
Endoplasmic Reticulum Stress and Related Pathological Processes
inferredcites →https://doi.org/10.4331/wjbc.v9.i1.1openalex-extracted
Mutual interaction between oxidative stress and endoplasmic reticulum stress in the pathogenesis of diseases specifically focusing on non-alcoholic fatty liver disease
inferredcites →https://doi.org/10.6084/m9.figshare.20525647.v1openalex-extracted
inferredcites →https://doi.org/10.7150/ijbs.59404openalex-extracted
Tagitinin C induces ferroptosis through PERK-Nrf2-HO-1 signaling pathway in colorectal cancer cells
inferredcites →https://doi.org/10.7150/jca.61622openalex-extracted
PERK Regulates the Sensitivity of Hepatocellular Carcinoma Cells to High-LET Carbon Ions via either Apoptosis or Ferroptosis
inferredcites →https://doi.org/10.6084/m9.figshare.20525647openalex-snapshot
Empagliflozin alleviates myocardial I/R injury and cardiomyocyte apoptosis via inhibiting ER stress-induced autophagy and the PERK/ATF4/Beclin1 pathway
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