Oxidative Stress and Diabetic Complications

The Effect of Intensive Treatment of Diabetes on the Development and Progression of Long-Term Complications in Insulin-Dependent Diabetes Mellitus

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Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33)

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Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). UK Prospective Diabetes Study (UKPDS) Group.

Turner, R. C., Fox, C., Matthews, McElroy, H. H., Cull, C. A., Holman, R. R., Neil, P., Hadden, D. R., Wright, D., Manley, E., et al. (1998) · The Lancet · Cited by 8,419

10-year follow-up of intensive glucose control in type 2 diabetes

Holman, R. R., Paul, S. K., Bethel, M. A., Matthews, D. R., & Neil, H. A. W. (2008) · New England Journal of Medicine · doi:10.1056/nejmoa0806470 · Cited by 7,751

Mortality from Coronary Heart Disease in Subjects with Type 2 Diabetes and in Nondiabetic Subjects with and without Prior Myocardial Infarction

Haffner, S. M., Lehto, S., Rönnemaa, T., Pyörälä, K., & Laakso, M. (1998) · New England Journal of Medicine · doi:10.1056/nejm199807233390404 · Cited by 7,000

The Pathobiology of Diabetic Complications

Brownlee, M. (2005) · Diabetes · doi:10.2337/diabetes.54.6.1615 · Cited by 5,339

Intensive diabetes treatment and cardiovascular disease in patients with type 1 diabetes

(2005) · New England Journal of Medicine · doi:10.1056/nejmoa052187 · Cited by 5,138

Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage

Nishikawa, T., Edelstein, D., Du, X. L., Yamagishi, S.-I., Matsumura, T., Kaneda, Y., Yorek, M. A., Beebe, D., Oates, P. J., Hammes, H.-P., et al. (2000) · Nature · doi:10.1038/35008121 · Cited by 4,277

The endothelium: influencing vascular smooth muscle in many ways

Triggle, C. R., Samuel, S. M., Ravishankar, S., Marei, I., Arunachalam, G., & Ding, H. (2012) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y2012-073 · Cited by 229

Roles of Hydrogen Sulfide in the Pathogenesis of Diabetes Mellitus and Its Complications

Szabó, C. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.4451 · Cited by 216

Thermosensitive Hydrogel Incorporating Prussian Blue Nanoparticles Promotes Diabetic Wound Healing via ROS Scavenging and Mitochondrial Function Restoration

Zhao, X., Liu, Y., Ma, R., Chen, J., Qiu, J., Du, S., Li, C., Wu, Z., Yang, X., Chen, Z., et al. (2022) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.1c24569 · Cited by 216

Mechanisms Leading to Differential Hypoxia-Inducible Factor Signaling in the Diabetic Kidney: Modulation by SGLT2 Inhibitors and Hypoxia Mimetics

Packer, M. (2020) · American Journal of Kidney Diseases · doi:10.1053/j.ajkd.2020.04.016 · Cited by 218

Natural Phyto-Bioactive Compounds for the Treatment of Type 2 Diabetes: Inflammation as a Target

Gothai, S., Ganesan, P., Park, S., Fakurazi, S., Choi, D., & Arulselvan, P. (2016) · Nutrients · doi:10.3390/nu8080461 · Cited by 226

Fibroblast Growth Factor in Diabetic Foot Ulcer: Progress and Therapeutic Prospects

Liu, Y., Liu, Y.-Q., Deng, J., Li, W., & Nie, X.-Q. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.744868 · Cited by 196

The impact of oxidative stress-induced mitochondrial dysfunction on diabetic microvascular complications

Zhang, Z., Huang, Q., Zhao, D., Lian, F., Li, X., & Qi, W. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1112363 · Cited by 236

Nanoparticle-Based Therapeutic Approach for Diabetic Wound Healing

Ezhilarasu, H., Dinesh, V., Dheen, S. T., Bay, B., & Srinivasan, D. K. (2020) · Nanomaterials · doi:10.3390/nano10061234 · Cited by 218

The role of inflammation in immune system of diabetic retinopathy: Molecular mechanisms, pathogenetic role and therapeutic implications

Yue, T., Shi, Y., Luo, S., Weng, J., Wu, Y., & Zheng, X. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1055087 · Cited by 230

How Effective Are Antioxidant Supplements in Obesity and Diabetes?

Abdali, D., Samson, S. E., & Grover, A. K. (2015) · Medical Principles and Practice · doi:10.1159/000375305 · Cited by 214

Tumor Microenvironment and Metabolic Synergy in Breast Cancers: Critical Importance of Mitochondrial Fuels and Function

Martinez‐Outschoorn, U., Sotgia, F., & Lisanti, M. P. (2014) · Seminars in Oncology · doi:10.1053/j.seminoncol.2014.03.002 · Cited by 211

In Vitro/In Vivo Toxicity Evaluation and Quantification of Iron Oxide Nanoparticles

Patil, U., Adireddy, S., Jaiswal, A. R., Mandava, S. H., Lee, B. G., & Chrisey, D. B. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms161024417 · Cited by 209

High Glucose Induced Alteration of SIRTs in Endothelial Cells Causes Rapid Aging in a p300 and FOXO Regulated Pathway

Mortuza, R., Chen, S., Feng, B., Sen, S., & Chakrabarti, S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054514 · Cited by 208

OxInflammation: From Subclinical Condition to Pathological Biomarker

Valacchi, G., Virgili, F., Cervellati, C., & Pecorelli, A. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00858 · Cited by 212

Glucagon-Like Peptide 1 Reduces Endothelial Dysfunction, Inflammation, and Oxidative Stress Induced by Both Hyperglycemia and Hypoglycemia in Type 1 Diabetes

Ceriello, A., Novials, A., Ortega, E., Canivell, S., La Sala, L., Pujadas, G., Esposito, K., Giugliano, D., & Genovese, S. (2013) · Diabetes Care · doi:10.2337/dc12-2469 · Cited by 204

Resveratrol alleviates diabetic cardiomyopathy in rats by improving mitochondrial function through PGC-1α deacetylation

Fang, W., Wang, C., He, Y., Zhou, Y., Peng, X., & Liu, S. (2017) · Acta Pharmacologica Sinica · doi:10.1038/aps.2017.50 · Cited by 207

Activation of Nrf2 signaling by natural products-can it alleviate diabetes?

Matzinger, M., Fischhuber, K., & Heiß, E. H. (2017) · Biotechnology Advances · doi:10.1016/j.biotechadv.2017.12.015 · Cited by 208

Modulation of Glucose Transporter Protein by Dietary Flavonoids in Type 2 Diabetes Mellitus

Hajiaghaalipour, F., Khalilpourfarshbafi, M., & Arya, A. (2015) · International Journal of Biological Sciences · doi:10.7150/ijbs.11241 · Cited by 215

Complications of Diabetes

Papatheodorou, K., Banach, M., EDMONDS, M. E., Παπάνας, Ν., & Papazoglou, D. (2015) · Journal of Diabetes Research · doi:10.1155/2015/189525 · Cited by 203

Antioxidant Activity, Metabolism, and Bioavailability of Polyphenols in the Diet of Animals

Bešlo, D., Golubić, N., Rastija, V., Agić, D., Karnaš, M., Šubarić, D., & Lučić, B. (2023) · Antioxidants · doi:10.3390/antiox12061141 · Cited by 226

TXNIP Links Innate Host Defense Mechanisms to Oxidative Stress and Inflammation in Retinal Muller Glia under Chronic Hyperglycemia: Implications for Diabetic Retinopathy

Devi, T. S., Lee, I., Hüttemann, M., Kumar, A., Nantwi, K. D., & Singh, L. P. (2012) · Experimental Diabetes Research · doi:10.1155/2012/438238 · Cited by 203

Principles of targeting endothelial cell metabolism to treat angiogenesis and endothelial cell dysfunction in disease

Goveia, J., Stapor, P. C., & Carmeliet, P. (2014) · EMBO Molecular Medicine · doi:10.15252/emmm.201404156 · Cited by 203

Molecular hydrogen is a novel antioxidant to efficiently reduce oxidative stress with potential for the improvement of mitochondrial diseases

Ohta, S. (2011) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2011.05.006 · Cited by 202

Molecular complexities underlying the vascular complications of diabetes mellitus – A comprehensive review

Paul, S., Ali, A., & Katare, R. (2020) · Journal of Diabetes and its Complications · doi:10.1016/j.jdiacomp.2020.107613 · Cited by 215

Is oxidative stress, a link between nephrolithiasis and obesity, hypertension, diabetes, chronic kidney disease, metabolic syndrome?

Khan, S. R. (2012) · Urological Research · doi:10.1007/s00240-011-0448-9 · Cited by 202

Diabetic retinopathy: a complex pathophysiology requiring novel therapeutic strategies

Whitehead, M. A., Wickremasinghe, S., Osborne, A., van Wijngaarden, P., & Martin, K. R. G. (2018) · Expert Opinion on Biological Therapy · doi:10.1080/14712598.2018.1545836 · Cited by 209

Diabetic Foot Ulcers: Pathophysiology, Immune Dysregulation, and Emerging Therapeutic Strategies

Dawi, J., Tumanyan, K., Tomas, K., Misakyan, Y., Gargaloyan, A., Gonzalez, E., Hammi, M., Tomas, S., & Venketaraman, V. (2025) · Biomedicines · doi:10.3390/biomedicines13051076 · Cited by 225

Diabetic nephropathy and antioxidants

Tavafi, M. (2013) · Journal of Nephropathology · doi:10.5812/nephropathol.9093 · Cited by 195

Thrombosis and Vascular Inflammation in Diabetes: Mechanisms and Potential Therapeutic Targets

Pechlivani, N., & Ajjan, R. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2018.00001 · Cited by 204

A bidirectional relationship between sleep and oxidative stress in Drosophila

Hill, V. M., O'Connor, R. M., Sissoko, G. B., Irobunda, I., Leong, S., Canman, J. C., Stavropoulos, N., & Shirasu‐Hiza, M. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2005206 · Cited by 200

Meal-induced oxidative stress and low-density lipoprotein oxidation in diabetes: The possible role of hyperglycemia

Ceriello, A., Bortolotti, N., Motz, E., Pieri, C., Marra, M., Tonutti, L., Lizzio, S., Feletto, F., Catone, B., & Taboga, C. (1999) · Metabolism · doi:10.1016/s0026-0495(99)90237-8 · Cited by 197

Oxidative Stress and MicroRNAs in Vascular Diseases

Magenta, A., Greco, S., Gaetano, C., & Martelli, F. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms140917319 · Cited by 198

Metallothionein Is Downstream of Nrf2 and Partially Mediates Sulforaphane Prevention of Diabetic Cardiomyopathy

Gu, J., Cheng, Y., Wu, H., Kong, L., Wang, S., Xu, Z., Zhang, Z., Tan, Y., Keller, B. B., Zhou, H., et al. (2016) · Diabetes · doi:10.2337/db15-1274 · Cited by 196

Salidroside ameliorates endothelial inflammation and oxidative stress by regulating the AMPK/NF-κB/NLRP3 signaling pathway in AGEs-induced HUVECs

Hu, R., Wang, M., Ni, S.-H., Wang, M., Liu, L., You, H., Wu, X., Wang, Y., Lu, L., & Wei, L. (2019) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2019.172797 · Cited by 199

Circulating Oxidative Stress Biomarkers in Clinical Studies on Type 2 Diabetes and Its Complications

Bigagli, E., & Lodovici, M. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/5953685 · Cited by 208

Journal of Pharmaceutical and Biomedical Sciences

(2016) · Journal of Pharmaceutical and Biomedical Sciences · doi:10.20936/jpbms · Cited by 193

Mitochondrial Hormesis and Diabetic Complications

Sharma, K. (2015) · Diabetes · doi:10.2337/db14-0874 · Cited by 194

Mitochondrial dysfunction and complications associated with diabetes

Blake, R., & Trounce, I. A. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.11.007 · Cited by 190

Ameliorative effect of kaempferol, a flavonoid, on oxidative stress in streptozotocin-induced diabetic rats

Al‐Numair, K. S., Govindasamy, C., Veeramani, C., & Alsaif, M. A. (2014) · Redox Report · doi:10.1179/1351000214y.0000000117 · Cited by 198

Attenuation of insulin resistance, metabolic syndrome and hepatic oxidative stress by resveratrol in fructose-fed rats

Bagul, P. K., Middela, H., Mattapally, S., Padiya, R., Bastia, T., Madhusudana, K., Reddy, B. R., Chakravarty, S., & Banerjee, S. (2012) · Pharmacological Research · doi:10.1016/j.phrs.2012.05.003 · Cited by 193

Endocrine Disruptors Leading to Obesity and Related Diseases

Petrakis, D., Vassilopoulou, L., Mamoulakis, C., Psycharakis, C., Anifantaki, A., Sifakis, S., Docea, A. O., Tsiaoussis, J., Makrigiannakis, A., & Tsatsakis, A. M. (2017) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph14101282 · Cited by 194

Role of Forkhead Transcription Factors in Diabetes-Induced Oxidative Stress

Ponugoti, B., Dong, G., & Graves, D. T. (2012) · Experimental Diabetes Research · doi:10.1155/2012/939751 · Cited by 196

Effects of resveratrol on biomarkers of oxidative stress and on the activity of delta aminolevulinic acid dehydratase in liver and kidney of streptozotocin-induced diabetic rats

Schmatz, R., Pereira, L. B., Stefanello, N., Mazzanti, C. M. D. A., Spanevello, R. M., Gutierres, J. M., Bagatini, M. D., Martins, C. C., Abdalla, F. H., Serres, J. D. D. S., et al. (2011) · Biochimie · doi:10.1016/j.biochi.2011.08.005 · Cited by 192

Long noncoding RNA-MEG3 is involved in diabetes mellitus-related microvascular dysfunction

Qiu, G.-Z., Tian, W., Fu, H., Li, C.-P., & Liu, B. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.01.164 · Cited by 191

High glucose-induced oxidative stress impairs proliferation and migration of human gingival fibroblasts

Buranasin, P., Mizutani, K., Iwasaki, K., Mahasarakham, C. P. N., Kido, D., Takeda, K., & Izumi, Y. (2018) · PLoS ONE · doi:10.1371/journal.pone.0201855 · Cited by 191

The role of cellular senescence in female reproductive aging and the potential for senotherapeutic interventions

Secomandi, L., Borghesan, M., Velarde, M., & Demaria, M. (2022) · Human Reproduction Update · doi:10.1093/humupd/dmab038 · Cited by 208

Diabetes Mellitus and Heart Failure

Lehrke, M., & Marx, N. (2017) · The American Journal of Medicine · doi:10.1016/j.amjmed.2017.04.010 · Cited by 196

A glance at the therapeutic potential of irisin against diseases involving inflammation, oxidative stress, and apoptosis: An introductory review

Askari, H., Rajani, S. F., Poorebrahim, M., Haghi‐Aminjan, H., Raeis-Abdollahi, E., & Abdollahi, M. R. (2018) · Pharmacological Research · doi:10.1016/j.phrs.2018.01.012 · Cited by 191

Diabetic‑induced alterations in hepatic glucose and lipid metabolism: The role of type 1 and type 2 diabetes mellitus (Review)

Jiang, S., Young, J. L., Wang, K., Qian, Y., & Cai, L. (2020) · Molecular Medicine Reports · doi:10.3892/mmr.2020.11175 · Cited by 206

Molecular Mechanisms of Mitochondrial Quality Control in Ischemic Cardiomyopathy

Chang, X., Liu, R., Li, R., Peng, Y., Zhu, P., & Zhou, H. (2022) · International Journal of Biological Sciences · doi:10.7150/ijbs.76223 · Cited by 196

Antioxidant peptides, the guardian of life from oxidative stress

Zhu, Y., Wang, K., Jia, X., Fu, C., Yu, H., & Wang, Y. (2023) · Medicinal Research Reviews · doi:10.1002/med.21986 · Cited by 198

Impact of Glycemic Variability on Chromatin Remodeling, Oxidative Stress, and Endothelial Dysfunction in Patients With Type 2 Diabetes and With Target HbA1c Levels

Costantino, S., Paneni, F., Battista, R., Castello, L., Capretti, G., Chiandotto, S., Tanese, L., Russo, G., Pitocco, D., Lanza, G. A., et al. (2017) · Diabetes · doi:10.2337/db17-0294 · Cited by 188

Retinal energy demands control vascular supply of the retina in development and disease: The role of neuronal lipid and glucose metabolism

Joyal, J., Gantner, M. L., & Smith, L. E. H. (2017) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2017.11.002 · Cited by 193

The cell biology of aging

DiLoreto, R., & Murphy, C. T. (2015) · Molecular Biology of the Cell · doi:10.1091/mbc.e14-06-1084 · Cited by 192

Oxidative Stress‐Related Mechanisms and Antioxidant Therapy in Diabetic Retinopathy

Li, C., Miao, X., Li, F., Wang, S., Liu, Q., Wang, Y., & Sun, J. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/9702820 · Cited by 191

Understanding Diabetic Neuropathy: Focus on Oxidative Stress

Pang, L., Lian, X., Liu, H., Zhang, Y., Li, Q., Cai, Y., Ma, H., & Yu, X. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/9524635 · Cited by 184

Inflammation and diabetic retinal microvascular complications

Zhang, W., Liu, H., Al‐Shabrawey, M., Caldwell, R. W., & Caldwell, R. B. (2011) · Journal of Cardiovascular Disease Research · doi:10.4103/0975-3583.83035 · Cited by 184

Beneficial roles of honey polyphenols against some human degenerative diseases: A review

Hossen, M. S., Ali, M. Y., Jahurul, M. H. A., Abdel‐Daim, M. M., Gan, S. H., & Khalil, M. I. (2017) · Pharmacological Reports · doi:10.1016/j.pharep.2017.07.002 · Cited by 185

Knockdown of Glyoxalase 1 Mimics Diabetic Nephropathy in Nondiabetic Mice

Giacco, F., Du, X., D’Agati, V. D., Milne, R. W., Sui, G., Geoffrion, M., & Brownlee, M. (2013) · Diabetes · doi:10.2337/db13-0316 · Cited by 184

The gut–renal axis: do incretin-based agents confer renoprotection in diabetes?

Muskiet, M. H. A., Smits, M. M., Morsink, L. M., & Diamant, M. (2013) · Nature Reviews Nephrology · doi:10.1038/nrneph.2013.272 · Cited by 187

Diabetic Kidney Disease

Bonner, R., Albajrami, O., Hudspeth, J. C., & Upadhyay, A. (2020) · Primary Care Clinics in Office Practice · doi:10.1016/j.pop.2020.08.004 · Cited by 200

The Investigation of the Oxidative Stress-Related Parameters in Type 2 Diabetes Mellitus

Aouacheri, O., Saka, S., Krim, M., Messaadia, A., & Maidi, I. (2014) · Canadian Journal of Diabetes · doi:10.1016/j.jcjd.2014.03.002 · Cited by 180

A review of the evidence for pathogenic mechanisms that may link periodontitis and diabetes

Taylor, J. J., Preshaw, P. M., & Lalla, E. (2013) · Journal of Periodontology · doi:10.1902/jop.2013.134005 · Cited by 183

Glucagon-Like Peptide-1 Protects Against Cardiac Microvascular Injury in Diabetes via a cAMP/PKA/Rho-Dependent Mechanism

Wang, D., Luo, P., Wang, Y., Li, W., Wang, C., Sun, D., Zhang, R., Su, T., Ma, X., Zeng, C., et al. (2013) · Diabetes · doi:10.2337/db12-1025 · Cited by 179

FoxOs Integrate Pleiotropic Actions of Insulin in Vascular Endothelium to Protect Mice from Atherosclerosis

Tsuchiya, K., Tanaka, J., Yu, S., Welch, C. L., DePinho, R. A., Tabas, I. A., Tall, A. R., Goldberg, I. J., & Accili, D. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.01.018 · Cited by 178

Glutathione metabolism in type 2 diabetes and its relationship with microvascular complications and glycemia

Lutchmansingh, F., Hsu, J. W.-C., Bennett, F. I., Badaloo, A. V., McFarlane‐Anderson, N., Gordon-Strachan, G. M., Wright-Pascoe, R. A., Jahoor, F., & Boyne, M. S. (2018) · PLoS ONE · doi:10.1371/journal.pone.0198626 · Cited by 187

Physiological and Pathological Roles of Aldose Reductase

Singh, M., Kapoor, A., & Bhatnagar, A. (2021) · Metabolites · doi:10.3390/metabo11100655 · Cited by 197

Anticholinergic, antidiabetic and antioxidant activities of cinnamon ( cinnamomum verum ) bark extracts: polyphenol contents analysis by LC-MS/MS

Gülçın, İ., Kaya, R., Gören, A. C., Akıncıoğlu, H., Topal, M., Bingöl, Z., Çakmak, K. C., Sarıkaya, S. B. Ö., Durmaz, L., & Alwasel, S. H. (2019) · International Journal of Food Properties · doi:10.1080/10942912.2019.1656232 · Cited by 178

Hyperglycemia and Endothelial Dysfunction in Atherosclerosis: Lessons from Type 1 Diabetes

Funk, S. D., Yurdagul, A., & Orr, A. W. (2012) · International Journal of Vascular Medicine · doi:10.1155/2012/569654 · Cited by 176

Advances in our understanding of diabetic retinopathy

Stitt, A. W., Lois, N., Medina, R. J., Adamson, P., & Curtis, T. M. (2013) · Clinical Science · doi:10.1042/cs20120588 · Cited by 182

Diabetes mellitus and stroke: A clinical update

Tun, N. N., Arunagirinathan, G., Munshi, S. K., & Pappachan, J. M. (2017) · World Journal of Diabetes · doi:10.4239/wjd.v8.i6.235 · Cited by 177

Extraglycemic Effects of SGLT2 Inhibitors: A Review of the Evidence

Bonora, B. M., Avogaro, A., & Fadini, G. P. (2020) · Diabetes Metabolic Syndrome and Obesity · doi:10.2147/dmso.s233538 · Cited by 199

Therapeutic potential of targeting oxidative stress in diabetic cardiomyopathy

Byrne, N. J., Rajasekaran, N. S., Abel, E. D., & Bugger, H. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.03.046 · Cited by 179

Postbiotics as potential new therapeutic agents for metabolic disorders management

Bourebaba, Y., Marycz, K., Mularczyk, M., & Bourebaba, L. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113138 · Cited by 191

Adverse Epigenetic Signatures by Histone Methyltransferase Set7 Contribute to Vascular Dysfunction in Patients With Type 2 Diabetes Mellitus

Paneni, F., Costantino, S., Battista, R., Castello, L., Capretti, G., Chiandotto, S., Scavone, G., Villano, A., Pitocco, D., Lanza, G. A., et al. (2014) · Circulation Cardiovascular Genetics · doi:10.1161/circgenetics.114.000671 · Cited by 177

The Role of Zinc and Copper in Insulin Resistance and Diabetes Mellitus

Bjørklund, G., Dadar, M., Pivina, L. M., Doşa, M. D., Semenova, Y. M., & Aaseth, J. (2019) · Current Medicinal Chemistry · doi:10.2174/0929867326666190902122155 · Cited by 178

Eryptosis and oxidative damage in type 2 diabetic mellitus patients with chronic kidney disease

Calderón-Salinas, J. V., Muñoz-Reyes, E. G., Guerrero-Romero, J. F., Rodríguez‐Morán, M., Bracho-Riquelme, R. L., Carrera-Gracia, M., & Escorza, M. A. Q. (2011) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-011-0887-1 · Cited by 174

Glutathione and infection

Morris, D., Khurasany, M., Nguyen, T., Kim, J., Guilford, F. T., Mehta, R. J., Gray, D., Saviola, B., & Venketaraman, V. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2012.10.012 · Cited by 178

Antihyperglycemic Effect ofGinkgo bilobaExtract in Streptozotocin-Induced Diabetes in Rats

Cheng, D., Liang, B., & Li, Y. (2012) · BioMed Research International · doi:10.1155/2013/162724 · Cited by 173

Catalase Deficiency Accelerates Diabetic Renal Injury Through Peroxisomal Dysfunction

Hwang, I., Lee, J., Huh, J. Y., Park, J., Lee, H. B., Ho, Y.-S., & Ha, H. (2012) · Diabetes · doi:10.2337/db11-0584 · Cited by 173

Enhanced ROS production and oxidative damage in subcutaneous white adipose tissue mitochondria in obese and type 2 diabetes subjects

Chattopadhyay, M., Khemka, V., Chatterjee, G., Ganguly, A., Mukhopadhyay, S., & Chakrabarti, S. (2014) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-014-2236-7 · Cited by 143

Regulation of Inflammatory Phenotype in Macrophages by a Diabetes-Induced Long Noncoding RNA

Reddy, M. A., Chen, Z., Park, J. T., Wang, M., Lanting, L. L., Zhang, Q., Bhatt, K. S., Leung, A., Wu, X., Putta, S., et al. (2014) · Diabetes · doi:10.2337/db14-0298 · Cited by 172

Recent advances in understanding the biochemical and molecular mechanism of diabetic retinopathy

Ola, M. S., Nawaz, M. I., Siddiquei, M. M., Al-Amro, S. A., & El‐Asrar, A. M. A. (2012) · Journal of Diabetes and its Complications · doi:10.1016/j.jdiacomp.2011.11.004 · Cited by 176

Regulation of eNOS Enzyme Activity by Posttranslational Modification

Heiß, E. H., & Dirsch, V. M. (2014) · Current Pharmaceutical Design · doi:10.2174/13816128113196660745 · Cited by 171

m 6 A reader YTHDC1 modulates autophagy by targeting SQSTM1 in diabetic skin

Liang, D., Lin, W., Ren, M., Qiu, J., Yang, C., Wang, X., Li, N., Zeng, T., Sun, K., You, L., et al. (2021) · Autophagy · doi:10.1080/15548627.2021.1974175 · Cited by 174

Role of free radical in atherosclerosis, diabetes and dyslipidaemia: larger‐than‐life

Singh, R., Devi, S., & Gollen, R. (2014) · Diabetes/Metabolism Research and Reviews · doi:10.1002/dmrr.2558 · Cited by 180

Diabetic retinopathy: Breaking the barrier

Eshaq, R. S., Aldalati, A. M. Z., Alexander, J. S., & Harris, N. R. (2017) · Pathophysiology · doi:10.1016/j.pathophys.2017.07.001 · Cited by 175

Pathophysiology of Coronary Microvascular Dysfunction

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Symbiotic Algae–Bacteria Dressing for Producing Hydrogen to Accelerate Diabetic Wound Healing

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