S-Nitrosation of the Insulin Receptor, Insulin Receptor Substrate 1, and Protein Kinase B/Akt

Adipose Expression of Tumor Necrosis Factor-α: Direct Role in Obesity-Linked Insulin Resistance

Hotamisligil, G. S., Shargill, N. S., & Spiegelman, B. M. (1993) · Science · doi:10.1126/science.7678183 · Cited by 7,518

Increased adipose tissue expression of tumor necrosis factor-alpha in human obesity and insulin resistance.

Hotamisligil, G. S., Arner, P., Caro, J. F., Atkinson, R. L., & Spiegelman, B. M. (1995) · Journal of Clinical Investigation · doi:10.1172/jci117936 · Cited by 3,543

A central role for JNK in obesity and insulin resistance

Hirosumi, J., Tuncman, G., Chang, L., Görgün, C. Z., Uysal, K. T., Maeda, K., Karin, M., & Hotamisligil, G. S. (2002) · Nature · doi:10.1038/nature01137 · Cited by 3,359

IRS-1-Mediated Inhibition of Insulin Receptor Tyrosine Kinase Activity in TNF-α- and Obesity-Induced Insulin Resistance

Hotamisligil, G. S., Peraldi, P., Budavari, A., Ellis, R., White, M. F., & Spiegelman, B. M. (1996) · Science · doi:10.1126/science.271.5249.665 · Cited by 2,630

C-Reactive Protein in Healthy Subjects: Associations With Obesity, Insulin Resistance, and Endothelial Dysfunction: A Potential Role for Cytokines Originating From Adipose Tissue?

Yudkin, J. S., Stehouwer, C. D. A., Emeis, J. J., & Coppack, S. W. (1999) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/01.atv.19.4.972 · Cited by 2,465

Increased Insulin Sensitivity and Obesity Resistance in Mice Lacking the Protein Tyrosine Phosphatase-1B Gene

Elchebly, M., Payette, P., Michaliszyn, E., Cromlish, W., Collins, S., Loy, A. L., Normandin, D., Cheng, A., Himms-Hagen, J., Chan, C.-C., et al. (1999) · Science · doi:10.1126/science.283.5407.1544 · Cited by 2,210

S-nitrosylation of proteins with nitric oxide: synthesis and characterization of biologically active compounds.

Stamler, J. S., Simon, D. I., Osborne, J. A., Mullins, M. E., Jaraki, O., Michel, T. M., Singel, D. J., & Loscalzo, J. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.1.444 · Cited by 1,471

Tumor Necrosis Factor α: A Key Component of the Obesity-Diabetes Link

Hotamışlıgil, G. S., & Spiegelman, B. M. (1994) · Diabetes · doi:10.2337/diab.43.11.1271 · Cited by 1,353

Lipotoxic heart disease in obese rats: Implications for human obesity

Zhou, Y.-T., Grayburn, P., Karim, A., Shimabukuro, M., Higa, M., Baetens, D., Orci, L., & Unger, R. H. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.4.1784 · Cited by 1,265

Untitled work

Stamler (2001) · doi:10.1016/s0092-8674(01)00495-0 · Cited by 1,261

Therapeutic Potential of GLP-1 Receptor Agonists in Heart Failure with Preserved Ejection Fraction (HFpEF) in Obese Patients

Patel, R., Kokori, E., Olatunji, G. D., Adejumo, F. A., Ukah, J. D., Babalola, A. E., Ndakotsu, A., Abraham, I. C., & Aderinto, N. (2025) · Current Heart Failure Reports · doi:10.1007/s11897-025-00704-1 · Cited by 7

Transient Insulin Resistance in Normal Subjects: Acute Hyperglycemia Inhibits Endothelial-Dependent Vasodilatation in Normal Subjects

Rammos, G., Peppes, V., & Zakopoulos, N. (2008) · Metabolic Syndrome and Related Disorders · doi:10.1089/met.2007.0036 · Cited by 7

New insight into the mechanism by which acute physical exercise ameliorates insulin resistance

Hoy, A. J., & Turner, N. A. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.152991 · Cited by 7

S-Nitrosoglutathione Reverts Dietary Sucrose-Induced Insulin Resistance

Sousa‐Lima, I., Fernandes, A. B., Patarrão, R. S., Kim, Y., & Macedo, M. P. (2020) · Antioxidants · doi:10.3390/antiox9090870 · Cited by 8

Gut Microbiota and Insulin Resistance: Understanding the Mechanism of Better Treatment of Type 2 Diabetes Mellitus

Al-Busaidi, A., Alabri, O., Alomairi, J., Elsharaawy, A., Lawati, A. A., Lawati, H. A., & Das, S. (2024) · Current Diabetes Reviews · doi:10.2174/0115733998281910231231051814 · Cited by 7

Hepatic nNOS impaired hepatic insulin sensitivity through the activation of p38 MAPK

Zhao, T., Li, Q., Mao, Q., Mu, K., & Wang, C. (2021) · Journal of Endocrinology · doi:10.1530/joe-20-0322 · Cited by 6

Heracleum dissectum Ledeb. ethanol extract attenuates metabolic syndrome symptoms in high-fat diet-induced obese mice by activating adiponectin/AMPK signaling

Son, Y., Jung, D. S., Shin, J. M., Erdenebileg, S., & Nho, C. W. (2021) · Journal of Functional Foods · doi:10.1016/j.jff.2021.104581 · Cited by 7

Impaired Nitric Oxide Metabolism in Type 2 Diabetes: At a Glance

Bahadoran, Z., Carlström, M., Mirmiran, P., & Ghasemi, A. (2022) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815079814122010006 · Cited by 6

Ghrelin Protects against the Detrimental Consequences ofPorphyromonas gingivalis-Induced Akt Inactivation through S-Nitrosylation on Salivary Mucin Synthesis

Slomiany, B. L., & Slomiany, A. (2011) · International Journal of Inflammation · doi:10.4061/2011/807279 · Cited by 6

Role of Oxidative Stress and Associated Alteration in Enzyme Activities in Obesity Comorbidities

Demerdash, H. M. (2017) · Obesity Research - Open Journal · doi:10.17140/oroj-4-131 · Cited by 5

Cysteine redoxome landscape in mouse brown adipose tissue under acute cold exposure

Oo, H. K., Galicia‐Medina, C. M., Nishiuchi, T., Tanida, R., Goto, H., Nakano, Y., Takeshita, Y., Saito, Y., Takayama, H., & Takamura, T. (2025) · iScience · doi:10.1016/j.isci.2025.112051 · Cited by 6

Nonalcoholic Fatty Liver Disease and the Gut Microbiota: Exploring the Connection

Oldfield, E. C., & Dong, R. (2014) · Journal of Gastrointestinal & Digestive System · doi:10.4172/2161-069x.1000245 · Cited by 5

Differential benefits of physical training associated or not with l-arginine supplementation in rats with metabolic syndrome: Evaluation of cardiovascular, autonomic and metabolic parameters

Reginato, G. D. S., de Jager, L., Martins, A. B., Lucchetti, B. F. C., de Campos, B. H., Lopes, F. N. C., Araújo, E. J. D. A., Zaia, C. T. B. V., Pinge‐Filho, P., & Martins‐Pinge, M. C. (2023) · Physiology & Behavior · doi:10.1016/j.physbeh.2023.114251 · Cited by 5

SILAM for quantitative proteomics of liver Akt1/PKBα after burn injury

Fischman, A. J. (2011) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2011.861 · Cited by 5

Non-alcoholic Fatty Liver Disease and the Gut Microbiota: Exploring the Connection

Oldfield, E. C., Dong, R., & Johnson, D. A. (2015) · Gastro - Open Journal · doi:10.17140/goj-1-107 · Cited by 4

Exogenous nitric oxide inhibits IRS-1 expression in rat hepatocytes and skeletal myocytes

Badal, S. A. M., Brown, P. D., & Ragoobirsingh, D. (2006) · Journal of Biomedical Science · doi:10.1007/s11373-006-9073-y · Cited by 5

Allergic activation of mast cells.

Parker, C. W. (1986) · PubMed · Cited by 5

Kumquat Fruit Administration Counteracts Dysmetabolism-Related Neurodegeneration and the Associated Brain Insulin Resistance in the High-Fat Diet-Fed Mice

Massaro, A., Calvi, P., Restivo, I., Giardina, M., Mulè, F., Tesoriere, L., Amato, A., Nuzzo, D., Picone, P., Terzo, S., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26073077 · Cited by 4

Microbial metabolism mediates the deteriorative effects of sedentary behaviour on insulin resistance

Ju, J., He, J., Ye, B., Li, S., Zhao, J., Chen, W., Zhang, Q., Zhao, W., Yang, J., Liu, L., et al. (2025) · Clinical and Translational Medicine · doi:10.1002/ctm2.70348 · Cited by 4

Palmitate-induced hepatic insulin resistance as an in vitro model for natural and synthetic drug screening: A scoping review of therapeutic candidates and mechanisms

Faria, B. Q., Calixto, P. S., Picheth, G., Ferreira, L. M., Rego, F. G. D. M., Guerra, J. F. D. C., & Sari, M. H. M. (2025) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2025.111717 · Cited by 4

Characterization of vascular dysregulation in meriones shawi after high-calorie diet feeding

Lyoussi, B., Cherkaoui-Tangi, K., Morel, N., & Wibo, M. (2018) · Clinical and Experimental Hypertension · doi:10.1080/10641963.2017.1377219 · Cited by 4

Enhancing Muscle Intracellular Ca2+ Homeostasis and Glucose Uptake: Passive Pulsatile Shear Stress Treatment in Type 2 Diabetes

Uryash, A., Umlas, J., Mijares, A., Adams, J. A., & Lopez, J. R. (2023) · Biomedicines · doi:10.3390/biomedicines11102596 · Cited by 4

A Novel L-Arginine/L-Glutamine Coupling Hypothesis: Implications for Type 1 Diabetes

de Bittencourt, P. I. H., & Newsholme, P. (2011) · InTech eBooks · doi:10.5772/20759 · Cited by 4

Role of ghrelin in modulation of s-nitrosylation-Dependent akt inactivation induced in salivary gland acinar cells by porphyromonas gingivalis

Slomiany, B. L., & Slomiany, A. (2010) · Health · doi:10.4236/health.2010.212215 · Cited by 4

Gut Microbiota and Type 2 Diabetes Mellitus : What is The Link ?

Ibrahim, N. A. (2018) · Afro-Egyptian Journal of Infectious and Endemic Diseases · doi:10.21608/aeji.2018.9950 · Cited by 3

Nitric Oxide and Type 2 Diabetes: Lessons from Genetic Studies

Bahadoran, Z., Mirmiran, P., Carlström, M., & Ghasemi, A. (2022) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815079814122010009 · Cited by 3

Is there any role of glucose-6-phosphate dehydrogenase in obesity induced metabolic disorder

Sankhla, M., Mathur, K., & Rathor, J. S. (2012) · Health · doi:10.4236/health.2012.412a219 · Cited by 3

TNF-α in obesity-associated colon cancer

Osório–Costa, F., & Carvalheira, J. B. C. (2013) · Translational gastrointestinal cancer · Cited by 3

MOLECULAR MECHANISMS OF INSULIN RESISTANCE IN OBESITY

Marette, A. (2008) · Cited by 3

Solid‐Phase Synthesis of Substrate‐Based Dipeptides and Heterocyclic Pseudo‐dipeptides as Potential NO Synthase Inhibitors

Touati‐Jallabe, Y., Tintillier, T., Mauchauffée, E., Boucher, J., Leroy, J., Ramassamy, B., Hamzé, A., Mezghenna, K., Bouzekrini, A., Verna, C., et al. (2020) · ChemMedChem · doi:10.1002/cmdc.201900659 · Cited by 2

Obesity, Cardiometabolic Risk, and Chronic Kidney Disease

Snyder, S., & Gangeri, N. (2015) · Springer eBooks · doi:10.1007/978-3-319-19821-7_14 · Cited by 2

Adipocyte Dysfunction, Inflammation, and Insulin Resistance in Obesity

Jahansouz, C. (2015) · Springer eBooks · doi:10.1007/978-1-4939-3220-7_5 · Cited by 2

Obesity, Diabetes, and Endothelium: Molecular Interactions

Saad, M. J. A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812348-5.00044-1 · Cited by 4

Insulin Resistance and Atherosclerosis

Singh, K., & Raghavan, V. A. (2013) · Contemporary diabetes · doi:10.1007/978-1-4614-7554-5_3 · Cited by 2

Potential Binding Sites for Taurine on the Insulin Receptor: A Molecular Docking Study

junior, J. A. D. S., & Ribeiro, R. A. (2022) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-93337-1_25 · Cited by 2

l -Arginine Binding to Human Inducible Nitric Oxide Synthase: An Antisymmetric Funnel Route toward Isoform-Specific Inhibitors?

Floquet, N., Hernandez, J., Boucher, J., & Martínez, J. (2011) · Journal of Chemical Information and Modeling · doi:10.1021/ci100422v · Cited by 2

Role of Inflammation in the Pathogenesis of Insulin Resistance in Obesity: Specific Role of Reactive Oxygen and Reactive Nitrogen Species

Issa, N. G. (2016) · Cited by 2

Pathological Nitric Oxide‐Triggered Microneedle Patch for Spatiotemporally Controlled Therapy of Acute and Chronic Inflammatory Disorders

Lee, S., Boo, Y., Park, S., Eom, S., Ryu, W., & Kim, W. J. (2026) · Advanced Healthcare Materials · doi:10.1002/adhm.202504714 · Cited by 1

The iNOS paradox: how high NO flux suppresses inflammation through S-nitrosylation and cGMP signaling under redox-buffered conditions

Lee, S.-S. (2026) · Medical Hypotheses · doi:10.1016/j.mehy.2026.111942 · Cited by 1

Neuronal nitric oxide synthase in hypothalamic leptin signaling

Hristov, M., Landzhov, B. V., & YAKIMOVA, K. S. (2026) · Neuroscience · doi:10.1016/j.neuroscience.2026.05.018 · Cited by 1

Efeitos do exercicio físico em parâmetros moleculares da via de sinalização da insulina e obesidade

de Farias, J. M. (2014) · Brazilian Journal of Kinanthropometry and Human Performance · doi:10.5007/1980-0037.2014v16n5p588 · Cited by 1

Translational research into gut microbiota: new horizons in obesity treatment Pesquisa translacional em microbiota intestinal: novos horizontes no tratamento da obesidade

Tsukumo, D. M. L., Filho, C., & Saad, M. J. A. (2009) · Cited by 1

S-Ethyl-Isothiocitrullin-Based Dipeptides and 1,2,4-Oxadiazole Pseudo-Dipeptides: Solid Phase Synthesis and Evaluation as NO Synthase Inhibitors

Mauchauffée, E., Leroy, J., Chamcham, J., Ejjoummany, A., Maurel, M., Nauton, L., Ramassamy, B., Mezghenna, K., Boucher, J., Lajoix, A., et al. (2023) · Molecules · doi:10.3390/molecules28135085 · Cited by 1

High sucrose/fat diet and isosorbide mononitrate increase insulin resistance, nitric oxide production and myocardial apoptosis in a hypertensive rat model

Li, T., Bai, B., Tian, C., Wang, H. H., Jiang, D., Ma, F., & Shan, M. (2018) · Molecular Medicine Reports · doi:10.3892/mmr.2018.8651 · Cited by 1

Investigação de polimorfismos em genes do sistema imune inato em uma população com diabetes tipo 2

Bagarolli, R. A. (2009) · doi:10.47749/t/unicamp.2009.440016

Purification and Characterization of Novel Denitrosylases from Yeast and Mammals

Anand, P. (2012) · DukeSpace (Duke University)

Post-Translational Modification Profiling of Burn-Induced — Insulin Resistance and Muscle Wasting

Lu, X., Ronald, G., & Alan, J. F. (2013) · InTech eBooks · doi:10.5772/54849

Efeito dos ácidos palmítico e palmitoléico sobre o metabolismo de glicose no músculo sóleo de ratos.

Nachbar, R. T. (2012) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2012.tde-29012013-102458

oxide synthase Obesity, insulin resistance, and skeletal muscle nitric

Pierce, J. R., Choi, M. D., Hickner, R. C., Kraus, R. M., Houmard, J. A., Kraus, W. E., & Tanner, C. J. (2015)

Preparação, caracterização e aplicações de biomateriais liberadores de oxido nitrico

Seabra, A. B. (2006) · doi:10.47749/t/unicamp.2006.368470

The anti-obesogenic effects of nitric oxide.

Sansbury, B. E. (2014) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/1262

MyD88: um modulador do perfil inflamatório e metabólico na obesidade experimental.

Castoldi, Â. (2015) · doi:10.11606/t.42.2015.tde-10122015-070834

Identification and functional studies of two novel serine phosphorylation sites of insulin receptor substrate (IRS)-2: Ser 675 and Ser 907

Naturwissenschaften, F. (2010)

Efeitos da suplementação com óleo de peixe sobre a resistência à insulina e a função mitocondrial no músculo esquelético de camundongos alimentados com dieta hiperlipídica

Paulo, S., & Hirabara, M. (2014)

AVALIAÇÃO DOS MECANISMOS ENVOLVIDOS NA REDUÇÃO DA CONTRAÇÃO VASCULAR EM AORTAS DE RATAS DIABÉTICAS: PAPEL DA

Insulina, I. E. (2013)

Asymmetric Dimethylarginine and Endothelial Dysfunction

Anderssohn, M., & Böger, R. H. (2013) · CRC Press eBooks · doi:10.1201/b14907-8

La régulation du transport du glucose dans le muscle squelettique : l'implication des protéines AMPK et iNOS

St-Amand, E. (2015) · Corpus Université Laval (Université Laval)

Rôle de la synthase inductible du monoxyde d'azote dans les maladies proinflammatoires et la résistance à l'insuline associée à l'obésité

Centeno-Baez, C. (2015)

Targeting obesity-related inflammation through nutritional and genetic approaches

LeMieux, M. J. (2015) · ThinkTech (Texas Tech University)

Obesity and inflammation: probiotics or pharmaceuticals intervention?

Graham, M. R., Davies, B., Pates, J. A., Evans, P. J., & Baker, J. S. (2015) · International Journal of Recent Scientific Research

Endotoxin and metabolically associated pathology

Fadieienko, G. D., Gridnyev, O., & Gridnieva, S. V. (2020) · Modern Gastroenterology · doi:10.30978/mg-2020-4-80

Signaling and Redox Regulation by Nitric Oxide, Superoxide and Carbon Monoxide

Frein, D. (2006)

Current literature in diabetes

(2005) · Diabetes/Metabolism Research and Reviews · doi:10.1002/dmrr.619

Differential Benefits of Physical Training Associated or Not with L-Arginine Supplementation in Rats with Metabolic Syndrome: Cardiovascular, Autonomic and Metabolic ParametersPreprint

Reginato, G. D. S., de Jager, L., Martins, A. B., Lucchetti, B. F. C., de Campos, B. H., Lopes, F. N. C., Araújo, E. J. D. A., Zaia, C. T. B. V., Pinge‐Filho, P., & Martins‐Pinge, M. C. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4062542

Stimulation of Akt Phosphorylation and Glucose Transport by Metalloporphyrins with Peroxynitrite Decomposition Catalytic Activity

Eccardt, A. M., Pelzel, R. J., Bell, T. P., & Fisher, J. S. (2022) · Catalysts · doi:10.3390/catal12080849

Brain Insulin Resistance, Nitric Oxide and Alzheimer’s Disease Pathology

Pei, Z., Lee, K.-C., Khan, A., & Wang, H.-Y. (2022) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815079814122010014

Establishment and evaluation of a model for clinical feature selection and prediction in gout patients with cardiovascular diseases: a retrospective cohort study

Fan, B., Ye, Y., Wang, Z., Xu, Y., Lu, M., Cong, W., & Ma, F. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1599028

Taurine depletion and Schwann cell dysfunction in diabetic neuropathy.

Askwith, T. (2010) · University of Birmingham Institutional Research Archive (University of Birmingham)

Une exposition à l'ozone induit une insulino-résistance via un stress oxydant systémique et un stress du réticulum endoplasmique musculaire : pollution à l'ozone et diabète de type 2 : peut-on imaginer une origine environnementale aux maladies métaboliques ?

Vella, R. (2013) · theses.fr (ABES) · doi:10.70675/5d6d7be0z4be0z4763z94a7z7426da9a6eb3

Emerging role of protein S-nitrosylation in diabetes and diabetes-associated diseases

Yu, M., He, J., Xu, M., 张真稳, Shang, W., & Fang, P. (2026) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2026.110823

GLX10, a Novel Immunometabolic Modulator, Enhances Glycemic Control and Suppresses Inflammatory Signaling in a High-Fat Diet and Streptozotocin-Induced Rat Model of Type 2 DiabetesPreprint

Abdelaziz, S., Kassem, K. F., & salah, M. S. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.16.718956

Gut microbiota contributes to protection against high-fat diet-induced insulin resistance in iNOS knockout mice

Zanotto, T. M., Santos, A., Vecina, J. F., Quaresma, P. G. F., Guadagnini, D., Rocha, G. Z., Brambilla, S. R., Carvalho, C. R. D. O., & Saad, M. J. A. (2026) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2026.112875

Therapeutic Modulation of Nitric Oxide Pathways to Address Insulin Resistance in Cardiovascular–Kidney–Metabolic Syndrome

Ceteraș, L.-M., Brata, V. D., Dobrotă, I. R., Borbei, R., Clim, M., Alexescu, T., Milaciu, M. V., Perné, M.-G., Gerdanovics, C.-A., Cozma, A., et al. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27177701

Endothelial nitric oxide signaling in cellular and systemic metabolism

Siragusa, M., Dunaway, L. S., Lammert, E., Fleming, I., Isakson, B. E., & Cortese-Krott, M. M. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104443

Resistència a la insulina i disfunció endotelial sinusoïdal a la malaltia hepàtica per dipòsit de greix

Pasarín, M. (2012) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

Modulation of skeletal muscle insulin sensitivity and SNAT2 amino acid transporter expression by fatty acid availability

Nardi, F. (2015) · Discovery Research Portal (University of Dundee)

S-nitrosação

Filho, C. (2005) · doi:10.47749/t/unicamp.2005.380971

Targeted disruption of iNOS prevents LPS-induced S-nitrosation of IRβ/IRS-1 and Akt and insulin resistance in muscle of mice

Carvalho-Filho, M. A., Ueno, M., Carvalheira, J. B. C., Velloso, L. A., & Saad, M. J. A. (2006) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00422.2005 · Cited by 84

S-Nitrosylation-dependent Inactivation of Akt/Protein Kinase B in Insulin Resistance

Yasukawa, T., Tokunaga, E., Ota, H., Sugita, H., Martyn, J. A. J., & Kaneki, M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m411871200 · Cited by 265

Peroxynitrite mediates muscle insulin resistance in mice via nitration of IRβ/IRS-1 and Akt

Zhou, J., & Huang, K. (2009) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2009.08.005 · Cited by 27

Nitrosative Stress and Pathogenesis of Insulin Resistance

Kaneki, M., Shimizu, N., Yamada, D., & Chang, K. (2007) · Antioxidants and Redox Signaling · doi:10.1089/ars.2006.1464 · Cited by 136