Review: Oxidative Stress and Disease

Apparent hydroxyl radical production by peroxynitrite: Implications for endothelial injury from nitric oxide and superoxide

Beckman, J. S., Beckman, T. W., Chen, J., Marshall, P. A., & Freeman, B. A. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.4.1620 · Cited by 7,029 · see citing works

Role of Oxidative Stress in Development of Complications in Diabetes

Baynes, J. (1991) · Diabetes · doi:10.2337/diab.40.4.405 · Cited by 3,791 · see citing works

Hydrogen peroxide mediates amyloid β protein toxicity

Behl, C. (1994) · Cell · doi:10.1016/0092-8674(94)90131-7 · Cited by 2,074 · see citing works

Oxidative Stress and Diabetic Vascular Complications

Giugliano, D., Ceriello, A., & Paolisso, G. (1996) · Diabetes Care · doi:10.2337/diacare.19.3.257 · Cited by 1,938 · see citing works

Oxidative stress‐induced cataract: mechanism of action

Spector, A. (1995) · The FASEB Journal · doi:10.1096/fasebj.9.12.7672510 · Cited by 896 · see citing works

A study of the reactivity of HO2/O2-with unsaturated fatty acids

Bielski, B. H., Arudi, R. L., & Sutherland, M. W. (1983) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)32488-8 · Cited by 546 · see citing works

Inactivation-reactivation of aconitase in Escherichia coli. A sensitive measure of superoxide radical.

Gardner, P. R., & Fridovich, I. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)50343-x · Cited by 346 · see citing works

National Outcomes of Cataract Extraction

Javitt, J. C., Tielsch, J. M., Canner, J. K., Kolb, M. M., Sommer, A. H., Steinberg, E. P., Steinberg, E. P., Bergner, M., Sommer, A. H., Anderson, G. F., et al. (1992) · Ophthalmology · doi:10.1016/s0161-6420(92)31775-0 · Cited by 302 · see citing works

Free and protein-bound glutathione in normal and cataractous human lenses

Harding, J. J. (1970) · Biochemical Journal · doi:10.1042/bj1170957 · Cited by 290 · see citing works

Nuclear cataract and myopia during hyperbaric oxygen therapy.

Palmquist, B. ‐., Philipson, B., & Barr, P. (1984) · British Journal of Ophthalmology · doi:10.1136/bjo.68.2.113 · Cited by 290 · see citing works

Reaction of No With O2−. Implications for the Action of Endothelium-Derived Relaxing Factor (EDRF)

Sarán, M., Michel, C., Bors, W., & Czapski, G. (1990) · Free Radical Research Communications · doi:10.3109/10715769009149890 · Cited by 269 · see citing works

Glutathione and its function in the lens—An overview

Reddy, V. N. (1990) · Experimental Eye Research · doi:10.1016/0014-4835(90)90127-g · Cited by 246 · see citing works

Lipoprotein glycation and its metabolic consequences

Lyons, T. J., & Jenkins, A. J. (1997) · Current Opinion in Lipidology · doi:10.1097/00041433-199706000-00008 · Cited by 232 · see citing works

Perhydroxyl radical (HOO.) initiated lipid peroxidation. The role of fatty acid hydroperoxides

Aikens, J., & Dix, T. A. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)98591-1 · Cited by 228 · see citing works

Amyloid β-protein toxicity and oxidative stress in Alzheimer's disease

Behl, C. (1997) · Cell and Tissue Research · doi:10.1007/s004410050955 · Cited by 211 · see citing works

Lipoprotein Glycation and Its Metabolic Consequences

Lyons, T. J. (1992) · Diabetes · doi:10.2337/diab.41.2.s67 · Cited by 141 · see citing works

Increased antioxidant enzyme activity in amyloid beta protein-resistant cells

Sagara, Y., Dargusch, R., Klier, F. G., Schubert, D. A., & Behl, C. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-02-00497.1996 · Cited by 126 · see citing works

Variation in Cellular Glutathione Peroxidase Activity in Lens Epithelial Cells, Transgenics and Knockouts Does Not Significantly Change the Response to H2O2Stress

Spector, A., Yang, Y., Ho, Y., Magnenat, J.-L., Wang, R.-R., Ma, W., & Li, W. (1996) · Experimental Eye Research · doi:10.1006/exer.1996.0063 · Cited by 66 · see citing works

Rat lens superoxide dismutase and glucose-6-phosphate dehydrogenase: Studies on the catalytic activity and the fate of enzyme antigen as a function of age

Dovrat, A., & Gershon, D. (1981) · Experimental Eye Research · doi:10.1016/s0014-4835(81)80105-4 · Cited by 55 · see citing works

Peroxide-Induced Damage in Lenses of Transgenic Mice with Deficient and Elevated Levels of Glutathione Peroxidase

Reddy, V. N., Lu, L., Ho, Y., Magnenat, J.-L., Ibaraki, N., Giblin, F. J., & Dang, L. (2010) · Ophthalmologica · doi:10.1159/000310788 · Cited by 54 · see citing works

Activity of glutathione peroxidase and glutathione reductase in the human lens related to age

Rathbun, W. B., & Bovis, M. G. (1986) · Current Eye Research · doi:10.3109/02713688609025177 · Cited by 45 · see citing works

National Outcomes of Cataract Extraction III. Corneal Edema and Transplant Following Inpatient Surgery

Canner, J. K. (1992) · Archives of Ophthalmology · doi:10.1001/archopht.1992.01080200117038 · Cited by 28 · see citing works

Microperoxidases Catalytically Degrade Reactive Oxygen Species and May Be Anti-Cataract Agents

Spector, A., Ma, W., Wang, R.-R., & Kleiman, N. J. (1997) · Experimental Eye Research · doi:10.1006/exer.1997.0336 · Cited by 24 · see citing works

HPLC analysis of lens GSH and GSSG

Chancy, W. G., & Spector, A. (1984) · Current Eye Research · doi:10.3109/02713688408997219 · Cited by 22 · see citing works

The Effect of Catalase Amplification on Immortal Lens Epithelial Cell Lines

Yang, Y., Spector, A., Ma, W., Wang, R.-R., Larsen, K., & Kleiman, N. J. (1998) · Experimental Eye Research · doi:10.1006/exer.1998.0560 · Cited by 18 · see citing works

Insulin Inhibits Intranuclear Nuclear Factor B and Stimulates I B in Mononuclear Cells in Obese Subjects: Evidence for an Anti-inflammatory Effect?

Dandona, P., Aljada, A., Mohanty, P., Ghanim, H., Hamouda, W., Assian, E., & Ahmad, S. (2001) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.86.7.7623 · Cited by 695 · see citing works

Curcumin and Turmeric Delay Streptozotocin-Induced Diabetic Cataract in Rats

Suryanarayana, P., Saraswat, M., Mrudula, T., Krishna, T. P., Krishnaswamy, K., & Reddy, G. B. (2005) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.04-1304 · Cited by 307 · see citing works

Antioxidants from Plants Protect against Skin Photoaging

Petruk, G., Del Giudice, R., Rigano, M. M., & Monti, D. M. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/1454936 · Cited by 283 · see citing works

Oxidative Stress, Lens Gap Junctions, and Cataracts

Berthoud, V. M., & Beyer, E. C. (2008) · Antioxidants and Redox Signaling · doi:10.1089/ars.2008.2119 · Cited by 259 · see citing works

Role of curcumin in health and disease

Pari, L., Tewas, D., & Eckel, J. (2008) · Archives of Physiology and Biochemistry · doi:10.1080/13813450802033958 · Cited by 248 · see citing works

ROS-Scavenging Therapeutic Hydrogels for Modulation of the Inflammatory Response

Kim, Y. E., & Kim, J. (2021) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.1c18261 · Cited by 229 · see citing works

Pharmacological prevention of diabetic cataract

Kyseľová, Z., Štefek, M., & Bauer, V. (2004) · Journal of Diabetes and its Complications · doi:10.1016/s1056-8727(03)00009-6 · Cited by 212 · see citing works

The Anti-inflammatory Effects of Selenium Are Mediated through 15-Deoxy-Δ12,14-prostaglandin J2 in Macrophages

Vunta, H., Davis, F. B., Palempalli, U. M. D., Bhat, D., Arner, R. J., Thompson, J. T., Peterson, D. G., Reddy, C. C., & Prabhu, K. S. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m703075200 · Cited by 211 · see citing works

The Pathomechanism, Antioxidant Biomarkers, and Treatment of Oxidative Stress-Related Eye Diseases

Hsueh, Y., Chen, Y., Tsao, Y., Cheng, C., Wu, W., & Chen, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031255 · Cited by 199 · see citing works

Antioxidative Effects of Carrot-Derived Nanovesicles in Cardiomyoblast and Neuroblastoma Cells

Kim, D. K., & Rhee, W. J. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13081203 · Cited by 186 · see citing works

Multiple and Additive Functions of ALDH3A1 and ALDH1A1

Lassen, N., Bateman, J., Estey, T., Kuszak, J. R., Nees, D. W., Piatigorsky, J., Duester, G., Day, B. J., Huang, J., Hines, L. M., et al. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702076200 · Cited by 175 · see citing works

Source Apportionment of in Vitro Reactive Oxygen Species Bioassay Activity from Atmospheric Particulate Matter

Zhang, Y., Schauer, J. J., Shafer, M. M., Hannigan, M., & Dutton, S. J. (2008) · Environmental Science & Technology · doi:10.1021/es800126y · Cited by 172 · see citing works

Hepatoprotective and antioxidant effects of the coffee diterpenes kahweol and cafestol on carbon tetrachloride-induced liver damage in mice

Lee, K. J., Choi, J. H., & Jeong, H. G. (2007) · Food and Chemical Toxicology · doi:10.1016/j.fct.2007.05.010 · Cited by 171 · see citing works

The Anti-Oxidant and Antitumor Properties of Plant Polysaccharides

Jiao, R., Liu, Y., Gao, H., Xiao, J., & So, K. (2016) · The American Journal of Chinese Medicine · doi:10.1142/s0192415x16500269 · Cited by 160 · see citing works

Exercise-Induced Oxidative Stress and Dietary Antoxidative

Yavari, A., Javadi, M., Mirmiran, P., & Bahadoran, Z. (2015) · Asian Journal of Sports Medicine · doi:10.5812/asjsm.24898 · Cited by 156 · see citing works

Selenium attenuates pro‐inflammatory gene expression in macrophages

Vunta, H., Belda, B. J., Arner, R. J., Reddy, C. C., Heuvel, J. P. V., & Prabhu, K. S. (2008) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.200700346 · Cited by 156 · see citing works

Tart Cherry Juice Decreases Oxidative Stress in Healthy Older Men and Women , ,

Traustadóttir, T., Davies, S. S., Stock, A. A., Su, Y., Heward, C. B., Roberts, L. J., & Harman, S. M. (2009) · Journal of Nutrition · doi:10.3945/jn.109.111716 · Cited by 151 · see citing works

Metallothionein Inhibits Peroxynitrite-induced DNA and Lipoprotein Damage

Cai, L., Klein, J. B., & Kang, Y. J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.c000593200 · Cited by 151 · see citing works

Chemical diversity of biologically active metabolites in the sclerotia of Inonotus obliquus and submerged culture strategies for up-regulating their production

Zheng, W., Miao, K., Liu, Y., Zhao, Y., Zhang, M., Pan, S., & Dai, Y. (2010) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-010-2682-4 · Cited by 136 · see citing works

Reactive oxygen species activity and chemical speciation of size-fractionated atmospheric particulate matter from Lahore, Pakistan: an important role for transition metals

Shafer, M. M., Perkins, D. A., Antkiewicz, D. S., Stone, E. A., Quraishi, T. A., & Schauer, J. J. (2010) · J. Environ. Monit. · doi:10.1039/b915008k · Cited by 131 · see citing works

Efficacy of Biodegradable Curcumin Nanoparticles in Delaying Cataract in Diabetic Rat Model

Grama, C. N., Suryanarayana, P., Patil, M. A., Ganugula, R., Balakrishna, N., Kumar, M. N. V. R., & Reddy, G. B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0078217 · Cited by 118 · see citing works

Toxic essential oils. Part II: Chemical, toxicological, pharmacological and microbiological profiles of Artemisia annua L. volatiles

Radulović, N. S., Randjelović, P. J., Stojanović, N. M., Blagojević, P. D., Stojanović-Radić, Z. Z., Ilić, I., & Djordjević, V. B. (2013) · Food and Chemical Toxicology · doi:10.1016/j.fct.2013.04.016 · Cited by 106 · see citing works

Reactive Oxygen Species and the Aging Eye

Babizhayev, M. A., & Yegorov, Y. E. (2010) · American Journal of Therapeutics · doi:10.1097/mjt.0b013e3181ea31ff · Cited by 103 · see citing works

A proteomic approach to identify early molecular targets of oxidative stress in human epithelial lens cells

Paron, I., D'Elia, A. V., DˈAmbrosio, C., Scaloni, A., D’Aurizio, F., Prescott, A. R., Damante, G., & Tell, G. (2004) · Biochemical Journal · doi:10.1042/bj20031190 · Cited by 97 · see citing works

Acute acidic exposure induces p53-mediated oxidative stress and DNA damage in tilapia (Oreochromis niloticus) blood cells

Mai, W., Yan, J.-L., Wang, L., Zheng, Y., Xin, Y., & Wang, W.-N. (2010) · Aquatic Toxicology · doi:10.1016/j.aquatox.2010.07.025 · Cited by 95 · see citing works

Proteomics study of oxidative stress and Src kinase inhibition in H9C2 cardiomyocytes: a cell model of heart ischemia–reperfusion injury and treatment

Chou, H., Chen, Y., Lee, T., Wu, F.-S., Chan, H.-T., Lyu, P. C., Timms, J. F., & Chan, H. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.04.001 · Cited by 92 · see citing works

Protective effect of saponins derived from roots of Platycodon grandiflorum on tert-butyl hydroperoxide-induced oxidative hepatotoxicity

Lee, K. (2004) · Toxicology Letters · doi:10.1016/j.toxlet.2003.12.002 · Cited by 91 · see citing works

The effect of oxidative stress on ERα and ERβ expression

Tamir, S., Izrael, S., & Vaya, J. (2002) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/s0960-0760(02)00115-2 · Cited by 90 · see citing works

Efficacy of N-Acetylcarnosine in the Treatment of Cataracts

Babizhayev, M. A., Deyev, A. I., Yermakova, V. N., Semiletov, Y. A., Davydova, N. G., Doroshenko, V. S., Zhukotskii, A. V., & Goldman, I. M. (2002) · Drugs in R&D · doi:10.2165/00126839-200203020-00004 · Cited by 89 · see citing works

Taurine protection of PC12 cells against endoplasmic reticulum stress induced by oxidative stress

Pan, C., Giraldo, G. S., Prentice, H. M., & Wu, J. (2010) · Journal of Biomedical Science · doi:10.1186/1423-0127-17-s1-s17 · Cited by 89 · see citing works

A transgenic mouse model for monitoring oxidative stress

Oikawa, D., Akai, R., Tokuda, M., & Iwawaki, T. (2012) · Scientific Reports · doi:10.1038/srep00229 · Cited by 88 · see citing works

Blood and lens lipid peroxidation and antioxidant status in normal individuals, senile and diabetic cataractous patients

Donma, O., Yorulmaz, E., Pekel, H., & Suyugül, N. (2002) · Current Eye Research · doi:10.1076/ceyr.25.1.9.9960 · Cited by 86 · see citing works

Cellular lipid peroxidation end-products induce apoptosis in human lens epithelial cells

Choudhary, S., Zhang, W., Zhou, F. L., Campbell, G. A., Chan, L.-N. L., Thompson, E. B., & Ansari, N. H. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(01)00810-3 · Cited by 86 · see citing works

Role of the unfolded protein response (UPR) in cataract formation

Ikesugi, K., Yamamoto, R., Mulhern, M. L., & Shinohara, T. (2006) · Experimental Eye Research · doi:10.1016/j.exer.2006.01.033 · Cited by 83 · see citing works

Urinary excretion of three nucleic acid oxidation adducts and isoprostane F2α measured by liquid chromatography-mass spectrometry in smokers, ex-smokers, and nonsmokers

Harman, S. M., Liang, L., Tsitouras, P. D., Gucciardo, F., Heward, C. B., Reaven, P. D., Ping, W., Ahmed, A. E., & Cutler, R. G. (2003) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2003.07.003 · Cited by 79 · see citing works

Functional constituents of six wild edible Silene species: A focus on their phytochemical profiles and bioactive properties

Zengin, G., Mahomoodally, M. F., Aktümsek, A., Ceylan, R., Uysal, Ş., Mocan, A., Yılmaz, M. A., Picot-Allain, C. M. N., Ćirić, A., Glamočlija, J., et al. (2018) · Food Bioscience · doi:10.1016/j.fbio.2018.03.010 · Cited by 75 · see citing works

Modulation of alpha-crystallin chaperone activity in diabetic rat lens by curcumin.

Kumar, P. A., Suryanarayana, P., Reddy, P. Y., & Reddy, G. B. (2005) · PubMed · Cited by 74 · see citing works

Reference ranges of urinary biomarkers of oxidized guanine in (2′-deoxy)ribonucleotides and nucleic acids

Andreoli, R., Mutti, A., Goldoni, M., Manini, P., Apostoli, P., & Palma, G. D. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.11.009 · Cited by 72 · see citing works

Oxidative stress in older adults: effects of physical fitness

Traustadóttir, T., Davies, S. S., Su, Y., Choi, L., Brown‐Borg, H. M., Roberts, L. J., & Harman, S. M. (2011) · AGE · doi:10.1007/s11357-011-9277-6 · Cited by 72 · see citing works

Environmental lipidomics: understanding the response of organisms and ecosystems to a changing world

Koelmel, J. P., Napolitano, M. P., Ulmer, C. Z., Vasiliou, V., Garrett, T. J., Yost, R. A., Prasad, M. N. V., Pollitt, K. J. G., & Bowden, J. A. (2020) · Metabolomics · doi:10.1007/s11306-020-01665-3 · Cited by 70 · see citing works

Effects of N-acetylcysteine and glutathione ethyl ester drops on streptozotocin-induced diabetic cataract in rats.

Zhang, S., Chai, F.-Y., YAN, H. H., Guo, Y. G., & Harding, J. J. (2008) · PubMed Central · Cited by 70 · see citing works

Update on uveal melanoma: Translational research from biology to clinical practice (Review)

Ortega, M. A., Fraile‐Μartinez, O., García‐Honduvilla, N., Coca, S., Álvarez‐Mon, M., Buján, J., & Teus, M. A. (2020) · International Journal of Oncology · doi:10.3892/ijo.2020.5140 · Cited by 70 · see citing works

Antioxidant activities and oxidative stress inhibitory effects of ethanol extracts from Cornus officinalis on raw 264.7 cells

Hwang, K., Hwang, Y.-J., & Song, J. (2016) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-016-1172-3 · Cited by 69 · see citing works

Age-related cataract progression in five mouse models for anti-oxidant protection or hormonal influence

Wolf, N. S., Penn, P., Pendergrass, W. R., Remmen, H. V., Bartke, A., Rabinovitch, P. S., & Martin, G. M. (2005) · Experimental Eye Research · doi:10.1016/j.exer.2005.01.024 · Cited by 65 · see citing works

Generation of reactive oxygen species in the anterior eye segment. Synergistic codrugs of N-acetylcarnosine lubricant eye drops and mitochondria-targeted antioxidant act as a powerful therapeutic platform for the treatment of cataracts and primary open-angle glaucoma

Babizhayev, M. A. (2016) · BBA Clinical · doi:10.1016/j.bbacli.2016.04.004 · Cited by 65 · see citing works

Ultraviolet Radiation–Induced Cataract in Mice: The Effect of Age and the Potential Biochemical Mechanism

Zhang, J., YAN, H. H., Löfgren, S., Tian, X., & Lou, M. F. (2012) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.12-10482 · Cited by 62 · see citing works

Antityrosinase, Antioxidant, and Cytotoxic Activities of Phytochemical Constituents from Manilkara zapota L. Bark

Chunhakant, S., & Chaicharoenpong, C. (2019) · Molecules · doi:10.3390/molecules24152798 · Cited by 61 · see citing works

Chloroacetic acid induced neuronal cells death through oxidative stress-mediated p38-MAPK activation pathway regulated mitochondria-dependent apoptotic signals

Chen, C., Chen, S.-J., Su, C., Yen, C., Tseng, T.-J., Jinn, T., Tang, F., Chen, K., Su, Y., Lee, K.-I., et al. (2012) · Toxicology · doi:10.1016/j.tox.2012.10.008 · Cited by 59 · see citing works

Uncoupling-mediated generation of reactive oxygen by halogenated aromatic hydrocarbons in mouse liver microsomes

Shertzer, H. G., Clay, C. D., Genter, M. B., Chames, M. C., Schneider, S. N., Oakley, G. G., Nebert, D. W., & Dalton, T. P. (2003) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2003.11.014 · Cited by 59 · see citing works

Grape seed proanthocyanidin extract protects human lens epithelial cells from oxidative stress via reducing NF-кB and MAPK protein expression.

(2011) · Europe PMC (PubMed Central) · Cited by 58 · see citing works

Development- and age-associated expression pattern of peroxiredoxin 6, and its regulation in murine ocular lens

Kubo, E., Miyazawa, T., Fatma, N., Akagi, Y., & Singh, D. P. (2005) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2005.10.003 · Cited by 54 · see citing works

Analytical and biological variation of biomarkers of oxidative stress during the menstrual cycle

Browne, R. W., Bloom, M. S., Schisterman, E. F., Hovey, K. M., Trevisan, M., Wu, C., Liu, A., & Wactawski‐Wende, J. (2008) · Biomarkers · doi:10.1080/13547500701775563 · Cited by 52 · see citing works

Antioxidant activity and DNA damage inhibition in vitro by a methanolic extract of Carissa carandas (Apocynaceae) leaves

Verma, K., Shrivastava, D., & Kumar, G. (2014) · Journal of Taibah University for Science · doi:10.1016/j.jtusci.2014.07.001 · Cited by 51 · see citing works

Fermentation Changes the Nutritive Value, Polyphenol Distribution, and Antioxidant Properties ofParkia biglobosaSeeds (African Locust Beans)

Oboh, G., Alabi, K. B., & Akindahunsi, A. A. (2008) · Food Biotechnology · doi:10.1080/08905430802463404 · Cited by 51 · see citing works

Protective Effect ofMesona procumbensagainsttert-Butyl Hydroperoxide-Induced Acute Hepatic Damage in Rats

Yen, G., Yeh, C., & Chen, Y.-J. (2004) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf049840d · Cited by 50 · see citing works

p53 is involved in shrimp survival via its regulation roles on MnSOD and GPx in response to acute environmental stresses

Qian, Z., Liu, T., Liu, Q., He, S., Liu, Y., Hou, F., Wang, X., Mi, X., Cai, C., & Liu, X. (2013) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2013.09.009 · Cited by 50 · see citing works

Metallo‐ROS in Alzheimer's Disease: Oxidation of Neurotransmitters by CuII‐β‐Amyloid and Neuropathology of the Disease

da Silva, G. F. Z., & Ming, L. (2007) · Angewandte Chemie International Edition · doi:10.1002/anie.200604421 · Cited by 50 · see citing works

Prevention and reversal of selenite-induced cataracts by N-acetylcysteine amide in Wistar rats

Maddirala, Y., Tobwala, S., Karacal, H., & Nuran Ercal, A. (2017) · BMC Ophthalmology · doi:10.1186/s12886-017-0443-1 · Cited by 48 · see citing works

Roles and regulation of lens epithelial cell connexins

Berthoud, V. M., Minogue, P. J., Osmolak, P., Snabb, J. I., & Beyer, E. C. (2014) · FEBS Letters · doi:10.1016/j.febslet.2013.12.024 · Cited by 47 · see citing works

Iron metabolism in the eye: A review

Goralska, M., Ferrell, J., Harned, J., Lall, M. M., Nagar, S., Fleisher, L. N., & McGahan, M. C. (2008) · Experimental Eye Research · doi:10.1016/j.exer.2008.10.026 · Cited by 47 · see citing works

Protein expression profiling of lens epithelial cells from Prdx6-depleted mice and their vulnerability to UV radiation exposure

Kubo, E., Hasanova, N., Tanaka, Y., Fatma, N., Takamura, Y., Singh, D. P., & Akagi, Y. (2009) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00336.2009 · Cited by 47 · see citing works

Evaluation of Antioxidant Activity and Characterization of Phenolic Constituents ofPhyllanthus amarusRoot

Maity, S., Chatterjee, S., Variyar, P. S., Sharma, A. K., Adhikari, S., & Mazumder, S. (2013) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf3046686 · Cited by 46 · see citing works

Evaluation of Neonatal Streptozotocin Induced Diabetic Rat Model for the Development of Cataract

Patil, M. A., Suryanarayana, P., Putcha, U. K., Srinivas, M., & Reddy, G. B. (2014) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2014/463264 · Cited by 45 · see citing works

Different experimental approaches in modelling cataractogenesis

Kyseľová, Z. (2010) · Interdisciplinary Toxicology · doi:10.2478/v10102-010-0005-3 · Cited by 45 · see citing works

The effect of a single Finnish sauna bath after aerobic exercise on the oxidative status in healthy men

Sutkowy, P., Woźniak, A., Boraczyński, T., Mila-Kierzenkowska, C., & Boraczyński, M. (2013) · Scandinavian Journal of Clinical and Laboratory Investigation · doi:10.3109/00365513.2013.860616 · Cited by 44 · see citing works

Potential pathways of zinc deficiency-promoted tumorigenesis

Zhang, Y., Tian, Y., Zhang, H., Xu, B., & Chen, H. (2020) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.110983 · Cited by 43 · see citing works

Preventive Effect of Zea mays L. (Purple Waxy Corn) on Experimental Diabetic Cataract

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The effect of stress withdrawal on gene expression and certain biochemical and cell biological properties of peroxide‐conditioned cell lines

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