Intracellular Redox State Alters NMDA Receptor Response during Aging through Ca2+/Calmodulin-Dependent Protein Kinase II

A synaptic model of memory: long-term potentiation in the hippocampus

Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566 · see citing works

The molecular basis of CaMKII function in synaptic and behavioural memory

Lisman, J., Schulman, H., & Cline, H. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn753 · Cited by 1,860 · see citing works

The essential role of hippocampal CA1 NMDA receptor-dependent synaptic plasticity in spatial memory.

Tsien, J. Z., Huerta, P. T., & Tonegawa, S. (1996) · Cell · doi:10.1016/s0092-8674(00)81827-9 · Cited by 1,782 · cited 1× · see citing works

Modulation of Protein Kinase Activity and Gene Expression by Reactive Oxygen Species and Their Role in Vascular Physiology and Pathophysiology

Griendling, K. K., Sorescu, D., Lassegue, B. P., & Ushio‐Fukai, M. (2000) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.20.10.2175 · Cited by 955 · see citing works

Impact of aging on hippocampal function: plasticity, network dynamics, and cognition

Rosenzweig, E. S., & Barnes, C. A. (2003) · Progress in Neurobiology · doi:10.1016/s0301-0082(02)00126-0 · Cited by 730 · see citing works

KN-62, 1-[N,O-bis(5-isoquinolinesulfonyl)-N-methyl-L-tyrosyl]-4-phenylpiperazi ne, a specific inhibitor of Ca2+/calmodulin-dependent protein kinase II.

Tokumitsu, H., Chijiwa, T., Hagiwara, M., Mizutani, A., Terasawa, M., & Hidaka, H. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)39565-1 · Cited by 624 · see citing works

Regulation of NMDA Receptors by an Associated Phosphatase-Kinase Signaling Complex

Westphal, R. S., Tavalin, S. J., Lin, J., Alto, N. M., Fraser, I. D. C., Langeberg, L. K., Sheng, M., & Scott, J. D. (1999) · Science · doi:10.1126/science.285.5424.93 · Cited by 492 · see citing works

Regulation of NMDA channel function by endogenous Ca2+-dependent phosphatase

Lieberman, D. N., & Mody, I. (1994) · Nature · doi:10.1038/369235a0 · Cited by 480 · see citing works

Selective modulation of NMDA responses by reduction and oxidation

Aizenman, E., Lipton, S. A., & Loring, R. H. (1989) · Neuron · doi:10.1016/0896-6273(89)90310-3 · Cited by 456 · see citing works

Cysteine regulation of protein function – as exemplified by NMDA-receptor modulation

Lipton, S. A., Choi, Y.-B., Takahashi, H., Zhang, D., Li, W., Godzik, A., & Bankston, L. A. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02245-2 · Cited by 375 · see citing works

Protein kinase C modulation of NMDA currents: an important link for LTP induction

Ben‐Ari, Y., Aniksztejn, L., & Bregestovski, P. D. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90049-e · Cited by 343 · see citing works

Involvement of hippocampal synaptic plasticity in age-related memory decline

Foster, T. C. (1999) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00017-x · Cited by 317 · see citing works

Cystine/Glutamate Exchange Modulates Glutathione Supply for Neuroprotection from Oxidative Stress and Cell Proliferation

Shih, A. Y., Erb, H., Sun, X., Toda, S., Kalivas, P. W., & Murphy, T. H. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3178-06.2006 · Cited by 315 · see citing works

Calcium homeostasis and modulation of synaptic plasticity in the aged brain

Foster, T. C. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00283.x · Cited by 302 · see citing works

Reversal of Age-Related Alterations in Synaptic Plasticity by Blockade of L-Type Ca2+ Channels

Norris, C., Halpain, S., & Foster, T. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-09-03171.1998 · Cited by 289 · see citing works

Regulation of NMDA receptors by cyclin-dependent kinase-5

Li, B., Sun, M., Zhang, L., Takahashi, S., Ma, W., Vinadé, L., Kulkarni, A. B., Brady, R. O., & Pant, H. C. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.211428098 · Cited by 260 · see citing works

Aging Differentially Alters Forms of Long-Term Potentiation in Rat Hippocampal Area CA1

Shankar, S., Teyler, T. J., & Robbins, N. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.1.334 · Cited by 225 · see citing works

Modulation of potassium channel function by methionine oxidation and reduction

Ciorba, M. A., Heinemann, S. H., Weissbach, H., Brot, N., & Hoshi, T. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.18.9932 · Cited by 224 · see citing works

Calcineurin Links Ca2+Dysregulation with Brain Aging

Foster, T. C., Sharrow, K., Masse, J. R., Norris, C. M., & Kumar, A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-11-04066.2001 · Cited by 214 · see citing works

Regulation of NMDA receptors in cultured hippocampal neurons by protein phosphatases 1 and 2A

Wang, L., Orser, B. A., Brautigan, D. L., & MacDonald, J. F. (1994) · Nature · doi:10.1038/369230a0 · Cited by 204 · see citing works

Oxygen free radicals regulate NMDA receptor function via a redox modulatory site

Aizenman, E., Hartnett, K. A., & Reynoldst, I. J. (1990) · Neuron · doi:10.1016/0896-6273(90)90343-e · Cited by 203 · see citing works

Superoxide-induced Stimulation of Protein Kinase C via Thiol Modification and Modulation of Zinc Content

Knapp, L. T., & Klann, E. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m002043200 · Cited by 201 · see citing works

Distinct triggering and expression mechanisms underlie LTD of AMPA and NMDA synaptic responses

Morishita, W., Marie, H., & Malenka, R. C. (2005) · Nature Neuroscience · doi:10.1038/nn1506 · Cited by 186 · see citing works

Interactions between the NR2B Receptor and CaMKII Modulate Synaptic Plasticity and Spatial Learning

Zhou, Y., Takahashi, E., Li, W., Halt, A., Wiltgen, B., Ehninger, D., Li, G.-D., Hell, J. W., Kennedy, M. B., & Silva, A. J. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4486-07.2007 · Cited by 179 · see citing works

Redox modulation of the NMDA receptor

Choi, Y., & Lipton, S. A. (2000) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000638 · Cited by 165 · see citing works

Potentiation of Hippocampal Synaptic Transmission by Superoxide Requires the Oxidative Activation of Protein Kinase C

Knapp, L. T., & Klann, E. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-03-00674.2002 · Cited by 148 · see citing works

Age-Related Decrease in the N-Methyl-d-AspartateR-Mediated Excitatory Postsynaptic Potential in Hippocampal Region CA1

Barnes, C. A., RAO, G. R., & Shen, J. (1997) · Neurobiology of Aging · doi:10.1016/s0197-4580(97)00044-4 · Cited by 145 · see citing works

Decreased NR2B Subunit Synaptic Levels Cause Impaired Long-Term Potentiation But Not Long-Term Depression

Gardoni, F., Mauceri, D., Malinverno, M., Polli, F., Costa, C., Tozzi, A., Siliquini, S., Picconi, B., Cattabeni, F., Calabresi, P., et al. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3921-08.2009 · Cited by 142 · see citing works

Multivalent Interactions of Calcium/Calmodulin-dependent Protein Kinase II with the Postsynaptic Density Proteins NR2B, Densin-180, and α-Actinin-2

Robison, A. J., Bass, M. A., Jiao, Y., MacMillan, L. B., Carmody, L. C., Bartlett, R. K., & Colbran, R. J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m502191200 · Cited by 134 · see citing works

Three Pairs of Cysteine Residues Mediate Both Redox and Zn²⁺Modulation of the NMDA Receptor

Choi, Y.-B., Chen, H.-S. V., & Lipton, S. A. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-02-00392.2001 · Cited by 132 · see citing works

Biological Markers of Age-Related Memory Deficits

Foster, T. C. (2006) · CNS Drugs · doi:10.2165/00023210-200620020-00006 · Cited by 119 · see citing works

Potential Adaptive Function for Altered Long-Term Potentiation Mechanisms in Aging Hippocampus

Boric, K., Muñoz, P., Gallagher, M., & Kirkwood, A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2036-08.2008 · Cited by 115 · see citing works

Reducing and Oxidizing Agents Sensitize Heat-Activated Vanilloid Receptor (TRPV1) Current

Sušánková, K., Tousova, K., Vyklický, L., Teisinger, J., & Vlachová, V. (2006) · Molecular Pharmacology · doi:10.1124/mol.106.023069 · Cited by 113 · see citing works

Alterations in the Balance of Protein Kinase/Phosphatase Activities Parallel Reduced Synaptic Strength During Aging

Norris, C. M., Halpain, S., & Foster, T. C. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.3.1567 · Cited by 104 · see citing works

Proteomics Analyses of Specific Protein Oxidation and Protein Expression in Aged Rat Brain and Its Modulation by L-Acetylcarnitine: Insights Into the Mechanisms of Action of This Proposed Therapeutic Agent for CNS Disorders Associated with Oxidative Stress

Poon, H. F., Calabrese, V., Calvani, M., & Butterfield, D. A. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2006.8.381 · Cited by 99 · see citing works

Ascorbate attenuates trimethyltin-induced oxidative burden and neuronal degeneration in the rat hippocampus by maintaining glutathione homeostasis

Shin, E., Suh, S. K., Lim, Y.-Y., Jhoo, W., Hjelle, O. P., Ottersen, O. P., Shin, C. Y., Ko, K. H., Kim, W.-K., Kim, D. S., et al. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.02.030 · Cited by 97 · see citing works

Deficit of NMDA receptor activation in CA1 hippocampal area of aged rats is rescued by d ‐cycloserine

Billard, J., & Rouaud, E. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05488.x · Cited by 91 · see citing works

Oxidation of a potassium channel causes progressive sensory function loss during aging

Cai, S., & Sesti, F. (2009) · Nature Neuroscience · doi:10.1038/nn.2291 · Cited by 72 · see citing works

Age‐related decreases in NAD(P)H and glutathione cause redox declines before ATP loss during glutamate treatment of hippocampal neurons

Parihar, M. S., Kunz, E. A., & Brewer, G. J. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21679 · Cited by 69 · see citing works

Alterations in the balance of protein kinase and phosphatase activities and age‐related impairments of synaptic transmission and long‐term potentiation

Hsu, K., Huang, C., Liang, Y., Wu, H., Chen, Y., Lo, S.-W., & Ho, W. (2002) · Hippocampus · doi:10.1002/hipo.10032 · Cited by 68 · see citing works

Red blood cell permeability to thiol compounds following oxidative stress

Mazor, D., Golan, E., Philip, V., Katz, M., Jafe, A., Ben‐Zvi, Z., & Meyerstein, N. (1996) · European Journal Of Haematology · doi:10.1111/j.1600-0609.1996.tb01370.x · Cited by 56 · see citing works

Regulation of synaptic plasticity in memory and memory decline with aging

Foster, T. C. (2002) · Progress in brain research · doi:10.1016/s0079-6123(02)38083-x · Cited by 51 · see citing works

Protein phosphatase inhibitors facilitate DHPG‐induced LTD in the CA1 region of the hippocampus

Schnabel, R., Kilpatrick, I. C., & Collingridge, G. L. (2001) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0703905 · Cited by 51 · see citing works

In vivo depletion of endogenous glutathione facilitates trimethyltin-induced neuronal damage in the dentate gyrus of mice by enhancing oxidative stress

Yoneyama, M., Nishiyama, N., Shuto, M., Sugiyama, C., Kawada, K., Seko, K., Nagashima, R., & Ogita, K. (2007) · Neurochemistry International · doi:10.1016/j.neuint.2007.09.003 · Cited by 49 · see citing works

Oxidation of calmodulin alters activation and regulation of CaMKII

Robison, A. J., Winder, D. G., Colbran, R. J., & Bartlett, R. K. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.02.087 · Cited by 46 · see citing works

Oxidative Modulation of Cyclic AMP-Dependent Protein Kinase in Human Fibroblasts: Possible Role in Psoriasis

Raynaud, F., Evain‐Brion, D., Gerbaud, P., Marciano, D., Gorin, I., Liapi, C. A., & Anderson, W. B. (1997) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(96)00353-x · Cited by 44 · see citing works

Hippocampal ‘zipper’ slice studies reveal a necessary role for calcineurin in the increased activity of L-type Ca2+ channels with aging

Norris, C. M., Blalock, E. M., Chen, K.-C., Porter, N. M., Thibault, O., Kraner, S. D., & Landfield, P. W. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2008.03.026 · Cited by 37 · see citing works

Age-related differences in NMDA responses in cultured rat hippocampal neurons

Cady, C., Evans, M. S., & Brewer, G. J. (2001) · Brain Research · doi:10.1016/s0006-8993(01)03063-3 · Cited by 35 · see citing works

Differential effects of aging on NMDA receptors in the intermediate versus the dorsal hippocampus

MAGNUSSON, K., Kresge, D. L., & Supon, J. (2005) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.01.012 · Cited by 34 · see citing works

Redox modulation of synaptic responses and plasticity in rat CA1 hippocampal neurons

Bernard, C., Hirsch, J. C., Khazipov, R., Ben‐Ari, Y., & GOZLAN, H. (1997) · Experimental Brain Research · doi:10.1007/bf02450332 · Cited by 33 · see citing works

In CA1 hippocampal neurons, the redox state of NMDA receptors determines LTP expressed by NMDA but not by AMPA receptors

GOZLAN, H., Khazipov, R., Diabira, D., & Ben‐Ari, Y. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.73.6.2612 · Cited by 30 · see citing works

Ischemia-elicited Oxidative Modulation of Ca2+/Calmodulin-dependent Protein Kinase II

Shetty, P. K., Huang, F. L., & Huang, K. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m708479200 · Cited by 27 · see citing works

The effects of aging on different C-terminal splice forms of the ζ1(NR1) subunit of the N-methyl-d-aspartate receptor in mice

Magnusson, K. R., Bai, L., & Zhao, X. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.12.012 · Cited by 26 · see citing works

Disulfide Bonding and Cysteine Accessibility in the α-Amino-3-hydroxy-5-methylisoxazole-4-propionic Acid Receptor Subunit GluRD

Abele, R., Lampinen, M., KEINÄNEN, K. P., & Madden, D. R. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.39.25132 · Cited by 26 · see citing works

Differential Effects of Methionine and Cysteine Oxidation on [Ca2+]i in Cultured Hippocampal Neurons

Long, L., Liu, J., Liu, R., Wang, F., Hu, Z., Xie, N., Fu, H. Q., & Chen, J. (2008) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-008-9289-7 · Cited by 18 · see citing works

Oxidative insult in sheep red blood cells induced by t-butyl hydroperoxide: The roles of glutathione and glutathione peroxidase

Zou, C., Agar, N. S., & Jones, G. L. (2001) · Free Radical Research · doi:10.1080/10715760100300051 · Cited by 16 · see citing works

The effects of aging in the hippocampus and cognitive decline

Bettio, L. E. B., Rajendran, L., & Gil‐Mohapel, J. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.04.030 · Cited by 654 · see citing works

Synaptic plasticity in depression: molecular, cellular and functional correlates.

Marsden, W. N. (2013) · Progress in Neuro-psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2012.12.012 · Cited by 321 · see citing works

Linking early-life NMDAR hypofunction and oxidative stress in schizophrenia pathogenesis

Hardingham, G. E., & Do, K. Q. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2015.19 · Cited by 304 · see citing works

Reactive Oxygen Species: Physiological and Physiopathological Effects on Synaptic Plasticity: Supplementary Issue: Brain Plasticity and Repair

Beckhauser, T. F., Francis-Oliveira, J., & De Pasquale, R. (2016) · Journal of Experimental Neuroscience · doi:10.4137/jen.s39887 · Cited by 301 · see citing works

The origin of NMDA receptor hypofunction in schizophrenia

Nakazawa, K., & Sapkota, K. (2019) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2019.107426 · Cited by 277 · see citing works

Redox dysregulation, neuroinflammation, and NMDA receptor hypofunction: A “central hub” in schizophrenia pathophysiology?

Steullet, P., Cabungcal, J. H., Monin, A., Dwir, D., O'Donnell, P., Cuenod, M., & Do, K. Q. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2014.06.021 · Cited by 262 · see citing works

Bioassay‐guided Evaluation of Antioxidant and Antinociceptive Activities of Carvacrol

Guimarães, A. G., Oliveira, G. F., Seabra, M. S. D. M., Cavalcanti, S. C. H., Antoniolli, Â. R., Bonjardim, L. R., Silva, F. A., dos Santos, J. P. A., da Rocha, R. F., Moreira, J. C. F., et al. (2010) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/j.1742-7843.2010.00609.x · Cited by 225 · see citing works

Vitamin D cell signalling in health and disease

Berridge, M. J. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.01.008 · Cited by 214 · see citing works

Glutamatergic Neurons in Rodent Models Respond to Nanoscale Particulate Urban Air Pollutants in Vivo and in Vitro

Morgan, T. E., Davis, D. A., Iwata, N., Tanner, J. A., Snyder, D., Ning, Z., Kam, W. W.-Y., Hsu, Y., Winkler, J. W., Chen, J., et al. (2011) · Environmental Health Perspectives · doi:10.1289/ehp.1002973 · Cited by 204 · see citing works

Long-Term Potentiation at CA3–CA1 Hippocampal Synapses with Special Emphasis on Aging, Disease, and Stress

Kumar, A. (2011) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2011.00007 · Cited by 169 · see citing works

Dissecting the age-related decline on spatial learning and memory tasks in rodent models: N-methyl-D-aspartate receptors and voltage-dependent Ca2+ channels in senescent synaptic plasticity

Foster, T. C. (2012) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.01.007 · Cited by 159 · see citing works

Aging, Synaptic Dysfunction, and Insulin-Like Growth Factor (IGF)-1

Deák, F., & Sonntag, W. E. (2012) · The Journals of Gerontology Series A · doi:10.1093/gerona/gls118 · Cited by 147 · see citing works

Insulin-like growth factor-1 in CNS and cerebrovascular aging

Sonntag, W. E., Deák, F., Ashpole, N. M., Tóth, P., Csiszár, A., Freeman, W. M., & Ungvari, Z. I. (2013) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2013.00027 · Cited by 136 · see citing works

Caught in vicious circles: a perspective on dynamic feed-forward loops driving oxidative stress in schizophrenia

Cuénod, M., Steullet, P., Cabungcal, J.-H., Dwir, D., Khadimallah, I., Klauser, P., Conus, P., & Kim, Q. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01374-w · Cited by 129 · see citing works

NMDA Receptor Function During Senescence: Implication on Cognitive Performance

Kumar, A. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00473 · Cited by 121 · see citing works

Influence of late-life exposure to environmental enrichment or exercise on hippocampal function and CA1 senescent physiology

Kumar, A., Rani, A., Tchigranova, O., Russell, W. L., & Foster, T. C. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.06.023 · Cited by 114 · see citing works

Redox Signaling in Neurotransmission and Cognition During Aging

Kumar, A., Yegla, B., & Foster, T. C. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7111 · Cited by 104 · see citing works

Potential Roles of Redox Dysregulation in the Development of Schizophrenia

Perkins, D. O., Jeffries, C. D., & Do, K. Q. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.03.016 · Cited by 103 · see citing works

Dysregulated phosphorylation of Ca2+/calmodulin‐dependent protein kinase II‐α in the hippocampus of subjects with mild cognitive impairment and Alzheimer’s disease

Reese, L. C., Laezza, F., Woltjer, R. L., & Taglialatela, G. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07447.x · Cited by 99 · see citing works

Central role for NMDA receptors in redox mediated impairment of synaptic function during aging and Alzheimer’s disease

Foster, T. C., Kyritsopoulos, C., & Kumar, A. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.05.012 · Cited by 92 · see citing works

APOE4 enhances age-dependent decline in cognitive function by down-regulating an NMDA receptor pathway in EFAD-Tg mice

Liu, D.-S., Pan, X.-D., Zhang, J., Shen, H., Collins, N. C., Cole, A. M., Koster, K. P., Ben Aissa, M., Dai, X.-M., Zhou, M., et al. (2015) · Molecular Neurodegeneration · doi:10.1186/s13024-015-0002-2 · Cited by 99 · see citing works

Glutathione Restores the Mechanism of Synaptic Plasticity in Aged Mice to That of the Adult

Robillard, J. M., Gordon, G. R., Choi, H. B., Christie, B. R., & MacVicar, B. A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020676 · Cited by 89 · see citing works

Reversal of age‐related oxidative stress prevents hippocampal synaptic plasticity deficits by protecting <scp>d</scp>‐serine‐dependent NMDA receptor activation

Haxaire, C., Turpin, F. R., Potier, B., Kervern, M., Sinet, P., Barbanel, G., Mothet, J., Dutar, P., & Billard, J. (2012) · Aging Cell · doi:10.1111/j.1474-9726.2012.00792.x · Cited by 88 · see citing works

NO-dependent CaMKII activation during β-adrenergic stimulation of cardiac muscle

Gutierrez, D. A., Fernández-Tenorio, M., Ogrodnik, J., & Ernst Niggli, A. (2013) · Cardiovascular Research · doi:10.1093/cvr/cvt201 · Cited by 87 · see citing works

Redox Sensitive Calcium Stores Underlie Enhanced After Hyperpolarization of Aged Neurons: Role for Ryanodine Receptor Mediated Calcium Signaling

Bodhinathan, K., Kumar, A., & Foster, T. C. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00577.2010 · Cited by 86 · see citing works

Loss of glutathione homeostasis associated with neuronal senescence facilitates TRPM2 channel activation in cultured hippocampal pyramidal neurons

Belrose, J. C., Xie, Y., Gierszewski, L. J., MacDonald, J. F., & Jackson, M. F. (2012) · Molecular Brain · doi:10.1186/1756-6606-5-11 · Cited by 86 · see citing works

Effects of pre-natal alcohol exposure on hippocampal synaptic plasticity: Sex, age and methodological considerations

Fontaine, C. J., Patten, A. R., Sickmann, H. M., Helfer, J. L., & Christie, B. R. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.02.014 · Cited by 79 · see citing works

Early Identification and Intervention of Schizophrenia: Insight From Hypotheses of Glutamate Dysfunction and Oxidative Stress

Lin, C., & Lane, H. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00093 · Cited by 80 · see citing works

Early pathogenesis in the adult‐onset neurodegenerative disease amyotrophic lateral sclerosis

van Zundert, B., Izaurieta, P., Fritz, E., & Álvarez, F. J. (2012) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24234 · Cited by 80 · see citing works

Linking Redox Regulation of NMDAR Synaptic Function to Cognitive Decline during Aging

Kumar, A., & Foster, T. C. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2176-13.2013 · Cited by 78 · see citing works

Enhancement of BDNF Expression and Memory by HDAC Inhibition Requires BET Bromodomain Reader Proteins

Sartor, G. C., Malvezzi, A. M., Kumar, A., Andrade, N. S., Wiedner, H. J., Vilca, S. J., Janczura, K. J., Bagheri, A., Al‐Ali, H., Powell, S. K., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1604-18.2018 · Cited by 77 · see citing works

Single-Cell Redox Imaging Demonstrates a Distinctive Response of Dopaminergic Neurons to Oxidative Insults

Horowitz, M. P., Milanese, C., Maio, R. D., Hu, X., Montero, L. M., Sanders, L. H., Tapias, V., Sepe, S., van Cappellen, W. A., Burton, E. A., et al. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3629 · Cited by 75 · see citing works

Calcium, Reactive Oxygen Species, and Synaptic Plasticity

Hidalgo, C., & Arias‐Cavieres, A. (2016) · Physiology · doi:10.1152/physiol.00038.2015 · Cited by 72 · see citing works

Calcium Signaling, Excitability, and Synaptic Plasticity Defects in a Mouse Model of Alzheimer's Disease

Zhang, H., Liu, J., Sun, S., Pchitskaya, E. I., Александровна, П. Е., & Борисович, Б. И. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-142427 · Cited by 73 · see citing works

Memory in aged mice is rescued by enhanced expression of the GluN2B subunit of the NMDA receptor

Brim, B. C., Haskell, R. E., Awedikian, R., Ellinwood, N. M., Jin, L. E., Kumar, A., Foster, T. C., & Magnusson, K. R. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.10.026 · Cited by 73 · see citing works

Oxidative Dysregulation in Early Life Stress and Posttraumatic Stress Disorder: A Comprehensive Review

Karanikas, E., Daskalakis, N. P., & Agorastos, A. (2021) · Brain Sciences · doi:10.3390/brainsci11060723 · Cited by 78 · see citing works

L-type Ca2+ currents at CA1 synapses, but not CA3 or dentate granule neuron synapses, are increased in 3xTgAD mice in an age-dependent manner

Wang, Y., & Mattson, M. P. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.07.007 · Cited by 72 · see citing works

Alteration in NMDA Receptor Mediated Glutamatergic Neurotransmission in the Hippocampus During Senescence

Kumar, A., & Foster, T. C. (2018) · Neurochemical Research · doi:10.1007/s11064-018-2634-4 · Cited by 72 · see citing works

Aging Impairs Hippocampal- Dependent Recognition Memory and LTP and Prevents the Associated RyR Up-regulation

Arias-Cavieres, A., Adasme, T., Sánchez, G., Muñoz, P., & Hidalgo, C. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00111 · Cited by 70 · see citing works

A HIF1a-Dependent Pro-Oxidant State Disrupts Synaptic Plasticity and Impairs Spatial Memory in Response to Intermittent Hypoxia

Arias‐Cavieres, A., Khuu, M. A., Nwakudu, C. U., Barnard, J. E., Dalgin, G., & Garcia, A. J. (2020) · eNeuro · doi:10.1523/eneuro.0024-20.2020 · Cited by 67 · see citing works

Melatonin alleviates inflammation-induced apoptosis in human umbilical vein endothelial cells via suppression of Ca2+-XO-ROS-Drp1-mitochondrial fission axis by activation of AMPK/SERCA2a pathway

Cui, J., Li, Z., Zhuang, S., Qi, S., Li, L., Zhou, J., Zhang, W., & Zhao, Y. (2018) · Cell Stress and Chaperones · doi:10.1007/s12192-017-0841-6 · Cited by 65 · see citing works

Effect of peripheral cellular senescence on brain aging and cognitive decline

Budamagunta, V., Kumar, A., Rani, A., Bean, L. A., Manohar‐Sindhu, S., Yang, Y., Zhou, D., & Foster, T. C. (2023) · Aging Cell · doi:10.1111/acel.13817 · Cited by 65 · see citing works

Impaired Attention and Synaptic Senescence of the Prefrontal Cortex Involves Redox Regulation of NMDA Receptors

Guidi, M., Kumar, A., & Foster, T. C. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.3523-14.2015 · Cited by 63 · see citing works

Dual action of L-Lactate on the activity of NR2B-containing NMDA receptors: from potentiation to neuroprotection

Jourdain, P., Rothenfusser, K., Benadiba, C., Allaman, I., Marquet, P. P., & Magistretti, P. J. (2018) · Scientific Reports · doi:10.1038/s41598-018-31534-y · Cited by 64 · see citing works

Stressor-induced NMDAR dysfunction as a unifying hypothesis for the aetiology, pathogenesis and comorbidity of clinical depression

Marsden, W. N. (2011) · Medical Hypotheses · doi:10.1016/j.mehy.2011.06.021 · Cited by 63 · see citing works

In Vivo Imaging with Genetically Encoded Redox Biosensors

Kostyuk, A. I., Panova, A. S., Kokova, A. D., Kotova, D. A., Maltsev, D. I., Podgorny, O. V., Belousov, V. V., & Bilan, D. S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21218164 · Cited by 63 · see citing works

Session III: Mechanisms of Age-Related Cognitive Change and Targets for Intervention: Inflammatory, Oxidative, and Metabolic Processes

Craft, S., Foster, T. C., Landfield, P. W., Maier, S. F., Resnick, S. M., & Yaffe, K. (2012) · The Journals of Gerontology Series A · doi:10.1093/gerona/gls112 · Cited by 61 · see citing works

The hypoxia-tolerant vertebrate brain: Arresting synaptic activity

Buck, L. T., & Pamenter, M. E. (2017) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2017.11.015 · Cited by 61 · see citing works

Role of Hydrogen Sulfide and Polysulfides in Neurological Diseases: Focus on Protein S-Persulfidation

Sun, H., Wu, Z., Nie, X.-W., & Bian, J. (2020) · Current Neuropharmacology · doi:10.2174/1570159x18666200905143550 · Cited by 62 · see citing works

Contribution of Ca 2+ Release Channels to Hippocampal Synaptic Plasticity and Spatial Memory: Potential Redox Modulation

Paula-Lima, A. C., Adasme, T., & Hidalgo, C. (2014) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5796 · Cited by 58 · see citing works

Dietary phytoestrogen intakes and cognitive function during the menopausal transition

Greendale, G. A., Huang, M.-H., Leung, K., Crawford, S. L., Gold, E. B., Wight, R. G., Waetjen, E., & Karlamangla, A. S. (2012) · Menopause The Journal of The North American Menopause Society · doi:10.1097/gme.0b013e318242a654 · Cited by 57 · see citing works

Tetrahydroxystilbene glucoside, a plant-derived cognitive enhancer, promotes hippocampal synaptic plasticity

Wang, T., Yang, Y., Wu, P., Wang, W., Hu, Z., Long, L., Xie, N., Fu, H. Q., Wang, F., & Chen, J. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.10.002 · Cited by 55 · see citing works

Short-term environmental enrichment enhances synaptic plasticity in hippocampal slices from aged rats

Stein, L. R., O’Dell, K. A., Funatsu, M., Zorumski, C. F., & Izumi, Y. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.05.020 · Cited by 55 · see citing works

Age-dependent alterations in cAMP signaling contribute to synaptic plasticity deficits following traumatic brain injury

Titus, D. J., Furones, C., Kang, Y. J., & Atkins, C. M. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.12.002 · Cited by 53 · see citing works

Re-Opening the Critical Window for Estrogen Therapy

Bean, L. A., Kumar, A., Rani, A., Guidi, M., Rosario, A. M., Cruz, P. E., Golde, T. E., & Foster, T. C. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1890-15.2015 · Cited by 53 · see citing works

‘Tagging’ along memories in aging: Synaptic tagging and capture mechanisms in the aged hippocampus

Shetty, M. S., & Sajikumar, S. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2016.12.008 · Cited by 53 · see citing works

Redox signaling and metabolism in Alzheimer's disease

Holubiec, M. I., Gellert, M., & Hanschmann, E.-M. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1003721 · Cited by 52 · see citing works

Schizophrenia Synaptic Pathology and Antipsychotic Treatment in the Framework of Oxidative and Mitochondrial Dysfunction: Translational Highlights for the Clinics and Treatment

De Simone, G., Mazza, B., Vellucci, L., Barone, A., Ciccarelli, M., & de Bartolomeis, A. (2023) · Antioxidants · doi:10.3390/antiox12040975 · Cited by 49 · see citing works

Multi-input Synapses, but Not LTP-Strengthened Synapses, Correlate with Hippocampal Memory Storage in Aged Mice

Aziz, W., Kraev, I., Mizuno, K., Kirby, A. J., Fang, T., Rupawala, H., Kasbi, K., Rothe, S., Jozsa, F., Rosenblum, K., et al. (2019) · Current Biology · doi:10.1016/j.cub.2019.08.064 · Cited by 44 · see citing works

Impairments in hippocampal synaptic plasticity following prenatal ethanol exposure are dependent on glutathione levels

Patten, A. R., Brocardo, P. S., Sakiyama, C., Wortman, R. C., Noonan, A., Gil‐Mohapel, J., & Christie, B. R. (2013) · Hippocampus · doi:10.1002/hipo.22199 · Cited by 45 · see citing works

Dual-energy precursor and nuclear erythroid–related factor 2 activator treatment additively improve redox glutathione levels and neuron survival in aging and Alzheimer mouse neurons upstream of reactive oxygen species

Ghosh, D., LeVault, K. R., & Brewer, G. J. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.06.023 · Cited by 43 · see citing works

Susceptibility of the cerebral cortex to spreading depolarization in neurological disease states: The impact of aging

Hertelendy, P., Varga, D. P., Menyhárt, Á., Bari, F., & Farkas, E. (2018) · Neurochemistry International · doi:10.1016/j.neuint.2018.10.010 · Cited by 43 · see citing works

Subunit contribution to NMDA receptor hypofunction and redox sensitivity of hippocampal synaptic transmission during aging

Kumar, A., Thinschmidt, J. S., & Foster, T. C. (2019) · Aging · doi:10.18632/aging.102108 · Cited by 39 · see citing works

Oxidation of ion channels in the aging nervous system

Patel, R., & Sesti, F. (2016) · Brain Research · doi:10.1016/j.brainres.2016.02.046 · Cited by 39 · see citing works

α-Tocopherol and Hippocampal Neural Plasticity in Physiological and Pathological Conditions

Ambrogini, P., Betti, M., Galati, C., Palma, M. D., Lattanzi, D., Savelli, D., Galli, F., Cuppini, R., & Minelli, A. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17122107 · Cited by 38 · see citing works

Redox Post-translational Modifications of Protein Thiols in Brain Aging and Neurodegenerative Conditions—Focus on S-Nitrosation

Finelli, M. J. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.00254 · Cited by 37 · see citing works

Targeting redox-altered plasticity to reactivate synaptic function: A novel therapeutic strategy for cognitive disorder

Wang, P., Wang, F., Ni, L., Wu, P., & Chen, J. (2020) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2020.11.012 · Cited by 37 · see citing works

Role of antioxidant enzymes in redox regulation of N-methyl-D-aspartate receptor function and memory in middle-aged rats

Russell, W. L., Kumar, A., Rani, A., & Foster, T. C. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.12.002 · Cited by 36 · see citing works

Influence of Viral Vector–Mediated Delivery of Superoxide Dismutase and Catalase to the Hippocampus on Spatial Learning and Memory During Aging

Russell, W. L., Kumar, A., Rani, A., Herrera, J., Xu, J., Someya, S., & Foster, T. C. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.4054 · Cited by 34 · see citing works

Impairments of Synaptic Plasticity in Aged Animals and in Animal Models of Alzheimer's Disease

Balietti, M., Tamagnini, F., Fattoretti, P., Burattini, C., Casoli, T., Platano, D., Lattanzio, F., & Aicardi, G. (2012) · Rejuvenation Research · doi:10.1089/rej.2012.1318 · Cited by 34 · see citing works

Activity-Dependent Sulfhydration Signal Controls N-Methyl-D-Aspartate Subtype Glutamate Receptor-Dependent Synaptic Plasticity via Increasing d -Serine Availability

Li, Y., Wu, P., Chen, J., Wang, S., Han, Q.-Q., Li, D., Wang, W., Guan, X., Li, D., Long, L., et al. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2016.6936 · Cited by 33 · see citing works

Scavenging ROS dramatically increases NMDA receptor whole cell currents in painted turtle cortical neurons

Dukoff, D. J., Hogg, D. W., Hawrsyh, P. J., & Buck, L. T. (2014) · Journal of Experimental Biology · doi:10.1242/jeb.105825 · Cited by 31 · see citing works

Glutathione depletion: Starting point of brain metabolic stress, neuroinflammation and cognitive impairment in rats

González-Fraguela, M. E., Blanco, L., Fernández, C. I., Lorigados, L., Serrano, T., & Fernández, J. L. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.11.015 · Cited by 32 · see citing works

Antinociceptive activities of Artocarpus lacucha Buch-ham (Moraceae) and its isolated phenolic compound, catechin, in mice

Islam, S., Shajib, M. S., Rashid, R. B., Khan, M. F., Al-Mansur, M. A., Datta, B. K., & Rashid, M. A. (2019) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-019-2565-x · Cited by 32 · see citing works

Enhanced expression of Pctk1, Tcf12 and Ccnd1 in hippocampus of rats: Impact on cognitive function, synaptic plasticity and pathology

Wu, K., Li, S., Bodhinathan, K., Meyers, C., Chen, W., Campbell‐Thompson, M., McIntyre, L. M., Foster, T. C., Muzyczka, N., & Kumar, A. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.09.006 · Cited by 32 · see citing works

Senolytic treatment alleviates doxorubicin‐induced chemobrain

Budamagunta, V., Kumar, A., Rani, A., Sindhu, S. M., Yang, Y., Zhou, D., & Foster, T. C. (2024) · Aging Cell · doi:10.1111/acel.14037 · Cited by 35 · see citing works

Human Serine Racemase: Key Residues/Active Site Motifs and Their Relation to Enzyme Function

Graham, D. L., Beio, M. L., Nelson, D. L., & Berkowitz, D. B. (2019) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2019.00008 · Cited by 31 · see citing works

Age-Induced Alterations in Hippocampal Function and Metabolism.

Shetty, P. K., Galeffi, F., & Turner, D. A. (2011) · PubMed Central · Cited by 31 · see citing works

Beta-amyloid short- and long-term synaptic entanglement

Lanni, C., Fagiani, F., Racchi, M., Preda, S., Pascale, A., Grilli, M., Allegri, N., & Govoni, S. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2018.11.018 · Cited by 29 · see citing works

Estradiol Acts Directly and Indirectly on Multiple Signaling Pathways to Phosphorylate cAMP-Response Element Binding Protein in GnRH Neurons

Cheong, R. Y., Kwakowsky, A., Barad, Z., Porteous, R. W., Herbison, A. E., & Ábrahám, I. M. (2012) · Endocrinology · doi:10.1210/en.2012-1232 · Cited by 30 · see citing works

Nonsteroidal anti-inflammatory drug, indomethacin improves spatial memory and NMDA receptor function in aged animals

Kumar, A., Rani, A., Scheinert, R. B., Ormerod, B. K., & Foster, T. C. (2018) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2018.06.026 · Cited by 30 · see citing works

Adulthood systemic inflammation accelerates the trajectory of age-related cognitive decline

Barter, J., Kumar, A., Bean, L. A., Ciesla, M. R., & Foster, T. C. (2021) · Aging · doi:10.18632/aging.203588 · Cited by 29 · see citing works

Antinociceptive effect of methanol extract of Celosia cristata Linn. in mice

Islam, S., Shajib, M. S., & Ahmed, T. (2016) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-016-1393-5 · Cited by 28 · see citing works

Changes in Serine Racemase-Dependent Modulation of NMDA Receptor: Impact on Physiological and Pathological Brain Aging

Billard, J. (2018) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2018.00106 · Cited by 28 · see citing works

Preclinical Magnetic Resonance Imaging and Spectroscopy Studies of Memory, Aging, and Cognitive Decline

Febo, M., & Foster, T. C. (2016) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2016.00158 · Cited by 27 · see citing works

Curcumin Rescues Aging-Related Loss of Hippocampal Synapse Input Specificity of Long Term Potentiation in Mice

Cheng, Y.-F., Guo, L., Xie, Y., Liu, Y., Zhang, J., Qingwen, W., & Li, J. (2012) · Neurochemical Research · doi:10.1007/s11064-012-0894-y · Cited by 27 · see citing works

Triclosan Impairs Hippocampal Synaptic Plasticity and Spatial Memory in Male Rats

Arias‐Cavieres, A., More, J., Vicente, J. M., Adasme, T., Hidalgo, J., Valdés, J. L., Humeres, A., Valdés-Undurraga, I., Sánchez, G., Hidalgo, C., et al. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00429 · Cited by 27 · see citing works

CoCl2-Induced Biochemical Hypoxia Down Regulates Activities and Expression of Super Oxide Dismutase and Catalase in Cerebral Cortex of Mice

Rani, A., & Prasad, S. (2014) · Neurochemical Research · doi:10.1007/s11064-014-1388-x · Cited by 25 · see citing works

Novel Biomarkers of Alzheimer's Disease: Based Upon N-methyl-D-aspartate Receptor Hypoactivation and Oxidative Stress

Chiang, T.-I., Yu, Y., Lin, C., & Lane, H. (2021) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2021.19.3.423 · Cited by 26 · see citing works

Calcium Signaling During Brain Aging and Its Influence on the Hippocampal Synaptic Plasticity

Kumar, A. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-12457-1_39 · Cited by 25 · see citing works

Age-Dependent Targeting of Protein Phosphatase 1 to Ca2+/Calmodulin-Dependent Protein Kinase II by Spinophilin in Mouse Striatum

Baucum, A. J., Strack, S., & Colbran, R. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031554 · Cited by 24 · see citing works

Proteome profiling in the hippocampus, medial prefrontal cortex, and striatum of aging rat

Hamezah, H. S., Durani, L. W., Yanagisawa, D., Ibrahim, N. F., Aizat, W. M., Bellier, J., Makpol, S., Ngah, W. Z. W., Damanhuri, H. A., & Tooyama, I. (2018) · Experimental Gerontology · doi:10.1016/j.exger.2018.07.002 · Cited by 24 · see citing works

Citrulline prevents age-related LTP decline in old rats

Ginguay, A., Regazzetti, A., Laprévôte, O., Moinard, C., Bandt, J. P. D., Cynober, L., Billard, J., Allinquant, B., & Dutar, P. (2019) · Scientific Reports · doi:10.1038/s41598-019-56598-2 · Cited by 23 · see citing works

Simultaneous intrathecal injection of muscimol and endomorphin‐1 alleviates neuropathic pain in rat model of spinal cord injury

Hosseini, M., Karami, Z., Yousefifard, M., Janzadeh, A., Zamani, E., & Nasirinezhad, F. (2020) · Brain and Behavior · doi:10.1002/brb3.1576 · Cited by 23 · see citing works

Modulation of GDF11 expression and synaptic plasticity by age and training

Domenico, E. D., D’Arcangelo, G., Faraoni, I., Palmieri, M., Tancredi, V., Graziani, G., Grimaldi, P., & Tentori, L. (2017) · Oncotarget · doi:10.18632/oncotarget.19854 · Cited by 22 · see citing works

Dopamine D4 receptor activation restores CA 1 LTP in hippocampal slices from aged mice

Guo, F., Zhao, J., Zhao, D., Wang, J., Wang, X., Feng, Z., Vreugdenhil, M., & Lu, C. (2017) · Aging Cell · doi:10.1111/acel.12666 · Cited by 22 · see citing works

Intermittent Hypoxia causes targeted disruption to NMDA receptor dependent synaptic plasticity in area CA1 of the hippocampus

Arias‐Cavieres, A., Fonteh, A., Castro-Rivera, C. I., & Garcia, A. J. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113808 · Cited by 22 · see citing works

The Role of Intracellular Ca2+ and Mitochondrial ROS in Small Aβ1-42 Oligomer-Induced Microglial Death

Jekabsone, A., Jankevičiūtė, S., Pampuščenko, K., Borutaitė, V., & Morkūnienė, R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241512315 · Cited by 21 · see citing works

Redox Sensitivity of Tyrosine Hydroxylase Activity and Expression in Dopaminergic Dysfunction

Giovanni, G. D., Pessia, M., & Maio, R. D. (2012) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/187152712800792938 · Cited by 21 · see citing works

Dose–Response Effect of Vibratory Stimulus on Synaptic and Muscle Plasticity in a Middle-Aged Murine Model

Cariati, I., Bonanni, R., Annino, G., Scimeca, M., Bonanno, E., D’Arcangelo, G., & Tancredi, V. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.678449 · Cited by 21 · see citing works

Subunit contribution to NMDA receptor hypofunction and redox sensitivity of hippocampal synaptic transmission during aging

Kumar, A., Thinschmidt, J. S., & Foster, T. C. (2019) · Aging · doi:10.18632/aging.102108 · Cited by 39 · see citing works

Linking Redox Regulation of NMDAR Synaptic Function to Cognitive Decline during Aging

Kumar, A., & Foster, T. C. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2176-13.2013 · Cited by 78 · see citing works

Age-related differences in NMDA responses in cultured rat hippocampal neurons

Cady, C., Evans, M. S., & Brewer, G. J. (2001) · Brain Research · doi:10.1016/s0006-8993(01)03063-3 · Cited by 35 · see citing works

Impaired Attention and Synaptic Senescence of the Prefrontal Cortex Involves Redox Regulation of NMDA Receptors

Guidi, M., Kumar, A., & Foster, T. C. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.3523-14.2015 · Cited by 63 · see citing works

NMDA receptor activation in the aged rat hippocampus

Potier, B., Poindessous‐Jazat, F., Dutar, P., & Billard, J. (2000) · Experimental Gerontology · doi:10.1016/s0531-5565(00)00122-4 · Cited by 70 · see citing works