Theta-gamma coupling increases during the learning of item-context associations

EEGLAB: an open source toolbox for analysis of single-trial EEG dynamics including independent component analysis

Delorme, A., & Makeig, S. (2004) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2003.10.009 · Cited by 24,371 · see citing works

Neuronal Oscillations in Cortical Networks

Buzsáki, G., & Draguhn, A. (2004) · Science · doi:10.1126/science.1099745 · Cited by 6,576 · see citing works

Rhythms of the Brain

Buzsáki, G. (2006) · doi:10.1093/acprof:oso/9780195301069.001.0001 · Cited by 4,873 · see citing works

High Gamma Power Is Phase-Locked to Theta Oscillations in Human Neocortex

Canolty, R. T., Edwards, E., Dalal, S. S., Soltani, M., Nagarajan, S. S., Kirsch, H. E., Berger, M. S., Barbaro, N. M., & Knight, R. T. (2006) · Science · doi:10.1126/science.1128115 · Cited by 2,650 · see citing works

The Medial Temporal Lobe and Recognition Memory

Eichenbaum, H., Yonelinas, A. P., & Ranganath, C. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094328 · Cited by 2,580 · see citing works

Low-frequency neuronal oscillations as instruments of sensory selection

Schroeder, C. E., & Lakatos, P. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2008.09.012 · Cited by 1,528 · see citing works

Gamma (40-100 Hz) oscillation in the hippocampus of the behaving rat

Bragin, A., Jando, G., Nadasdy, Z., Hetke, J., Wise, K., & Buzsaki, G. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00047.1995 · Cited by 1,527 · see citing works

Storage of 7 +/- 2 short-term memories in oscillatory subcycles

Lisman, J. E., & Idiart, M. A. P. (1995) · Science · doi:10.1126/science.7878473 · Cited by 1,471 · see citing works

An Oscillatory Hierarchy Controlling Neuronal Excitability and Stimulus Processing in the Auditory Cortex

Lakatos, P., Shah, A. S., Knuth, K. H., Ulbert, I., Karmos, G., & Schroeder, C. E. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00263.2005 · Cited by 1,241 · see citing works

The Hippocampus, Memory, and Place Cells

Eichenbaum, H., Dudchenko, P., Wood, E., Shapiro, M., & Tanila, H. (1999) · Neuron · doi:10.1016/s0896-6273(00)80773-4 · Cited by 1,064 · see citing works

Entrainment of Neocortical Neurons and Gamma Oscillations by the Hippocampal Theta Rhythm

Sirota, A., Montgomery, S., Fujisawa, S., Isomura, Y., Zugaro, M., & Buzsáki, G. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.014 · Cited by 1,015 · see citing works

Cross-frequency coupling between neuronal oscillations

Jensen, O., & Colgin, L. L. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.05.003 · Cited by 991 · see citing works

Dynamic cross-frequency couplings of local field potential oscillations in rat striatum and hippocampus during performance of a T-maze task

Tort, A. B. L., Kramer, M., Thorn, C. A., Gibson, D. J., Kubota, Y., Graybiel, A. M., & Kopell, N. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810524105 · Cited by 842 · see citing works

Relating Hippocampal Circuitry to Function

Lisman, J. E. (1999) · Neuron · doi:10.1016/s0896-6273(00)81085-5 · Cited by 607 · see citing works

Hippocampal network patterns of activity in the mouse

Buzsáki, G., Buhl, D. L., Harris, K. D., Csicsvari, J., Czéh, B., & Morozov, A. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00669-3 · Cited by 486 · see citing works

The theta/gamma discrete phase code occuring during the hippocampal phase precession may be a more general brain coding scheme

Lisman, J. (2005) · Hippocampus · doi:10.1002/hipo.20121 · Cited by 435 · see citing works

A Neural Coding Scheme Formed by the Combined Function of Gamma and Theta Oscillations

Lisman, J. E., & Buzsáki, G. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn060 · Cited by 433 · see citing works

Hippocampal theta rhythm and its coupling with gamma oscillations require fast inhibition onto parvalbumin-positive interneurons

Wulff, P., Ponomarenko, A. A., Bartos, M., Korotkova, T. M., Fuchs, E. C., Bähner, F., Both, M., Tort, A. B. L., Kopell, N. J., Wisden, W., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0813176106 · Cited by 400 · see citing works

Robust Conjunctive Item–Place Coding by Hippocampal Neurons Parallels Learning What Happens Where

Komorowski, R. W., Manns, J. R., & Eichenbaum, H. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.1378-09.2009 · Cited by 372 · see citing works

Learning-related coordination of striatal and hippocampal theta rhythms during acquisition of a procedural maze task

DeCoteau, W. E., Thorn, C. A., Gibson, D. J., Courtemanche, R., Mitra, P. P., Kubota, Y., & Graybiel, A. M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700818104 · Cited by 239 · see citing works

Hippocampal ensemble activity during spatial delayed-nonmatch-to-sample performance in rats

Deadwyler, S., Bunn, T., & Hampson, R. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-01-00354.1996 · Cited by 234 · see citing works

Oscillatory Activity and Phase–Amplitude Coupling in the Human Medial Frontal Cortex during Decision Making

Cohen, M. X., Elger, C. E., & Fell, J. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.21020 · Cited by 218 · see citing works

The Statistical Analysis of Discrete Data

Santner, T. J., & Duffy, D. E. (1989) · Springer texts in statistics · doi:10.1007/978-1-4612-1017-7 · Cited by 199 · see citing works

Good Vibrations: Cross-frequency Coupling in the Human Nucleus Accumbens during Reward Processing

Cohen, M. X., Axmacher, N., Lenartz, D., Elger, C. E., Sturm, V., & Schlaepfer, T. E. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21062 · Cited by 197 · see citing works

The Statistical Analysis of Discrete Data.

Iyer, R. K., Santner, T. J., & Duffy, D. E. (1991) · Journal of the Royal Statistical Society Series D (The Statistician) · doi:10.2307/2348290 · Cited by 196 · see citing works

On the formation of gamma-coherent cell assemblies by oriens lacunosum-moleculare interneurons in the hippocampus

Tort, A. B. L., Rotstein, H. G., Dugladze, T., Gloveli, T., & Kopell, N. J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705708104 · Cited by 192 · see citing works

Behavior-Dependent Coordination of Multiple Theta Dipoles in the Hippocampus

Montgomery, S. M., Betancur, M. I., & Buzsáki, G. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4339-08.2009 · Cited by 190 · see citing works

Physiologically realistic formation of autoassociative memory in networks with theta/gamma oscillations: role of fast NMDA channels.Preprint

Jensen, O. B., Idiart, M. A., & Lisman, J. E. (1996) · Learning & Memory · doi:10.1101/lm.3.2-3.243 · Cited by 188 · see citing works

Novel lists of 7 +/- 2 known items can be reliably stored in an oscillatory short-term memory network: interaction with long-term memory.Preprint

Jensen, O. B., & Lisman, J. E. (1996) · Learning & Memory · doi:10.1101/lm.3.2-3.257 · Cited by 183 · see citing works

Gamma Oscillatory Firing Reveals Distinct Populations of Pyramidal Cells in the CA1 Region of the Hippocampus

Senior, T. J., Huxter, J. R., Allen, K. L., O'Neill, J., & Csicsvari, J. L. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4669-07.2008 · Cited by 180 · see citing works

Theta/gamma networks with slow NMDA channels learn sequences and encode episodic memory: role of NMDA channels in recall.Preprint

Jensen, O. B., & Lisman, J. E. (1996) · Learning & Memory · doi:10.1101/lm.3.2-3.264 · Cited by 152 · see citing works

Recall of memory sequences by interaction of the dentate and CA3: A revised model of the phase precession

Lisman, J. E., Talamini, L. M., & Raffone, A. (2005) · Neural Networks · doi:10.1016/j.neunet.2005.08.008 · Cited by 151 · see citing works

The Role of CA3 Hippocampal NMDA Receptors in Paired Associate Learning

Rajji, T. K., Chapman, D. E., Eichenbaum, H., & Greene, R. W. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4194-05.2006 · Cited by 105 · see citing works

Cross-frequency coupling of brain oscillations indicates the success in visual motion discrimination

Händel, B., & Haarmeier, T. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.12.013 · Cited by 94 · see citing works

Muscarinic blockade weakens interaction of gamma with theta rhythms in mouse hippocampus

Hentschke, H., Perkins, M. G., Pearce, R. A., & Banks, M. I. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05779.x · Cited by 66 · see citing works

Memory, navigation and theta rhythm in the hippocampal-entorhinal system

Buzsáki, G., & Moser, E. I. (2013) · Nature Neuroscience · doi:10.1038/nn.3304 · Cited by 1,847 · see citing works

Comorbidity: a network perspective

Cramer, A. O. J., Waldorp, L. J., van der Maas, H. L. J., & Borsboom, D. (2010) · Behavioral and Brain Sciences · doi:10.1017/s0140525x09991567 · Cited by 1,575 · see citing works

The role of phase synchronization in memory processes

Fell, J., & Axmacher, N. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2979 · Cited by 1,620 · see citing works

The theta-gamma neural code

Lisman, J. E., & Jensen, O. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.007 · Cited by 1,609 · see citing works

Network abnormalities and interneuron dysfunction in Alzheimer disease

Palop, J. J., & Mucke, L. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.141 · Cited by 1,022 · see citing works

Cross-Frequency Phase–Phase Coupling between Theta and Gamma Oscillations in the Hippocampus

Belluscio, M. A., Mizuseki, K., Schmidt, R., Kempter, R., & Buzsáki, G. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4122-11.2012 · Cited by 784 · see citing works

Therapeutic deep brain stimulation reduces cortical phase-amplitude coupling in Parkinson's disease

de Hemptinne, C., Swann, N. C., Ostrem, J. L., Ryapolova-Webb, E. S., San Luciano, M., Galifianakis, N. B., & Starr, P. A. (2015) · Nature Neuroscience · doi:10.1038/nn.3997 · Cited by 623 · see citing works

Rhythms of the hippocampal network

Colgin, L. L. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.21 · Cited by 654 · see citing works

Schema-dependent gene activation and memory encoding in neocortex

Tse, D., Takeuchi, T., Kakeyama, M., Kajii, Y., Okuno, H., Tohyama, C., Bito, H., & Morris, R. G. M. (2011) · Science · doi:10.1126/science.1205274 · Cited by 618 · see citing works

Nasal Respiration Entrains Human Limbic Oscillations and Modulates Cognitive Function

Zelano, C., Jiang, H., Zhou, G., Arora, N., Schuele, S., Rosenow, J., & Gottfried, J. A. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.2586-16.2016 · Cited by 599 · see citing works

Dynamic Network Communication as a Unifying Neural Basis for Cognition, Development, Aging, and Disease

Voytek, B., & Knight, R. T. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.04.016 · Cited by 556 · see citing works

Brain rhythms and neural syntax: implications for efficient coding of cognitive content and neuropsychiatric disease.

Buzsáki, G., & Watson, B. O. (2012) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2012.14.4/gbuzsaki · Cited by 579 · see citing works

Theta Phase Segregation of Input-Specific Gamma Patterns in Entorhinal-Hippocampal Networks

Schomburg, E. W., Fernández-Ruiz, A., Mizuseki, K., Berényi, A., Anastassiou, C. A., Koch, C., & Buzsáki, G. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.051 · Cited by 465 · see citing works

Direct ventral hippocampal-prefrontal input is required for anxiety-related neural activity and behavior

Padilla-Coreano, N., Bolkan, S. S., Pierce, G. M., Blackman, D. R., Hardin, W. D., Garcia-Garcia, A. L., Spellman, T. J., & Gordon, J. A. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.011 · Cited by 463 · see citing works

Temporal coding organized by coupled alpha and gamma oscillations prioritize visual processing

Jensen, O., Gips, B., Bergmann, T. O., & Bonnefond, M. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.04.001 · Cited by 389 · see citing works

Episodic sequence memory is supported by a theta-gamma phase code

Heusser, A. C., Poeppel, D., Ezzyat, Y., & Davachi, L. (2016) · Nature Neuroscience · doi:10.1038/nn.4374 · Cited by 290 · see citing works

Past, present and future of therapeutic strategies against amyloid-β peptides in Alzheimer’s disease: a systematic review

Jeremic, D., Jiménez-Díaz, L., & Navarro-López, J. D. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101496 · Cited by 306 · see citing works

Fear and safety engage competing patterns of theta-gamma coupling in the basolateral amygdala

Stujenske, J. M., Likhtik, E., Topiwala, M. A., & Gordon, J. A. (2014) · Neuron · doi:10.1016/j.neuron.2014.07.026 · Cited by 303 · see citing works

Site-specific phosphorylation of tau inhibits amyloid-β toxicity in Alzheimer’s mice

Ittner, A., Chua, S. W., Bertz, J., Volkerling, A., van der Hoven, J., Gladbach, A., Przybyla, M., Bi, M., van Hummel, A., Stevens, C. H., et al. (2016) · Science · doi:10.1126/science.aah6205 · Cited by 263 · see citing works

Breathing as a fundamental rhythm of brain function.

Heck, D. H., McAfee, S. S., Liu, Y., Babajani-Feremi, A., Rezaie, R., Freeman, W. J., Wheless, J. W., Papanicolaou, A. C., Ruszinkó, M., Sokolov, Y., et al. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00115 · Cited by 272 · see citing works

Successful memory encoding is associated with increased cross-frequency coupling between frontal theta and posterior gamma oscillations in human scalp-recorded EEG

Friese, U., Köster, M., Hassler, U., Martens, U., Trujillo-Barreto, N., & Gruber, T. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.11.002 · Cited by 233 · see citing works

Bidirectional changes to hippocampal theta-gamma comodulation predict memory for recent spatial episodes

Shirvalkar, P. R., Rapp, P. R., & Shapiro, M. L. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911184107 · Cited by 235 · see citing works

Interneuronal mechanisms of hippocampal theta oscillations in a full-scale model of the rodent CA1 circuit

Bezaire, M. J., Raikov, I., Burk, K., Vyas, D., & Soltesz, I. (2016) · eLife · doi:10.7554/elife.18566 · Cited by 198 · see citing works

Activity-dependent switch of GABAergic inhibition into glutamatergic excitation in astrocyte-neuron networks

Perea, G., Gómez, R., Mederos, S., Covelo, A., Ballesteros, J. J., Schlosser, L., Hernández-Vivanco, A., Martín-Fernández, M., Quintana, R., Rayan, A., et al. (2016) · eLife · doi:10.7554/elife.20362 · Cited by 194 · see citing works

Slow Oscillations in the Mouse Hippocampus Entrained by Nasal Respiration

Yanovsky, Y., Ciatipis, M., Draguhn, A., Tort, A. B. L., & Brankačk, J. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.5287-13.2014 · Cited by 175 · see citing works

Bidirectional prefrontal-hippocampal interactions support context-guided memory

Place, R., Farovik, A., Brockmann, M., & Eichenbaum, H. (2016) · Nature Neuroscience · doi:10.1038/nn.4327 · Cited by 200 · see citing works

The Functional Role of Dreaming in Emotional Processes

Scarpelli, S., Bartolacci, C., D'Atri, A., Gorgoni, M., & De Gennaro, L. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.00459 · Cited by 190 · see citing works

No consolidation without representation: Correspondence between neural and psychological representations in recent and remote memory

Gilboa, A., & Moscovitch, M. (2021) · Neuron · doi:10.1016/j.neuron.2021.04.025 · Cited by 174 · see citing works

Selective entrainment of gamma subbands by different slow network oscillations

Zhong, W., Ciatipis, M., Wolfenstetter, T., Jessberger, J., Müller, C., Ponsel, S., Yanovsky, Y., Brankačk, J., Tort, A. B. L., & Draguhn, A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1617249114 · Cited by 155 · see citing works

The brain's resting-state activity is shaped by synchronized cross-frequency coupling of neural oscillations

Florin, E., & Baillet, S. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.01.054 · Cited by 184 · see citing works

Mapping Multiplex Hubs in Human Functional Brain Networks

De Domenico, M., Sasai, S., & Arenas, A. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00326 · Cited by 144 · see citing works

Sleep-Dependent Facilitation of Episodic Memory Details

van der Helm, E., Gujar, N., Nishida, M., & Walker, M. P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027421 · Cited by 138 · see citing works

Early Cognitive Experience Prevents Adult Deficits in a Neurodevelopmental Schizophrenia Model

Lee, H., Dvorak, D., Kao, H.-Y., Duffy, Á. M., Scharfman, H. E., & Fenton, A. A. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.016 · Cited by 122 · see citing works

Expected reward modulates encoding-related theta activity before an event

Gruber, M. J., Watrous, A. J., Ekstrom, A. D., Ranganath, C., & Otten, L. J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.07.064 · Cited by 108 · see citing works

Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity

Murthy, S., Kane, G. A., Katchur, N. J., Lara Mejia, P. S., Obiofuma, G., Buschman, T. J., McEwen, B. S., & Gould, E. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.02.021 · Cited by 118 · see citing works

Shifting the spotlight of attention: evidence for discrete computations in cognition

Buschman, T. J., & Miller, E. K. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00194 · Cited by 87 · see citing works

Binding by random bursts: a computational model of cognitive control

Verguts, T. (2017) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01117 · Cited by 76 · see citing works

Functional connectivity between the amygdala and prefrontal cortex underlies processing of emotion ambiguity

Sun, S., Yu, H., Yu, R., & Wang, S. (2023) · Translational Psychiatry · doi:10.1038/s41398-023-02625-w · Cited by 69 · see citing works

Roles of multiscale brain activity fluctuations in shaping the variability and dynamics of psychophysical performance

Palva, J. M., & Palva, S. (2011) · Progress in Brain Research · doi:10.1016/b978-0-444-53839-0.00022-3 · Cited by 63 · see citing works

Preservation and Changes in Oscillatory Dynamics across the Cortical Hierarchy

Lundqvist, M., Bastos, A. M., & Miller, E. K. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01600 · Cited by 58 · see citing works

Distinct features of fast oscillations in phasic and tonic rapid eye movement sleep

BRANKAČK, J., SCHEFFZÜK, C., KUKUSHKA, V. I., VYSSOTSKI, A. L., TORT, A. B. L., & DRAGUHN, A. (2012) · Journal of Sleep Research · doi:10.1111/j.1365-2869.2012.01037.x · Cited by 53 · see citing works

Altered Hippocampal-Prefrontal Neural Dynamics in Mouse Models of Down Syndrome

Chang, P., Bush, D., Schorge, S., Good, M., Canonica, T., Shing, N., Noy, S., Wiseman, F. K., Burgess, N., Tybulewicz, V. L. J., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2019.12.065 · Cited by 47 · see citing works

A bird-brain view of episodic memory

Rattenborg, N. C., & Martinez-Gonzalez, D. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.03.030 · Cited by 45 · see citing works

Dream to Predict? REM Dreaming as Prospective Coding

Llewellyn, S. (2016) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01961 · Cited by 45 · see citing works

Early psychosocial neglect adversely impacts developmental trajectories of brain oscillations and their interactions

Stamoulis, C., Vanderwert, R. E., Zeanah, C. H., Fox, N. A., & Nelson, C. A. (2015) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00877 · Cited by 39 · see citing works

Differential Impact of Acute and Chronic Stress on CA1 Spatial Coding and Gamma Oscillations

Tomar, A., Polygalov, D., & McHugh, T. J. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.710725 · Cited by 21 · see citing works

Spatial learning impairments and discoordination of entorhinal‐hippocampal circuit coding following prolonged febrile seizures

Kloc, M. L., Chen, Y., Daglian, J. M., Holmes, G. L., Baram, T. Z., & Barry, J. M. (2023) · Hippocampus · doi:10.1002/hipo.23541 · Cited by 21 · see citing works

Neural mechanisms of mental schema: a triplet of delta, low beta/spindle and ripple oscillations

Ohki, T., & Takei, Y. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13844 · Cited by 20 · see citing works

Neural Mechanisms of Memory

Amer, T., & Davachi, L. (2022) · doi:10.31234/osf.io/32egy · Cited by 3 · see citing works

RESPOSTAS FISIOLÓGICAS PARA DETECTAR O OVERTRAINING - DOI: 10.4025/reveducfis.v19i2.5558

de Araújo, G. G., Gobatto, C. A., Hirata, R. D. C., et al. (2008) · journal of physical education

RESPOSTAS FISIOLÓGICAS PARA DETECTAR O OVERTRAINING

Gobatto, C. A., de Araújo, G. G., Hirata, R. D. C., et al. (2008) · journal of physical education · doi:10.4025/reveducfis.v19i2.5558 · Cited by 4 · see citing works

Impact of Overtraining and Glutamine Supplementation on TNF-α,its mRNA and NF-κB in Hippocampus and Frontal Cortex of Rat Brain

Chen, P. (2010) · Tiyu kexue

Effects of subtotal hippocampal lesions upon hippocampal electrical activity

Helmes, E., & Vanderwolf, C. H. (1976) · Physiology & Behavior · doi:10.1016/0031-9384(76)90143-8 · Cited by 3 · see citing works

Comparison of the effect of β-amyloid peptide 25-35 on hippocampal and septal neurons in vitroi

Zhao, Y. (2004)