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Calcium-binding protein (calbindin-D28K) and parvalbumin immunocytochemistry in the normal and epileptic human hippocampus.
Abstract
The calcium‐binding proteins calbindin‐D28K (CaBP) and parvalbumin (PV) were localized in the “normal” and “epileptic” human hippocampus to address the possible relationship between the expression of these constitutive cytosolic calcium‐binding proteins and the resistance or selective vulnerability of different hippocampal neuron populations in temporal lobe epilepsy. Compared to rodents and a baboon ( Papio papio ), the pattern of CaBP‐like immunoreactivity (LI) in the “normal” human hippocampus is unique. CaBP‐LI is present in the dentate granule cells, neurons of the “resistant zone” (area CA2), and presumed interneurons of all regions. Unlike rodent and baboon CA1 pyramidal cells, human CA1 pyramidal cells appear to be devoid of CaBP‐LI. Thus, the relatively resistant dentate granule cells and CA2 pyramidal cells are the only human hippocampal principal cells that contain CaBP‐LI normally. As in lower mammals, PV‐LI is present exclusively in interneurons of all human hippocampal subregions. CaBP‐ and PV‐LI were localized in hippocampi surgically removed in the treatment of intractable temporal lobe epilepsy to determine whether surviving hippocampal cells were those that express these calcium‐binding proteins. Hippocampi removed from patients with tumors or arteriovenous malformations that were associated with complex partial seizures arising from this region appeared relatively normal histologically. CaBP‐ and PV‐LI in this patient group appeared similar to that seen in autopsy controls. Conversely, “cryptogenic” epileptics, who exhibit hippocampal sclerosis as the only lesion associated with the epilepsy, exhibited a preferential survival of hippocampal cells that were CaBP‐ or PV‐immunoreactive. In the dentate hilus, which normally contains few CaBP‐LI neurons, most of the few surviving hilar neurons were CaBP‐immunoreactive. Their number and darkness of staining suggests that CaBP synthesis may be increased in cells that survive. Despite an obvious decrease of PV‐LI specifically in the damaged parts of the sclerotic hippocampi, PV‐immunoreactive interneurons were often among the few surviving cells. Nevertheless, large expanses of the surviving granule cell layer appeared to have lost the PV‐immunoreactive axosomatic fiber plexus. These results reveal a unique and striking correlation between the human hippocampal cells that normally express these calcium‐binding proteins and those that survive in the sclerotic epileptic hippocampus.
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“Analysis of post-mortem human brain tissues demonstrated reduced PV cell density and immunoreactivity at epileptic foci in the hippocampus and neocortex (Sloviter et al., 1991; Ferrer et al., 1994; Andrioli et al., 2007).”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Sloviter et al., 1991
In the citing paper
“Epilepsy [63,64] and prion disease [65] are among other disorders that are associated with alterations in PV-INs.”
From Parvalbumin interneuron vulnerability and brain disorders (2021) · cites this paper as [63]
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Cites
de Nó, R. L. (1934) · Cited by 1,974
EPILEPSY AND THE TEMPORAL LOBES
Margerison, J. H., & Corsellis, J. (1966) · Brain · doi:10.1093/brain/89.3.499 · Cited by 1,260
Lantos, P. L. (1985) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.48.5.496 · Cited by 1,156
Decreased Hippocampal Inhibition and a Selective Loss of Interneurons in Experimental Epilepsy
Sloviter, R. S. (1987) · Science · doi:10.1126/science.2879352 · Cited by 1,082
Self-citationSloviter, R. S. (1991) · Hippocampus · doi:10.1002/hipo.450010106 · Cited by 707
Self-citationSloviter, R. S. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902800203 · Cited by 686
Self-citationGranule cell dispersion in the dentate gyrus of humans with temporal lobe epilepsy
Houser, C. R. (1990) · Brain Research · doi:10.1016/0006-8993(90)91601-c · Cited by 604
Kosaka, T., Katsumaru, H., Hama, K., Wu, J.-Y., & Heizmann, C. W. (1987) · Brain Research · doi:10.1016/0006-8993(87)90575-0 · Cited by 536
Baimbridge, K. G., & Miller, J. J. (1982) · Brain Research · doi:10.1016/0006-8993(82)90804-6 · Cited by 487
The Neuropathology of Temporal Lobe Epilepsy
Bruton, C. J. (1988) · Medical Entomology and Zoology · Cited by 398
Research works printed but not linked: 1
- Sloviter R. S., 1989, Calcium‐binding protein (calbindin) and parvalbumin‐like immunoreactivity (LI) in the “normal” and “epileptic” hippocampus, Epilepsia, 30, 719
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Parent, J. M., Yu, T. W., Leibowitz, R. T., Geschwind, D. H., Sloviter, R. S., & Lowenstein, D. H. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-10-03727.1997 · Cited by 1,872
Self-citationA survey of human brain transcriptome diversity at the single cell level
Darmanis, S., Sloan, S. A., Zhang, Y., Enge, M., Caneda, C., Shuer, L. M., Hayden Gephart, M. G., Barres, B. A., & Quake, S. R. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1507125112 · Cited by 1,401
Calcium-binding proteins in the nervous system
Baimbridge, K. G., Celio, M. R., & ROGERS, J. H. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90081-i · Cited by 1,329
Calcium-binding proteins: selective markers of nerve cells
Andressen, C., Bl�mcke, I., & Celio, M. R. (1993) · Cell and Tissue Research · doi:10.1007/bf00318606 · Cited by 701
Scharfman, H. E., Goodman, J. H., & Sollas, A. L. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-16-06144.2000 · Cited by 605
Self-citationReview: Hippocampal sclerosis in epilepsy: a neuropathology review
Thom, M. (2014) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12150 · Cited by 565
Buckmaster, P. S., & Dudek, F. E. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970901)385:3 · Cited by 528
Gulyás, A. I., Hájos, N., & Freund, T. F. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-10-03397.1996 · Cited by 512
Sloviter, R. S. (1994) · Annals of Neurology · doi:10.1002/ana.410350604 · Cited by 454
Self-citationChanges in Ca2+-binding proteins in human neurodegenerative disorders
Heizmann, C. W., & Braun, K. A. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90067-i · Cited by 409
Witter, M. P., & Amaral, D. G. (2004) · Elsevier eBooks · doi:10.1016/b978-012547638-6/50022-5 · Cited by 361
Rediscovering area CA2: unique properties and functions
Dudek, S. M., Alexander, G. M., & Farris, S. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2015.22 · Cited by 333
Buckmaster, P. S., Zhang, G. F., & Yamawaki, R. M. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06650.2002 · Cited by 311
Selective Alterations in GABA A Receptor Subtypes in Human Temporal Lobe Epilepsy
Loup, F., Wieser, H. G., Yonekawa, Y., Aguzzi, A., & Fritschy, J. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-14-05401.2000 · Cited by 308
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Carstens, K. E., Phillips, M. L., Pozzo-Miller, L., Weinberg, R. J., & Dudek, S. M. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.0245-16.2016 · Cited by 271
Gorter, J. A., van Vliet, E. A., Aronica, E., & Lopes, F. H. D. S. (2001) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2001.01428.x · Cited by 289
Cendes, F., Andermann, F., GLOOR, P., Lopes‐Cendes, Í., Andermann, E., Melanson, D., Jones‐Gotman, M., Robitaille, Y., Evans, A. C., & Peters, T. M. (1993) · Annals of Neurology · doi:10.1002/ana.410340607 · Cited by 269
Insausti, R., & Amaral, D. G. (2004) · Elsevier eBooks · doi:10.1016/b978-012547626-3/50024-7 · Cited by 256
Quantitative Architecture Distinguishes Prefrontal Cortical Systems in the Rhesus Monkey
Dombrowski, S. M. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.10.975 · Cited by 240
Sloviter, R. S., Zappone, C. A., Harvey, B. D., Bumanglag, A. V., Bender, R. A., & Frotscher, M. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10630 · Cited by 244
Self-citationSperk, G., Marksteiner, J., Gruber, B., Bellmann, R., Mahata, M., & Ortler, M. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90207-i · Cited by 241
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Impaired and repaired inhibitory circuits in the epileptic human hippocampus
Maglóczky, Z., & Freund, T. F. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.04.002 · Cited by 222
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Arellano, J. I. (2003) · Brain · doi:10.1093/brain/awh004 · Cited by 210
Houser, C. R. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)63013-1 · Cited by 202
Pathophysiogenesis of Mesial Temporal Lobe Epilepsy: Is Prevention of Damage Antiepileptogenic?
Curia, G., Lucchi, C., Vinet, J., Gualtieri, F., Marinelli, C., Torsello, A., Costantino, L., & Biagini, G. (2014) · Current Medicinal Chemistry · doi:10.2174/0929867320666131119152201 · Cited by 216
Age-related deficits in the ability to encode contextual change: A place cell analysis
Oler, J. A., & Markus, E. J. (2000) · Hippocampus · doi:10.1002/1098-1063(2000)10:3 · Cited by 58
Peña‐Ortega, F., & Tapia, R. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00400-0 · Cited by 195
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Ruden, J. B., Dugan, L. L., & Konradi, C. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-020-0778-9 · Cited by 194
Molecular neuropathology of human mesial temporal lobe epilepsy
Blümcke, I., Beck, H., Lie, A. A., & Wiestler, O. D. (1999) · Epilepsy Research · doi:10.1016/s0920-1211(99)00052-2 · Cited by 192
The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders
Wen, T. H., Binder, D. K., Ethell, I. M., & Razak, K. A. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00270 · Cited by 170
Preservation of perisomatic inhibitory input of granule cells in the epileptic human dentate gyrus
Wittner, L., Maglóczky, Z., Borhegyi, Z., Halász, P., Tóth, S., Erőss, L., Szabó, Z., & Freund, T. F. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00446-8 · Cited by 185
Samland, H., Huitrón‐Reséndiz, S., Masliah, E., Criado, J. R., Henriksen, S. J., & Campbell, I. L. (2003) · Journal of Neuroscience Research · doi:10.1002/jnr.10635 · Cited by 178
Febrile seizures and mesial temporal sclerosis
Cendes, F. (2004) · Current Opinion in Neurology · doi:10.1097/00019052-200404000-00013 · Cited by 176
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Maglóczky, Z., Wittner, L., Borhegyi, Z., Halász, P., Vajda, J., Czirják, S., & Freund, T. F. (2000) · Neuroscience · doi:10.1016/s0306-4522(99)00474-1 · Cited by 174
Excitotoxicity and Selective Neuronal Loss in Epilepsy
Meldrum, B. S. (1993) · Brain Pathology · doi:10.1111/j.1750-3639.1993.tb00768.x · Cited by 174
GABAergic neurons and GABAA-receptors in temporal lobe epilepsy
Fritschy, J., Kiener, T., Bouilleret, V., & Loup, F. (1999) · Neurochemistry International · doi:10.1016/s0197-0186(99)00040-6 · Cited by 172
Calretinin-immunoreactive neocortical interneurons are unaffected in Alzheimer's disease
Hof, P. R., Nimchinsky, E. A., Celio, M. R., Bouras, C., & Morrison, J. H. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90504-e · Cited by 172
Serrano, G. E., Lelutiu, N. B., Rojas, A., Cochi, S., Shaw, R. N., Makinson, C. D., Wang, D., FitzGerald, G. A., & Dingledine, R. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3922-11.2011 · Cited by 169
Parvalbumin-, calbindin-, and calretinin-immunoreactive hippocampal interneuron density in autism
Lawrence, Y. A., Kemper, T. L., Bauman, M. L., & Blatt, G. J. (2009) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.2009.01234.x · Cited by 165
Lein, E. S., Callaway, E. M., Albright, T. D., & Gage, F. H. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20426 · Cited by 158
Populations of hippocampal inhibitory neurons express different levels of cytochrome c
Gulyás, A. I., Buzsáki, G., Freund, T. F., & Hirase, H. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04814.x · Cited by 142
Sloviter, R. S., & Lowenstein, D. H. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-08-03004.1992 · Cited by 155
Self-citationQuantitative analysis of parvalbumin-immunoreactive cells in the human epileptic hippocampus.
Andrioli, A., Alonso-Nanclares, L., Arellano, J. I., & DeFelipe, J. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.07.029 · Cited by 147
Hippocampal pyramidal cells: the reemergence of cortical lamination
Slomianka, L., Amrein, I., Knuesel, I., Sørensen, J. C. H., & Wolfer, D. P. (2011) · Brain Structure and Function · doi:10.1007/s00429-011-0322-0 · Cited by 153
Hippocampal neurogenesis and neural stem cells in temporal lobe epilepsy
Kuruba, R., Hattiangady, B., & Shetty, A. K. (2008) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2008.08.020 · Cited by 144
Wittner, L. (2004) · Brain · doi:10.1093/brain/awh339 · Cited by 140
Brain somatostatin: a candidate inhibitory role in seizures and epileptogenesis
Vezzani, A., & Hoyer, D. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00838.x · Cited by 140
Pauls, T. L., Cox, J. A., & Berchtold, M. W. (1996) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/0167-4781(95)00221-9 · Cited by 139
Connection matrix of the hippocampal formation: I. The dentate gyrus
Patton, P. E., & McNaughton, B. L. (1995) · Hippocampus · doi:10.1002/hipo.450050402 · Cited by 130
Zhao, L., Nagao, T., Desjardins, G. C., GLOOR, P., & Avoli, M. (1994) · Epilepsy Research · doi:10.1016/0920-1211(94)90054-x · Cited by 128
Seress, L., Gulyás, A. I., Ferrer, I., Tuñón, T., Soriano, E., & Freund, T. F. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903370204 · Cited by 130
Loss and reorganization of calretinin-containing interneurons in the epileptic human hippocampus
Tóth, K., Erőss, L., Vajda, J., Halász, P., Freund, T. F., & Maglóczky, Z. (2010) · Brain · doi:10.1093/brain/awq149 · Cited by 126
Parvalbumin-immunoreactive neurons in the hippocampal formation of Alzheimer’s diseased brain
Brady, D. R., & Mufson, E. J. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00068-7 · Cited by 125
Loss of Calbindin-D28K immunoreactivity from dentate granule cells in human temporal lobe epilepsy
Maglóczky, Z., Halász, P., Vajda, J., Czirják, S., & Freund, T. F. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00440-x · Cited by 119
Bhaskaran, M. D., & Smith, B. N. (2010) · Experimental Neurology · doi:10.1016/j.expneurol.2010.01.021 · Cited by 116
Cappaert, N. L. M., van Strien, N. M., & Witter, M. P. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-374245-2.00020-6 · Cited by 120
Distribution of parvalbumin‐immunoreactive cells and fibers in the human amygdaloid complex
Sorvari, H., Soininen, H., Paljärvi, L., Karkola, K. O., & Pitkänen, A. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903600202 · Cited by 114
Martin, B., Brenneman, R., Becker, K. G., Guček, M., Cole, R. N., & Maudsley, S. R. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002750 · Cited by 113
VANVLIET, E. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.01.016 · Cited by 112
Thind, K. K., Yamawaki, R. M., Phanwar, I., Zhang, G., Wen, X., & Buckmaster, P. S. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22235 · Cited by 111
Loss of GABAergic neurons in the subiculum and its functional implications in temporal lobe epilepsy
Knopp, A., Frahm, C., Fidzinski, P., Witte, O. W., & Behr, J. (2008) · Brain · doi:10.1093/brain/awn095 · Cited by 110
Hippocampal sclerosis revisited
Fisher, P. D., Sperber, E. F., & Moshé, S. L. (1998) · Brain and Development · doi:10.1016/s0387-7604(98)00069-2 · Cited by 110
Inhibitory Circuits in Human Dysplastic Tissue
Spreafico, R., Tassi, L., Colombo, N., Bramerio, M., GALLI, C., Garbelli, R., Ferrario, A., Russo, G. L., & Munari, C. (2000) · Epilepsia · doi:10.1111/j.1528-1157.2000.tb01576.x · Cited by 110
Topical Review: Functional Anatomy of Human Hippocampal Formation and Related Structures
Braak, H., Braak, E., Yilmazer‐Hanke, D., & Böhl, J. (1996) · Journal of Child Neurology · doi:10.1177/088307389601100402 · Cited by 110
Krebs, C., Fernandes, H. B., Sheldon, C. A., Raymond, L. A., & Baimbridge, K. G. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03364.2003 · Cited by 112
Adrenal Steroid Regulation of Neurotrophic Factor Expression in the Rat Hippocampus
Chao, H. M., Sakai, R. R., Li, Y., & McEwen, B. S. (1998) · Endocrinology · doi:10.1210/endo.139.7.6114 · Cited by 108
Scharfman, H. E., & Gray, W. (2007) · Epilepsia · doi:10.1111/j.1528-1167.2007.01065.x · Cited by 108
Selden, N. R. W., Geula, C., Hersh, L. B., & Mesulam, M. M. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90491-x · Cited by 107
Bouilleret, V., Schwaller, B., Schurmans, S., Celio, M. R., & Fritschy, J. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00017-8 · Cited by 105
Wittner, L., Erőss, L., Szabó, Z., Tóth, S., Czirják, S., Halász, P., Freund, T. F., & Maglóczky, Z. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00264-6 · Cited by 104
Differential vulnerability of interneurons in the epileptic hippocampus
Marx, M., Haas, C. A., & Häussler, U. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00167 · Cited by 104
Seress, L., Nitsch, R., & Léránth, C. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90441-h · Cited by 104
Parvalbumin and calbindin-D28k immunocytochemistry in human neocortical epileptic foci.
Ferrer, I., Oliver, B., Russi, A., Casas, R., & Rivera, R. (1994) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(94)90198-8 · Cited by 100
Leuba, G., Kraftsik, R., & Saini, K. (1998) · Experimental Neurology · doi:10.1006/exnr.1998.6838 · Cited by 101
Figueredo-Cardenas, G., Harris, C. L., Anderson, K. D., & Reiner, A. J. (1998) · Experimental Neurology · doi:10.1006/exnr.1997.6724 · Cited by 100
Functional Implications of Seizure-Induced Neurogenesis
Scharfman, H. E. (2004) · Advances in experimental medicine and biology · doi:10.1007/978-1-4757-6376-8_14 · Cited by 103
Wittner, L., Huberfeld, G., Clémenceau, S., Erőss, L., Dezamis, E., Entz, L., Ulbert, I., Baulac, M., Freund, T. F., Maglóczky, Z., et al. (2009) · Brain · doi:10.1093/brain/awp238 · Cited by 98
Neurochemical and morphological changes associated with human epilepsy
Glass, M., & Dragunow, M. (1995) · Brain Research Reviews · doi:10.1016/0165-0173(95)00005-n · Cited by 98
Experimental and clinical findings from physical exercise as complementary therapy for epilepsy
Arida, R. M., de Almeida, A.-C. G., Cavalheiro, É. A., & Scorza, F. A. (2012) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2012.07.025 · Cited by 98
Goodman, J. H., Wasterlain, C. G., Massarweh, W. F., Dean, E., Sollas, A. L., & Sloviter, R. S. (1993) · Brain Research · doi:10.1016/0006-8993(93)90999-4 · Cited by 98
Self-citationFarris, S., Ward, J. M., Carstens, K. E., Samadi, M., Wang, Y., & Dudek, S. M. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.08.093 · Cited by 94
Pierce, J. P., Melton, J. T., Punsoni, M., McCloskey, D. P., & Scharfman, H. E. (2005) · Experimental Neurology · doi:10.1016/j.expneurol.2005.08.007 · Cited by 97
Insausti, R., & Amaral, D. G. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374236-0.10024-0 · Cited by 101
Heterogeneity of layer II neurons in human entorhinal cortex
Beall, M. J., & Lewis, D. A. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903210206 · Cited by 97
Mesial temporal sclerosis: Pathogenesis and significance
Liu, Z., Mikati, M. A., & Holmes, G. L. (1995) · Pediatric Neurology · doi:10.1016/0887-8994(94)00122-i · Cited by 97
Lavenex, P., Lavenex, P. B., Bennett, J. L., & Amaral, D. G. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21906 · Cited by 89
Emery, D. L., Fulp, C. T., Saatman, K. E., Schütz, C., Neugebauer, E. A. M., & McIntosh, T. K. (2005) · Journal of Neurotrauma · doi:10.1089/neu.2005.22.978 · Cited by 89
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Williamson, A., Spencer, D. D., & Shepherd, G. M. (1993) · Brain Research · doi:10.1016/0006-8993(93)90819-9 · Cited by 85
Nitsch, R., & Léránth, C. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90442-i · Cited by 86
Clinical neuropathology practice guide 5-2013: markers of neuronal maturation
Sarnat, H. B. (2013) · Clinical Neuropathology · doi:10.5414/np300638 · Cited by 86
Pitkänen, A., & Amaral, D. G. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903310104 · Cited by 85
Tortosa, A., & Ferrer, I. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90452-l · Cited by 84
Ochiishi, T., Saitoh, Y., Yukawa, A., Saji, M., Ren, Y., Shirao, T., Miyamoto, H., Nakata, H., & Sekino, Y. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00179-7 · Cited by 83
Bhaskaran, M. D., & Smith, B. N. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010683 · Cited by 82
The dentate gyrus in Alzheimer's disease
Ohm, T. G. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)63039-8 · Cited by 78
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Tescarollo, F. C., Rombo, D. M., DeLiberto, L. K., Fedele, D., Alharfoush, E., Tomé, Â. R., Cunha, R. A., Sebastião, A. M., & Boison, D. (2020) · Journal of Caffeine and Adenosine Research · doi:10.1089/caff.2019.0022 · Cited by 80
Schwaller, B. (2012) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2011.11.008 · Cited by 75
Metadata
- Authors
- Sloviter, R. S., Sollas, A. L., Barbaro, N. M., & Laxer, K. D.
- Affiliations
- New York State Department of Health (US)
- University of California, San Francisco (US)
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1991-06-15
- Volume
- 308
- Issue
- 3
- Pages
- 381-396
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2072648531
- Semantic Scholar
- f5fd95ae0f455c333152f81068245b21495c2179
- Cited by
- 349
- References
- 18
- Citations by year
- 2026: 6 · 2025: 6 · 2024: 3 · 2023: 6 · 2022: 7 · 2021: 5 · 2020: 32 · 2019: 6 · 2018: 8 · 2017: 6 · 2016: 4 · 2015: 4 · 2014: 5 · 2013: 7 · 2012: 10
- FWCI
- 16.16
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (NS18201, R01NS018201)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Epilepsy research and treatment
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › S100 Proteins and Annexins
- Keywords
- calbindin-D28k, parvalbumin, calcium-binding proteins, human hippocampus, temporal lobe epilepsy, hippocampal sclerosis, dentate gyrus granule cells, interneurons, neuronal survival, immunoreactivity, complex partial seizures, arteriovenous malformation, dentate hilus
- MeSH terms
- Adult, Epilepsy, Female, Hippocampus, Humans, Male, Middle Aged, Parvalbumins, Calbindins, S100 Calcium Binding Protein G, Calbindin 1
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