Folia Biologica
Journal of Cellular and Molecular Biology, Charles University 

Crossref Cited-by Linking

• Keskin Aysenur, Acar Gozde, Aladag Tugce, Onal Ummugulsum, Baltaci Saltuk Bugra, Mogulkoc Rasim, Baltaci Abdulkerim Kasim: Effect of 2 Weeks Naringin Application on Neurological Function and Neurogenesis After Brain Ischemia\u2013Reperfusion in Ovariectomized Rats. Mol Neurobiol 2025. <https://doi.org/10.1007/s12035-025-05050-w>
• Al-Redouan Azzat, Busch Aaron, Salaj Martin, Kubova Hana, Druga Rastislav: Dorsal Striatum Is Compromised by Status Epilepticus Induced in Immature Developing Animal Experimental Model of Mesial Temporal Lobe Epilepsy. IJMS 2025, 26, 3349. <https://doi.org/10.3390/ijms26073349>
• Parka Aleksandra, Degel Caroline, Dreyer Jakob, Richter Ulrike, Hall Benjamin, Bastlund Jesper F., Laursen Bettina, Nedergaard Maiken, Sotty Florence, Botta Paolo: Early impairments of visually-driven neuronal ensemble dynamics in the rTg4510 tauopathy mouse model. Neurobiology of Disease 2023, 178, 106012. <https://doi.org/10.1016/j.nbd.2023.106012>
• Kim Kang-Ho, Son Jae-Rim, Kwon Oh-Ju, Jeon Chang-Jin: Immunocytochemical Localization of Cholinergic Amacrine Cells in the Mongolian Gerbil Retina: Colocalization with Calcium-Binding Protein Calretinin. jkoos 2023, 28, 27. <https://doi.org/10.14479/jkoos.2023.28.1.27>
• Son Jae-Rim, Lee Myung-Jun, Jeon Chang-Jin: Changes in Starburst Amacrine Cells in Mice with Diabetic Retinopathy. Front. Biosci. (Landmark Ed) 2023, 28. <https://doi.org/10.31083/j.fbl2805092>
• Shin Jean, French Leon, Xu Ting, Leonard Gabriel, Perron Michel, Pike G Bruce, Richer Louis, Veillette Suzanne, Pausova Zdenka, Paus Tomá\u0161: Cell-Specific Gene-Expression Profiles and Cortical Thickness in the Human Brain. Cerebral Cortex 2018, 28, 3267. <https://doi.org/10.1093/cercor/bhx197>
• Matukhno A. E., Lysenko L. V., Andreeva Ya. V., Sukhov A. G.: Effects of a GABAC Receptor Blocker on the Formation of Evoked Potentials in Neuronal Columns in the Rat Somatosensory Cortex. Neurosci Behav Physi 2017, 47, 235. <https://doi.org/10.1007/s11055-016-0389-4>
• Chen Y-H, Lan Y-J, Zhang S-R, Li W-P, Luo Z-Y, Lin S, Zhuang J-P, Li X-W, Li S-J, Yang J-M, Gao T-M: ErbB4 signaling in the prelimbic cortex regulates fear expression. Transl Psychiatry 2017, 7, e1168. <https://doi.org/10.1038/tp.2017.139>
• Nakagawa Julia M., Donkels Catharina, Fauser Susanne, Schulze\u2010Bonhage Andreas, Prinz Marco, Zentner Josef, Haas Carola A.: Characterization of focal cortical dysplasia with balloon cells by layer\u2010specific markers: Evidence for differential vulnerability of interneurons. Epilepsia 2017, 58, 635. <https://doi.org/10.1111/epi.13690>
• Jacobs Bob, Lee Laura, Schall Matthew, Raghanti Mary Ann, Lewandowski Albert H., Kottwitz Jack J., Roberts John F., Hof Patrick R., Sherwood Chet C.: Neocortical neuronal morphology in the newborn giraffe (Giraffa camelopardalis tippelskirchi) and African elephant (Loxodonta africana). J of Comparative Neurology 2016, 524, 257. <https://doi.org/10.1002/cne.23841>
• Sukhov A. G., Kirichenko E. Yu., Belichenko L. A.: Structural Characteristics and Spatial Organization of Parvalbumin-Containing Neurons in Somatosensory Zone SI of the Cerebral Cortex in Rats. Neurosci Behav Physi 2016, 46, 863. <https://doi.org/10.1007/s11055-016-0323-9>
• Xu Jiansong, Potenza Marc N., Calhoun Vince D., Zhang Rubin, Yip Sarah W., Wall John T., Pearlson Godfrey D., Worhunsky Patrick D., Garrison Kathleen A., Moran Joseph M.: Large-scale functional network overlap is a general property of brain functional organization: Reconciling inconsistent fMRI findings from general-linear-model-based analyses. Neuroscience & Biobehavioral Reviews 2016, 71, 83. <https://doi.org/10.1016/j.neubiorev.2016.08.035>
• Hervig Mona E., Thomsen Morten S., Kalló Imre, Mikkelsen Jens D.: Acute phencyclidine administration induces c-Fos-immunoreactivity in interneurons in cortical and subcortical regions. Neuroscience 2016, 334, 13. <https://doi.org/10.1016/j.neuroscience.2016.07.028>
• Larsson Martin, Lietzau Grazyna, Nathanson David, Östenson Claes-Göran, Mallard Carina, Johansson Maria E., Nyström Thomas, Patrone Cesare, Darsalia Vladimer: Diabetes negatively affects cortical and striatal GABAergic neurons: an effect that is partially counteracted by exendin-4. Bioscience Reports 2016, 36. <https://doi.org/10.1042/BSR20160437>
• Medici Valentina, Rossini Laura, Deleo Francesco, Tringali Giovanni, Tassi Laura, Cardinale Francesco, Bramerio Manuela, de Curtis Marco, Garbelli Rita, Spreafico Roberto: Different parvalbumin and GABA expression in human epileptogenic focal cortical dysplasia. Epilepsia 2016, 57, 1109. <https://doi.org/10.1111/epi.13405>
• Harris Erin P., Abel Jean M., Tejada Lucia D., Rissman Emilie F.: Calbindin Knockout Alters Sex-Specific Regulation of Behavior and Gene Expression in Amygdala and Prefrontal Cortex. Endocrinology 2016, 157, 1967. <https://doi.org/10.1210/en.2016-1055>
• Kress Sigrid, Biechl Daniela, Wullimann Mario F.: Combinatorial analysis of calcium-binding proteins in larval and adult zebrafish primary olfactory system identifies differential olfactory bulb glomerular projection fields. Brain Struct Funct 2015, 220, 1951. <https://doi.org/10.1007/s00429-014-0765-1>
• Butti Camilla, Janeway Caroline M., Townshend Courtney, Wicinski Bridget A., Reidenberg Joy S., Ridgway Sam H., Sherwood Chet C., Hof Patrick R., Jacobs Bob: The neocortex of cetartiodactyls: I. A comparative Golgi analysis of neuronal morphology in the bottlenose dolphin (Tursiops truncatus), the minke whale (Balaenoptera acutorostrata), and the humpback whale (Megaptera novaeangliae). Brain Struct Funct 2015, 220, 3339. <https://doi.org/10.1007/s00429-014-0860-3>
• Wu Connie, Sun Dandan: GABA receptors in brain development, function, and injury. Metab Brain Dis 2015, 30, 367. <https://doi.org/10.1007/s11011-014-9560-1>
• Osterop Samira F., Virtanen Mari A., Loepke Johanna R., Joseph Bernadin, Loepke Andreas W., Vutskits Laszlo: Developmental stage\u2010dependent impact of midazolam on calbindin, calretinin and parvalbumin expression in the immature rat medial prefrontal cortex during the brain growth spurt. Intl J of Devlp Neuroscience 2015, 45, 19. <https://doi.org/10.1016/j.ijdevneu.2015.04.002>
• Pirone Andrea, Magliaro Chiara, Giannessi Elisabetta, Ahluwalia Arti: Parvalbumin expression in the claustrum of the adult dog. An immunohistochemical and topographical study with comparative notes on the structure of the nucleus. Journal of Chemical Neuroanatomy 2015, 64-65, 33. <https://doi.org/10.1016/j.jchemneu.2015.02.004>
• Xu Jiansong, Calhoun Vince D., Potenza Marc N.: The absence of task-related increases in BOLD signal does not equate to absence of task-related brain activation. Journal of Neuroscience Methods 2015, 240, 125. <https://doi.org/10.1016/j.jneumeth.2014.11.002>
• Xu Jiansong: Implications of cortical balanced excitation and inhibition, functional heterogeneity, and sparseness of neuronal activity in fMRI. Neuroscience & Biobehavioral Reviews 2015, 57, 264. <https://doi.org/10.1016/j.neubiorev.2015.08.018>
• Pereira P.A., Vilela M., Sousa S., Neves J., Paula-barbosa M.M., Madeira M.D.: Lesions of the laterodorsal tegmental nucleus alter the cholinergic innervation and neuropeptide Y expression in the medial prefrontal cortex and nucleus accumbens. Neuroscience 2015, 284, 707. <https://doi.org/10.1016/j.neuroscience.2014.10.054>
• Pistillo Francesco, Clementi Francesco, Zoli Michele, Gotti Cecilia: Nicotinic, glutamatergic and dopaminergic synaptic transmission and plasticity in the mesocorticolimbic system: Focus on nicotine effects. Progress in Neurobiology 2015, 124, 1. <https://doi.org/10.1016/j.pneurobio.2014.10.002>
• Wimmer Verena C., Li Melody Y.-S., Berkovic Samuel F., Petrou Steven: Cortical microarchitecture changes in genetic epilepsy. Neurology 2015, 84, 1308. <https://doi.org/10.1212/WNL.0000000000001415>
• Xu Jiansong, Calhoun Vince D., Worhunsky Patrick D., Xiang Hui, Li Jian, Wall John T., Pearlson Godfrey D., Potenza Marc N., Chialvo Dante R.: Functional Network Overlap as Revealed by fMRI Using sICA and Its Potential Relationships with Functional Heterogeneity, Balanced Excitation and Inhibition, and Sparseness of Neuron Activity. PLoS ONE 2015, 10, e0117029. <https://doi.org/10.1371/journal.pone.0117029>
• Freire Marco Aurelio M., Faber Jean, Lemos Nelson Alessandretti M., Santos Jose Ronaldo, Cavalcanti Pedro França, Lima Ramon Hypolito, Morya Edgard, Sugihara Izumi: Distribution and Morphology of Calcium-Binding Proteins Immunoreactive Neurons following Chronic Tungsten Multielectrode Implants. PLoS ONE 2015, 10, e0130354. <https://doi.org/10.1371/journal.pone.0130354>
• Prauss Katharina, Varatharajan Ramya, Joseph Kevin, Moser Andreas: Transmitter self-regulation by extracellular glutamate in fresh human cortical slices. J Neural Transm 2014, 121, 1321. <https://doi.org/10.1007/s00702-014-1215-1>
• Wachter B., Caradonna S., Gittinger K., Schläger A., Küppers E.: Intraventricular injection of 6-hydroxydopamine results in an increased number of tyrosine hydroxylase immune-positive cells in the rat cortex. Neuroscience 2014, 280, 99. <https://doi.org/10.1016/j.neuroscience.2014.09.010>
• Endo Toshiaki, Yanagawa Yuchio, Komatsu Yukio: Substance P Activates Ca2+-Permeable Nonselective Cation Channels through a Phosphatidylcholine-Specific Phospholipase C Signaling Pathway in nNOS-Expressing GABAergic Neurons in Visual Cortex. Cereb. Cortex 2014, bhu233. <https://doi.org/10.1093/cercor/bhu233>
• \u041c\u044b\u0446\u0438\u043a, Mytsik A., \u0410\u043a\u0443\u043b\u0438\u043d\u0438\u043d, Akulinin V., \u0421\u0435\u0440\u0433\u0435\u0435\u0432, Sergeev A., \u0421\u0442\u0435\u043f\u0430\u043d\u043e\u0432, Stepanov S.: Modern problems of morphological studying of the human cortex cytoarchitecture in norm and during ischemia. Journal of New Medical Technologies. eJournal 2014, 8, 1. <https://doi.org/10.12737/4789>
• Rudolph Judith, Gerstmann Katrin, Zimmer Geraldine, Steinecke André, Döding Annika, Bolz Jürgen: A dual role of EphB1/ephrin-B3 reverse signaling on migrating striatal and cortical neurons originating in the preoptic area: should I stay or go away?. Front. Cell. Neurosci. 2014, 8. <https://doi.org/10.3389/fncel.2014.00185>
• Byron Craig D., Vanvalkinburgh Daniel, Northcutt Katharine, Young Virginia: Plasticity in the Cerebellum and Primary Somatosensory Cortex Relating to Habitual and Continuous Slender Branch Climbing in Laboratory Mice (Mus musculus). The Anatomical Record 2013, 296, 822. <https://doi.org/10.1002/ar.22685>
• Rath Martin F., Rohde Kristian, Fahrenkrug Jan, Møller Morten: Circadian clock components in the rat neocortex: daily dynamics, localization and regulation. Brain Struct Funct 2013, 218, 551. <https://doi.org/10.1007/s00429-012-0415-4>
• Roberts Eleanor S., Chana Gursharan, Nguyen Timothy B., Perera Gayathri, Landau Sabine, Rabe-Hesketh Sophia, Glass Jonathan D., McArthur Justin, Everall Ian Paul: The spatial relationship between neurons and astrocytes in HIV-associated dementia. J. Neurovirol. 2013, 19, 123. <https://doi.org/10.1007/s13365-013-0149-y>
• Barbaresi Paolo, Mensà Emanuela, Lariccia Vincenzo, Pugnaloni Armanda, Amoroso Salvatore, Fabri Mara: Differential distribution of parvalbumin- and calbindin-D28K-immunoreactive neurons in the rat periaqueductal gray matter and their colocalization with enzymes producing nitric oxide. Brain Research Bulletin 2013, 99, 48. <https://doi.org/10.1016/j.brainresbull.2013.09.004>
• Hiraishi Tetsuya, Kitaura Hiroki, Oishi Makoto, Fukuda Masafumi, Kameyama Shigeki, Takahashi Hitoshi, Kakita Akiyoshi, Fujii Yukihiko: Significance of horizontal propagation of synchronized activities in human epileptic neocortex investigated by optical imaging and immunohistological study. Epilepsy Research 2013, 104, 59. <https://doi.org/10.1016/j.eplepsyres.2012.09.014>
• Hoffmann Nadine A, Dorostkar Mario M, Blumenstock Sonja, Goedert Michel, Herms Jochen: Impaired plasticity of cortical dendritic spines in P301S tau transgenic mice. acta neuropathol commun 2013, 1. <https://doi.org/10.1186/2051-5960-1-82>
• Bae Jong Seok, Simon Neil G., Menon Parvathi, Vucic Steve, Kiernan Matthew C.: The Puzzling Case of Hyperexcitability in Amyotrophic Lateral Sclerosis. J Clin Neurol 2013, 9, 65. <https://doi.org/10.3988/jcn.2013.9.2.65>
• Varvatsoulias George: The Physiological Processes Underpinning PET and fMRI Techniques With an Emphasis on the Temporal and Spatial Resolution of These Methods. Psychol. Thought 2013, 6, 173. <https://doi.org/10.5964/psyct.v6i2.75>
• Langer Dominik, Helmchen Fritjof: Post hoc immunostaining of GABAergic neuronal subtypes following in vivo two-photon calcium imaging in mouse neocortex. Pflugers Arch - Eur J Physiol 2012, 463, 339. <https://doi.org/10.1007/s00424-011-1048-9>
• Barinka Filip, Salaj Martin, Rybá\u0159 Jan, Kraj\u010dovi\u010dová Eva, Kubová Hana, Druga Rastislav: Calretinin, parvalbumin and calbindin immunoreactive interneurons in perirhinal cortex and temporal area Te3V of the rat brain: Qualitative and quantitative analyses. Brain Research 2012, 1436, 68. <https://doi.org/10.1016/j.brainres.2011.12.014>
• Sakakibara T., Sukigara S., Otsuki T., Takahashi A., Kaneko Y., Kaido T., Saito Y., Sato N., Nakagawa E., Sugai K., Sasaki M., Goto Y., Itoh M.: Imbalance of interneuron distribution between neocortex and basal ganglia: Consideration of epileptogenesis of focal cortical dysplasia. Journal of the Neurological Sciences 2012, 323, 128. <https://doi.org/10.1016/j.jns.2012.08.035>
• Freire M.A.M., Faber J., Picanço-Diniz C.W., Franca J.G., Pereira A.: Morphometric variability of nicotinamide adenine dinucleotide phosphate diaphorase neurons in the primary sensory areas of the rat. Neuroscience 2012, 205, 140. <https://doi.org/10.1016/j.neuroscience.2011.12.029>
• Song Juan, Christian Kimberly M, Ming Guo-li, Song Hongjun: Life or death: developing cortical interneurons make their own decision. The EMBO Journal 2012, 31, 4373. <https://doi.org/10.1038/emboj.2012.290>
• Herrera\u2010Rincon Celia, Torets Carlos, Sanchez\u2010Jimenez Abel, Avendaño Carlos, Panetsos Fivos: Chronic electrical stimulation of transected peripheral nerves preserves anatomy and function in the primary somatosensory cortex. Eur J of Neuroscience 2012, 36, 3679. <https://doi.org/10.1111/ejn.12000>
• Molina\u2010Hernández Anayansi, Díaz Néstor Fabián, Arias\u2010Montaño José\u2010Antonio: Histamine in brain development. Journal of Neurochemistry 2012, 122, 872. <https://doi.org/10.1111/j.1471-4159.2012.07863.x>
• Desgent Sébastien, Ptito Maurice: Cortical GABAergic Interneurons in Cross-Modal Plasticity following Early Blindness. Neural Plasticity 2012, 2012, 1. <https://doi.org/10.1155/2012/590725>
• Jacobs Bob, Lubs Jessica, Hannan Markus, Anderson Kaeley, Butti Camilla, Sherwood Chet C., Hof Patrick R., Manger Paul R.: Neuronal morphology in the African elephant (Loxodonta africana) neocortex. Brain Struct Funct 2011, 215, 273. <https://doi.org/10.1007/s00429-010-0288-3>
• Wang Yanmei, Zhan Lixuan, Zeng Wei, Li Ke, Sun Weiwen, Xu Zao C., Xu En: Downregulation of Hippocampal GABA after Hypoxia-Induced Seizures in Neonatal Rats. Neurochem Res 2011, 36, 2409. <https://doi.org/10.1007/s11064-011-0565-4>
• Matsuda Yoshiki, Inoue Yuki, Izumi Hitomi, Kaga Makiko, Inagaki Masumi, Goto Yu-ichi: Fewer GABAergic interneurons, heightened anxiety and decreased high-frequency electroencephalogram components in Bronx waltzer mice, a model of hereditary deafness. Brain Research 2011, 1373, 202. <https://doi.org/10.1016/j.brainres.2010.12.006>
• Takano Tomoyuki: Seizure susceptibility in polymicrogyria: Clinical and experimental approaches. Epilepsy Research 2011, 96, 1. <https://doi.org/10.1016/j.eplepsyres.2011.06.010>