Glia and volume transmission during physiological and pathological states

Proteoglycans: many forms and many functions

Hardingham, T., & Fosang, A. (1992) · The FASEB Journal · doi:10.1096/fasebj.6.3.1740236 · Cited by 1,203 · see citing works

Extracellular space structure revealed by diffusion analysis

Nicholson, C., & Syková, E. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01261-2 · Cited by 914 · see citing works

Regulation and Modulation of pH in the Brain

Chesler, M. (2003) · Physiological Reviews · doi:10.1152/physrev.00010.2003 · Cited by 891 · see citing works

Ion diffusion modified by tortuosity and volume fraction in the extracellular microenvironment of the rat cerebellum.

Nicholson, C., & Phillips, J. M. (1981) · The Journal of Physiology · doi:10.1113/jphysiol.1981.sp013981 · Cited by 785 · see citing works

Intercellular communication in the brain: Wiring versus volume transmission

Agnati, L. F., Zoli, M., Strömberg, I., & Fuxé, K. (1995) · Neuroscience · doi:10.1016/0306-4522(95)00308-6 · Cited by 569 · see citing works

Time-dependent diffusion of water in a biologicalmodel system.

Latour, L. L., Svoboda, K., Mitra, P. P., & Sotak, C. H. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.4.1229 · Cited by 517 · see citing works

Mechanism of detection of acute cerebral ischemia in rats by diffusion-weighted magnetic resonance microscopy.

Benveniste, H., Hedlund, L. W., & Johnson, G. A. (1992) · Stroke · doi:10.1161/01.str.23.5.746 · Cited by 509 · see citing works

Perineuronal nets: past and present

Celio, M. R., Spreafico, R., De Biasi, S., & Vitellaro-Zuccarello, L. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01298-3 · Cited by 497 · see citing works

Diffusion and related transport mechanisms in brain tissue

Nicholson, C. (2001) · Reports on Progress in Physics · doi:10.1088/0034-4885/64/7/202 · Cited by 491 · see citing works

Extrasynaptic Glutamate Spillover in the Hippocampus: Dependence on Temperature and the Role of Active Glutamate Uptake

Asztély, F., Erdemli, G., & Kullmann, D. M. (1997) · Neuron · doi:10.1016/s0896-6273(00)80268-8 · Cited by 417 · see citing works

Volume transmission in the brain. Novel mechanisms for neural transmission

(1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90031-2 · Cited by 383 · see citing works

LTP of AMPA and NMDA receptor-mediated signals: evidence for presynaptic expression and extrasynaptic glutamate spill-over.

Kullmann, D., Erdemli, G., & Asztely, F. (1996) · Neuron · doi:10.1016/s0896-6273(00)80178-6 · Cited by 299 · see citing works

Extracellular space parameters in the rat neocortex and subcortical white matter during postnatal development determined by diffusion analysis

Lehmenkühler, A., Syková, E., Svoboda, J., Zilles, K., & Nicholson, C. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90503-8 · Cited by 298 · see citing works

Dynamic changes in water ADC, energy metabolism, extracellular space volume, and tortuosity in neonatal rat brain during global ischemia

van der Toorn, A., Syková, E., Dijkhuizen, R. M., Voříšek, I., Vargová, L., Škobisová, E., Campagne, M. V. L., Reese, T., & Nicolay, K. (1996) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910360110 · Cited by 270 · see citing works

Nervous tissue proteoglycans

Margolis, R. K., & Margolis, R. U. (1993) · Cellular and Molecular Life Sciences · doi:10.1007/bf01923587 · Cited by 265 · see citing works

Modification of extracellular matrix by enzymatic removal of chondroitin sulfate and by lack of tenascin-R differentially affects several forms of synaptic plasticity in the hippocampus

Bukalo, O., Schachner, M., & Dityatev, A. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00082-3 · Cited by 236 · see citing works

Diffusion barriers evoked in the rat cortex by reactive astrogliosis

Roitbak, T., & Sykov�, E. (1999) · Glia · doi:10.1002/(sici)1098-1136(199910)28:1 · Cited by 208 · see citing works

The Extracellular Space in the CNS: Its Regulation, Volume and Geometry in Normal and Pathological Neuronal Function

Syková, E. (1997) · The Neuroscientist · doi:10.1177/107385849700300113 · Cited by 155 · see citing works

Healthy and infarcted brain tissues studied at short diffusion times: The origins of apparent restriction and the reduction in apparent diffusion coefficient

Norris, D. G., Niendorf, T., & Leibfritz, D. (1994) · NMR in Biomedicine · doi:10.1002/nbm.1940070703 · Cited by 142 · see citing works

Glial diffusion barriers during aging and pathological states

Syková, E. (2001) · Progress in brain research · doi:10.1016/s0079-6123(01)32087-3 · Cited by 124 · see citing works

Evolution of anisotropic diffusion in the developing rat corpus callosum

Voříšek, I., & Syková, E. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.2.912 · Cited by 113 · see citing works

Diffusion constraints and neuron–glia interaction during aging

Syková, E., Mazel, T., & Šimonová, Z. (1998) · Experimental Gerontology · doi:10.1016/s0531-5565(98)00038-2 · Cited by 110 · see citing works

Anisotropic and heterogeneous diffusion in the turtle cerebellum: implications for volume transmission

Rice, M. E., Okada, Y., & Nicholson, C. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.70.5.2035 · Cited by 105 · see citing works

Learning deficits in aged rats related to decrease in extracellular volume and loss of diffusion anisotropy in hippocampus

Syková, E., Mazel, T., Hasenöhrl, R. U., Harvey, A. R., Šimonová, Z., Mulders, W. H. A. M., & Huston, J. P. (2002) · Hippocampus · doi:10.1002/hipo.1101 · Cited by 102 · see citing works

Glial cells and volume transmission in the CNS

Syková, E., & Chvátal, A. (2000) · Neurochemistry International · doi:10.1016/s0197-0186(99)00131-x · Cited by 93 · see citing works

Water ADC, extracellular space volume, and tortuosity in the rat cortex after traumatic injury

Voříšek, I., Hájek, M., Tintěra, J., Nicolay, K., & Syková, E. (2002) · Magnetic Resonance in Medicine · doi:10.1002/mrm.10305 · Cited by 84 · see citing works

Extracellular space diffusion and pathological states

Syková, E., Mazel, T., Vargová, L., Voříšek, I., & Prokopová-Kubinová, Š. (2000) · Progress in brain research · doi:10.1016/s0079-6123(00)25008-5 · Cited by 72 · see citing works

The relationship between changes in intrinsic optical signals and cell swelling in rat spinal cord slices

Syková, E., Vargová, L., Kubinová, Š., Jendelová, P., & Chvátal, A. (2003) · NeuroImage · doi:10.1016/s1053-8119(02)00014-9 · Cited by 63 · see citing works

Heterogeneous and anisotropic diffusion in the developing rat spinal cord

Prokopová, Š., Vargová, L., & Syková, E. (1997) · Neuroreport · doi:10.1097/00001756-199711100-00022 · Cited by 62 · see citing works

Ionic and Volume Changes in the Microenvironment of Nerve and Receptor Cells

Syková, E. (1992) · Cited by 58 · see citing works

X-irradiation-induced changes in the diffusion parameters of the developing rat brain

Syková, E., Svoboda, J., Šimonová, Z., Lehmenkühler, A., & Lassmann, H. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00361-4 · Cited by 41 · see citing works

Changes of extracellular space volume and tortuosity in the spinal cord of Lewis rats with experimental autoimmune encephalomyelitis.

Šimonová, Z., Svoboda, J., Orkand, P. M., Bernard, C. C. A., Lassmann, H., & Syková, E. (1996) · PubMed · Cited by 40 · see citing works

Glutamate, NMDA, and AMPA Induced Changes in Extracellular Space Volume and Tortuosity in the Rat Spinal Cord

Vargová, L., Jendelová, P., Chvátal, A., & Syková, E. (2001) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200109000-00005 · Cited by 35 · see citing works

Diffusion Parameters of the Extracellular Space

Syková, E. (2003) · Israel Journal of Chemistry · doi:10.1560/11ga-dqd7-dc41-q1u7 · Cited by 12 · see citing works

Glia and Extracellular Space Diffusion Parameters in the Injured and Aging Brain

Syková, E. (2002) · Humana Press eBooks · doi:10.1007/978-1-59259-105-3_5 · Cited by 6 · see citing works

Association of human, rat, and rabbit apolipoprotein E with β‐amyloid

LaDu, M. J., Lukens, J. R., Reardon, C. A., & Getz, G. S. (1997) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19970701)49:1

Multi-target strategies for the improved treatment of depressive states: Conceptual foundations and neuronal substrates, drug discovery and therapeutic application

Millan, M. J. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2005.11.006 · Cited by 549 · see citing works

Pathogenetic mechanisms of hepatic encephalopathy

Häussinger, D., & Schliess, F. (2008) · Gut · doi:10.1136/gut.2007.122176 · Cited by 391 · see citing works

Astrocytes in the Epileptic Brain

Wetherington, J. P., Serrano, G. E., & Dingledine, R. J. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.002 · Cited by 391 · see citing works

Spinal glial activation contributes to pathological pain states

Cao, H., & Zhang, Y. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.03.009 · Cited by 248 · see citing works

Compartmentalization from the outside: the extracellular matrix and functional microdomains in the brain

Dityatev, A. E., Seidenbecher, C. I., & Schachner, M. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.08.003 · Cited by 229 · see citing works

Characterization of Developmental Neurotoxicity of As, Cd, and Pb Mixture: Synergistic Action of Metal Mixture in Glial and Neuronal Functions

Rai, A., Maurya, S. K., Khare, P., Srivastava, A., & Bandyopadhyay, S. (2010) · Toxicological Sciences · doi:10.1093/toxsci/kfq266 · Cited by 203 · see citing works

The acute effects of NMDA antagonism: from the rodent to the human brain.

Gunduz-Bruce, H. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2008.07.006 · Cited by 182 · see citing works

Interoception and the origin of feelings: A new synthesis

Carvalho, G. B., & Damasio, A. (2021) · BioEssays · doi:10.1002/bies.202000261 · Cited by 132 · see citing works

Gangliosides Trigger Inflammatory Responses via TLR4 in Brain Glia

Jou, I., Lee, J. H., Park, S. Y., Yoon, H. J., Joe, E.-H., & Park, E. J. (2006) · American Journal Of Pathology · doi:10.2353/ajpath.2006.050924 · Cited by 136 · see citing works

Gene therapy and transplantation in CNS repair: The visual system

Harvey, A. R., Hu, Y. J., Leaver, S. G., Mellough, C., Park, K. K., Verhaagen, J., Plant, G. W., & Cui, Q. (2006) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2006.07.002 · Cited by 110 · see citing works

Could chronic pain and spread of pain sensation be induced and maintained by glial activation?

Hansson, E. (2006) · Acta Physiologica · doi:10.1111/j.1748-1716.2006.01568.x · Cited by 108 · see citing works

Cell volume regulation: physiology and pathophysiology

Lambert, I. H., Hoffmann, E. K., & Pedersen, S. F. (2008) · Acta Physiologica · doi:10.1111/j.1748-1716.2008.01910.x · Cited by 103 · see citing works

Coupled Changes in Brain White Matter Microstructure and Fluid Intelligence in Later Life

Ritchie, S. J., Bastin, M. E., Tucker–Drob, E. M., Maniega, S. M., Engelhardt, L. E., Cox, S. R., Royle, N. A., Gow, A. J., Corley, J., Pattie, A., et al. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0862-15.2015 · Cited by 98 · see citing works

Time and space profiling of NMDA receptor co‐agonist functions

Mothet, J., Bail, M. L., & Billard, J. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13204 · Cited by 98 · see citing works

Perineuronal nets and schizophrenia: The importance of neuronal coatings

Bitanihirwe, B. K. Y., & Woo, T.-U. W. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.03.018 · Cited by 95 · see citing works

Multiple Diffusion Mechanisms Due to Nanostructuring in Crowded Environments

Sanabria, H., Kubota, Y., & Waxham, M. N. (2006) · Biophysical Journal · doi:10.1529/biophysj.106.090498 · Cited by 92 · see citing works

Pathogenetic interplay between osmotic and oxidative stress: the hepatic encephalopathy paradigm

Schliess, F., Görg, B., & Häussinger, D. (2006) · Biological Chemistry · doi:10.1515/bc.2006.171 · Cited by 85 · see citing works

Omega‐3 fatty acids deficiency aggravates glutamatergic synapse and astroglial aging in the rat hippocampal CA 1

Latour, A., Grintal, B., Champeil‐Potokar, G., Hennebelle, M., Lavialle, M., Dutar, P., Potier, B., Billard, J., Vancassel, S., & Denis, I. (2012) · Aging Cell · doi:10.1111/acel.12026 · Cited by 82 · see citing works

Age-related changes in glutamate release in the CA3 and dentate gyrus of the rat hippocampus

Humeidan, M., Quintero, J. E., Pomerleau, F., Huettl, P. F., & Gerhardt, G. A. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.05.009 · Cited by 81 · see citing works

Detecting microstructural properties of white matter based on compartmentalization of magnetic susceptibility

Chen, W. C., Foxley, S., & Miller, K. L. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.12.032 · Cited by 79 · see citing works

Dynamic Volume Changes in Astrocytes Are an Intrinsic Phenomenon Mediated by Bicarbonate Ion Flux

Florence, C. M., Baillie, L. D., & Mulligan, S. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051124 · Cited by 73 · see citing works

Molecular targets of opiate drug abuse in neuro AIDS

Hauser, K. F., El‐Hage, N., Buch, S. K., Berger, J. R., Tyor, W. R., Nath, A., Bruce‐Keller, A. J., & Knapp, P. E. (2005) · Neurotoxicity Research · doi:10.1007/bf03033820 · Cited by 73 · see citing works

Implications for glycine receptors and astrocytes in ethanol-induced elevation of dopamine levels in the nucleus accumbens

Adermark, L., Clarke, R. B. C., Olsson, T., Hansson, E., Söderpalm, B., & Ericson, M. (2010) · Addiction Biology · doi:10.1111/j.1369-1600.2010.00206.x · Cited by 71 · see citing works

Bioimpedance modeling to monitor astrocytic response to chronically implanted electrodes

McConnell, G. C., Butera, R. J., & Bellamkonda, R. V. (2009) · Journal of Neural Engineering · doi:10.1088/1741-2560/6/5/055005 · Cited by 67 · see citing works

Three‐dimensional confocal morphometry reveals structural changes in astrocyte morphology in situ

Chvátal, A., ̆rová, M. A., Hock, M., Prajerová, I., Neprašová, H., Chvátal, V., Kirchhoff, F., & Syková, E. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.21113 · Cited by 68 · see citing works

A longitudinal diffusion tensor imaging study in symptomatic Huntington's disease

Sritharan, A., Egan, G. F., Johnston, L. A., Horne, M. K., Bradshaw, J. L., Bohanna, I., Asadi, H., Cunnington, R., Churchyard, A., Chua, P. M.-L., et al. (2009) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2007.142786 · Cited by 66 · see citing works

Calcium-induced outgrowth of astrocytic peripheral processes requires actin binding by Profilin-1

Molotkov, D. A., Николаевна, З. С., Arcas, J. M., & Khiroug, L. S. (2013) · Cell Calcium · doi:10.1016/j.ceca.2013.03.001 · Cited by 64 · see citing works

Feelings Are the Source of Consciousness

Damasio, A., & Damasio, H. (2023) · Neural Computation · doi:10.1162/neco_a_01521 · Cited by 60 · see citing works

Brain metabolism and diffusion in the rat cerebral cortex during pilocarpine-induced status epilepticus

Šlais, K., Voříšek, I., Zoremba, N., Homola, A., Dmytrenko, L., & Syková, E. (2007) · Experimental Neurology · doi:10.1016/j.expneurol.2007.09.008 · Cited by 60 · see citing works

Quantification of astrocyte volume changes during ischemia in situ reveals two populations of astrocytes in the cortex of GFAP/EGFP mice

Benešová, J., Hock, M., Butenko, O., Prajerová, I., Anděrová, M., & Chvátal, A. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21828 · Cited by 56 · see citing works

Lipopolysaccharide repeated challenge followed by chronic mild stress protocol introduces a combined model of depression in rats: Reversibility by imipramine and pentoxifylline

Elgarf, A. A., Aboul‐Fotouh, S., Abd-Alkhalek, H. A., El‐Tabbal, M., Hassan, A. N. E.-D., Kassim, S. K., Hammouda, G. A., Farrag, K. A. E.-R., & Abdel-Tawab, A. M. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2014.09.014 · Cited by 57 · see citing works

Interactions of HIV and Drugs of Abuse

Hauser, K. F., & Knapp, P. E. (2014) · International review of neurobiology · doi:10.1016/b978-0-12-801284-0.00009-9 · Cited by 55 · see citing works

Gangliosides induce autophagic cell death in astrocytes

Hwang, J., Lee, S., Lee, J. T., Kwon, T. K., Kim, D. R., Kim, H., Park, H., & Suk, K. (2010) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2009.00563.x · Cited by 54 · see citing works

Three‐dimensional confocal morphometry – a new approach for studying dynamic changes in cell morphology in brain slices

Chvátal, A., Anděrová, M., & Kirchhoff, F. (2007) · Journal of Anatomy · doi:10.1111/j.1469-7580.2007.00724.x · Cited by 54 · see citing works

Morphine and gp120 Toxic Interactions in Striatal Neurons are Dependent on HIV-1 Strain

Podhaizer, E. M., Zou, S., Fitting, S., Samano, K. L., El‐Hage, N., Knapp, P. E., & Hauser, K. F. (2011) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-011-9326-z · Cited by 49 · see citing works

Pathological potential of astroglia

Chvátal, A., Anděrová, M., Neprašová, H., Prajerová, I., Benešová, J., Butenko, O., & Verkhratsky, A. (2008) · Physiological Research · doi:10.33549/physiolres.931604 · Cited by 41 · see citing works

Changes in diffusion parameters, energy-related metabolites and glutamate in the rat cortex after transient hypoxia/ischemia

Homola, A., Zoremba, N., Šlais, K., Kuhlen, R., & Syková, E. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.05.028 · Cited by 41 · see citing works

The effects of chronic corticosterone on hippocampal astrocyte numbers: A comparison of male and female Wistar rats

Bridges, N., Šlais, K., & Syková, E. (2008) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2008-1682 · Cited by 37 · see citing works

High extracellular K+ evokes changes in voltage-dependent K+ and Na+ currents and volume regulation in astrocytes

Neprašová, H., Anděrová, M., Petřík, D., Vargová, L., Kubinová, Š., Chvátal, A., & Syková, E. (2006) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-006-0151-9 · Cited by 35 · see citing works

Neurobiological aspects of depressive disorder and antidepressant treatment: role of glia

Páv, M., Kovárů, H., Fišerová, A., Havrdová, E., & Lisá, V. (2008) · Physiological Research · doi:10.33549/physiolres.930990 · Cited by 34 · see citing works

Extracellular space diffusion and extrasynaptic transmission

Vargová, L., & Syková, E. (2008) · Physiological Research · doi:10.33549/physiolres.931603 · Cited by 34 · see citing works

A transcriptome‐based assessment of the astrocytic dystrophin‐associated complex in the developing human brain

Simon, M. J., Murchison, C., & Iliff, J. J. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.24082 · Cited by 31 · see citing works

Bloodless fMRI

Jasanoff, A. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.08.002 · Cited by 28 · see citing works

Homeostatic Feelings and the Emergence of Consciousness

Damasio, A., & Damasio, H. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02119 · Cited by 26 · see citing works

Does rapid and physiological astrocyte–neuron signalling amplify epileptic activity?

Henneberger, C. (2016) · The Journal of Physiology · doi:10.1113/jp271958 · Cited by 25 · see citing works

Extrasynaptic glutamate NMDA receptors: Key players in striatal function

Garcia-Munoz, M., López-Huerta, V. G., Carrillo‐Reid, L., & Arbuthnott, G. W. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.09.013 · Cited by 24 · see citing works

Clinical and Genetic Aspects of Epilepsy

Heron, S., & Mulley, J. (2011) · InTech eBooks · doi:10.5772/1138 · Cited by 24 · see citing works

The Omega-3 Polyunsaturated Fatty Acid Docosahexaenoic Acid (DHA) Reverses Corticosterone-Induced Changes in Cortical Neurons

Pusceddu, M. M., Nolan, Y. M., Green, H. F., Robertson, R. C., Stanton, C., Kelly, P. M., Cryan, J. F., & Dinan, T. G. (2015) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyv130 · Cited by 23 · see citing works

Measuring diffusion parameters in the brain: comparing the real‐time iontophoretic method and diffusion‐weighted magnetic resonance

Vorisek, I., & Syková, E. (2008) · Acta Physiologica · doi:10.1111/j.1748-1716.2008.01924.x · Cited by 20 · see citing works

Blockade of AMPA-receptors attenuates 4-aminopyridine seizures, decreases the activation of inhibitory neurons but is ineffective against seizure-related astrocytic swelling

Weiczner, R., Krisztin‐Péva, B., & Mihály, A. (2007) · Epilepsy Research · doi:10.1016/j.eplepsyres.2007.10.004 · Cited by 18 · see citing works

Modulation of Excitation by Metabotropic Glutamate Receptors

Knöpfel, T., & Uusisaari, M. Y. (2007) · Springer eBooks · doi:10.1007/400_2007_035 · Cited by 18 · see citing works

A Role for The P2Y1 Receptor in Nonsynaptic Cross-depolarization in the Rat Dorsal Root Ganglia

Carvalho, G. B., Mulpuri, Y., Damásio, A. R., & Spigelman, I. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.09.038 · Cited by 17 · see citing works

Vascular dementia and the cholinergic pathways

Engelhardt, E., Moreira, D. M., & Laks, J. (2007) · Dementia & Neuropsychologia · doi:10.1590/s1980-57642008dn10100002 · Cited by 16 · see citing works

Multimodal and multifunctional stealth polymer nanospheres for sustained drug delivery

Evans, C. W., Latter, M. J., Ho, D., Peerzade, S. A. M. A., Clemons, T. D., Fitzgerald, M., Dunlop, S. A., & Iyer, K. S. (2012) · New Journal of Chemistry · doi:10.1039/c2nj40016b · Cited by 14 · see citing works

Neurologic Presentations of Hepatic Disease

Harris, M. K., Elliott, D. G., Schwendimann, R. N., Minagar, A., & Jaffe, S. L. (2009) · Neurologic Clinics · doi:10.1016/j.ncl.2009.09.016 · Cited by 12 · see citing works

The influence of the chloride currents on action potential firing and volume regulation of excitable cells studied by a kinetic model

Berndt, N., Hoffmann, S., Benda, J., & Holzhütter, H. (2011) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2011.01.022 · Cited by 12 · see citing works

The Extracellular Space in the Edematous Human Cerebral Cortex: An Electron Microscopic Study Using Cortical Biopsies

Castejón, O. J. (2009) · Ultrastructural Pathology · doi:10.1080/01913120902787076 · Cited by 10 · see citing works

Structural Magnetic Resonance Imaging Markers of Alzheimer’s Disease and Its Retranslation to Rodent Models

Kincses, Z. T., Király, A., Veréb, D., & Vécsei, L. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-143195 · Cited by 10 · see citing works

Long-lasting dephosphorylation of connexin 43 in acute seizures is regulated by NMDA receptors in the rat cerebral cortex

Zádor (2008) · Molecular Medicine Reports · doi:10.3892/mmr_00000019 · Cited by 9 · see citing works

Neuroimaging assessment of memory‐related brain structures in a rat model of acute space‐like radiation

Huang, L., Smith, A., Cummings, P. T., Kendall, E. J., & Obenaus, A. (2009) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.21661 · Cited by 9 · see citing works

The Biotic-Abiotic Interface

Tresco, P. A., & Gerhardt, G. A. (2008) · Springer eBooks · doi:10.1007/978-1-4020-8705-9_3 · Cited by 8 · see citing works

Cell–Cell Communication Through the Extracellular Space

Fuxé, K., & Agnati, L. F. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.01739-3 · Cited by 8 · see citing works

Astrogliosis is temporally correlated with enhanced neurogenesis in adult rat hippocampus following a glucoprivic insult

Estrada, F. S., Hernández, V. S., Medina‐Pizarro, M., Corona-Morales, A. A., González-Pérez, Ó., Vega‐González, A., & Zhang, L. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.05.016 · Cited by 7 · see citing works

The emerging role of 12/15-lipoxygenase in ischemic stroke

Wang, X., Shao, Q., & Gao, Y. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111194 · Cited by 6 · see citing works

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