The roles of perineuronal nets and the perinodal extracellular matrix in neuronal function

Structural basis of long-term potentiation in single dendritic spines

Matsuzaki, M., Honkura, N., Ellis-Davies, G. C. R., & Kasai, H. (2004) · Nature · doi:10.1038/nature02617 · Cited by 2,483

Chondroitinase ABC promotes functional recovery after spinal cord injury

Bradbury, E. J., Moon, L. D. F., Popat, R. J., King, V. R., Bennett, G. S., Patel, P. N., Fawcett, J. W., & McMahon, S. B. (2002) · Nature · doi:10.1038/416636a · Cited by 2,357

Reactivation of Ocular Dominance Plasticity in the Adult Visual Cortex

Pizzorusso, T., Medini, P., Berardi, N., Chierzi, S., Fawcett, J. W., & Maffei, L. (2002) · Science · doi:10.1126/science.1072699 · Cited by 1,679

Critical period regulation

Hensch, T. K. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144327 · Cited by 1,300

Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder

Gandal, M. J., Zhang, P., Hadjimichael, E., Walker, R. L., Chen, C., Liu, S., Won, H., van Bakel, H., Varghese, M., Wang, Y., et al. (2018) · Science · doi:10.1126/science.aat8127 · Cited by 1,247

Cortical parvalbumin interneurons and cognitive dysfunction in schizophrenia

Lewis, D. A., Curley, A. A., Glausier, J. R., & Volk, D. W. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2011.10.004 · Cited by 1,071

CNS injury, glial scars, and inflammation: Inhibitory extracellular matrices and regeneration failure

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Genome-wide association studies of brain imaging phenotypes in UK Biobank

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Abundant Tau Filaments and Nonapoptotic Neurodegeneration in Transgenic Mice Expressing Human P301S Tau Protein

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Glycosaminoglycans in mucopolysaccharidoses and other disorders

Khan, S. A., Nidhi, F., Leal, A. F., Çelik, B., Herreño-Pachón, A. M., Saikia, S., Benincore-Flórez, E., Ago, Y., & Tomatsu, S. (2024) · Advances in clinical chemistry · doi:10.1016/bs.acc.2024.06.011 · Cited by 15

Transcriptomic profiling of murine GnRH neurons reveals developmental trajectories linked to human reproduction and infertility

Zouaghi, Y., Alpern, D., Gardeux, V., Russeil, J., Deplancke, B., Santoni, F. A., Pitteloud, N., & Messina, A. (2025) · Theranostics · doi:10.7150/thno.91873 · Cited by 16

Reorganization of the Brain Extracellular Matrix in Hippocampal Sclerosis

Sitaš, B., Bobić‐Rasonja, M., Mrak, G., Trnski, S., Skorić, M. K., Orešković, D., Knezović, V., Gadže, Ž. P., Petanjek, Z., Šimić, G., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158197 · Cited by 16

Resilience to Alzheimer's disease associates with alterations in perineuronal nets

de Vries, L. E., Bahnerth, A., Swaab, D. F., Verhaagen, J., & Carulli, D. (2024) · Alzheimer s & Dementia · doi:10.1002/alz.14504 · Cited by 16

Modulatory Effects of Monoamines and Perineuronal Nets on Output of Cerebellar Purkinje Cells

Hirono, M., Karube, F., & Yanagawa, Y. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.661899 · Cited by 16

The secret world in the gaps between brain cells

Nicholson, C. (2022) · Physics Today · doi:10.1063/pt.3.4999 · Cited by 14

Astrocyte depletion alters extracellular matrix composition in the demyelinating phase of Theiler’s murine encephalomyelitis

Allnoch, L., Leitzen, E., Zdora, I., Baumgärtner, W., & Hansmann, F. (2022) · PLoS ONE · doi:10.1371/journal.pone.0270239 · Cited by 15

Signatures of adaptive evolution in platyrrhine primate genomes

Byrne, H., Webster, T. H., Brosnan, S. F., Izar, P., & Lynch, J. W. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2116681119 · Cited by 14

High-Content Screening and Analysis of Stem Cell-Derived Neural Interfaces Using a Combinatorial Nanotechnology and Machine Learning Approach

Yang, L., Conley, B. M., Yoon, J., Rathnam, C., Pongkulapa, T., Conklin, B., Hou, Y., & Lee, K. (2022) · Research · doi:10.34133/2022/9784273 · Cited by 14

Reorganization of the Primate Dorsal Horn in Response to a Deafferentation Lesion Affecting Hand Function

Fisher, K. M., Garner, J. P., & Darian‐Smith, C. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2330-19.2020 · Cited by 14

Impact of Perineuronal Net Removal in the Rat Medial Prefrontal Cortex on Parvalbumin Interneurons After Reinstatement of Cocaine Conditioned Place Preference

Gonzalez, A. E., Jorgensen, E. T., Ramos, J. D., Harkness, J. H., Aadland, J. A., Brown, T. E., & Sorg, B. A. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.932391 · Cited by 14

Critical functions of extracellular matrix in brain metastasis seeding

Yuzhalin, A. E., & Yu, D. (2023) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-04944-z · Cited by 15

Electroacupuncture promotes the repair of the damaged spinal cord in mice by mediating neurocan‐perineuronal net

Hu, R., He, K., Chen, B., Chen, Y., Zhang, J., Wu, X., Shi, M., Wu, L., & Ma, R. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14468 · Cited by 14

Intersectional strategy to study cortical inhibitory parvalbumin-expressing interneurons

Palicz, R., Pater, B. A., Truschow, P., Witte, M., & Staiger, J. F. (2024) · Scientific Reports · doi:10.1038/s41598-024-52901-y · Cited by 13

Perineuronal Net Alterations Following Early-Life Stress: Are Microglia Pulling Some Strings?

Rahimian, R., Belliveau, C., Simard, S., Turecki, G., & Mechawar, N. (2024) · Biomolecules · doi:10.3390/biom14091087 · Cited by 18

Glial Control of Cortical Neuronal Circuit Maturation and Plasticity

Faust, T. E., Devlin, B. A., Farhy-Tselnicker, I., Ferro, A., Postolache, M., & Xin, W. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1208-24.2024 · Cited by 13

A Lipid-Raft Theory of Alzheimer's Disease

Rappoport, A. (2024) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-052024-115455 · Cited by 15

Disruption of Extracellular Matrix and Perineuronal Nets Modulates Extracellular Space Volume and Geometry

Syková, E., Voříšek, I., Starčuk, Z., Kratochvíla, J., Pavlova, I., Ichikawa, Y., Kwok, J. C. F., Kmonı́čková, E., Myronchenko, S., Hromádka, T., et al. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0517-24.2024 · Cited by 13

Neurocan regulates axon initial segment organization and neuronal activity

Baidoe‐Ansah, D., Mirzapourdelavar, H., Aleshin, S. E., Schott, B. H., Seidenbecher, C. I., Kaushik, R., & Dityatev, A. E. (2025) · Matrix Biology · doi:10.1016/j.matbio.2025.01.001 · Cited by 14

Dysregulation of astrocyte-derived matrix gla protein impairs dendritic spine development in pyridoxine-dependent epilepsy

Wu, J., Qin, D., Liang, Z., Liu, Q., Wang, M., Guo, Y., & Guo, W. (2025) · Molecular Therapy · doi:10.1016/j.ymthe.2025.02.027 · Cited by 13

Does maternal separation accelerate maturation of perineuronal nets and parvalbumin-containing inhibitory interneurons in male and female rats?

Richardson, R., Bowers, J., Callaghan, B. L., & Baker, K. (2020) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2020.100905 · Cited by 16

Early Chronic Memantine Treatment-Induced Transcriptomic Changes in Wild-Type and Shank2-Mutant Mice

Yoo, Y.-E., Lee, S., Kim, W., Kim, H., Chung, C., Ha, S., Park, J., Chung, Y., Kang, H., & Kim, E. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.712576 · Cited by 12

Synapse Formation and Function Across Species: Ancient Roles for CCP, CUB, and TSP-1 Structural Domains

González-Calvo, I., Cizeron, M., Bessereau, J., & Selimi, F. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.866444 · Cited by 12

Altered Activity-Regulated H3K9 Acetylation at TGF-Beta Signaling Genes During Egocentric Memory in Huntington's Disease

Alcalá‐Vida, R., Lotz, C., Brulé, B., Séguin, J., Decraene, C., Awada, A., Bombardier, A., Cosquer, B., de Vasconcelos, A. P., Brouillet, E., et al. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102363 · Cited by 16

Responses in fast-spiking interneuron firing rates to parameter variations associated with degradation of perineuronal nets

Hanssen, K. Ø., Grødem, S., Fyhn, M., Hafting, T., Einevoll, G. T., Ness, T. V., & Halnes, G. (2023) · Journal of Computational Neuroscience · doi:10.1007/s10827-023-00849-9 · Cited by 10

Extracellular Matrix Recycling as a Novel Plasticity Mechanism With a Potential Role in Disease

Dankovich, T. M., & Rizzoli, S. O. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.854897 · Cited by 12

Aberrant perineuronal nets alter spinal circuits, impair motor function, and increase plasticity

Sánchez-Ventura, J., Canal, C., Hidalgo, J., Penas, C., Navarro, X., Espin, A. T., Fouad, K., & Udina, E. (2022) · Experimental Neurology · doi:10.1016/j.expneurol.2022.114220 · Cited by 12

Rethinking the First Episode of Schizophrenia: Identifying Convergent Mechanisms During Development and Moving Toward Prediction

Forsyth, J. K., & Bearden, C. E. (2023) · American Journal of Psychiatry · doi:10.1176/appi.ajp.20230736 · Cited by 12

Choice impulsivity after repeated social stress is associated with increased perineuronal nets in the medial prefrontal cortex

Martinez, C. A., Pantazopoulos, H., Gisabella, B., Stephens, E. T., Garteiser, J., & Arco, A. D. (2024) · Scientific Reports · doi:10.1038/s41598-024-57599-6 · Cited by 11

Extracellular matrix integrity regulates GABAergic plasticity in the hippocampus

Jabłońska, J., Wiera, G., & Mozrzymas, J. W. (2024) · Matrix Biology · doi:10.1016/j.matbio.2024.11.001 · Cited by 12

Glycosaminoglycans in Neurodegenerative Diseases

Jin, W., Zhang, F., & Linhardt, R. J. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-70115-4_9 · Cited by 13

Transcriptomic analysis of isolated and pooled human postmortem cerebellar Purkinje cells in autism spectrum disorders

Brandenburg, C., Griswold, A. J., Booven, D. J. V., Kilander, M. B. C., Frei, J. A., Nestor, M. W., Dykxhoorn, D. M., Pericak‐Vance, M. A., & Blatt, G. J. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.944837 · Cited by 12

The brain's polymath: Emerging roles of microglia throughout brain development

Wong, F. K., & Favuzzi, E. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102700 · Cited by 12

Age-Dependent Sex Differences in Perineuronal Nets in an APP Mouse Model of Alzheimer’s Disease Are Brain Region-Specific

Rahmani, R., Rambarack, N., Singh, J., Constanti, A., & Ali, A. B. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914917 · Cited by 11

Acute damage to the blood–brain barrier and perineuronal net integrity in a clinically-relevant rat model of traumatic brain injury

Vita, S. M., Grayson, B. E., & Grill, R. J. (2020) · Neuroreport · doi:10.1097/wnr.0000000000001531 · Cited by 12

Adiposity‐related insulin resistance and thickness of the cerebral cortex in middle‐aged adults

Shin, J., Pelletier, S., Richer, L., Pike, G. B., Gaudet, D., Paus, T., & Pausová, Z. (2020) · Journal of Neuroendocrinology · doi:10.1111/jne.12921 · Cited by 13

Editorial: Perineuronal Nets as Therapeutic Targets for the Treatment of Neuropsychiatric Disorders

Browne, C. A., Conant, K. E., Lasek, A. W., & Nácher, J. (2022) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2022.889800 · Cited by 11

Extracellular matrix dysfunction and synaptic alterations in schizophrenia

Unzueta‐Larrinaga, P., Cuesta-Vega, E., Barrena-Barbadillo, R., Olabarrieta, E., Recio-Barbero, M., Horrillo, I., Mentxaka, O., Segarra, R., Meana, J. J., Nácher, J., et al. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03154-2 · Cited by 11

Experience-regulated molecular mechanisms in cortical GABAergic interneurons: from cellular functions to control over circuit plasticity

Spiegel, I. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.11.013 · Cited by 12

The cochlear matrisome: Importance in hearing and deafness

Pressé, M. T., Malgrange, B., & Delacroix, L. (2023) · Matrix Biology · doi:10.1016/j.matbio.2023.12.002 · Cited by 12

Astrocytes and Alcohol Throughout the Lifespan

Guizzetti, M., Mangieri, R. A., Ezerskiy, L. A., Hashimoto, J. G., Bajo, M., Farris, S. P., Homanics, G. E., Lasek, A. W., Mayfield, R. D., Messing, R. O., et al. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.04.013 · Cited by 13

Removal of Perineuronal Nets Leads to Altered Neuronal Excitability and Synaptic Transmission in Visual Cortex with Distinct Time Courses

Liu, L., Zhang, Y., & Ju, J. (2022) · Neuroscience Letters · doi:10.1016/j.neulet.2022.136763 · Cited by 10

Longitudinal in vivo imaging of perineuronal nets

Benbenishty, A., Peled-Hajaj, S., Krishnaswamy, V. R., Har-Gil, H., Havusha-Laufer, S., Ruggiero, A., Slutsky, I., Blinder, P., & Sagi, I. (2023) · Neurophotonics · doi:10.1117/1.nph.10.1.015008 · Cited by 11

Evidence of microglial involvement in the childhood abuse-associated increase in perineuronal nets in the ventromedial prefrontal cortex

Belliveau, C., Rahimian, R., Fakhfouri, G., Hosdey, C., Simard, S., Davoli, M. A., Mirault, D., Giros, B., Turecki, G., & Mechawar, N. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.12.013 · Cited by 14

Aggrecan modulates the expression and phosphorylation of tau in a novel bigenic TauP301L ‐ Acan mouse model

Schmidt, S., Stapf, C. D., Schmutzler, S., Lachmann, I., Arendt, T., Holzer, M., Sonntag, M., & Morawski, M. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14923 · Cited by 11

A Highly Translatable Dual‐arm Local Delivery Strategy To Achieve Widespread Therapeutic Coverage in Healthy and Tumor‐bearing Brain Tissues

Negrón, K., Kwak, G., Wang, H., Li, H., Huang, Y., Chen, S.-W., Tyler, B., Eberhart, C. G., Hanes, J. S., & Suk, J. S. (2023) · Small · doi:10.1002/smll.202207278 · Cited by 12

1-Methyltryptophan treatment ameliorates high-fat diet-induced depression in mice through reversing changes in perineuronal nets

Hu, J., Zhang, S., Wu, H., Wang, L., Zhang, Y., Gao, H., Li, M., Ren, H. G., Xiao, H., Guo, K., et al. (2024) · Translational Psychiatry · doi:10.1038/s41398-024-02938-4 · Cited by 10

Modulation of stress-, pain-, and alcohol-related behaviors by perineuronal nets

Aguilar, J. S., & Lasek, A. W. (2024) · Neurobiology of Stress · doi:10.1016/j.ynstr.2024.100692 · Cited by 11

Fast-spiking parvalbumin-positive interneurons: new perspectives of treatment and future challenges in dementia

Zhang, X., Wu, M., Cheng, L., Cao, W., Liu, Z., Yang, S., & Kim, M. S. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02756-6 · Cited by 13

Sugar as a therapeutic target for the cognitive restoration following traumatic brain injury

Kumar, A. (2019) · Current Opinion in Neurology · doi:10.1097/wco.0000000000000752 · Cited by 10

Development of parvalbumin neurons and perineuronal nets in the visual cortex of normal and dark‐exposed cats

Aronitz, E. M., Kamermans, B. A., & Duffy, K. R. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25127 · Cited by 11

Strategies for engineering neural cell alignment and their biomedical applications

Xia, N. L., Liu, R., Chen, W., Wang, D., & Sun, L. (2023) · Engineered Regeneration · doi:10.1016/j.engreg.2023.09.002 · Cited by 11

The Role of Perineuronal Nets in the Contralateral Hemisphere in the Electroacupuncture-Mediated Rehabilitation of Poststroke Dysphagia Mice

Yuan, S., Shi, J., Tang, X., Deng, B., Wu, Z., Qiu, B., Lin, S., Ji, C., Wang, L., Cui, S., et al. (2023) · eNeuro · doi:10.1523/eneuro.0234-23.2023 · Cited by 10

Glial cells undergo rapid changes following acute chemogenetic manipulation of cortical layer 5 projection neurons

Vadišiūtė, A., Meijer, E. J., Therpurakal, R. N., Mueller, M., Szabó, F., Messore, F., Juršėnas, A., Bredemeyer, O., Krone, L. B., Mann, E. O., et al. (2024) · Communications Biology · doi:10.1038/s42003-024-06994-w · Cited by 10

Cholinergic boutons are closely associated with excitatory cells and four subtypes of inhibitory cells in the inferior colliculus

Beebe, N. L., & Schofield, B. R. (2021) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2021.101998 · Cited by 10

Co-Expression Analysis of microRNAs and Proteins in Brain of Alzheimer’s Disease Patients

Watson, C. N., Begum, G., Ashman, E., Thorn, D., Yakoub, K. M., Hariri, M. A., Nehme, A., Mondello, S., Kobeissy, F. H., Belli, A., et al. (2022) · Cells · doi:10.3390/cells11010163 · Cited by 12

Postpartum scarcity-adversity inflicts sex-specific cerebellar adaptations and reward behaviors in adolescence

Maulik, M., Looschen, K., Smith, C., Johnson, K., Carman, A. F., Nagisetty, C., Corriveau, K., Salisbury, C., DeSchepper, K. M., Michels, M., et al. (2023) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2023.173620 · Cited by 9

Therapeutic approaches to microglial dysfunction in Alzheimer's disease: Enhancing phagocytosis and metabolic regulation

Almalki, W. H., & Almujri, S. S. (2024) · Pathology - Research and Practice · doi:10.1016/j.prp.2024.155614 · Cited by 9

Increased levels of extracellular matrix proteins associated with extracellular vesicles from brains of aged mice

Kaplelach, A. K., Murchison, C., Kojima, K., Mobley, J. A., & Arrant, A. E. (2024) · Aging Cell · doi:10.1111/acel.14359 · Cited by 9

Connexin 43 contributes to perioperative neurocognitive disorder by attenuating perineuronal net of hippocampus in aged mice

Zhang, Q., Zhang, Y., Cong, P., Wu, Q., Wan, H., Huang, X., Li, X., Li, Z., Li, J., Wu, H., et al. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-024-05530-7 · Cited by 9

Chronic treatment with fluoxetine regulates mitochondrial features and plasticity-associated transcriptomic pathways in parvalbumin-positive interneurons of prefrontal cortex

Jetsonen, E., Didio, G., Suleymanova, I., Teino, I., Ċastrén, E., & Umemori, J. (2025) · Neuropsychopharmacology · doi:10.1038/s41386-025-02219-8 · Cited by 11

Ventral tegmental area GABA neurons integrate positive and negative valence

Stelzner, M. E., Wolff, A. R., & Saunders, B. T. (2025) · Nature Communications · doi:10.1038/s41467-025-65345-3 · Cited by 13

The parental umwelt: Effects of parenthood on sensory processing in rodents

Wilson, K. M., Arquilla, A. M., & Wendy Saltzman, A. (2023) · Journal of Neuroendocrinology · doi:10.1111/jne.13237 · Cited by 11

Functional bioengineered tissue models of neurodegenerative diseases

Mullis, A. S., & Kaplan, D. L. (2023) · Biomaterials · doi:10.1016/j.biomaterials.2023.122143 · Cited by 10

Enhanced expression of parvalbumin and perineuronal nets in the medial prefrontal cortex after extended‐access cocaine self‐administration in rats

Wingert, J. C., Anguiano, J. N., Ramos, J. D., Blacktop, J. M., Gonzalez, A. E., Churchill, L., & Sorg, B. A. (2023) · Addiction Biology · doi:10.1111/adb.13334 · Cited by 9

Increased expression of chondroitin sulfate proteoglycans in dentate gyrus and amygdala causes postinfectious seizures

Patel, D. C., Swift, N. A., Tewari, B. P., Browning, J. L., Prim, C. E., Chaunsali, L., Kimbrough, I. F., Olsen, M. L., & Sontheimer, H. W. (2023) · Brain · doi:10.1093/brain/awad430 · Cited by 10

A disinhibitory microcircuit of the orbitofrontal cortex mediates cocaine preference in mice

Huang, Z., Wei, X., Tian, J., Fu, Y., Dong, J., Wang, Y., Shi, J., Lü, L., & Zhang, W. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02579-5 · Cited by 10

Combined loss of brevican, neurocan, tenascin-C and tenascin-R leads to impaired fear retrieval due to perineuronal net loss

Mueller-Buehl, C., Pakusch, J., Bader, V., Winklhofer, K. F., Mark, M. D., & Faissner, A. (2025) · Scientific Reports · doi:10.1038/s41598-025-89580-2 · Cited by 10

Microglial depletion increases aggrecan and hyaluronan levels in the diffuse and aggregated extracellular matrix of the mouse brain

Egorova, D., Kerever, A., Inada, M., Itoh, Y., Arikawa‐Hirasawa, E., & Miyata, S. (2025) · Scientific Reports · doi:10.1038/s41598-025-94224-6 · Cited by 11

Neuronal pericellular baskets: neurotransmitter convergence and regulation of network excitability

Senft, R. A., & Dymecki, S. M. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.08.006 · Cited by 10

Erythropoietin restrains the inhibitory potential of interneurons in the mouse hippocampus

Curto, Y., Carceller, H., Klimczak, P., Pérez-Rando, M., Wang, Q., Grewe, K., Kawaguchi, R., Rizzoli, S. O., Geschwind, D. H., Nave, K., et al. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02528-2 · Cited by 8

Advancement in modulation of brain extracellular space and unlocking its potential for intervention of neurological diseases

Yong, Y., Cai, Y., Lin, J., Ma, L., Han, H., & Li, F. (2024) · Med-X · doi:10.1007/s44258-024-00021-7 · Cited by 10

Therapeutic actions of terpenes in neurodegenerative disorders and their correlations with the regulation and remodeling of the extracellular matrix

Carneiro, R. D. S., da Costa, M. H. D. A., SANTOS, J. Z. L. V., Mendes, A. N., Uchôa, V. T., & LOPES, L. D. S. (2025) · Biocell · doi:10.32604/biocell.2024.058405 · Cited by 8

Identification of Novel Biomarkers for Ischemic Stroke Through Integrated Bioinformatics Analysis and Machine Learning

Jia, J., Niu, L., Feng, P., Liu, S., Han, H., Zhang, B., Wang, Y., & Wang, M. (2025) · Journal of Molecular Neuroscience · doi:10.1007/s12031-025-02309-8 · Cited by 8

Neuroglia and extracellular matrix molecules

Dzyubenko, E., & Hermann, D. M. (2025) · Handbook of clinical neurology · doi:10.1016/b978-0-443-19104-6.00010-3 · Cited by 8

The role of microglia in neuropathic pain: A systematic review of animal experiments

Long, J., Tian, G., He, K., Su, Y., Wang, Z., Huang, L., Yao, Y., Li, X., & Yi, L. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111410 · Cited by 11

Orchestrating the Matrix: The Role of Glial Cells and Systemic Signals in Perineuronal Net Dynamics

Totaro, V., Pizzorusso, T., & Tognini, P. (2025) · Neurochemical Research · doi:10.1007/s11064-025-04506-8 · Cited by 9

Pairing with Enriched Sound Exposure Restores Auditory Processing Degraded by an Antidepressant

Cheng, Y., Chen, R., Su, B., Zhang, G., Sun, Y., An, P., Fang, Y., Zhang, Y., Shan, Y., de Villers‐Sidani, E., et al. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.2027-22.2023 · Cited by 8

Cortical matrix remodeling as a hallmark of relapsing–remitting neuroinflammation in MR elastography and quantitative MRI

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Activational and Organizational Effects of Sex Hormones on Hippocampal Inhibitory Neurons

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