The blood-brain barrier and immune function and dysfunction

Microbial translocation is a cause of systemic immune activation in chronic HIV infection

Brenchley, J. M., Price, D. A., Schacker, T. W., Asher, T. E., Silvestri, G., Rao, S., Kazzaz, Z., Bornstein, E., Lambotte, O., Altmann, D., et al. (2006) · Nature Medicine · doi:10.1038/nm1511 · Cited by 3,559

FINE STRUCTURAL LOCALIZATION OF A BLOOD-BRAIN BARRIER TO EXOGENOUS PEROXIDASE

Reese, T. S., & Karnovsky, M. J. (1967) · The Journal of Cell Biology · doi:10.1083/jcb.34.1.207 · Cited by 2,629

Systemic LPS causes chronic neuroinflammation and progressive neurodegeneration

Qin, L., Wu, X., Block, M. L., Liu, Y., Breese, G. R., Hong, J., Knapp, D. J., & Crews, F. T. (2007) · Glia · doi:10.1002/glia.20467 · Cited by 2,144

Multiplicity of cerebrospinal fluid functions: new challenges in health and disease

Johanson, C. E., Duncan, J. A., Klinge, P. M., Brinker, T., Stopa, E. G., & Silverberg, G. D. (2008) · Cerebrospinal Fluid Research · doi:10.1186/1743-8454-5-10 · Cited by 861

Passage of cytokines across the blood–brain barrier

Banks, W. A., Kastin, A. J., & Broadwell, R. D. (1996) · Neuroimmunomodulation · doi:10.1159/000097202 · Cited by 778

Chylomicrons promote intestinal absorption of lipopolysaccharides

Ghoshal, S., Witta, J., Zhong, J., de Villiers, W., & Eckhardt, E. (2009) · Journal of Lipid Research · doi:10.1194/jlr.m800156-jlr200 · Cited by 662

Brain-immune communication pathways

Quan, N., & Banks, W. A. (2007) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2007.05.005 · Cited by 626

Physiology of the cerebro-spinal fluid

(1967) · Postgraduate Medical Journal · doi:10.1136/pgmj.43.501.508 · Cited by 620

Energy intake is associated with endotoxemia in apparently healthy men

Amar, J., Burcelin, R., Ruidavets, J. B., Cani, P. D., Fauvel, J., Alessi, M., Chamontin, B., & Ferrières, J. (2008) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/87.5.1219 · Cited by 610

The gut-brain barrier in major depression: intestinal mucosal dysfunction with an increased translocation of LPS from gram negative enterobacteria (leaky gut) plays a role in the inflammatory pathophysiology of depression.

Maes, M. H. J., Kubera, M., & Leunis, J. (2008) · PubMed · Cited by 609

Pathophysiological mechanisms linking osteoarthritis and neurodegenerative disease risk

Prasoon, P., Nguyen, K. L., Fathi, P. A., Gupta, S., Arnab, S., Jones, E. C., Meyyappan, A., Stehle, E. J., & Bethea, J. R. (2025) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2025.10.009 · Cited by 4

Developing interferon-β as a safe in vivo experimental-medicine model of human inflammation

Periche-Tomas, E., Underwood, J., MacIver, C., Leach, H., Bone, C., Guy, C., Triantafilou, K., Szomolay, B., Jones, S. A., & Harrison, N. A. (2025) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2025.106173 · Cited by 4

Investigation of putative antimicrobial peptides in Carassius gibel, revealing a practical approach to screening antimicrobials

Zhang, Y., Deng, P., Dai, C., Wu, M., Liu, X., Li, L., Pan, X., & Yuan, J. (2022) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2021.12.050 · Cited by 4

Complex gut–brain interactions underlying inflammatory bowel disease-related depression have translational implications in regenerative medicine: a narrative review

Fu, H., & Liu, Y. (2024) · Regenerative medicine reports . · doi:10.4103/regenmed.regenmed-d-24-00006 · Cited by 5

Sex-Specific Inflammatory Profiles Affect Neuropsychiatric Issues in COVID-19 Survivors

Palladini, M., Mazza, M. G., Bravi, B., Bessi, M., Lorenzi, C., Spadini, S., LORENZO, R. D., Rovere, P. Q., Furlan, R., & Benedetti, F. (2025) · Biomolecules · doi:10.3390/biom15040600 · Cited by 4

Neuropsychiatric Systemic Lupus Erythematosus: Mechanisms of Injury

Mackay, M. C., Uluğ, A. M., & Volpe, B. T. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-374994-9.10028-2 · Cited by 4

The Influence of the Microbiota on Brain Structure and Function: Implications for Stress-Related Neuropsychiatric Disorders

Sterrett, J. D., Andersen, N. D., & Lowry, C. A. (2022) · Progress in inflammation research · doi:10.1007/978-3-030-91051-8_10 · Cited by 4

Amyloid‐β concentration and structure influences the transport and immunomodulatory effects of IVIG

Wuest, D., & Lee, K. H. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12678 · Cited by 4

Stimulation of neuronal cells by culture supernatant of T lymphocytes triggered by anti‐CD3 mAb followed by propagation in the presence of interleukin‐2

Ishiguro, M., Okada, A. K., Asai, K., Kojima, K., & Okada, H. (2015) · Microbiology and Immunology · doi:10.1111/1348-0421.12346 · Cited by 4

FUNDAMENTAL AND APPLIED ASPECTS OF THE BLOOD-BRAIN BARRIER RESEARCH

Chekhonin, V. P., Baklaushev, V. P., Yusubalieva, G. M., Volgina, N. E., & Gurina, O. I. (2012) · Annals of the Russian academy of medical sciences · doi:10.15690/vramn.v67i8.352 · Cited by 4

Genetic Associations Among Inflammation, White Matter Architecture, and Extracellular Free Water

Rodrigue, A., Knowles, E. E. M., Mollon, J., Mathias, S. R., Peralta, J. M., Leandro, A. C., Fox, P. T., Kochunov, P., Olvera, R. L., Almasy, L. A., et al. (2025) · Human Brain Mapping · doi:10.1002/hbm.70101 · Cited by 3

An organ-on-a-chip investigation into dose-dependent, temporal dynamic effects of radiosurgery on the blood–brain barrier and its immunological response

Yock, A. D., Brown, J. A., Eley, J. G., Lwin, C., Liu, D., & Wikswo, J. P. (2025) · Brain Research · doi:10.1016/j.brainres.2025.150092 · Cited by 3

La interacción inmuno-neuro-endocrina en enfermedades reumáticas autoinmunes: un nuevo desafio para el reumatólogo

Jara, L. J. (2011) · Reumatología Clínica · doi:10.1016/j.reuma.2011.02.002 · Cited by 3

Neuroimmunoendocrine interaction in autoimmune rheumatic diseases: a new challenge for the rheumatologist

Jara, L. J. (2011) · Reumatología Clínica (English Edition) · doi:10.1016/s2173-5743(11)70017-x · Cited by 3

EFFECTS OF VITAMIN E AND COENZYME Q10 SUPPLEMENTATION AGAINST DOXORUBICIN-INDUCED NEUROTOXICITY IN RATS

Ibrahim, M. A., & Al-Shawi, N. N. (2018) · Asian Journal of Pharmaceutical and Clinical Research · doi:10.22159/ajpcr.2018.v11i9.27851 · Cited by 3

Brain targeting drug delivery systems for the management of brain disorders

Kaur, M., Sodhi, R. K., Jyothi, V. G. S. S., Sree, V. H., Shubhra, Singh, P. K., Mehra, N. K., Khatri, D. K., Srivastava, S., Singh, S. B., et al. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-85041-4.00012-3 · Cited by 4

CECOG educational illustrations: the blood–brain barrier and its relevance for targeted cancer therapies and immuno-oncology

Preusser, M., Berghoff, A. S., Thallinger, C., & Zielinski, C. C. (2017) · ESMO Open · doi:10.1136/esmoopen-2017-000194 · Cited by 3

Cellular and Molecular Mechanisms of Neuroinflammation in Drug-Resistant Epilepsy

Mercado-Gómez, O. F., Arriaga-Ávila, V. S., Vega-García, A., Sánchez-Hernández, J., Jiménez, A., Organista‐Juárez, D., Guzmán‐Ruiz, M. A., & Guevara‐Guzmán, R. (2023) · Springer eBooks · doi:10.1007/978-3-031-36526-3_8 · Cited by 2

Interplay between immune cells and metabolites in epilepsy: insights from a Mendelian randomization analysis

Wang, K., Yang, J., Xu, W., Wang, L., & Wang, Y. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1400426 · Cited by 2

Pathophysiological Divergence Between Vascular and Post-Stroke Dementia: Bridging Human and Experimental Perspectives

Ahn, J. H., Shin, M. C., Kim, D. W., Yoo, K., & Won, M. (2025) · Journal of Integrative Neuroscience · doi:10.31083/jin45565 · Cited by 2

Imaging Neuroimmune Dysfunction: From TSPO to Emerging Positron Emission Tomography Targets

Bonomi, R. E., Raval, N. R., Hillmer, A. T., & Cosgrove, K. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.11.010 · Cited by 3

Neuroimmune regulation of behavior: Focus on sensory circumventricular organs and associated cell circuit mechanisms

Mancz, E., Peach, T., & Sah, R. (2026) · The Journal of Immunology · doi:10.1093/jimmun/vkaf337 · Cited by 2

Comorbidities and Inflammation: How Chronic Diseases Prime the Host Response in Sepsis

Miguel, M. V. O., Santos, R. M., de Oliveira, M. M., Pelosi, G. G., & de Freitas, A. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27167395 · Cited by 2

Brain–Gut Relationship on Mucosal Inflammation in the Gastrointestinal Tract

Gyires, K., & Fehér, Á. (2017) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789813148574_0001 · Cited by 2

The Factors Associated with the Blood–Brain Barrier Dysfunction in Tick-Borne Encephalitis

Grygorczuk, S., Czupryna, P., Martonik, D., Adamczuk, J., Parfieniuk‐Kowerda, A., Grzeszczuk, A., Pawlak-Zalewska, W., Dunaj, J., Mielczak, K., Parczewski, M., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26041503 · Cited by 2

Effect of Alcohol on Brain Development

Patel, F., & Mandal, P. (2018) · InTech eBooks · doi:10.5772/intechopen.73693 · Cited by 2

Common infectious morbidity and white blood cell count in middle childhood predict behavior problems in adolescence

Beer, R. J., Dent, K. R., Robinson, S. L., Oliveros, H., Mora‐Plazas, M., Marín, C., & Villamor, E. (2021) · Development and Psychopathology · doi:10.1017/s0954579421000675 · Cited by 2

Tick-borne encephalitis : clinical and pathogenetic aspects

Mickienė, A. (2015) · Figshare · Cited by 2

Immune Functional Capability Dynamics Determine Disease Outcomes as in Cancer, Heart Diseases, COVID-19, Etc.Preprint

Wu, J., & Zha, P. (2021) · OSF Preprints (OSF Preprints) · doi:10.31219/osf.io/skf8e · Cited by 2

An Overview of the Blood-Brain Barrier

Barichello, T., Generoso, J. S., & Dal‐Pizzol, F. (2025) · Neuromethods · doi:10.1007/978-1-0716-4474-4_1 · Cited by 1

Preliminary associations between brain metabolites and oral microbiome profiles during adolescence

Browning, B. D., Kirkland, A. E., Perica, M. I., Engevik, M. A., Alekseyenko, A. V., & Squeglia, L. M. (2025) · Scientific Reports · doi:10.1038/s41598-025-09818-x · Cited by 1

Impact of physical activity and cardiorespiratory fitness on brain morphology among overweight and obese populations: A systematic review and meta-analysis of neuroimaging studies

Shettigar, D., Sukumar, S., Kadavigere, R., Vaishali, K., Panakkal, N. C., Dkhar, W., Pradhan, A., Chandrasekaran, B., Palaniswamy, H. P., Paramashiva, P. S., et al. (2025) · Neuroscience Informatics · doi:10.1016/j.neuri.2025.100224 · Cited by 1

Curcumin-enhanced elvitegravir therapy mitigates neuroinflammation and cognitive deficits in EcoHIV mice

Godse, S., Zhou, L., Sinha, N., Salman, M., Ishrat, T., & Kumar, S. (2025) · Experimental Biology and Medicine · doi:10.3389/ebm.2025.10758 · Cited by 1

The Nonlinear Relationship Between the Aggregate Index of Systemic Inflammation and Serum Neurofilament Light Chain Levels in U.S. Adults: A Cross‐Sectional Study

Wei, J., Liu, Y., & Zhang, J. (2026) · Mediators of Inflammation · doi:10.1155/mi/6698474 · Cited by 1

Syphilis infection and incident dementia in two real-world cohorts: A harmonized propensity-matched analysis in Taiwan NHIRD and TriNetX Asia-Pacific

Huang, W., Pang, C., Hsu, J.-Z., Wang, J., Chang, W., & Teh, S.-H. (2026) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2026.106781 · Cited by 1

Disease Influence on BBB Transport in Inflammatory Disorders

Schenk, G. J., Kooij, G., Reijerkerk, A., & de Vries, H. E. (2013) · AAPS advances in the pharmaceutical sciences series · doi:10.1007/978-1-4614-9105-7_21 · Cited by 1

Increased intake of fat and cholesterol as a pathogenetic factor of depression: A possible molecular mechanism

Veniaminova, E. A., & Strekalova, T. V. (2016) · Neurochemical Journal · doi:10.1134/s1819712416010153 · Cited by 1

The Behavioural Immune System of Lower Vertebrates

Rakus, K. Ł., Widziołek, M., Kemenade, B. M. L. V.-V., & Chadzińska, M. (2023) · Masterclass in neuroendocrinology · doi:10.1007/978-3-031-21358-8_3 · Cited by 1

Sistema imunológico e fadiga no exercício: uma relação pouco conhecida

Schöler, C. M., & Castro, F. A. D. S. (2014) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · Cited by 1

Ethnopharmacological Importance of Western Medicinal Herb, Scutellaria lateriflora

Lohani, M., Patel, M., Majrashi, M., Joshi, S., Kemppainen, B. W., Mulabagal, V., & Dhanasekaran, M. (2016) · Springer eBooks · doi:10.1007/978-981-10-1085-9_2 · Cited by 1

Gut Microbiota in Brain Development and Disorders of the CNS: Therapeutic Strategies Involving Dietary Modification, Pro- and Prebiotic Intervention, and Fecal Microbiota Transplantation (FMT) Therapy

Tungland, B. C. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-814649-1.00012-0 · Cited by 1

Omega-3 effects on electrocorticographic patterns of adult Wistar rats exposed to ionizing radiation

Lima, H., Lopes, I. M. S. D. S., Oliveira, A. P. B., Costa, E. V. L., Aguiar, L. A. A., Lindoso, B. P. A., Silva, M. C. O., Silva, J. E. S., & Nogueira, R. A. (2021) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2021.100992 · Cited by 1

Psychobiotics: A Newer Approach Toward the Treatment of Neurodevelopmental Disorders

Chakraborty, T., Begum, J., Mandal, D., & Sengupta, A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822909-5.00013-7 · Cited by 1

Novel pathomechanisms in chronic fatigue syndrome/myalgic encephalomyelitis: do purinergic signalling perturbations and gliosis play a role?

Staines, D., Brenu, E. W., & Marshall‐Gradisnik, S. (2010) · Griffith Research Online · Cited by 1

The use of modern metabolomics and proteomics to address the health challenges facing the Canadian cattle industry

Saleem, F. (2013) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3tt3q · Cited by 1

Interaktion des Frühsommer-Meningoenzephalitis- Virus mit antigenpräsentierenden Zellen

Dörrbecker, B. (2011) · doi:10.53846/goediss-474

An in vitro approach to unravel the modulation of the hypothalamic system by blood-circulating factors

Martins, J. P., Alves, C. J., Neto, E., Leite, D. M., Xavier, M., Sousa, D. M., Alencastre, I. S., & Lamghari, M. (2015) · IEEE Portuguese Meeting on Bioengineering · doi:10.1109/enbeng.2015.7088886

Overenthousiast immuunsysteem pakt ongelukkig uit

Korte, S. M., van Heesch, F., Prins, J., Oosting, R. S., Kraneveld, A. D., Garssen, J., & Olivier, B. (2013) · Neuropraxis · doi:10.1007/s12474-013-0030-z

Ionenkanalmodulation durch Interferon in Layer V Pyramidenneuronen des somatosensorischen Cortex

Stadler, K. (2012) · Universitätsbibliothek der FU Berlin Hochschulschriftenstelle u. Dokumentenserver · doi:10.17169/refubium-7605

Delirium in the elderly: biomarkers and outcomes

Witlox, J. (2012) · UvA-DARE (University of Amsterdam)

Angefertigt mit Genehmigung der Mathematisch-Naturwissenschaftlichen Fakultät der

Bonn, R. F.-W.-U. (2012)

Tumour necrosis FA cTor - ALPHA mediAT ed mecHAnisms oF cogniT ive dysF unc Tion 1 Discipline of Psychiatry, School of Medicine,

Baune, B. T., Camara, M.-L., Eyre, H. A., Jawahar, M. C., Anscomb, H., & Körner, H. (2012)

Coadministração de aminoácidos de cadeia ramificada e lipopolissacarídeo causam quebra da barreira hematoencefálica

Morais, M. O. D. S. (2013)

Four Narcolepsy Cases after H1N1 Infection or Vaccination

Kim, T. W., Kim, H. J., Kang, D. W., Kwak, H. J., & Hong, S. (2015) · Sleep Medicine Research · doi:10.17241/smr.2015.6.1.38

A Role for Orexin Neuron Activity in Cytotoxic Chemotherapy-Induced Fatigue

Weymann, K. B. (2013) · doi:10.6083/m4n29vnp

Role of Mitochondria in TNF-alpha Neurotoxicity in Stroke

Doll, D. N. (2015) · doi:10.33915/etd.5502

Immunotherapy for High-Grade Gliomas

Schaller, T. H., & Sampson, J. H. (2016) · Springer eBooks · doi:10.1007/978-3-319-49864-5_12

Contemporary anti-inflammatory treatment approaches

Reza, H. M., & Al-Amin, M. M. (2014)

Microglial Location, Morphology, and Cognitive Performance in Mold-Exposed Mice

Marmon, K. (2017) · CUNY Academic Works (City University of New York)

Molecular Mimicry may Underlie a Worm-Associated Epilepsy Syndrome

Lyman, K. A., & Chetkovich, D. M. (2018) · Epiliepsy currents/Epilepsy currents · doi:10.5698/1535-7597.18.3.180

Discrepancy in Microglia and Peripheral Monocytic Cells - A scope in the Pathophysiology of Psychiatric maladies

Jes, P. (2018) · Journal of Neuroscience and Neurological Disorders · doi:10.29328/journal.jnnd.1001011

Relationship of inflammatory response and mood to high-intensity interval exercise

Kemp, R. N., Loh, R., Howe, C. C. F., & Moir, H. J. (2018) · Translational Sports Medicine · doi:10.1002/tsm2.50

Análise transcriptômica em estruturas encefálicas de ratos jovens e idosos submetidos ao modelo de ligadura e perfuração cecal

Hamasaki, M. Y. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2018.tde-11092018-154135

PENINGKATAN EKSPRESI LAMININ NAMUN TIDAK VE-CADHERIN PADA SAWAR DARAH OTAK SETELAH INFEKSI Mycobacterium tuberculosis INTRAPULMONALIS

Widayati, A., Wulandari, L., & Riawan, W. (2018) · majalah kesehatan · doi:10.21776/ub.majalahkesehatan.005.03.3

Perioperative Neurocognitive Disorder Mitigation Strategies

Eckenhoff, R. G., & Terrando, N. (2019) · Cambridge University Press eBooks · doi:10.1017/9781316402504.017

Brain-gut axis: From the conditioned reflex to the microbiota-gut-brain communication system

Gyires, K. (2020) · Integrative Physiology · doi:10.33910/2687-1270-2020-1-4-266-276

Köpeklerde ve Kedilerde Epilepsi ve Etiyopatogenezisi

ARIBURNU, N., & Tunç, A. S. (2021) · Cumhuriyet Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi · doi:10.51754/cusbed.871042

Therapeutic role and importance of gut microbiota in brain and related disorder: A review

Kundu Smita, S., & Rana, D. G. (2021) · Asian Journal of Pharmacy and Pharmacology · doi:10.31024/ajpp.2021.7.1.6

Investigation of the endocannabinoid system using in vivo and in vitro models

Ternes, S. (2013) · bonndoc (University of Bonn)

POTENTIAL USE OF SULFORAPHANE AS A NEUROPROTECTOR

Tsiumpala, S. A., Starchevska, K. M., & Lushchak, V. I. (2021) · Medical and Clinical Chemistry · doi:10.11603/mcch.2410-681x.2021.i2.12048

The effect of tert-butylhydroquinone, an Nrf2-ARE signaling pathway inducer, on oxidative stress-related neurodegeneration

Sun, J. (2015) · doi:10.33915/etd.6742

Alcohol

(2021) · Elsevier eBooks · doi:10.1016/b978-0-12-816793-9.00001-3

Influence of psychoactive substances on the immune system and involvement of the brain through immunologically-mediated mechanisms

Famitafreshi, H., & Karimian, M. (2021) · Alcoholism and Drug Addiction · doi:10.5114/ain.2021.113514

Dual-modal Assessment for in Vivo Investigation of Neurovascular Characteristic of Cerebral Edema Induced by LipopolysaccharidePreprint

Li, W., Zhang, Y., Xie, Q., Yang, Y., Yao, L., Ning, X., & Qian, Z. (2021) · Research Square · doi:10.21203/rs.3.rs-944735/v1

A role for LRRK2 and Neuroinflammatory Processes in Multi-Hit Toxicant Models of Parkinson’s Disease

Rudyk, C. (2018) · doi:10.22215/etd/2018-14444

Immune Responses in Infections of the Central Nervous System

Win, K. K., & Parmasivam, P. A. L. (2023) · Springer eBooks · doi:10.1007/978-981-99-6445-1_4 · Cited by 1

Insights in the Cross-Talk Between Microbiota-Gut-Brain Axis: A Focus on Alzheimer’s Disease

Soni, T., Jawanda, I. K., Kumari, S., & Prabha, V. (2023) · Springer eBooks · doi:10.1007/978-981-99-3126-2_22

Cytokine Expression Profiles in Children and Adolescents with Tic Disorders.Preprint

Kütük, Ö., Kütük, M. Ö., Tufan, A. E., Kılıçaslan, F., Gökçen, C., Aksu, G. G., Yektaş, Ç., Kandemır, H., Celik, F., Mutluer, T., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-3813261/v1

Additional file 3 of Regulation of blood–brain barrier integrity by microbiome-associated methylamines and cognition by trimethylamine N-oxide

Hoyles, L., Pontifex, M. G., Rodríguez‐Ramiro, I., Anis-Alavi, M. A., Jelane, K. S., Snelling, T., Solito, E., Fonseca, S., Carvalho, A. L., Carding, S. R., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17086980

Gut-Microbiota as a Therapeutic Intervention for Cognitive Damage

Hamdalla, H. M., Abdul‐Hamid, M., & Zaky, M. Y. (2024) · Springer eBooks · doi:10.1007/978-981-99-8803-7_11

Mecanismos moleculares de la epilepsia farmacorresistente

Lagger, I. A., Burgueño, A. L., (BIOMED)., L. P. I. D. I. B. U.-C., Garino, E., Martínez, O., Knorre, F., & Ernst, G. (2023) · Fronteras en Medicina · doi:10.31954/rfem/202301/0029-0036

Probiotic Supplements For Depression In Parkinson’s Disease (Pro-Park): A Randomized, Triple-Blind, Placebo-Controlled, Phase Iib Trial Protocol

Farina, G. S., Nirta, L., de Oliveira, L. M. L., Rospigliosi, O. L. C., Vespasiano, C. F. P., Woite, N. L., Zahran, I., Checo, M., Fernandes, K. B. P., Blinov, D., et al. (2024) · Principles and Practice of Clinical Research Journal · doi:10.21801/ppcrj.2024.102.5

Nanoparticle-mediated drug delivery for neurodegenerative diseases

Parhi, R. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-28822-7.00013-1

Crosstalk between gut-brain axis and brain components along with associated neurological disorders

Bindal, P., Kaushal, S., Singh, C., & Singh, A. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-21680-0.00005-5

CNS Targets of Adipokines

Beall, C., Hanna, L., & Ellacott, K. L. J. (2017) · Comprehensive physiology · doi:10.1002/j.2040-4603.2017.tb00781.x

Hypothèse immuno-inflammatoire dans les troubles bipolaires

Petit, A., & Gaillard, R. (2023) · Elsevier eBooks · doi:10.1016/b978-2-294-77180-4.00038-x

Arbutin improves spatial learning and memory in a lipopolysaccharide-induced neuroinflammation model via attenuating of astrocytes activation and oxidative stress

Pouramir, A., Nosratiyan, N., Askari, H., Ghasemi‐Kasman, M., Shirzad, M., & Pouramir, M. (2025) · Neuroscience Letters · doi:10.1016/j.neulet.2025.138356

The Role of Oral Microbiota and Glial Cell Dynamics in Relation to Gender in Cardiovascular Disease Risk

Ghosh, D., & Kumar, A. (2025) · Neuroglia · doi:10.3390/neuroglia6030030

USO DA BIOINFORMÁTICA PARA SELECIONAR MOLÉCULAS CANDIDATAS A FÁRMACOS

Costa, J. B., Santos, T. S. D., Franconi, L., Sathler, A. D. A., Pereira, M. B. D. M., & Antunes, J. E. (2025) · LUMEN ET VIRTUS · doi:10.56238/levv16n53-039

Histohematic Barriers

Shevlyuk, N. N., Blinova, E. V., & Фирдатович, Р. М. (2025) · Journal of Anatomy and Histopathology · doi:10.18499/2225-7357-2025-14-3-84-93

Antimicrobial Resistance and the Blood–Brain Barrier: Complex Interactions and Implications for Neurological Health

Semenova, Y., Dadar, M., Makalkina, L., Lim, L., & Bjørklund, G. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-05448-6 · Cited by 1

Talking to the Brain at the Blood-Brain Barrier through Inflammation-Induced Prostaglandin E2

Vasilache, A. M. (2015) · Linköping University medical dissertations · doi:10.3384/diss.diva-114378

Etude des interfaces sang/cerveau dans la région tubérale de l'hypothalamus médiobasal (rôle des tanycytes de l'éminence médiane)

Mullier, A., & Bouret, S. G. (2009) · OpenGrey (Institut de l'Information Scientifique et Technique)

Additional file 3 of Metabotropic glutamate receptor 5 inhibits α-synuclein-induced microglia inflammation to protect from neurotoxicity in Parkinson’s disease

Zhang, Y.-N., Fan, J.-K., Gu, L., Yang, H.-M., Zhan, S.-Q., & Zhang, H. (2021) · Figshare · doi:10.6084/m9.figshare.13605718

Additional file 2 of Metabotropic glutamate receptor 5 inhibits α-synuclein-induced microglia inflammation to protect from neurotoxicity in Parkinson’s disease

Zhang, Y.-N., Fan, J.-K., Gu, L., Yang, H.-M., Zhan, S.-Q., & Zhang, H. (2021) · Figshare · doi:10.6084/m9.figshare.13605715

Additional file 1 of Metabotropic glutamate receptor 5 inhibits α-synuclein-induced microglia inflammation to protect from neurotoxicity in Parkinson’s disease

Zhang, Y.-N., Fan, J.-K., Gu, L., Yang, H.-M., Zhan, S., & Zhang, H. (2021) · Figshare · doi:10.6084/m9.figshare.13605712

Additional file 2 of Regulation of blood–brain barrier integrity by microbiome-associated methylamines and cognition by trimethylamine N-oxide

Hoyles, L., Pontifex, M. G., Rodríguez‐Ramiro, I., Anis-Alavi, M. A., Jelane, K. S., Snelling, T., Solito, E., Fonseca, S., Carvalho, A. L., Carding, S. R., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17086974

Genome‐Wide Association Studies Data and Transcriptomics Data Link Herpes Simplex Virus 1 Infection and Parkinson’s Disease

Lu, C., CAI, X., Simula, E. R., Ercoli, T., Solla, P., & Sechi, L. A. (2025) · Parkinson s Disease · doi:10.1155/padi/4044371

Minor cannabinoids have pleiotropic effects on human brain microvascular endothelial activation and barrier functionPreprint

Qin, S., Ghazali, F., Nguyen, N. T., Tsutsui, K., Schumacher, M. A., Bonet, I. J. M., Lloyd, E., Xu, F., & Hellman, J. (2026) · Research Square · doi:10.21203/rs.3.rs-8982679/v1

The Blood–Brain Barriers

Banks, W. A., & Erickson, M. A. (2024) · Springer eBooks · doi:10.1007/978-3-031-68237-7_13

The blood-brain barrier in neuroimmunology: Tales of separation and assimilation

Banks, W. A. (2015) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2014.08.007 · Cited by 292

The Blood–Brain Barrier in Psychoneuroimmunology

Banks, W. A. (2009) · Immunology and Allergy Clinics of North America · doi:10.1016/j.iac.2009.02.001 · Cited by 37

The Blood Brain Barrier

Banks, W. A. (2008) · Springer eBooks · doi:10.1007/978-0-387-72573-4_4 · Cited by 16

Neuroimmune Axes of the Blood–Brain Barriers and Blood–Brain Interfaces: Bases for Physiological Regulation, Disease States, and Pharmacological Interventions

Erickson, M. A., & Banks, W. A. (2018) · Pharmacological Reviews · doi:10.1124/pr.117.014647 · Cited by 398