“Inflammatory” Cytokines: Neuromodulators in Normal Brain?

A metalloproteinase disintegrin that releases tumour-necrosis factor-α from cells

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Identification of a common nucleotide sequence in the 3'-untranslated region of mRNA molecules specifying inflammatory mediators.

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Cloning of a disintegrin metalloproteinase that processes precursor tumour-necrosis factor-α

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Regulation of the Hypothalamic-Pituitary-Adrenal Axis by Cytokines: Actions and Mechanisms of Action

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NF-kB: a crucial transcription factor for glial and neuronal cell function

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Interleukin-1 Type II Receptor: A Decoy Target for IL-1 That Is Regulated by IL-4

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Altered neuronal and microglial responses to excitotoxic and ischemic brain injury in mice lacking TNF receptors

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Cytokines and the nervous system II: actions and mechanisms of action

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Tumor Necrosis Factor-α: A Mediator of Focal Ischemic Brain Injury

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Cytokines and the nervous system I: expression and recognition

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NF-kappaB-associated MnSOD induction protects against beta-amyloid-induced neuronal apoptosis.

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Neuroinflammation in l-DOPA-induced dyskinesia: beyond the immune function

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BiP/GRP78-Induced Production of Cytokines and Uptake of Amyloid-β(1-42) Peptide in Microglia

Kakimura, J., Kitamura, Y., Taniguchi, T., Shimohama, S., & Gebicke‐Haerter, P. J. (2001) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2001.4299 · Cited by 48

Widely expressed transcripts for chemokine receptor CXCR1 in identified glutamatergic, γ‐aminobutyric acidergic, and cholinergic neurons and astrocytes of the rat brain: A single‐cell reverse transcription‐multiplex polymerase chain reaction study

Danik, M., Puma, C., Quirion, R., & Williams, S. (2003) · Journal of Neuroscience Research · doi:10.1002/jnr.10744 · Cited by 48

Cytokine and Inducible Nitric Oxide Synthase mRNA Expression during Experimental Murine Cryptococcal Meningoencephalitis

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Inflammation and clinical presentation in neurodegenerative disease: a volatile relationship

Bettcher, B. M., & Kramer, J. H. (2012) · Neurocase · doi:10.1080/13554794.2011.654227 · Cited by 49

Microglial self-defence mediated through GLT-1 and glutathione

Persson, M., & Rönnbäck, L. (2011) · Amino Acids · doi:10.1007/s00726-011-0865-7 · Cited by 47

Involvement of pro-inflammatory cytokines and microglia in an age-associated neurodegeneration model, the SAMP10 mouse

Kumagai, N., Chiba, Y., Hosono, M., Fujii, M., Kawamura, N., Keino, H., Yoshikawa, K., Ishii, S., Saitoh, Y., Satoh, M., et al. (2007) · Brain Research · doi:10.1016/j.brainres.2007.09.021 · Cited by 47

The immune system: a new look at pain

Zhang, J., & Huang, Y. (2006) · Chinese Medical Journal · doi:10.1097/00029330-200606010-00009 · Cited by 46

Disruption of the astrocytic TNFR1-GDNF axis accelerates motor neuron degeneration and disease progression in amyotrophic lateral sclerosis

Brambilla, L., Guidotti, G., Martorana, F., Iyer, A. M., Aronica, E., Valori, C. F., & Rossi, D. (2016) · Human Molecular Genetics · doi:10.1093/hmg/ddw161 · Cited by 47

Potentiating role of interleukin 2 (IL-2) receptors in the midbrain periaqueductal gray (PAG) upon defensive rage behavior in the cat: Role of neurokinin NK1 receptors

Bhatt, S., & Siegel, A. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.09.011 · Cited by 46

Interleukin‐1β, but not IL‐1α, mediates nerve growth factor secretion from rat astrocytes via type I IL‐1 receptor

Jurič, D. M., & Čarman‐Kržan, M. (2001) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(01)00044-2 · Cited by 46

Hippocampal Interleukin‐1β Gene Expression during Long‐Term Potentiation Decays with Age

Balschun, D., Randolf, A., Pitossi, F. J., Schneider, H., del Rey, A., & Besedovsky, H. O. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb03132.x · Cited by 46

The Role of Pro-inflammatory Cytokines in Memory Processes and Neural Plasticity

Goshen, I., & Yirmiya, R. (2007) · Elsevier eBooks · doi:10.1016/b978-012088576-3/50021-6 · Cited by 47

The analysis of correlation between IL-1B gene expression and genotyping in multiple sclerosis patients

Heidary, M., Rakhshi, N., Kakhki, M. P., Behmanesh, M., Sanati, M. H., Sanadgol, N., Kamaladini, H., & Nikravesh, A. (2014) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2014.05.013 · Cited by 51

Tumor Necrosis Factor Alpha in Amyotrophic Lateral Sclerosis: Friend or Foe?

Guidotti, G., Scarlata, C., Brambilla, L., & Rossi, D. (2021) · Cells · doi:10.3390/cells10030518 · Cited by 42

Reduced Immobility in the Forced Swim Test in Mice with a Targeted Deletion of the Leukemia Inhibitory Factor (LIF) Gene

Pechnick, R. N., Chesnokova, V., Kariagina, A., Price, S., Bresee, C. J., & Poland, R. E. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300402 · Cited by 43

Multiple lipopolysaccharide (LPS) injections alter interleukin 6 (IL-6), IL-7, IL-10 and IL-6 and IL-7 receptor mRNA in CNS and spleen.

Szot, P., Franklin, A., Figlewicz, D., Beuca, T. P., Bullock, K. M., Hansen, K., Banks, W., Raskind, M., & Peskind, E. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.04.028 · Cited by 39

Evaluation of IL-1β levels in epilepsy and traumatic brain injury in dogs

Kostic, D., Carlson, R., Henke, D., Röhn, K., & Tipold, A. (2019) · BMC Neuroscience · doi:10.1186/s12868-019-0509-5 · Cited by 41

Acute IL-1RA treatment suppresses the peripheral and central inflammatory response to spinal cord injury

Yates, A. G., Jogia, T., Gillespie, E. R., Couch, Y., Ruitenberg, M. J., & Anthony, D. C. (2021) · Journal of Neuroinflammation · doi:10.1186/s12974-020-02050-6 · Cited by 42

Selective increases in the cytokine, TNFα, in the prefrontal cortex of PCP-treated rats and human schizophrenic subjects: influence of antipsychotic drugs

Paterson, G., Ohashi, Y., Reynolds, G. P., Pratt, J. A., & MORRIS, B. J. (2006) · Journal of Psychopharmacology · doi:10.1177/0269881106062025 · Cited by 41

Interleukin-1α regulates substance P expression and release in adult sensory neurons

Skoff, A. M., Zhao, C., & Adler, J. E. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.03.022 · Cited by 40

Effects of Serotonergic Activation by 5-Hydroxytryptophan on Sleep and Body Temperature of C57BL/6J and Interleukin-6-Deficient Mice are Dose and Time Related

Morrow, J. D., Vikraman, S., Imeri, L., & Opp, M. R. (2008) · SLEEP · doi:10.1093/sleep/31.1.21 · Cited by 40

Upregulation of type I interleukin−1 receptor after traumatic spinal cord injury in adult rats

Wang, X., Huang, L.-D., Yu, P.-P., Hu, J., Yin, L., Wang, L., Xu, X., & Lu, P. (2006) · Acta Neuropathologica · doi:10.1007/s00401-005-0016-x · Cited by 41

Acute Cocaine Increases Interleukin-1β mRNA and Immunoreactive Cells in the Cortex and Nucleus Accumbens

Cearley, C. N., Blindheim, K., Sorg, B. A., Krueger, J. M., & Churchill, L. (2011) · Neurochemical Research · doi:10.1007/s11064-011-0410-9 · Cited by 40

Pathophysiology of Nasal Symptoms

Eccles, R. (2000) · American Journal of Rhinology · doi:10.2500/105065800781329528 · Cited by 39

Cytokine production as a putative biological mechanism underlying stress sensitization in high combat exposed soldiers

Smid, G. E., van Zuiden, M., Geuze, E., Kavelaars, A., Heijnen, C. J., & Vermetten, E. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2014.07.010 · Cited by 38

Distinct cytokine profile in SIDS brain

Kadhim, H. J., Kahn, A., & Sébire, G. (2003) · Neurology · doi:10.1212/01.wnl.0000092014.14997.47 · Cited by 38

Interleukin-1β and Interleukin-1 Receptor Antagonist Appear in Grey Matter Additionally to White Matter Lesions during Experimental Multiple Sclerosis

Prins, M., Eriksson, C., Wierinckx, A., Bol, J. G. J. M., Binnekade, R., Tilders, F. J. H., & van Dam, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0083835 · Cited by 37

Brain homeostasis is maintained by “danger” signals stimulating a supportive immune response within the brain’s borders

Ron‐Harel, N., Cardon, M., & Schwartz, M. (2010) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2010.12.011 · Cited by 37

Alterations in the Interplay between Neurons, Astrocytes and Microglia in the Rat Dentate Gyrus in Experimental Models of Neurodegeneration

Lana, D., Ugolini, F., Nosi, D., Wenk, G. L., & Giovannini, M. G. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00296 · Cited by 39

Interleukin-1β mediates GDNF up-regulation upon dopaminergic injury in ventral midbrain cell cultures

Saavedra, A., Baltazar, G., & Duarte, E. P. (2006) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.08.019 · Cited by 37

Slit modulates cerebrovascular inflammation and mediates neuroprotection against global cerebral ischemia

Altay, T., McLaughlin, B., Wu, J. Y., Park, T. S., & Gidday, J. M. (2007) · Experimental Neurology · doi:10.1016/j.expneurol.2007.06.028 · Cited by 36

Inhibition of caspase-1 in rat brain reduces spontaneous nonrapid eye movement sleep and nonrapid eye movement sleep enhancement induced by lipopolysaccharide

Imeri, L., Bianchi, S., & Opp, M. R. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00828.2005 · Cited by 36

Microglia modulate TNFα ‐mediated synaptic plasticity

Kleidonas, D., Kirsch, M., Andrieux, G., Pfeifer, D., Boerries, M., & Vlachos, A. (2023) · Glia · doi:10.1002/glia.24383 · Cited by 37

Changes in Serum Tumor Necrosis Factor (TNF-α) with Kami-Shoyo-San Administration in Depressed Climacteric Patients

Ushiroyama, T., Ikeda, A., Sakuma, K., & Ueki, M. (2004) · The American Journal of Chinese Medicine · doi:10.1142/s0192415x04002259 · Cited by 35

Up-regulation of A2A adenosine receptors by proinflammatory cytokines in rat PC12 cells

Trincavelli, M. L., Costa, B., Tuscano, D., Lucacchini, A., & Martini, C. (2002) · Biochemical Pharmacology · doi:10.1016/s0006-2952(02)01222-4 · Cited by 35

Brain Arteriovenous Malformations Are Associated With Interleukin-1 Cluster Gene Polymorphisms

Fontanella, M. M., Rubino, E., Crobeddu, E., Gallone, S., Gentile, S., Garbossa, D., Ducati, A., Pinessi, L., & Rainero, I. (2011) · Neurosurgery · doi:10.1227/neu.0b013e31822d9881 · Cited by 35

Neuroprotective effect of TNFα against the β-amyloid neurotoxicity mediated by CDK5 kinase

Orellana, D. I., Quintanilla, R. A., & Maccioni, R. B. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.10.010 · Cited by 36

Increased expression of ICAM-1 among symptomatic neurocysticercosis

Prasad, A., Prasad, K. N., Gupta, R. K., & Pradhan, S. (2008) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2008.09.015 · Cited by 34

REM sleep deprivation increases the expression of interleukin genes in mice hypothalamus

Kang, W. S., Park, H. J., Chung, J.-H., & Kim, J. W. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2013.09.050 · Cited by 33

Cytokine mRNA induction by interleukin-1β or tumor necrosis factor α in vitro and in vivo

Taishi, P., Churchill, L., De, A., Obál, F., & Krueger, J. M. (2008) · Brain Research · doi:10.1016/j.brainres.2008.05.067 · Cited by 33

Application of Nucleus Pulposus to L5Dorsal Root Ganglion in Rats Enhances Nociceptive Dorsal Horn Neuronal Windup

Cuéllar, J. M., Montesano, P. X., Antognini, J. F., & Carstens, E. E. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00762.2004 · Cited by 32

Regulation of the cyclooxygenase-2 system by interleukin-1β through mitogen-activated protein kinase signaling pathways: A comparative study of human neuroglioma and neuroblastoma cells

Moolwaney, A. S., & Igwe, O. J. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2005.03.010 · Cited by 32

Comorbidity of depressive and dermatologic disorders - therapeutic aspects.

Filaković, P., Petek, A., Koić, O., Radanović-Grgurić, L., & Degmečić, D. (2009) · PubMed · Cited by 31

Fundamental role of pan-inflammation and oxidative-nitrosative pathways in neuropathogenesis of Alzheimer's disease in focal cerebral ischemic rats.

Daulatzai, M. A. (2016) · Europe PMC (PubMed Central) · Cited by 31

Associations between systemic pro-inflammatory markers, cognitive function and cognitive complaints in a population-based sample of working adults

Stenfors, C. U. D., Jónsdóttir, I. H., Hanson, L. L. M., & Theorell, T. (2017) · Journal of Psychosomatic Research · doi:10.1016/j.jpsychores.2017.03.010 · Cited by 32

Why inflammation and the activities of the immune system matter for social and personality psychology (and not only for those who study health)

Gassen, J., & Hill, S. E. (2019) · Social and Personality Psychology Compass · doi:10.1111/spc3.12471 · Cited by 34

A Molecular Perspective on Understanding and Modulating the Performance of Chronic Central Nervous System (CNS) Recording Electrodes

He, W. J., & Bellamkonda, R. V. (2007) · Frontiers in neuroengineering series/Frontiers in neuroengineering · doi:10.1201/9781420009309.pt4 · Cited by 32

Antidepressant drugs and cytokines in mood disorders

Nishida, A., Hisaoka, K., Zensho, H., Uchitomi, Y., Morinobu, S., & Yamawaki, S. (2002) · International Immunopharmacology · doi:10.1016/s1567-5769(02)00190-x · Cited by 31

Effects of Central Injection of Anti-LPS Antibody and Blockade of TLR4 on GnRH/LH Secretion during Immunological Stress in Anestrous Ewes

Haziak, K., Herman, A. P., & Tomaszewska-Zaremba, D. (2014) · Mediators of Inflammation · doi:10.1155/2014/867170 · Cited by 31

Cytokine mRNA levels in brain and peripheral tissues of the rat: relationships with plus-maze behavior

Pawlak, C. R., Schwarting, R. K. W., & Bauhofer, A. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2005.03.002 · Cited by 31

The association of genetic variants in interleukin-1 genes with cognition: Findings from the cardiovascular health study

Benke, K. S., Carlson, M. C., Doan, B. Q., Walston, J. D., Xue, Q., Reiner, A. P., Fried, L. P., Arking, D. E., Chakravarti, A., & Fallin, M. D. (2011) · Experimental Gerontology · doi:10.1016/j.exger.2011.09.005 · Cited by 31

Influenza A(H1N1) vaccination during early pregnancy transiently promotes hippocampal neurogenesis and working memory. Involvement of Th1/Th2 balance

Xia, Y., Qi, F., Zou, J., & Yao, Z. (2014) · Brain Research · doi:10.1016/j.brainres.2014.09.076 · Cited by 29

Peripheral Injection of SB203580 Inhibits the Inflammatory-Dependent Synthesis of Proinflammatory Cytokines in the Hypothalamus

Herman, A. P., Krawczyńska, A., Bochenek, J., Antushevich, H., Herman, A., & Tomaszewska-Zaremba, D. (2014) · BioMed Research International · doi:10.1155/2014/475152 · Cited by 30

IL-1β inhibits axonal growth of developing sympathetic neurons

Nolan, A. M., Nolan, Y. M., & O’Keeffe, G. W. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2011.07.003 · Cited by 29

Monocytes infected withMycobacterium tuberculosisregulate MAP kinase-dependent astrocyte MMP-9 secretion

Harris, J. E., Green, J. A., Elkington, P. T., & Friedland, J. S. (2006) · Journal of Leukocyte Biology · doi:10.1189/jlb.0806512 · Cited by 29

Involvement of nitric oxide in lipopolysaccharide induced anorexia

Riediger, T., Cordani, C., Potes, C. S., & Lutz, T. A. (2010) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2010.04.015 · Cited by 29

Development of functional units within trigeminal ganglia correlates with increased expression of proteins involved in neuron–glia interactions

Durham, P. L., & Garrett, F. G. (2010) · Neuron Glia Biology · doi:10.1017/s1740925x10000232 · Cited by 29

Haplotypes in the expression quantitative trait locus of interleukin-1β gene are associated with schizophrenia

Yoshida, M., Shiroiwa, K., Mouri, K., Ishiguro, H., Supriyanto, I., Ratta‐apha, W., Eguchi, N., Okazaki, S., Sasada, T., Fukutake, M., et al. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.06.031 · Cited by 31

Time-dependent in-vivo effects of interleukin-2 on neurotransmitters in various cortices: Relationships with depressive-related and anxiety-like behaviour

Karrenbauer, B. D., Müller, C. P., Ho, Y., Spanagel, R., Huston, J. P., Schwarting, R. K. W., & Pawlak, C. R. (2011) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2011.05.011 · Cited by 30

Recombinant Human TNF α Induces Concentration-Dependent and Reversible Alterations in the Electrophysiological Properties of Axons in Mammalian Spinal Cord

Davies, A. L., Hayes, K. C., & Shi, R. (2006) · Journal of Neurotrauma · doi:10.1089/neu.2006.23.1261 · Cited by 29

Recent advances in psychoneuroimmunology: Inflammation in psychiatric disorders

Debnath, M., Doyle, K., Langan, C., McDonald, C., Leonard, B., & Cannon, D. (2011) · Translational Neuroscience · doi:10.2478/s13380-011-0019-0 · Cited by 28

Persistent Neuroinflammation and Brain-Specific Immune Priming in a Novel Survival Model of Murine Pneumosepsis

Denstaedt, S. J., Spencer-Segal, J. L., Newstead, M. W., Laborc, K. F., Zeng, X., Standiford, T. J., & Singer, B. H. (2019) · Shock · doi:10.1097/shk.0000000000001435 · Cited by 28

G-CSF attenuates neuroinflammation and neuronal apoptosis via the mTOR/p70SK6 signaling pathway in neonatal Hypoxia-Ischemia rat model

Dumbuya, J. S., Chen, L., Shu, S., Ma, L., Luo, W., Li, F., Wu, J., & Wang, B. (2020) · Brain Research · doi:10.1016/j.brainres.2020.146817 · Cited by 28

Expression of Interleukin (IL)‐1β and IL‐1 Receptors Genes in the Hypothalamus of Anoestrous Ewes after Lipopolysaccharide Treatment

Herman, A. P., Misztal, T., Herman, A., & Tomaszewska-Zaremba, D. (2010) · Reproduction in Domestic Animals · doi:10.1111/j.1439-0531.2010.01595.x · Cited by 27

DJ-1 mutation decreases astroglial release of inflammatory mediators

Ashley, A. K., Hinds, A., Hanneman, W. H., Tjalkens, R. B., & Legare, M. E. (2015) · NeuroToxicology · doi:10.1016/j.neuro.2015.12.007 · Cited by 28

Essential Dietary Bioactive Lipids in Neuroinflammatory Diseases

Catani, M. V., Gasperi, V., Bisogno, T., & Maccarrone, M. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2016.6958 · Cited by 28

Emerging Importance of Neuron-Satellite Glia Interactions within Trigeminal Ganglia in Craniofacial Pain

Durham, P. L., & Garrett, F. G. (2010) · The Open Pain Journal · doi:10.2174/1876386301003010003 · Cited by 27

Investigation of the effects of short-term inhalation of carbon nanoparticles on brains and lungs of c57bl/6j and p47phox−/− mice

van Berlo, D., Hullmann, M., Wessels, A., Scherbart, A. M., Cassee, F. R., Gerlofs-Nijland, M. E., Albrecht, C., & Schins, R. P. F. (2014) · NeuroToxicology · doi:10.1016/j.neuro.2014.04.008 · Cited by 26

Thermal stress induces a positive phenotypic and molecular feedback loop in zebrafish embryos

Feugere, L., Scott, V. F., Rodriguez‐Barucg, Q., Beltrán-Álvarez, P., & Valero, K. C. W. (2021) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2021.103114 · Cited by 26

Lack of association between the interleukin-1alpha gene C(−889)T polymorphism and Alzheimer's disease in a Chinese population

Tsai, S., Liu, H.-C., Liu, T., WANG, K.-Y., & Hong, C. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(03)00333-1 · Cited by 26

Neuromodulatory role of endogenous interleukin-1β in acute seizures: Possible contribution of cyclooxygenase-2

Claycomb, R., Hewett, S. J., & Hewett, J. A. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.08.007 · Cited by 26

Effects of Electroconvulsive Therapy on Some Inflammatory Factors in Patients With Treatment-Resistant Schizophrenia

Kartalcı, Ş., Karabulut, A. B., Erbay, L. G., & Acar, C. (2016) · Journal of Ect · doi:10.1097/yct.0000000000000303 · Cited by 26

Biologically active neutrophil chemokine pattern in tonsillitis

Rudack, C., JÖRG, S., & Sachse, F. B. (2004) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2003.02390.x · Cited by 26

Propofol anesthesia induces proapoptotic tumor necrosis factor‐α and pro‐nerve growth factor signaling and prosurvival Akt and XIAP expression in neonatal rat brain

Milanović, D., Pešić, V., Popić, J., Tanić, N., Kanazir, S., Jevtović‐Todorović, V., & Ruždijić, S. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23409 · Cited by 25

Cytokines and memory across the mature life span of women

Lekander, M., von Essen, J., Schultzberg, M., Andréasson, A., Garlind, A., Hansson, L., & Nilsson, L. (2011) · Scandinavian Journal of Psychology · doi:10.1111/j.1467-9450.2010.00865.x · Cited by 25

A Neurologist’s Guide to TNF Biology and to the Principles behind the Therapeutic Removal of Excess TNF in Disease

Clark, I. A., & Vissel, B. (2015) · Neural Plasticity · doi:10.1155/2015/358263 · Cited by 25

Immunobiology of Organ Transplantation

Wilkes, D. S., & Burlingham, W. J. (2004) · Springer eBooks · doi:10.1007/978-1-4419-8999-4 · Cited by 25

Neuroimmmune interactions of cannabinoids in neurogenesis: focus on interleukin-1β (IL-1β) signalling

García‐Ovejero, D., Arévalo‐Martín, Á., Navarro‐Galve, B., Pinteaux, E., Molina‐Holgado, E., & Molina‐Holgado, F. (2013) · Biochemical Society Transactions · doi:10.1042/bst20130198 · Cited by 26

The Immune System and the Developing Brain

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Inflammatory markers associated with electroconvulsive therapy response in patients with depression: A meta-analysis

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