Brain Tissue Homogenizer & Homogenization Protocol

Ideal for Brain Tissue Homogenization

Do you spend lots of time and effort homogenizing brain tissue samples? The Bullet Blender® tissue homogenizer delivers high quality and superior yields. No other homogenizer comes close to delivering the Bullet Blender’s winning combination of top-quality performance and budget-friendly affordability. See below for a brain tissue homogenization protocol.

Save Time, Effort and Get Superior Results with

The Bullet Blender Homogenizer

Consistent and High Yield Results

Run up to 24 samples at the same time under microprocessor-controlled conditions, ensuring experimental reproducibility and high yield. Process samples from 10mg or less up to 3.5g.

No Cross Contamination

No part of the Bullet Blender ever touches the tissue – the sample tubes are kept closed during homogenization. There are no probes to clean between samples.

Samples Stay Cool

The Bullet Blenders’ innovative and elegant design provides convective cooling of the samples, so they do not heat up more than several degrees. In fact, our Gold+ models hold the sample temperature to about 4ºC.

Easy and Convenient to Use

Just place beads and buffer along with your tissue sample in standard tubes, load tubes directly in the Bullet Blender, select time and speed, and press start.

Risk Free Purchase

Thousands of peer-reviewed journal articles attest to the consistency and quality of the Bullet Blender homogenizer. We offer a 2 year warranty, extendable to 4 years, because our Bullet Blenders are reliable and last for many years.  

Brain Tissue Homogenization Protocol

Sample Tube Protocol
1.5 mL tubes 1.5 mL tubes Brain Protocol
1.5/2 mL tubes using 5 mL adapters 1.5/2 mL tubes using 5 mL adapters Brain Protocol
5 mL tubes 5 mL tubes Brain Protocol

What Else Can You Homogenize? Tough or Soft, No Problem! 

The Bullet Blender can process a wide range of samples including organ tissue, cell culture, plant tissue, and small organisms. You can homogenize samples as tough as mouse femur or for gentle applications such as tissue dissociation or organelle isolation.

the Bullet Blender high-throughput tissue homogenizer

Brain tissue pieces (on beads in upper photo) are completely homogenized into the buffer (slightly darker in lower photo).

Want more guidance? Need a quote? Contact us:



    Bullet Blender Models

    Select Publications using the Bullet Blender to Homogenize Brain Tissue

    O’Leary, S., Prasai, A., Robledo, A., Thang, C., Wang, Y., Deshpande, R. R., Russell, W. K., Murton, A. J., Wolf, S. E., & El Ayadi, A. (2025). Altered lipid profiles in the prefrontal cortex are associated with neuroinflammation after severe burn injury. Frontiers in Immunology, 16, 1709256. https://doi.org/10.3389/fimmu.2025.1709256
    Štefková-Mazochová, K., Danda, H., Mazoch, V., Olejníková-Ladislavová, L., Šíchová, K., Paškanová, N., Vágnerová, M., Jurásek, B., Ryšánek, P., Šíma, M., Šafanda, A., Bui, Q. H., Kuchař, M., & Páleníček, T. (2025). The acute effects of methoxphenidine on behaviour and pharmacokinetics profile in animal model. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 137, 111285. https://doi.org/10.1016/j.pnpbp.2025.111285
    Aloui, L., Greene, E. S., Tabler, T., Lassiter, K., Thompson, K., Bottje, W. G., Orlowski, S., & Dridi, S. (2024). Effect of heat stress on the hypothalamic expression profile of water homeostasis‐associated genes in low‐ and high‐water efficient chicken lines. Physiological Reports, 12(5), e15972. https://doi.org/10.14814/phy2.15972
    Kimble, A. L., Silva, J., Omar, O. M., Murphy, M., Hensel, J. A., Nicholas, S.-A. E., Jellison, E. R., Reese, B., & Murphy, P. A. (2022). A method for rapid flow-cytometric isolation of endothelial nuclei and RNA from archived frozen brain tissue. Laboratory Investigation, 102(2), 204–211. https://doi.org/10.1038/s41374-021-00698-z
    Gallart-Palau, X., Guo, X., Serra, A., & Sze, S. K. (2020). Alzheimer’s disease progression characterized by alterations in the molecular profiles and biogenesis of brain extracellular vesicles. Alzheimer’s Research & Therapy, 12(1), 54. https://doi.org/10.1186/s13195-020-00623-4
    Reichard, A., & Asosingh, K. (2019). Best Practices for Preparing a Single Cell Suspension from Solid Tissues for Flow Cytometry. Cytometry Part A, 95(2), 219–226. https://doi.org/10.1002/cyto.a.23690
    Mahinrad, S., Bulk, M., van der Velpen, I., Mahfouz, A., van Roon-Mom, W., Fedarko, N., Yasar, S., Sabayan, B., van Heemst, D., & van der Weerd, L. (2018). Natriuretic Peptides in Post-mortem Brain Tissue and Cerebrospinal Fluid of Non-demented Humans and Alzheimer’s Disease Patients. Frontiers in Neuroscience, 12, 864. https://doi.org/10.3389/fnins.2018.00864
    Volovitz, I., Shapira, N., Ezer, H., Gafni, A., Lustgarten, M., Alter, T., Ben-Horin, I., Barzilai, O., Shahar, T., Kanner, A., Fried, I., Veshchev, I., Grossman, R., & Ram, Z. (2016). A non-aggressive, highly efficient, enzymatic method for dissociation of human brain-tumors and brain-tissues to viable single-cells. BMC Neuroscience, 17(1), 30. https://doi.org/10.1186/s12868-016-0262-y
    Pinacho, R., Vila, E., Prades, R., Tarragó, T., Castro, E., Ferrer, I., & Ramos, B. (2016). The glial phosphorylase of glycogen isoform is reduced in the dorsolateral prefrontal cortex in chronic schizophrenia. Schizophrenia Research. https://doi.org/10.1016/j.schres.2016.04.024
    Kim, J. M., Park, S. K., Guo, T. J., Kang, J. Y., Ha, J. S., Lee, D. S., Lee, U., & Heo, H. J. (2016). Anti-amnesic effect of Dendropanax morbifera via JNK signaling pathway on cognitive dysfunction in high-fat diet-induced diabetic mice. Behavioural Brain Research, 312, 39–54. https://doi.org/10.1016/j.bbr.2016.06.013
    Hubbard, J. A., Szu, J. I., Yonan, J. M., & Binder, D. K. (2016). Regulation of astrocyte glutamate transporter-1 (GLT1) and aquaporin-4 (AQP4) expression in a model of epilepsy. Experimental Neurology. https://doi.org/10.1016/j.expneurol.2016.05.003
    Murray, H. C., Low, V. F., Swanson, M. E. V., Dieriks, B. V., Turner, C., Faull, R. L. M., & Curtis, M. A. (2016). Distribution of PSA-NCAM in normal, Alzheimer’s and Parkinson’s disease human brain. Neuroscience, 330, 359–375. https://doi.org/10.1016/j.neuroscience.2016.06.003
    David, C. N., Frias, E. S., Szu, J. I., Vieira, P. A., Hubbard, J. A., Lovelace, J., Michael, M., Worth, D., McGovern, K. E., Ethell, I. M., Stanley, B. G., Korzus, E., Fiacco, T. A., Binder, D. K., & Wilson, E. H. (2016). GLT-1-Dependent Disruption of CNS Glutamate Homeostasis and Neuronal Function by the Protozoan Parasite Toxoplasma gondii. PLOS Pathog, 12(6), e1005643. https://doi.org/10.1371/journal.ppat.1005643
    Perland, E., Lekholm, E., Eriksson, M. M., Bagchi, S., Arapi, V., & Fredriksson, R. (2016). The Putative SLC Transporters Mfsd5 and Mfsd11 Are Abundantly Expressed in the Mouse Brain and Have a Potential Role in Energy Homeostasis. PLOS ONE, 11(6), e0156912. https://doi.org/10.1371/journal.pone.0156912
    Kumar, M., Belcaid, M., & Nerurkar, V. R. (2016). Identification of host genes leading to West Nile virus encephalitis in mice brain using RNA-seq analysis. Scientific Reports, 6. https://doi.org/10.1038/srep26350
    Vadnie, C. A., Ayers-Ringler, J., Oliveros, A., Abulseoud, O. A., Choi, S., Hitschfeld, M. J., & Choi, D.-S. (2016). Antipsychotic-like effects of a neurotensin receptor type 1 agonist. Behavioural Brain Research, 305, 8–17. https://doi.org/10.1016/j.bbr.2016.02.019
    Hoover, C. E., Davenport, K. A., Henderson, D. M., Pulscher, L. A., Mathiason, C. K., Zabel, M. D., & Hoover, E. A. (2016). Detection and Quantification of CWD Prions in Fixed Paraffin Embedded Tissues by Real-Time Quaking-Induced Conversion. Scientific Reports, 6. https://doi.org/10.1038/srep25098
    Lui, H., Zhang, J., Makinson, S. R., Cahill, M. K., Kelley, K. W., Huang, H.-Y., Shang, Y., Oldham, M. C., Martens, L. H., Gao, F., Coppola, G., Sloan, S. A., Hsieh, C. L., Kim, C. C., Bigio, E. H., Weintraub, S., Mesulam, M.-M., Rademakers, R., Mackenzie, I. R., … Huang, E. J. (2016). Progranulin Deficiency Promotes Circuit-Specific Synaptic Pruning by Microglia via Complement Activation. Cell, 165(4), 921–935. https://doi.org/10.1016/j.cell.2016.04.001
    Zeng, X., Wang, H., Xing, X., Wang, Q., & Li, W. (2016). Dexmedetomidine Protects against Transient Global Cerebral Ischemia/Reperfusion Induced Oxidative Stress and Inflammation in Diabetic Rats. PLOS ONE, 11(3), e0151620. https://doi.org/10.1371/journal.pone.0151620
    Ayers-Ringler, J. R., Oliveros, A., Qiu, Y., Lindberg, D. M., Hinton, D. J., Moore, R. M., Dasari, S., & Choi, D.-S. (2016). Label-Free Proteomic Analysis of Protein Changes in the Striatum during Chronic Ethanol Use and Early Withdrawal. Frontiers in Behavioral Neuroscience, 10. https://doi.org/10.3389/fnbeh.2016.00046
    Bosch, M., Fajardo, A., Alcalá-Vida, R., Fernández-Vidal, A., Tebar, F., Enrich, C., Cardellach, F., Pérez-Navarro, E., & Pol, A. (2016). Hepatic Primary and Secondary Cholesterol Deposition and Damage in Niemann-Pick Disease. The American Journal of Pathology, 186(3), 517–523. https://doi.org/10.1016/j.ajpath.2015.12.002
    Bakmiwewa, S. M., Weiser, S., Grey, M., Heng, B., Guillemin, G. J., Ball, H. J., & Hunt, N. H. (2016). Synergistic induction of CXCL10 by interferon-gamma and lymphotoxin-alpha in astrocytes: Possible role in cerebral malaria. Cytokine, 78, 79–86. https://doi.org/10.1016/j.cyto.2015.11.024
    Viader, A., Ogasawara, D., Joslyn, C. M., Sanchez-Alavez, M., Mori, S., Nguyen, W., Conti, B., & Cravatt, B. F. (2016). A chemical proteomic atlas of brain serine hydrolases identifies cell type-specific pathways regulating neuroinflammation. eLife, 5, e12345. https://doi.org/10.7554/eLife.12345
    Luethy, L. N., Erickson, A. K., Jesudhasan, P. R., Ikizler, M., Dermody, T. S., & Pfeiffer, J. K. (2016). Comparison of three neurotropic viruses reveals differences in viral dissemination to the central nervous system. Virology, 487, 1–10. https://doi.org/10.1016/j.virol.2015.09.019
    Gallart-Palau, X., Lee, B. S. T., Adav, S. S., Qian, J., Serra, A., Park, J. E., Lai, M. K. P., Chen, C. P., Kalaria, R. N., & Sze, S. K. (2016). Gender differences in white matter pathology and mitochondrial dysfunction in Alzheimer’s disease with cerebrovascular disease. Molecular Brain, 9, 27. https://doi.org/10.1186/s13041-016-0205-7
    Gallart-Palau, X., Serra, A., & Sze, S. K. (2016). Enrichment of extracellular vesicles from tissues of the central nervous system by PROSPR. Molecular Neurodegeneration, 11, 41. https://doi.org/10.1186/s13024-016-0108-1
    Kim, J., Shim, J., Lee, S., Cho, W.-H., Hong, E., Lee, J. H., Han, J.-S., Lee, H. J., & Lee, K. W. (2016). Rg3-enriched ginseng extract ameliorates scopolamine-induced learning deficits in mice. BMC Complementary and Alternative Medicine, 16, 66. https://doi.org/10.1186/s12906-016-1050-z
    Hallgren, S., & Viberg, H. (2016). Postnatal exposure to PFOS, but not PBDE 99, disturb dopaminergic gene transcription in the mouse CNS. Environmental Toxicology and Pharmacology, 41, 121–126. https://doi.org/10.1016/j.etap.2015.11.016
    Tristán-Noguero, A., Díez, H., Jou, C., Pineda, M., Ormazábal, A., Sánchez, A., Artuch, R., & Garcia-Cazorla, À. (2015). Study of a fetal brain affected by a severe form of tyrosine hydroxylase deficiency, a rare cause of early parkinsonism. Metabolic Brain Disease. https://doi.org/10.1007/s11011-015-9780-z
    Hajkova, K., Jurasek, B., Sykora, D., Palenicek, T., Miksatkova, P., & Kuchar, M. (2015). Salting-out-assisted liquid–liquid extraction as a suitable approach for determination of methoxetamine in large sets of tissue samples. Analytical and Bioanalytical Chemistry. https://doi.org/10.1007/s00216-015-9221-1
    Wang, Y., Billon, C., Walker, J. K., & Burris, T. P. (2015). Therapeutic Effect of a Synthetic RORα/γ Agonist in an Animal Model of Autism. ACS Chemical Neuroscience. https://doi.org/10.1021/acschemneuro.5b00159
    Evers, M. M., Schut, M. H., Pepers, B. A., Atalar, M., van Belzen, M. J., Faull, R. L., Roos, R. A., & van Roon-Mom, W. M. (2015). Making (anti-) sense out of huntingtin levels in Huntington disease. Molecular Neurodegeneration, 10(1). https://doi.org/10.1186/s13024-015-0018-7
    Doldur-Balli, F., Ozel, M. N., Gulsuner, S., Tekinay, A. B., Ozcelik, T., Konu, O., & Adams, M. M. (2015). Characterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ). BMC Neuroscience, 16(1). https://doi.org/10.1186/s12868-015-0229-4
    Kumar, M., Roe, K., O’Connell, M., & Nerurkar, V. R. (2015). Induction of virus-specific effector immune cell response limits virus replication and severe disease in mice infected with non-lethal West Nile virus Eg101 strain. Journal of Neuroinflammation, 12(1). https://doi.org/10.1186/s12974-015-0400-y
    Khademi, S., Frye, M. A., Jeckel, K. M., Schroeder, T., Monnet, E., Irwin, D. C., Cole, P. A., Bell, C., Miller, B. F., & Hamilton, K. L. (2015). Hypoxia mediated pulmonary edema: potential influence of oxidative stress, sympathetic activation and cerebral blood flow. BMC Physiology, 15(1). https://doi.org/10.1186/s12899-015-0018-4
    Semple, B. D., Noble-Haeusslein, L. J., Gooyit, M., Tercovich, K. G., Peng, Z., Nguyen, T. T., Schroeder, V. A., Suckow, M. A., Chang, M., Raber, J., & Trivedi, A. (2015). Early Gelatinase Activity Is Not a Determinant of Long-Term Recovery after Traumatic Brain Injury in the Immature Mouse. PLOS ONE, 10(11), e0143386. https://doi.org/10.1371/journal.pone.0143386
    Falendysz, E. A., Lopera, J. G., Lorenzsonn, F., Salzer, J. S., Hutson, C. L., Doty, J., Gallardo-Romero, N., Carroll, D. S., Osorio, J. E., & Rocke, T. E. (2015). Further Assessment of Monkeypox Virus Infection in Gambian Pouched Rats (Cricetomys gambianus) Using In Vivo Bioluminescent Imaging. PLOS Neglected Tropical Diseases, 9(10), e0004130. https://doi.org/10.1371/journal.pntd.0004130
    Lee, M., Chen, Z., Tomlinson, B. N., Gooyit, M., Hesek, D., Juárez, M. R., Nizam, R., Boggess, B., Lastochkin, E., Schroeder, V. A., Wolter, W. R., Suckow, M. A., Cui, J., Mobashery, S., Gu, Z., & Chang, M. (2015). Water-Soluble MMP-9 Inhibitor Reduces Lesion Volume after Severe Traumatic Brain Injury. ACS Chemical Neuroscience, 6(10), 1658–1664. https://doi.org/10.1021/acschemneuro.5b00140
    Yuan, Z.-X., & Rapoport, S. I. (2015). Transient postnatal fluoxetine decreases brain concentrations of 20-HETE and 15-epi-LXA4, arachidonic acid metabolites in adult mice. Prostaglandins, Leukotrienes and Essential Fatty Acids (PLEFA), 101, 9–14. https://doi.org/10.1016/j.plefa.2015.07.002
    Yau, B., Mitchell, A. J., Too, L. K., Ball, H. J., & Hunt, N. H. (2015). Interferon-γ-Induced Nitric Oxide Synthase-2 Contributes to Blood/Brain Barrier Dysfunction and Acute Mortality in Experimental Streptococcus pneumoniae Meningitis. Journal of Interferon & Cytokine Research. https://doi.org/10.1089/jir.2015.0078
    Wong, R. Y., & Godwin, J. (2015). Neurotranscriptome profiles of multiple zebrafish strains. Genomics Data, 5, 206–209. https://doi.org/10.1016/j.gdata.2015.06.004
    Hallgren, S., Fredriksson, A., & Viberg, H. (2015). More signs of neurotoxicity of surfactants and flame retardants – Neonatal PFOS and PBDE 99 cause transcriptional alterations in cholinergic genes in the mouse CNS. Environmental Toxicology and Pharmacology, 40(2), 409–416. https://doi.org/10.1016/j.etap.2015.06.014
    Crowell, J., Hughson, A., Caughey, B., & Bessen, R. A. (2015). Host determinants of prion strain diversity independent of prion protein genotype. Journal of Virology, JVI.01586-15. https://doi.org/10.1128/JVI.01586-15
    Zhou, J., Coles, L. D., Kartha, R. V., Nash, N., Mishra, U., Lund, T. C., & Cloyd, J. C. (2015). Intravenous Administration of Stable-Labeled N-Acetylcysteine Demonstrates an Indirect Mechanism for Boosting Glutathione and Improving Redox Status. Journal of Pharmaceutical Sciences, 104(8), 2619–2626. https://doi.org/10.1002/jps.24482
    Xu, X.-F., Li, T., Wang, D.-D., Chen, B., Wang, Y., & Chen, Z.-Y. (2015). Integrin-linked Kinase is Essential for Environmental Enrichment Enhanced Hippocampal Neurogenesis and Memory. Scientific Reports, 5, 11456. https://doi.org/10.1038/srep11456
    Razafsky, D., & Hodzic, D. (2015). A variant of Nesprin1 giant devoid of KASH domain underlies the molecular etiology of autosomal recessive cerebellar ataxia type I. Neurobiology of Disease, 78, 57–67. https://doi.org/10.1016/j.nbd.2015.03.027
    Grasso, C. S., Tang, Y., Truffaux, N., Berlow, N. E., Liu, L., Debily, M.-A., Quist, M. J., Davis, L. E., Huang, E. C., Woo, P. J., Ponnuswami, A., Chen, S., Johung, T. B., Sun, W., Kogiso, M., Du, Y., Qi, L., Huang, Y., Hütt-Cabezas, M., … Monje, M. (2015). Functionally defined therapeutic targets in diffuse intrinsic pontine glioma. Nature Medicine, 21(6), 555–559. https://doi.org/10.1038/nm.3855
    Ciesielska, A., Sharma, N., Beyer, J., Forsayeth, J., & Bankiewicz, K. (2015). Carbidopa-Based Modulation of the Functional Effect of the AAV2-hAADC Gene Therapy in 6-OHDA Lesioned Rats. PLOS ONE, 10(4), e0122708. https://doi.org/10.1371/journal.pone.0122708
    Aryal, M., Vykhodtseva, N., Zhang, Y.-Z., & McDannold, N. (2015). Multiple sessions of liposomal doxorubicin delivery via focused ultrasound mediated blood–brain barrier disruption: A safety study. Journal of Controlled Release, 204, 60–69. https://doi.org/10.1016/j.jconrel.2015.02.033
    Crowell, J., Wiley, J. A., & Bessen, R. A. (2015). Lesion of the Olfactory Epithelium Accelerates Prion Neuroinvasion and Disease Onset when Prion Replication Is Restricted to Neurons. PLOS ONE, 10(3), e0119863. https://doi.org/10.1371/journal.pone.0119863
    Drew, P. D., Johnson, J. W., Douglas, J. C., Phelan, K. D., & Kane, C. J. M. (2015). Pioglitazone Blocks Ethanol Induction of Microglial Activation and Immune Responses in the Hippocampus, Cerebellum, and Cerebral Cortex in a Mouse Model of Fetal Alcohol Spectrum Disorders. Alcoholism: Clinical and Experimental Research, 39(3), 445–454. https://doi.org/10.1111/acer.12639
    Hägglund, M. G. A., Hellsten, S. V., Bagchi, S., Philippot, G., Löfqvist, E., Nilsson, V. C. O., Almkvist, I., Karlsson, E., Sreedharan, S., Tafreshiha, A., & Fredriksson, R. (2015). Transport of l-Glutamine, l-Alanine, l-Arginine and l-Histidine by the Neuron-Specific Slc38a8 (SNAT8) in CNS. Journal of Molecular Biology, 427(6), 1495–1512. https://doi.org/10.1016/j.jmb.2014.10.016
    Wang, H., Yang, Y., Li, Y., Bai, B., Wang, X., Tan, H., Liu, T., Beach, T. G., Peng, J., & Wu, Z. (2015). Systematic Optimization of Long Gradient Chromatography Mass Spectrometry for Deep Analysis of Brain Proteome. Journal of Proteome Research, 14(2), 829–838. https://doi.org/10.1021/pr500882h
    Burrell-Saward, H. (2015). Development of an imaging model of a CNS infection with African trypanosomes. [London School of Hygeine and Tropical Medicine]. http://researchonline.lshtm.ac.uk/2222110/1/2015_ITD_PhD_Burrell-Saward_H.pdf
    Eriksson, A., Williams, M. J., Voisin, S., Hansson, I., Krishnan, A., Philippot, G., Yamskova, O., Herisson, F. M., Dnyansagar, R., Moschonis, G., Manios, Y., Chrousos, G. P., Olszewski, P. K., Frediksson, R., & Schiöth, H. B. (2015). Implication of coronin 7 in body weight regulation in humans, mice and flies. BMC Neuroscience, 16(1), 13. https://doi.org/10.1186/s12868-015-0151-9
    Hu, V. W., Sarachana, T., Sherrard, R. M., & Kocher, K. M. (2015). Investigation of sex differences in the expression of RORA and its transcriptional targets in the brain as a potential contributor to the sex bias in autism. Molecular Autism, 6(1), 7. https://doi.org/10.1186/2040-2392-6-7
    Yoshida, Y., Ozawa, T., Yao, T.-W., Shen, W., Brown, D., Parsa, A. T., Raizer, J. J., Cheng, S.-Y., Stegh, A. H., Mazar, A. P., Giles, F. J., Sarkaria, J. N., Butowski, N., Nicolaides, T., & James, C. D. (2014). NT113, a Pan-ERBB Inhibitor with High Brain Penetrance, Inhibits the Growth of Glioblastoma Xenografts with EGFR Amplification. Molecular Cancer Therapeutics, 13(12), 2919–2929. https://doi.org/10.1158/1535-7163.MCT-14-0306
    Zhou, C., Chen, J., Zhang, X., Costa, L. G., & Guizzetti, M. (2014). Prenatal Ethanol Exposure Up-Regulates the Cholesterol Transporters ATP-Binding Cassette A1 and G1 and Reduces Cholesterol Levels in the Developing Rat Brain. Alcohol and Alcoholism, 49(6), 626–634. https://doi.org/10.1093/alcalc/agu049
    Pinacho, R., Valdizán, E. M., Pilar-Cuellar, F., Prades, R., Tarragó, T., Haro, J. M., Ferrer, I., & Ramos, B. (2014). Increased SP4 and SP1 transcription factor expression in the postmortem hippocampus of chronic schizophrenia. Journal of Psychiatric Research, 58, 189–196. https://doi.org/10.1016/j.jpsychires.2014.08.006
    Terryn, S., Francart, A., Lamoral, S., Hultberg, A., Rommelaere, H., Wittelsberger, A., Callewaert, F., Stohr, T., Meerschaert, K., Ottevaere, I., Stortelers, C., Vanlandschoot, P., Kalai, M., & Van Gucht, S. (2014). Protective Effect of Different Anti-Rabies Virus VHH Constructs against Rabies Disease in Mice. PLoS ONE, 9(10), e109367. https://doi.org/10.1371/journal.pone.0109367
    Shibuya, Y., Chang, C. C. Y., Huang, L.-H., Bryleva, E. Y., & Chang, T.-Y. (2014). Inhibiting ACAT1/SOAT1 in Microglia Stimulates Autophagy-Mediated Lysosomal Proteolysis and Increases A 1-42 Clearance. Journal of Neuroscience, 34(43), 14484–14501. https://doi.org/10.1523/JNEUROSCI.2567-14.2014
    Borschensky, C. M., & Reinacher, M. (2014). Mutations in the 3c and 7b genes of feline coronavirus in spontaneously affected FIP cats. Research in Veterinary Science, 97(2), 333–340. https://doi.org/10.1016/j.rvsc.2014.07.016
    Boskovic, Z., Alfonsi, F., Rumballe, B. A., Fonseka, S., Windels, F., & Coulson, E. J. (2014). The Role of p75NTR in Cholinergic Basal Forebrain Structure and Function. Journal of Neuroscience, 34(39), 13033–13038. https://doi.org/10.1523/JNEUROSCI.2364-14.2014
    Colton, C. A., Wilson, J. G., Everhart, A., Wilcock, D. M., Puoliväli, J., Heikkinen, T., Oksman, J., Jääskeläinen, O., Lehtimäki, K., Laitinen, T., Vartiainen, N., & Vitek, M. P. (2014). mNos2 Deletion and Human NOS2 Replacement in Alzheimer Disease Models: Journal of Neuropathology & Experimental Neurology, 73(8), 752–769. https://doi.org/10.1097/NEN.0000000000000094
    Too, L. K., Ball, H. J., McGregor, I. S., & Hunt, N. H. (2014). The pro-inflammatory cytokine interferon-gamma is an important driver of neuropathology and behavioural sequelae in experimental pneumococcal meningitis. Brain, Behavior, and Immunity, 40, 252–268. https://doi.org/10.1016/j.bbi.2014.02.020
    Hill, A. J., Drever, N., Yin, H., Tamayo, E., Saade, G., & Bytautiene, E. (2014). The role of NADPH oxidase in a mouse model of fetal alcohol syndrome. American Journal of Obstetrics and Gynecology, 210(5), 466.e1-466.e5. https://doi.org/10.1016/j.ajog.2013.12.019
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