Brain lipid binding protein (FABP7) as modulator of astrocyte function

A serum autoantibody marker of neuromyelitis optica: distinction from multiple sclerosis

Lennon, V. A., Wingerchuk, D. M., Kryzer, T. J., Pittock, S. J., Lucchinetti, C. F., Fujihara, K., Nakashima, I., & Weinshenker, B. G. (2004) · The Lancet · doi:10.1016/s0140-6736(04)17551-x · Cited by 3,239 · see citing works

Mode of cell migration to the superficial layers of fetal monkey neocortex

Rakic, P. (1972) · Journal of Comparative Neurology · doi:10.1002/cne.901450105 · Cited by 2,170 · see citing works

Astrocyte activation and reactive gliosis

Pekny, M., & Nilsson, M. (2005) · Glia · doi:10.1002/glia.20207 · Cited by 1,611 · see citing works

Reactive Astrocytes Protect Tissue and Preserve Function after Spinal Cord Injury

Faulkner, J., Herrmann, J., Woo, M. J., Tansey, K., Doan, N., & Sofroniew, M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3547-03.2004 · Cited by 1,600 · see citing works

Remyelination in the CNS: from biology to therapy

Franklin, R. J. M., & ffrench-Constant, C. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2480 · Cited by 1,544 · see citing works

Neuron‐glia relationship during granule cell migration in developing cerebellar cortex. A Golgi and electonmicroscopic study in Macacus rhesus

RAKIC, P. T. (1971) · The Journal of Comparative Neurology · doi:10.1002/cne.901410303 · Cited by 1,343 · see citing works

Neural Stem Cells and the Origin of Gliomas

Sanai, N., Álvarez-Buylla, A., & Berger, M. S. (2005) · New England Journal of Medicine · doi:10.1056/nejmra043666 · Cited by 1,049 · see citing works

Understanding pathogenesis and therapy of multiple sclerosis via animal models: 70 years of merits and culprits in experimental autoimmune encephalomyelitis research

Gold, R. (2006) · Brain · doi:10.1093/brain/awl075 · Cited by 1,017 · see citing works

TNFα promotes proliferation of oligodendrocyte progenitors and remyelination

Arnett, H. A., Mason, J., Marino, M., Suzuki, K., Matsushima, G. K., & Ting, J. P.-Y. (2001) · Nature Neuroscience · doi:10.1038/nn738 · Cited by 1,012 · see citing works

Premyelinating Oligodendrocytes in Chronic Lesions of Multiple Sclerosis

Chang, A., Tourtellotte, W. W., Rudick, R., & Trapp, B. D. (2002) · New England Journal of Medicine · doi:10.1056/nejmoa010994 · Cited by 991 · see citing works

Docosahexaenoic acid: Membrane properties of a unique fatty acid

Stillwell, W., & Wassall, S. R. (2003) · Chemistry and Physics of Lipids · doi:10.1016/s0009-3084(03)00101-4 · Cited by 872 · see citing works

Remyelination is extensive in a subset of multiple sclerosis patients

Patrikios, P., Stadelmann, C., Kutzelnigg, A., Rauschka, H., Schmidbauer, M., Laursen, H., Sorensen, P. S., Bruck, W., Lucchinetti, C., & Lassmann, H. (2006) · Brain · doi:10.1093/brain/awl217 · Cited by 807 · see citing works

Environmental risk factors for multiple sclerosis. Part II: Noninfectious factors

Ascherio, A., & Munger, K. L. (2007) · Annals of Neurology · doi:10.1002/ana.21141 · Cited by 714 · see citing works

NG2-Positive Oligodendrocyte Progenitor Cells in Adult Human Brain and Multiple Sclerosis Lesions

Chang, A., Nishiyama, A., Peterson, J. W., Prineas, J. W., & Trapp, B. D. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-17-06404.2000 · Cited by 711 · see citing works

Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

Brenner, M., Johnson, T., Boespflug‐Tanguy, O., Rodriguez, D., Goldman, J. E., & Messing, A. (2001) · Nature Genetics · doi:10.1038/83679 · Cited by 689 · see citing works

Hyaluronan accumulates in demyelinated lesions and inhibits oligodendrocyte progenitor maturation

Back, S. A., Tuohy, T. M. F., Chen, H., Wallingford, N., Craig, A., Struve, J., Luo, N. L., Banine, F., Liu, Y., Chang, A., et al. (2005) · Nature Medicine · doi:10.1038/nm1279 · Cited by 612 · see citing works

Multiple sclerosis: Remyelination of nascent lesions: Remyelination of nascent lesions

Prineas, J. W., Barnard, R. O., Kwon, E. E., Sharer, L. R., & Cho, E. ‐. (1993) · Annals of Neurology · doi:10.1002/ana.410330203 · Cited by 574 · see citing works

Brain lipid-binding protein (BLBP): A novel signaling system in the developing mammalian CNS

Feng, L., Hatten, M. E., & Heintz, N. (1994) · Neuron · doi:10.1016/0896-6273(94)90341-7 · Cited by 572 · see citing works

Gene expression profiling reveals molecularly and clinically distinct subtypes of glioblastoma multiforme

Liang, Y., Diehn, M., Watson, N. P., Bollen, A. W., Aldape, K. D., Nicholas, M. K., Lamborn, K. R., Berger, M. S., Botstein, D., Brown, P. O., et al. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402870102 · Cited by 503 · see citing works

Interleukin-1β Promotes Repair of the CNS

Mason, J. L., Suzuki, K., Chaplin, D. D., & Matsushima, G. K. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-18-07046.2001 · Cited by 502 · see citing works

Chronic stage multiple sclerosis lesions contain a relatively quiescent population of oligodendrocyte precursor cells

Wolswijk, G. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-02-00601.1998 · Cited by 498 · see citing works

The cuprizone animal model: new insights into an old story

Kipp, M., Clarner, T., Dang, J., Copray, S., & Beyer, C. (2009) · Acta Neuropathologica · doi:10.1007/s00401-009-0591-3 · Cited by 481 · see citing works

Multiple sclerosis: Re-expression of a developmental pathway that restricts oligodendrocyte maturation

John, G. R., Shankar, S. L., Shafit‐Zagardo, B., Massimi, A. B., Lee, S. C., Raine, C. S., & Brosnan, C. F. (2002) · Nature Medicine · doi:10.1038/nm781 · Cited by 478 · see citing works

Differentiation of mouse embryonic stem cells into a defined neuronal lineage

Bibel, M., Richter, J., Schrenk, K., Tucker, K. L., Staiger, V., Korte, M., Goetz, M., & Barde, Y.-A. (2004) · Nature Neuroscience · doi:10.1038/nn1301 · Cited by 450 · see citing works

Cell-Specific Expression of Connexins and Evidence of Restricted Gap Junctional Coupling between Glial Cells and between Neurons

Rash, J. E., Yasumura, T., Dudek, F. E., & Nagy, J. I. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-06-01983.2001 · Cited by 432 · see citing works

AQP4 antibodies in neuromyelitis optica: diagnostic and pathogenetic relevance

Jarius, S., & Wildemann, B. (2010) · Nature Reviews Neurology · doi:10.1038/nrneurol.2010.72 · Cited by 424 · see citing works

Remyelination protects axons from demyelination-associated axon degeneration

Irvine, K. A., & Blakemore, W. F. (2008) · Brain · doi:10.1093/brain/awn080 · Cited by 420 · see citing works

Mice lacking glial fibrillary acidic protein display astrocytes devoid of intermediate filaments but develop and reproduce normally.

Pekny, M., Levéen, P., Pekna, M., Eliasson, C., Berthold, C. H., Westermark, B., & Betsholtz, C. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb07147.x · Cited by 336 · see citing works

Mechanisms of Disease: aquaporin-4 antibodies in neuromyelitis optica

Jarius, S., Paul, F., Franciotta, D. M., Waters, P. J., Zipp, F., Hohlfeld, R., Vincent, A. C., & Wildemann, B. (2008) · Nature Clinical Practice Neurology · doi:10.1038/ncpneuro0764 · Cited by 335 · see citing works

Central remyelination restores secure conduction

Smith, K. J., Blakemore, W. F., & MCDONALD, W. I. (1979) · Nature · doi:10.1038/280395a0 · Cited by 332 · see citing works

Remyelination can be extensive in multiple sclerosis despite a long disease course

Patani, R., Balaratnam, M. S., Vora, A., & Reynolds, R. (2007) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.2007.00805.x · Cited by 315 · see citing works

Staging of multiple sclerosis (MS) lesions: pathology of the time frame of MS

van der Valk, P., & Groot, C. J. A. D. (2000) · Neuropathology and Applied Neurobiology · doi:10.1046/j.1365-2990.2000.00217.x · Cited by 304 · see citing works

Oligodendrocyte progenitors are present in the normal adult human CNS and in the lesions of multiple sclerosis

Scolding, N. J. (1998) · Brain · doi:10.1093/brain/121.12.2221 · Cited by 293 · see citing works

Grey matter pathology in multiple sclerosis.

Geurts, J., & Barkhof, F. (2008) · Lancet Neurology · doi:10.1016/s1474-4422(08)70191-1 · Cited by 290 · see citing works

Re-expression of PSA-NCAM by demyelinated axons: an inhibitor of remyelination in multiple sclerosis?

Charles, P. (2002) · Brain · doi:10.1093/brain/awf216 · Cited by 289 · see citing works

Regulation of Cellular and Humoral Immune Responses by the SLAM and SAP Families of Molecules

Ma, C. S., Nichols, K. E., & Tangye, S. G. (2007) · Annual Review of Immunology · doi:10.1146/annurev.immunol.25.022106.141651 · Cited by 263 · see citing works

Fatal encephalopathy with astrocyte inclusions in GFAP transgenic mice.

Messing, A., Head, M. W., Galles, K., Galbreath, E. J., Goldman, J. E., & Brenner, M. (1998) · Europe PMC (PubMed Central) · Cited by 242 · see citing works

Multiple sclerosis

Prineas, J. W., Barnard, R. O., Révész, T., Kwon, E. E., Sharer, L. R., & Cho, E.-S. (1993) · Brain · doi:10.1093/brain/116.3.681 · Cited by 240 · see citing works

Interferon-γ inhibits central nervous system remyelination through a process modulated by endoplasmic reticulum stress

Lin, W., Kemper, A., Dupree, J. L., Harding, H. P., Ron, D., & Popko, B. (2006) · Brain · doi:10.1093/brain/awl044 · Cited by 222 · see citing works

Crystal Structure and Thermodynamic Analysis of Human Brain Fatty Acid-binding Protein

Balendiran, G. K., Schnütgen, F., Scapin, G., Börchers, T., Xhong, N., Lim, K., Godbout, R., Spener, F., & Sacchettini, J. C. (2000) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)61478-x · Cited by 217 · see citing works

GFAP and its role in Alexander disease

Quinlan, R. A., Brenner, M., Goldman, J. E., & Messing, A. (2007) · Experimental Cell Research · doi:10.1016/j.yexcr.2007.04.004 · Cited by 207 · see citing works

Functional Genomic Analysis of Remyelination Reveals Importance of Inflammation in Oligodendrocyte Regeneration

Arnett, H. A., Wang, Y., Matsushima, G. K., Suzuki, K., & Ting, J. P.-Y. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-30-09824.2003 · Cited by 190 · see citing works

Effects of eicosapentaenoic acid and docosahexaenoic acid on plasma membrane fluidity of aortic endothelial cells

Hashimoto, M., Hossain, M. S., Yamasaki, H., Yazawa, K., & Masumura, S. (1999) · Lipids · doi:10.1007/s11745-999-0481-6 · Cited by 189 · see citing works

How factors secreted from astrocytes impact myelin repair

Moore, C. S., Abdullah, S. L., Brown, A. D., Arulpragasam, A. R., & Crocker, S. J. (2010) · Journal of Neuroscience Research · doi:10.1002/jnr.22482 · Cited by 172 · see citing works

Recovery from Chronic Demyelination by Thyroid Hormone Therapy: Myelinogenesis Induction and Assessment by Diffusion Tensor Magnetic Resonance Imaging

Harsan, L. A., Steibel, J., Zaremba, A., Agin, A., Sapin, R., Poulet, P., Guignard, B., Parizel, N., Grucker, D., Boehm, N., et al. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4453-08.2008 · Cited by 171 · see citing works

Insulin-Like Growth Factor I

Kooijman, R., Sarre, S., Michotte, Y. M., & Keyser, J. D. (2009) · Stroke · doi:10.1161/strokeaha.108.528356 · Cited by 152 · see citing works

GFAP mutations in Alexander disease

Li, R., Messing, A., Goldman, J. E., & Brenner, M. (2002) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(02)00019-9 · Cited by 137 · see citing works

Chronic toxic demyelination in the central nervous system leads to axonal damage despite remyelination

Lindner, M., Fokuhl, J., Linsmeier, F., Trebst, C., & Stangel, M. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.02.004 · Cited by 136 · see citing works

Fatty Acid-Binding Proteins of Nervous Tissue

Veerkamp, J. H., & Zimmerman, A. W. (2001) · Journal of Molecular Neuroscience · doi:10.1385/jmn:16:2-3:133 · Cited by 135 · see citing works

Differentiation of radial glia from radial precursor cells and transformation into astrocytes in the developing rat spinal cord

Barry, D., & McDermott, K. W. G. (2005) · Glia · doi:10.1002/glia.20166 · Cited by 132 · see citing works

Multiple Sclerosis Pathology: Evolution of Pathogenetic Concepts

Lassmann, H. (2005) · Brain Pathology · doi:10.1111/j.1750-3639.2005.tb00523.x · Cited by 130 · see citing works

Gray matter pathology in (chronic) MS: modern views on an early observation.

Geurts, J., Stys, P., Minagar, A., Amor, S., & Zivadinov, R. (2009) · Journal of Neurological Sciences · doi:10.1016/j.jns.2009.01.018 · Cited by 123 · see citing works

Cuprizone treatment induces demyelination and astrocytosis in the mouse hippocampus

Norkute, A., Hieble, A., Braun, A., Johann, S., Clarner, T., Baumgartner, W., Beyer, C., & Kipp, M. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.21946 · Cited by 123 · see citing works

Reactive changes of retinal astrocytes and Müller glial cells in kainate‐induced neuroexcitotoxicity

Chang, M., Wu, C., Jiang‐Shieh, Y., Shieh, J.-Y., & Wen, C.-Y. (2006) · Journal of Anatomy · doi:10.1111/j.1469-7580.2006.00671.x · Cited by 120 · see citing works

Cuprizone Treatment Induces Distinct Demyelination, Astrocytosis, and Microglia Cell Invasion or Proliferation in the Mouse Cerebellum

Groebe, A., Clarner, T., Baumgartner, W., Dang, J., Beyer, C., & Kipp, M. (2009) · The Cerebellum · doi:10.1007/s12311-009-0099-3 · Cited by 116 · see citing works

Astrogliosis in EAE spinal cord: Derivation from radial glia, and relationships to oligodendroglia

Bannerman, P. G. C., Hahn, A., Soulika, A. M., Gallo, V., & Pleasure, D. (2006) · Glia · doi:10.1002/glia.20437 · Cited by 112 · see citing works

Platelet-Derived Growth Factor Promotes Repair of Chronically Demyelinated White Matter

Vana, A. C., Flint, N. C., Harwood, N. E., Le, T. Q., Fruttiger, M., & Armstrong, R. C. (2007) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e3181587d46 · Cited by 101 · see citing works

Regional heterogeneity in astrocyte responses following contusive spinal cord injury in mice

White, R., McTigue, D. M., & Jakeman, L. B. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22282 · Cited by 95 · see citing works

Brain-Region-Specific Astroglial Responses In Vitro After LPS Exposure

Kipp, M., Norkutė, A., Johann, S., Lorenz, L., Braun, A., Hieble, A., Gingele, S., Pott, F., Richter, J., & Beyer, C. (2008) · Journal of Molecular Neuroscience · doi:10.1007/s12031-008-9057-7 · Cited by 86 · see citing works

Reelin and Notch1 Cooperate in the Development of the Dentate Gyrus

Sibbe, M., Forster, E., Başak, O., Taylor, V., & Frotscher, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0958-09.2009 · Cited by 86 · see citing works

Cuprizone effect on myelination, astrogliosis and microglia attraction in the mouse basal ganglia

Pott, F., Gingele, S., Clarner, T., Dang, J., Baumgartner, W., Beyer, C., & Kipp, M. (2009) · Brain Research · doi:10.1016/j.brainres.2009.09.084 · Cited by 85 · see citing works

Correlation of B-FABP and GFAP expression in malignant glioma

Godbout, R., Bisgrove, D. A., Shkolny, D. L., & Day, R. S. (1998) · Oncogene · doi:10.1038/sj.onc.1201740 · Cited by 84 · see citing works

Oestrogen Regulates the Expression and Function of Dopamine Transporters in Astrocytes of the Nigrostriatal System

Karakaya, S., Kipp, M., & Beyer, C. (2007) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2007.01575.x · Cited by 82 · see citing works

B-FABP-Expressing Radial Glial Cells: The Malignant Glioma Cell of Origin?

Mita, R., Coles, J. E., Glubrecht, D. D., Sung, R., Sun, X., & Godbout, R. (2007) · Neoplasia · doi:10.1593/neo.07439 · Cited by 82 · see citing works

Models of multiple sclerosis: new insights into pathophysiology and repair

Lassmann, H. (2008) · Current Opinion in Neurology · doi:10.1097/wco.0b013e3282fee94a · Cited by 81 · see citing works

Homotypic and Heterotypic Coupling Mediated by Gap Junctions During Glial Cell Differentiation In Vitro

Venance, L., Cordier, J., Monge, M., Zalc, B., Glowinski, J., & Giaume, C. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb00341.x · Cited by 74 · see citing works

Activation of Inflammatory Response by a Combination of Growth Factors in Cuprizone-Induced Demyelinated Brain Leads to Myelin Repair

Biancotti, J. C., Kumar, S., & de Vellis, J. (2008) · Neurochemical Research · doi:10.1007/s11064-008-9792-8 · Cited by 69 · see citing works

Review of Alexander disease: Beyond the classical concept of leukodystrophy

Sawaishi, Y. (2009) · Brain and Development · doi:10.1016/j.braindev.2009.03.006 · Cited by 67 · see citing works

Gene Expression Analysis in Human Fetal Retinal Explants Treated with Docosahexaenoic Acid

Rojas, C., ́nez, J. I. M., Flores, I., Hoffman, D. R., & Uauy, R. D. (2003) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.02-1138 · Cited by 64 · see citing works

Anti-aquaporin-4 auto-antibodies orchestrate the pathogenesis in neuromyelitis optica

Saikali, P., Cayrol, R., & Vincent, T. (2009) · Autoimmunity Reviews · doi:10.1016/j.autrev.2009.04.004 · Cited by 63 · see citing works

Effects of dietary intervention on MRI activity, de- and remyelination in the cuprizone model for demyelination

Torkildsen, Ø., Brunborg, L. A., Thorsen, F. A., Mørk, S. J., Stangel, M., Myhr, K., & Bø, L. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2008.09.026 · Cited by 56 · see citing works

Generation and characterization of brain lipid‐binding protein promoter‐based transgenic mouse models for the study of radial glia

Schmid, R. S., Yokota, Y., & Anton, E. S. (2005) · Glia · doi:10.1002/glia.20274 · Cited by 51 · see citing works

Expression of Enzymes Involved in the Prostanoid Metabolism by Cortical Astrocytes after LPS-induced Inflammation

Johann, S., Kampmann, E., Denecke, B., Arnold, S., Kipp, M., Mey, J., & Beyer, C. (2008) · Journal of Molecular Neuroscience · doi:10.1007/s12031-007-9028-4 · Cited by 51 · see citing works

Deleterious Role of IFNγ in a Toxic Model of Central Nervous System Demyelination

Maña, P., Liñares, D., Fordham, S., Staykova, M., & Willenborg, D. (2006) · The American Journal of Pathology · doi:10.2353/ajpath.2006.050799 · Cited by 48 · see citing works

Occurrence of Oligodendrocytes within Astrocytes in Demyelinating Lesions

Ghatak, N. R. (1992) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-199201000-00006 · Cited by 44 · see citing works

Selective regulation of growth factor expression in cultured cortical astrocytes by neuro-pathological toxins

Braun, A., Dang, J., Johann, S., Beyer, C., & Kipp, M. (2009) · Neurochemistry International · doi:10.1016/j.neuint.2009.06.004 · Cited by 42 · see citing works

Visual evoked potentials in demyelinating disease.

Am, H. (1981) · PubMed · Cited by 34 · see citing works

Absence of Spontaneous Central Nervous System Remyelination in Class ll-deficient Mice Infected with Theilerʼs Virus

Njenga, M. K., Murray, P. D., McGavern, D. B., Lin, X., Drescher, K. M., & Rodriguez, M. (1999) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-199901000-00009 · Cited by 33 · see citing works

Cellular localization of epidermal‐type and brain‐type fatty acid‐binding proteins in adult hippocampus and their response to cerebral ischemia

Ma, D., Zhang, M., Mori, Y., Yao, C., Larsen, C. P., Yamashima, T., & Zhou, L. (2009) · Hippocampus · doi:10.1002/hipo.20682 · Cited by 31 · see citing works

Glial Amyloid Precursor Protein Expression is Restricted to Astrocytes in an Experimental Toxic Model of Multiple Sclerosis

Clarner, T., Buschmann, J., Beyer, C., & Kipp, M. (2010) · Journal of Molecular Neuroscience · doi:10.1007/s12031-010-9419-9 · Cited by 29 · see citing works

A salmon based diet protects mice from behavioural changes in the cuprizone model for demyelination

Torkildsen, Ø., Brunborg, L. A., Milde, A. M., Mørk, S. J., Myhr, K.-M., & Bø, L. (2009) · Clinical Nutrition · doi:10.1016/j.clnu.2008.10.015 · Cited by 28 · see citing works

Oligodendrogenesis is differentially regulated in gray and white matter of jimpy mice

Baracskay, K. L., Duchala, C., Miller, R. H., Macklin, W., & Trapp, B. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10418 · Cited by 27 · see citing works

Lymphocyte Emperipolesis in Human Glial Cells

FURER, M., Hartloper, V., Wilkins, J. A., & Nath, A. (1993) · Cell Communication & Adhesion · doi:10.3109/15419069309097256 · Cited by 20 · see citing works

Glial response during cuprizone-induced de- and remyelination in the CNS: lessons learned

Gudi, V., Gingele, S., Skripuletz, T., & Stangel, M. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00073 · Cited by 375 · see citing works

eIF2B activator prevents neurological defects caused by a chronic integrated stress response

Wong, Y. L., LeBon, L., Basso, A. M., Kohlhaas, K. L., Nikkel, A. L., Robb, H. M., Donnelly-Roberts, D. L., Prakash, J., Swensen, A. M., Rubinstein, N. D., et al. (2019) · eLife · doi:10.7554/elife.42940 · Cited by 236 · see citing works

On the Neuroprotective Effects of Naringenin: Pharmacological Targets, Signaling Pathways, Molecular Mechanisms, and Clinical Perspective

Nouri, Z., Fakhri, S., El‐Senduny, F. F., Sanadgol, N., Abdel‐Ghani, G. E., Farzaei, M. H., & Chen, J. (2019) · Biomolecules · doi:10.3390/biom9110690 · Cited by 168 · see citing works

CXCL10 Triggers Early Microglial Activation in the Cuprizone Model

Clarner, T., Janssen, K., Nellessen, L., Stangel, M., Skripuletz, T., Krauspe, B., Hess, F.-M., Denecke, B., Beutner, C., Linnartz-Gerlach, B., et al. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1401459 · Cited by 150 · see citing works

Inflammatory Response and Chemokine Expression in the White Matter Corpus Callosum and Gray Matter Cortex Region During Cuprizone-Induced Demyelination

Buschmann, J. P., Berger, K., Awad, H., Clarner, T., Beyer, C., & Kipp, M. (2012) · Journal of Molecular Neuroscience · doi:10.1007/s12031-012-9773-x · Cited by 133 · see citing works

Sildenafil (Viagra) Protective Effects on Neuroinflammation: The Role of iNOS/NO System in an Inflammatory Demyelination Model

Rapôso, C., Nunes, A. K. S., Luna, R. L. D. A., Araújo, S. M. D. R., da Cruz‐Höfling, M. A., & Peixoto, C. A. (2013) · Mediators of Inflammation · doi:10.1155/2013/321460 · Cited by 62 · see citing works

Metabolic role of fatty acid binding protein 7 in mediating triple-negative breast cancer cell death via PPAR-α signaling

Kwong, S. C., Jamil, A. H. A., Rhodes, A., Taib, N. A. M., & Chung, I. (2019) · Journal of Lipid Research · doi:10.1194/jlr.m092379 · Cited by 54 · see citing works

Intracellular fibril formation, calcification, and enrichment of chaperones, cytoskeletal, and intermediate filament proteins in the adult hippocampus CA1 following neonatal exposure to the nonprotein amino acid BMAA

Karlsson, O., Berg, A., Hanrieder, J., Arnerup, G., Lindström, A.-K., & Brittebo, E. B. (2014) · Archives of Toxicology · doi:10.1007/s00204-014-1262-2 · Cited by 50 · see citing works

Astrocyte-derived fatty acid-binding protein 7 protects blood-brain barrier integrity through a caveolin-1/MMP signaling pathway following traumatic brain injury

Qin, R., Ni, H., Lin, X., Zhu, X., Li, D., Liu, H., & Chen, G. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113044 · Cited by 51 · see citing works

Naringenin: its chemistry and roles in neuroprotection

Atoki, A. V., Aja, P. M., Shinkafi, T. S., Ondari, E. N., & Awuchi, C. G. (2023) · Nutritional Neuroscience · doi:10.1080/1028415x.2023.2243089 · Cited by 46 · see citing works

Addiction and reward-related genes show altered expression in the postpartum nucleus accumbens

Zhao, C., Eisinger, B. E., Driessen, T. M., & Gammie, S. C. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00388 · Cited by 39 · see citing works

Absence of CCL2 and CCL3 Ameliorates Central Nervous System Grey Matter But Not White Matter Demyelination in the Presence of an Intact Blood–Brain Barrier

Janssen, K., Rickert, M., Clarner, T., Beyer, C., & Kipp, M. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9113-6 · Cited by 38 · see citing works

Expression Pattern of Fatty Acid Binding Proteins in Celiac Disease Enteropathy

Arias, N. M. B., García, M., Bondar, C., Guzmán, L., Redondo, A., Chopita, N., Córsico, B., & Chirdo, F. G. (2015) · Mediators of Inflammation · doi:10.1155/2015/738563 · Cited by 31 · see citing works

The fatty acid binding protein FABP7 is required for optimal oligodendrocyte differentiation during myelination but not during remyelination

Foerster, S., de la Fuente, A. G., Kagawa, Y., Bartels, T., Owada, Y., & Franklin, R. J. M. (2020) · Glia · doi:10.1002/glia.23789 · Cited by 29 · see citing works

Dose-dependent effect of cannabinoid WIN-55,212-2 on myelin repair following a demyelinating insult

Tomàs-Roig, J., Agbemenyah, H. Y., Celarain, N., Quintana, E., Ramió‐Torrentà, L., & Havemann‐Reinecke, U. (2020) · Scientific Reports · doi:10.1038/s41598-019-57290-1 · Cited by 26 · see citing works

Effects of FABP7 on functional recovery after spinal cord injury in adult mice

Senbokuya, N., Yoshioka, H., Yagi, T., Owada, Y., & Kinouchi, H. (2019) · Journal of Neurosurgery Spine · doi:10.3171/2019.2.spine18844 · Cited by 18 · see citing works

Astroglial Redistribution of Aquaporin 4 During Spongy Degeneration in a Canavan Disease Mouse Model

Clarner, T., Wieczorek, N., Krauspe, B., Jansen, K., Beyer, C., & Kipp, M. (2013) · Journal of Molecular Neuroscience · doi:10.1007/s12031-013-0184-4 · Cited by 17 · see citing works

Differential hippocampal protein expression between normal aged rats and aged rats with postoperative cognitive dysfunction: A proteomic analysis

Li, Y., Wang, S., RAN, K., Hu, Z., Liu, Z., & Duan, K. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.3697 · Cited by 16 · see citing works

Brain lipid binding protein mediates the proliferation of human glioblastoma cells by regulating ERK1/2 signaling pathway in vitro

Tian, W., Shi, J., Qin, J., Jin, G., Han, X., & Li, H. (2017) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-017-0220-8 · Cited by 14 · see citing works

Oligodendrocyte Lineage Marker Expression in eGFP-GFAP Transgenic Mice

Behrangi, N., Lorenz, P., & Kipp, M. (2020) · Journal of Molecular Neuroscience · doi:10.1007/s12031-020-01771-w · Cited by 14 · see citing works

Exploring the Role of Lipid-Binding Proteins and Oxidative Stress in Neurodegenerative Disorders: A Focus on the Neuroprotective Effects of Nutraceutical Supplementation and Physical Exercise

Scarfò, G., Piccarducci, R., Daniele, S., Franzoni, F., & Martini, C. (2022) · Antioxidants · doi:10.3390/antiox11112116 · Cited by 16 · see citing works

The neuroprotective action of naringenin on oseltamivir (Tamiflu) treated male rats

Hegazy, H. G., Ali, E. H. A., & Sabry, H. A. (2016) · The Journal of Basic and Applied Zoology · doi:10.1016/j.jobaz.2016.12.006 · Cited by 12 · see citing works

TSG-6–Mediated Extracellular Matrix Modifications Regulate Hypoxic–Ischemic Brain Injury

Srivastava, T., Nguyen, H., Haden, G., Diba, P., Sowa, S. W., LaNguyen, N., Reed-Dustin, W., Zhu, W., Gong, X., Harris, E. N., et al. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.2215-23.2024 · Cited by 10 · see citing works

Low-dose DHA-induced astrocyte proliferation can be attenuated by insufficient expression of BLBP in vitro

Li, H., Yang, Q., Han, X., Tan, X., Qin, J., & Jin, G. (2017) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2017.09.003 · Cited by 10 · see citing works

Targeting the FABP Axis: Interplay Between Lipid Metabolism, Neuroinflammation, and Neurodegeneration

Wu, C., Lin, J., Chen, Q., Zhao, W., Kawahata, K., & Cheng, A. (2025) · Cells · doi:10.3390/cells14191502 · Cited by 9 · see citing works

Diurnal proteome profile of the mouse cerebral cortex: Conditional deletion of the Bmal1 circadian clock gene elevates astrocyte protein levels and cell abundance in the neocortex and hippocampus

Bering, T., Gadgaard, C., Vorum, H., Honoré, B., & Rath, M. F. (2023) · Glia · doi:10.1002/glia.24443 · Cited by 9 · see citing works

Secretomics Alterations and Astrocyte Dysfunction in Human iPSC of Leukoencephalopathy with Vanishing White Matter

Deng, J., Zhang, J., Gao, K., Yan, W., Zhou, L., Jiang, Y., Wang, J., & Wu, Y. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03765-z · Cited by 8 · see citing works

Brain lipid-binding protein promotes proliferation and modulates cell cycle in C6 rat glioma cells

Han, X., Li, H., Zhang, Y., Qin, J., Yang, Q., Wang, L., Yuan, M., & Xia, C. (2017) · International Journal of Oncology · doi:10.3892/ijo.2017.4132 · Cited by 6 · see citing works

The Role of Fatty Acid Binding Proteins in Neuropsychiatric Diseases: A Narrative Review

Powell, A., Yamaguchi, N., Lu, H., Pareek, O., Elman, I., Gold, M. S., Pinhasov, A., Blum, K., & Thanos, P. K. (2025) · Frontiers in Bioscience-Landmark · doi:10.31083/fbl26812 · Cited by 5 · see citing works

Proteomic analysis of murine Tsc1-deficient neural stem progenitor cells

Chiaradia, E., Miller, I., Renzone, G., Tognoloni, A., Polchi, A., Marco, F. D., Tancini, B., Scaloni, A., & Magini, A. (2023) · Journal of Proteomics · doi:10.1016/j.jprot.2023.104928 · Cited by 4 · see citing works

β-hydroxybutyrate attenuates demyelination, modulates microglial phenotype and supports blood-brain barrier integrity in a cuprizone-induced mouse model of demyelination

Zhang, N., Li, L., Li, S., Khan, M. A., Tahir, A. H., Rahim, M. F., Wang, T., Zhao, J.-Y., & Zhang, R.-Y. (2023) · Journal of Functional Foods · doi:10.1016/j.jff.2023.105580 · Cited by 4 · see citing works

Effect of carotid endarterectomy on brain damage markers

Iłżecki, M., Iłżecka, J., Przywara, S., Terlecki, P., Grabarska, A., Stepulak, A., & Zubilewicz, T. (2016) · Acta Neurologica Scandinavica · doi:10.1111/ane.12607 · Cited by 4 · see citing works

Genetic dissection of the M ss4 locus mediating sex‐biased cancer resistance in the rat peripheral nervous system

van den Berg, L., Koelsch, B. U., Winzen‐Reichert, B., Fischer, C., Kutritz, A., & Kindler‐Röhrborn, A. (2014) · International Journal of Cancer · doi:10.1002/ijc.29256 · Cited by 4 · see citing works

Potential effects of brain lipid binding protein in the pathogenesis of amyotrophic lateral sclerosis

Zhou, Q., Kang, Q., Chen, W., & Xu, R. (2023) · Science Progress · doi:10.1177/00368504231184320 · Cited by 3 · see citing works

Effects of cuprizone on mitochondria

McDonough, J. A., & Sternbach, S. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-88462-4.00011-0 · Cited by 1 · see citing works

Single-cell analysis reveals the diversity of human fetal membrane and adjacent placental cells with preterm premature rupture of membranes

Sun, C. M., Wu, M., Zheng, Z., Wang, L., Xu, X., Hu, Y., Chen, H., Hu, X., Zhou, Q., Chen, L., et al. (2025) · Human Molecular Genetics · doi:10.1093/hmg/ddaf143 · Cited by 1 · see citing works

The cuprizone model and multiple sclerosis : disparities and similarities

Kipp, M., & Baumgärtner, W. (2011) · RWTH Publications (RWTH Aachen)

Region specific characterization of the cuprizone model for Multiple Sclerosis and impairment of remyelination by corticosteroids

Clarner, T., & Beyer, C. (2011) · RWTH Publications (RWTH Aachen)

Enhancing Remyelination by Blockade of Astrocytic P2X1 Receptors Signaling in Cuprizone‐Induced Demyelination Mouse Model

Xu, Z., Gao, T., Xie, H. Q., He, Y., Luo, H., Mo, Z., Yang, Y., Peng, W., & Xiao, L. (2025) · Glia · doi:10.1002/glia.70121

Oligodendrocytes as active modulators of neuroinflammation

Janssen, K., & Beyer, C. (2014) · RWTH Publications (RWTH Aachen)

Fatty acid–binding proteins as emerging immunometabolic regulators and therapeutic targets in multiple sclerosis and neurodegeneration: Promise, mechanistic gaps, and translational hurdles

Mhatre, A., Prasad, A., & Naqvi, S. (2026) · ASPET Discovery · doi:10.1016/j.aspetd.2026.100033

Proteins that show aggregation in the brains of patients with schizophrenia and other chronic mental illnesses

Zaharija, B., Stanivuk, I., Kršanac, M., Juković, M., Radonja, A. P., & Bradshaw, N. J. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-34176-2.00009-2

The role of fatty acid binding protein 7 in spinal cord astrocytes in a mouse model of experimental autoimmune encephalomyelitis

Kamizato, K., Sato, S., Shil, S. K., Umaru, B. A., Kagawa, Y., Yamamoto, Y., Ogata, M., Yasumoto, Y., Okuyama, Y., Ishii, N., et al. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.03.050 · Cited by 29 · see citing works

FABP7 upregulation induces a neurotoxic phenotype in astrocytes

Killoy, K. M., Harlan, B. A., Pehar, M., & Vargas, M. R. (2020) · Glia · doi:10.1002/glia.23879 · Cited by 67 · see citing works

Fatty Acid Binding Protein 7 is Involved in the Proliferation of Reactive Astrocytes, but not in Cell Migration and Polarity

Hara, T., Umaru, B. A., Sharifi, K., Yoshikawa, T., Owada, Y., & Kagawa, Y. (2020) · ACTA HISTOCHEMICA ET CYTOCHEMICA · doi:10.1267/ahc.20001 · Cited by 20 · see citing works

A novel fatty acid-binding protein 5 and 7 inhibitor ameliorates oligodendrocyte injury in multiple sclerosis mouse models

Cheng, A., Jia, W., Kawahata, K., & Fukunaga, K. (2021) · EBioMedicine · doi:10.1016/j.ebiom.2021.103582 · Cited by 60 · see citing works

FABP7 is increased in progressive multiple sclerosis and induces a pro-inflammatory phenotype in monocytes through a glycolytic switch

Patel, R. P., King, D. A., LaBarre, B. A., Lokhande, H. A., Caefer, D., Varghese, J. F., Warner, K., Bouffard, M. A., Saxena, S., Zhirova, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60747-9 · Cited by 6 · see citing works