An acidic protein isolated from fibrous astrocytes

Colchicine-binding protein of mammalian brain and its relation to microtubules

Weisenberg, R. C., Broisy, G. G., & Taylor, E. W. (1968) · Biochemistry · doi:10.1021/bi00852a043 · Cited by 1,164 · see citing works

Maturation of human white matter myelin. Fractionation of the myelin membrane proteins

Eng, L. F., Chao, F.-C., Gerstl, B., Pratt, D. R., & Tavaststjerna, M. G. (1968) · Biochemistry · doi:10.1021/bi00852a042 · Cited by 344 · see citing works

Precipitation of Proteins by Vinblastine and Calcium Ions

Wilson, L., Bryan, J., Ruby, A., & Mazia, D. (1970) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.66.3.807 · Cited by 224 · see citing works

The cellular localization of the two brain specific proteins, S-100 and 14-3-2

Cicero, T. J., Cowan, W. M., Moore, B. W., & Suntzeff, V. (1970) · Brain Research · doi:10.1016/0006-8993(70)90454-3 · Cited by 209 · see citing works

Fibrillar proteins from squid axons

Huneeus, F. C., & Davison, P. F. (1970) · Journal of Molecular Biology · doi:10.1016/0022-2836(70)90410-9 · Cited by 143 · see citing works

Fibrillar proteins from squid axons

Davison, P. F., & Huneeus, F. C. (1970) · Journal of Molecular Biology · doi:10.1016/0022-2836(70)90411-0 · Cited by 51 · see citing works

Proteins of Keratin and their Synthesis

Fraser, I. (1969) · Australian Journal of Biological Sciences · doi:10.1071/bi9690213 · Cited by 27 · see citing works

Reactive astrocyte nomenclature, definitions, and future directions

Escartin, C., Galea, E., Lakatos, A., O’Callaghan, J. P., Petzold, G. C., Serrano-Pozo, A., Steinhäuser, C., Volterra, A., Carmignoto, G., Agarwal, A., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-020-00783-4 · Cited by 2,533 · see citing works

Reactive Astrocytes: Production, Function, and Therapeutic Potential

Liddelow, S. A., & Barres, B. A. (2017) · Immunity · doi:10.1016/j.immuni.2017.06.006 · Cited by 2,336 · see citing works

Physiology of Astroglia

Verkhratsky, A., & Nedergaard, M. (2018) · Physiological Reviews · doi:10.1152/physrev.00042.2016 · Cited by 1,678 · see citing works

Protoplasmic Astrocytes in CA1 Stratum Radiatum Occupy Separate Anatomical Domains

Bushong, E. A., Martone, M. E., Jones, Y. Z., & Ellisman, M. H. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-01-00183.2002 · Cited by 1,578 · see citing works

Localization of the glial fibrillary acidic protein in astrocytes by immunofluorescence

Bignami, A., Eng, L. F., Dahl, D. R., & Uyeda, C. T. (1972) · Brain Research · doi:10.1016/0006-8993(72)90398-8 · Cited by 1,456 · see citing works

Glial Fibrillary Acidic Protein: GFAP-Thirty-One Years (1969–2000)

Eng, L. F., Ghirnikar, R. S., & Lee, Y. L. (2000) · Neurochemical Research · doi:10.1023/a:1007677003387 · Cited by 1,368 · see citing works

GFAP in health and disease

Middeldorp, J., & Hol, E. M. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.01.005 · Cited by 1,080 · see citing works

GFAP and Astrogliosis

Eng, L. F., & Ghirnikar, R. S. (1994) · Brain Pathology · doi:10.1111/j.1750-3639.1994.tb00838.x · Cited by 864 · see citing works

Galactocerebroside is a specific cell-surface antigenic marker for oligodendrocytes in culture

RAFF, M. C., Mirsky, R., Fields, K. L., Lisak, R. P., Dorfman, S. H., Silberberg, D. H., Gregson, N. A., Leibowitz, S., & KENNEDY, M. C. (1978) · Nature · doi:10.1038/274813a0 · Cited by 808 · see citing works

Blood GFAP as an emerging biomarker in brain and spinal cord disorders

Abdelhak, A., Foschi, M., Abu-Rumeileh, S., Yue, J. K., D’Anna, L., Huss, A., Oeckl, P., Ludolph, A. C., Kuhle, J., Petzold, A., et al. (2022) · Nature Reviews Neurology · doi:10.1038/s41582-021-00616-3 · Cited by 807 · see citing works

Cell-type-specific markers for distinguishing and studying neurons and the major classes of glial cells in culture

RAFF, M. C., Fields, K. L., Hakomori, S., Mirsky, R., Pruss, R. M., & Winter, J. (1979) · Brain Research · doi:10.1016/0006-8993(79)90851-5 · Cited by 800 · see citing works

Retinoic acid induces embryonal carcinoma cells to differentiate into neurons and glial cells.

Jones-Villeneuve, E. M., McBurney, M. W., Rogers, K. A., & Kalnins, V. I. (1982) · The Journal of cell biology · doi:10.1083/jcb.94.2.253 · Cited by 645 · see citing works

Glial fibrillary acidic protein (GFAP): the major protein of glial intermediate filaments in differentiated astrocytes

Eng, L. F. (1985) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(85)80063-1 · Cited by 737 · see citing works

Immunoperoxidase localization of glial fibrillary acidic protein in radial glial cells and astrocytes of the developing rhesus monkey brain

Levitt, P., & Rakic, P. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901930316 · Cited by 704 · see citing works

Immunocytochemical demonstration of vimentin in astrocytes and ependymal cells of developing and adult mouse nervous system

Schnitzer, J., Franke, W. W., & Schachner, M. (1981) · The Journal of Cell Biology · doi:10.1083/jcb.90.2.435 · Cited by 637 · see citing works

The topographical distribution of S‐100 and GFA proteins in the adult rat brain: An immunohistochemical study using horseradish peroxidase‐labelled antibodies

Ludwin, S. K., Kosek, J. C., & Eng, L. F. (1976) · The Journal of Comparative Neurology · doi:10.1002/cne.901650206 · Cited by 575 · see citing works

Cell lineage in the cerebral cortex of the mouse studied in vivo and in vitro with a recombinant retrovirus.

Luskin, M. B., Pearlman, A., & Sanes, J. (1988) · Neuron · doi:10.1016/0896-6273(88)90163-8 · Cited by 554 · see citing works

Quantitative aspects of reactive gliosis: A review

Norton, W. T., Aquino, D. A., Hozumi, I., Chiu, F., & Brosnan, C. F. (1992) · Neurochemical Research · doi:10.1007/bf00993263 · Cited by 549 · see citing works

Time Course and Diagnostic Accuracy of Glial and Neuronal Blood Biomarkers GFAP and UCH-L1 in a Large Cohort of Trauma Patients With and Without Mild Traumatic Brain Injury

Papa, L., Brophy, G. M., Welch, R. D., Lewis, L. M., Braga, C. F., Tan, C. N., Ameli, N. J., López, M. A., Haeussler, C. A., Giordano, D. M., et al. (2016) · JAMA Neurology · doi:10.1001/jamaneurol.2016.0039 · Cited by 542 · see citing works

GFAP Is Necessary for the Integrity of CNS White Matter Architecture and Long-Term Maintenance of Myelination

(1996) · doi:10.1016/s0896-6273(00)80194-4 · Cited by 538 · see citing works

The astrocyte odyssey

Wang, D. D., & Bordey, A. (2008) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2008.09.015 · Cited by 517 · see citing works

Astrocyte‐specific protein and neuroglial differentiation. An immunofluorescence study with antibodies to the glial fibrillary acidic protein

Bignami, A., & Dahl, D. R. (1974) · The Journal of Comparative Neurology · doi:10.1002/cne.901530104 · Cited by 491 · see citing works

Induction of calcium-independent nitric oxide synthase activity in primary rat glial cultures.

Galea, E., Feinstein, D. L., & Reis, D. J. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.22.10945 · Cited by 478 · see citing works

Brain Enolases as Specific Markers of Neuronal and Glial Cells

Schmechel, D. E., Marangos, P. J., Zis, A. P., Brightman, M., & Goodwin, F. K. (1978) · Science · doi:10.1126/science.339349 · Cited by 461 · see citing works

Adult bone marrow stromal stem cells express germline, ectodermal, endodermal, and mesodermal genes prior to neurogenesis

Woodbury, D., Reynolds, K., & Black, I. B. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10365 · Cited by 460 · see citing works

Identification of a Novel Phosphorylation Site on Histone H3 Coupled with Mitotic Chromosome Condensation

Goto, H., Kosako, H., Tomono, Y., Ajiro, K., Fujita, M., Sakurai, M., Okawa, K., Iwamatsu, A., Okigaki, T., Takahashi, T., et al. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.36.25543 · Cited by 458 · see citing works

Elusive roles for reactive astrocytes in neurodegenerative diseases

Ben Haim, L., Carrillo-de Sauvage, M.-A., Ceyzériat, K., & Escartin, C. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00278 · Cited by 453 · see citing works

Excitatory amino acids activate calpain I and induce structural protein breakdown in vivo

Siman, R. G., & Noszek, J. C. (1988) · Neuron · doi:10.1016/0896-6273(88)90076-1 · Cited by 434 · see citing works

Astrocyte intermediate filaments in CNS pathologies and regeneration

Pekny, M., & Pekna, M. (2004) · The Journal of Pathology · doi:10.1002/path.1645 · Cited by 420 · see citing works

GFAP mRNA increases with age in rat and human brain

Nichols, N. R., Day, J. R., Laping, N. J., Johnson, S. A., & Finch, C. E. (1993) · Neurobiology of Aging · doi:10.1016/0197-4580(93)90100-p · Cited by 413 · see citing works

GFAP promoter elements required for region‐specific and astrocyte‐specific expression

Lee, Y., Messing, A., Su, M., & Brenner, M. (2008) · Glia · doi:10.1002/glia.20622 · Cited by 406 · see citing works

Antibodies to neurofilament, glial filament, and fibroblast intermediate filament proteins bind to different cell types of the nervous system.

Yen, S. H., & Fields, K. L. (1981) · The Journal of Cell Biology · doi:10.1083/jcb.88.1.115 · Cited by 405 · see citing works

Fibrillary astrocytes proliferate in response to brain injury

Latov, N., Nilaver, G., Zimmerman, E. A., Johnson, W. G., Silverman, A., Defendini, R., & COTE, L. J. (1979) · Developmental Biology · doi:10.1016/0012-1606(79)90127-1 · Cited by 397 · see citing works

Coexistence of neuronal and glial precursor cells in the cerebral ventricular zone of the fetal monkey: an ultrastructural immunoperoxidase analysis

Levitt, P. R., Cooper, M., & RAKIC, P. T. (1981) · Journal of Neuroscience · doi:10.1523/jneurosci.01-01-00027.1981 · Cited by 395 · see citing works

GFAP Versus S100B in Serum after Traumatic Brain Injury: Relationship to Brain Damage and Outcome

Pelinka, L. E., Kroepfl, A., Leixnering, M., Buchinger, W., Raabe, A., & Redl, H. R. (2004) · Journal of Neurotrauma · doi:10.1089/neu.2004.21.1553 · Cited by 388 · see citing works

Studies on the function and composition of the 10-nm(100- å) filaments of vertebrate smooth muscle

Small, J. V., & Sobieszek, A. (1977) · Journal of Cell Science · doi:10.1242/jcs.23.1.243 · Cited by 388 · see citing works

Up-Regulation of Glial Fibrillary Acidic Protein in Response to Retinal Injury: Its Potential Role in Glial Remodeling and a Comparison to Vimentin Expression

Lewis, G. P., & Fisher, S. K. (2003) · International review of cytology · doi:10.1016/s0074-7696(03)30005-1 · Cited by 380 · see citing works

Localization of vimentin, the nonspecific intermediate filament protein, in embryonal glia and in early differentiating neurons

Bignami, A., Raju, T. R., & Dahl, D. R. (1982) · Developmental Biology · doi:10.1016/0012-1606(82)90035-5 · Cited by 376 · see citing works

Quantitative real-time RT-PCR assessment of spinal microglial and astrocytic activation markers in a rat model of neuropathic pain

Tanga, F. Y., Raghavendra, V., & DeLeo, J. A. (2004) · Neurochemistry International · doi:10.1016/j.neuint.2003.06.002 · Cited by 375 · see citing works

The L2/HNK-1 carbohydrate of neural cell adhesion molecules is involved in cell interactions.

Künemund, V. H., Jungalwala, F. B., Fischer, G., Chou, D. K. H., Keilhauer, G., & Schachner, M. (1988) · The Journal of Cell Biology · doi:10.1083/jcb.106.1.213 · Cited by 375 · see citing works

The radial glia of Müller in the rat retina and their response to injury. An immunofluorescence study with antibodies to the glial fibrillary acidic (GFA) protein

Dahl, D. R. (1979) · Experimental Eye Research · doi:10.1016/0014-4835(79)90106-4 · Cited by 358 · see citing works

UPTAKE AND METABOLISM OF GLUTAMATE IN ASTROCYTES CULTURED FROM DISSOCIATED MOUSE BRAIN HEMISPHERES

Schousboe, A., Svenneby, G., & Hertz, L. (1977) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1977.tb06503.x · Cited by 346 · see citing works

The Two Patterns of Reactive Astrocytosis in Postischemic Rat Brain

Petito, C. K., Morgello, S., Felix, J. C., & LESSER, M. L. (1990) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1990.141 · Cited by 337 · see citing works

GAT-1, a high-affinity GABA plasma membrane transporter, is localized to neurons and astroglia in the cerebral cortex

Minelli, A., Brecha, N., Karschin, C., Debiasi, S., & Conti, F. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-11-07734.1995 · Cited by 333 · see citing works

Elevated levels of serum glial fibrillary acidic protein breakdown products in mild and moderate traumatic brain injury are associated with intracranial lesions and neurosurgical intervention

Papa, L., Lewis, L. M., Falk, J. L., Zhang, Z., Silvestri, S., Giordano, P., Brophy, G. M., Demery, J. A., Dixit, N. K., Ferguson, I., et al. (2012) · Annals of Emergency Medicine · doi:10.1016/j.annemergmed.2011.08.021 · Cited by 332 · see citing works

Contribution of immunohistochemistry to diagnostic problems of human cerebral tumors.

Eng, L. F., & Rubinstein, L. J. (1978) · Journal of Histochemistry & Cytochemistry · doi:10.1177/26.7.357640 · Cited by 317 · see citing works

Ultrastructural localization of glial fibrillary acidic protein in mouse cerebellum by immunoperoxidase labeling.

Schachner, M., Hedley‐Whyte, E. T., Hsu, D., Schoonmaker, G., & Bignami, A. (1977) · The Journal of Cell Biology · doi:10.1083/jcb.75.1.67 · Cited by 316 · see citing works

Intermediate filament proteins in the developing chick spinal cord

Tapscott, S. J., Bennett, G. S., Toyama, Y., Kleinbart, F. A., & Holtzer, H. (1981) · Developmental Biology · doi:10.1016/0012-1606(81)90313-4 · Cited by 313 · see citing works

The 180-kD component of the neural cell adhesion molecule N-CAM is involved in cell-cell contacts and cytoskeleton-membrane interactions

Pollerberg, G. E., Burridge, K., Krebs, K. E., Goodman, S. R., & Schachner, M. (1987) · Cell and Tissue Research · doi:10.1007/bf00214676 · Cited by 300 · see citing works

Astrocytes in cerebral ischemic injury: Morphological and general considerations

Panickar, K. S., & Norenberg, M. D. (2005) · Glia · doi:10.1002/glia.20181 · Cited by 297 · see citing works

Human immunodeficiency virus can productively infect cultured human glial cells.

Cheng‐Mayer, C., Rutka, J. T., Rosenblum, M. L., McHugh, T. M., Stites, D. P., & Levy, J. A. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.10.3526 · Cited by 297 · see citing works

A new class of drug carriers: micelles of poly(oxyethylene)-poly(oxypropylene) block copolymers as microcontainers for drug targeting from blood in brain

Kabanov, A. V., Batrakova, E. V., Melik-Nubarov, N. S., Fedoseev, N. A., Dorodnich, T. Y., Alakhov, V. Y., Chekhonin, V. P., Nazarova, I. R., & Kabanov, V. A. (1992) · Journal of Controlled Release · doi:10.1016/0168-3659(92)90199-2 · Cited by 295 · see citing works

Biochemical and immunological analysis of rapidly purified 10-nm filaments from baby hamster kidney (BHK-21) cells.

Starger, J. M., Brown, W. E., Goldman, A. E., & Goldman, R. D. (1978) · The Journal of Cell Biology · doi:10.1083/jcb.78.1.93 · Cited by 286 · see citing works

Astrocytes: Form, Functions, and Roles in Disease

Montgomery, D. L. (1994) · Veterinary Pathology · doi:10.1177/030098589403100201 · Cited by 279 · see citing works

Radial glia in the human fetal cerebrum: A combined golgi, immunofluorescent and electron microscopic study

Choi, B. H., & Lapham, L. W. (1978) · Brain Research · doi:10.1016/0006-8993(78)90721-7 · Cited by 277 · see citing works

J1-160 and J1-180 are oligodendrocyte-secreted nonpermissive substrates for cell adhesion.

Pesheva, P., Spieß, E., & Schachner, M. (1989) · The Journal of Cell Biology · doi:10.1083/jcb.109.4.1765 · Cited by 270 · see citing works

Astrocytes increase in glial fibrillary acidic protein during retrograde changes of facial motor neurons

Grabber, M. B., & Kreutzberg, G. W. (1986) · Journal of Neurocytology · doi:10.1007/bf01611438 · Cited by 255 · see citing works

Fibroblast growth factor stimulates the proliferation and differentiation of neural precursor cells in vitro

Murphy, M., Drago, J., & Bartlett, P. F. (1990) · Journal of Neuroscience Research · doi:10.1002/jnr.490250404 · Cited by 255 · see citing works

Cytoimitiunotherapy for persistent virus infection reveals a unique clearance pattern from the central nervous system

Oldstone, M. B. A., Blount, P., Southern, P. J., & Lampert, P. W. (1986) · Nature · doi:10.1038/321239a0 · Cited by 247 · see citing works

The problem of astrocyte identity

Kimelberg, H. K. (2004) · Neurochemistry International · doi:10.1016/j.neuint.2003.08.015 · Cited by 244 · see citing works

Differentiation of astrocytes in the cerebellar cortex and the pyramidal tracts of the newborn rat. An immunofluorescence study with antibodies to a protein specific to astrocytes

Bignami, A., & Dahl, D. R. (1973) · Brain Research · doi:10.1016/0006-8993(73)90430-7 · Cited by 245 · see citing works

Organization of radial glial cells during the development of the rat dentate gyrus

Rickmann, M., Amaral, D. G., & Cowan, W. M. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902640403 · Cited by 243 · see citing works

Neurofilament and glial fibrillary acidic protein in multiple sclerosis

Norgren, N., Sundström, P., Svenningsson, A., Rosengren, L., Stigbrand, T. I., & Gunnarsson, M. (2004) · Neurology · doi:10.1212/01.wnl.0000142988.49341.d1 · Cited by 241 · see citing works

The role of glial fibrillary acidic protein in the diagnosis of central nervous system tumors

Deck, J. H. N., Eng, L. F., Bigbee, J. W., & Woodcock, S. M. (1978) · Acta Neuropathologica · doi:10.1007/bf00690355 · Cited by 241 · see citing works

Serum GFAP is a diagnostic marker for glioblastoma multiforme

Jung, C. S., Foerch, C., Schänzer, A., Heck, A., Plate, K. H., Seifert, V., Steinmetz, H., Raabe, A., & Sitzer, M. (2007) · Brain · doi:10.1093/brain/awm263 · Cited by 238 · see citing works

Neuropathological and computerized tomographic findings in experimental brain abscess

Britt, R. H., Enzmann, D. R., & Yeager, A. S. (1981) · Journal of neurosurgery · doi:10.3171/jns.1981.55.4.0590 · Cited by 239 · see citing works

GLIOSIS FOLLOWING CNS INJURY: THE ANATOMY OF ASTROCYTIC SCARS AND THEIR INFLUENCES ON AXONAL ELONGATION

Reier, P. J. (1986) · Elsevier eBooks · doi:10.1016/b978-0-12-250453-2.50014-1 · Cited by 234 · see citing works

Glial Fibrillary Acidic Protein (GFA) in Normal Neural Cells and in Pathological Conditions

Bignami, A., Dahl, D. R., & Rueger, D. C. (1980) · Advances in cellular neurobiology · doi:10.1016/b978-0-12-008301-5.50012-1 · Cited by 230 · see citing works

EAAC1, a high-affinity glutamate tranporter, is localized to astrocytes and gabaergic neurons besides pyramidal cells in the rat cerebral cortex

Conti, F. (1998) · Cerebral Cortex · doi:10.1093/cercor/8.2.108 · Cited by 227 · see citing works

Retinal and epiretinal glia--an immunohistochemical study.

Hiscott, P. S., Grierson, I., Trombetta, C. J., Rahi, A. H. S., Marshall, J., & McLeod, D. (1984) · British Journal of Ophthalmology · doi:10.1136/bjo.68.10.698 · Cited by 223 · see citing works

Neuronal–glial interactions and behaviour

Laming, P. R., Kimelberg, H. K., Robinson, S. R., Salm, A. K., Hawrylak, N., Müller, C. M., Roots, B. I., & Ng, K. (2000) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(99)00080-9 · Cited by 220 · see citing works

GFAP and S100B in the acute phase of mild traumatic brain injury

Metting, Z., Wilczak, N., Rödiger, L. A., Schaaf, J. M., & van der Naalt, J. (2012) · Neurology · doi:10.1212/wnl.0b013e318253d5c7 · Cited by 219 · see citing works

Benign lipoblastomatosis ultrastructure and histogenesis

GRECO, M. A., Garcia, R. L., & Vuletin, J. C. (1980) · Cancer · doi:10.1002/1097-0142(19800201)45:3 · Cited by 43 · see citing works

Astrocyte-specific protein and radial glia in the cerebral cortex of newborn rat

Bignami, A., & Dahl, D. R. (1974) · Nature · doi:10.1038/252055a0 · Cited by 209 · see citing works

Expression of neurofilament subunits in neurons of the central and peripheral nervous system: an immunohistochemical study with monoclonal antibodies

Trojanowski, J. Q., Walkenstein, N., & Lee, V. (1986) · Journal of Neuroscience · doi:10.1523/jneurosci.06-03-00650.1986 · Cited by 208 · see citing works

NERVOUS SYSTEM SPECIFIC PROTEINS

Bock, E. (1978) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1978.tb07028.x · Cited by 208 · see citing works

Immunocytochemical demonstration of early appearing astroglial structures that form boundaries and pathways along axon tracts in the fetal brain

Silver, J., Edwards, M. A., & Levitt, P. R. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903280308 · Cited by 206 · see citing works

GFAP Out-Performs S100β in Detecting Traumatic Intracranial Lesions on Computed Tomography in Trauma Patients with Mild Traumatic Brain Injury and Those with Extracranial Lesions

Papa, L., Silvestri, S., Brophy, G. M., Giordano, P., Falk, J. L., Braga, C. F., Tan, C. N., Ameli, N. J., Demery, J. A., Dixit, N. K., et al. (2014) · Journal of Neurotrauma · doi:10.1089/neu.2013.3245 · Cited by 206 · see citing works

Measurement of Glial Fibrillary Acidic Protein in Human Blood: Analytical Method and Preliminary Clinical Results

Missler, U., Wiesmann, M., Wittmann, G., Magerkurth, O., & Hagenström, H. (1999) · Clinical Chemistry · doi:10.1093/clinchem/45.1.138 · Cited by 204 · see citing works

Determination of glial fibrillary acidic protein (GFAP) in human brain tumors

Jacque, C., Vinner, C., Kujas, M., Raoul, M. M., Racadot, J., & Baumann, N. (1978) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(78)90107-7 · Cited by 204 · see citing works

αII-Spectrin Breakdown Products (SBDPs): Diagnosis and Outcome in Severe Traumatic Brain Injury Patients

Mondello, S., Robicsek, S. A., Gabrielli, A., Brophy, G. M., Papa, L., Tepas, J. J., Robertson, C. S., Büki, A., Scharf, D., Mo, J., et al. (2010) · Journal of Neurotrauma · doi:10.1089/neu.2010.1278 · Cited by 204 · see citing works

The multifaceted role of astrocytes in regulating myelination

Kıray, H., Lindsay, S. L., Hosseinzadeh, S., & Barnett, S. C. (2016) · Experimental Neurology · doi:10.1016/j.expneurol.2016.03.009 · Cited by 200 · see citing works

Purification of individual components of the neurofilament triplet: filament assembly from the 70000-dalton subunit

Liem, R. K. H., & Hutchison, S. B. (1982) · Biochemistry · doi:10.1021/bi00256a029 · Cited by 201 · see citing works

Glial Fibrillary Acidic Protein and the Mesolimbic Dopamine System: Regulation by Chronic Morphine and Lewis‐Fischer Strain Differences in the Rat Ventral Tegmental Area

Beitner‐Johnson, D., Guitart, X., & Nestler, E. J. (1993) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1993.tb09814.x · Cited by 197 · see citing works

Increased glial fibrillary acidic protein synthesis in astrocytes during retrograde reaction of the rat facial nucleus

Tetzlaff, W., Graeber, M. B., Bisby, M. A., & Kreutzberg, G. W. (1988) · Glia · doi:10.1002/glia.440010110 · Cited by 198 · see citing works

Hormones and growth factors induce the synthesis of glial fibrillary acidic protein in rat brain astrocytes

Morrison, R. S., de Vellis, J., Lee, Y. L., Bradshaw, R. A., & Eng, L. F. (1985) · Journal of Neuroscience Research · doi:10.1002/jnr.490140202 · Cited by 196 · see citing works

Immunohistochemical demonstration of S-100 protein and GFA protein in interstitial cells of rat pineal gland

Møller, M., Ingild, A., & Bock, E. (1978) · Brain Research · doi:10.1016/0006-8993(78)90234-2 · Cited by 195 · see citing works

Toxoplasma gondii infection of the central nervous system

Conley, F. K., Jenkins, K. A., & Remington, J. S. (1981) · Human Pathology · doi:10.1016/s0046-8177(81)80170-0 · Cited by 193 · see citing works

Selective expression of the 180-kD component of the neural cell adhesion molecule N-CAM during development.

Pollerberg, E. G., Sadoul, R., Goridis, C., & Schachner, M. (1985) · The Journal of Cell Biology · doi:10.1083/jcb.101.5.1921 · Cited by 191 · see citing works

Glial fibrillary acidic protein: a potential biomarker for progression in multiple sclerosis

Axelsson, M., Malmeström, C., Nilsson, S., Haghighi, S., Rosengren, L., & Lycke, J. (2010) · Journal of Neurology · doi:10.1007/s00415-010-5863-2 · Cited by 190 · see citing works

Immunological study of the glial fibrillary acidic protein

Uyeda, C. T., Eng, L. F., & Bignami, A. (1972) · Brain Research · doi:10.1016/0006-8993(72)90347-2 · Cited by 190 · see citing works

Biomarkers for the Clinical Differential Diagnosis in Traumatic Brain Injury-A Systematic Review

Yokobori, S., Hosein, K., Burks, S. S., Sharma, I., Gajavelli, S., & Bullock, R. M. (2013) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12127 · Cited by 189 · see citing works

Glial fibrillary acidic protein (GFAP): modulation by growth factors and its implication in astrocyte differentiation

Gomes, F. C. A., Paulin, D., & Moura‐Neto, V. (1999) · Brazilian Journal of Medical and Biological Research · doi:10.1590/s0100-879x1999000500016 · Cited by 189 · see citing works

Mesenchymal Stem Cell-Derived Exosomes Reduce A1 Astrocytes via Downregulation of Phosphorylated NFκB P65 Subunit in Spinal Cord Injury

Wang, L., Pei, S., Han, L., Guo, B., Li, Y., Duan, R., Yao, Y., Xue, B., Chen, X., & Jia, Y. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000494652 · Cited by 188 · see citing works

Blood-based diagnostics of traumatic brain injuries

Mondello, S., Muller, U., Jeromin, A., Streeter, J., Hayes, R., & Wang, K. K. W. (2011) · Expert Review of Molecular Diagnostics · doi:10.1586/erm.10.104 · Cited by 181 · see citing works

Glial fibrillary acidic protein increases in Müller cells after retinal detachment

Erickson, P. A., Fisher, S. K., Guérin, C. J., Anderson, D. H., & Kaska, D. D. (1987) · Experimental Eye Research · doi:10.1016/s0014-4835(87)80023-4 · Cited by 185 · see citing works

Change in body fat, but not body weight or metabolic correlates of obesity, is related to symptomatic relief of obese patients with knee osteoarthritis after a weight control program.

Toda, Y., Toda, T., Takemura, S., Wada, T., Morimoto, T., & Ogawa, R. (1998) · PubMed · Cited by 184 · see citing works

Delayed astrocyte reaction following facial nerve axotomy

Graeber, M. B., & Kreutzberg, G. W. (1988) · Journal of Neurocytology · doi:10.1007/bf01674208 · Cited by 183 · see citing works

Cytokeratins in certain endothelial and smooth muscle cells of two taxonomically distant vertebrate species, Xenopus laevis and man

Jahn, L., Fouquet, B., Rohe, K., & Franke, W. W. (1987) · Differentiation · doi:10.1111/j.1432-0436.1987.tb00198.x · Cited by 180 · see citing works

Immunochemical and immunofluorescence studies of the glial fibrillary acidic protein in vertebrates

Dahl, D. R., & Bignami, A. (1973) · Brain Research · doi:10.1016/0006-8993(73)90533-7 · Cited by 179 · see citing works

Reactive astrocytes express acidic fibroblast growth factor in Alzheimer's disease brain

Yasuhara, O. (1992) · doi:10.11501/3061100

Proteomic analysis of Abeta-associated proteins in cultured astrocytes

Hsu, C.-P. (. (2014) · University of Southern California Digital Library · doi:10.25549/usctheses-c16-308030

astrocytic cytoskeletal proteins

Sampson, D., Pickard, M., Sinha, A., Evans, I. M., Leonard, A., & Ekins, R. P. (2013)

Glial fibrillary acidic protein in primary astroglial cell cultures derived from newborn rat brain

Bock, E. (1977) · FEBS Letters · doi:10.1016/0014-5793(77)81006-5 · Cited by 131 · see citing works

Identity of the major protein in ‘native’ glial fibrillary acidic protein preparation with tubulin

Liem, R. K. H., & Shelanski, M. L. (1978) · Brain Research · doi:10.1016/0006-8993(78)90811-9 · Cited by 22 · see citing works