Cited by 1,230Neuroscience and Neuropharmacology ResearchNeuroinflammation and Neurodegeneration MechanismsS100 Proteins and Annexins

The DOI matches its Crossref record; 7 of the 8 references it cites were found in a registry or an index.

An acidic protein isolated from fibrous astrocytes

Eng, L.F., Vanderhaeghen, J.J., Bignami, A., Gerstl, B.·1971·Brain Research

DOI 10.1016/0006-8993(71)90668-8

Open this paper in CoChat — free account

Integrity signals

Registry

Crossref · 10.1016/0006-8993(71)90668-8

Cites

7 of 7 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

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 1,161
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
Self-citation
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
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
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
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
Proteins of Keratin and their Synthesis
Fraser, I. (1969) · Australian Journal of Biological Sciences · doi:10.1071/bi9690213 · Cited by 27

Show all 8 references

Research works printed but not linked: 3

Bairati, 1957, Propriétés biophysiques des fibres névrogliques, C.R. Ass. Anat., 44, 113
Eng, L.F., Bond, P., and Gerstl, B., Isolation of myelin proteins from disc acrylamide gels electrophoresed in phenol-formic acid water, Neurobiology, in press.
Moore, 1969, Acidic proteins, Vol. 1, 93

Sorted by citations

Items 201–300 of 1,000

Immunocytochemical study of the glial fibrillary acidic protein in human neoplasms of the central nervous system
Tascos, N. A., Parr, J., & Gonatas, N. K. (1982) · Human Pathology · doi:10.1016/s0046-8177(82)80028-2 · Cited by 109
Chapter 37 Astrocyte activation and fibrous gliosis: glial fibrillary acidic protein immunostaining of astrocytes following intraspinal cord grafting of fetal CNS tissue
Eng, L. F., Reier, P. J., & Houlé, J. D. (1987) · Progress in brain research · doi:10.1016/s0079-6123(08)61845-2 · Cited by 109
Self-citation
Glial fibrillary acidic protein from normal human brain. Purification and properties
Dahl, D. R., & Bignami, A. (1973) · Brain Research · doi:10.1016/0006-8993(73)90141-8 · Cited by 109
Self-citation
Immunohistochemical characterization of oligodendrogliomas: an analysis of multiple markers
Nakagawa, Y., Perentes, E., & Rubinstein, L. J. (1986) · Acta Neuropathologica · doi:10.1007/bf00687942 · Cited by 106
Distinct Populations of Identified Glial Cells in the Developing Rat Spinal Cord Slice: Ion Channel Properties and Cell Morphology
Chvátal, A., Pastor, A., Mauch, M., Syková, E., & Kettenmann, H. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb01027.x · Cited by 106
Effects of prolonged ethanol exposure on the glial fibrillary acidic protein-containing intermediate filaments of astrocytes in primary culture: a quantitative immunofluorescence and immunogold electron microscopic study.
Renau‐Piqueras, J., Zaragozá, R., de Paz, P., Báguena-Cervellera, R., Megias, L. D. R., & Guerri, C. (1989) · Journal of Histochemistry & Cytochemistry · doi:10.1177/37.2.2642942 · Cited by 106
Developmental Expression of the Glial Fibrillary Acidic Protein mRNA in the Central Nervous System and in Cultured Astrocytes
Tardy, M., Fages, C., Riol, H., Prince, G. L., Rataboul, P., Charrière‐Bertrand, C., & Nunez, J. (1989) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1989.tb10911.x · Cited by 106
Biomarkers of Traumatic Brain Injury: Temporal Changes in Body Fluids
Harel, A., Kvist, M., Salla, N., & Välimaa, L. (2016) · eNeuro · doi:10.1523/eneuro.0294-16.2016 · Cited by 105
Purification of murine endothelial cell cultures by flow cytometry using fluorescein-labeled griffonia simplicifolia agglutinin.
Sahagun, G., Moore, S. A., Fábry, Z., Schelper, R. L., & HART, M. N. (1989) · PubMed Central · Cited by 105
The development of bergmann glia in mutant mice with cerebellar malformations: Reeler, staggerer and weaver. 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.901550207 · Cited by 104
Self-citation
Glial reaction in aging and Alzheimer's disease
Unger, J. W. (1998) · Microscopy Research and Technique · doi:10.1002/(sici)1097-0029(19981001)43:1 · Cited by 103
Blood biomarkers for traumatic brain injury: A narrative review of current evidence
Hossain, I., Marklund, N., Czeiter, E., Hutchinson, P. J., & Büki, A. (2023) · Brain and Spine · doi:10.1016/j.bas.2023.102735 · Cited by 103
Degradation of glial fibrillary acidic protein protein by a calcium dependent proteinase: an electroblot study
DeArmond, S. J., Fajardo, M., Naughton, S. A., & Eng, L. F. (1983) · Brain Research · doi:10.1016/0006-8993(83)91018-1 · Cited by 103
Self-citation
Astroglial architecture of the carp ( Cyprinus carpio ) brain as revealed by immunohistochemical staining against glial fibrillary acidic protein (GFAP)
Kálmán, M. (1998) · Anatomy and Embryology · doi:10.1007/s004290050193 · Cited by 102
Astroglial response in the excitotoxically lesioned neostriatum and its projection areas in the rat
Ole Isacson, A., Fischer, W., Wictorin, K., Dawbarn, D., & Björklund, A. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90262-4 · Cited by 100
The Challenge of Mild Traumatic Brain Injury: Role of Biochemical Markers in Diagnosis of Brain Damage
Mondello, S., Schmid, K. E., Berger, R. P., Kobeissy, F. H., Italiano, D., Jeromin, A., Hayes, R. L., Tortella, F. C., & Büki, A. (2013) · Medicinal Research Reviews · doi:10.1002/med.21295 · Cited by 104
Combining Biochemical and Imaging Markers to Improve Diagnosis and Characterization of Mild Traumatic Brain Injury in the Acute Setting: Results from a Pilot Study
Kou, Z., Gattu, R., Kobeissy, F. H., Welch, R. D., O’Neil, B. J., Woodard, J. L., Ayaz, S. I., Kulek, A. R., Kas-Shamoun, R., Mika, V. H., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080296 · Cited by 100
Immunocytochemical Studies of Astrocytes in Normal Development and Disease
Eng, L. F., & DeArmond, S. J. (1982) · Advances in cellular neurobiology · doi:10.1016/b978-0-12-008303-9.50009-8 · Cited by 101
Self-citation
Intermediate (skeletin) filaments in heart Purkinje fibers. A correlative morphological and biochemical identification with evidence of a cytoskeletal function.
Eriksson, A., & Thornell, L. (1979) · The Journal of Cell Biology · doi:10.1083/jcb.80.2.231 · Cited by 101
Bone marrow: a possible alternative source of cells in the adult nervous system
Mezey, É., & Chandross, K. J. (2000) · European Journal of Pharmacology · doi:10.1016/s0014-2999(00)00561-6 · Cited by 100
The distribution of glial fibrillary acidic protein in the adult rat brain is influenced by the neonatal levels of sex steroids
García‐Segura, L. M., Suarez, I., Segovia, S., Tranque, P., Calés, J. M., Aguilera, P., Olmos, G., & Guillamón, A. (1988) · Brain Research · doi:10.1016/0006-8993(88)90239-9 · Cited by 102
Taurine uptake in astrocytes cultured from dissociated mouse brain hemispheres
Schousboe, A., Fosmark, H., & Svenneby, G. (1976) · Brain Research · doi:10.1016/0006-8993(76)90258-4 · Cited by 100
Immunological Markers for Central Nervous System Glia
Huang, H., He, W., Tang, T., & Qiu, M. S. (2022) · Neuroscience Bulletin · doi:10.1007/s12264-022-00938-2 · Cited by 103
Neurofilament expression in vagal neural crest-derived precursors of enteric neurons
Payette, R. F., Bennett, G. S., & Gershon, M. D. (1984) · Developmental Biology · doi:10.1016/0012-1606(84)90285-9 · Cited by 99
Protein Synthesis in Postischemic Rat Brain: A Two-Dimensional Electrophoretic Analysis
Kiessling, M., Dienel, G. A., Jacewicz, M., & Pulsinelli, W. A. (1986) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1986.119 · Cited by 99
The importance of intermediate filaments in the adaptation of tissues to mechanical stress: Evidence from gene knockout studies
Galou, M., Gao, J., Humbert, J., Mericskay, M., Li, Z., Paulin, D., & Vicart, P. (1997) · Biology of the Cell · doi:10.1111/j.1768-322x.1997.tb00997.x · Cited by 98
Growth Kinetics, Cell Shape, and the Cytoskeleton of Primary Astrocyte Cultures
Goldman, J. E., & Chiu, F. (1984) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1984.tb09714.x · Cited by 98
Biomarker-based dissection of neurodegenerative diseases
Olsson, B., Zetterberg, H., Hampel, H. J., & Blennow, K. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.04.006 · Cited by 102
Neuro–glia interaction effects on GFAP gene: a novel role for transforming growth factor‐β1
Spohr, T. C. L. D. S. E., Martinez, R., Silva, E. F. D., Moura‐Neto, V., & Gomes, F. C. A. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02283.x · Cited by 97
Identification of the pituicytes as astroglial cells by indirect immunofluorescence-staining for the glial fibrillary acidic protein
Suess, U., & Pliška, V. (1981) · Brain Research · doi:10.1016/0006-8993(81)91061-1 · Cited by 97
Determination in human cerebrospinal fluid of glial fibrillary acidic protein, S-100 and myelin basic protein as indices of non-specific or specific central nervous tissue pathology
Noppe, M., Crols, R., Andries, D., & Löwenthal, A. (1986) · Clinica Chimica Acta · doi:10.1016/0009-8981(86)90275-5 · Cited by 96
Cellular localization and laminar distribution of AMPA glutamate receptor subunits mRNAs and proteins in the rat cerebral cortex
Conti, F., Minelli, A., & Brecha, N. C. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903500208 · Cited by 96
ADRENERGIC α‐ AND β‐RECEPTORS EXPRESSED BY THE SAME CELL TYPE IN PRIMARY CULTURE OF PERINATAL MOUSE BRAIN
van Calker, D., Müller, M., & Hamprecht, B. (1978) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1978.tb10776.x · Cited by 96
Investigating regeneration and functional integration of CNS neurons: Lessons from zebrafish genetics and other fish species
Fleisch, V. C., Fraser, B., & Allison, W. T. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2010.10.012 · Cited by 93
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
Differential effect of gamma-vinyl GABA and valproate on GABA-transaminase from cultured neurones and astrocytes
Larsson, O. M., Gram, L., Schusboe, I., & Schousboe, A. (1986) · Neuropharmacology · doi:10.1016/0028-3908(86)90214-5 · Cited by 95
Coexpression patterns of vimentin and glial filament protein with cytokeratins in the normal, hyperplastic, and neoplastic breast.
Gould, V. E., Koukoulis, G. Κ., Jansson, D. S., Nagle, R. B., Franke, W. W., & Moll, R. (1990) · Europe PMC (PubMed Central) · Cited by 95
Thorough overview of ubiquitin C‐terminal hydrolase‐L1 and glial fibrillary acidic protein as tandem biomarkers recently cleared by US Food and Drug Administration for the evaluation of intracranial injuries among patients with traumatic brain injury
Wang, K., Kobeissy, F. H., Shakkour, Z., & Tyndall, J. A. (2021) · Acute Medicine & Surgery · doi:10.1002/ams2.622 · Cited by 101
Astrocytic intermediate filaments: lessons from GFAP and vimentin knock-out mice
Pekny, M. (2001) · Progress in brain research · doi:10.1016/s0079-6123(01)32062-9 · Cited by 93
New Immunohistochemical Markers in the Evaluation of Central Nervous System Tumors: A Review of 7 Selected Adult and Pediatric Brain Tumors
Takei, H., Bhattacharjee, M. B., Rivera, A. L., Dancer, Y., & Powell, S. Z.-E. (2007) · Archives of Pathology & Laboratory Medicine · doi:10.5858/2007-131-234-nimite · Cited by 93
Fluid Biomarkers of Traumatic Brain Injury and Intended Context of Use
Bogoslovsky, T., Gill, J., Jeromin, A., Davis, C., & Diaz-Arrastia, R. R. (2016) · Diagnostics · doi:10.3390/diagnostics6040037 · Cited by 93
Astrocyte heterogeneity across the brain and spinal cord occurs developmentally, in adulthood and in response to demyelination
Yoon, H., Walters, G. C., Paulsen, A. R., & Scarisbrick, I. A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0180697 · Cited by 101
Glial Fibrillary Acidic Protein and Ubiquitin C-Terminal Hydrolase-L1 Are Not Specific Biomarkers for Mild CT-Negative Traumatic Brain Injury
Posti, J. P., Hossain, I., Takala, R. S. K., Liedes, H., Newcombe, V., Outtrim, J. G., Katila, A. J., Frantzén, J., Ala-Seppälä, H. M., Coles, J., et al. (2016) · Journal of Neurotrauma · doi:10.1089/neu.2016.4442 · Cited by 92
M�ller cells in detached human retina express glial fibrillary acidic protein and vimentin
Okada, M., Matsumura, M., Ogino, N., & Honda, Y. (1990) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/bf00927264 · Cited by 92
Localization of sodium/potassium adenosine triphosphatase in multiple cell types of the murine nervous system with antibodies raised against the enzyme from kidney
Ariyasu, R., Nichol, J., & Ellisman, M. H. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-10-02581.1985 · Cited by 92
Diversity of Reactive Astrogliosis in CNS Pathology: Heterogeneity or Plasticity?
Moulson, A. J., Squair, J. W., Franklin, R. J. M., Tetzlaff, W., & Assinck, P. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.703810 · Cited by 97
Glycine‐ and GABA‐activated Currents in Identified Glial Cells of the Developing Rat Spinal Cord Slice
Pastor, A., Chvátal, A., Syková, E., & Kettenmann, H. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb01109.x · Cited by 91
Postnatal development of dye‐coupling among astrocytes in rat visual cortex
Binmöller, F.-J., & Müller, C. M. (1992) · Glia · doi:10.1002/glia.440060207 · Cited by 92
Modification of astrocytes in the spinal cord following dorsal root or peripheral nerve lesions
Murray, M., Wang, S., Goldberger, M. E., & Levitt, P. R. (1990) · Experimental Neurology · doi:10.1016/0014-4886(90)90036-r · Cited by 91
Intermediate Filaments from Bovine, Rat, and Human CNS: Mapping Analysis of the Major Proteins
Chiu, F., Korey, B., & Norton, W. T. (1980) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1980.tb09954.x · Cited by 91
Glial fibrillary acidic protein in ependymomas and other brain tumors
Duffy, P. E., Graf, L., Huang, Y., & Rapport, M. M. (1979) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(79)90199-0 · Cited by 90
Estradiol — induced redistribution of glial fibrillary acidic protein immunoreactivity in the rat brain
Trangue, P. A., Suarez, I., Olmos, G., Fernández, B., & García‐Segura, L. M. (1987) · Brain Research · doi:10.1016/0006-8993(87)90805-5 · Cited by 91
Effects of primary antiserum dilution on staining of "antigenrich" tissues with the peroxidase antiperoxidase technique.
Bigbee, J. W., Kosek, J. C., & Eng, L. F. (1977) · Journal of Histochemistry & Cytochemistry · doi:10.1177/25.6.69655 · Cited by 90
Self-citation
Selective down‐regulation of the astrocyte glutamate transporters GLT‐1 and GLAST within the medial thalamus in experimental Wernicke's encephalopathy
Hazell, A. S., Rao, K. V. R., Danbolt, N. C., Pow, D. V., & Butterworth, R. F. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00436.x · Cited by 89
An ELISA for glial fibrillary acidic protein
Petzold, A., Keir, G., Green, A. J. E., Giovannoni, G., & Thompson, E. J. (2004) · Journal of Immunological Methods · doi:10.1016/j.jim.2004.01.015 · Cited by 89
Glial fibrillary acidic protein messenger RNA and glutamine synthetase activity after nervous system injury
Condorelli, D. F., Dell’Albani, P., Kaczmarek, L., Messina, L., Spampinato, G., Avola, R., Messina, A., & Stella, A. M. G. (1990) · Journal of Neuroscience Research · doi:10.1002/jnr.490260216 · Cited by 89
Oligodendrocyte-derived J1-160/180 extracellular matrix glycoproteins are adhesive or repulsive depending on the partner cell type and time of interaction
Morganti, M. C., Taylor, J., Pesheva, P., & Schachner, M. (1990) · Experimental Neurology · doi:10.1016/s0014-4886(05)80012-3 · Cited by 89
Glial Fibrillary Acidic Protein Increases in the Spinal Cord of Lewis Rats with Acute Experimental Autoimmune Encephalomyelitis
Aquino, D. A., Chiu, F., Brosnan, C. F., & Norton, W. T. (1988) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1988.tb03072.x · Cited by 89
GLIAL CELL LINES
Pfeiffer, S. E., Betschart, B., COOK, J., Mancini, P. E., & Morris, R. J. (1977) · Elsevier eBooks · doi:10.1016/b978-0-12-250450-1.50019-3 · Cited by 89
Simultaneous Separation and Purification of Neurofilament and Glial Filament Proteins from Brain
Liem, R. K. H. (1982) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1982.tb10865.x · Cited by 88
Alzheimer's Disease and Related Conditions.
Calne, D. B. (1971) · Annals of Internal Medicine · doi:10.7326/0003-4819-75-5-826_1 · Cited by 87
Astrocitos en las enfermedades neurodegenerativas (I): función y caracterización molecular
Guillamón-Vivancos, T., Gómez‐Pinedo, U., & Matías‐Guiu, J. (2013) · Neurología · doi:10.1016/j.nrl.2012.12.007 · Cited by 98
Expression of microtubule-associated protein 2 by reactive astrocytes.
Geisert, E. E., Johnson, H. G., & Binder, L. I. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.10.3967 · Cited by 86
Subclass of astroglia in mouse cerebellum recognized by monoclonal antibody
Lagenaur, C. F., Sommer, I., & Schachner, M. (1980) · Developmental Biology · doi:10.1016/0012-1606(80)90122-0 · Cited by 86
Comparing Glial Fibrillary Acidic Protein (GFAP) in Serum and Plasma Following Mild Traumatic Brain Injury in Older Adults
Huebschmann, N. A., Luoto, T. M., Karr, J. E., Berghem, K., Blennow, K., Zetterberg, H., Ashton, N. J., Simrén, J., Posti, J. P., Gill, J. M., et al. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.01054 · Cited by 85
The Discovery of the Matrix Cell, the Identification of the Multipotent Neural Stem Cell and the Development of the Central Nervous System
Fujita, S. (2003) · Cell Structure and Function · doi:10.1247/csf.28.205 · Cited by 85
Co‐expression of nestin and vimentin intermediate filaments in invasive human astrocytoma cells
Rutka, J. T., Ivanchuk, S. M., Mondal, S., Taylor, M. D., Sakai, K., Dirks, P. B., Jun, P. Y., Jung, S., Becker, L. E., & Ackerley, C. A. (1999) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(99)00049-0 · Cited by 85
Cellular heterogeneity in primary cultures of brain cells revealed by immunocytochemical localization of glutamine synthetase
Hallermayer, K., & Hamprecht, B. (1984) · Brain Research · doi:10.1016/0006-8993(84)90810-2 · Cited by 85
Should We Stop Saying ‘Glia’ and ‘Neuroinflammation’?
Masgrau, R., Guaza, C., Ransohoff, R. M., & Galea, E. (2017) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2017.04.005 · Cited by 88
Differential splicing of MAG transcripts during CNS and PNS development
Tropak, M. B., Johnson, P. W., Dunn, R. J., & Roder, J. (1988) · Molecular Brain Research · doi:10.1016/0169-328x(88)90006-x · Cited by 84
The Diversity of Intermediate Filaments in Astrocytes
Potokar, M., Morita, M., Wiche, G., & Jorgačevski, J. (2020) · Cells · doi:10.3390/cells9071604 · Cited by 91
Glial fibrillary acidic protein in Alzheimer’s disease: a narrative review
Leipp, F., Vialaret, J., Mohaupt, P., Coppens, S., Jaffuel, A., Niehoff, A., Lehmann, S., & Hirtz, C. (2024) · Brain Communications · doi:10.1093/braincomms/fcae396 · Cited by 88
Regulation of glial fibrillary acidic protein (GFAP) expression in CNS development and in pathological states
Chiu, F., & Goldman, J. E. (1985) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(85)80067-9 · Cited by 83
Mice lacking NT-3, and its receptor TrkC, exhibit profound deficiencies in CNS glial cells
Kahn, M. A., Kumar, S., Liebl, D. J., Chang, R., Parada, L. F., & de Vellis, J. (1999) · Glia · doi:10.1002/(sici)1098-1136(199904)26:2 · Cited by 99
The blood-brain barrier protects foreign antigens in the brain from immune attack
Pollack, I. F., & Lund, R. D. (1990) · Experimental Neurology · doi:10.1016/0014-4886(90)90017-m · Cited by 82
Expression of glial fibrillary acidic protein and its relation to tract formation in embryonic zebrafish (Danio rerio)
Marcus, R. C., & Easter, S. S. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903590302 · Cited by 81
Spinal cord multiple sclerosis lesions in Japanese patients: Schwann cell remyelination occurs in areas that lack glial fibrillary acidic protein (GFAP)
Itoyama, Y., Ohnishi, A., Tateishi, J., Kuroiwa, Y., & de Webster, H. F. (1985) · Acta Neuropathologica · doi:10.1007/bf00687001 · Cited by 81
Cytokine-stimulated astrocytes damage human neurons via a nitric oxide mechanism
Chao, C. C., Hu, S., Sheng, W. S., Bu, D.-F., Bukrinsky, M., & Peterson, P. K. (1996) · Glia · doi:10.1002/(sici)1098-1136(199603)16:3 · Cited by 273
Effect of Homo‐β‐Proline and Other Heterocyclic GAB A Analogues on GABA Uptake in Neurons and Astroglial Cells and on GABA Receptor Binding
Larsson, O. M., Thorbek, P., Krogsgaard‐Larsen, P., & Schousboe, A. (1981) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1981.tb06320.x · Cited by 80
Subcellular localization and molecular topology of the dopamine transporter in the striatum and substantia nigra
Hersch, S. M., Yi, H. L., Heilman, C. J., Edwards, R. H., & Levey, A. I. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19971117)388:2 · Cited by 290
Multiple marker analysis in the avian optic tectum reveals three classes of neuroglia and carbonic anhydrase-containing neurons
Linser, P. J. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-09-02388.1985 · Cited by 80
The Immunological Identification of Brain Proteins on Cellulose Nitrate in Human Demyelinating Disease
Newcombe, J., Glynn, P., & Cuzner, M. L. (1982) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1982.tb10880.x · Cited by 80
Bilateral Injections of Amyloid-β 25-35 into the Amygdala of Young Fischer Rats: Behavioral, Neurochemical, and Time Dependent Histopathological Effects
Sigurdsson, E. M., Lee, J. M., Dong, X.-W., Hejna, M. J., & Lorens, S. A. (1997) · Neurobiology of Aging · doi:10.1016/s0197-4580(97)00154-1 · Cited by 81
Malignant peripheral nerve sheath tumors of the buttock and lower extremity. A study of 43 cases
Hruban, R. H., Shiu, M. H., Senie, R. T., & Woodruff, J. M. (1990) · Cancer · doi:10.1002/1097-0142(19900915)66:6 · Cited by 364
Inhibition of growth and induction of differentiation in a malignant human glioma cell line by normal leptomeningeal extracellular matrix proteins.
Rutka, J. T., Giblin, J. R., Apodaca, G., DeArmond, S. J., Stern, R., & Rosenblum, M. L. (1987) · PubMed · Cited by 79
Astrocyte phenotypes and their relationship to myelination
Nash, B., Ioannidou, K., & Barnett, S. C. (2010) · Journal of Anatomy · doi:10.1111/j.1469-7580.2010.01330.x · Cited by 77
Radial glia and astrocytes in developing and adult telencephalon of the lizard Gallotia galloti as revealed by immunohistochemistry with anti‐GFAP and anti‐vimentin antibodies
Yanes, C. M., Monzón-Mayor, M., Ghandour, M. S., de Barry, J., & Gombos, G. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902950405 · Cited by 78
Characterization of human cDNA and genomic clones for glial fibrillary acidic protein
Brenner, M., Lampel, K. A., Nakatani, Y., Mill, J. F., Banner, C., Mearow, K. M., Dohadwala, M., Lipsky, R. H., & Freese, E. (1990) · Molecular Brain Research · doi:10.1016/0169-328x(90)90078-r · Cited by 78
Effects of propofol on ischemia-reperfusion and traumatic brain injury
Hausburg, M. A., Banton, K. L., Roman, P. E., Salgado, F., Baek, P., Waxman, M., Tanner, A. H., Yoder, J., & Bar‐Or, D. (2019) · Journal of Critical Care · doi:10.1016/j.jcrc.2019.12.021 · Cited by 77
Vimentin and glial fibrillary acidic protein in human brain tumors
Yung, W.-K., Luna, M. A., & Borit, A. (1985) · Journal of Neuro-Oncology · doi:10.1007/bf00165169 · Cited by 77
The relationship of glial fibrillary acidic protein to the shape, motility, and differentiation of human astrocytoma cells
Duffy, P. E., Huang, Y., & Rapport, M. M. (1982) · Experimental Cell Research · doi:10.1016/0014-4827(82)90328-7 · Cited by 77
Immunofluorescent Visualization of 100 Å Filaments in Different Cultured Chick Embryo Cell Types
Bennett, G. S., FELLINI, S. A., & Holtzer, H. (1979) · Differentiation · doi:10.1111/j.1432-0436.1979.tb00992.x · Cited by 77
Developmental expression of the Glial fibrillary acidic protein (GFAP) gene in the mouse retina
Sarthy, P. V., Fu, M., & Huang, J. (1991) · Cellular and Molecular Neurobiology · doi:10.1007/bf00741450 · Cited by 76
Connexin expression in the retina
Söhl, G., Güldenagel, M., Traub, O., & Willecke, K. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00074-0 · Cited by 76
Interactive properties of human glioblastoma cells with brain neurons in culture and neuronal modulation of glial laminin organization
Faria, J., Romão, L. F., Martins, S. C. D. S., Alves, T. R., Mendes, F. A., de Faria, G. P., Hollanda, R., Takiya, C. M., Chimelli, L. M. C., Morandi, V., et al. (2006) · Differentiation · doi:10.1111/j.1432-0436.2006.00090.x · Cited by 76
Grafts of fetal central nervous system tissue rescue axotomized clarke's nucleus neurons in adult and neonatal operates
Himes, B. T., Goldberger, M. E., & Tessler, A. R. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903390111 · Cited by 76
Glial fibrillary acidic protein and intermediate filaments in human glioma cells
Paetau, A. E., Viranen, I., Stenman, S., Kurki, P., Linder, E., Vaheri, A., Westermark, B., Dahl, D. R., & Haltia, M. (1979) · Acta Neuropathologica · doi:10.1007/bf00698276 · Cited by 76
Preferential phosphorylation of the 150,000 molecular weight component of neurofilaments by a cyclic AMP-dependent, microtubule-associated protein kinase.
Leterrier, J. F., Liem, R. K. H., & Shelanski, M. L. (1981) · The Journal of Cell Biology · doi:10.1083/jcb.90.3.755 · Cited by 76
Focal ependymal differentiation in choroid plexus papillomas
Rubinstein, L. J., & Brucher, J.-M. (1981) · Acta Neuropathologica · doi:10.1007/bf00697181 · Cited by 75
Tau, Glial Fibrillary Acidic Protein, and Neurofilament Light Chain as Brain Protein Biomarkers in Cerebrospinal Fluid and Blood for Diagnosis of Neurobiological Diseases
Park, Y., Nirajan, K. C., Paneque, A., & Cole, P. D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126295 · Cited by 78

Authors: Eng, L. F., Vanderhaeghen, J. J., Bignami, A., & Gerstl, B.
Affiliations: United States Department of Veterans Affairs (US)
Venue: Brain Research
Publisher: Elsevier BV
Published: 1971-05
Volume: 28
Issue: 2
Pages: 351-354
ISSN: 0006-8993 (ISSN-L)
DOI: 10.1016/0006-8993(71)90668-8
OpenAlex: W2055390759
Cited by: 1,230
References: 8
Citations by year: 2026: 16 · 2025: 22 · 2024: 21 · 2023: 21 · 2022: 23 · 2021: 23 · 2020: 16 · 2019: 13 · 2018: 13 · 2017: 16 · 2016: 16 · 2015: 28 · 2014: 12 · 2013: 23 · 2012: 15
FWCI: 3.99
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Brain Research (publishedVersion)
PubMed (publishedVersion)
Dépôt institutionnel de l'Université libre de Bruxelles (Université Libre de Bruxelles) (submittedVersion)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › S100 Proteins and Annexins
Keywords: acidic proteins, fibrous astrocytes, astrocytes, protein extraction, glial cells
MeSH terms: Aged, Amino Acids, Brain, Electrophoresis, Disc, Gliosis, Humans, Hydrocephalus, Hydrogen-Ion Concentration, Multiple Sclerosis, Nerve Tissue Proteins, Neuroglia

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

An acidic protein isolated from fibrous astrocytes

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks