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

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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

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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
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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

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Self-citation
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Self-citation
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Self-citation
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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

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