Cited by 381Microtubule and mitosis dynamicsNeuroscience and Neuropharmacology ResearchNeurogenesis and neuroplasticity mechanisms

The DOI matches its Crossref record; 58 of the 61 references it cites were found in a registry or an index.

Distribution of microtubule-associated protein 2 in the nervous system of the rat studied by immunofluorescence

De Camilli, P., Miller, P.E., Navone, F., Theurkauf, W.E., Vallee, R.B.·1984·Neuroscience

DOI 10.1016/0306-4522(84)90194-5

Open this paper in CoChat — free account

Abstract

It has recently been reported that high molecular weight microtubule-associated proteins are differently distributed in dendrites and axons of neurons [ Matus Bernhardt and Hugh-Jones (1981), Proc. natn Acad. Sci. U.S.A. 78, 3010-3014; Vallee (1982), J. Cell Biol. 92, 435-442]. We have reported earlier in a preliminary form [Miller, Walter, Theurkauf , Vallee and De Camilli (1982), Proc. natn Acad. Sci. U.S.A. 79, 5562-5566] that an antiserum specific for microtubule-associated protein 2, one of the most prominent high molecular weight microtubule-associated proteins in brain and a major brain phosphoprotein, stains specifically neuronal dendrites and perikarya. We have now extended those observations by performing a detailed analysis of the distribution of microtubule-associated protein 2 throughout the nervous system of the rat. We found that microtubule-associated protein 2 is present at high concentrations in the great majority of neurons. Under our conditions of immunostaining microtubule-associated protein 2 was not detected in nonneuronal cells. In all neurons it was compartmentalized in perikarya and dendrites. In most cases, the latter were more heavily stained than perikarya. The pattern of staining (overall intensity, relative intensity in dendrites vs perikarya, and in proximal vs distal segments of the dendritic tree), varied in different classes of neurons but was identical for all neurons with similar geometry in the same brain region. Different patterns of sta…

Integrity signals

Registry

Crossref · 10.1016/0306-4522(84)90194-5

Cites

58 of 58 references verified0 citation errors · 0 not checkable

Statistics

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

Claims the paper makes

This paper’s full text isn’t openly available, 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?

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961
Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.
Towbin, H., Staehelin, T., & Gordon, J. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.9.4350 · Cited by 53,218
Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane
Fairbanks, G., Steck, T. L., & Wallach, D. F. H. (1971) · Biochemistry · doi:10.1021/bi00789a030 · Cited by 8,526
The Synaptic Organization of the Brain
(2004) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195159561.001.1 · Cited by 3,574
A protein factor essential for microtubule assembly
Weingarten, M. D., Lockwood, A. H., Hwo, S. Y., & Kirschner, M. W. (1975) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.72.5.1858 · Cited by 3,089
Cerebellar Cortex: Cytology and Organization
Palay, S. L., & Chan‐Palay, V. (1974) · Medical Entomology and Zoology · Cited by 1,679
Untitled work
(1976) · Medical Entomology and Zoology · Cited by 1,328
The neurosciences. Fourth study program
Hughes, J. R. (1980) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(80)90242-4 · Cited by 1,166
Branching dendritic trees and motoneuron membrane resistivity
Rall, W. (1959) · Experimental Neurology · doi:10.1016/0014-4886(59)90046-9 · Cited by 1,013
The Synaptic Organization of the Brain
Freemon, F. R. (1980) · JAMA · doi:10.1001/jama.1980.03300440052037 · Cited by 709

Show all 61 references

Research works printed but not linked: 8

Aamodt, 1983, MAPs mediate association of microtubules and neurofilaments in vitro, Biophys. J., 41, 86a
Golgi, 1883, Sulla fine anatomia degli organi centrali del sistema nervoso. IV. Sulla fine anatomia delle circonvoluzioni cerebellari, Riv. sper. Freniat. Med. leg. Alien. Ment., 9, 1
Kandel, 1977, Neuronal plasticity and the modification of behaviour, Vol. 1, 1137
Papasozomenos, 1972, A monoclonal antibody to microtubule-associated protein (MAP2) localizes with neurofilaments in the b,b′-iminodiproprionitrile (IDPN) model, J. Cell Biol., 95, 341a
Peloquin, 1979, Cell and tissue distribution of the major high molecular weight microtubule-associated protein from brain, J. Cell Biol., 83, 338a
Ramón, 1911, Vol. 1,II
Theurkauf, 1982, Phosphorylation of MAP2 by cAMP-dependent protein kinase, J. Cell Biol., 95, 340a
Vallee, 1982, Identification of MAPs from diverse sources using taxol, J. Cell Biol., 95, 339a

Sorted by citations

Items 301–381 of 381

Histopathologic changes induced by the microtubule‐stabilizing agent Taxol in the rat hippocampus in vivo
Mercado-Gómez, O. F., Ferrera, P., & Arias, C. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20264 · Cited by 12
Differential localization of high‐ and low‐molecular‐weight variants of microtubule‐associated protein 2 in the developing rat telencephalon
Fujimori, K. E., Takauji, R., & Tamamaki, N. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10286 · Cited by 12
Wiring dendrites in layers and columns
Luo, J., McQueen, P. G., Shi, B., Lee, C., & Ting, C. (2016) · Journal of Neurogenetics · doi:10.3109/01677063.2016.1173038 · Cited by 12
Isolation and Characterization of Two Rat Alpha‐Tubulin Isotypesa
Ginzburg, I., TEICHMAN, A., & Littauer, U. Z. (1986) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1986.tb38382.x · Cited by 12
The Cerebellar Cortex and the Dentate Nucleus in Hereditary Ataxia
Koeppen, A. H., & Turok, D. I. (1992) · Foundations of neurology · doi:10.1007/978-1-4615-3510-2_9 · Cited by 12
Protein phosphorylation systems in postmortem human brain
Walaas, S. I., Perdahl, E., Winblad, B. G., & Greengard, P. (1989) · Journal of Molecular Neuroscience · doi:10.1007/bf02896894 · Cited by 12
[17] Type II cAMP-dependent protein kinase regulatory subunit-binding proteins
Lohmann, S. M., Camilli, P. V. D., & Walter, U. (1988) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(88)59019-5 · Cited by 12
Gelatin methacrylate hydrogel loaded with brain‐derived neurotrophic factor enhances small molecule‐induced neurogenic differentiation of stem cells from apical papilla
Zou, T., Jiang, S., Yi, B., Chen, Q., Heng, B. C., & Zhang, C. (2021) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.37315 · Cited by 12
Microtubule-Associated Proteins
Olmsted, J. (1986) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.2.1.421 · Cited by 11
Neuronal Tip Growth
Heidemann, S. R. (1990) · Elsevier eBooks · doi:10.1016/b978-0-12-335845-5.50014-8 · Cited by 11
Norepinephrine-Dependent Neuronal Plasticity in Kitten Visual Cortex
Kasamatsu, T., & Shirokawa, T. (1988) · Springer eBooks · doi:10.1007/978-1-4757-9610-0_41 · Cited by 11
Construction of a decellularized spinal cord matrix/GelMA composite scaffold and its effects on neuronal differentiation of neural stem cells
He, W., Wang, H., Zhang, X., Mao, T., Lu, Y., Gu, Y., Ju, D., Qi, L., Wang, Q., & Dong, C. (2022) · Journal of Biomaterials Science Polymer Edition · doi:10.1080/09205063.2022.2102275 · Cited by 10
Microtubule‐Associated Cyclic AMP‐Dependent Protein Kinase in Drosophila melanogaster
Ádám, G., & Friedrich, P. (1988) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1988.tb03062.x · Cited by 10
Pyramidal Cell Modules in Rat Visual Cortex: Their Structure and Development
Peters, A. (1993) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4899-6707-7_9 · Cited by 10
Recent cytoarchitechtonic changes in the prefrontal cortex of schizophrenics
Liesl, B. J. (2001) · Frontiers in bioscience · doi:10.2741/jones · Cited by 10
A primary culture system of rat olfactory bulb forming many synapses similar to intact ones and spontaneously generating synchronous intracellular calcium oscillations
Muramoto, K., Kato, M., Matsuoka, M., Kuroda, Y., & Ichikawa, M. (2001) · Anatomy and Embryology · doi:10.1007/pl00008245 · Cited by 10
Changes in Cytoskeletal Elements during Postnatal Development of Cerebral Cortex
Cronly-Dillon, J. R., & Nona, S. N. (1988) · Cerebral cortex · doi:10.1007/978-1-4615-6619-9_9 · Cited by 10
Three-dimensional visualization of cerebral blood vessels and neural changes in thick ischemic rat brain slices using tissue clearing
Lee, E. H., Hong, S.-K., Choi, D., Gum, S.-I., Hwang, M. Y., Kim, D. S., Oh, J. W., & Lee, E.-S. (2022) · Scientific Reports · doi:10.1038/s41598-022-19575-w · Cited by 8
Murine BC1 RNA in dendritic fields of the retinal inner plexiform layer
Tiedge, H., Dräger, U. C., & Brosius, J. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90879-c · Cited by 9
α-Tubulin is not detyrosylated during axonal transport
Burgoyne, R. D., & Norman, K.-M. (1986) · Brain Research · doi:10.1016/0006-8993(86)90697-9 · Cited by 9
Immunocytochemical localization of tropomyosin in rat cerebellum
Burgoyne, R. D., & Norman, K.-M. (1985) · Brain Research · doi:10.1016/0006-8993(85)91287-9 · Cited by 9
Olivopontocerebellar Atrophy in Two Adult Cats, Sporadic Cases or New Genetic Entity
Résibois, A., & Poncelet, L. (2004) · Veterinary Pathology · doi:10.1354/vp.41-1-20 · Cited by 9
Spatial distributions of cytoskeletal proteins and the nerve growth factor receptor in septal transplants in oculo: Protection from abnormal immunoreactivity by hippocampal co-grafts
Doering, L. C., Eriksdotter, M., & Olson, L. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90063-t · Cited by 9
Cyclic modulation of cross-linking interactions of microtubule-associated protein-2 with actin and microtubules by protein kinase FA
Yang, S.-D., Song, J., Liu, H., & Chan, W. (1993) · Journal of Protein Chemistry · doi:10.1007/bf01025039 · Cited by 9
Morphology of neurons cultured from subdivisions of the mouse cochlear nucleus
Fitzakerley, J. L., & Schweitzer, L. (2003) · Cell and Tissue Research · doi:10.1007/s00441-002-0690-0 · Cited by 8
Cytoskeletal Protein Immunoexpression in Fetal Neural Grafts: Distribution of Phosphorylated and Nonphosphorylated Neurofilament Protein and Microtubule-Associated Protein 2 (Map-2)
Rosenstein, J. M., & Krum, J. M. (1996) · Cell Transplantation · doi:10.1016/0963-6897(95)02031-4 · Cited by 8
α1-Antichymotrypsin supports short-term survival of cerebral neurons in culture
Mizuguchi, M., & Kim, S. U. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90085-8 · Cited by 8
Monoclonal antibodies against larval nervous system of Xenopus laevis: Their specificities and application to analysis of neural development
Mitani, S., & Okamoto, H. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90027-9 · Cited by 8
A microfluidic model of the first sensory synapse for analgesic target discovery
Kimourtzis, G., & Raouf, R. (2024) · Molecular Pain · doi:10.1177/17448069241293286 · Cited by 6
Erythropoietin Production in Embryonic Neural Cells is Controlled by Hypoxia Signaling and Histone Deacetylases with an Undifferentiated Cellular State
Iwamura, Y., Nakai, T., Kato, K., Ishioka, H., Yamamoto, M. P., Hirano, I., & Suzuki, N. (2024) · Molecular and Cellular Biology · doi:10.1080/10985549.2024.2428717 · Cited by 8
Perinatal lamb mortality: an assessment of gross, histological and immunohistochemical changes in the central nervous system
Lashley, V., Roe, W. D., Kenyon, P. R., & Thompson, K. (2013) · New Zealand Veterinary Journal · doi:10.1080/00480169.2013.875980 · Cited by 7
Compartmentation of α-tubulin in neurons: Identification of a somatodendritic-specific variant of α-tubulin
Baas, P. W., & Black, M. M. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90170-x · Cited by 7
Sorting of Sox1-GFP Mouse Embryonic Stem Cells Enhances Neuronal Identity Acquisition upon Factor-Free Monolayer Differentiation
Incitti, T., Messina, A., Bozzi, Y., & Casarosa, S. (2014) · BioResearch open access · doi:10.1089/biores.2014.0009 · Cited by 7
Differential localization of microtubules in cerebellar cells
Ginzburg, I., Behar, L., Littauer, U. Z., & Griffin, W. S. T. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-06-01961.1989 · Cited by 7
Cytotypic Specialization of the Neuronal Cytoskeleton and the Cytomatrix: Implications for Neuronal Growth and Regeneration
Brady, S. T. (1988) · Springer eBooks · doi:10.1007/978-3-642-73148-8_27 · Cited by 7
Some neuronal properties of PC12 cells differentiated by the K-ras oncogene
Brightman, M., SIMPSON, D. L., Tao-Cheng, J.-H., Bressler, J. P., Okuda, O., & Chang, L. H. (1990) · Journal of Neurocytology · doi:10.1007/bf01188045 · Cited by 7
Immunolocalization of MAP-2 in Routinely Formalin-Fixed, Paraffin-Embedded Guinea Pig Brain Sections Using Microwave Irradiation: A Comparison of Different Combinations of Antibody Clones and Antigen Retrieval Buffer Solutions
Kan, R. K., Pleva, C. M., Hamilton, T. A., & Petrali, J. P. (2005) · Microscopy and Microanalysis · doi:10.1017/s1431927605050191 · Cited by 6
MICROTUBULE FORMATION AND KINESIN‐DRIVEN MICROTUBULE GLIDING IN VITRO IN THE PRESENCE OF LIPOPOLYSACCHARIDE
Böhm, K. J., Rußwurm, S., Ghaleb, N., Reinhart, K., & Unger, E. (1999) · Cell Biology International · doi:10.1006/cbir.1999.0382 · Cited by 6
Control of microtubule polymerization and stability
Ávila, J., & Díaz‐Nido, J. (1995) · The Cytoskeleton · doi:10.1016/s1874-6020(06)80005-4 · Cited by 6
Immunocytochemical demonstration of tubulin microheterogeneity within rat cortical and hippocampal pyramidal neurons
Hajós, F., & Gallatz, K. (1985) · Histochemistry and Cell Biology · doi:10.1007/bf02450485 · Cited by 6
The effect of circulatory arrest and retrograde cerebral perfusion on microtubule-associated protein 2: an immunohistochemical study in pig hippocampus
Ye, J., Yang, L., Bigio, M. R. D., Summers, R., Salerno, T. A., & Deslauriers, R. (1997) · Neuroscience Letters · doi:10.1016/s0304-3940(97)13328-6 · Cited by 6
Neonatal NLRP3 Inflammasome Activation Leads to Perineuronal Net Deficits in Early Adulthood
Tarakcioglu, E., Genc, B., Tüfekçi, K. U., & Genç, Ş. (2025) · Developmental Neurobiology · doi:10.1002/dneu.22986 · Cited by 6
Impaired Synaptic Plasticity and Dendritic Damage of Hippocampal CA1 Pyramidal Cells in Chronic Hydrocephalus
Katayama, Y., Tsubokawa, T., Kinoshita, K., Koshinaga, M., Kawamata, T., & Miyazaki, S. (1991) · Springer eBooks · doi:10.1007/978-4-431-68156-4_6 · Cited by 5
Effects of SARA on Oxygen–Glucose Deprivation in PC12 Cell Line
Wang, J., He, J., Du, Z., Li, Z.-S., Liu, Y., Mang, J., & Xu, Z. (2013) · Neurochemical Research · doi:10.1007/s11064-013-1004-5 · Cited by 6
The correlation between microtubule-associated protein 2 in the brainstem of SIDS victims and physiological data on sleep apnea
Sawaguchi, T., Franco, P., Kadhim, H. J., Groswasser, J., Sottiaux, M., Nishida, H., & Kahn, A. (2003) · Early Human Development · doi:10.1016/j.earlhumdev.2003.08.012 · Cited by 5
Diminished Expression of Microtubule-Associated Protein (MAP-2) and β-Tubulin as a Putative Marker for Ischemic Injury in Neocortical Transplants
Rosenstein, J. M. (1995) · Cell Transplantation · doi:10.1177/096368979500400112 · Cited by 5
Loss of Spines and Neuropil
Jones, L. B. (2004) · International review of neurobiology · doi:10.1016/s0074-7742(04)59001-3 · Cited by 5
Aging of cholinergic synapses in the avian iris. Part I—Biochemical studies
Giacobini, E., Mattio, T. G., & Mussini, I. (1987) · Neurobiology of Aging · doi:10.1016/0197-4580(87)90021-2 · Cited by 5
V. The Structure of Neurons
Pannese, E. (2014) · Springer eBooks · doi:10.1007/978-3-319-06856-5_5 · Cited by 4
Protein Dephosphorylation as a Mediator of NMDA Receptor Signal Transduction
Halpain, S., & Greengard, P. (1991) · Springer eBooks · doi:10.1007/978-3-662-22666-7_9 · Cited by 4
A novel heat-stable 205 kDa microtubule-associated protein is involved in the neural development of the rat brain
Shiomura, Y., & Hirokawa, N. (1989) · Brain Research · doi:10.1016/0006-8993(89)90632-x · Cited by 4
Immunocytochemistry as a tool in the study of neurotransmitter actions
Camilli, P. V. D., & Navone, F. (1984) · Trends in Pharmacological Sciences · doi:10.1016/0165-6147(84)90451-6 · Cited by 4
Self-citation
Microtubule-associated protein 2 (MAP2) deficiency causes high-frequency hearing loss
Shin'ya, K. T., Miyasaka, T., Ukaji, T., Harada, A., & Kobayashi, K. I. (2025) · Frontiers in Audiology and Otology · doi:10.3389/fauot.2025.1605980 · Cited by 3
Sex Steroid Hormones Regulate the Expression of Growth-associated Protein 43, Microtubule-associated Protein 2, Synapsin 1 and Actin in the Ventromedial Nucleus of the Hypothalamus
Sá, S. I., & Madeira, M. D. (2011) · Journal of Molecular Neuroscience · doi:10.1007/s12031-011-9650-z · Cited by 3
[Morphometric analysis of the differentiation process of hippocampal neurons in vitro].
Correa, G., & Longart, M. (2010) · PubMed · Cited by 3
Embryology and neuropathological examination of central nervous system malformations
Sarnat, H. B. (2007) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)87029-1 · Cited by 3
Microtubule-Associated Proteins in Cerebellar Morphogenesis
Matus, A. I., Tucker, R. P., & Viereck, C. (1992) · Springer eBooks · doi:10.1007/978-1-4612-2840-0_4 · Cited by 3
Developmentally regulated epitopes on a neurofilament protein visualized by monoclonal antibodies
Thorey, I. S., & Seifert, W. E. (1989) · Developmental Brain Research · doi:10.1016/0165-3806(89)90024-2 · Cited by 3
A novel monoclonal antibody K1 recognises early neurones in the rat cortex
Ishii, K., Murata, A., Yoshimura, K., & Uyemura, K. (2001) · Neuroscience Research · doi:10.1016/s0168-0102(00)00197-8 · Cited by 3
A new type of neuronal cytoplasmic inclusion: histological, ultrastructural, and immunocytochemical studies
Lew, E. O., Rozdilsky, B., Muñoz, D. G., & Perry, G. L. (1989) · Acta Neuropathologica · doi:10.1007/bf00687887 · Cited by 3
Chicken optic tract cells showing GABA‐like immunoreactivity: Morphological and immunocytochemical studies
Granda, R. H., Eyck, G. R. T., & Crossland, W. J. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903030308 · Cited by 3
Microfilament Involvement in Hirano Body Formation
Galloway, P. G., & Perry, G. L. (1987) · Advances in behavioral biology · doi:10.1007/978-1-4613-1657-2_15 · Cited by 3
The microtubule cytoskeleton in neuronal development and degeneration
Ávila, J., Correas, I., de Ancos, J. G., Ledesma, D., Ulloa, L., de Garcini, E. M., & Díaz‐Nido, J. (1993) · Elsevier eBooks · doi:10.1016/b978-0-444-81470-8.50010-7 · Cited by 3
The correlation between microtubule-associated protein 2 in the brainstem of SIDS victims and physiological data on sleep apnea
Sawaguchi, T., Franco, P., Kadhim, H. J., Groswasser, J., Sottiaux, M., Nishida, H., & Kahn, A. (2004) · Pathophysiology · doi:10.1016/j.pathophys.2004.01.011 · Cited by 2
Protein phosphorylation in rat cerebral cortex after desipramine treatment
Pérez, J., Tinelli, D., Zanotti, M., & Racagni, G. (1987) · Pharmacological Research Communications · doi:10.1016/0031-6989(87)90052-x · Cited by 2
Dendritic pathology and overexpression of MAP2 in Purkinje cells from mice inoculated with rabies virus
Porras, A. O., Morales, M. P., Santamaría, G., & Torres‐Fernández, O. (2024) · Journal of Molecular Histology · doi:10.1007/s10735-024-10348-5 · Cited by 1
The ontogeny and phylogenetic conservation of MAP 2 forms
Tucker, R. P., Viereck, C., & Matus, A. I. (1988) · PROTOPLASMA · doi:10.1007/bf01349359 · Cited by 1
Cypin binds to tubulin heterodimers and microtubule protofilaments and regulates microtubule spacing in developing hippocampal neurons
Sweet, E. S., Lange, K. R., Fenner, M. R., Tseng, C., Akum, B. F., & Firestein, B. L. (2022) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2022.103783 · Cited by 1
The Expression of Microtubule Proteins During the Development of the Nervous System
Ginzburg, I., & Littauer, U. Z. (1986) · Topics in the neurosciences · doi:10.1007/978-1-4613-2321-1_8 · Cited by 1
Protein products of the bacterial reporter gene are found within axon terminals in the brain of transgenic mice
Arai, R., Karasawa, N., Deura, S., Kobayashi, K., Nagatsu, T., & Nagatsu, I. (1994) · Neuroscience Letters · doi:10.1016/0304-3940(94)90420-0 · Cited by 1
Proteomic profiling of IDH-wildtype Glioblastoma Tissue and Serum uncovers prognostic Subtypes and Marker CandidatesPreprint
Werner, T., Schäfer, A., Hennes, M., Cosenza‐Contreras, M., Espadas, G., Sabidó, E., Cook, L., Pagenstecher, A., Pinter, N., Feilen, T., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.29.582688 · Cited by 1
Active transport by cytoplasmic dynein sustains dendritic MAP2 localization in developing neurons
Yonemura, Y., Sakai, Y., Nakata, R., Hagita-Tatsumoto, A., Miyasaka, T., & Misonou, H. (2026) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2026.113407
Neurobiology and Neural Systems
Ikezu, T., & Gendelman, H. E. (2008) · Springer eBooks · doi:10.1007/978-0-387-72573-4_14
Immunohistopathology in the Guinea Pig Following Chronic Low-Level Exposure to Chemical Warfare Agents
Kan, R. K., Tompkins, C. P., Fath, D. M., & Hamilton, T. A. (2005)
Visualization of the Ca2+-dependent regulation of voltage-gated Ether-à-go-go channels by FRET microscopy
Gonçalves, J. T. (2006) · doi:10.53846/goediss-3227
The role of early Ca[2+] influx in the pathogenesis of delayed neuronal death after brief forebrain ischemia in gerbils
中村, 貢. (1993) · doi:10.11501/3093436
Effekte der milden Hypothermie auf das traumatisierte Gehirn und extrazerebrale Organe des juvenilen Schweines
Fritz, H. (2008) · Digitalen Hochschulbibliothek Sachsen-Anhalt (Universitäts- und Landesbibliothek Sachsen-Anhalt) · doi:10.25673/2434
Resolving the Ultrastructural Organization of Synaptic Vesicle Pools at Hippocampal Mossy Fiber and Schaffer Collateral Synapses
Maus, L. (2021) · doi:10.53846/goediss-1
Selective Death of Cholinergic Septohippocampal Neurons Induced by Colchicine: the Role of Axoplasmic Transport
Ginn, S. R., & Peterson, G. M. (1992) · Advances in behavioral biology · doi:10.1007/978-1-4615-3432-7_34
Faculty Opinions recommendation of Parkinson sac domain mutation in synaptojanin 1 impairs clathrin uncoating at synapses and triggers dystrophic changes in dopaminergic axons.
Dickson, E. J. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.727333457.793557099
Structure and Function of Cytoplasmic Dynein: a Thesis
Paschal, B. M. (1992) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/zk8v-xy13

Authors: De Camilli, P., Miller, P. E., Navone, F., Theurkauf, W. E., & Vallee, R. B.
Affiliations: Yale University (US)
University of Milan (IT)
ORCID: Navone, F.
Theurkauf, W.E.
Venue: Neuroscience
Publisher: Elsevier BV
Published: 1984-04
Volume: 11
Issue: 4
Pages: 819-846
ISSN: 0306-4522 (ISSN-L)
DOI: 10.1016/0306-4522(84)90194-5
OpenAlex: W2030804101
Cited by: 381
References: 61
Citations by year: 2026: 1 · 2025: 2 · 2024: 4 · 2022: 4 · 2021: 2 · 2020: 1 · 2019: 1 · 2018: 1 · 2017: 3 · 2016: 2 · 2015: 1 · 2014: 4 · 2013: 5 · 2012: 4
FWCI: 13.20
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Neuroscience (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords: MAP2, dendrites, perikarya, neuronal localization, dendritic microtubules, axons, axon terminals, primary sensory neurons, dendritic branching, nervous system, rat brain, phosphoproteins, neuronal ultrastructure, dendritic growth, dendritic plasticity
MeSH terms: Animals, Autonomic Nervous System, Brain Stem, Cerebellum, Cerebral Cortex, Fluorescent Antibody Technique, Ganglia, Spinal, Hippocampus, Microtubule-Associated Proteins, Nervous System, Proteins, Rats, Inbred Strains, Retina, Spinal Cord, Rats

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

Distribution of microtubule-associated protein 2 in the nervous system of the rat studied by immunofluorescence

Abstract

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