The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Kinesin associates with anterogradely transported membranous organelles in vivo.
Open accessAbstract
Biochemical, pharmacological and immunocytochemical studies have implicated the microtubule-activated ATPase, kinesin, in the movement of membrane bounded organelles in fast axonal transport. In vitro studies suggested that kinesin moves organelles preferentially in the anterograde direction, but data about the function and precise localization of kinesin in the living axon were lacking. The current study was undertaken to establish whether kinesin associates with anterograde or retrograde moving organelles in vivo. Peripheral nerves were ligated to produce accumulations of organelles moving in defined directions. Regions proximal (anterograde) and distal (retrograde) to the ligation were analyzed for kinesin localization by immunofluorescence, and by immunogold electron microscopy using ultracryomicrotomy. Substantial amounts of kinesin were associated with anterograde moving organelles on the proximal side, while significantly less kinesin was detected distally. Statistical analyses indicated that kinesin was mostly associated with membrane-bounded organelles. These observations indicate that axonal kinesin is primarily associated with anterograde moving organelles in vivo.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Identification of a novel force-generating protein, kinesin, involved in microtubule-based motility
VALE, R., REESE, T., & SHEETZ, M. (1985) · Cell · doi:10.1016/s0092-8674(85)80099-4 · Cited by 1,993
Hirokawa, N., Pfister, K. K., Yorifuji, H., Wagner, M. C., Brady, S. T., & Bloom, G. S. (1989) · Cell · doi:10.1016/0092-8674(89)90691-0 · Cited by 477
Self-citationThe molecular structure of adrenal medulla kinesin
Hisanaga, S., Murofushi, H., Okuhara, K., Sato, R., Masuda, Y., Sakai, H., & Hirokawa, N. (1989) · Cell Motility · doi:10.1002/cm.970120407 · Cited by 63
Self-citation
Cited by
Axonal transport: cargo-specific mechanisms of motility and regulation
Maday, S., Twelvetrees, A. E., Moughamian, A. J., & Holzbaur, E. L. F. (2014) · Neuron · doi:10.1016/j.neuron.2014.10.019 · Cited by 683
Tanaka, Y., Kanai, Y., Okada, Y., Nonaka, S., Takeda, S., Harada, A., & Hirokawa, N. (1998) · Cell · doi:10.1016/s0092-8674(00)81459-2 · Cited by 654
Self-citationHurd, D. D., & Saxton, W. M. (1996) · Genetics · doi:10.1093/genetics/144.3.1075 · Cited by 379
Martin, M., Iyadurai, S. J., Gassman, A., Gindhart, J. G., Hays, T. S., & Saxton, W. M. (1999) · Molecular Biology of the Cell · doi:10.1091/mbc.10.11.3717 · Cited by 365
The Chlamydomonas FLA10 gene encodes a novel kinesin-homologous protein.
Walther, Z., Vashishtha, M., & Hall, J. L. (1994) · The Journal of cell biology · doi:10.1083/jcb.126.1.175 · Cited by 226
Kinesin Light Chains Are Essential for Axonal Transport in Drosophila
Gindhart, J. G., Desai, C. J., Beushausen, S., Zinn, K., & Goldstein, L. S. B. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.141.2.443 · Cited by 179
Cloning and localization of a conventional kinesin motor expressed exclusively in neurons
Niclas, J., Navone, F., Hom-Booker, N., & Vale, R. D. (1994) · Neuron · doi:10.1016/0896-6273(94)90314-x · Cited by 153
Cargo binding and regulatory sites in the tail of fungal conventional kinesin
Seiler, S., Kirchner, J., Horn, C., Kallipolitou, A., Woehlke, G., & Schliwa, M. (2000) · Nature Cell Biology · doi:10.1038/35014022 · Cited by 147
Immunochemical analysis of kinesin light chain function
Stenoien, D. L., & Brady, S. T. (1997) · Molecular Biology of the Cell · doi:10.1091/mbc.8.4.675 · Cited by 143
Self-citationCanty, J. T., Hensley, A., Aslan, M., Jack, A., & Yildiz, A. (2023) · Nature Communications · doi:10.1038/s41467-023-36945-8 · Cited by 131
Kinesin participates in melanosomal movement along melanocyte dendrites
Hara, M., Yaar, M., Byers, H. R., Goukassian, D., Gonsalves, J., Gilchrest, B. A., & Fine, R. E. (2000) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.2000.00894.x · Cited by 127
Two Kinesin Light Chain Genes in Mice
Rahman, A., Friedman, D. S., & Goldstein, L. S. B. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.25.15395 · Cited by 123
Hagiwara, H., Yorifuji, H., Sato-Yoshitake, R., & Hirokawa, N. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)41903-x · Cited by 115
Self-citationThe Drosophila kinesin light chain. Primary structure and interaction with kinesin heavy chain
Gauger, A. K., & Goldstein, L. S. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)38698-3 · Cited by 105
Defective kinesin heavy chain behavior in mouse kinesin light chain mutants
Rahman, A., Kamal, A., Roberts, E. A., & Goldstein, L. S. B. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.146.6.1277 · Cited by 102
Association of kinesin with the Golgi apparatus in rat hepatocytes
Marks, D. L., Larkin, J. M., & McNiven, M. A. (1994) · Journal of Cell Science · doi:10.1242/jcs.107.9.2417 · Cited by 84
Microtubule-associated protein-dependent binding of phagosomes to microtubules
Blocker, A., Severin, F. F., Habermann, A., Hyman, A. A., Griffiths, G., & Burkhardt, J. K. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.7.3803 · Cited by 81
Yoshiyama, Y., Zhang, B., Bruce, J., Trojanowski, J. Q., & Lee, V. M.-Y. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-33-10662.2003 · Cited by 72
A cryo-ET survey of microtubules and intracellular compartments in mammalian axons
Foster, H. E., Ventura Santos, C., & Carter, A. P. (2022) · Journal of Cell Biology · doi:10.1083/jcb.202103154 · Cited by 69
Hirling, H., Steiner, P., Chaperon, C., Marsault, R., Regazzi, R., & Catsicas, S. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00076.x · Cited by 69
Mechanisms of trafficking in axons and dendrites: implications for development and neurodegeneration
Sheetz, M. P., Pfister, K. K., Bulinski, J. C., & Cotman, C. W. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00021-5 · Cited by 55
Self-citationWoll, K. A., Guzik-Lendrum, S., Bensel, B. M., Bhanu, N. V., Dailey, W. P., Garcia, B. A., Gilbert, S. P., & Eckenhoff, R. G. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.002182 · Cited by 23
Metadata
- Authors
- Hirokawa, N., Sato-Yoshitake, R., Kobayashi, N., Pfister, K. K., Bloom, G. S., & Brady, S. T.
- Venue
- The Journal of cell biology
- Publisher
- Rockefeller University Press
- Published
- 1991-07-15
- Volume
- 114
- Issue
- 2
- Pages
- 295-302
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- OpenAlex
- W1981791822
- Cited by
- 260
- References
- 3
- FWCI
- 6.64
- Type
- journal article
- Language
- en
- Open access
- green
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.