The DOI matches its Crossref record; 58 of the 58 references it cites were found in a registry or an index.
Cytoplasmic Dynein, the Dynactin Complex, and Kinesin Are Interdependent and Essential for Fast Axonal Transport
Open accessAbstract
In axons, organelles move away from (anterograde) and toward (retrograde) the cell body along microtubules. Previous studies have provided compelling evidence that conventional kinesin is a major motor for anterograde fast axonal transport. It is reasonable to expect that cytoplasmic dynein is a fast retrograde motor, but relatively few tests of dynein function have been reported with neurons of intact organisms. In extruded axoplasm, antibody disruption of kinesin or the dynactin complex (a dynein activator) inhibits both retrograde and anterograde transport. We have tested the functions of the cytoplasmic dynein heavy chain (cDhc64C) and the p150(Glued) (Glued) component of the dynactin complex with the use of genetic techniques in Drosophila. cDhc64C and Glued mutations disrupt fast organelle transport in both directions. The mutant phenotypes, larval posterior paralysis and axonal swellings filled with retrograde and anterograde cargoes, were similar to those caused by kinesin mutations. Why do specific disruptions of unidirectional motor systems cause bidirectional defects? Direct protein interactions of kinesin with dynein heavy chain and p150(Glued) were not detected. However, strong dominant genetic interactions between kinesin, dynein, and dynactin complex mutations in axonal transport were observed. The genetic interactions between kinesin and either Glued or cDhc64C mutations were stronger than those between Glued and cDhc64C mutations themselves. The shared bidirectional disruption phenotypes and the dominant genetic interactions demonstrate that cytoplasmic dynein, the dynactin complex, and conventional kinesin are interdependent in fast axonal transport.
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.
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?
In the citing paper
“Thus, our data is consistent with a model for bidirectional coordination in which activities of Kinesin-1 and dynein might be linked via physical contacts (Martin et al., 1999), and points to a role of KLCs in this linkage.”
From Stable kinesin and dynein assemblies drive the axonal transport of mammalian prion protein vesicles (2011) · cites this paper as Martin et al., 1999
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
Molecular Cloning: A Laboratory Manual
Sambrook, J., Fritsch, E., & Maniatis, T. (1989) · UCLA - Biblioteca de Ciencias de la Salud · Cited by 133,589
The Genome of Drosophila Melanogaster
Lindsley, D. L., & Zimm, G. G. (1992) · Cited by 3,098
Kinesin and Dynein Superfamily Proteins and the Mechanism of Organelle Transport
Hirokawa, N. (1998) · Science · doi:10.1126/science.279.5350.519 · Cited by 1,689
Baas, P. W., Deitch, J. S., Black, M. M., & Banker, G. A. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.21.8335 · Cited by 742
Kaiser, C. A., & Schekman, R. W. (1990) · Cell · doi:10.1016/0092-8674(90)90483-u · Cited by 730
Gill, S. R., Schroer, T. A., Szilak, I., Steuer, E. R., Sheetz, M. P., & Cleveland, D. W. (1991) · The Journal of Cell Biology · doi:10.1083/jcb.115.6.1639 · Cited by 487
The design plan of kinesin motors
Vale, R. D., & Fletterick, R. J. (1997) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.13.1.745 · Cited by 474
Vaughan, K. T., & Vallee, R. B. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.131.6.1507 · Cited by 469
ALLEN, R. D., Weiss, D. G., Hayden, J. H., Brown, D. T., Fujiwake, H., & Simpson, M. (1985) · The Journal of Cell Biology · doi:10.1083/jcb.100.5.1736 · Cited by 440
Developmental Regulation of Vesicle Transport in Drosophila Embryos: Forces and Kinetics
Welte, M. A., Gross, S. P., Postner, M. A., Block, S. M., & Wieschaus, E. F. (1998) · Cell · doi:10.1016/s0092-8674(00)80947-2 · Cited by 389
Research works printed but not linked: 1
- Bowman A.B., 1999, J. Cell. Biol., 146, 165
Cited by
Sorted by citations
Items 201–300 of 365
Monteiro, M. I., Ahlawat, S., Kowalski, J. R., Malkin, E., Koushika, S. P., & Juo, P. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-04-0334 · Cited by 36
Nudel Promotes Axonal Lysosome Clearance and Endo‐lysosome Formation via Dynein‐Mediated Transport
Zhang, Q., Wang, F., Cao, J., Shen, Y., Huang, Q., Bao, L., & Zhu, X. (2009) · Traffic · doi:10.1111/j.1600-0854.2009.00945.x · Cited by 35
Kif5b is an essential forward trafficking motor for the Kv1.5 cardiac potassium channel
Zadeh, A. D., Cheng, Y., Xu, H., Wong, N. C., Wang, Z., Goonasekara, C. L., Steele, D. F., & Fedida, D. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.178442 · Cited by 35
Axon Biology in ALS: Mechanisms of Axon Degeneration and Prospects for Therapy
Coleman, M. P. (2022) · Neurotherapeutics · doi:10.1007/s13311-022-01297-6 · Cited by 33
“For example, pathogenic variants of the anterograde and retrograde motors or associated proteins KIF5A and dynactin subunit 1 (DCTN1; p150Glued) both disrupt axonal transport [50, 51], and ALS-associated variants of the heavily phosphorylated repeat region of the heavy neurofilament subunit (NEFH) are likely to cause…”
BackgroundDistinct functional roles of cytoplasmic dynein defined by the intermediate chain isoforms
Pfister, K. K. (2015) · Experimental Cell Research · doi:10.1016/j.yexcr.2014.12.013 · Cited by 33
Kif5 regulates mitochondrial movement, morphology, function and neuronal survival
Iworima, D. G., Pasqualotto, B. A., & Rintoul, G. L. (2016) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2015.12.014 · Cited by 32
Steinman, J. B., Santarossa, C., Miller, R. M., Yu, L. S., Serpinskaya, A. S., Furukawa, H., Morimoto, S., Tanaka, Y., Nishitani, M., Asano, M., et al. (2017) · eLife · doi:10.7554/elife.25174 · Cited by 36
A minimal hydrodynamic model for a traffic jam in an axon
Kuznetsov, A. V., & Avramenko, A. A. (2008) · International Communications in Heat and Mass Transfer · doi:10.1016/j.icheatmasstransfer.2008.09.004 · Cited by 32
A macroscopic model of traffic jams in axons
Kuznetsov, A. V., & Avramenko, A. A. (2009) · Mathematical Biosciences · doi:10.1016/j.mbs.2009.01.005 · Cited by 31
The Gene for the Intermediate Chain Subunit of Cytoplasmic Dynein Is Essential in Drosophila
Boylan, K. L. M., & Hays, T. S. (2002) · Genetics · doi:10.1093/genetics/162.3.1211 · Cited by 30
Self-citationMitochondrial dysfunction and traffic jams in amyotrophic lateral sclerosis
Jhanji, R., Behl, T., Sehgal, A., & BUNGAU, S. G. (2021) · Mitochondrion · doi:10.1016/j.mito.2021.02.008 · Cited by 29
Bao, H., Berlanga, M. L., Xue, M., Hapip, S. M., Daniels, R. W., Mendenhall, J. M., Alcantara, A. A., & Zhang, B. (2007) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2007.01.007 · Cited by 29
Hung, C., & Coleman, M. P. (2016) · Traffic · doi:10.1111/tra.12428 · Cited by 30
Valakh, V., Naylor, S. A., Berns, D. S., & DiAntonio, A. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.04.008 · Cited by 28
Soustelle, L., Aimond, F., López-Andrés, C., Brugioti, V., Raoul, C., & Layalle, S. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0562-23.2023 · Cited by 27
Fabian, L., & Forer, A. (2005) · PROTOPLASMA · doi:10.1007/s00709-005-0094-6 · Cited by 28
Eade, K., & Allan, D. W. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0213-09.2009 · Cited by 28
Li, A., & Zhang, Y. J. (2022) · Computer Methods in Applied Mechanics and Engineering · doi:10.1016/j.cma.2022.115757 · Cited by 27
Dynein and dynactin move long-range but are delivered separately to the axon tip
Fellows, A. D., Bruntraeger, M. B., Burgold, T., Bassett, A. R., & Carter, A. P. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202309084 · Cited by 27
Bearer, E. L., Zhang, X., & Jacobs, R. E. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.05.010 · Cited by 27
Moua, P., Fullerton, D., Serbus, L. R., Warrior, R., & Saxton, W. M. (2011) · Development · doi:10.1242/dev.048645 · Cited by 26
Self-citationTranscriptional control of synaptic differentiation by retrograde signals
Kalinovsky, A., & Scheiffele, P. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.05.011 · Cited by 27
KIF1C activates and extends dynein movement through the FHF cargo adapter
Abid Ali, F., Zwetsloot, A. J., Stone, C. E., Morgan, T. E., Wademan, R. F., Carter, A. P., & Straube, A. (2025) · Nature Structural & Molecular Biology · doi:10.1038/s41594-024-01418-z · Cited by 30
Motil, J., Dubey, M., Chan, W. K. ‐., & Shea, T. B. (2007) · Brain Research · doi:10.1016/j.brainres.2006.09.108 · Cited by 25
Modeling traffic jams in intracellular transport in axons
Kuznetsov, A. V., & Hooman, K. (2008) · International Journal of Heat and Mass Transfer · doi:10.1016/j.ijheatmasstransfer.2008.04.022 · Cited by 25
Jing, X., & Malicki, J. J. (2009) · Development · doi:10.1242/dev.037739 · Cited by 24
Louie, K., Russo, G. J., Salkoff, D. B., Wellington, A. J., & Zinsmaier, K. E. (2008) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2008.06.023 · Cited by 24
Abl Tyrosine Kinase and Its Substrate Ena/VASP Have Functional Interactions with Kinesin-1
Martin, M., Ahern-Djamali, S. M., Hoffmann, F. M., & Saxton, W. M. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-02-0116 · Cited by 24
Self-citationDynactin polices two-way organelle traffic
Dell, K. R. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200301040 · Cited by 24
Organizational Dynamics, Functions, and Pathobiological Dysfunctions of Neurofilaments
SHEA, T. B., Chan, W. K. ‐., Kushkuley, J., & Lee, S. (2009) · Results and problems in cell differentiation · doi:10.1007/400_2009_8 · Cited by 23
Cytoskeleton-dependent transport and localization of mRNA
Stebbings, H. (2001) · International review of cytology · doi:10.1016/s0074-7696(01)11016-8 · Cited by 23
A Functional Misexpression Screen Uncovers a Role for Enabled in Progressive Neurodegeneration
Rezával, C., Berni, J., Gorostiza, E. A., Werbajh, S., Fagilde, M. M., Fernandez, M. P., Beckwith, E. J., Aranovich, E. J., y García, C. A. S., & Ceriani, M. F. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003332 · Cited by 23
Djagaeva, I., Rose, D. J., Lim, A. P. C., Venter, C. E., Brendza, K. M., Moua, P., & Saxton, W. M. (2012) · Genetics · doi:10.1534/genetics.112.140798 · Cited by 19
Self-citationMolecular pathogenesis of peripheral neuropathies: insights from Drosophila models
Bussmann, J., & Storkebaum, E. (2017) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2017.01.011 · Cited by 20
Jones, M. D., & Naylor, K. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23169402 · Cited by 18
Kinesin passing permanent blockages along its protofilament track
Dreblow, K., Kalchishkova, N., & Böhm, K. J. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.04.035 · Cited by 18
Speech- and language-linked FOXP2 mutation targets protein motors in striatal neurons
Kuo, H., Chen, S.-Y., Huang, R.-C., Takahashi, H., Lee, Y., Pang, H.-Y., Wu, C.-H., Graybiel, A. M., & Liu, F. (2023) · Brain · doi:10.1093/brain/awad090 · Cited by 18
Spastin regulates VAMP7-containing vesicles trafficking in cortical neurons
Plaud, C., Joshi, V., Marinello, M., Pastré, D., Galli, T., Curmi, P. A., & Burgo, A. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2017.04.007 · Cited by 18
Mitochondria: how eminent in ageing and neurodegenerative disorders?
Bamshad, C., Najafi-Ghalehlou, N., Pourmohammadi-Bejarpasi, Z., Tomita, K., Kuwahara, Y., Sato, T., Feizkhah, A., Roushnadeh, A. M., & Roudkenar, M. H. (2022) · Human Cell · doi:10.1007/s13577-022-00833-y · Cited by 20
Oocyte Patterning: Dynein and Kinesin, Inc.
Cohen, R. S. (2002) · Current Biology · doi:10.1016/s0960-9822(02)01310-6 · Cited by 18
Cargo distributions differentiate pathological axonal transport impairments
Mitchell, C. S., & Lee, R. H. (2012) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2012.01.019 · Cited by 17
Sivagurunathan, S., Schnittker, R. R., Razafsky, D. S., Nandini, S., Plamann, M. D., & King, S. J. (2012) · Genetics · doi:10.1534/genetics.112.141580 · Cited by 17
Synaptic Vesicle Distribution by Conveyor Belt
Moughamian, A. J., & Holzbaur, E. L. F. (2012) · Cell · doi:10.1016/j.cell.2012.02.007 · Cited by 17
Mycalolide B dissociates dynactin and abolishes retrograde axonal transport of dense-core vesicles
Cavolo, S. L., Zhou, C., Ketcham, S. A., Suzuki, M. M., Ukalovic, K., Silverman, M. A., Schroer, T. A., & Levitan, E. S. (2015) · Molecular Biology of the Cell · doi:10.1091/mbc.e14-11-1564 · Cited by 16
The Drosophila LC8 homolog cut up specifies the axonal transport of proteasomes
Kreko‐Pierce, T., & Eaton, B. A. (2017) · Journal of Cell Science · doi:10.1242/jcs.207027 · Cited by 17
The Generation of Dynein Networks by Multi-Layered Regulation and Their Implication in Cell Division
Torisawa, T., & Kimura, A. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00022 · Cited by 16
Chi, H., Lee, S., Shiu, R.-H., Han, R., Hsieh, C.-P., Wei, T.-M., Lo, C., Chang, H.-Y., & Sang, T. (2020) · Scientific Reports · doi:10.1038/s41598-020-70423-1 · Cited by 17
Uptake and transport of clostridial neurotoxins
Schmieg, N., Bercsényi, K., & Schiavo, G. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800188-2.00012-4 · Cited by 16
Chang, L., Kreko‐Pierce, T., Davison, H., Cusmano, T., Wu, Y., Rothenfluh, A., & Eaton, B. A. (2013) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-09-0697 · Cited by 15
Ye, F., Zangenehpour, S., & Chaudhuri, A. (2000) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)61494-8 · Cited by 15
Fast intra-axonal transport: Beginning, development and post-genome advances
Dahlström, A. B. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.11.004 · Cited by 14
Microtubule motor proteins and the organization of the pollen tube cytoplasm
Romagnoli, S., Cresti, M., & Cai, G. (2001) · Sexual Plant Reproduction · doi:10.1007/s004970100089 · Cited by 14
Nagpal, S., Swaminathan, K., Beaudet, D., Verdier, M., Wang, S., Berger, C. L., Berger, F., & Hendricks, A. G. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114649 · Cited by 13
Ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon
Segal, M., Soifer, I., Petzold, H., Howard, J., Elbaum, M., & Reiner, O. (2012) · Biology Open · doi:10.1242/bio.2012307 · Cited by 13
Dynein catch bond as a mediator of codependent bidirectional cellular transport
Puri, P., Gupta, N., Chandel, S., Naskar, S., Nair, A., Chaudhuri, A., Mitra, M. K., & Muhuri, S. (2019) · Physical Review Research · doi:10.1103/physrevresearch.1.023019 · Cited by 14
A stochastic model that explains axonal organelle pileups induced by a reduction of molecular motors
Lai, X., Brown, A., & Xue, C. (2018) · Journal of The Royal Society Interface · doi:10.1098/rsif.2018.0430 · Cited by 12
Axonal transport dysfunction of mitochondria in traumatic brain injury: A novel therapeutic target
Shin, S. S., Karlsson, M., Mazandi, V. M., Ranganathan, A., Hallowell, T., Delso, N., & Kilbaugh, T. J. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113311 · Cited by 13
Effect of the degree of polar mismatching on traffic jam formation in fast axonal transport
Kuznetsov, A. V. (2010) · Computer Methods in Biomechanics & Biomedical Engineering · doi:10.1080/10255840903505154 · Cited by 13
ACTIVE BIO-SYSTEMS: FROM SINGLE MOTOR MOLECULES TO COOPERATIVE CARGO TRANSPORT
Lipowsky, R., Beeg, J., Dimova, R., Klumpp, S., Liepelt, S., Müller, M. J. I., & Valleriani, A. (2009) · Biophysical Reviews and Letters · doi:10.1142/s1793048009000946 · Cited by 13
Nemtsova, Y., Steinert, B. L., & Wharton, K. A. (2023) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2023.103834 · Cited by 12
Banerjee, S., & Riordan, M. (2018) · Scientific Reports · doi:10.1038/s41598-018-35618-7 · Cited by 12
Rawson, J. M., Kreko‐Pierce, T., Davison, H., Mahoney, R. E., Bokov, A. F., Chang, L., Gelfond, J., Macleod, G. T., & Eaton, B. A. (2012) · Aging Cell · doi:10.1111/j.1474-9726.2012.00799.x · Cited by 12
The Drosophila kinesin‐I associated protein YETI binds both kinesin subunits
Wisniewski, T., Tanzi, C. L., & Gindhart, J. G. (2003) · Biology of the Cell · doi:10.1016/j.biolcel.2003.10.004 · Cited by 12
Self-citationTau Protein: Function and Pathology
Rosenmann, H., Blum, D. L., Kayed, R., & Ittner, L. M. (2012) · International Journal of Alzheimer s Disease · doi:10.1155/2012/707482 · Cited by 12
Effect of vesicle traps on traffic jam formation in fast axonal transport
Kuznetsov, A. V. (2010) · Mathematical Biosciences · doi:10.1016/j.mbs.2010.05.003 · Cited by 12
Uptake and transport of Clostridium neurotoxins
Bohnert, S., Deinhardt, K., Salinas, S., & Schiavo, G. (2006) · Elsevier eBooks · doi:10.1016/b978-012088445-2/50025-1 · Cited by 12
Gassman, A., Hao, L. T., Bhoite, L. T., Bradford, C. L., Chien, C.-B., Beattie, C. E., & Manfredi, J. P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074325 · Cited by 11
Self-citationKurup, N. S., Yan, D., Kono, K., & Jin, Y. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006844 · Cited by 9
Hansen, T., Thant, C. N., White, J. A., Banerjee, R., Thuamsang, B., & Gunawardena, S. (2019) · APOPTOSIS · doi:10.1007/s10495-019-01520-4 · Cited by 9
VEGF Axonal Transport Dependent on Kinesin-1B and Microtubules Dynamics
Yang, P., Sun, X., Kou, Z., Wu, K., Huang, Y.-L., & Sun, F. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00424 · Cited by 9
Pedrazzi, M., Nash, B., Meucci, O., & Brandimarti, R. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104634 · Cited by 9
Blasier, K. R., Humsi, M. K., Ha, J., Ross, M. W., Smiley, W. R., Inamdar, N. A., Mitchell, D. J., Lo, K. W. ‐., & Pfister, K. K. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23388 · Cited by 8
A force-sensitive mutation reveals a non-canonical role for dynein in anaphase progression
Salvador-Garcia, D., Jin, L., Hensley, A. M., Gölcük, M., Gallaud, E., Chaaban, S., Port, F., Vagnoni, A., Planelles-Herrero, V. J., McClintock, M. A., et al. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202310022 · Cited by 7
Axonal transport disruption in peripheral nerve disease
Lloyd, T. E. (2012) · Journal of the Peripheral Nervous System · doi:10.1111/j.1529-8027.2012.00431.x · Cited by 8
Spatial and Temporal Characteristics of Normal and Perturbed Vesicle Transport
Iacobucci, G. J., Rahman, N. A., Valtueña, A. A., Nayak, T. K., & Gunawardena, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0097237 · Cited by 8
Neisch, A. L., Avery, A. W., Machamer, J. B., Li, M.-G., & Hays, T. S. (2015) · Methods in cell biology · doi:10.1016/bs.mcb.2015.06.015 · Cited by 8
Self-citationNeurobiological Mechanisms Involved in the Pathogenesis of Alzheimer’s Disease
Mir, F. A., & Rizvi, Z. A. (2019) · Springer eBooks · doi:10.1007/978-981-13-9636-6_13 · Cited by 8
Cytoplasmic Dynein Function Defined by Subunit Composition
Pfister, K. K., & Lo, K. W. ‐. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-382004-4.10015-9 · Cited by 8
Halo: A Guiding Light for Transport
Cohen, R. S. (2003) · Current Biology · doi:10.1016/j.cub.2003.10.046 · Cited by 8
Synaptic-mitochondrial transport: mechanisms in neural adaptation and degeneration
Ding, Y., Yang, H., Gao, J., Tang, C. L., Peng, Y.-Y., Ma, X., Li, S., Wang, H., Lu, X., & Wang, Y. (2025) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-025-05209-y · Cited by 7
Fu, D., Zhang, L., Tang, B., Du, L., Li, J., Ao, J., Zhang, Z., Wang, Z., Liu, S., & Pang, D. (2024) · ACS Nano · doi:10.1021/acsnano.4c10564 · Cited by 7
Cooperation and Competition Coexist in Bidirectional Transport by Motor Proteins
Xie, K., & Wang, Q. (2022) · The Journal of Physical Chemistry Letters · doi:10.1021/acs.jpclett.2c01659 · Cited by 7
Tug-of-War and Coordination in Bidirectional Transport by Molecular Motors
Muñoz, O., & Klumpp, S. (2022) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.2c05194 · Cited by 6
Grimaud, B., Frétaud, M., Terras, F., Bénassy, A., Duroure, K., Bercier, V., Trippé-Allard, G., Mohammedi, R., Gacoin, T., Bene, F. D., et al. (2022) · ACS Nano · doi:10.1021/acsnano.2c06799 · Cited by 7
Fan, S.-S. (2004) · Journal of Biomedical Sciences · doi:10.1007/bf02254441 · Cited by 10
Xu, Y., Wang, B., Bush, I., Saunders, H. A. J., Wildonger, J., & Han, C. (2024) · Science Advances · doi:10.1126/sciadv.adp0138 · Cited by 8
KINESIN BYPASSING BLOCKAGES ON MICROTUBULE RAILS
Dreblow, K., Kalchishkova, N., & Böhm, K. J. (2009) · Biophysical Reviews and Letters · doi:10.1142/s1793048009000958 · Cited by 6
Animal models of amyotrophic lateral sclerosis and Huntington’s disease
Islam, A. M. T., Kwak, J., Jung, Y. J., & Kee, Y. (2014) · Genes & Genomics · doi:10.1007/s13258-014-0188-7 · Cited by 5
DNA tensiometer reveals catch-bond detachment kinetics of kinesin-1, -2, and -3
Noell, C. R., Ma, T.-C., Jiang, R., McKinley, S. A., & Hancock, W. O. (2026) · eLife · doi:10.7554/elife.108837.4 · Cited by 10
Cytoplasmic Dynein Dysfunction and Neurodegenerative Disease
Moughamian, A. J., & Holzbaur, E. L. F. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-382004-4.10023-8 · Cited by 5
Kinesin transport: driving kinesin in the neuron
Hays, T. S., & Li, M. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00061-6 · Cited by 5
Self-citationKerendi, H., Rahmati, M., Mirnasuri, R., & Kazemi, A. (2019) · Gene · doi:10.1016/j.gene.2019.04.027 · Cited by 5
Effect of the width of regions with severed microtubules on transport of organelles down the axon
Kuznetsov, A. V. (2010) · International Communications in Heat and Mass Transfer · doi:10.1016/j.icheatmasstransfer.2009.12.008 · Cited by 5
The ALS-associated KIF5A P986L variant is not pathogenic for Drosophila motoneurons
Layalle, S., Aimond, F., Brugioti, V., Guissart, C., Raoul, C., & Soustelle, L. (2024) · Scientific Reports · doi:10.1038/s41598-024-70543-y · Cited by 4
Altered expression of KLC3 may affect semen parameters
Kargar-Dastjerdy, P., Tavalaee, M., Salehi, M., Falahati, M., Izadi, T., & Nasr‐Esfahani, M. H. (2016) · International Journal of Reproductive BioMedicine (IJRM) · doi:10.29252/ijrm.14.1.15 · Cited by 4
Axonal Transport Mechanisms in Cytoskeleton Formation and Regulation
Yuan, A., & Nixon, R. A. (2010) · Advances in neurobiology · doi:10.1007/978-1-4419-6787-9_21 · Cited by 4
Neurofilament Dynamics: A Tug of War by Microtubule Motors
Shea, T. B., Lee, S., Kushkuley, J., Dubey, M., & Chan, W. K. ‐. (2009) · Future Neurology · doi:10.2217/fnl.09.4 · Cited by 4
Analytical investigation of transient molecular-motor-assisted transport in elongated cells
Kuznetsov, A. V., & Avramenko, A. A. (2008) · Open Physics · doi:10.2478/s11534-008-0009-1 · Cited by 4
Tanaka, Y., & Hirokawa, N. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.20060-6 · Cited by 4
Motors and Membrane Trafficking
Verhey, K. J. (2002) · Wiley eBooks · doi:10.1002/3527601503.ch16 · Cited by 4
Metadata
- Authors
- Martin, M., Iyadurai, S. J., Gassman, A., Gindhart, J. G., Hays, T. S., & Saxton, W. M.
- Affiliations
- Indiana University Bloomington (US)
- University of Minnesota (US)
- University of Massachusetts Boston (US)
- Venue
- Molecular Biology of the Cell
- Published
- 1999-11
- Volume
- 10
- Issue
- 11
- Pages
- 3717-3728
- ISSN
- 1059-1524 (ISSN-L)
- 1939-4586
- PMC
- PMC25669
- OpenAlex
- W2144151547
- Cited by
- 365
- References
- 58
- Citations by year
- 2026: 3 · 2025: 7 · 2024: 7 · 2023: 8 · 2022: 13 · 2021: 5 · 2020: 11 · 2019: 8 · 2018: 9 · 2017: 21 · 2016: 9 · 2015: 11 · 2014: 14 · 2013: 14 · 2012: 26
- FWCI
- 3.90
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular Biology of the Cell (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Howard Hughes Medical Institute
- American Heart Association
- National Institutes of Health
- National Institute of General Medical Sciences (GM-44757, R01GM044757, R56GM044757, R01GM046295, GM-46295)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- cytoplasmic dynein, dynactin, kinesin, fast axonal transport, anterograde transport, retrograde transport, microtubule motor proteins, dynein heavy chain, p150Glued, axonal swellings, Drosophila neurons
- MeSH terms
- Dynactin Complex, Animals, Axons, Cytoplasm, Drosophila, Dyneins, Microscopy, Electron, Microtubule-Associated Proteins, Mutation, Phenotype, Precipitin Tests, Kinesins, Microscopy, Confocal, Microscopy, Video
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