Axonal transport: Driving synaptic function

Molecular anatomy of a trafficking organelle

Takamori, S., Holt, M., Stenius, K., Lemke, E. A., Grønborg, M., Riedel, D., Urlaub, H., Schenck, S., Brügger, B., Ringler, P., et al. (2006) · Cell · doi:10.1016/j.cell.2006.10.030 · Cited by 2,373

Kinesin Transports RNA

Kanai, Y., Dohmae, N., & Hirokawa, N. (2004) · Neuron · doi:10.1016/j.neuron.2004.07.022 · Cited by 1,109

Differential Regulation of Dynein and Kinesin Motor Proteins by Tau

Dixit, R., Ross, J. L., Goldman, Y. E., & Holzbaur, E. L. F. (2008) · Science · doi:10.1126/science.1152993 · Cited by 1,012

Quantitative ultrastructural analysis of hippocampal excitatory synapses

Schikorski, T., & Stevens, C. F. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-15-05858.1997 · Cited by 997

Mutant dynactin in motor neuron disease

Puls, I., Jonnakuty, C., LaMonte, B. H., Holzbaur, E. L. F., Tokito, M. K., MANN, E. A., Floeter, M. K., Bidus, K., Drayna, D. T., Oh, S. J., et al. (2003) · Nature Genetics · doi:10.1038/ng1123 · Cited by 973

The Biology of Huntingtin

Saudou, F., & Humbert, S. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.003 · Cited by 945

Control of microtubule organization and dynamics: Two ends in the limelight

Akhmanova, A., & Steinmetz, M. O. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm4084 · Cited by 895

The Mechanism of Ca2+-Dependent Regulation of Kinesin-Mediated Mitochondrial Motility

Wang, X., & Schwarz, T. L. (2009) · Cell · doi:10.1016/j.cell.2008.11.046 · Cited by 871

Activity-driven local ATP synthesis is required for synaptic function

Rangaraju, V., Calloway, N., & Ryan, T. A. (2014) · Cell · doi:10.1016/j.cell.2013.12.042 · Cited by 836

Neuropeptide Transmission in Brain Circuits

van den Pol, A. N. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.014 · Cited by 810

Axonal injury mediated by neuronal p75NTR/TRAF6/JNK pathway contributes to cognitive impairment after repetitive mTBI

Liu, G., He, M., Wu, C., Lv, P., Sun, H., Wang, H., Xin, X., & Liao, H. (2023) · Experimental Neurology · doi:10.1016/j.expneurol.2023.114618 · Cited by 5

Extreme-value analysis in nano-biological systems: applications and implications

Hayashi, K., TAKAMATSU, N., & Takaramoto, S. (2024) · Biophysical Reviews · doi:10.1007/s12551-024-01239-w · Cited by 4

UNC-10/SYD-2 links kinesin-3 to RAB-3-containing vesicles in the absence of the motor's PH domain

Bayansan, O., Bhan, P., Chang, C.-Y., Barmaver, S. N., Shen, C.-P., & Wagner, O. I. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106766 · Cited by 5

Genetic Insights into Brain Morphology: a Genome-Wide Association Study of Cortical Thickness and T1-Weighted MRI Gray Matter-White Matter Intensity Contrast

Kim, N. J., Chowdhury, N. F., Buetow, K. H., Thompson, P. M., & Andrei Irimia, A. (2025) · Neuroinformatics · doi:10.1007/s12021-025-09722-9 · Cited by 5

Role of LRRK2 in axonal transport and Parkinson’s disease

Twellsieck, B., & Boecker, C. A. (2025) · Biochemical Journal · doi:10.1042/bcj20253133 · Cited by 7

Structural basis of kinesin-1 autoinhibition and its control of microtubule-based motility

Ashaduzzaman, M., Tang, Y., Okada, K., Fried, S. D., McKenney, R. J., & Al-Bassam, J. (2026) · Science Advances · doi:10.1126/sciadv.aeg1267 · Cited by 8

Intellectual disability-causing mutations in KIF11 impair microtubule dynamics and dendritic arborization

Wingfield, J. L., Niese, L., Avchalumov, Y., Liu, X., Grover, R., Nakahata, Y., Raveendra, B., González-Santiago, A., Carter, J. P., Yasuda, R., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-70522-z · Cited by 5

Live-Cell Superresolution Imaging of Retrograde Axonal Trafficking Using Pulse–Chase Labeling in Cultured Hippocampal Neurons

Wang, T., & Meunier, F. A. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2209-4_9 · Cited by 4

The long-loop recycling (LLR) of synaptic components as a question of economics

Georgiev, S. V., & Rizzoli, S. O. (2023) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2023.103862 · Cited by 4

Effects of dynein inhibitor on the number of motor proteins transporting synaptic cargos

Hayashi, K., Miyamoto, M. G., & Niwa, S. (2021) · Biophysical Journal · doi:10.1016/j.bpj.2021.02.018 · Cited by 4

High-Resolution Imaging of Mitochondria and Mitochondrial Nucleoids in Differentiated SH-SY5Y Cells

Annuario, E., Ng, K., & Vagnoni, A. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-1990-2_15 · Cited by 4

Number of kinesins engaged in axonal cargo transport: A novel biomarker for neurological disorders

Hayashi, K., & Sasaki, K. (2023) · Neuroscience Research · doi:10.1016/j.neures.2023.09.004 · Cited by 4

Functional Inhibition of Katanin Affects Synaptic Plasticity

Lombino, F. L., Schwarz, J. R., Pechmann, Y., Schweizer, M., Jark, R., Stange, O., Glatzel, M., Gee, C. E., Hausrat, T. J., Gromova, K. V., et al. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0374-23.2023 · Cited by 4

Functional specialisation and coordination of myonuclei

Korb, A., Tajbakhsh, S., & Comai, G. (2024) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.13063 · Cited by 5

VLK drives extracellular phosphorylation of EphB2 to govern the EphB2-NMDAR interaction and injury-induced painPreprint

Srikanth, K. D., Elahi, H., Chander, P., Washburn, H. R., Hassler, S. N., Mwirigi, J. M., Kume, M., Loucks, J., Arjarapu, R., Hodge, R., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.18.585314 · Cited by 4

Neuronal autophagosomes are transported to astrocytes for degradationPreprint

Linda, K., Schuurmans, I. M. E., Smeenk, H., Vints, K., Negwer, M., Peredo, N., Lewerissa, E., Swerts, J., Hoekstra, M. M., Mordelt, A., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.03.610698 · Cited by 4

Different Mechanisms Link Gain and Loss of Kinesin Functions to Axonal DegenerationPreprint

Liew, Y.-T., Bailey, D. M., Cairns, W., Day, M., Dajas‐Bailador, F., Jones, E., McCann, S., Landgraf, M., Lorenzo-Cisneros, L., Murphy, T., et al. (2025) · SSRN Electronic Journal · doi:10.1101/2024.12.31.630930 · Cited by 4

Cell type transcriptomics reveal shared genetic mechanisms in Alzheimer’s and Parkinson’s diseasePreprint

Bhattacharya, A., Fon, E. A., Dagher, A., Iturria‐Medina, Y., Stratton, J. A., Savignac, C., Stanley, J., Hodgson, L. M., Hammou, B. A., Bennett, D. A., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.17.638647 · Cited by 4

Transcriptome Analysis of Left Versus Right Intrinsic Laryngeal Muscles Associated with Innervation

Kemfack, A. M., Hernández‐Morato, I., Moayedi, Y., & Pitman, M. J. (2024) · The Laryngoscope · doi:10.1002/lary.31487 · Cited by 3

Direct observation of importin α family member KPNA1 in axonal transport with or without a schizophrenia-related mutation

Mizuno, K., Sugahara, M., Kutomi, O., Kato, R., Itoh, T., Fujita, S., & Yamada, M. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.108343 · Cited by 3

Quantum mechanisms in the brain: from conjectures and theories to experimental evidence

Craddock, T. J. A. (2025) · Quantum Effects and Measurement Techniques in Biology and Biophotonics · doi:10.1117/12.3043206 · Cited by 3

Sex and regional differences in gene expression across the striatum in psychosis

Perez, M. S., Yin, R., Scott, M. R., Zong, W., Seney, M. L., Xue, X., Hildebrand, M. A., Shankar, V. G., Glausier, J. R., Lewis, D. A., et al. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03395-3 · Cited by 3

Linking neuron-axon-synapse architecture to white matter vasculature using high-resolution multimodal MRI in primate brain

Kimura, I., Hayashi, T., & Autio, J. A. (2025) · Imaging Neuroscience · doi:10.1162/imag.a.77 · Cited by 3

Enigmatic tubular ultrastructure in the bacterial defensive symbiont of the Asian citrus psyllid Diaphorina citri

Song, C., Maruyama, J., Murata, K., Suzaki, T., & Nakabachi, A. (2025) · npj Imaging · doi:10.1038/s44303-025-00107-w · Cited by 3

Integrated Profiling of DEHP-Induced Hippocampal Neurotoxicity in Adult Female Rats Based on Transcriptomic and Neurobiological Analyses

Bai, J., Li, J., Tang, L., Sun, W., Gao, F., Zhang, X., Bian, R., & Wang, R. (2026) · Toxics · doi:10.3390/toxics14010079 · Cited by 4

Lanthanide carriers: biomedical imaging redefined

Liu, Y., Chen, Z., Sui, M., Wang, H., Bettinelli, M., Carlos, L. D., Jaque, D., Malta, O. L., Méndez‐Ramos, J., Richard, C., et al. (2026) · Frontiers in Science · doi:10.3389/fsci.2026.1856377 · Cited by 3

Neuronal Cytoskeleton: Presynaptic Boutons as Hotspots for Activity-Dependent Microtubule Nucleation

Freal, A., & Hoogenraad, C. C. (2019) · Current Biology · doi:10.1016/j.cub.2019.11.011 · Cited by 3

Cdc42 Promotes Axonogenesis of Primary Hippocampal Neurons by Inhibiting Glycogen Synthase Kinase-3β

Li, Y., Chen, F.-Z., Chen, W., Zhu, H.-M., Chen, Y., Li, Z., Yan, F., Liu, Z., Dong, W.-R., Zhang, L., et al. (2022) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2105133 · Cited by 3

Advances in the study of axon–associated vesicles

Liu, Y., Shuai, K., Sun, Y., Zhu, L., & Wu, X. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.1045778 · Cited by 3

Neurodegeneration in a novel invertebrate model system: Failed microtubule‐mediated cell adhesion and unraveling of macroglia

Fabian‐Fine, R., Aiken, A. M., Aug, J. R., Boucher, J. D., Butler, D. C., Clancy, L. J., Clem, S. A., Crotty, S. C., Dalpe, A. M., Donzello‐Jewett, E. J., et al. (2023) · The Journal of Comparative Neurology · doi:10.1002/cne.25450 · Cited by 5

Multiscale Computational Analysis of the Effect of Taxol on Microtubule Mechanics

Cannariato, M., Zizzi, E. A., Tuszyński, J. A., & Deriu, M. A. (2024) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.4c00847 · Cited by 3

AP2A1 activates Rab7 to promote axonal autophagosome transport and slow the progression of Alzheimer’s disease

Wang, Y., Li, S.-Y., Liang, X., Fan, J.-N., Li, S.-J., Zhou, F., Li, X., Lai, M., Feng, D., & Li, Y. (2025) · Alzheimer's Research & Therapy · doi:10.1186/s13195-025-01771-1 · Cited by 5

Spatiotemporal Insights Into RNA–Organelle Interactions in Neurons

Kharod, S. C., Hwang, D.-W., Das, S., & Yoon, Y. J. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.663367 · Cited by 3

New cell biological explanations for kinesin-linked axon degenerationPreprint

Liew, Y.-T., Voelzmann, A., Pinho-Correia, L. M., Murphy, T., Tortoishell, H., Parkin, J., Bailey, D. M., Landgraf, M., & Prokop, A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.23.473961 · Cited by 3

A novel antidepressant mechanism of baicalin: enhancing KIF5A-mediated axoplasmic transport and vesicular trafficking in glutamatergic neurons

Lu, S., Shen, J.-D., Jin, X., Zhang, C., Wang, B., Liu, X., Bai, M., Xu, E., Yan, X., & Li, Y. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1577676 · Cited by 2

Sciatic Integrity Is Necessary for Fast and Efficient Scrapie Infection After Footpad Injection

Cardone, F., Porreca, F., Sbriccoli, M., Poleggi, A., Ladogana, A., Lü, M., Pocchiari, M., & Giamberardino, L. D. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26157273 · Cited by 2

Itch

Heul, A. V., & Kim, B. (2025) · Immunology and Allergy Clinics of North America · doi:10.1016/j.iac.2025.06.005 · Cited by 2

Connectome-constrained ligand-receptor interaction analysis for understanding brain network communication

Du, Z., Chu, C., Shi, W., Luo, N., Lu, Y., Wang, H., Zhao, B., Xiong, H., Yang, Z., & Jiang, T. (2025) · Nature Communications · doi:10.1038/s41467-025-63204-9 · Cited by 2

KIF5A upregulation by FAK ‐mediated downregulation of epigenetic modifiers promotes mitochondrial dynamics in neuronal differentiation

Manna, S., Kirtana, R., Mishra, J., & Patra, S. K. (2025) · FEBS Letters · doi:10.1002/1873-3468.70177 · Cited by 2

A system for high-throughput axonal imaging of induced pluripotent stem cell-derived human i 3 Neurons

Whittaker, S. A. C., McKenna, E. D., Sarbanes, S. L., Fernandopulle, M. S., Ward, M. E., & Roll‐Mecak, A. (2025) · Molecular Biology of the Cell · doi:10.1091/mbc.e25-06-0300 · Cited by 4

Integrated Plasma and Glial Cell Evidence Indicates a Functional Role for hsa-miR-342-5p in Spinocerebellar Ataxia Type 7 and Its Potential Use as a Biomarker

Borgonio‐Cuadra, V. M., Meza‐Dorantes, A., Rodríguez-Pérez, J. M., García‐Aguirre, I., Murillo-Melo, N. M., Pérez‐Hernández, N., Hernández‐Hernández, Ó., Hernández-Ortega, M., Herrera-Carrillo, Z., Cisneros, B., et al. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27020683 · Cited by 3

Auxin-inducible degradation of UNC-116 in C. elegans inhibits bidirectional dense core vesicle transport and worm locomotion on different timescales

Boström, A., Gavrilova, A., Herzig, J. C., Poulin, G. B., & Allan, V. (2026) · Journal of Cell Science · doi:10.1242/jcs.264245 · Cited by 2

Cell type transcriptomic modules reveal shared molecular mechanisms in Alzheimer’s and Parkinson’s disease

Bhattacharya, A., Fon, E. A., Dagher, A., Iturria‐Medina, Y., Stratton, J. A., Savignac, C., Stanley, J., Hodgson, L. M., Hammou, B. A., Bennett, D. A. A., et al. (2026) · GigaScience · doi:10.1093/gigascience/giag059 · Cited by 9

Aberrant tau accumulation caused by MAPT mutations induces early pathological changes in axonal transport that are rescued by p38α inhibition

Moretto, E., Masato, A., Panzi, C., Lopes, A. T., Stuart, S., De La-Rocque, S., Caso, M. G., White, I. J., Harris, S. S., Busche, M. A., et al. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02266-4 · Cited by 4

Single‐particle fluorescence tracking combined with TrackMate assay reveals highly heterogeneous and discontinuous lysosomal transport in freely orientated axons

Liu, Y., Lu, Y., Tang, Z., Cao, Y., Huang, D., Wu, F. H., Zhang, Y., Li, C., Chen, G., & Wang, Q. (2022) · Biotechnology Journal · doi:10.1002/biot.202200006 · Cited by 2

Multiple Labeling of Compartmentalized Cortical Neurons in Microfluidic Chambers

Moya‐Alvarado, G., Aguirre-Soto, A. A., & Bronfman, F. C. (2024) · BIO-PROTOCOL · doi:10.21769/bioprotoc.4911 · Cited by 2

Visualization and Quantification of Organelle Axonal Transport in Cultured Neurons

Aiken, J., & Holzbaur, E. L. F. (2024) · Methods in molecular biology · doi:10.1007/978-1-0716-3969-6_15 · Cited by 2

A novel neurodevelopmental-neurodegenerative syndrome that cosegregates with a homozygous SPAG9/JIP4 stop-codon deletion

Acosta‐Baena, N., Moreno, J., Soto-Ospina, A., Mejía‐García, A., Preciado, M., Nanclares-Torres, J., Antonieta, M., Rojas, W., Cardona‐Gómez, G. P., Madrigal, L., et al. (2024) · Genomic psychiatry : · doi:10.61373/gp024a.0052 · Cited by 2

Modeling of ATP transport in an axon: Effects of spontaneous neuron firing and mitochondrial transfer via tunneling nanotubes

Kuznetsov, A. V. (2025) · International Journal of Heat and Mass Transfer · doi:10.1016/j.ijheatmasstransfer.2025.126790 · Cited by 2

Exploring the potential role of microtubule associated proteins-2 in the pathogenesis of HIV associated neurocognitive disorders

Becher, M. K., Avdoshina, V., Campbell, L. A., & Mocchetti, I. (2025) · Neurotoxicity Research · doi:10.1007/s12640-025-00739-1 · Cited by 2

Computational investigation of the effect of reduced dynein velocity and reduced cargo diffusivity on slow axonal transport

Kuznetsov, I. A., & Kuznetsov, A. V. (2023) · Proceedings of the Royal Society A Mathematical Physical and Engineering Sciences · doi:10.1098/rspa.2022.0672 · Cited by 2

KIF3A accelerates KIF3C within the kinesin-2 heterodimer to generate symmetrical phosphate release rates for each processive step

Quinn, S. M., Vargason, T., Pokhrel, N., Antony, E., Hahn, J., & Gilbert, S. P. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.015272 · Cited by 2

AP-4 mediates vesicular transport of the 2-AG endocannabinoid producing enzyme DAGLBPreprint

Davies, A. K., Ziegler, M., Jumo, H., Saber, W. A., Ebrahimi‐Fakhari, D., & Borner, G. H. H. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.25.353995 · Cited by 2

Editorial: Microtubule-associated molecular motors: Transport mechanisms and role in disease

Soppina, V., Xiang, X., & Arumugam, S. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1106435 · Cited by 3

Neuroscience Scaffolded by Informatics: A Raging Interdisciplinary Field

Papageorgiou, I. E. (2023) · Symmetry · doi:10.3390/sym15010153 · Cited by 2

Rab11 suppresses neuronal stress signaling by localizing dual leucine zipper kinase to axon terminals for protein turnoverPreprint

Kim, S., Quagraine, Y., Singh, M., & Kim, J. H. (2024) · eLife · doi:10.7554/elife.96592 · Cited by 2

Enhanced axonal transport in large vertebrates: KIF5A adaptations in giraffes and pythonsPreprint

Kambara, T., Rao, L., Yamagishi, Y., Ikeda, K., Taniguchi, D., Imasaki, T., Shigematsu, H., Sakai, N., Gennerich, A., Nitta, R., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.04.652084 · Cited by 2

Self-renewal of neuronal mitochondria through asymmetric divisionPreprint

Waingankar, T. P., Zurita, C., Lang, A. E., Vuong, C., Shami, A., Bautista, D. M., Drerup, C. M., & Lewis, S. C. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.17.694973 · Cited by 2

A Protein-Centric View of in Vitro Biological Model Systems for Schizophrenia

Chandrasekaran, A., Jensen, P., Mohamed, F. A., Lancaster, M. A., Benros, M. E., Larsen, M. R., & Freude, K. (2021) · Stem Cells · doi:10.1002/stem.3447 · Cited by 1

Navigating the pathways: TAR-DNA-binding-protein-43 aggregation, axonal transport, and local synthesis in amyotrophic lateral sclerosis pathology

Avi, O. B., & Perlson, E. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-00726 · Cited by 1

Human ATP-binding proteins: Structural features, functional diversity, and pharmacotherapeutic potential in disease: A review

Li, L., Wang, S., Fu, S., Chen, Z., Wang, P., & Zhao, Y. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.142303 · Cited by 1

Nose-to-Glioblastoma Axonal Transport of Manganese Ferrite Nanoparticles under the Influence of Olfactory Stimulation

Sharapova, M. B., Zuev, D. S., Silvanovich, E. K., Ibraeva, A. Z., Morozova, K. N., Владимировна, К. Е., Chernozem, P. V., Urakova, A. O., Wagner, D. V., Gerasimov, E. Y., et al. (2025) · ACS Applied Nano Materials · doi:10.1021/acsanm.4c07085 · Cited by 1

Engine breakdown of lysosomes and related organelles and the resulting physiology

Bakker, N., Jongsma, M. L. M., & Neefjes, J. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1575571 · Cited by 1

The Plus End-Directed Microtubule (Kinesin-3 Family) Motor Protein KIF13B Is Associated with the Photoreceptor Synaptic Ribbon Complex

Suiwal, S., Schwarz, K., Maxeiner, S., & Schmitz, F. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26136044 · Cited by 1

Ccp1 depletion disrupts network integration of hippocampal parvalbumin interneurons

Bail, R. L., Lakaye, B., Espuny-Camacho, I., Janke, C., Magiera, M. M., Engel, D., Silva, C. G., & Nguyen, L. (2025) · iScience · doi:10.1016/j.isci.2025.113215 · Cited by 1

Neural transmission in the wired brain, new insights into an encoding-decoding-based neuronal communication model

Kinreich, S. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03506-0 · Cited by 1

New insights into the influence of temperature on axonal transport and function in myelinated regions of Schwann cells

Zeng, C., & Kamei, Y. (2025) · iScience · doi:10.1016/j.isci.2025.113467 · Cited by 1

Cytoskeletal disintegration in cardiovascular disease-related neurodegeneration

Atasever, E., Cebe, T., Turgut, Ş., Andican, G., & Çakatay, U. (2025) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2025.10.030 · Cited by 1

Flicker-Suppressed Neuromorphic Unit for Dynamic Vision Processing

Xie, P., Shi, S., Ran, L., Wang, C., Li, D., Zhang, Y., Wei, Y., Quan, Q., Li, B., Meng, Y., et al. (2026) · ACS Nano · doi:10.1021/acsnano.5c18939 · Cited by 1

Axonal injury signaling is restrained by a spared synaptic branch

Smithson, L. J., Zang, J. L., Junginger, L. M., Waller, T. J., Jankowiak, R., Khan, S. A., Li, Y., Cai, D., & Collins, C. A. (2025) · eLife · doi:10.7554/elife.104896.3 · Cited by 1

Heterogeneous model for superdiffusive movement of dense core vesicles in C. elegans

Gavrilova, A., Nickolay Korabel, A., Allan, V., & Fedotov, S. P. (2025) · Scientific Reports · doi:10.1038/s41598-024-83602-1 · Cited by 1

Live-Imaging of Axonal Cargoes in Drosophila Brain Explants Using Confocal Microscopy

Médioni, C., Ephrussi, A., & Besse, F. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-1916-2_2 · Cited by 1

Why slow axonal transport is bidirectional – can axonal transport of tau protein rely only on motor-driven anterograde transport?

Kuznetsov, I. A., & Kuznetsov, A. V. (2023) · Computer Methods in Biomechanics & Biomedical Engineering · doi:10.1080/10255842.2023.2197541 · Cited by 1

UNC-10/SYD-2 links kinesin-3 to RAB-3-containing vesicles in the absence of the motor’s PH domainPreprint

Bayansan, O., Bhan, P., Chang, C.-Y., Barmaver, S. N., Shen, C.-P., & Wagner, O. I. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/723247 · Cited by 1

NAD homeostasis maintained by NMNAT2 supports vesicular glycolysis and fuels fast axonal transport in distal axons of cortical glutamatergic neurons in micePreprint

Yang, S., Niou, Z., Enriquez, A., LaMar, J., Huang, J.-Y., Ling, K., Jafar‐Nejad, P., Gilley, J., Coleman, M. P., Tennessen, J. M., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.06.479307 · Cited by 2

Concepts | No Membrane, No Problem: Cellular Organization by Biomolecular Condensates

Sang, C. C., Moore, G., & Lee, H. O. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819460-7.00329-7 · Cited by 1

Neuronal Transport and Spatial Signaling Mechanisms in Neural Repair

Hines, T. J., Smith, D. S., Twiss, J. L., Roossien, D. H., & Kalinski, A. L. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00161-9 · Cited by 1

Dyneins

Yıldız, A., & Ishikawa, T. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00094-8 · Cited by 1

NMNAT2 supports vesicular glycolysis via NAD homeostasis to fuel fast axonal transportPreprint

Yang, S., Niou, Z., Enriquez, A., LaMar, J., Huang, J.-Y., Ling, K., Jafar‐Nejad, P., Gilley, J., Coleman, M. P., Tennessen, J. M., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-2859584/v1 · Cited by 1

Editorial: Cytoskeletal alterations in aging and disease

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