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Opposite-polarity motors activate one another to trigger cargo transport in live cells

https://doi.org/10.1083/jcb.200908075

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Microtubule polarity and axis formation in the Drosophila oocyte

inferredcites →https://doi.org/10.1006/jmbi.1997.1319openalex-snapshot

Kinetic evidence for low chemical processivity in ncd and Eg5

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Load-dependent release limits the processive stepping of the tetrameric Eg5 motor

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Obstacles on the Microtubule Reduce the Processivity of Kinesin-1 in a Minimal In Vitro System and in Cell Extract

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To step or not to step? How biochemistry and mechanics influence processivity in Kinesin and Eg5

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Consequences of Motor Copy Number on the Intracellular Transport of Kinesin-1-Driven Lipid Droplets

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

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Molecular motors in neuronal development, intracellular transport and diseases

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A Determinant for Directionality of Organelle Transport in Drosophila Embryos

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Halo: A Guiding Light for Transport

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Monastrol stabilises an attached low-friction mode of Eg5

inferredcites →https://doi.org/10.1016/j.cub.2004.06.045openalex-snapshot

Bidirectional Transport along Microtubules

inferredcites →https://doi.org/10.1016/j.cub.2005.08.027openalex-snapshot

Microtubule Motors: LSD2 Trips the Toggle

inferredcites →https://doi.org/10.1016/j.cub.2007.06.062openalex-snapshot

Control of a Kinesin-Cargo Linkage Mechanism by JNK Pathway Kinases

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Minus-End-Directed Motor Ncd Exhibits Processive Movement that Is Enhanced by Microtubule Bundling In Vitro

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ARF6 Interacts with JIP4 to Control a Motor Switch Mechanism Regulating Endosome Traffic in Cytokinesis

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Multiple Kinesin Motors Coordinate Cytoplasmic RNA Transport on a Subpopulation of Microtubules in Xenopus Oocytes

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Molecular Dissection of the Inhibitor Binding Pocket of Mitotic Kinesin Eg5 Reveals Mutants that Confer Resistance to Antimitotic Agents

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Kinesin: walking, crawling or sliding along?

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Huntingtin as an essential integrator of intracellular vesicular trafficking

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Role of Phosphatidylinositol(4,5)bisphosphate Organization in Membrane Transport by the Unc104 Kinesin Motor

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Role of the kinesin neck linker and catalytic core in microtubule-based motility

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The Cytoplasmic Dynein and Kinesin Motors Have Interdependent Roles in Patterning the Drosophila Oocyte

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Kinetic Studies of Dimeric Ncd: Evidence That Ncd Is Not Processive

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Direction determination in the minus-end-directed kinesin motor ncd

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Dynamic instability of microtubule growth

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Microtubule motors in mitosis

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A bipolar kinesin

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Huntingtin phosphorylation acts as a molecular switch for anterograde/retrograde transport in neurons

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The bipolar mitotic kinesin Eg5 moves on both microtubules that it crosslinks

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Individual dimers of the mitotic kinesin motor Eg5 step processively and support substantial loads in vitro

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Allosteric inhibition of kinesin-5 modulates its processive directional motility

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A Drosophila kinesin required for synaptic bouton formation and synaptic vesicle transport

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A structural model for monastrol inhibition of dimeric kinesin Eg5

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Transport of Drosophila fragile X mental retardation protein-containing ribonucleoprotein granules by kinesin-1 and cytoplasmic dynein

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Probing the kinesin reaction cycle with a 2D optical force clamp

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Two modes of microtubule sliding driven by cytoplasmic dynein

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Huntingtin facilitates dynein/dynactin-mediated vesicle transport

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Tug-of-war as a cooperative mechanism for bidirectional cargo transport by molecular motors

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Tug-of-war between dissimilar teams of microtubule motors regulates transport and fission of endosomes

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Use of double-stranded RNA interference in Drosophila cell lines to dissect signal transduction pathways

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The interaction between cytoplasmic dynein and dynactin is required for fast axonal transport

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S-Trityl-L-cysteine Is a Reversible, Tight Binding Inhibitor of the Human Kinesin Eg5 That Specifically Blocks Mitotic Progression

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Heterotrimeric Kinesin II Is the Microtubule Motor Protein Responsible for Pigment Dispersion in Xenopus Melanophores

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Cargo of Kinesin Identified as Jip Scaffolding Proteins and Associated Signaling Molecules

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Interactions and regulation of molecular motors in Xenopus melanophores

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Coordination of opposite-polarity microtubule motors

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The roles of microtubule-based motor proteins in mitosis

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Cytoplasmic Dynein, the Dynactin Complex, and Kinesin Are Interdependent and Essential for Fast Axonal Transport

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Kinesin-1 and Dynein Are the Primary Motors for Fast Transport of Mitochondria in Drosophila Motor Axons

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Tight Functional Coupling of Kinesin-1A and Dynein Motors in the Bidirectional Transport of Neurofilaments

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Bicaudal D induces selective dynein‐mediated microtubule minus end‐directed transport

inferredcites →https://doi.org/10.1126/science.1073386openalex-snapshot

Conversion of Unc104/KIF1A Kinesin into a Processive Motor After Dimerization

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Kinesin Walks Hand-Over-Hand

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Kinesin and Dynein Move a Peroxisome in Vivo: A Tug-of-War or Coordinated Movement?

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β-Arrestin–Mediated Localization of Smoothened to the Primary Cilium

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Herpesvirus Interactions with the Host Cytoskeleton

inferredcites →https://doi.org/10.1128/mcb.25.7.2733-2743.2005openalex-snapshot

Role of the JIP4 Scaffold Protein in the Regulation of Mitogen-Activated Protein Kinase Signaling Pathways

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Mechanical Signaling in Networks of Motor and Cytoskeletal Proteins

inferredcites →https://doi.org/10.1152/physrev.00023.2007openalex-snapshot

Intracellular Transport and Kinesin Superfamily Proteins, KIFs: Structure, Function, and Dynamics

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Milton controls the early acquisition of mitochondria byDrosophilaoocytes

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The axonal transport of mitochondria

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Ncd motor binding and transport in the spindle

inferredcites →https://doi.org/10.1242/jcs.053850openalex-snapshot

The axonal transport of mitochondria

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Tau/PTL-1 associates with kinesin-3 KIF1A/UNC-104 and affects the motor's motility characteristics in C. elegans neurons

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KIF1A is the primary anterograde motor protein required for the axonal transport of dense-core vesicles in cultured hippocampal neurons

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The role of the cytoskeleton and molecular motors in endosomal dynamics

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Teamwork in microtubule motors

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Hitchhiking: A Non-Canonical Mode of Microtubule-Based Transport

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Activation and Regulation of Cytoplasmic Dynein

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Lysosome-associated membrane proteins (LAMPs) regulate intracellular positioning of mitochondria in MC3T3-E1 cells

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Adapter Proteins for Opposing Motors Interact Simultaneously with Nuclear Pore Protein Nup358

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Manipulation and Motion of Organelles and Single Molecules in Living Cells

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Tug-of-War and Coordination in Bidirectional Transport by Molecular Motors

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Cooperation and Competition Coexist in Bidirectional Transport by Motor Proteins

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Single-Molecule Fluorescence and in Vivo Optical Traps: How Multiple Dyneins and Kinesins Interact

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Coupling viruses to dynein and kinesin‐1

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Load-induced enhancement of Dynein force production by LIS1–NudE in vivo and in vitro

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Rotational dynamics of cargos at pauses during axonal transport

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HIV-1 capsids bind and exploit the kinesin-1 adaptor FEZ1 for inward movement to the nucleus

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In brief

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Bidirectional cargo transport: moving beyond tug of war

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The cellular mechanisms that maintain neuronal polarity

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Axonal transport and neurological disease

inferred← citeshttps://doi.org/10.1038/s41594-024-01418-zopenalex-snapshot

KIF1C activates and extends dynein movement through the FHF cargo adapter

inferred← citeshttps://doi.org/10.1038/s41594-025-01524-6openalex-snapshot

Microtubule motors of opposite polarity cooperate rather than compete in cargo transport

inferred← citeshttps://doi.org/10.1038/s41598-018-29818-4openalex-snapshot

The actin capping protein in Aspergillus nidulans enhances dynein function without significantly affecting Arp1 filament assembly

inferred← citeshttps://doi.org/10.1039/c0sm00927jopenalex-snapshot

Crosstalk between non-processive myosin motors mediated by the actin filament elasticity

inferred← citeshttps://doi.org/10.1039/c5sm01609fopenalex-snapshot

Collective dynamics of processive cytoskeletal motors

inferred← citeshttps://doi.org/10.1042/bst0391126openalex-snapshot

Bidirectional intracellular transport: utility and mechanism

inferred← citeshttps://doi.org/10.1042/bst0391169openalex-snapshot

Cytoplasmic dynein

inferred← citeshttps://doi.org/10.1042/cbi20110413openalex-snapshot

Bidirectional transport of organelles: unity and struggle of opposing motors

inferred← citeshttps://doi.org/10.1063/1.4921591openalex-snapshot

Real-time investigation of dynamic protein crystallization in living cells

inferred← citeshttps://doi.org/10.1063/1.4921591.4openalex-snapshot

10.1063/1.4921591.4

inferred← citeshttps://doi.org/10.1063/1.4921591.7openalex-snapshot

10.1063/1.4921591.7

inferred← citeshttps://doi.org/10.1073/pnas.1004736107openalex-snapshot

Kinesin-1 heavy chain mediates microtubule sliding to drive changes in cell shape

inferred← citeshttps://doi.org/10.1073/pnas.1015839108openalex-snapshot

Transient binding of dynein controls bidirectional long-range motility of early endosomes

inferred← citeshttps://doi.org/10.1073/pnas.1104298108openalex-snapshot

Myosin Va and myosin VI coordinate their steps while engaged in an in vitro tug of war during cargo transport

inferred← citeshttps://doi.org/10.1073/pnas.1107841108openalex-snapshot

Mechanical stochastic tug-of-war models cannot explain bidirectional lipid-droplet transport

inferred← citeshttps://doi.org/10.1073/pnas.1201390110openalex-snapshot

Measuring collective transport by defined numbers of processive and nonprocessive kinesin motors

inferred← citeshttps://doi.org/10.1073/pnas.1219961110openalex-snapshot

In vivo optical trapping indicates kinesin’s stall force is reduced by dynein during intracellular transport

inferred← citeshttps://doi.org/10.1073/pnas.1522424113openalex-snapshot

Microtubule–microtubule sliding by kinesin-1 is essential for normal cytoplasmic streaming in Drosophila oocytes

inferred← citeshttps://doi.org/10.1073/pnas.2113795119openalex-snapshot

De novo mutations in KIF1A-associated neuronal disorder (KAND) dominant-negatively inhibit motor activity and axonal transport of synaptic vesicle precursors

inferred← citeshttps://doi.org/10.1074/jbc.m111.296582openalex-snapshot

Cooperative Responses of Multiple Kinesins to Variable and Constant Loads

inferred← citeshttps://doi.org/10.1080/10255842.2011.607445openalex-snapshot

Analytical modelling of retrograde transport of nerve growth factors in an axon: a transient problem

inferred← citeshttps://doi.org/10.1080/10255842.2011.632376openalex-snapshot

An analytical solution describing the propagation of positive injury signals in an axon: effect of dynein velocity distribution

inferred← citeshttps://doi.org/10.1080/10255842.2012.662679openalex-snapshot

An exact solution of transient equations describing slow axonal transport

inferred← citeshttps://doi.org/10.1083/jcb.1877iti1openalex-snapshot

Opposing motors take the strain

inferred← citeshttps://doi.org/10.1083/jcb.201004118openalex-snapshot

Kinesin-1 and dynein at the nuclear envelope mediate the bidirectional migrations of nuclei

inferred← citeshttps://doi.org/10.1083/jcb.201104076openalex-snapshot

High-resolution imaging reveals indirect coordination of opposite motors and a role for LIS1 in high-load axonal transport

inferred← citeshttps://doi.org/10.1083/jcb.201112101openalex-snapshot

Lis1 is an initiation factor for dynein-driven organelle transport

inferred← citeshttps://doi.org/10.1083/jcb.201307116openalex-snapshot

PKA-dependent dynein switching from lysosomes to adenovirus: A novel form of host–virus competition

inferred← citeshttps://doi.org/10.1083/jcb.201708122openalex-snapshot

New splicing variants of mitochondrial Rho GTPase-1 (Miro1) transport peroxisomes

inferred← citeshttps://doi.org/10.1083/jcb.201709174openalex-snapshot

Ooplasmic flow cooperates with transport and anchorage in Drosophila oocyte posterior determination

inferred← citeshttps://doi.org/10.1083/jcb.202205136openalex-snapshot

Kinesin-1 autoinhibition facilitates the initiation of dynein cargo transport

inferred← citeshttps://doi.org/10.1083/jcb.202309084openalex-snapshot

Dynein and dynactin move long-range but are delivered separately to the axon tip

inferred← citeshttps://doi.org/10.1083/jcb.202405032openalex-snapshot

Nesprin-2 coordinates opposing microtubule motors during nuclear migration in neurons

inferred← citeshttps://doi.org/10.1088/0953-8984/25/46/463101openalex-snapshot

Motor proteins and molecular motors: how to operate machines at the nanoscale

inferred← citeshttps://doi.org/10.1088/1478-3975/10/1/016003openalex-snapshot

Characterization of bidirectional molecular motor-assisted transport models

inferred← citeshttps://doi.org/10.1088/1478-3975/aba5e5openalex-snapshot

Getting around the cell: physical transport in the intracellular world

inferred← citeshttps://doi.org/10.1091/mbc.e10-09-0741openalex-snapshot

CK1 activates minus-end–directed transport of membrane organelles along microtubules

inferred← citeshttps://doi.org/10.1091/mbc.e11-03-0217openalex-snapshot

Kinesin-3 and dynein cooperate in long-range retrograde endosome motility along a nonuniform microtubule array

inferred← citeshttps://doi.org/10.1091/mbc.e11-11-0938openalex-snapshot

Molecular motor function in axonal transport in vivo probed by genetic and computational analysis inDrosophila

inferred← citeshttps://doi.org/10.1091/mbc.e12-12-0858openalex-snapshot

Amyloid-β oligomers induce tau-independent disruption of BDNF axonal transport via calcineurin activation in cultured hippocampal neurons

inferred← citeshttps://doi.org/10.1091/mbc.e14-10-1423openalex-snapshot

Kinesin-1–powered microtubule sliding initiates axonal regeneration in Drosophila cultured neurons

inferred← citeshttps://doi.org/10.1091/mbc.e23-01-0020openalex-snapshot

Tubulin CFEOM mutations both inhibit or activate kinesin motor activity

inferred← citeshttps://doi.org/10.1093/brain/awu097openalex-snapshot

DYNC1H1 mutation alters transport kinetics and ERK1/2-cFos signalling in a mouse model of distal spinal muscular atrophy

inferred← citeshttps://doi.org/10.1096/fj.14-250019openalex-snapshot

Microtubule‐dependent transport of vimentin filament precursors is regulated by actin and by the concerted action of Rho‐ and p21‐activated kinases

inferred← citeshttps://doi.org/10.1098/rsob.120183openalex-snapshot

Kinesin-1 and mitochondrial motility control by discrimination of structurally equivalent but distinct subdomains in Ran-GTP-binding domains of Ran-binding protein 2

inferred← citeshttps://doi.org/10.1098/rspa.2012.0061openalex-snapshot

An exact solution describing slow axonal transport of cytoskeletal elements: the effect of a finite half-life

inferred← citeshttps://doi.org/10.1101/2021.05.06.443034openalex-snapshot

Coil-to-Helix Transition at the Nup358-BicD2 Interface Activates BicD2 for Dynein Recruitment

inferred← citeshttps://doi.org/10.1101/2021.05.15.444169openalex-snapshot

A lipid-mTORC1 nutrient sensing pathway regulates animal development by peroxisome-derived hormones

inferred← citeshttps://doi.org/10.1101/2021.06.10.447989openalex-snapshot

Cargo-mediated mechanisms reduce inter-motor mechanical interference, promote load-sharing and enhance processivity in teams of molecular motors

inferred← citeshttps://doi.org/10.1101/2023.03.19.533383openalex-snapshot

Mutant Prion Protein Endoggresomes are Hubs for Local Axonal Organelle-Cytoskeletal Remodeling

inferred← citeshttps://doi.org/10.1101/250175openalex-snapshot

Dynein catch bond as a mediator of codependent bidirectional cellular transport

inferred← citeshttps://doi.org/10.1103/physreve.101.062416openalex-snapshot

Intracellular motor-driven transport of rodlike smooth organelles along microtubules

inferred← citeshttps://doi.org/10.1103/physrevresearch.1.023019openalex-snapshot

Dynein catch bond as a mediator of codependent bidirectional cellular transport

inferred← citeshttps://doi.org/10.1111/tra.12037openalex-snapshot

Endogenous GSK ‐3/Shaggy Regulates Bidirectional Axonal Transport of the Amyloid Precursor Protein

inferred← citeshttps://doi.org/10.1111/tra.12070openalex-snapshot

Distinct Functions of Nuclear Distribution Proteins LIS1 , Ndel1 and NudCL in Regulating Axonal Mitochondrial Transport

inferred← citeshttps://doi.org/10.1111/tra.12475openalex-snapshot

Regulation of dynein‐dynactin‐driven vesicular transport

inferred← citeshttps://doi.org/10.1111/tra.12537openalex-snapshot

Tau directs intracellular trafficking by regulating the forces exerted by kinesin and dynein teams

inferred← citeshttps://doi.org/10.1115/1.4056915openalex-snapshot

Dynein Dysfunction Prevents Maintenance of High Concentrations of Slow Axonal Transport Cargos at the Axon Terminal: A Computational Study

inferred← citeshttps://doi.org/10.1134/s0006297917070057openalex-snapshot

Intracellular cargo transport by kinesin-3 motors

inferred← citeshttps://doi.org/10.1142/s021951941100468xopenalex-snapshot

A THREE-KINETIC-STATE MODEL OF AXONAL TRANSPORT DRUG DELIVERY

inferred← citeshttps://doi.org/10.1146/annurev-biophys-042910-155310openalex-snapshot

Kinesin Assembly and Movement in Cells

inferred← citeshttps://doi.org/10.1146/annurev-biophys-051013-022746openalex-snapshot

Biophysical Challenges to Axonal Transport: Motor-Cargo Deficiencies and Neurodegeneration

inferred← citeshttps://doi.org/10.1146/annurev-micro-092611-150051openalex-snapshot

Herpesvirus Transport to the Nervous System and Back Again

inferred← citeshttps://doi.org/10.1152/ajpgi.00118.2013openalex-snapshot

Rab1a regulates sorting of early endocytic vesicles

inferred← citeshttps://doi.org/10.1152/ajpregu.00002.2010openalex-snapshot

Mechanisms of proximal tubule sodium transport regulation that link extracellular fluid volume and blood pressure

inferred← citeshttps://doi.org/10.1152/physrev.00023.2007openalex-snapshot

Intracellular Transport and Kinesin Superfamily Proteins, KIFs: Structure, Function, and Dynamics

inferred← citeshttps://doi.org/10.1242/bio.2012307openalex-snapshot

Ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon

inferred← citeshttps://doi.org/10.1242/bio.20147633openalex-snapshot

Opposing microtubule motors control motility, morphology and cargo segregation during ER-to-Golgi transport

inferred← citeshttps://doi.org/10.1242/dmm.052405openalex-snapshot

14-3-3θ phosphorylation at S232 reduces its interactome and regulates axonal trafficking

inferred← citeshttps://doi.org/10.1242/jcs.053850openalex-snapshot

The axonal transport of mitochondria

inferred← citeshttps://doi.org/10.1242/jcs.062208openalex-snapshot

Towards a quantitative understanding of mitotic spindle assembly and mechanics

inferred← citeshttps://doi.org/10.1242/jcs.075259openalex-snapshot

The microtubule plus-end localization ofAspergillusdynein is important for dynein–early-endosome interaction but not for dynein ATPase activation

inferred← citeshttps://doi.org/10.1242/jcs.097675openalex-snapshot

Functional coupling of microtubules to membranes – implications for membrane structure and dynamics

inferred← citeshttps://doi.org/10.1242/jcs.115030openalex-snapshot

Microtubule-based transport – basic mechanisms, traffic rules and role in neurological pathogenesis

inferred← citeshttps://doi.org/10.1242/jcs.122317openalex-snapshot

Microtubule motors mediate endosomal sorting by maintaining functional domain organization.

inferred← citeshttps://doi.org/10.1242/jcs.123885openalex-snapshot

Protein kinase Darkener of apricot and its substrate EF1γ regulate organelle transport along microtubules

inferred← citeshttps://doi.org/10.1242/jcs.237016openalex-snapshot

The role of microtubules in secretory protein transport

inferred← citeshttps://doi.org/10.1242/jcs.249938openalex-snapshot

Stable tug-of-war between kinesin-1 and cytoplasmic dynein upon different ATP and roadblock concentrations

inferred← citeshttps://doi.org/10.1242/jcs.262148openalex-snapshot

The role of kinesin-1 in neuronal dense core vesicle transport, locomotion and lifespan regulation in C. elegans

inferred← citeshttps://doi.org/10.1242/jcs.264245openalex-snapshot

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

inferred← citeshttps://doi.org/10.1371/journal.pbio.1001551openalex-snapshot

Directional Transport Is Mediated by a Dynein-Dependent Step in an RNA Localization Pathway

inferred← citeshttps://doi.org/10.1371/journal.pbio.3002273openalex-snapshot

Optogenetic cleavage of the Miro GTPase reveals the direct consequences of real-time loss of function in Drosophila

inferred← citeshttps://doi.org/10.1371/journal.pcbi.1010217openalex-snapshot

Cargo surface fluidity can reduce inter-motor mechanical interference, promote load-sharing and enhance processivity in teams of molecular motors

inferred← citeshttps://doi.org/10.1371/journal.pgen.1003066openalex-snapshot

Spastic Paraplegia Mutation N256S in the Neuronal Microtubule Motor KIF5A Disrupts Axonal Transport in a Drosophila HSP Model

inferred← citeshttps://doi.org/10.1371/journal.pone.0024479openalex-snapshot

Roles of Dynein and Dynactin in Early Endosome Dynamics Revealed Using Automated Tracking and Global Analysis

inferred← citeshttps://doi.org/10.1371/journal.ppat.1007055openalex-snapshot

Role of kinesins in directed adenovirus transport and cytoplasmic exploration

inferred← citeshttps://doi.org/10.1523/jneurosci.1074-10.2010openalex-snapshot

Amyloid- Peptide Oligomers Disrupt Axonal Transport through an NMDA Receptor-Dependent Mechanism That Is Mediated by Glycogen Synthase Kinase 3 in Primary Cultured Hippocampal Neurons

inferred← citeshttps://doi.org/10.1523/jneurosci.1233-11.2012openalex-snapshot

Mitochondrial Dynamics and Bioenergetic Dysfunction Is Associated with Synaptic Alterations in Mutant SOD1 Motor Neurons

inferred← citeshttps://doi.org/10.17116/molgen2019370113openalex-snapshot

mRNP transport. mRNP transport in the cytoplasm

inferred← citeshttps://doi.org/10.2147/dnnd.s57502openalex-snapshot

Axonal transport and neurodegenerative disease: vesicle-motor complex formation and their regulation

inferred← citeshttps://doi.org/10.2478/s11534-011-0051-2openalex-snapshot

Analytical investigation of various regimes of retrograde trafficking of neurotropic viruses in axons

inferred← citeshttps://doi.org/10.2478/s11534-011-0070-zopenalex-snapshot

Merging of viral concentration waves in retrograde viral transport in axons

inferred← citeshttps://doi.org/10.2478/s11534-011-0116-2openalex-snapshot

A model of axonal transport drug delivery

inferred← citeshttps://doi.org/10.2478/s11534-012-0051-xopenalex-snapshot

Effect of kinesin velocity distribution on slow axonal transport

inferred← citeshttps://doi.org/10.3103/s089141681901004xopenalex-snapshot

mRNP Transport in Eukaryots: Transport of mRNP Particles in Cytoplasm

inferred← citeshttps://doi.org/10.3109/10409238.2011.572861openalex-snapshot

Molecular motors: directing traffic during RNA localization

inferred← citeshttps://doi.org/10.31274/td-20240329-164openalex-snapshot

Consequences of pathogenic tubulin-mutations on molecular motor proteins and their implications in tubulinopathies

inferred← citeshttps://doi.org/10.3389/fcell.2020.00022openalex-snapshot

The Generation of Dynein Networks by Multi-Layered Regulation and Their Implication in Cell Division

inferred← citeshttps://doi.org/10.3389/fcell.2020.00835openalex-snapshot

Rosy Beginnings: Studying Peroxisomes in Drosophila

inferred← citeshttps://doi.org/10.3389/fncel.2019.00470openalex-snapshot

Crowd Control: Effects of Physical Crowding on Cargo Movement in Healthy and Diseased Neurons

inferred← citeshttps://doi.org/10.3389/fncel.2023.1215945openalex-snapshot

Axonal transport during injury on a theoretical axon

inferred← citeshttps://doi.org/10.3389/fnmol.2017.00424openalex-snapshot

VEGF Axonal Transport Dependent on Kinesin-1B and Microtubules Dynamics

inferred← citeshttps://doi.org/10.3389/fnsyn.2016.00003openalex-snapshot

The Roles of Microtubule-Based Transport at Presynaptic Nerve Terminals

inferred← citeshttps://doi.org/10.3390/cells10020262openalex-snapshot

Mechanisms and Therapeutic Implications of GSK-3 in Treating Neurodegeneration

inferred← citeshttps://doi.org/10.3390/md14050102openalex-snapshot

Axonal Transport and Neurodegeneration: How Marine Drugs Can Be Used for the Development of Therapeutics

inferred← citeshttps://doi.org/10.3390/v3030233openalex-snapshot

The Dynactin Complex Enhances the Speed of Microtubule-Dependent Motions of Adenovirus Both Towards and Away from the Nucleus

inferred← citeshttps://doi.org/10.3410/f.717497850.792902901openalex-snapshot

Faculty Opinions recommendation of Lis1 is an initiation factor for dynein-driven organelle transport.

inferred← citeshttps://doi.org/10.3791/50838openalex-snapshot

Organelle Transport in Cultured Drosophila Cells: S2 Cell Line and Primary Neurons.

inferred← citeshttps://doi.org/10.4161/bioa.1.1.14629openalex-snapshot

Watching nuclei move

inferred← citeshttps://doi.org/10.4161/cib.13780openalex-snapshot

Bi-directional transport of the nucleus by dynein and kinesin-1

inferred← citeshttps://doi.org/10.48550/arxiv.1006.5161openalex-snapshot

A hopping mechanism for cargo transport by molecular motors in crowded microtubules

inferred← citeshttps://doi.org/10.48550/arxiv.1107.1507openalex-snapshot

Jamming of molecular motors as a tool for transport cargos along microtubules

inferred← citeshttps://doi.org/10.64898/2026.01.17.700114openalex-snapshot

Structural characterization of a minimal KLC2/Nup358/BicD2 complex

inferred← citeshttps://doi.org/10.70675/1d94d1cdze6b7z41ccz80baz3c7fa8e55e69openalex-snapshot

Etude de l'implication des microtubules dans le trafic intracellulaire

inferred← citeshttps://doi.org/10.70675/25af38bbz9dd0z48fbzb24cza35d0a181013openalex-snapshot

Understanding internal cell coordination during migration

inferred← citeshttps://doi.org/10.70675/5a5d3bacz6b6ez4a35z9159z6459b40efcdfopenalex-snapshot

Huntingtin functions in the regulation of axonal transport : consequences on neuronal network homeostasis and behavior, in health and disease

inferred← citeshttps://doi.org/10.70675/c735a183z2524z4e97z8d81ze3f04b47a7eeopenalex-snapshot

Application of statistical physics tools to intracellular transport

showing the first 200 of 205

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