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Bidirectional cargo transport: moving beyond tug of war

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inferredcites →https://doi.org/10.1002/1097-4547(20001215)62:6<830::aid-jnr10>3.0.co;2-eopenalex-snapshot

Isolation and characterization of substance P-containing dense core vesicles from rabbit optic nerve and termini

inferredcites →https://doi.org/10.1002/cm.20196openalex-snapshot

Direct interaction of Gas11 with microtubules: Implications for the dynein regulatory complex

inferredcites →https://doi.org/10.1016/j.bbadis.2006.04.002openalex-snapshot

Axonal transport and neurodegenerative disease

inferredcites →https://doi.org/10.1016/j.bpj.2010.02.037openalex-snapshot

Bidirectional Transport by Molecular Motors: Enhanced Processivity and Response to External Forces

inferredcites →https://doi.org/10.1016/j.bpj.2010.07.055openalex-snapshot

Probing Intracellular Motor Protein Activity Using an Inducible Cargo Trafficking Assay

inferredcites →https://doi.org/10.1016/j.bpj.2010.08.025openalex-snapshot

Two Kinesins Transport Cargo Primarily via the Action of One Motor: Implications for Intracellular Transport

inferredcites →https://doi.org/10.1016/j.bpj.2011.05.067openalex-snapshot

Productive Cooperation among Processive Motors Depends Inversely on Their Mechanochemical Efficiency

inferredcites →https://doi.org/10.1016/j.bpj.2012.05.037openalex-snapshot

Force-Dependent Detachment of Kinesin-2 Biases Track Switching at Cytoskeletal Filament Intersections

inferredcites →https://doi.org/10.1016/j.ceb.2007.11.006openalex-snapshot

Cargo transport: molecular motors navigate a complex cytoskeleton

inferredcites →https://doi.org/10.1016/j.ceb.2009.01.005openalex-snapshot

The diffusive interaction of microtubule binding proteins

inferredcites →https://doi.org/10.1016/j.cell.2008.10.021openalex-snapshot

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

inferredcites →https://doi.org/10.1016/j.cell.2008.11.046openalex-snapshot

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

inferredcites →https://doi.org/10.1016/j.cell.2010.02.035openalex-snapshot

LIS1 and NudE Induce a Persistent Dynein Force-Producing State

inferredcites →https://doi.org/10.1016/j.cell.2011.01.021openalex-snapshot

Stable Kinesin and Dynein Assemblies Drive the Axonal Transport of Mammalian Prion Protein Vesicles

inferredcites →https://doi.org/10.1016/j.cell.2012.07.022openalex-snapshot

Lis1 Acts as a “Clutch” between the ATPase and Microtubule-Binding Domains of the Dynein Motor

inferredcites →https://doi.org/10.1016/j.cell.2012.11.044openalex-snapshot

Molecular Adaptations Allow Dynein to Generate Large Collective Forces inside Cells

inferredcites →https://doi.org/10.1016/j.conb.2014.03.015openalex-snapshot

Axon and dendritic trafficking

inferredcites →https://doi.org/10.1016/j.cub.2003.08.032openalex-snapshot

A Determinant for Directionality of Organelle Transport in Drosophila Embryos

inferredcites →https://doi.org/10.1016/j.cub.2003.10.027openalex-snapshot

Switching between Microtubule- and Actin-Based Transport Systems in Melanophores Is Controlled by cAMP Levels

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

Bidirectional Transport along Microtubules

inferredcites →https://doi.org/10.1016/j.cub.2005.06.062openalex-snapshot

Regulation of Lipid-Droplet Transport by the Perilipin Homolog LSD2

inferredcites →https://doi.org/10.1016/j.cub.2005.10.047openalex-snapshot

APLIP1, a Kinesin Binding JIP-1/JNK Scaffold Protein, Influences the Axonal Transport of Both Vesicles and Mitochondria in Drosophila

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

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

inferredcites →https://doi.org/10.1016/j.cub.2008.07.027openalex-snapshot

Stepping, Strain Gating, and an Unexpected Force-Velocity Curve for Multiple-Motor-Based Transport

inferredcites →https://doi.org/10.1016/j.cub.2010.02.058openalex-snapshot

Motor Coordination via a Tug-of-War Mechanism Drives Bidirectional Vesicle Transport

inferredcites →https://doi.org/10.1016/j.cub.2010.03.065openalex-snapshot

Neck Linker Length Determines the Degree of Processivity in Kinesin-1 and Kinesin-2 Motors

inferredcites →https://doi.org/10.1016/j.cub.2012.10.017openalex-snapshot

She1-Mediated Inhibition of Dynein Motility along Astral Microtubules Promotes Polarized Spindle Movements

inferredcites →https://doi.org/10.1016/j.cub.2013.05.015openalex-snapshot

Local Cytoskeletal and Organelle Interactions Impact Molecular-Motor-Driven Early Endosomal Trafficking

inferredcites →https://doi.org/10.1016/j.devcel.2011.10.007openalex-snapshot

Arl8 and SKIP Act Together to Link Lysosomes to Kinesin-1

inferredcites →https://doi.org/10.1016/j.jbiomech.2009.09.006openalex-snapshot

The mechanochemistry of integrated motor protein complexes

inferredcites →https://doi.org/10.1016/j.molcel.2008.01.004openalex-snapshot

Phosphorylation Relieves Autoinhibition of the Kinetochore Motor Cenp-E

inferredcites →https://doi.org/10.1016/j.neuron.2009.01.030openalex-snapshot

Miro1 Is a Calcium Sensor for Glutamate Receptor-Dependent Localization of Mitochondria at Synapses

inferredcites →https://doi.org/10.1016/j.neuron.2010.09.039openalex-snapshot

Molecular Motors in Neurons: Transport Mechanisms and Roles in Brain Function, Development, and Disease

inferredcites →https://doi.org/10.1016/j.neuron.2012.02.025openalex-snapshot

Dynactin Is Required for Transport Initiation from the Distal Axon

inferredcites →https://doi.org/10.1016/j.neuron.2012.11.027openalex-snapshot

TRAK/Milton Motor-Adaptor Proteins Steer Mitochondrial Trafficking to Axons and Dendrites

inferredcites →https://doi.org/10.1016/j.tcb.2009.01.005openalex-snapshot

Huntingtin as an essential integrator of intracellular vesicular trafficking

inferredcites →https://doi.org/10.1016/j.tcb.2013.06.003openalex-snapshot

Teamwork in microtubule motors

inferredcites →https://doi.org/10.1016/s0006-3495(03)74926-1openalex-snapshot

Equilibrium and Transition between Single- and Double-Headed Binding of Kinesin as Revealed by Single-Molecule Mechanics

inferredcites →https://doi.org/10.1016/s0021-9258(18)42499-4openalex-snapshot

Kinesin undergoes a 9 S to 6 S conformational transition.

inferredcites →https://doi.org/10.1016/s0074-7696(01)04005-0openalex-snapshot

Regulation of molecular motor proteins

inferredcites →https://doi.org/10.1016/s0076-6879(98)98032-6openalex-snapshot

[30] In Vitro motility assay for melanophore pigment organelles

inferredcites →https://doi.org/10.1016/s0092-8674(00)00162-8openalex-snapshot

Kinesin-Dependent Axonal Transport Is Mediated by the Sunday Driver (SYD) Protein

inferredcites →https://doi.org/10.1016/s0092-8674(00)80947-2openalex-snapshot

Developmental Regulation of Vesicle Transport in Drosophila Embryos: Forces and Kinetics

inferredcites →https://doi.org/10.1016/s0092-8674(00)81459-2openalex-snapshot

Targeted Disruption of Mouse Conventional Kinesin Heavy Chain kif5B, Results in Abnormal Perinuclear Clustering of Mitochondria

inferredcites →https://doi.org/10.1016/s0092-8674(00)81705-5openalex-snapshot

Randomization of Left–Right Asymmetry due to Loss of Nodal Cilia Generating Leftward Flow of Extraembryonic Fluid in Mice Lacking KIF3B Motor Protein

inferredcites →https://doi.org/10.1016/s0092-8674(02)00708-0openalex-snapshot

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

inferredcites →https://doi.org/10.1016/s0167-4889(00)00015-xopenalex-snapshot

Understanding the functions of kinesin-II

inferredcites →https://doi.org/10.1016/s0896-6273(00)00124-0openalex-snapshot

Axonal Transport of Amyloid Precursor Protein Is Mediated by Direct Binding to the Kinesin Light Chain Subunit of Kinesin-I

inferredcites →https://doi.org/10.1016/s0955-0674(01)00295-2openalex-snapshot

Principles of cargo attachment to cytoplasmic motor proteins

inferredcites →https://doi.org/10.1016/s0960-9822(01)00484-5openalex-snapshot

Localization of intraflagellar transport protein IFT52 identifies basal body transitional fibers as the docking site for IFT particles

inferredcites →https://doi.org/10.1016/s0960-9822(03)00237-9openalex-snapshot

Dynactin: Coordinating Motors with Opposite Inclinations

inferredcites →https://doi.org/10.1016/s0960-9822(98)70063-6openalex-snapshot

Myosin cooperates with microtubule motors during organelle transport in melanophores

inferredcites →https://doi.org/10.1016/s0960-9822(98)70064-8openalex-snapshot

Functional coordination of microtubule-based and actin-based motility in melanophores

inferredcites →https://doi.org/10.1016/s1534-5807(03)00094-7openalex-snapshot

JNK1 Is Required for Maintenance of Neuronal Microtubules and Controls Phosphorylation of Microtubule-Associated Proteins

inferredcites →https://doi.org/10.1021/bi701169wopenalex-snapshot

The Effector Domain of Human Dlg Tumor Suppressor Acts as a Switch That Relieves Autoinhibition of Kinesin-3 Motor GAKIN/KIF13B

inferredcites →https://doi.org/10.1021/j100540a008openalex-snapshot

Exact stochastic simulation of coupled chemical reactions

inferredcites →https://doi.org/10.1038/13001openalex-snapshot

Kinesin’s tail domain is an inhibitory regulator of the motor domain

inferredcites →https://doi.org/10.1038/13008openalex-snapshot

Single-molecule analysis of kinesin motility reveals regulation by the cargo-binding tail domain

inferredcites →https://doi.org/10.1038/35010525openalex-snapshot

Kinesin’s IAK tail domain inhibits initial microtubule-stimulated ADP release

inferredcites →https://doi.org/10.1038/35036345openalex-snapshot

Force production by single kinesin motors

inferredcites →https://doi.org/10.1038/41111openalex-snapshot

Kinesin hydrolyses one ATP per 8-nm step

inferredcites →https://doi.org/10.1038/emboj.2008.133openalex-snapshot

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

inferredcites →https://doi.org/10.1038/nature01804openalex-snapshot

Processivity of the single-headed kinesin KIF1A through biased binding to tubulin

inferredcites →https://doi.org/10.1038/nature03528openalex-snapshot

Mechanics of the kinesin step

inferredcites →https://doi.org/10.1038/ncb1186openalex-snapshot

Two anterograde intraflagellar transport motors cooperate to build sensory cilia on C. elegans neurons

inferredcites →https://doi.org/10.1038/ncb1370openalex-snapshot

A microtubule-binding domain in dynactin increases dynein processivity by skating along microtubules

inferredcites →https://doi.org/10.1038/nmeth.2287openalex-snapshot

Quantitative optical trapping on single organelles in cell extract

inferredcites →https://doi.org/10.1038/nn.2346openalex-snapshot

Pathogenic huntingtin inhibits fast axonal transport by activating JNK3 and phosphorylating kinesin

inferredcites →https://doi.org/10.1038/nrm2060openalex-snapshot

Powering membrane traffic in endocytosis and recycling

inferredcites →https://doi.org/10.1038/nrm2774openalex-snapshot

Kinesin superfamily motor proteins and intracellular transport

inferredcites →https://doi.org/10.1038/nrm2804openalex-snapshot

Regulators of the cytoplasmic dynein motor

inferredcites →https://doi.org/10.1038/nsb911openalex-snapshot

Loading direction regulates the affinity of ADP for kinesin

inferredcites →https://doi.org/10.1038/nsmb.1728openalex-snapshot

Catalysis of the microtubule on-rate is the major parameter regulating the depolymerase activity of MCAK

inferredcites →https://doi.org/10.1039/b900964gopenalex-snapshot

Negative interference dominates collective transport of kinesin motors in the absence of load

inferredcites →https://doi.org/10.1039/c0cp00117aopenalex-snapshot

Coupling between motor proteins determines dynamic behaviors of motor protein assemblies

inferredcites →https://doi.org/10.1042/bst0370343openalex-snapshot

An end to 40 years of mistakes in DNA–protein association kinetics?

inferredcites →https://doi.org/10.1042/bst0370991openalex-snapshot

Fat on the move: intracellular motion of lipid droplets

inferredcites →https://doi.org/10.1073/pnas.0408114101openalex-snapshot

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

inferredcites →https://doi.org/10.1073/pnas.0507363102openalex-snapshot

Cooperative cargo transport by several molecular motors

inferredcites →https://doi.org/10.1073/pnas.0610628104openalex-snapshot

Huntingtin facilitates dynein/dynactin-mediated vesicle transport

inferredcites →https://doi.org/10.1073/pnas.0611471104openalex-snapshot

Myosin Va maneuvers through actin intersections and diffuses along microtubules

inferredcites →https://doi.org/10.1073/pnas.0706825105openalex-snapshot

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

inferredcites →https://doi.org/10.1073/pnas.0711531105openalex-snapshot

Myosin V and Kinesin act as tethers to enhance each others' processivity

inferredcites →https://doi.org/10.1073/pnas.0906524106openalex-snapshot

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

inferredcites →https://doi.org/10.1073/pnas.092546199openalex-snapshot

Kinesin–microtubule binding depends on both nucleotide state and loading direction

inferredcites →https://doi.org/10.1073/pnas.1006869107openalex-snapshot

Deficits in axonal transport precede ALS symptoms in vivo

inferredcites →https://doi.org/10.1073/pnas.1107841108openalex-snapshot

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

inferredcites →https://doi.org/10.1073/pnas.1121180109openalex-snapshot

Axon injury and stress trigger a microtubule-based neuroprotective pathway

inferredcites →https://doi.org/10.1073/pnas.1219961110openalex-snapshot

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

inferredcites →https://doi.org/10.1073/pnas.79.15.4818openalex-snapshot

Microinjection into an identified axon to study the mechanism of fast axonal transport.

inferredcites →https://doi.org/10.1073/pnas.90.12.5519openalex-snapshot

A motility in the eukaryotic flagellum unrelated to flagellar beating.

inferredcites →https://doi.org/10.1073/pnas.94.22.12180openalex-snapshot

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

inferredcites →https://doi.org/10.1073/pnas.94.8.3720openalex-snapshot

Regulated bidirectional motility of melanophore pigment granules along microtubules in vitro

inferredcites →https://doi.org/10.1073/pnas.97.2.640openalex-snapshot

Mechanism of the single-headed processivity: Diffusional anchoring between the K-loop of kinesin and the C terminus of tubulin

inferredcites →https://doi.org/10.1074/jbc.274.21.14617openalex-snapshot

Formation of the Compact Confomer of Kinesin Requires a COOH-terminal Heavy Chain Domain and Inhibits Microtubule-stimulated ATPase Activity

inferredcites →https://doi.org/10.1074/jbc.m109.007906openalex-snapshot

Kinesin-1 Regulates Microtubule Dynamics via a c-Jun N-terminal Kinase-dependent Mechanism

inferredcites →https://doi.org/10.1074/jbc.m111.296582openalex-snapshot

Cooperative Responses of Multiple Kinesins to Variable and Constant Loads

inferredcites →https://doi.org/10.1074/jbc.m113.515510openalex-snapshot

Motor Domain Phosphorylation Modulates Kinesin-1 Transport

inferredcites →https://doi.org/10.1074/jbc.m313472200openalex-snapshot

A Direct Interaction between Cytoplasmic Dynein and Kinesin I May Coordinate Motor Activity

inferredcites →https://doi.org/10.1074/jbc.m802951200openalex-snapshot

Regulatory ATPase Sites of Cytoplasmic Dynein Affect Processivity and Force Generation

inferredcites →https://doi.org/10.1083/jcb.119.6.1589openalex-snapshot

Directional instability of microtubule transport in the presence of kinesin and dynein, two opposite polarity motor proteins.

inferredcites →https://doi.org/10.1083/jcb.124.3.223openalex-snapshot

Motile kinetochores and polar ejection forces dictate chromosome position on the vertebrate mitotic spindle

inferredcites →https://doi.org/10.1083/jcb.133.3.585openalex-snapshot

Cell cycle regulation of dynein association with membranes modulates microtubule-based organelle transport.

inferredcites →https://doi.org/10.1083/jcb.141.4.979openalex-snapshot

A Dynein Light Chain Is Essential for the Retrograde Particle Movement of Intraflagellar Transport (IFT)

inferredcites →https://doi.org/10.1083/jcb.141.4.993openalex-snapshot

Chlamydomonas Kinesin-II–dependent Intraflagellar Transport (IFT): IFT Particles Contain Proteins Required for Ciliary Assembly in Caenorhabditis elegans Sensory Neurons

inferredcites →https://doi.org/10.1083/jcb.142.3.803openalex-snapshot

Regulation of Organelle Movement in Melanophores by Protein Kinase A (PKA), Protein Kinase C (PKC), and Protein Phosphatase 2A (PP2A)

inferredcites →https://doi.org/10.1083/jcb.143.6.1547openalex-snapshot

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

inferredcites →https://doi.org/10.1083/jcb.146.6.1265openalex-snapshot

Regulation of Melanosome Movement in the Cell Cycle by Reversible Association with Myosin V

inferredcites →https://doi.org/10.1083/jcb.148.5.945openalex-snapshot

Dynein-Mediated Cargo Transport in Vivo

inferredcites →https://doi.org/10.1083/jcb.151.3.709openalex-snapshot

Chlamydomonas IFT 88 and Its Mouse Homologue, Polycystic Kidney Disease Gene Tg 737, Are Required for Assembly of Cilia and Flagella

inferredcites →https://doi.org/10.1083/jcb.152.5.959openalex-snapshot

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

inferredcites →https://doi.org/10.1083/jcb.153.1.13openalex-snapshot

Protein Particles inChlamydomonasFlagella Undergo a Transport Cycle Consisting of Four Phases

inferredcites →https://doi.org/10.1083/jcb.200105055openalex-snapshot

Interactions and regulation of molecular motors in Xenopus melanophores

inferredcites →https://doi.org/10.1083/jcb.200109047openalex-snapshot

Coordination of opposite-polarity microtubule motors

inferredcites →https://doi.org/10.1083/jcb.200210066openalex-snapshot

Dynactin is required for bidirectional organelle transport

inferredcites →https://doi.org/10.1083/jcb.200511055openalex-snapshot

JNK1 phosphorylation of SCG10 determines microtubule dynamics and axodendritic length

inferredcites →https://doi.org/10.1083/jcb.200605099openalex-snapshot

Two binding partners cooperate to activate the molecular motor Kinesin-1

inferredcites →https://doi.org/10.1083/jcb.200606003openalex-snapshot

Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors

inferredcites →https://doi.org/10.1083/jcb.200801145openalex-snapshot

Microtubule cross-linking triggers the directional motility of kinesin-5

inferredcites →https://doi.org/10.1083/jcb.200908075openalex-snapshot

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

inferredcites →https://doi.org/10.1083/jcb.201001057openalex-snapshot

Autoinhibition of the kinesin-2 motor KIF17 via dual intramolecular mechanisms

inferredcites →https://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

inferredcites →https://doi.org/10.1083/jcb.201106120openalex-snapshot

Autophagosomes initiate distally and mature during transport toward the cell soma in primary neurons

inferredcites →https://doi.org/10.1083/jcb.201112101openalex-snapshot

Lis1 is an initiation factor for dynein-driven organelle transport

inferredcites →https://doi.org/10.1083/jcb.201302078openalex-snapshot

JIP1 regulates the directionality of APP axonal transport by coordinating kinesin and dynein motors

inferredcites →https://doi.org/10.1088/1478-3967/1/2/r01openalex-snapshot

Hither and yon: a review of bi-directional microtubule-based transport

inferredcites →https://doi.org/10.1088/1478-3975/3/1/005openalex-snapshot

Finite-particle tracking reveals submicroscopic-size changes of mitochondria during transport in mitral cell dendrites

inferredcites →https://doi.org/10.1088/1478-3975/7/1/016012openalex-snapshot

Robust transport by multiple motors with nonlinear force–velocity relations and stochastic load sharing

inferredcites →https://doi.org/10.1091/mbc.10.11.3717openalex-snapshot

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

inferredcites →https://doi.org/10.1091/mbc.e05-06-0526openalex-snapshot

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

inferredcites →https://doi.org/10.1091/mbc.e06-08-0695openalex-snapshot

Dynactin Is Required for Coordinated Bidirectional Motility, but Not for Dynein Membrane Attachment

inferredcites →https://doi.org/10.1091/mbc.e07-03-0261openalex-snapshot

Identification of an Axonal Kinesin-3 Motor for Fast Anterograde Vesicle Transport that Facilitates Retrograde Transport of Neuropeptides

inferredcites →https://doi.org/10.1091/mbc.e09-04-0304openalex-snapshot

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

inferredcites →https://doi.org/10.1091/mbc.e09-11-0967openalex-snapshot

Global Up-Regulation of Microtubule Dynamics and Polarity Reversal during Regeneration of an Axon from a Dendrite

inferredcites →https://doi.org/10.1091/mbc.e10-03-0233openalex-snapshot

Huntingtin coordinates the dynein-mediated dynamic positioning of endosomes and lysosomes

inferredcites →https://doi.org/10.1091/mbc.e11-11-0938openalex-snapshot

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

inferredcites →https://doi.org/10.1101/cshperspect.a011304openalex-snapshot

Mitochondrial Trafficking in Neurons

inferredcites →https://doi.org/10.1111/j.1471-4159.2008.05393.xopenalex-snapshot

Retrograde axonal transport and motor neuron disease

inferredcites →https://doi.org/10.1111/j.1600-0854.2009.00964.xopenalex-snapshot

Diffusive Movement of Processive Kinesin‐1 on Microtubules

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

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

inferredcites →https://doi.org/10.1126/science.1108408openalex-snapshot

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

inferredcites →https://doi.org/10.1126/science.1152993openalex-snapshot

Differential Regulation of Dynein and Kinesin Motor Proteins by Tau

inferredcites →https://doi.org/10.1126/science.1204824openalex-snapshot

The Structure of the Kinesin-1 Motor-Tail Complex Reveals the Mechanism of Autoinhibition

inferredcites →https://doi.org/10.1126/science.1226734openalex-snapshot

Tug-of-War in Motor Protein Ensembles Revealed with a Programmable DNA Origami Scaffold

inferredcites →https://doi.org/10.1126/science.146.3642.347openalex-snapshot

Strong Inference

inferredcites →https://doi.org/10.1126/science.283.5405.1152openalex-snapshot

A Processive Single-Headed Motor: Kinesin Superfamily Protein KIF1A

inferredcites →https://doi.org/10.1126/science.347575openalex-snapshot

Models for the Specific Adhesion of Cells to Cells

inferredcites →https://doi.org/10.1146/annurev.biophys.30.1.105openalex-snapshot

Probing the Relation Between Force—Lifetime—and Chemistry in Single Molecular Bonds

inferredcites →https://doi.org/10.1146/annurev.cellbio.19.111401.091318openalex-snapshot

Intraflagellar Transport

inferredcites →https://doi.org/10.1146/annurev.neuro.31.061307.090711openalex-snapshot

Role of Axonal Transport in Neurodegenerative Diseases

inferredcites →https://doi.org/10.1242/bio.2012307openalex-snapshot

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

inferredcites →https://doi.org/10.1242/jcs.00168openalex-snapshot

Molecular structure of cytoplasmic dynein 2 and its distribution in neuronal and ciliated cells

inferredcites →https://doi.org/10.1242/jcs.02745openalex-snapshot

The axonal transport of mitochondria

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

The axonal transport of mitochondria

inferredcites →https://doi.org/10.1242/jcs.059337openalex-snapshot

Functional interplay between LIS1, NDE1 and NDEL1 in dynein-dependent organelle positioning

inferredcites →https://doi.org/10.1242/jcs.115.7.1453openalex-snapshot

Cytoplasmic dynein-associated structures move bidirectionallyin vivo

inferredcites →https://doi.org/10.1242/jcs.1991.supplement_14.21openalex-snapshot

Kinesin interactions with membrane bounded organelles in vivo and in vitro

inferredcites →https://doi.org/10.1371/journal.pbio.1000072openalex-snapshot

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inferredcites →https://doi.org/10.1371/journal.pbio.1000216openalex-snapshot

Single Molecule Imaging Reveals Differences in Microtubule Track Selection Between Kinesin Motors

inferredcites →https://doi.org/10.1371/journal.pcbi.1000459openalex-snapshot

Strong Inference for Systems Biology

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inferredcites →https://doi.org/10.1529/biophysj.105.067843openalex-snapshot

Organelle Transport along Microtubules in Xenopus Melanophores: Evidence for Cooperation between Multiple Motors

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Cooperation and Competition Coexist in Bidirectional Transport by Motor Proteins

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Intraflagellar transport dynein is autoinhibited by trapping of its mechanical and track-binding elements

inferred← citeshttps://doi.org/10.1038/s41467-019-10644-9openalex-snapshot

PTPN21 and Hook3 relieve KIF1C autoinhibition and activate intracellular transport

inferred← citeshttps://doi.org/10.1038/s41467-019-11056-5openalex-snapshot

Dopey1-Mon2 complex binds to dual-lipids and recruits kinesin-1 for membrane trafficking

inferred← citeshttps://doi.org/10.1038/s41467-019-13838-3openalex-snapshot

Quantitative live cell imaging reveals influenza virus manipulation of Rab11A transport through reduced dynein association

inferred← citeshttps://doi.org/10.1038/s41467-020-14527-2openalex-snapshot

Naturally-occurring cholesterol analogues in lipid nanoparticles induce polymorphic shape and enhance intracellular delivery of mRNA

inferred← citeshttps://doi.org/10.1038/s41467-021-24862-7openalex-snapshot

Mitochondrial adaptor TRAK2 activates and functionally links opposing kinesin and dynein motors

inferred← citeshttps://doi.org/10.1038/s41467-022-34004-2openalex-snapshot

Subcellular spatial transcriptomics identifies three mechanistically different classes of localizing RNAs

inferred← citeshttps://doi.org/10.1038/s41467-023-36945-8openalex-snapshot

TRAK adaptors regulate the recruitment and activation of dynein and kinesin in mitochondrial transport

inferred← citeshttps://doi.org/10.1038/s41467-023-42605-8openalex-snapshot

Vesicles driven by dynein and kinesin exhibit directional reversals without regulators

inferred← citeshttps://doi.org/10.1038/s41556-018-0213-1openalex-snapshot

The cryo-EM structure of intraflagellar transport trains reveals how dynein is inactivated to ensure unidirectional anterograde movement in cilia

inferred← citeshttps://doi.org/10.1038/s41567-018-0107-yopenalex-snapshot

The physics of cooperative transport in groups of ants

inferred← citeshttps://doi.org/10.1038/s41567-025-03105-2openalex-snapshot

Mechanical origin for non-equilibrium ultrasensitivity in the bacterial flagellar motor

inferred← citeshttps://doi.org/10.1038/s41580-018-0004-3openalex-snapshot

The cytoplasmic dynein transport machinery and its many cargoes

inferred← citeshttps://doi.org/10.1038/s41580-022-00491-wopenalex-snapshot

Selective motor activation in organelle transport along axons

inferred← citeshttps://doi.org/10.1038/s41586-022-05186-yopenalex-snapshot

Structure of dynein–dynactin on microtubules shows tandem adaptor binding

inferred← citeshttps://doi.org/10.1038/s41594-024-01212-xopenalex-snapshot

Tropomyosin 1-I/C coordinates kinesin-1 and dynein motors during oskar mRNA transport

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/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/10.1038/s41598-018-31656-3openalex-snapshot

Small-scale displacement fluctuations of vesicles in fibroblasts

inferred← citeshttps://doi.org/10.1038/s41598-018-37126-0openalex-snapshot

Force sharing and force generation by two teams of elastically coupled molecular motors

inferred← citeshttps://doi.org/10.1038/s41598-021-82836-7openalex-snapshot

Distinguishing synaptic vesicle precursor navigation of microtubule ends with a single rate constant model

inferred← citeshttps://doi.org/10.1038/s41598-024-83602-1openalex-snapshot

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

inferred← citeshttps://doi.org/10.1038/s41598-025-90222-wopenalex-snapshot

Cloning of nf-profilin and intercellular interaction with nf-actin in Naegleria fowleri cysts

inferred← citeshttps://doi.org/10.1038/s44319-025-00458-wopenalex-snapshot

Molecular basis for assembly and activation of the Hook3 − KIF1C complex-dependent transport machinery

inferred← citeshttps://doi.org/10.1038/s44385-025-00056-4openalex-snapshot

Targeted amplification of alternating electric fields using ferroelectric nanoparticles

inferred← citeshttps://doi.org/10.1038/srep28940openalex-snapshot

Cargo binding promotes KDEL receptor clustering at the mammalian cell surface

inferred← citeshttps://doi.org/10.1038/srep37162openalex-snapshot

Run-and-pause dynamics of cytoskeletal motor proteins

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

Collective dynamics of processive cytoskeletal motors

inferred← citeshttps://doi.org/10.1039/c6lc01349jopenalex-snapshot

Modulating motility of intracellular vesicles in cortical neurons with nanomagnetic forces on-chip

inferred← citeshttps://doi.org/10.1039/c7nr00604gopenalex-snapshot

Label-free, ultrahigh-speed, 3D observation of bidirectional and correlated intracellular cargo transport by coherent brightfield microscopy

inferred← citeshttps://doi.org/10.1039/c7sc02339aopenalex-snapshot

De novo vesicle formation and growth: an integrative approach to artificial cells

inferred← citeshttps://doi.org/10.1039/c9sc05149jopenalex-snapshot

Influenza as a molecular walker

inferred← citeshttps://doi.org/10.1039/c9sm01904aopenalex-snapshot

Tuning molecular motor transport through cytoskeletal filament network organization

inferred← citeshttps://doi.org/10.1039/d2sm00900eopenalex-snapshot

Spontaneous formation and growth kinetics of lipid nanotubules induced by passive nanoparticles

inferred← citeshttps://doi.org/10.1039/d3sm01122dopenalex-snapshot

Theoretical analysis of cargo transport by catch bonded motors in optical trapping assays

inferred← citeshttps://doi.org/10.1039/d4sc04925jopenalex-snapshot

Dynamic satellite–parent liposome networks for quantitative microreactions

inferred← citeshttps://doi.org/10.1039/d5sm01174dopenalex-snapshot

The influence of cellular energy status, microtubules, and crowding on mitochondrial motion

inferred← citeshttps://doi.org/10.1042/bsr20180208openalex-snapshot

Retraction of rod-like mitochondria during microtubule-dependent transport

inferred← citeshttps://doi.org/10.1042/bst20170568openalex-snapshot

Emerging mechanisms of dynein transport in the cytoplasm versus the cilium

inferred← citeshttps://doi.org/10.1063/1.5064867openalex-snapshot

eGFRD in all dimensions

inferred← citeshttps://doi.org/10.1063/1.5113880openalex-snapshot

Hydrodynamic interaction facilitates the unsteady transport of two neighboring vesicles

inferred← citeshttps://doi.org/10.1063/1.5133645openalex-snapshot

Mechanobiology of dynamic enzyme systems

inferred← citeshttps://doi.org/10.1063/9780735425279_002openalex-snapshot

Multiscale Theoretical Studies for Molecular Motors

inferred← citeshttps://doi.org/10.1073/pnas.1508514112openalex-snapshot

p27 kip1 controls H-Ras/MAPK activation and cell cycle entry via modulation of MT stability

inferred← citeshttps://doi.org/10.1073/pnas.1708157114openalex-snapshot

Intraflagellar transport velocity is governed by the number of active KIF17 and KIF3AB motors and their motility properties under load

inferred← citeshttps://doi.org/10.1073/pnas.1710328114openalex-snapshot

Molecular origin of the weak susceptibility of kinesin velocity to loads and its relation to the collective behavior of kinesins

inferred← citeshttps://doi.org/10.1073/pnas.1711088114openalex-snapshot

Dynein/dynactin is necessary for anterograde transport of Mbp mRNA in oligodendrocytes and for myelination in vivo

inferred← citeshttps://doi.org/10.1073/pnas.1806189115openalex-snapshot

Single-molecule analysis of endogenous β-actin mRNA trafficking reveals a mechanism for compartmentalized mRNA localization in axons

inferred← citeshttps://doi.org/10.1073/pnas.1900416116openalex-snapshot

Active cargo positioning in antiparallel transport networks

inferred← citeshttps://doi.org/10.1073/pnas.2101391118openalex-snapshot

Three-color single-molecule imaging reveals conformational dynamics of dynein undergoing motility

inferred← citeshttps://doi.org/10.1073/pnas.2103383118openalex-snapshot

On and off controls within dynein–dynactin on native cargoes

inferred← citeshttps://doi.org/10.1073/pnas.2206677119openalex-snapshot

The ubiquitous microtubule-associated protein 4 (MAP4) controls organelle distribution by regulating the activity of the kinesin motor

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