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Posttranslational Modifications of Tubulin and the Polarized Transport of Kinesin-1 in Neurons

https://doi.org/10.1091/mbc.e09-01-0044
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What this work says

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

inferredcites →https://doi.org/10.1002/jnr.490300115openalex-snapshot
Microtubule dynamics in axons and dendrites
inferredcites →https://doi.org/10.1016/j.ceb.2007.11.010openalex-snapshot
Tubulin modifications and their cellular functions
inferredcites →https://doi.org/10.1016/j.cell.2004.11.012openalex-snapshot
GSK-3β Regulates Phosphorylation of CRMP-2 and Neuronal Polarity
inferredcites →https://doi.org/10.1016/j.cell.2004.12.033openalex-snapshot
Both the Establishment and the Maintenance of Neuronal Polarity Require Active Mechanisms
inferredcites →https://doi.org/10.1016/j.cell.2007.03.023openalex-snapshot
Spinophilin Facilitates Dephosphorylation of Doublecortin by PP1 to Mediate Microtubule Bundling at the Axonal Wrist
inferredcites →https://doi.org/10.1016/j.cell.2008.11.043openalex-snapshot
Elongator Controls the Migration and Differentiation of Cortical Neurons through Acetylation of α-Tubulin
inferredcites →https://doi.org/10.1016/j.conb.2008.05.003openalex-snapshot
New insights into the molecular mechanisms specifying neuronal polarity in vivo
inferredcites →https://doi.org/10.1016/j.cub.2006.09.014openalex-snapshot
Microtubule Acetylation Promotes Kinesin-1 Binding and Transport
inferredcites →https://doi.org/10.1016/j.cub.2008.01.025openalex-snapshot
The JIP1 Scaffold Protein Regulates Axonal Development in Cortical Neurons
inferredcites →https://doi.org/10.1016/j.cub.2008.06.026openalex-snapshot
Plasticity of Polarization: Changing Dendrites into Axons in Neurons Integrated in Neuronal Circuits
inferredcites →https://doi.org/10.1016/j.molcel.2007.04.012openalex-snapshot
A Targeted Multienzyme Mechanism for Selective Microtubule Polyglutamylation
inferredcites →https://doi.org/10.1016/j.neuron.2006.02.005openalex-snapshot
A Change in the Selective Translocation of the Kinesin-1 Motor Domain Marks the Initial Specification of the Axon
inferredcites →https://doi.org/10.1016/j.neuron.2006.10.031openalex-snapshot
Essential Roles for GSK-3s and GSK-3-Primed Substrates in Neurotrophin-Induced and Hippocampal Axon Growth
inferredcites →https://doi.org/10.1016/s0076-6879(98)98024-7openalex-snapshot
[22] Use of drugs to study role of microtubule assembly dynamics in living cells
inferredcites →https://doi.org/10.1016/s1044-7431(03)00095-2openalex-snapshot
Inhibition of glycogen synthase kinase 3β in sensory neurons in culture alters filopodia dynamics and microtubule distribution in growth cones
inferredcites →https://doi.org/10.1038/330254a0openalex-snapshot
Experimentally induced alteration in the polarity of developing neurons
inferredcites →https://doi.org/10.1038/417455aopenalex-snapshot
HDAC6 is a microtubule-associated deacetylase
inferredcites →https://doi.org/10.1038/nbt1191openalex-snapshot
Engineering of a monomeric green-to-red photoactivatable fluorescent protein induced by blue light
inferredcites →https://doi.org/10.1038/nn.2314openalex-snapshot
Tubulin tyrosination navigates the kinesin-1 motor domain to axons
inferredcites →https://doi.org/10.1038/nprot.2006.356openalex-snapshot
Culturing hippocampal neurons
inferredcites →https://doi.org/10.1038/nrn2056openalex-snapshot
Neuronal polarity: from extracellular signals to intracellular mechanisms
inferredcites →https://doi.org/10.1073/pnas.0430973100openalex-snapshot
Domain-selective small-molecule inhibitor of histone deacetylase 6 (HDAC6)-mediated tubulin deacetylation
inferredcites →https://doi.org/10.1073/pnas.0611547104openalex-snapshot
Loss of α-tubulin polyglutamylation in ROSA22 mice is associated with abnormal targeting of KIF1A and modulated synaptic function
inferredcites →https://doi.org/10.1074/jbc.271.36.22117openalex-snapshot
Interaction of Kinesin Motor Domains with α- and β-Tubulin Subunits at a Tau-independent Binding Site
inferredcites →https://doi.org/10.1074/jbc.273.16.9797openalex-snapshot
Kinesin Is a Candidate for Cross-bridging Microtubules and Intermediate Filaments
inferredcites →https://doi.org/10.1074/jbc.274.49.35113openalex-snapshot
Interaction of c-Jun Amino-terminal Kinase Interacting Protein-1 with p190 rhoGEF and Its Localization in Differentiated Neurons
inferredcites →https://doi.org/10.1074/jbc.m603984200openalex-snapshot
TTLL7 Is a Mammalian β-Tubulin Polyglutamylase Required for Growth of MAP2-positive Neurites
inferredcites →https://doi.org/10.1083/jcb.108.4.1507openalex-snapshot
Experimental observations on the development of polarity by hippocampal neurons in culture.
inferredcites →https://doi.org/10.1083/jcb.109.6.3085openalex-snapshot
Changes in microtubule polarity orientation during the development of hippocampal neurons in culture.
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.200302175openalex-snapshot
Microtubules provide directional cues for polarized axonal transport through interaction with kinesin motor head
inferredcites →https://doi.org/10.1083/jcb.200604160openalex-snapshot
Shootin1: a protein involved in the organization of an asymmetric signal for neuronal polarization
inferredcites →https://doi.org/10.1083/jcb.200707042openalex-snapshot
Microtubule stabilization specifies initial neuronal polarization
inferredcites →https://doi.org/10.1091/mbc.e05-10-0914openalex-snapshot
The Formin mDia Regulates GSK3β through Novel PKCs to Promote Microtubule Stabilization but Not MTOC Reorientation in Migrating Fibroblasts
inferredcites →https://doi.org/10.1093/emboj/cdf682openalex-snapshot
In vivo destabilization of dynamic microtubules by HDAC6‐mediated deacetylation
inferredcites →https://doi.org/10.1111/j.1365-2443.2008.01235.xopenalex-snapshot
N‐acetyltransferase ARD1‐NAT1 regulates neuronal dendritic development
inferredcites →https://doi.org/10.1126/science.1113010openalex-snapshot
Tubulin Polyglutamylase Enzymes Are Members of the TTL Domain Protein Family
inferredcites →https://doi.org/10.1242/jcs.01531openalex-snapshot
Tau interaction with microtubules in vivo
inferredcites →https://doi.org/10.1242/jcs.026492openalex-snapshot
Differential trafficking of Kif5c on tyrosinated and detyrosinated microtubules in live cells
inferredcites →https://doi.org/10.1242/jcs.03159openalex-snapshot
Neuronal polarity is regulated by glycogen synthase kinase-3 (GSK-3β) independently of Akt/PKB serine phosphorylation
inferredcites →https://doi.org/10.1242/jcs.048975openalex-snapshot
The NIMA-family kinase Nek3 regulates microtubule acetylation in neurons
inferredcites →https://doi.org/10.1254/fpj.119.163openalex-snapshot
Culturing hippocampal neurons.
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/10.1523/jneurosci.0037-07.2007openalex-snapshot
Histone Deacetylase 6 Inhibition Compensates for the Transport Deficit in Huntington's Disease by Increasing Tubulin Acetylation
inferredcites →https://doi.org/10.1523/jneurosci.07-11-03695.1987openalex-snapshot
Taxol interferes with the interaction of microtubule-associated proteins with microtubules in cultured neurons
inferredcites →https://doi.org/10.1523/jneurosci.08-04-01454.1988openalex-snapshot
The establishment of polarity by hippocampal neurons in culture
inferredcites →https://doi.org/10.4161/cc.6.17.4633openalex-snapshot
The Tubulin Code

What points at this work

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

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The Motility of Axonemal Dynein Is Regulated by the Tubulin Code
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Acetylated Microtubules Are Preferentially Bundled Leading to Enhanced Kinesin-1 Motility
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No Pasaran! Role of the axon initial segment in the regulation of protein transport and the maintenance of axonal identity
inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.12.006openalex-snapshot
The detyrosination/re-tyrosination cycle of tubulin and its role and dysfunction in neurons and cardiomyocytes
inferred← citeshttps://doi.org/10.1016/j.tcb.2014.05.002openalex-snapshot
Integrated regulation of motor-driven organelle transport by scaffolding proteins
inferred← citeshttps://doi.org/10.1016/j.tcb.2014.10.004openalex-snapshot
Post-translational modifications of tubulin: pathways to functional diversity of microtubules
inferred← citeshttps://doi.org/10.1016/j.tcb.2015.10.001openalex-snapshot
Right Time, Right Place: Probing the Functions of Organelle Positioning
inferred← citeshttps://doi.org/10.1016/j.tcb.2016.06.001openalex-snapshot
The Tubulin Code: A Navigation System for Chromosomes during Mitosis
inferred← citeshttps://doi.org/10.1016/j.tcb.2018.08.003openalex-snapshot
The Tubulin Detyrosination Cycle: Function and Enzymes
inferred← citeshttps://doi.org/10.1016/j.tins.2010.05.001openalex-snapshot
Tubulin post-translational modifications: encoding functions on the neuronal microtubule cytoskeleton
inferred← citeshttps://doi.org/10.1016/j.ydbio.2022.03.009openalex-snapshot
Microtubule polarity is instructive for many aspects of neuronal polarity
inferred← citeshttps://doi.org/10.1016/j.yexcr.2015.02.016openalex-snapshot
Kinesin superfamily proteins (KIFs): Various functions and their relevance for important phenomena in life and diseases
inferred← citeshttps://doi.org/10.1016/j.ymthe.2025.09.028openalex-snapshot
Epigenetic mechanisms of HIV and opioid-induced neuropathology: Potential therapies and interventions
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.0c02210openalex-snapshot
Tetrahydroquinoline-Capped Histone Deacetylase 6 Inhibitor SW-101 Ameliorates Pathological Phenotypes in a Charcot–Marie–Tooth Type 2A Mouse Model
inferred← citeshttps://doi.org/10.1021/acschemneuro.8b00600openalex-snapshot
Brain Penetrable Histone Deacetylase 6 Inhibitor SW-100 Ameliorates Memory and Learning Impairments in a Mouse Model of Fragile X Syndrome
inferred← citeshttps://doi.org/10.1021/acsmedchemlett.9b00560openalex-snapshot
Structural and in Vivo Characterization of Tubastatin A, a Widely Used Histone Deacetylase 6 Inhibitor
inferred← citeshttps://doi.org/10.1021/jm4001659openalex-snapshot
Development and Therapeutic Implications of Selective Histone Deacetylase 6 Inhibitors
inferred← citeshttps://doi.org/10.1038/cddis.2012.96openalex-snapshot
Selective loss of RPGRIP1-dependent ciliary targeting of NPHP4, RPGR and SDCCAG8 underlies the degeneration of photoreceptor neurons
inferred← citeshttps://doi.org/10.1038/gt.2012.77openalex-snapshot
Highly acetylated tubulin permits enhanced interactions with and trafficking of plasmids along microtubules
inferred← citeshttps://doi.org/10.1038/ncb3406openalex-snapshot
Self-repair promotes microtubule rescue
inferred← citeshttps://doi.org/10.1038/nchembio.2456openalex-snapshot
Optogenetic control of kinetochore function
inferred← citeshttps://doi.org/10.1038/ncomms15496openalex-snapshot
Exploiting the kinesin-1 molecular motor to generate a virus membrane penetration site
inferred← citeshttps://doi.org/10.1038/ncomms2962openalex-snapshot
αTAT1 is the major α-tubulin acetyltransferase in mice
inferred← citeshttps://doi.org/10.1038/ncomms9526openalex-snapshot
Detyrosinated microtubules modulate mechanotransduction in heart and skeletal muscle
inferred← citeshttps://doi.org/10.1038/nrm3227openalex-snapshot
Post-translational regulation of the microtubule cytoskeleton: mechanisms and functions
inferred← citeshttps://doi.org/10.1038/nrn.2016.100openalex-snapshot
The cellular mechanisms that maintain neuronal polarity
inferred← citeshttps://doi.org/10.1038/nrn.2017.100openalex-snapshot
The impact of cytoskeletal organization on the local regulation of neuronal transport
inferred← citeshttps://doi.org/10.1038/nrn.2017.129openalex-snapshot
The nano-architecture of the axonal cytoskeleton
inferred← citeshttps://doi.org/10.1038/nrn2852openalex-snapshot
The axon initial segment and the maintenance of neuronal polarity
inferred← citeshttps://doi.org/10.1038/nrn3176openalex-snapshot
Assembly of a new growth cone after axotomy: the precursor to axon regeneration
inferred← citeshttps://doi.org/10.1038/s41419-019-1920-7openalex-snapshot
Histone deacetylase 6 inhibition rescues axonal transport impairments and prevents the neurotoxicity of HIV-1 envelope protein gp120
inferred← citeshttps://doi.org/10.1038/s41467-024-46379-5openalex-snapshot
Microtubule damage shapes the acetylation gradient
inferred← citeshttps://doi.org/10.1038/s41467-024-52729-0openalex-snapshot
Metabolic regulation of cytoskeleton functions by HDAC6-catalyzed α-tubulin lactylation
inferred← citeshttps://doi.org/10.1038/s41467-025-56098-0openalex-snapshot
Tubulin tyrosination/detyrosination regulate the affinity and sorting of intraflagellar transport trains on axonemal microtubule doublets
inferred← citeshttps://doi.org/10.1038/s41467-025-56951-2openalex-snapshot
Doublecortin restricts neuronal branching by regulating tubulin polyglutamylation
inferred← citeshttps://doi.org/10.1038/srep16869openalex-snapshot
New HDAC6-mediated deacetylation sites of tubulin in the mouse brain identified by quantitative mass spectrometry
inferred← citeshttps://doi.org/10.1042/bse0530055openalex-snapshot
Crucial polarity regulators in axon specification
inferred← citeshttps://doi.org/10.1042/bst0391126openalex-snapshot
Bidirectional intracellular transport: utility and mechanism
inferred← citeshttps://doi.org/10.1042/bst20240841openalex-snapshot
How does the tubulin code facilitate directed cell migration?
inferred← citeshttps://doi.org/10.1073/pnas.1016396108openalex-snapshot
Tubulin acetyltransferase discovered: Ciliary role in the ancestral eukaryote expanded to neurons in metazoans
inferred← citeshttps://doi.org/10.1073/pnas.2300322120openalex-snapshot
Microtubule detyrosination drives symmetry breaking to polarize cells for directed cell migration
inferred← citeshttps://doi.org/10.1074/jbc.c112.421222openalex-snapshot
Crystal Structures of Tubulin Acetyltransferase Reveal a Conserved Catalytic Core and the Plasticity of the Essential N Terminus
inferred← citeshttps://doi.org/10.1074/jbc.m110.121491openalex-snapshot
RHAMM Promotes Interphase Microtubule Instability and Mitotic Spindle Integrity through MEK1/ERK1/2 Activity
inferred← citeshttps://doi.org/10.1074/jbc.m111.292987openalex-snapshot
The Nucleotide-binding State of Microtubules Modulates Kinesin Processivity and the Ability of Tau to Inhibit Kinesin-mediated Transport
inferred← citeshttps://doi.org/10.1074/jbc.m113.464792openalex-snapshot
Mice Lacking α-Tubulin Acetyltransferase 1 Are Viable but Display α-Tubulin Acetylation Deficiency and Dentate Gyrus Distortion
inferred← citeshttps://doi.org/10.1074/jbc.m113.489328openalex-snapshot
Inhibition of HDAC6 Deacetylase Activity Increases Its Binding with Microtubules and Suppresses Microtubule Dynamic Instability in MCF-7 Cells
inferred← citeshttps://doi.org/10.1074/jbc.m113.507400openalex-snapshot
Reactive Oxygen Species, AMP-activated Protein Kinase, and the Transcription Cofactor p300 Regulate α-Tubulin Acetyltransferase-1 (αTAT-1/MEC-17)-dependent Microtubule Hyperacetylation during Cell Stress
inferred← citeshttps://doi.org/10.1074/jbc.m113.515510openalex-snapshot
Motor Domain Phosphorylation Modulates Kinesin-1 Transport
inferred← citeshttps://doi.org/10.1074/jbc.m115.651885openalex-snapshot
JIP3 Activates Kinesin-1 Motility to Promote Axon Elongation
inferred← citeshttps://doi.org/10.1074/jbc.ra118.005765openalex-snapshot
Polyglutamylation of tubulin's C-terminal tail controls pausing and motility of kinesin-3 family member KIF1A
inferred← citeshttps://doi.org/10.1080/01677063.2020.1823385openalex-snapshot
Molecular mechanisms governing axonal transport: a C. elegans perspective
inferred← citeshttps://doi.org/10.1080/19420889.2017.1288771openalex-snapshot
Differential retraction of axonal arbor terminals mediated by microtubule and kinesin motor
inferred← citeshttps://doi.org/10.1083/jcb.200911024openalex-snapshot
ER sliding dynamics and ER–mitochondrial contacts occur on acetylated microtubules
inferred← citeshttps://doi.org/10.1083/jcb.201104034openalex-snapshot
Preferential binding of a kinesin-1 motor to GTP-tubulin–rich microtubules underlies polarized vesicle transport
inferred← citeshttps://doi.org/10.1083/jcb.201702157openalex-snapshot
The actin-MRTF-SRF transcriptional circuit controls tubulin acetylation via α-TAT1 gene expression
inferred← citeshttps://doi.org/10.1083/jcb.201708096openalex-snapshot
Autoinhibition of kinesin-1 is essential to the dendrite-specific localization of Golgi outposts
inferred← citeshttps://doi.org/10.1083/jcb.202006151openalex-snapshot
Lysine acetylation of cytoskeletal proteins: Emergence of an actin code
inferred← citeshttps://doi.org/10.1083/jcb.202206143openalex-snapshot
StableMARK-decorated microtubules in cells have expanded lattices
inferred← citeshttps://doi.org/10.1091/mbc.e10-03-0269openalex-snapshot
Soluble levels of cytosolic tubulin regulate ciliary length control
inferred← citeshttps://doi.org/10.1091/mbc.e10-06-0519openalex-snapshot
The posttranslational modification of tubulin undergoes a switch from detyrosination to acetylation as epithelial cells become polarized
inferred← citeshttps://doi.org/10.1091/mbc.e14-08-1313openalex-snapshot
Effects of kinesin-5 inhibition on dendritic architecture and microtubule organization
inferred← citeshttps://doi.org/10.1091/mbc.e19-03-0183openalex-snapshot
Regulatory mechanisms for the axonal localization of tau protein in neurons
inferred← citeshttps://doi.org/10.1091/mbc.e23-10-0401openalex-snapshot
Polarized transport requires AP-1-mediated recruitment of KIF13A and KIF13B at the trans-Golgi
inferred← citeshttps://doi.org/10.1093/brain/awab436openalex-snapshot
Tubulin tyrosination regulates synaptic function and is disrupted in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1093/brain/awt153openalex-snapshot
Beyond taxol: microtubule-based treatment of disease and injury of the nervous system
inferred← citeshttps://doi.org/10.1093/hmg/ddr326openalex-snapshot
The Sirtuin 2 microtubule deacetylase is an abundant neuronal protein that accumulates in the aging CNS
inferred← citeshttps://doi.org/10.1093/hmg/ddz186openalex-snapshot
Defective tubulin detyrosination causes structural brain abnormalities with cognitive deficiency in humans and mice
inferred← citeshttps://doi.org/10.1093/jmicro/dfr051openalex-snapshot
From electron microscopy to molecular cell biology, molecular genetics and structural biology: intracellular transport and kinesin superfamily proteins, KIFs: genes, structure, dynamics and functions
inferred← citeshttps://doi.org/10.1101/111484openalex-snapshot
α -tubulin acetylation and detyrosination correlate with starvation-induced autophagy in tobacco cells
inferred← citeshttps://doi.org/10.1101/2021.03.29.437471openalex-snapshot
A cryo-ET study of microtubules in axons
inferred← citeshttps://doi.org/10.1101/2021.04.09.439170openalex-snapshot
Motor usage imprints microtubule stability in the shaft
inferred← citeshttps://doi.org/10.1101/2021.05.17.443847openalex-snapshot
Impaired α-tubulin re-tyrosination leads to synaptic dysfunction and is a feature of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1101/2021.09.01.458567openalex-snapshot
Microtubule retrograde flow retains neuronal polarization in a fluctuating state
inferred← citeshttps://doi.org/10.1101/2022.12.01.518806openalex-snapshot
Running Kinesin-1 shapes the microtubule acetylation gradient
inferred← citeshttps://doi.org/10.1101/2023.04.26.538370openalex-snapshot
Active Transport by Cytoplasmic Dynein Maintains the Localization of MAP2 in Developing Neurons
inferred← citeshttps://doi.org/10.1101/2023.12.01.569616openalex-snapshot
Spatial Relationships Matter: Kinesin-1 Molecular Motors Transport Liposome Cargo Through 3D Microtubule Intersections In Vitro
inferred← citeshttps://doi.org/10.1101/2024.05.03.592312openalex-snapshot
Tubulin tyrosination/detyrosination governs the spatial segregation of intraflagellar transport trains on axonemal microtubule doublets
inferred← citeshttps://doi.org/10.1101/410860openalex-snapshot
Regulation of KIF1A motility via polyglutamylation of tubulin C-terminal tails
inferred← citeshttps://doi.org/10.1101/cshperspect.a025817openalex-snapshot
Microtubule-Based Transport and the Distribution, Tethering, and Organization of Organelles
inferred← citeshttps://doi.org/10.1101/cshperspect.a027896openalex-snapshot
Microtubule Motors in Establishment of Epithelial Cell Polarity
inferred← citeshttps://doi.org/10.1111/boc.201300012openalex-snapshot
MAPping out distribution routes for kinesin couriers
inferred← citeshttps://doi.org/10.1111/j.1600-0854.2011.01325.xopenalex-snapshot
The Translocation Selectivity of the Kinesins that Mediate Neuronal Organelle Transport
inferred← citeshttps://doi.org/10.1111/jnc.12001openalex-snapshot
Differential neurite outgrowth is required for axon specification by cultured hippocampal neurons
inferred← citeshttps://doi.org/10.1111/jnc.14015openalex-snapshot
The viral protein gp120 decreases the acetylation of neuronal tubulin: potential mechanism of neurotoxicity
inferred← citeshttps://doi.org/10.1111/tra.70002openalex-snapshot
Computational Modeling Reveals a Catch‐and‐Guide Interaction Between Kinesin‐1 and Tubulin C‐Terminal Tails
inferred← citeshttps://doi.org/10.1126/sciadv.abo2336openalex-snapshot
Microtubule retrograde flow retains neuronal polarization in a fluctuating state
inferred← citeshttps://doi.org/10.1126/sciadv.abo6333openalex-snapshot
The core PCP protein Prickle2 regulates axon number and AIS maturation by binding to AnkG and modulating microtubule bundling
inferred← citeshttps://doi.org/10.1126/sciadv.adi5548openalex-snapshot
Loss of function of the ALS-associated NEK1 kinase disrupts microtubule homeostasis and nuclear import
inferred← citeshttps://doi.org/10.1126/sciadv.adi7838openalex-snapshot
A family of carboxypeptidases catalyzing α- and β-tubulin tail processing and deglutamylation
inferred← citeshttps://doi.org/10.1126/science.aaa5175openalex-snapshot
Microtubule detyrosination guides chromosomes during mitosis
inferred← citeshttps://doi.org/10.1128/mcb.00612-17openalex-snapshot
Cilium Length and Intraflagellar Transport Regulation by Kinases PKG-1 and GCK-2 in Caenorhabditis elegans Sensory Neurons
inferred← citeshttps://doi.org/10.1146/annurev-biophys-042910-155310openalex-snapshot
Kinesin Assembly and Movement in Cells
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-101011-155711openalex-snapshot
Microtubules in Cell Migration
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