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Tuba1a is uniquely important for axon guidance through midline commissural structures

https://doi.org/10.1101/2020.05.05.079376

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

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Comparison of the expression of a T?1:nlacZ transgene and T?1 ?-tubulin mRNA in the mature central nervous system

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Early induction of T?1 ?-tubulin transcription in neurons of the developing nervous system

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Microtubule organization and the effects of GFP-tubulin expression inDictyostelium discoideum

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Subdiffraction‐Resolution Fluorescence Imaging with Conventional Fluorescent Probes

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Stability properties of neuronal microtubules

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Tubulin mutations in brain development disorders: Why haploinsufficiency does not explain TUBA1A tubulinopathies

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Differential localisation of tyrosinated, detyrosinated, and acetylated α‐tubulins in neurites and growth cones of dorsal root ganglion neurons

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Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A)

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Participation of structural microtubule‐associated proteins (MAPs) in the development of neuronal polarity

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The Microtubule-Associated Protein MAP1B Is Involved in Local Stabilization of Turning Growth Cones

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Measuring the Effects of Microtubule-Associated Proteins on Microtubule Dynamics In Vitro

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Dynamic post-translational modification of tubulin in rat cerebral cortical neurons extending neurites in culture: Effects of taxol

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Ueber den Bau des vollständig balkenlosen Gross-hirnes sowie über Mikrogyrie und Heterotopie der grauen Substanz

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Human lissencephaly with cerebellar hypoplasia due to mutations in TUBA1A: expansion of the foetal neuropathological phenotype

inferredcites →https://doi.org/10.1007/s12264-014-1444-6openalex-snapshot

Microtubule dynamics in axon guidance

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Acetylated Microtubules Are Preferentially Bundled Leading to Enhanced Kinesin-1 Motility

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Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans

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.cell.2009.04.065openalex-snapshot

An EB1-Binding Motif Acts as a Microtubule Tip Localization Signal

inferredcites →https://doi.org/10.1016/j.celrep.2015.11.057openalex-snapshot

FMRP-Mediated Axonal Delivery of miR-181d Regulates Axon Elongation by Locally Targeting Map1b and Calm1

inferredcites →https://doi.org/10.1016/j.conb.2007.01.008openalex-snapshot

Commissure formation in the mammalian forebrain

inferredcites →https://doi.org/10.1016/j.conb.2016.11.010openalex-snapshot

Timing temporal transitions during brain development

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Windows of opportunity: timing in neurodevelopmental disorders

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MAP1B Is Required for Netrin 1 Signaling in Neuronal Migration and Axonal Guidance

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.2016.10.040openalex-snapshot

Dynamic mRNA Transport and Local Translation in Radial Glial Progenitors of the Developing Brain

inferredcites →https://doi.org/10.1016/j.gde.2011.01.003openalex-snapshot

Phenotypic spectrum of the tubulin-related disorders and functional implications of disease-causing mutations

inferredcites →https://doi.org/10.1016/j.mcn.2011.10.003openalex-snapshot

MAP1B enhances microtubule assembly rates and axon extension rates in developing neurons

inferredcites →https://doi.org/10.1016/j.molcel.2012.06.025openalex-snapshot

Molecular Basis for Specific Regulation of Neuronal Kinesin-3 Motors by Doublecortin Family Proteins

inferredcites →https://doi.org/10.1016/j.neuron.2015.05.046openalex-snapshot

Building the Neuronal Microtubule Cytoskeleton

inferredcites →https://doi.org/10.1016/j.neuroscience.2007.08.017openalex-snapshot

Agrin induced morphological and structural changes in growth cones of cultured hippocampal neurons

inferredcites →https://doi.org/10.1016/j.tcb.2009.08.006openalex-snapshot

Control of neuronal polarity and plasticity – a renaissance for microtubules?

inferredcites →https://doi.org/10.1016/j.tins.2010.05.001openalex-snapshot

Tubulin post-translational modifications: encoding functions on the neuronal microtubule cytoskeleton

inferredcites →https://doi.org/10.1016/j.ydbio.2015.11.022openalex-snapshot

Novel α-tubulin mutation disrupts neural development and tubulin proteostasis

inferredcites →https://doi.org/10.1016/j.ygeno.2007.04.008openalex-snapshot

A revised nomenclature for the human and rodent α-tubulin gene family

inferredcites →https://doi.org/10.1016/s0092-8674(00)81795-xopenalex-snapshot

Netrin-1 Is Required for Commissural Axon Guidance in the Developing Vertebrate Nervous System

inferredcites →https://doi.org/10.1016/s0962-8924(97)01168-9openalex-snapshot

The α- and β-tubulin folding pathways

inferredcites →https://doi.org/10.1021/bi2005174openalex-snapshot

Design, Overexpression, and Purification of Polymerization-Blocked Yeast αβ-Tubulin Mutants

inferredcites →https://doi.org/10.1038/421230aopenalex-snapshot

Tubulin acetylation and cell motility

inferredcites →https://doi.org/10.1038/ncb2920openalex-snapshot

Regulation of microtubule motors by tubulin isotypes and post-translational modifications

inferredcites →https://doi.org/10.1038/s41429-019-0141-8openalex-snapshot

Lactacystin: first-in-class proteasome inhibitor still excelling and an exemplar for future antibiotic research

inferredcites →https://doi.org/10.1073/pnas.0404995101openalex-snapshot

The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development

inferredcites →https://doi.org/10.1073/pnas.1900441116openalex-snapshot

Effects of α-tubulin acetylation on microtubule structure and stability

inferredcites →https://doi.org/10.1074/jbc.m011380200openalex-snapshot

Differential Binding Regulation of Microtubule-associated Proteins MAP1A, MAP1B, and MAP2 by Tubulin Polyglutamylation

inferredcites →https://doi.org/10.1083/jcb.105.5.2167openalex-snapshot

Posttranslational modification and microtubule stability.

inferredcites →https://doi.org/10.1083/jcb.105.6.3065openalex-snapshot

Isotypes of alpha-tubulin are differentially regulated during neuronal maturation.

inferredcites →https://doi.org/10.1083/jcb.151.6.1169openalex-snapshot

Map1b Is Required for Axon Guidance and Is Involved in the Development of the Central and Peripheral Nervous System

inferredcites →https://doi.org/10.1083/jcb.201001024openalex-snapshot

Tubulin polyglutamylation stimulates spastin-mediated microtubule severing

inferredcites →https://doi.org/10.1083/jcb.201604108openalex-snapshot

Motor axon navigation relies on Fidgetin-like 1–driven microtubule plus end dynamics

inferredcites →https://doi.org/10.1083/jcb.201607074openalex-snapshot

Mutation of the α-tubulin Tuba1a leads to straighter microtubules and perturbs neuronal migration

inferredcites →https://doi.org/10.1083/jcb.92.2.435openalex-snapshot

A taxol-dependent procedure for the isolation of microtubules and microtubule-associated proteins (MAPs).

inferredcites →https://doi.org/10.1091/mbc.10.7.2309openalex-snapshot

Polymerizing Microtubules Activate Site-directed F-Actin Assembly in Nerve Growth Cones

inferredcites →https://doi.org/10.1091/mbc.12.12.3973openalex-snapshot

Dominant-Lethal α-Tubulin Mutants Defective in Microtubule Depolymerization in Yeast

inferredcites →https://doi.org/10.1091/mbc.12.7.2087openalex-snapshot

Evidence for the Role of MAP1B in Axon Formation

inferredcites →https://doi.org/10.1091/mbc.e07-09-0861openalex-snapshot

A Pachygyria-causing α-Tubulin Mutation Results in Inefficient Cycling with CCT and a Deficient Interaction with TBCB

inferredcites →https://doi.org/10.1091/mbc.e17-02-0124openalex-snapshot

Tubulin isoform composition tunes microtubule dynamics

inferredcites →https://doi.org/10.1093/brain/awn155openalex-snapshot

Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A

inferredcites →https://doi.org/10.1093/brain/aws338openalex-snapshot

Overlapping cortical malformations and mutations in TUBB2B and TUBA1A

inferredcites →https://doi.org/10.1093/cercor/bhs395openalex-snapshot

Netrin-DCC Signaling Regulates Corpus Callosum Formation Through Attraction of Pioneering Axons and by Modulating Slit2-Mediated Repulsion

inferredcites →https://doi.org/10.1093/cercor/bhx225openalex-snapshot

α-Tubulin Acetylation Restricts Axon Overbranching by Dampening Microtubule Plus-End Dynamics in Neurons

inferredcites →https://doi.org/10.1093/gbe/evu187openalex-snapshot

Six Subgroups and Extensive Recent Duplications Characterize the Evolution of the Eukaryotic Tubulin Protein Family

inferredcites →https://doi.org/10.1093/hmg/ddq182openalex-snapshot

TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins

inferredcites →https://doi.org/10.1093/hmg/ddq276openalex-snapshot

Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway

inferredcites →https://doi.org/10.1093/hmg/ddv250openalex-snapshot

Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes

inferredcites →https://doi.org/10.1093/hmg/ddy416openalex-snapshot

TUBA1A mutations identified in lissencephaly patients dominantly disrupt neuronal migration and impair dynein activity

inferredcites →https://doi.org/10.1098/rsob.130061openalex-snapshot

Microtubule dynamics in neuronal morphogenesis

inferredcites →https://doi.org/10.1101/cshperspect.a001800openalex-snapshot

The Growth Cone Cytoskeleton in Axon Outgrowth and Guidance

inferredcites →https://doi.org/10.1104/pp.15.01173openalex-snapshot

Affinity Purification and Characterization of Functional Tubulin from Cell Suspension Cultures of Arabidopsis and Tobacco

inferredcites →https://doi.org/10.1111/jnc.12621openalex-snapshot

Microtubules in neurons as information carriers

inferredcites →https://doi.org/10.1128/mcb.4.2.371openalex-snapshot

Direct Isolation of Neuronal Microtubule Skeletons

inferredcites →https://doi.org/10.1128/mcb.7.10.3799openalex-snapshot

Insertions of up to 17 amino acids into a region of alpha-tubulin do not disrupt function in vivo.

inferredcites →https://doi.org/10.1128/mcb.7.10.3799-3805.1987openalex-snapshot

Insertions of up to 17 Amino Acids into a Region of α-Tubulin Do Not Disrupt Function In Vivo

inferredcites →https://doi.org/10.1155/2013/149060openalex-snapshot

Axon Guidance Mechanisms for Establishment of Callosal Connections

inferredcites →https://doi.org/10.1159/000319663openalex-snapshot

The Role of Tuba1a in Adult Hippocampal Neurogenesis and the Formation of the Dentate Gyrus

inferredcites →https://doi.org/10.1186/s13041-016-0246-yopenalex-snapshot

In vitro characterization of neurite extension using induced pluripotent stem cells derived from lissencephaly patients with TUBA1A missense mutations

inferredcites →https://doi.org/10.1186/s13064-015-0031-0openalex-snapshot

Differential requirement of F-actin and microtubule cytoskeleton in cue-induced local protein synthesis in axonal growth cones

inferredcites →https://doi.org/10.1242/dev.127.22.4797openalex-snapshot

Aberrant development of hippocampal circuits and altered neural activity in netrin 1-deficient mice

inferredcites →https://doi.org/10.1242/jcs.122184openalex-snapshot

Direct binding of TUBB3 with DCC couples netrin-1 signaling to intracellular microtubule dynamics in axon outgrowth and guidance

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The tubulin code at a glance

inferredcites →https://doi.org/10.1242/jcs.203455openalex-snapshot

The formin DAAM is required for coordination of the actin and microtubule cytoskeleton in axonal growth cones

inferredcites →https://doi.org/10.1242/jcs.224311openalex-snapshot

XMAP215 promotes microtubule–F-actin interactions to regulate growth cone microtubules during axon guidance in Xenopus laevis

inferredcites →https://doi.org/10.1248/yakushi1947.120.10_935openalex-snapshot

Lactacystin, a Proteasome Inhibitor : Discovery and its Application in Cell Biology

inferredcites →https://doi.org/10.1371/journal.pbio.1001439openalex-snapshot

Growth Cone MKK7 mRNA Targeting Regulates MAP1b-Dependent Microtubule Bundling to Control Neurite Elongation

inferredcites →https://doi.org/10.1371/journal.pgen.1007314openalex-snapshot

Brain Tumor promotes axon growth across the midline through interactions with the microtubule stabilizing protein Apc2

inferredcites →https://doi.org/10.1371/journal.pgen.1008243openalex-snapshot

Differential requirements of tubulin genes in mammalian forebrain development

inferredcites →https://doi.org/10.1523/eneuro.0045-20.2020openalex-snapshot

Reduced TUBA1A Tubulin Causes Defects in Trafficking and Impaired Adult Motor Behavior

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Netrin-1-Induced Local -Actin Synthesis and Growth Cone Guidance Requires Zipcode Binding Protein 1

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Microtubule-associated protein 1b (MAP1b) is concentrated in the distal region of growing axons

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The T alpha 1 alpha-tubulin promoter specifies gene expression as a function of neuronal growth and regeneration in transgenic mice

inferredcites →https://doi.org/10.1523/jneurosci.1510-13.2013openalex-snapshot

Zebrafish Embryonic Neurons Transport Messenger RNA to Axons and Growth ConesIn Vivo

inferredcites →https://doi.org/10.1523/jneurosci.21-24-09757.2001openalex-snapshot

Axon Branching Requires Interactions between Dynamic Microtubules and Actin Filaments

inferredcites →https://doi.org/10.1523/jneurosci.22-06-02106.2002openalex-snapshot

Microtubule-Associated Protein 1A (MAP1A) and MAP1B: Light Chains Determine Distinct Functional Properties

inferredcites →https://doi.org/10.1523/jneurosci.22-21-09358.2002openalex-snapshot

Growth Cone Turning Induced by Direct Local Modification of Microtubule Dynamics

inferredcites →https://doi.org/10.1523/jneurosci.22-23-10346.2002openalex-snapshot

The Netrin 1 Receptors Unc5h3 and Dcc Are Necessary at Multiple Choice Points for the Guidance of Corticospinal Tract Axons

inferredcites →https://doi.org/10.1523/jneurosci.2281-17.2017openalex-snapshot

The Microtubule-Associated Protein Tau Mediates the Organization of Microtubules and Their Dynamic Exploration of Actin-Rich Lamellipodia and Filopodia of Cortical Growth Cones

inferredcites →https://doi.org/10.3389/fncel.2018.00195openalex-snapshot

Neuronal Growth Cone Size-Dependent and -Independent Parameters of Microtubule Polymerization

inferredcites →https://doi.org/10.3389/fncel.2018.00300openalex-snapshot

Cue-Polarized Transport of β-actin mRNA Depends on 3′UTR and Microtubules in Live Growth Cones

inferredcites →https://doi.org/10.3389/fncel.2018.00394openalex-snapshot

Model for Coordination of Microtubule and Actin Dynamics in Growth Cone Turning

inferredcites →https://doi.org/10.3389/fncel.2018.00447openalex-snapshot

An Integrated Cytoskeletal Model of Neurite Outgrowth

inferredcites →https://doi.org/10.3390/ijms18102207openalex-snapshot

Tubulin Post-Translational Modifications and Microtubule Dynamics

inferredcites →https://doi.org/10.3390/jdb5030008openalex-snapshot

The α-Tubulin gene TUBA1A in Brain Development: A Key Ingredient in the Neuronal Isotype Blend

inferredcites →https://doi.org/10.7554/elife.51992openalex-snapshot

The speed of GTP hydrolysis determines GTP cap size and controls microtubule stability

What points at this work

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

inferred← citeshttps://doi.org/10.31274/td-20240329-517openalex-snapshot

Molecular and functional characterization of tubulin isotypes in budding yeast (Saccharomyces cerevisiae)

inferred← citeshttps://doi.org/10.3389/fnmol.2021.759404openalex-snapshot

With the Permission of Microtubules: An Updated Overview on Microtubule Function During Axon Pathfinding

inferred← citeshttps://doi.org/10.7554/elife.76189openalex-snapshot

TUBA1A tubulinopathy mutants disrupt neuron morphogenesis and override XMAP215/Stu2 regulation of microtubule dynamics

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