The Role of the Microtubule Cytoskeleton in Neurodevelopmental Disorders
Open accessAbstract
Neurons depend on the highly dynamic microtubule (MT) cytoskeleton for many different processes during early embryonic development including cell division and migration, intracellular trafficking and signal transduction, as well as proper axon guidance and synapse formation. The coordination and support from MTs is crucial for newly formed neurons to migrate appropriately in order to establish neural connections. Once connections are made, MTs provide structural integrity and support to maintain neural connectivity throughout development. Abnormalities in neural migration and connectivity due to genetic mutations of MT-associated proteins can lead to detrimental developmental defects. Growing evidence suggests that these mutations are associated with many different neurodevelopmental disorders, including intellectual disabilities (ID) and autism spectrum disorders (ASD). In this review article, we highlight the crucial role of the MT cytoskeleton in the context of neurodevelopment and summarize genetic mutations of various MT related proteins that may underlie or contribute to neurodevelopmental disorders.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Missense de novo mutations in all four enriched domain families have previously been associated with developmental disorders.
“Missense DNMs in all four enriched domain families have previously been associated with DD (Supplementary Table 8)16–18.”
From Evidence for 28 genetic disorders discovered by combining healthcare and research data (2020) · cites this paper as [17]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Dynamic instability of microtubule growth
Mitchison, T., & Kirschner, M. (1984) · Nature · doi:10.1038/312237a0 · Cited by 3,337 · see citing works
Tau in physiology and pathology
Wang, Y., & Mandelkow, E. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2015.1 · Cited by 2,251 · see citing works
The cell biology of neurogenesis
Götz, M., & Huttner, W. B. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1739 · Cited by 2,130 · see citing works
Filopodia: molecular architecture and cellular functions
Mattila, P. K., & Lappalainen, P. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2406 · Cited by 1,699 · see citing works
Hirokawa, N., Niwa, S., & Tanaka, Y. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.039 · Cited by 1,138 · see citing works
A developmental and genetic classification for malformations of cortical development: update 2012
Barkovich, A. J., Guerrini, R., Kuzniecky, R., Jackson, G. D., & Dobyns, W. B. (2012) · Brain · doi:10.1093/brain/aws019 · Cited by 1,110 · see citing works
Gleeson, J. G., Allen, K. M., Fox, J. W., Lamperti, E. D., Berkovic, S. F., Scheffer, I. E., Cooper, E. C., Dobyns, W. B., Minnerath, S., Ross, M. E., et al. (1998) · Cell · doi:10.1016/s0092-8674(00)80899-5 · Cited by 1,091 · see citing works
Microtubule assembly, organization and dynamics in axons and dendrites
Conde, C., & Cáceres, A. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2631 · Cited by 1,086 · see citing works
Isolation of a Miller–Dicker lissencephaly gene containing G protein β-subunit-like repeats
Reiner, O., Carrozzo, R., Shen, Y. H., Wehnert, M., Faustinella, F., Dobyns, W. B., Caskey, C. T., & Ledbetter, D. H. (1993) · Nature · doi:10.1038/364717a0 · Cited by 1,057 · see citing works
Tracking the ends: a dynamic protein network controls the fate of microtubule tips
Akhmanova, A., & Steinmetz, M. O. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2369 · Cited by 1,047 · see citing works
The MAP1 family of microtubule-associated proteins.
Dehmelt (2004) · Genome biology · doi:10.1186/gb-2004-6-1-204 · Cited by 972 · see citing works
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Pinto, D., Delaby, E., Merico, D., Barbosa, M., Merikangas, A., Klei, L., Thiruvahindrapuram, B., Xu, X., Ziman, R., Wang, Z., et al. (2014) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2014.03.018 · Cited by 969 · see citing works
Drewes, G., Ebneth, A., Preuss, U., Mandelkow, E.-M., & Mandelkow, E. (1997) · Cell · doi:10.1016/s0092-8674(00)80208-1 · Cited by 878 · see citing works
The trip of the tip: understanding the growth cone machinery
Lowery, L. A., & Vactor, D. V. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2679 · Cited by 788 · see citing works
Self-citationMutations in Dynein Link Motor Neuron Degeneration to Defects in Retrograde Transport
Hafezparast, M., Klocke, R., Ruhrberg, C., Marquardt, A., Ahmad‐Annuar, A., Bowen, S., Lalli, G., Witherden, A. S., Hummerich, H., Nicholson, S. J., et al. (2003) · Science · doi:10.1126/science.1083129 · Cited by 684 · see citing works
Axonal transport: cargo-specific mechanisms of motility and regulation
Maday, S., Twelvetrees, A. E., Moughamian, A. J., & Holzbaur, E. L. F. (2014) · Neuron · doi:10.1016/j.neuron.2014.10.019 · Cited by 683 · see citing works
The Growth Cone Cytoskeleton in Axon Outgrowth and GuidancePreprint
Dent, E. W., Gupton, S. L., & Gertler, F. B. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a001800 · Cited by 646 · see citing works
Building the Neuronal Microtubule Cytoskeleton
Kapitein, L. C., & Hoogenraad, C. C. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.046 · Cited by 643 · see citing works
Dynamic microtubules regulate dendritic spine morphology and synaptic plasticity
Jaworski, J., Kapitein, L. C., Gouveia, S. M., Dortland, B. R., Wulf, P. S., Grigoriev, I., Camera, P., Spangler, S. A., Di Stefano, P., Demmers, J., et al. (2009) · Neuron · doi:10.1016/j.neuron.2008.11.013 · Cited by 643 · see citing works
Hazan, J., Fonknechten, N., Mavel, D., Paternotte, C., Samson, D. S., Artiguenave, F., Davoine, C.-S., Cruaud, C., Dürr, A., Wincker, P., et al. (1999) · Nature Genetics · doi:10.1038/15472 · Cited by 632 · see citing works
Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance
Tischfield, M. A., Baris, H. N., Wu, C., Rudolph, G., Maldergem, L. V., He, W., Chan, W. M., Andrews, C. V., Demer, J. L., Robertson, R. L., et al. (2010) · Cell · doi:10.1016/j.cell.2009.12.011 · Cited by 597 · see citing works
Hirotsune, S., Fleck, M. W., Gambello, M. J., Bix, G. J., Chen, A. Y.-C., Clark, G., Ledbetter, D. H., McBain, C. J., & Wynshaw-Boris, A. J. (1998) · Nature Genetics · doi:10.1038/1221 · Cited by 575 · see citing works
A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size
Bond, J., Roberts, E., Springell, K., Lizarraga, S., Scott, S., Higgins, J. W., Hampshire, D. J., Morrison, E. E., Leal, G. F., Silva, E. O., et al. (2005) · Nature Genetics · doi:10.1038/ng1539 · Cited by 564 · see citing works
Microtubule stabilization specifies initial neuronal polarization
Witte, H., Neukirchen, D., & Bradke, F. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200707042 · Cited by 564 · see citing works
RNAi reveals doublecortin is required for radial migration in rat neocortex
Bai, J., Ramos, R. L., Ackman, J. B., Thomas, A. M., Lee, R. V., & LoTurco, J. J. (2003) · Nature Neuroscience · doi:10.1038/nn1153 · Cited by 538 · see citing works
Poirier, K., Lebrun, N., Broix, L., Tian, G., Saillour, Y., Boscheron, C., Parrini, E., Valence, S., Saintpierre, B., Oger, M., et al. (2013) · Nature Genetics · doi:10.1038/ng.2613 · Cited by 479 · see citing works
Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans
Keays, D. A., Tian, G., Poirier, K., Huang, G., Siebold, C., Cleak, J., Oliver, P. L., Fray, M., Harvey, R. J., Molnár, Z., et al. (2007) · Cell · doi:10.1016/j.cell.2006.12.017 · Cited by 454 · see citing works
Dual subcellular roles for LIS1 and dynein in radial neuronal migration in live brain tissue
Tsai, J., Bremner, K. H., & Vallee, R. B. (2007) · Nature Neuroscience · doi:10.1038/nn1934 · Cited by 442 · see citing works
Kaminsky, E. B., Kaul, V., Paschall, J., Church, D. M., Bunke, B., Kunig, D., Moreno-De-Luca, D., Moreno-De-Luca, A., Mulle, J. G., Warren, S. T., et al. (2011) · Genetics in Medicine · doi:10.1097/gim.0b013e31822c79f9 · Cited by 437 · see citing works
Specification of synaptic connectivity by cell surface interactions
de Wit, J., & Ghosh, A. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn.2015.3 · Cited by 410 · see citing works
Defects in Axonal Elongation and Neuronal Migration in Mice with Disrupted tau and map1b Genes
Takei, Y., Teng, J., Harada, A., & Hirokawa, N. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.150.5.989 · Cited by 408 · see citing works
Axon Branching Requires Interactions between Dynamic Microtubules and Actin Filaments
Dent, E. W., & Kalil, K. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-24-09757.2001 · Cited by 399 · see citing works
Regulation of cytoplasmic dynein behaviour and microtubule organization by mammalian Lis1
Smith, D. S., Niethammer, M., Ayala, R., Zhou, Y., Gambello, M. J., Wynshaw-Boris, A. J., & Tsai, L. (2000) · Nature Cell Biology · doi:10.1038/35041000 · Cited by 380 · see citing works
Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria
Jaglin, X. H., Poirier, K., Saillour, Y., Buhler, E., Tian, G., Bahi‐Buisson, N., Fallet‐Bianco, C., Tuy, F. P. D., Kong, X., Bomont, P., et al. (2009) · Nature Genetics · doi:10.1038/ng.380 · Cited by 380 · see citing works
Harada, A., Teng, J., Takei, Y., Oguchi, K., & Hirokawa, N. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200110134 · Cited by 366 · see citing works
Shu, T., Ayala, R., Nguyen, M.-D., Xie, Z., Gleeson, J. G., & Tsai, L. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.030 · Cited by 361 · see citing works
Pilz, D. T. (1998) · Human Molecular Genetics · doi:10.1093/hmg/7.13.2029 · Cited by 360 · see citing works
A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP
Helsmoortel, C., Vulto-van Silfhout, A. T., Coe, B. P., Vandeweyer, G., Rooms, L., van den Ende, J., Schuurs-Hoeijmakers, J. H. M., Marcelis, C. L., Willemsen, M. H., Vissers, L. E. L. M., et al. (2014) · Nature Genetics · doi:10.1038/ng.2899 · Cited by 354 · see citing works
Molecular mechanisms of dendrite stability
Koleske, A. J. (2013) · Nature reviews. Neuroscience · doi:10.1038/nrn3486 · Cited by 351 · see citing works
Microtubule behavior in the growth cones of living neurons during axon elongation.
Tanaka, E. M., & Kirschner, M. W. (1991) · The Journal of Cell Biology · doi:10.1083/jcb.115.2.345 · Cited by 349 · see citing works
KIF5C, a Novel Neuronal Kinesin Enriched in Motor Neurons
Kanai, Y., Okada, Y., Tanaka, Y., Harada, A., Terada, S., & Hirokawa, N. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-17-06374.2000 · Cited by 334 · see citing works
Ori-McKenney, K. M., Jan, L. Y., & Jan, Y. N. (2012) · Neuron · doi:10.1016/j.neuron.2012.10.008 · Cited by 325 · see citing works
Doublecortin Is Required in Mice for Lamination of the Hippocampus But Not the Neocortex
Corbo, J. C., Deuel, T. A., Long, J. M., LaPorte, P., Tsai, E., Wynshaw-Boris, A. J., & Walsh, C. A. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-17-07548.2002 · Cited by 324 · see citing works
The wide spectrum of tubulinopathies: what are the key features for the diagnosis?
Bahi‐Buisson, N., Poirier, K., Fourniol, F. J., Saillour, Y., Valence, S., Lebrun, N., Hully, M., Fallet‐Bianco, C., Boddaert, N., Elie, C., et al. (2014) · Brain · doi:10.1093/brain/awu082 · Cited by 324 · see citing works
Mixed microtubules steer dynein-driven cargo transport into dendrites
Kapitein, L. C., Schlager, M. A., Kuijpers, M., Wulf, P. S., van Spronsen, M., MacKintosh, F. C., & Hoogenraad, C. C. (2010) · Current Biology · doi:10.1016/j.cub.2009.12.052 · Cited by 320 · see citing works
Nakata, T., & Hirokawa, N. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200302175 · Cited by 311 · see citing works
Filopodia are required for cortical neurite initiation
Dent, E. W., Kwiatkowski, A. V., Mebane, L. M., Philippar, U., Barzik, M., Rubinson, D. A., Gupton, S. L., van Veen, J. E., Furman, C., Zhang, J., et al. (2007) · Nature Cell Biology · doi:10.1038/ncb1654 · Cited by 309 · see citing works
Differentiation between oppositely oriented microtubules controls polarized neuronal transport
Tas, R. P., Chazeau, A., Cloin, B. M. C., Lambers, M. L. A., Hoogenraad, C. C., & Kapitein, L. C. (2017) · Neuron · doi:10.1016/j.neuron.2017.11.018 · Cited by 306 · see citing works
Teng, J., Takei, Y., Harada, A., Nakata, T., Chen, J., & Hirokawa, N. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.200106025 · Cited by 305 · see citing works
Branch management: mechanisms of axon branching in the developing vertebrate CNS
Kalil, K., & Dent, E. W. (2013) · Nature reviews. Neuroscience · doi:10.1038/nrn3650 · Cited by 300 · see citing works
Sapir, T., Elbaum, M., & Reiner, O. (1997) · The EMBO Journal · doi:10.1093/emboj/16.23.6977 · Cited by 297 · see citing works
The in vivo roles of STEF/Tiam1, Rac1 and JNK in cortical neuronal migration
Kawauchi, T., Chihama, K., Nabeshima, Y., & Hoshino, M. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg413 · Cited by 297 · see citing works
Axon Extension Occurs Independently of Centrosomal Microtubule Nucleation
Stieß, M., Maghelli, N., Kapitein, L. C., Gomis-Rüth, S., Wilsch‐Bräuninger, M., Hoogenraad, C. C., Tolić, I. M., & Bradke, F. (2010) · Science · doi:10.1126/science.1182179 · Cited by 290 · see citing works
Dynein is required for polarized dendritic transport and uniform microtubule orientation in axons
Zheng, Y., Wildonger, J., Ye, B., Zhang, Y., Kita, A. M., Younger, S. H., Zimmerman, S., Jan, L. Y., & Jan, Y. N. (2008) · Nature Cell Biology · doi:10.1038/ncb1777 · Cited by 290 · see citing works
Deuel, T. A., Liu, J. S.-H., Corbo, J. C., Yoo, S.-Y., Rorke-Adams, L. B., & Walsh, C. A. (2006) · Neuron · doi:10.1016/j.neuron.2005.10.038 · Cited by 287 · see citing works
Yu, W., Qiang, L., Solowska, J. M., Karabay, A., Korulu, Ş., & Baas, P. W. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-09-0878 · Cited by 283 · see citing works
Kinesin Superfamily Protein 2A (KIF2A) Functions in Suppression of Collateral Branch Extension
Homma, N., Takei, Y., Tanaka, Y., Nakata, T., Terada, S., Kikkawa, M., Noda, Y., & Hirokawa, N. (2003) · Cell · doi:10.1016/s0092-8674(03)00522-1 · Cited by 281 · see citing works
The genetic basis of non-syndromic intellectual disability: a review
Kaufman, L., Ayub, M., & Vincent, J. B. (2010) · Journal of Neurodevelopmental Disorders · doi:10.1007/s11689-010-9055-2 · Cited by 280 · see citing works
Jacobson, C., Schnapp, B. J., & Banker, G. A. (2006) · Neuron · doi:10.1016/j.neuron.2006.02.005 · Cited by 278 · see citing works
Poirier, K., Saillour, Y., Bahi‐Buisson, N., Jaglin, X. H., Fallet‐Bianco, C., Nabbout, R., Castelnau, L., Roubertie, A., Attié‐Bitach, T., Desguerre, I., et al. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq377 · Cited by 273 · see citing works
CDK5RAP2 stimulates microtubule nucleation by the γ-tubulin ring complex
Choi, Y.-K., Liu, P., Sze, S. K., Dai, C., & Qi, R. Z. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201007030 · Cited by 273 · see citing works
Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors
Lizarraga, S. B., Margossian, S. P., Harris, M. H., Campagna, D. R., Han, A., Blevins, S., Mudbhary, R., Barker, J. E., Walsh, C. A., & Fleming, M. D. (2010) · Development · doi:10.1242/dev.040410 · Cited by 270 · see citing works
Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation
Trimborn, M., Bell, S. M., Felix, C., Rashid, Y. A., Jafri, H., Griffiths, P. D., Neumann, L. M., Krebsová, A., Reis, A., Sperling, K., et al. (2004) · The American Journal of Human Genetics · doi:10.1086/422855 · Cited by 269 · see citing works
Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH)
Portes, V. D., Francis, F., Pinard, J.-M., Desguerre, I., Moutard, M., Snoeck, I. N., Meiners, L. C., Capron, F., Cusmai, R., Ricci, S., et al. (1998) · Human Molecular Genetics · doi:10.1093/hmg/7.7.1063 · Cited by 266 · see citing works
Dent, E. W., Callaway, J. L., Szebenyi, G., Baas, P. W., & Kalil, K. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-20-08894.1999 · Cited by 265 · see citing works
Shi, S., Cheng, T., Jan, L. Y., & Jan, Y. N. (2004) · Current Biology · doi:10.1016/j.cub.2004.11.009 · Cited by 259 · see citing works
Intellectual disability and autism spectrum disorders: Causal genes and molecular mechanisms
Srivastava, A. K., & Schwartz, C. E. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.02.015 · Cited by 251 · see citing works
Poirier, K., Keays, D. A., Francis, F., Saillour, Y., Bahi‐Buisson, N., Manouvrier‐Hanu, S., Fallet‐Bianco, C., Pasquier, L., Toutain, A., Tuy, F. P. D., et al. (2007) · Human Mutation · doi:10.1002/humu.20572 · Cited by 246 · see citing works
Mechanism of Microtubule Stabilization by Doublecortin
Moores, C. A., Perderiset, M., Francis, F., Chelly, J., Houdusse, A., & Milligan, R. A. (2004) · Molecular Cell · doi:10.1016/j.molcel.2004.06.009 · Cited by 242 · see citing works
LIS1, CLIP-170's Key to the Dynein/Dynactin Pathway
Coquelle, F. M., Caspi, M., Cordelières, F. P., Dompierre, J., Dujardin, D., Koifman, C., Martin, P., Hoogenraad, C. C., Akhmanova, A. S., Galjart, N., et al. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.9.3089-3102.2002 · Cited by 240 · see citing works
Which way to go? Cytoskeletal organization and polarized transport in neurons
Kapitein, L. C., & Hoogenraad, C. C. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.08.015 · Cited by 239 · see citing works
MARK/PAR1 kinase is a regulator of microtubule-dependent transport in axons
Mandelkow, E.-M., Thies, E., Trinczek, B., Biernat, J., & Mandelkow, E. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200401085 · Cited by 236 · see citing works
Mutations in STIL, Encoding a Pericentriolar and Centrosomal Protein, Cause Primary Microcephaly
Kumar, A., Girimaji, S. C., Duvvari, M. R., & Blanton, S. H. (2009) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2009.01.017 · Cited by 231 · see citing works
Gruber, R., Zhou, Z., Sukchev, M., Jörß, T., Frappart, P., & Wang, Z. (2011) · Nature Cell Biology · doi:10.1038/ncb2342 · Cited by 230 · see citing works
Increased LIS1 expression affects human and mouse brain development
Bi, W., Sapir, T., Shchelochkov, O. A., Zhang, F., Withers, M. A., Hunter, J. V., Levy, T., Shinder, V., Peiffer, D. A., Gunderson, K. L., et al. (2009) · Nature Genetics · doi:10.1038/ng.302 · Cited by 223 · see citing works
Microtubules in Dendritic Spine Development
Gu, J., Firestein, B. L., & Zheng, J. Q. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2509-08.2008 · Cited by 220 · see citing works
Vulih-Shultzman, I., Pinhasov, A., Mandel, S., Grigoriadis, N., Touloumi, O., Pittel, Z., & Gozes, I. (2007) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.129551 · Cited by 219 · see citing works
Microtubule Minus-End Binding Protein CAMSAP2 Controls Axon Specification and Dendrite Development
Yau, K. W., van Beuningen, S. F. B., Cunha‐Ferreira, I., Cloin, B. M. C., van Battum, E. Y., Will, L., Schätzle, P., Tas, R. P., van Krugten, J., Katrukha, E. A., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.019 · Cited by 218 · see citing works
Schaar, B. T., Kinoshita, K., & McConnell, S. K. (2004) · Neuron · doi:10.1016/s0896-6273(03)00843-2 · Cited by 210 · see citing works
Kouprina, N., Pavlı́ček, A., Collins, N. K., Nakano, M., Noskov, V. N., Ohzeki, J., Mochida, G. H., Risinger, J. I., Goldsmith, P. K., Gunsior, M., et al. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi220 · Cited by 208 · see citing works
Tubulin-related cortical dysgeneses: microtubule dysfunction underlying neuronal migration defects
Jaglin, X. H., & Chelly, J. (2009) · Trends in Genetics · doi:10.1016/j.tig.2009.10.003 · Cited by 194 · see citing works
Yau, K. W., Schätzle, P., Tortosa, E., Pagès, S., Holtmaat, A. J. D. G., Kapitein, L. C., & Hoogenraad, C. C. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2430-15.2016 · Cited by 194 · see citing works
Axonal Transport RatesIn VivoAre Unaffected by Tau Deletion or Overexpression in Mice
Yuan, A., Kumar, A. R., Peterhoff, C. M., Duff, K., & Nixon, R. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5242-07.2008 · Cited by 187 · see citing works
Gumy, L. F., Katrukha, E. A., Grigoriev, I., Jaarsma, D., Kapitein, L. C., Akhmanova, A., & Hoogenraad, C. C. (2017) · Neuron · doi:10.1016/j.neuron.2017.03.046 · Cited by 186 · see citing works
Multiple Dose-Dependent Effects of Lis1 on Cerebral Cortical Development
Gambello, M. J., Darling, D. L., Yingling, J., Tanaka, T., Gleeson, J. G., & Wynshaw-Boris, A. J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-05-01719.2003 · Cited by 184 · see citing works
Initial Neurite Outgrowth in Drosophila Neurons Is Driven by Kinesin-Powered Microtubule Sliding
Lü, W., Fox, P., Lakonishok, M., Davidson, M. W., & Gelfand, V. I. (2013) · Current Biology · doi:10.1016/j.cub.2013.04.050 · Cited by 183 · see citing works
STIL is required for centriole duplication in human cells
Vulprecht, J., David, A., Tibelius, A., Castiel, A., Konotop, G., Liu, F., Bestvater, F., Raab, M. S., Zentgraf, H., Izraeli, S., et al. (2012) · Journal of Cell Science · doi:10.1242/jcs.104109 · Cited by 183 · see citing works
Synaptic Regulation of Microtubule Dynamics in Dendritic Spines by Calcium, F-Actin, and Drebrin
Merriam, E. B., Millette, M. M., Lumbard, D., Saengsawang, W., Fothergill, T., Hu, X., Ferhat, L., & Dent, E. W. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0661-13.2013 · Cited by 177 · see citing works
Lis1 is an initiation factor for dynein-driven organelle transport
Egan, M. J., Tan, K., & Reck‐Peterson, S. L. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201112101 · Cited by 177 · see citing works
Control of neuronal polarity and plasticity – a renaissance for microtubules?
Hoogenraad, C. C., & Bradke, F. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2009.08.006 · Cited by 173 · see citing works
Lee, H., Engel, U., Rusch, J., Scherrer, S., Sheard, K., & Vactor, D. V. (2004) · Neuron · doi:10.1016/j.neuron.2004.05.020 · Cited by 173 · see citing works
Mutation of the Variant α-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia
Abdollahi, M. R., Morrison, E. E., Sirey, T., Molnár, Z., Hayward, B. E., Carr, I., Springell, K., Woods, C. G., Ahmed, M., Hattingh, L., et al. (2009) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2009.10.007 · Cited by 170 · see citing works
Poultney, C. S., Goldberg, A. P., Drapeau, E., Kou, Y., Harony-Nicolas, H., Kajiwara, Y., De Rubeis, S., Durand, S., Stevens, C., Rehnström, K., et al. (2013) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2013.09.001 · Cited by 169 · see citing works
Janning, D., Igaev, M., Sündermann, F., Brühmann, J., Beutel, O., Heinisch, J. J., Bakota, L., Piehler, J., Junge, W., & Brandt, R. (2014) · Molecular Biology of the Cell · doi:10.1091/mbc.e14-06-1099 · Cited by 168 · see citing works
Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP
Dijck, A. V., Silfhout, A. T. V., Cappuyns, E., van der Werf, I. M., Mancini, G. M. S., Tzschach, A., Bernier, R., Gozes, I., Eichler, E. E., Romano, C., et al. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.02.1173 · Cited by 168 · see citing works
Function and Regulation of AUTS2, a Gene Implicated in Autism and Human Evolution
Oksenberg, N., Stevison, L., Wall, J. D., & Ahituv, N. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003221 · Cited by 167 · see citing works
Mandel, S., Rechavi, G., & Gozes, I. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2006.11.039 · Cited by 167 · see citing works
Neuronal polarization: The cytoskeleton leads the way
Stieß, M., & Bradke, F. (2010) · Developmental Neurobiology · doi:10.1002/dneu.20849 · Cited by 166 · see citing works
Microtubule minus-end regulation at spindle poles by an ASPM–katanin complex
Jiang, K., Řežábková, L., Hua, S., Liu, Q., Capitani, G., Altelaar, M. A. F., Heck, A. J. R., Kammerer, R. A., Steinmetz, M. O., & Akhmanova, A. S. (2017) · Nature Cell Biology · doi:10.1038/ncb3511 · Cited by 164 · see citing works
Lee, J.-R., Srour, M., Kim, D., Hamdan, F. F., Lim, S.-H., Brunel‐Guitton, C., Décarie, J., Rossignol, E., Mitchell, G. A., Schreiber, A., et al. (2014) · Human Mutation · doi:10.1002/humu.22709 · Cited by 160 · see citing works
Moughamian, A. J., Osborn, G. E., Lazarus, J. E., Maday, S., & Holzbaur, E. L. F. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0935-13.2013 · Cited by 158 · see citing works
Grabham, P. W., Seale, G. E., Bennecib, M., Goldberg, D. J., & Vallee, R. B. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1135-07.2007 · Cited by 158 · see citing works
Nakata, T., Niwa, S., Okada, Y., Perez, F., & Hirokawa, N. (2011) · Journal of Cell Biology · doi:10.1083/jcb.201104034 · Cited by 156 · see citing works
Two domains of p80 katanin regulate microtubule severing and spindle pole targeting by p60 katanin
Perry, K. L., Bazirgan, O. A., & McNally, F. J. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.9.1623 · Cited by 156 · see citing works
The microtubule-severing protein Spastin is essential for axon outgrowth in the zebrafish embryo
Wood, J. D. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl212 · Cited by 153 · see citing works
Kondo, M., Takei, Y., & Hirokawa, N. (2012) · Neuron · doi:10.1016/j.neuron.2011.12.020 · Cited by 151 · see citing works
Overlapping cortical malformations and mutations in TUBB2B and TUBA1A
Cushion, T. D., Dobyns, W. B., Mullins, J. G. L., Stoodley, N., Chung, S., Fry, A. E., Hehr, U., Gunny, R. S., Aylsworth, A. S., Prabhakar, P., et al. (2013) · Brain · doi:10.1093/brain/aws338 · Cited by 150 · see citing works
Bouquet, C., Soares, S., von Boxberg, Y., Ravaille‐Veron, M., Propst, F., & Nothias, F. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2254-04.2004 · Cited by 149 · see citing works
Axonal Growth Is Sensitive to the Levels of Katanin, a Protein That Severs Microtubules
Karabay, A., Yu, W., Solowska, J. M., Baird, D. H., & Baas, P. W. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1382-04.2004 · Cited by 147 · see citing works
Microtubule fragmentation and partitioning in the axon during collateral branch formation
Yu, W., Ahmad, F., & Baas, P. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-10-05872.1994 · Cited by 145 · see citing works
The emerging role of the tubulin code: From the tubulin molecule to neuronal function and disease
Chakraborti, S., Natarajan, K., Curiel, J., Janke, C., & Liu, J. S.-H. (2016) · Cytoskeleton · doi:10.1002/cm.21290 · Cited by 144 · see citing works
Centrosomes, microtubules and neuronal development
Kuijpers, M., & Hoogenraad, C. C. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2011.05.004 · Cited by 143 · see citing works
Oz, S., Kapitansky, O., Ivashko‐Pachima, Y., Malishkevich, A., Giladi, E., Skalka, N., Rosin‐Arbesfeld, R., Mittelman, L. A., Segev, O., Hirsch, J. A., et al. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.97 · Cited by 142 · see citing works
Doublecortin Recognizes the 13-Protofilament Microtubule Cooperatively and Tracks Microtubule Ends
Bechstedt, S., & Brouhard, G. J. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.05.006 · Cited by 141 · see citing works
Hippocampal Abnormalities and Enhanced Excitability in a Murine Model of Human Lissencephaly
Fleck, M. W., Hirotsune, S., Gambello, M. J., Phillips‐Tansey, E., Suares, G., Mervis, R. F., Wynshaw-Boris, A. J., & McBain, C. J. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02439.2000 · Cited by 138 · see citing works
Of microtubules and memory: implications for microtubule dynamics in dendrites and spines
Dent, E. W. (2016) · Molecular Biology of the Cell · doi:10.1091/mbc.e15-11-0769 · Cited by 136 · see citing works
Identification of a Microtubule-associated Motor Protein Essential for Dendritic Differentiation
Sharp, D. J., Yu, W., Ferhat, L., Kuriyama, R., Rueger, D. C., & Baas, P. W. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.138.4.833 · Cited by 133 · see citing works
Cytoskeletal Regulation by AUTS2 in Neuronal Migration and Neuritogenesis
Hori, K., Nagai, T., Shan, W., Sakamoto, A., Taya, S., Hashimoto, R., Hayashi, T., Abe, M., Yamazaki, M., Nakao, K., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.11.045 · Cited by 133 · see citing works
Microtubules in health and degenerative disease of the nervous system
Matamoros, A. J., & Baas, P. W. (2016) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2016.06.016 · Cited by 133 · see citing works
Polymicrogyria: A common and heterogeneous malformation of cortical development
Stutterd, C., & Leventer, R. J. (2014) · American Journal of Medical Genetics Part C Seminars in Medical Genetics · doi:10.1002/ajmg.c.31399 · Cited by 128 · see citing works
Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation
Kalscheuer, V. M., FitzPatrick, D. R., Tommerup, N., Bugge, M., Niebuhr, E., Neumann, L. M., Tzschach, A., Shoichet, S. A., Menzel, C., Erdogan, F., et al. (2007) · Human Genetics · doi:10.1007/s00439-006-0284-0 · Cited by 128 · see citing works
Genotypically Defined Lissencephalies Show Distinct Pathologies
Forman, M. S., Squier, W., Dobyns, W. B., & Golden, J. A. (2005) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/01.jnen.0000182978.56612.41 · Cited by 123 · see citing works
Biswas, S., & Kalil, K. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2281-17.2017 · Cited by 119 · see citing works
Gallo, G., & Letourneau, P. C. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-10-03860.1999 · Cited by 118 · see citing works
Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly
Kerjan, G., & Gleeson, J. G. (2007) · Trends in Genetics · doi:10.1016/j.tig.2007.09.003 · Cited by 118 · see citing works
Mechanisms and Disturbances of Neuronal Migration
Gressèns, P. (2000) · Pediatric Research · doi:10.1203/00006450-200012000-00004 · Cited by 116 · see citing works
Depletion of a microtubule-associated motor protein induces the loss of dendritic identity
Yu, W., Cook, C., Sauter, C., Kuriyama, R., Kaplan, P. L., & Baas, P. W. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-15-05782.2000 · Cited by 116 · see citing works
Fry, A. E., Cushion, T. D., & Pilz, D. T. (2014) · American Journal of Medical Genetics Part C Seminars in Medical Genetics · doi:10.1002/ajmg.c.31402 · Cited by 116 · see citing works
Youn, Y. H., Pramparo, T., Hirotsune, S., & Wynshaw-Boris, A. J. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4630-09.2009 · Cited by 115 · see citing works
Neuronal migration disorders: Focus on the cytoskeleton and epilepsy
Stouffer, M. A., Golden, J. A., & Francis, F. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2015.08.003 · Cited by 114 · see citing works
Alves‐Silva, J., Sánchez‐Soriano, N., Beaven, R., Klein, M., Parkin, J., Millard, T. H., Bellen, H. J., Venken, K. J. T., Ballestrem, C., Kammerer, R. A., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0416-12.2012 · Cited by 109 · see citing works
The mouse fidgetin gene defines a new role for AAA family proteins in mammalian development
Cox, G. A., Mahaffey, C. L., Nystuen, A., Letts, V. A., & Frankel, W. N. (2000) · Nature Genetics · doi:10.1038/79923 · Cited by 109 · see citing works
CLIP-170 and IQGAP1 Cooperatively Regulate Dendrite Morphology
Swiech, L. J., Błażejczyk, M., Urbańska, M., Pietruszka, P., Dortland, B. R., Malik, A. R., Wulf, P. S., Hoogenraad, C. C., & Jaworski, J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6582-10.2011 · Cited by 107 · see citing works
Kitagawa, D., Kohlmaier, G., Keller, D., Strnad, P., Balestra, F. R., Flückiger, I., & Gönczy, P. (2011) · Journal of Cell Science · doi:10.1242/jcs.089888 · Cited by 107 · see citing works
Sapir, T., Sapoznik, S., Levy, T., Finkelshtein, D., Shmueli, A., Timm, T., Mandelkow, E., & Reiner, O. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0911-08.2008 · Cited by 106 · see citing works
Cytoskeletal and signaling mechanisms of neurite formation
Sainath, R., & Gallo, G. (2015) · Cell and Tissue Research · doi:10.1007/s00441-014-1955-0 · Cited by 103 · see citing works
NudEL targets dynein to microtubule ends through LIS1
Li, J., Lee, W., & Cooper, J. A. (2005) · Nature Cell Biology · doi:10.1038/ncb1273 · Cited by 102 · see citing works
Ivashko‐Pachima, Y., Sayas, C. L., Malishkevich, A., & Gozes, I. (2017) · Molecular Psychiatry · doi:10.1038/mp.2016.255 · Cited by 102 · see citing works
Tint, I. S., Jean, D. C., Baas, P. W., & Black, M. M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3399-09.2009 · Cited by 100 · see citing works
Willemsen, M. H., Ba, W., Wissink-Lindhout, W. M., de Brouwer, A. P. M., Haas, S. A., Bienek, M., Hu, H., Vissers, L. E. L. M., van Bokhoven, H., Kalscheuer, V. M., et al. (2014) · Journal of Medical Genetics · doi:10.1136/jmedgenet-2013-102182 · Cited by 99 · see citing works
Microtubule plus-end tracking proteins in neuronal development
van de Willige, D., Hoogenraad, C. C., & Akhmanova, A. S. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2168-3 · Cited by 93 · see citing works
Mitotic Motors Coregulate Microtubule Patterns in Axons and Dendrites
Lin, S., Liu, M., Mozgova, O. I., Yu, W., & Baas, P. W. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3070-12.2012 · Cited by 93 · see citing works
Impaired Learning and Motor Behavior in Heterozygous Pafah1b1 (Lis1) Mutant MicePreprint
Paylor, R. E., Hirotsune, S., Gambello, M. J., Yuva‐Paylor, L. A., Crawley, J. N., & Wynshaw-Boris, A. J. (1999) · Learning & Memory · doi:10.1101/lm.6.5.521 · Cited by 92 · see citing works
Doublecortin-like Kinase Is Associated with Microtubules in Neuronal Growth Cones
Burgess, H. A., & Reiner, O. (2000) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2000.0891 · Cited by 90 · see citing works
Lis1 Has Two Opposing Modes of Regulating Cytoplasmic Dynein
DeSantis, M. E., Cianfrocco, M. A., Htet, Z. M., Tran, P. T., Reck‐Peterson, S. L., & Leschziner, A. E. (2017) · Cell · doi:10.1016/j.cell.2017.08.037 · Cited by 90 · see citing works
Tau's role in the developing brain: implications for intellectual disability
Sapir, T., Frotscher, M., Levy, T., Mandelkow, E., & Reiner, O. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddr603 · Cited by 89 · see citing works
Rehberg, M., Kleylein-Sohn, J., Faix, J., Ho, T.-H., Schulz, I., & Gräf, R. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-01-0069 · Cited by 88 · see citing works
Fiorillo, C., Moro, F., Yi, J., Weil, S. J., Brisca, G., Astrea, G., Severino, M., Romano, A., Battini, R., Rossi, A., et al. (2013) · Human Mutation · doi:10.1002/humu.22491 · Cited by 87 · see citing works
Oz, S., Ivashko‐Pachima, Y., & Gozes, I. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051458 · Cited by 86 · see citing works
Role of kinesin-1–based microtubule sliding in Drosophila nervous system development
Winding, M., Kelliher, M. T., Lü, W., Wildonger, J., & Gelfand, V. I. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1522416113 · Cited by 85 · see citing works
Maussion, G., Carayol, J., Lepagnol-Bestel, A.-M., Torès, F., Loe-Mie, Y., Milbreta, U., Rousseau, F., Fontaine, K., Renaud, J., Moalic, J., et al. (2008) · Human Molecular Genetics · doi:10.1093/hmg/ddn154 · Cited by 84 · see citing works
Neukirchen, D., & Bradke, F. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3983-10.2011 · Cited by 83 · see citing works
Microtubules and Growth Cones: Motors Drive the Turn
Kahn, O. I., & Baas, P. W. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.04.009 · Cited by 83 · see citing works
Armijo‐Weingart, L., & Gallo, G. (2017) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2017.03.007 · Cited by 82 · see citing works
Dynamic Microtubules Promote Synaptic NMDA Receptor-Dependent Spine Enlargement
Merriam, E. B., Lumbard, D., Viesselmann, C., Ballweg, J., Stevenson, M., Pietila, L., Hu, X., & Dent, E. W. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027688 · Cited by 81 · see citing works
MAP1B enhances microtubule assembly rates and axon extension rates in developing neurons
Tymanskyj, S. R., Scales, T. M. E., & Gordon‐Weeks, P. R. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2011.10.003 · Cited by 79 · see citing works
Cytoplasmic Dynein Transports Axonal Microtubules in a Polarity-Sorting Manner
Rao, A. N., Patil, A., Black, M. M., Craig, E. M., Myers, K. A., Yeung, H. T., & Baas, P. W. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.05.064 · Cited by 79 · see citing works
Dehmelt, L., Nalbant, P., Steffen, W., & Halpain, S. (2007) · Journal of Neurocytology · doi:10.1007/s11068-006-9001-0 · Cited by 78 · see citing works
Actin filament-microtubule interactions in axon initiation and branching
Pacheco, A., & Gallo, G. (2016) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2016.07.013 · Cited by 78 · see citing works
Zollo, M., Ahmed, M., Ferrucci, V., Salpietro, V., Asadzadeh, F., Carotenuto, M., Maroofian, R., Al-Amri, A. H., Singh, R., Scognamiglio, I., et al. (2017) · Brain · doi:10.1093/brain/awx014 · Cited by 77 · see citing works
Cammarata, G. M., Bearce, E. A., & Lowery, L. A. (2016) · Cytoskeleton · doi:10.1002/cm.21272 · Cited by 75 · see citing works
Self-citationJudkins, A. R., Martínez, D., Ferreira, P. C. L., Dobyns, W. B., & Golden, J. A. (2011) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31821ccf1c · Cited by 74 · see citing works
Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development
Whitman, M. C., Andrews, C. V., Chan, W. M., Tischfield, M. A., Stasheff, S. F., Brancati, F., Ortiz-Gonzalez, X. R., Nuovo, S., Garaci, F., MacKinnon, S. E., et al. (2015) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.37362 · Cited by 74 · see citing works
McVicker, D. P., Awe, A. M., Richters, K. E., Wilson, R. L., Cowdrey, D. A., Hu, X., Chapman, E. R., & Dent, E. W. (2016) · Nature Communications · doi:10.1038/ncomms12741 · Cited by 74 · see citing works
Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated children
Gozes, I., Dijck, A. V., Hacohen-Kleiman, G., Grigg, I., Karmon, G., Giladi, E., Eger, M., Gabet, Y., Pasmanik-Chor, M., Cappuyns, E., et al. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.27 · Cited by 74 · see citing works
Erratum: Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated children
Gozes, I., Dijck, A. V., Hacohen-Kleiman, G., Grigg, I., Karmon, G., Giladi, E., Eger, M., Gabet, Y., Pasmanik-Chor, M., Cappuyns, E., et al. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.128 · Cited by 71 · see citing works
Transport of dendritic microtubules establishes their nonuniform polarity orientation.
Sharp, D. J., Yu, W., & Baas, P. W. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.130.1.93 · Cited by 67 · see citing works
Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria
Poirier, K., Saillour, Y., Fourniol, F. J., Francis, F., Souville, I., Valence, S., Desguerre, I., Lepage, J. M., Boddaert, N., Jacquemont, M. L., et al. (2012) · European Journal of Human Genetics · doi:10.1038/ejhg.2012.195 · Cited by 67 · see citing works
Mukherjee, S., Díaz‐Valencia, J. D., Stewman, S. F., Metz, J., Monnier, S., Rath, U., Asenjo, A. B., Charafeddine, R. A., Sosa, H., Ross, J. L., et al. (2012) · Cell Cycle · doi:10.4161/cc.20849 · Cited by 67 · see citing works
Ohba, C., Haginoya, K., Osaka, H., Kubota, K., Ishiyama, A., Hiraide, T., Komaki, H., Sasaki, M., Miyatake, S., Nakashima, M., et al. (2015) · Journal of Human Genetics · doi:10.1038/jhg.2015.108 · Cited by 67 · see citing works
Vagnoni, A., Hoffmann, P. C., & Bullock, S. L. (2015) · Journal of Cell Science · doi:10.1242/jcs.179184 · Cited by 65 · see citing works
Marlin-1, a Novel RNA-binding Protein Associates with GABA Receptors
Couve, A., Restituito, S., Brandon, J. M., Charles, K. J., Bawagan, H., Freeman, K. B., Pangalos, M. N., Calver, A. R., & Moss, S. J. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m311737200 · Cited by 63 · see citing works
Microtubule plus-end tracking proteins in differentiated mammalian cells
Jaworski, J., Hoogenraad, C. C., & Akhmanova, A. S. (2007) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2007.10.015 · Cited by 62 · see citing works
Garcez, P. P., Díaz-Alonso, J., Crespo‐Enríquez, I., Castro, D. S., Bell, D. M., & Guillemot, F. (2015) · Nature Communications · doi:10.1038/ncomms7474 · Cited by 62 · see citing works
Vertebrate Fidgetin Restrains Axonal Growth by Severing Labile Domains of Microtubules
Leo, L., Yu, W., D’Rozario, M., Waddell, E. A., Marenda, D. R., Baird, M. A., Davidson, M. W., Zhou, B., Wu, B., Baker, L. M., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.08.017 · Cited by 61 · see citing works
TIPsy tour guides: how microtubule plus-end tracking proteins (+TIPs) facilitate axon guidance
Bearce, E. A., Erdoğan, B., & Lowery, L. A. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00241 · Cited by 60 · see citing works
Self-citationLIS1 is a microtubule‐associated phosphoprotein
Sapir, T., Cahana, A., Seger, R., Nekhai, S. A., & Reiner, O. (1999) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.1999.00711.x · Cited by 60 · see citing works
Mutations in the Microtubule-Associated Protein 1A ( Map1a ) Gene Cause Purkinje Cell Degeneration
Liu, Y., Lee, J.-W., & Ackerman, S. L. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2757-14.2015 · Cited by 58 · see citing works
Schirer, Y., Malishkevich, A., Ophir, Y., Lewis, J. M., Giladi, E., & Gozes, I. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087383 · Cited by 57 · see citing works
Nwagbara, B. U., Faris, A. E. R., Bearce, E. A., Erdoğan, B., Ebbert, P. T., Evans, M. F., Rutherford, E. L., Enzenbacher, T. B., & Lowery, L. A. (2014) · Molecular Biology of the Cell · doi:10.1091/mbc.e14-06-1121 · Cited by 57 · see citing works
Self-citationKoester, M. P., Müller, O., & Pollerberg, G. E. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2250-07.2007 · Cited by 56 · see citing works
A novel role for doublecortin and doublecortin-like kinase in regulating growth cone microtubules
Jean, D. C., Baas, P. W., & Black, M. M. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds395 · Cited by 55 · see citing works
Building Blocks of Functioning Brain: Cytoskeletal Dynamics in Neuronal Development
Menon, S., & Gupton, S. L. (2016) · International review of cytology · doi:10.1016/bs.ircmb.2015.10.002 · Cited by 55 · see citing works
Jamip1 (Marlin-1) Defines a Family of Proteins Interacting with Janus Kinases and Microtubules
Steindler, C., Li, Z., Algarté-Génin, M., Alcover, A., Libri, V., Ragimbeau, J., & Pellegrini, S. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m401915200 · Cited by 54 · see citing works
Mao, C., Xiong, Y., Xiong, Z., Wang, Q., Zhang, Y., & Jin, S. (2014) · Development · doi:10.1242/dev.097774 · Cited by 53 · see citing works
Gozes, I., Patterson, M. C., Dijck, A. V., Kooy, R. F., Peeden, J., Eichenberger, J. A., Zawacki-Downing, A., & Bedrosian‐Sermone, S. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00107 · Cited by 50 · see citing works
Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci
Hedges, D. J., Hamilton‐Nelson, K. L., Sacharow, S. J., Nations, L. D., Beecham, G. W., Kozhekbaeva, Z. M., Butler, B., Cukier, H. N., Whitehead, P. L., Ma, D., et al. (2012) · Molecular Autism · doi:10.1186/2040-2392-3-2 · Cited by 49 · see citing works
Li, L., Fothergill, T., Hutchins, B. I., Dent, E. W., & Kalil, K. (2013) · Developmental Neurobiology · doi:10.1002/dneu.22102 · Cited by 48 · see citing works
Ketschek, A., Spillane, M., Dun, X., Hardy, H., Chilton, J. K., & Gallo, G. (2016) · Developmental Neurobiology · doi:10.1002/dneu.22377 · Cited by 46 · see citing works
Berg, J. M., Lee, C., Chen, L., Galvan, L., Cepeda, C., Chen, J. Y., Peñagarikano, O., Stein, J. L., Li, A., Oguro-Ando, A., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.10.031 · Cited by 45 · see citing works
Takei, Y., Kikkawa, Y. S., Atapour, N., Hensch, T. K., & Hirokawa, N. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2671-15.2015 · Cited by 45 · see citing works
Mutation of Kinesin-6 Kif20b causes defects in cortical neuron polarization and morphogenesis
McNeely, K. C., Cupp, T. D., Little, J. N., Janisch, K. M., Shrestha, A., & Dwyer, N. D. (2017) · Neural Development · doi:10.1186/s13064-017-0082-5 · Cited by 44 · see citing works
The third wave: Intermediate filaments in the maturing nervous system
Kirkcaldie, M., & Dwyer, S. (2017) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2017.05.010 · Cited by 44 · see citing works
The Doublecortin and Doublecortin-Like Kinase 1 Genes Cooperate in Murine Hippocampal Development
Tanaka, T., Koizumi, H., & Gleeson, J. G. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhk005 · Cited by 43 · see citing works
Marx, A., Godinez, W. J., Tsimashchuk, V., Bankhead, P., Rohr, K., & Engel, U. (2013) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-08-0573 · Cited by 43 · see citing works
Bodaleo, F. J., Montenegro‐Venegas, C., Henríquez, D. R., Court, F. A., & González-Billault, C. E. (2016) · Scientific Reports · doi:10.1038/srep30069 · Cited by 42 · see citing works
A missense mutation in Katnal1 underlies behavioural, neurological and ciliary anomalies
Banks, G. T., Lassi, G., Hoerder‐Suabedissen, A., Tinarelli, F., Simon, M. M., Wilcox, A. J., Lau, P., Lawson, T. N., Johnson, S., Rutman, A., et al. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.54 · Cited by 42 · see citing works
Microtubules Modulate F-actin Dynamics during Neuronal Polarization
Zhao, B. Q., Meka, D. P., Scharrenberg, R., König, T., Schwanke, B., Kobler, O., Windhorst, S., Kreutz, M. R., Mikhaylova, M., & de Anda, F. C. (2017) · Scientific Reports · doi:10.1038/s41598-017-09832-8 · Cited by 42 · see citing works
The Compassionate Side of Neuroscience: Tony Sermone’s Undiagnosed Genetic Journey—ADNP Mutation
Gozes, I., Helsmoortel, C., Vandeweyer, G., der Aa, N. V., Kooy, R. F., & Bedrosian‐Sermone, S. (2015) · Journal of Molecular Neuroscience · doi:10.1007/s12031-015-0586-6 · Cited by 41 · see citing works
Neuronal migration defects in the Loa dynein mutant mouse
Ori-McKenney, K. M., & Vallee, R. B. (2011) · Neural Development · doi:10.1186/1749-8104-6-26 · Cited by 40 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Evidence for 28 genetic disorders discovered by combining healthcare and research data
Kaplanis, J., Samocha, K. E., Wiel, L., Zhang, Z., Arvai, K. J., Eberhardt, R. Y., Gallone, G., Lelieveld, S. H., Martin, H. C., McRae, J. F., et al. (2020) · Nature · doi:10.1038/s41586-020-2832-5 · Cited by 615 · see citing works
Hereditary Spastic Paraplegia: An Update
Meyyazhagan, A., & Orlacchio, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031697 · Cited by 171 · see citing works
Genome-wide association study identifies 48 common genetic variants associated with handedness
Cuéllar-Partida, G., Tung, J. Y., Eriksson, N., Albrecht, E., Alıev, F., Andreassen, O. A., Barroso, I., Beckmann, J. S., Boks, M. P., Boomsma, D. I., et al. (2020) · Nature Human Behaviour · doi:10.1038/s41562-020-00956-y · Cited by 155 · see citing works
Copper Toxicity Links to Pathogenesis of Alzheimer’s Disease and Therapeutics Approaches
Ijaz, H. W., Wang, W., & Lang, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21207660 · Cited by 146 · see citing works
Dell’Italia, J., Sanguinetti, J. L., Monti, M. M., Bystritsky, A., & Reggente, N. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.872639 · Cited by 115 · see citing works
Saudubray, J., & Garcia-Cazorla, A. (2018) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2018.20.4/jmsaudubray · Cited by 115 · see citing works
Carmona, A., Roudeau, S., & Ortega, R. (2021) · Toxics · doi:10.3390/toxics9090198 · Cited by 116 · see citing works
The Epigenome in Neurodevelopmental Disorders
Reichard, J., & Zimmer‐Bensch, G. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.776809 · Cited by 112 · see citing works
Towards Realizing the Vision of Precision Medicine: AI Based Prediction of Clinical Drug Response
de Jong, J., Cutcutache, I., Page, M., Elmoufti, S., Dilley, C., Fröhlich, H., & Armstrong, M. (2020) · Brain · doi:10.1093/brain/awab108 · Cited by 112 · see citing works
Triple negative breast cancer: approved treatment options and their mechanisms of action
Mandapati, A., & Lukong, K. E. (2022) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-022-04189-6 · Cited by 108 · see citing works
Willsey, H. R., Exner, C. R. T., Xu, Y., Everitt, A., Sun, N., Wang, B., Dea, J., Schmunk, G., Zaltsman, Y., Teerikorpi, N., et al. (2021) · Neuron · doi:10.1016/j.neuron.2021.01.002 · Cited by 97 · see citing works
The role of microtubules in secretory protein transport
Fourrière, L., Jiménez, A. J., Perez, F., & Boncompain, G. (2020) · Journal of Cell Science · doi:10.1242/jcs.237016 · Cited by 91 · see citing works
Germline AGO2 mutations impair RNA interference and human neurological development
Lessel, D., Zeitler, D. M., Reijnders, M. R. F., Kazantsev, A., Nia, F. H., Bartholomäus, A., Martens, V., Bruckmann, A., Graus, V., McConkie‐Rosell, A., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-19572-5 · Cited by 90 · see citing works
Synaptic Mitochondria: An Early Target of Amyloid-β and Tau in Alzheimer’s Disease
Torres, A. K., Jara, C., Park-Kang, H. S., Polanco, C. M., Tapia, D., Alarcón, F., de la Peña, A., Llanquinao, J., Vargas-Mardones, G., Álvarez‐Indo, J., et al. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-215139 · Cited by 79 · see citing works
Neurogenesis, neuronal migration, and axon guidance
Accogli, A., Addour-Boudrahem, N., & Srour, M. (2020) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64150-2.00004-6 · Cited by 72 · see citing works
The microtubule cytoskeleton at the synapse
Parato, J., & Bartolini, F. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135850 · Cited by 60 · see citing works
A novel method for generating glutamatergic SH-SY5Y neuron-like cells utilizing B-27 supplement
Martin, E.-R., Gandawijaya, J., & Oguro‐Ando, A. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.943627 · Cited by 62 · see citing works
Prem, S., Millonig, J. H., & DiCicco-Bloom, E. M. (2020) · Advances in neurobiology · doi:10.1007/978-3-030-45493-7_5 · Cited by 57 · see citing works
Ivashko‐Pachima, Y., Ganaiem, M., Ben-Horin-Hazak, I., Lobyntseva, A., Bellaiche, N., Fischer, I., Levy, G., Sragovich, S., Karmon, G., Giladi, E., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01603-w · Cited by 58 · see citing works
Excitatory‐inhibitory modulation of transcranial focus ultrasound stimulation on human motor cortex
Zhang, T., Guo, B., Zuo, Z., Long, X., Hu, S., Li, S., Su, X., Wang, Y., & Liu, C. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14303 · Cited by 55 · see citing works
The Mechanical Role of Microtubules in Tissue Remodeling
Matis, M. (2020) · BioEssays · doi:10.1002/bies.201900244 · Cited by 55 · see citing works
Mencer, S., Kartawy, M., Lendenfeld, F. V., Soluh, H., Tripathi, M. K., Халиулин, И. Г., & Amal, H. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01578-2 · Cited by 55 · see citing works
Gąssowska-Dobrowolska, M., Kolasa, A., Cieślik, M., Dominiak, A., Friedland, K., & Adamczyk, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22063209 · Cited by 45 · see citing works
Kaplanis, J., Samocha, K. E., Wiel, L., Zhang, Z., Arvai, K. J., Eberhardt, R. Y., Gallone, G., Lelieveld, S. H., Martin, H. C., McRae, J. F., et al. (2019) · doi:10.1101/797787 · Cited by 36 · see citing works
Mechanism of ribosome-associated mRNA degradation during tubulin autoregulation
Höpfler, M., Absmeier, E., Peak-Chew, S.-Y., Vartholomaiou, E., Passmore, L. A., Gasic, I., & Hegde, R. S. (2023) · Molecular Cell · doi:10.1016/j.molcel.2023.05.020 · Cited by 41 · see citing works
Liaci, C., Camera, M., Caslini, G., Rando, S., Contino, S., Romano, V., & Merlo, G. R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22116167 · Cited by 39 · see citing works
Cellular cartography: Towards an atlas of the neuronal microtubule cytoskeleton
Iwanski, M. K., & Kapitein, L. C. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1052245 · Cited by 38 · see citing works
Lorenzo, D. D. (2024) · ChemMedChem · doi:10.1002/cmdc.202400180 · Cited by 40 · see citing works
Beyond Neuronal Microtubule Stabilization: MAP6 and CRMPS, Two Converging Stories
Cuveillier, C., Boulan, B., Ravanello, C., Denarier, É., Deloulme, J., Gory‐Fauré, S., Delphin, C., Bosc, C., Arnal, I., & Andrieux, A. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.665693 · Cited by 35 · see citing works
Hu, Y., Yang, G., Liang, X.-S., Ding, X.-S., Xu, D.-E., Li, Z. Y., Ma, Q., Chen, R., & Sun, Y. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1117188 · Cited by 37 · see citing works
Taran, A., Belikova, L. D., Lagarkova, M. A., & Alieva, I. B. (2020) · Cells · doi:10.3390/cells9061514 · Cited by 35 · see citing works
Inborn errors of metabolism leading to neuronal migration defects
Schiller, S. A., Rosewich, H., Grünewald, S., & Gärtner, J. (2019) · Journal of Inherited Metabolic Disease · doi:10.1002/jimd.12194 · Cited by 37 · see citing works
Axonal mRNA translation in neurological disorders
Lin, J. Q., van Tartwijk, F. W., & Holt, C. E. (2020) · RNA Biology · doi:10.1080/15476286.2020.1822638 · Cited by 33 · see citing works
Endosomal trafficking defects in patient cells with KIAA1109 biallelic variants
Kane, M. S., Diamonstein, C. J., Hauser, N., Deeken, J. F., Niederhuber, J. E., & Vilboux, T. (2019) · Genes & Diseases · doi:10.1016/j.gendis.2018.12.004 · Cited by 32 · see citing works
Placental DNA methylation changes and the early prediction of autism in full-term newborns
Bahado-Singh, R. O., Vishweswaraiah, S., Aydas, B., & Radhakrishna, U. (2021) · PLoS ONE · doi:10.1371/journal.pone.0253340 · Cited by 32 · see citing works
Wu, Y., Stewart, A. G., & Lee, P. V. S. (2021) · Lab on a Chip · doi:10.1039/d1lc00186h · Cited by 31 · see citing works
Microtubules: A Key to Understand and Correct Neuronal Defects in CDKL5 Deficiency Disorder?
Barbiero, I., Rosa, R. D., & Kilstrup‐Nielsen, C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20174075 · Cited by 27 · see citing works
Microtubule remodelling as a driving force of axon guidance and pruning
Atkins, M., Nicol, X., & Fassier, C. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.05.030 · Cited by 30 · see citing works
Nahas, L. D., Datta, A., Alsamman, A. M., Adly, M. H., Al-Dewik, N. I. E., Sekaran, K., Sasikumar, K., Verma, K., Doss, C. G. P., & Zayed, H. (2023) · Metabolic Brain Disease · doi:10.1007/s11011-023-01322-3 · Cited by 30 · see citing works
Jurgens, J. A., Barry, B. J., Lemire, G., Chan, W. M., Whitman, M. C., Shaaban, S., Robson, C. D., MacKinnon, S. E., England, E. M., McMillan, H. J., et al. (2021) · European Journal of Human Genetics · doi:10.1038/s41431-020-00804-7 · Cited by 29 · see citing works
Pleiotropy of autism-associated chromatin regulators
Lasser, M. C., Sun, N., Xu, Y., Wang, S., Drake, S., Law, K., Gonzalez, S., Wang, B., Drury, V., Castillo, O., et al. (2023) · Development · doi:10.1242/dev.201515 · Cited by 29 · see citing works
Self-citationPresynaptic perspective: Axonal transport defects in neurodevelopmental disorders
Xiong, G.-J., & Sheng, Z. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202401145 · Cited by 26 · see citing works
Sánchez-Huertas, C., & Herrera, E. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.759404 · Cited by 28 · see citing works
Nucleating microtubules in neurons: Challenges and solutions
Lüders, J. (2020) · Developmental Neurobiology · doi:10.1002/dneu.22751 · Cited by 27 · see citing works
Kodani, A., Kenny, C. J., Lai, A., Gonzalez, D. M., Stronge, E., Sejourne, G. M., Isacco, L., Partlow, J. N., O’Donnell‐Luria, A., McWalter, K. M., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.01.030 · Cited by 27 · see citing works
Ivashko‐Pachima, Y., & Gozes, I. (2020) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2020.07.008 · Cited by 25 · see citing works
Wilkes, O. R., & Moore, A. W. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.594199 · Cited by 24 · see citing works
Recent Advances in Handedness Genetics
Paracchini, S. (2021) · Symmetry · doi:10.3390/sym13101792 · Cited by 23 · see citing works
Kulminski, A. M., Loiko, E., Loika, Y., & Culminskaya, I. V. (2021) · GeroScience · doi:10.1007/s11357-021-00484-1 · Cited by 23 · see citing works
The Many Faces of Xenopus: Xenopus laevis as a Model System to Study Wolf–Hirschhorn Syndrome
Lasser, M. C., Pratt, B. C., Monahan, C., Kim, S. W., & Lowery, L. A. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00817 · Cited by 23 · see citing works
Self-citationRaman, S. N. T., Latreille, E., Gao, J., Zhang, W., Wu, J., Russell, M. S., Walrond, L. D., Cyr, T. D., Lavoie, J. R., Safronetz, D., et al. (2020) · Emerging Microbes & Infections · doi:10.1080/22221751.2020.1818631 · Cited by 22 · see citing works
Mees, I., Tran, H., Roberts, A. M., Lago, L., Li, S., Roberts, B. R., Hannan, A. J., & Renoir, T. (2022) · Molecular Neurobiology · doi:10.1007/s12035-021-02698-y · Cited by 20 · see citing works
Bittencourt, L. O., Dionizio, A. S., Ferreira, M. K. M., Aragão, W. A. B., Cartágenes, S. D. C., Puty, B., Maia, C. D. S. F., Zohoori, F. V., Buzalaf, M. A. R., & Lima, R. R. (2023) · Scientific Reports · doi:10.1038/s41598-023-38096-8 · Cited by 20 · see citing works
βPix-d promotes tubulin acetylation and neurite outgrowth through a PAK/Stathmin1 signaling pathway
Kwon, Y., Jeon, Y., Kwon, M., Cho, Y., Park, D., & Shin, J. E. (2020) · PLoS ONE · doi:10.1371/journal.pone.0230814 · Cited by 20 · see citing works
Abraham, J. R., Barnard, J., Wang, H., Noritz, G. H., Yeganeh, M., Buhaş, D., & Natowicz, M. R. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.02.149 · Cited by 20 · see citing works
Hoff, K. J., Aiken, J., Gutierrez, M. A., Franco, S. J., & Moore, J. K. (2022) · eLife · doi:10.7554/elife.76189 · Cited by 19 · see citing works
The autophagy inducer SMER28 attenuates microtubule dynamics mediating neuroprotection
Kirchenwitz, M., Stahnke, S., Grunau, K., Melcher, L., van Ham, M., Rottner, K., Steffen, A., & Stradal, T. E. B. (2022) · Scientific Reports · doi:10.1038/s41598-022-20563-3 · Cited by 19 · see citing works
PET Imaging of [11C]MPC-6827, a Microtubule-Based Radiotracer in Non-Human Primate Brains
Damuka, N., Czoty, P. W., Davis, A., Nader, M. A., Nader, S. H., Craft, S., Macauley, S. L., Galbo, L. K., Epperly, P. M., Whitlow, C. T., et al. (2020) · Molecules · doi:10.3390/molecules25102289 · Cited by 19 · see citing works
Autism genes converge on microtubule biology and RNA-binding proteins during excitatory neurogenesisPreprint
Sun, N., Teyssier, N., Wang, B., Drake, S., Seyler, M., Zaltsman, Y., Everitt, A., Teerikorpi, N., Willsey, H. R., Goodarzi, H., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.22.573108 · Cited by 19 · see citing works
Neurodevelopmental phenotypes in individuals with pathogenic variants in CHAMP1Preprint
Garrity, M., Kavuş, H., Rojas‐Vasquez, M., Valenzuela, I., Larson, A. A., Reed, S., Bellus, G. A., Mignot, C., Münnich, A., Isidor, B., et al. (2021) · Molecular Case Studies · doi:10.1101/mcs.a006092 · Cited by 18 · see citing works
Lower plasma total tau in adolescent psychosis: Involvement of the orbitofrontal cortex
Andreou, D., Jørgensen, K. N., Nerland, S., Smelror, R. E., Wedervang‐Resell, K., Johannessen, C. H., Myhre, A. M., Andreassen, O. A., Blennow, K., Zetterberg, H., et al. (2021) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2021.10.031 · Cited by 17 · see citing works
Drastichová, Z., Hejnová, L., Trubacova, R., & Novotný, J. (2021) · Life · doi:10.3390/life11070683 · Cited by 16 · see citing works
Barbiero, I., Bianchi, M., & Kilstrup‐Nielsen, C. (2021) · Journal of Neuroendocrinology · doi:10.1111/jne.13033 · Cited by 16 · see citing works
The RNA-binding protein EIF4A3 promotes axon development by direct control of the cytoskeleton
Alsina, F. C., Lupan, B. M., Lin, L. J., Musso, C. M., Mosti, F., Newman, C. R., Wood, L. M., Suzuki, A., Agostino, M., Moore, J. K., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114666 · Cited by 15 · see citing works
Medyanik, A. D., Anisimova, P. E., Kustova, A. O., Tarabykin, V. S., & Kondakova, E. V. (2025) · Biomolecules · doi:10.3390/biom15010133 · Cited by 17 · see citing works
From the North Sea to Drug Repurposing, the Antiseizure Activity of Halimide and Plinabulin
Copmans, D., Kildgaard, S., Roux, E., Partoens, M., Steurs, G., Wang, X., Borggraeve, W. M. D., Esguerra, C. V., Crawford, A. D., Larsen, T. O., et al. (2022) · Pharmaceuticals · doi:10.3390/ph15020247 · Cited by 14 · see citing works
Structure of the Huntingtin F-actin complex reveals its role in cytoskeleton organization
Carpentier, R., Kim, J., Capizzi, M., Kim, H., Fäßler, F., Hansen, J. M., Kim, M. J., Denarier, É., Blot, B., Degennaro, M., et al. (2025) · Science Advances · doi:10.1126/sciadv.adw4124 · Cited by 13 · see citing works
Lorenzati, M., Boda, E., Parolisi, R., Bonato, M., Borsello, T., Herdegen, T., Buffo, A., & Vercelli, A. (2021) · Scientific Reports · doi:10.1038/s41598-021-86673-6 · Cited by 13 · see citing works
Establishing neuronal polarity: microtubule regulation during neurite initiation
Higgs, V. E., & Das, R. M. (2022) · Oxford Open Neuroscience · doi:10.1093/oons/kvac007 · Cited by 14 · see citing works
A critical review of the impact of candidate copy number variants on autism spectrum disorder
Abedini, S. S., Akhavantabasi, S., Liang, Y., Heng, J. I., Alizadehsani, R., Dehzangi, A., Bauer, D. C., & Alinejad‐Rokny, H. (2024) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2024.108509 · Cited by 16 · see citing works
Gholami, D., Riazi, G. H., Fathi, R., Sharafi, M., & Shahverdi, A. (2019) · BMC Molecular and Cell Biology · doi:10.1186/s12860-019-0224-1 · Cited by 13 · see citing works
Gąssowska-Dobrowolska, M., Kolasa, A., Beversdorf, D. Q., & Adamczyk, A. (2022) · Biomedicines · doi:10.3390/biomedicines10123031 · Cited by 13 · see citing works
Morozov, Y. M., Mackie, K., & RAKIC, P. T. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21228657 · Cited by 13 · see citing works
Kimura, T., Saito, H., Kawasaki, M., & Takeichi, M. (2021) · Development · doi:10.1242/dev.195073 · Cited by 13 · see citing works
Transient changes in white matter microstructure during general anesthesia
Tang, C. Y., Wang, V. X., Lun, M., Mincer, J. S., Ng, J., Brallier, J. W., Schwartz, A. E., Ahn, H., McCormick, P. J., Nir, T., et al. (2021) · PLoS ONE · doi:10.1371/journal.pone.0247678 · Cited by 13 · see citing works
Characterization of PARP6 Function in Knockout Mice and Patients with Developmental Delay
Vermehren‐Schmaedick, A., Huang, J. Y., Levinson, M., Pomaville, M. B., Reed, S., Bellus, G. A., Gilbert, F., Keren, B., Héron, D., Haye, D., et al. (2021) · Cells · doi:10.3390/cells10061289 · Cited by 13 · see citing works
Kliuchnikov, E., Klyshko, E., Kelly, M. S., Zhmurov, A. A., Dima, R. I., Marx, K. A., & Barsegov, V. A. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.01.028 · Cited by 12 · see citing works
Zocchi, R., Compagnucci, C., Bertini, E., & Sferra, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032781 · Cited by 12 · see citing works
Alvarez, J. R., Asselin, L., Tilly, P., Benoit, R., Batisse, C., Richert, L., Batisse, J., Morlet, B., Levet, F., Schwaller, N., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112744 · Cited by 12 · see citing works
Rossi, S., Barresi, S., Colafati, G. S., Genovese, S., Tancredi, C., Costabile, V., Patrizi, S. T., Giovannoni, I., Asioli, S., Poliani, P. L., et al. (2023) · Modern Pathology · doi:10.1016/j.modpat.2023.100387 · Cited by 12 · see citing works
Butto, T., Chongtham, M. C., Mungikar, K., Hartwich, D., Linke, M., Ruffini, N., Radyushkin, K., Schweiger, S., Winter, J., & Gerber, S. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02555-z · Cited by 10 · see citing works
McInerney, C. E., Lynn, J. A., Gilmore, A. R., Flannery, T., & Prise, K. M. (2022) · Current Issues in Molecular Biology · doi:10.3390/cimb44070206 · Cited by 12 · see citing works
Anderson, A. M. L., Ma, Q., Letendre, S. L., & Iudicello, J. E. (2021) · Current HIV/AIDS Reports · doi:10.1007/s11904-021-00581-y · Cited by 12 · see citing works
Cullin-RING E3 ubiquitin ligase 4 regulates neurite morphogenesis during neurodevelopment
Shim, T., Kim, J. Y., Kim, W.-C., Lee, Y., Cho, B., & Moon, C. (2024) · iScience · doi:10.1016/j.isci.2024.108933 · Cited by 10 · see citing works
Disease-associated mutations in human TUBB3 disturb netrin repulsive signaling
Shao, Q., Yang, T., Huang, H., Majumder, T., Khot, B., Khouzani, M. M., Alarmanazi, F., Gore, Y. K., & Liu, G. (2019) · PLoS ONE · doi:10.1371/journal.pone.0218811 · Cited by 11 · see citing works
Alachkar, A. (2022) · Physics of Life Reviews · doi:10.1016/j.plrev.2022.07.002 · Cited by 12 · see citing works
Zocchi, R., Bellacchio, E., Piccione, M., Scardigli, R., Doria, V., Petrini, S., Baranano, K. W., Bertini, E., & Sferra, A. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1162363 · Cited by 11 · see citing works
Barman, S., Das, G., Mondal, P., Pradhan, K., Bhunia, D., Khan, J., Kar, C., & Ghosh, S. (2018) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.8b00497 · Cited by 11 · see citing works
Ashitha, S. N. M., & Ramachandra, N. B. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.04.051 · Cited by 10 · see citing works
Gąssowska-Dobrowolska, M., Czapski, G. A., Cieślik, M., Zajdel, K., Frontczak-Baniewicz, M., Babiec, L., & Adamczyk, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24087303 · Cited by 10 · see citing works
TUBB3 M323V Syndrome Presents with Infantile Nystagmus
Jin, S., Park, S.-E., Won, D., Lee, S., Han, S., & Han, J. (2021) · Genes · doi:10.3390/genes12040575 · Cited by 10 · see citing works
Suciu, I., Delp, J., Gutbier, S., Suess, J., Henschke, L., Celardo, I., Mayer, T. U., Amelio, I., & Leist, M. (2023) · Antioxidants · doi:10.3390/antiox13010049 · Cited by 12 · see citing works
Yousefzadeh, S. A., Jarah, M., & Riazi, G. H. (2020) · Journal of Molecular Neuroscience · doi:10.1007/s12031-019-01457-y · Cited by 10 · see citing works
Drongitis, D., Caterino, M., Verrillo, L., Santonicola, P., Costanzo, M., Poeta, L., Attianese, B., Barra, A., Terrone, G., Lioi, M. B., et al. (2022) · Human Molecular Genetics · doi:10.1093/hmg/ddac028 · Cited by 10 · see citing works
Akrioti, E.-K., Karamitros, T., Gkaravelas, P., Kouroupi, G., Matsas, R., & Taoufik, E. (2022) · Biomolecules · doi:10.3390/biom12070876 · Cited by 10 · see citing works
Chou, V., Johnson, S. A., Long, J. B., Vounatsos, M. V., & Vactor, D. V. (2019) · Cytoskeleton · doi:10.1002/cm.21578 · Cited by 7 · see citing works
Bhoopal, B., Gollapelli, K. K., Damuka, N., Miller, M. D., Krizan, I. M., Bansode, A. H., Register, T. C., Frye, B. M., Kim, J., Mintz, A., et al. (2023) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.3c00527 · Cited by 9 · see citing works
Martín-Guerrero, S. M., Martín‐Estebané, M., Ordóñez, A. J. L., Cánovas, M., Martín‐Oliva, D., González‐Maeso, J., Cutillas, P. R., & López‐Giménez, J. F. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-02905-5 · Cited by 9 · see citing works
Spatial and Temporal Single-Cell Profiling of RNA Compartmentalization in Neurons with Nanotweezers
Sahota, A., Nadappuram, B. P., Kwan, Z., Lesept, F., Howden, J. H., Claxton, S., Kittler, J. T., Devine, M. J., Edel, J. B., & Ivanov, A. P. (2025) · ACS Nano · doi:10.1021/acsnano.5c02056 · Cited by 9 · see citing works
Polyglutamylation of microtubules drives neuronal remodeling
Gavoci, A., Zhiti, A., Rusková, M., Magiera, M. M., Wang, M., Ziegler, K. A., Hausrat, T. J., Ugwuja, A. I., Chakraborty, S., Engelhardt, S. H., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60855-6 · Cited by 10 · see citing works
- Authors
- Lasser, M., Tiber, J., & Lowery, L. A.
- Affiliations
- Boston College (US)
- Corresponding author
- Lowery, Laura Anne
- Venue
- Frontiers in Cellular Neuroscience
- Publisher
- Frontiers Media SA
- Published
- 2018-06-14
- Volume
- 12
- Pages
- 165-165
- ISSN
- 1662-5102 (ISSN-L)
- PMC
- PMC6010848
- OpenAlex
- W2806503585
- Cited by
- 201
- References
- 219
- Citations by year
- 2026: 15 · 2025: 22 · 2024: 24 · 2023: 30 · 2022: 32 · 2021: 35 · 2020: 29 · 2019: 12 · 2018: 2
- FWCI
- 2.18
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Frontiers in Cellular Neuroscience (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Institutes of Health (R01 MH109651, R01 GM121907)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- microtubule cytoskeleton, neurodevelopmental disorders, neuronal migration, intellectual disability, autism spectrum disorder, genetic mutations, axon guidance, synaptogenesis, neuronal connectivity, intracellular trafficking
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review