The DOI matches its Crossref record; 162 of the 162 references it cites were found in a registry or an index.
Branching out: mechanisms of dendritic arborization
Open accessAbstract
Type-specific dendrite morphology is a hallmark of the neuron and has important functional implications in determining what signals a neuron receives and how these signals are integrated. During the past two decades, studies on dendritic arborization neurons in Drosophila melanogaster have started to identify mechanisms of dendrite morphogenesis that may have broad applicability to vertebrate species. Transcription factors, receptor-ligand interactions, various signalling pathways, local translational machinery, cytoskeletal elements, Golgi outposts and endosomes have been identified as contributors to the organization of dendrites of individual neurons and the placement of these dendrites in the neuronal circuitry. Further insight into these mechanisms will improve our understanding of how the nervous system functions and might help to identify the underlying causes of some neurological and neurodevelopmental disorders.
Overview
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
Verification
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Dendritic morphogenesis, synaptogenesis and continued activity-dependent remodelling of synaptic connections are critical for the development and maintenance of functional neuronal networks.11, 12, 13, 14, 15”
From The autism and schizophrenia associated gene CYFIP1 is critical for the maintenance of dendritic complexity and the stabilization of mature spines (2014) · cites this paper as [11]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
RHO GTPASES: Biochemistry and Biology
Jaffe, A. B., & Hall, A. (2005) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.21.020604.150721 · Cited by 3,009 · cited 1×
“These small GTPases also influence the dynamics and plus-end capture of microtubule”
BackgroundLee, T., & Luo, L. (1999) · Neuron · doi:10.1016/s0896-6273(00)80701-1 · Cited by 2,540 · cited 1×
“dar5 encodes a transferin-like factor and functions non-cell autonomously, whereas the other four function cell autonomously and regulate dendrite growth, as determined by studies using MARCM (mosaic analysis with a repressible cell marker”
Experience-dependent structural synaptic plasticity in the mammalian brain
Holtmaat, A., & Svoboda, K. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2699 · Cited by 1,934 · cited 1×
“, and NMDA ( N -methyl- D -aspartate) receptor-mediated signalling that affects dendrite organization in the somatosensory cortex during development and in the mature nervous syste”
BackgroundAdvances in autism genetics: on the threshold of a new neurobiology
Abrahams, B. S., & Geschwind, D. H. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2346 · Cited by 1,866
Pyramidal neurons: dendritic structure and synaptic integration
Spruston, N. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2286 · Cited by 1,688 · cited 1×
“Second, the branching pattern and density of dendrites must be suitable for sampling and processing the signals that converge onto the dendritic fiel”
BackgroundIntellectual ability and cortical development in children and adolescents
Shaw, P., Greenstein, D., Lerch, J., Clasen, L., Lenroot, R., Gogtay, N., Evans, A., Rapoport, J., & Giedd, J. (2006) · Nature · doi:10.1038/nature04513 · Cited by 1,543
Long-term dendritic spine stability in the adult cortex
Grutzendler, J., Kasthuri, N., & Gan, W.-B. (2002) · Nature · doi:10.1038/nature01276 · Cited by 1,198 · cited 1×
“Extended time-lapse analyses of mouse cortical neurons have revealed that, following a period of juvenile plasticity during which neurons establish normal dendritic fields, dendrites become stable with most neurons maintaining their dendritic fields for the remainder of their lifespa”
BackgroundDrosophila Dscam Is an Axon Guidance Receptor Exhibiting Extraordinary Molecular Diversity
Schmucker, D., Clemens, J. C., Shu, H., Worby, C. A., Xiao, J. Y., Muda, M., Dixon, J. E., & Zipursky, S. L. (2000) · Cell · doi:10.1016/s0092-8674(00)80878-8 · Cited by 1,105 · cited 1×
“Extensive alternative splicing can potentially generate over 38,000 isoform”
BackgroundFunctional architecture of the mammalian retina
Wässle, H., & Boycott, B. B. (1991) · Physiological Reviews · doi:10.1152/physrev.1991.71.2.447 · Cited by 1,093 · cited 1×
“First, a neuron's dendrites need to cover the area (its dendritic field ) that encompasses its sensory and/or synaptic input”
BackgroundNeuregulin 1 in neural development, synaptic plasticity and schizophrenia
Mei, L., & Xiong, W.-C. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2392 · Cited by 1,030
Neurotrophins regulate dendritic growth in developing visual cortex
McAllister, A. K., Lo, D. C., & Katz, L. C. (1995) · Neuron · doi:10.1016/0896-6273(95)90171-x · Cited by 959 · cited 1×
“org/uniprot/P23560">BDNF ) and nerve growth factor (NGF) influence the dendrite morphology of cortical neuron”
BackgroundBI-DIRECTIONAL PROTEIN TRANSPORT BETWEEN THE ER AND GOLGI
Lee, M. C. S., Miller, E. A., Goldberg, J., Orci, L., & Schekman, R. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.010403.105307 · Cited by 813 · cited 1×
“The three proteins encoded by these genes are crucial regulators of endoplasmic reticulum (ER) to Golgi transport mediated by coat protein complex II vesicle”
BackgroundThe many faces of actin: matching assembly factors with cellular structures
Chhabra, E. S., & Higgs, H. N. (2007) · Nature Cell Biology · doi:10.1038/ncb1007-1110 · Cited by 779 · cited 1×
“RAC1 and CDC42 activate the Arp2/3 complex, which binds to existing actin filaments and nucleates branched growth, whereas RHOA activates formins that mediate unbranched actin filament extensio”
BackgroundDendritic Anomalies in Disorders Associated with Mental Retardation
Kaufmann, W. E. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.10.981 · Cited by 746
Baas, P. W., Deitch, J. S., Black, M. M., & Banker, G. A. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.21.8335 · Cited by 742
Reduced dendritic spine density on cerebral cortical pyramidal neurons in schizophrenia
Garey, L. J., Ong, W., Patel, T. S., Kanani, M., Davis, A., Mortimer, A. M., Barnes, T., & Hirsch, S. R. (1998) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.65.4.446 · Cited by 719
Craig, A. M., & Banker, G. A. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.001411 · Cited by 704
Hippo signaling in organ size controlPreprint
Pan, D. (2007) · Genes & Development · doi:10.1101/gad.1536007 · Cited by 665 · cited 1×
“Hippo , a kinase of the STE20 family, is a major regulator of organ size in flies and mammal”
BackgroundActin Cytoskeleton Regulation in Neuronal Morphogenesis and Structural Plasticity
Luo, L. (2002) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.18.031802.150501 · Cited by 658
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 · cited 1×
“Third, dendrites need to have the flexibility for adjustment in development and in response to experience — as indicated, for example, by dynamic microtubule invasion of spine”
BackgroundBourgeron, T. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.06.003 · Cited by 637
Activity-dependent regulation of dendritic growth and patterning
Wong, R. O. L., & Ghosh, A. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn941 · Cited by 635 · cited 1×
“Presynaptic inputs and neuronal activity probably also influence dendrite morphogenesis — a topic that is outside the scope of this article, and reviewed elsewher”
BackgroundA genome-wide linkage and association scan reveals novel loci for autism
The Gene Discovery Project of Johns Hopkins & the Autism Consortium, Weiss, L. A., & Arking, D. E. (2009) · Nature · doi:10.1038/nature08490 · Cited by 619
Molecular mechanisms of dendritic spine morphogenesis
Tada, T., & Sheng, M. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.12.001 · Cited by 615 · cited 1×
“RHOA has opposing effects to the small GTPases RAS-related C3 botulinum toxin substrate 1 ( RAC1 ) and CDC42 in controlling the growth and stability of actin-rich spines in mammalian neuron”
BackgroundThe Autistic Neuron: Troubled Translation?
Kelleher, R. J., & Bear, M. F. (2008) · Cell · doi:10.1016/j.cell.2008.10.017 · Cited by 598
Compartmentalized dendritic plasticity and input feature storage in neurons
Losonczy, A., Makara, J. K., & Magee, J. C. (2008) · Nature · doi:10.1038/nature06725 · Cited by 598 · cited 1×
“Second, the branching pattern and density of dendrites must be suitable for sampling and processing the signals that converge onto the dendritic fiel”
BackgroundJaworski, J., Spangler, S. A., Seeburg, D. P., Hoogenraad, C. C., & Sheng, M. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2270-05.2005 · Cited by 597
Regulation of Dendritic Morphogenesis by Ras–PI3K–Akt–mTOR and Ras–MAPK Signaling Pathways
Kumar, V., Zhang, M.-X., Swank, M. W., Kunz, J., & Wu, G.-Y. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2284-05.2005 · Cited by 588
Tiling of theDrosophilaepidermis by multidendritic sensory neurons
Grueber, W. B., Jan, L. Y., & Jan, Y. N. (2002) · Development · doi:10.1242/dev.129.12.2867 · Cited by 580
Self-citationOpposing Roles for Endogenous BDNF and NT-3 in Regulating Cortical Dendritic Growth
McAllister, A. K., Katz, L. C., & Lo, D. C. (1997) · Neuron · doi:10.1016/s0896-6273(00)80316-5 · Cited by 570 · cited 1×
“The same neurotrophic factor can either inhibit or promote dendrite outgrowth in cortical slices, depending on the neuronal typ”
BackgroundHistology of the nervous system of man and vertebrates
y Cajal, S. R. (1995) · Cited by 553
Pardo, C. A., & Eberhart, C. G. (2007) · Brain Pathology · doi:10.1111/j.1750-3639.2007.00102.x · Cited by 514
Neurogenesis in adult primate neocortex: an evaluation of the evidence
RAKIC, P. T. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn700 · Cited by 494
Wnt signaling through Dishevelled, Rac and JNK regulates dendritic development
Rosso, S. B., Sussman, D., Wynshaw-Boris, A., & Salinas, P. C. (2005) · Nature Neuroscience · doi:10.1038/nn1374 · Cited by 485
From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome
Bagni, C., & Greenough, W. T. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1667 · Cited by 475
Extreme Diversity among Amacrine Cells: Implications for Function
MacNeil, M. A., & Masland, R. H. (1998) · Neuron · doi:10.1016/s0896-6273(00)80478-x · Cited by 472 · cited 1×
“First, a neuron's dendrites need to cover the area (its dendritic field ) that encompasses its sensory and/or synaptic input”
BackgroundWayman, G. A., Impey, S., Marks, D., Saneyoshi, T., Grant, W. F., Derkach, V., & Soderling, T. R. (2006) · Neuron · doi:10.1016/j.neuron.2006.05.008 · Cited by 466
Calcium Regulation of Dendritic Growth via CaM Kinase IV and CREB-Mediated Transcription
Redmond, L., Kashani, A. H., & Ghosh, A. (2002) · Neuron · doi:10.1016/s0896-6273(02)00737-7 · Cited by 462
β-catenin is critical for dendritic morphogenesis
Yu, X., & Malenka, R. C. (2003) · Nature Neuroscience · doi:10.1038/nn1132 · Cited by 459
Polarized Secretory Trafficking Directs Cargo for Asymmetric Dendrite Growth and Morphogenesis
Horton, A. C., Rácz, B., Monson, E. E., Lin, A. L., Weinberg, R. J., & Ehlers, M. (2005) · Neuron · doi:10.1016/j.neuron.2005.11.005 · Cited by 440 · cited 1×
“is important for dendrite arborization of both vertebrate and invertebrate neuron”
BackgroundDindot, S. V., Antalffy, B. A., Bhattacharjee, M. B., & Beaudet, A. L. (2007) · Human Molecular Genetics · doi:10.1093/hmg/ddm288 · Cited by 418
Choice of cranial window type for in vivo imaging affects dendritic spine turnover in the cortex
Xu, H., Pan, F., Yang, G., & Gan, W. (2007) · Nature Neuroscience · doi:10.1038/nn1883 · Cited by 412 · cited 1×
“Extended time-lapse analyses of mouse cortical neurons have revealed that, following a period of juvenile plasticity during which neurons establish normal dendritic fields, dendrites become stable with most neurons maintaining their dendritic fields for the remainder of their lifespa”
BackgroundFailure of neuronal homeostasis results in common neuropsychiatric phenotypes
Ramocki, M. B., & Zoghbi, H. Y. (2008) · Nature · doi:10.1038/nature07457 · Cited by 399
Regulation of Dendritic Development by Neuron-Specific Chromatin Remodeling Complexes
Wu, J. I., Lessard, J. A., Olave, I. A., Qiu, Z., Ghosh, A., Graef, I. A., & Crabtree, G. R. (2007) · Neuron · doi:10.1016/j.neuron.2007.08.021 · Cited by 398 · cited 1×
“, is physically associated with the neuron-specific BRG1-associated factor (nBAF) chromatin remodelling complexes that distinguish neurons from neural progenitor”
BackgroundCyclic AMP/GMP-dependent modulation of Ca2+ channels sets the polarity of nerve growth-cone turning
Nishiyama, M., Hoshino, A., Tsai, L., Henley, J. R., Goshima, Y., Tessier‐Lavigne, M., Poo, M.-M., & Hong, K. (2003) · Nature · doi:10.1038/nature01751 · Cited by 387 · cited 1×
“In vertebrates, the secreted form of semaphorins that are the ligands for the Plexin–Neuropilin receptors can be either chemorepellent or chemoattractant in axon guidanc”
BackgroundStochastic spineless expression creates the retinal mosaic for colour vision
Wernet, M. F., Mazzoni, E. O., Çelik, A., Duncan, D. M., Duncan, I., & Desplan, C. (2006) · Nature · doi:10.1038/nature04615 · Cited by 383 · cited 1×
“Spineless might allow dendritic arborization neurons to take on specific dendrite patterns as dictated by other transcription factors and signalling molecules, perhaps analogously to its ability to endow alternative cell fat”
BackgroundGrowing Dendrites and Axons Differ in Their Reliance on the Secretory Pathway
Ye, B., Zhang, Y., Song, W., Younger, S. H., Jan, L. Y., & Jan, Y. N. (2007) · Cell · doi:10.1016/j.cell.2007.06.032 · Cited by 381
Self-citationDscam and Sidekick proteins direct lamina-specific synaptic connections in vertebrate retina
Yamagata, M., & Sanes, J. R. (2008) · Nature · doi:10.1038/nature06469 · Cited by 379 · cited 1×
“DSCAM not only mediates homotypic repulsion but also homotypic adhesion, such as controlling the layer-specific synapse formation in the chick retin”
BackgroundCdh1-APC Controls Axonal Growth and Patterning in the Mammalian Brain
Konishi, Y., Stegmüller, J., Matsuda, T., Bonni, S., & Bonni, A. (2004) · Science · doi:10.1126/science.1093712 · Cited by 363
Hand, R., Bortone, D. S., Mattar, P. A., Nguyen, L., Heng, J. I., Guerrier, S., Boutt, E., Peters, E. C., Barnes, A. P., Parras, C. M., et al. (2005) · Neuron · doi:10.1016/j.neuron.2005.08.032 · Cited by 363 · cited 1×
“The basic helix–loop–helix (bHLH) transcription factor Neurogenin 2 has a crucial role in the specification of dendrite morphology of pyramidal neurons in the neocortex: it promotes the outgrowth of a polarized leading process during the initiation of radial migratio”
BackgroundRho GTPases, dendritic structure, and mental retardation
Newey, S. E., Velamoor, V., Govek, E., & Van Aelst, L. (2005) · Journal of Neurobiology · doi:10.1002/neu.20153 · Cited by 351
Dendrite Self-Avoidance Is Controlled by Dscam
Matthews, B. J., Kim, M. E., Flanagan, J. J., Hattori, D., Clemens, J. C., Zipursky, S. L., & Grueber, W. B. (2007) · Cell · doi:10.1016/j.cell.2007.04.013 · Cited by 351 · cited 1×
“As neighbouring neurons are unlikely to express the same set of DSCAM isoform”
BackgroundEvidence for dendritic competition in the developing retina
Perry, V. H., & Linden, R. (1982) · Nature · doi:10.1038/297683a0 · Cited by 343
Rac GTPases control axon growth, guidance and branching
Ng, J., Nardine, T. M., Harms, M. B., Tzu, J., Goldstein, A. Y. N., Sun, Y., Dietzl, G., Dickson, B. J., & Luo, L. (2002) · Nature · doi:10.1038/416442a · Cited by 340 · cited 1×
“By contrast, loss of all three Rac homologues in central neurons of the mushroom body causes a reduction of dendrite size and complexit”
BackgroundWojtowicz, W. M., Flanagan, J. J., Millard, S. S., Zipursky, S. L., & Clemens, J. C. (2004) · Cell · doi:10.1016/j.cell.2004.08.021 · Cited by 332 · cited 1×
“The stochastic expression of a small subset of DSCAM isoforms in each neuron mediates neurite self-recognition by isoform-specific homophilic bindin”
BackgroundNeuronal diversity in the retina
Masland, R. H. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00230-0 · Cited by 330 · cited 1×
“and the more than 50 types of neurons in the mammalian retin”
BackgroundGrueber, W. B., Jan, L. Y., & Jan, Y. N. (2003) · Cell · doi:10.1016/s0092-8674(03)00160-0 · Cited by 315
Self-citationActivity-Dependent Dynamic Microtubule Invasion of Dendritic Spines
Hu, X., Viesselmann, C., Nam, S., Merriam, E. B., & Dent, E. W. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3074-08.2008 · Cited by 299 · cited 1×
“Third, dendrites need to have the flexibility for adjustment in development and in response to experience — as indicated, for example, by dynamic microtubule invasion of spine”
BackgroundDendritic territories of cat retinal ganglion cells
Wässle, H., Peichl, L., & Boycott, B. B. (1981) · Nature · doi:10.1038/292344a0 · Cited by 297
Dendritic spine formation and stabilization
Yoshihara, Y., De Roo, M., & Muller, D. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.05.013 · Cited by 292
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 · cited 1×
“In addition, motors that mediate the transport of building blocks and organelles to dendrites are crucial for dendrite morpholog”
BackgroundSelf-citationLee, T., Winter, C. G., Marticke, S., Lee, A. M., & Luo, L. (2000) · Neuron · doi:10.1016/s0896-6273(00)80896-x · Cited by 287 · cited 1×
“melanogaster , RHOA mutant clones display excessive dendrite extensio”
BackgroundDendrite Development Regulated by CREST, a Calcium-Regulated Transcriptional Activator
Aizawa, H., Hu, S., Bobb, K., Balakrishnan, K., Ince-Dunn, G., Gurevich, I., Cowan, M., & Ghosh, A. (2004) · Science · doi:10.1126/science.1089845 · Cited by 282 · cited 1×
“, as well as Ca 2+ -responsive transactivator (CREST”
BackgroundNeurite arborization and mosaic spacing in the mouse retina require DSCAM
Fuerst, P. G., Koizumi, A., Masland, R. H., & Burgess, R. W. (2008) · Nature · doi:10.1038/nature06514 · Cited by 281 · cited 1×
“melanogaster Down syndrome cell adhesion molecule ( DSCAM ) splice variants and the stochastic expression of a small subset of such isoforms in each dendritic arborization neuron ensure self-avoidance without compromising coexistence; mammalian DSCAM also mediates self-avoidance, indicating conservation of the functio…”
BackgroundGrueber, W. B., Ye, B., Moore, A. W., Jan, L. Y., & Jan, Y. N. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00207-0 · Cited by 274 · cited 1×
“Furthermore, dendrites of different neuronal types can cover the same region (coexistence”
BackgroundSelf-citationPetanjek, Z., Judas, M., Kostovic, I., & Uylings, H. B. M. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm124 · Cited by 273
Plasma membrane expansion: a neuron's Herculean task
Pfenninger, K. H. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2593 · Cited by 268 · cited 1×
“melanogaster dendritic arborization neurons and cultured hippocampal neurons, Golgi outposts reside in dendrites but not in axons and are often found at branch points of dendritic arbor”
BackgroundDSCAM Is a Netrin Receptor that Collaborates with DCC in Mediating Turning Responses to Netrin-1
Ly, A., Nikolaev, A. Y., Suresh, G., Zheng, Y., Tessier‐Lavigne, M., & Stein, E. (2008) · Cell · doi:10.1016/j.cell.2008.05.030 · Cited by 265
Homophilic Dscam Interactions Control Complex Dendrite Morphogenesis
Hughes, M. E., Bortnick, R., Tsubouchi, A., Bäumer, P., Kondo, M., Uemura, T., & Schmucker, D. (2007) · Neuron · doi:10.1016/j.neuron.2007.04.013 · Cited by 261 · cited 1×
“As neighbouring neurons are unlikely to express the same set of DSCAM isoform”
BackgroundGeometric and functional organization of cortical circuits
Shepherd, G. M., Stepanyants, A., Bureau, I., Chklovskii, D. B., & Svoboda, K. (2005) · Nature Neuroscience · doi:10.1038/nn1447 · Cited by 259 · cited 1×
“Physiological requirements of dendrite patterns A balance between the metabolic costs of dendrite elaboration and the need to cover the receptive field presumably determines the size and shape of dendrite”
BackgroundSoba, P., Zhu, S., Emoto, K., Younger, S. H., Yang, S.-J., Yu, H., Lee, T., Jan, L. Y., & Jan, Y. N. (2007) · Neuron · doi:10.1016/j.neuron.2007.03.029 · Cited by 258 · cited 1×
“As neighbouring neurons are unlikely to express the same set of DSCAM isoform”
BackgroundSelf-citationMechanisms that Regulate Establishment, Maintenance, and Remodeling of Dendritic Fields
Parrish, J. Z., Emoto, K., Kim, M. D., & Jan, Y. N. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112907 · Cited by 255 · cited 1×
“melanogaster larval peripheral nervous system (PNS) acquire their distinct dendrite morpholog”
BackgroundSelf-citationA CaMKII-NeuroD Signaling Pathway Specifies Dendritic Morphogenesis
Gaudilliere, B. L., Konishi, Y., de la Iglesia, N., Yao, G.-L., & Bonni, A. (2004) · Neuron · doi:10.1016/s0896-6273(03)00841-9 · Cited by 245 · cited 1×
“In addition, neuronal activity-dependent dendrite development is under the control of the bHLH transcription factor termed neurogenic differentiation factor 1 ( NEUROD1”
BackgroundCalcium Signaling and the Control of Dendritic Development
Konur, S., & Ghosh, A. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.022 · Cited by 245
Osteogenic protein-1 induces dendritic growth in rat sympathetic neurons
Lein, P. J., Johnson, M. I., Guo, X., Rueger, D. C., & Higgins, D. M. (1995) · Neuron · doi:10.1016/0896-6273(95)90148-5 · Cited by 239 · cited 1×
“Dendrite arborization of cultured sympathetic neurons can also be modulated by bone morphogenetic proteins in conjunction with NG”
BackgroundEmoto, K., He, Y., Ye, B., Grueber, W. B., Adler, P. N., Jan, L. Y., & Jan, Y.-N. (2004) · Cell · doi:10.1016/j.cell.2004.09.036 · Cited by 235 · cited 1×
“melanogaster dendritic arborization neurons remain largely unknown, two intracellular signalling molecules were identified several years ago: Tricornered ( TRC ), a kinase of the NDR family; and a positive regulator of TRC encoded by the furry ( fry ) gen”
BackgroundSelf-citationJossin, Y., & Goffinet, A. M. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.00928-07 · Cited by 235
GRIP1 controls dendrite morphogenesis by regulating EphB receptor trafficking
Hoogenraad, C. C., Milstein, A. D., Ethell, I. M., Henkemeyer, M. J., & Sheng, M. (2005) · Nature Neuroscience · doi:10.1038/nn1487 · Cited by 233 · cited 1×
“Another multi-PDZ domain scaffold protein located within the PSD, glutamate receptor interaction protein 1 (GRIP1), functions as an adaptor for the microtubule-based motor kinesin-related protein 5 to facilitate trafficking of the receptor tyrosine kinase ephrin type B receptor 2 (Ref”
BackgroundLee, A., Li, W., Xu, K., Bogert, B. A., Su, K., & Gao, F. (2003) · Development · doi:10.1242/dev.00792 · Cited by 233 · cited 1×
“In larval class IV dendritic arborization neurons, RAC1 (Ref”
BackgroundDevelopment of Continuous and Discrete Neural Maps
Luo, L., & Flanagan, J. G. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.014 · Cited by 232 · cited 1×
“melanogaster antennal lobe, Semaphorin 1A ( SEMA1A ) is expressed in a graded fashion along the dendrites of projection neurons and functions as a receptor for an as yet unknown ligand that targets these dendrites to the appropriate glomerul”
BackgroundDSCAM and DSCAML1 Function in Self-Avoidance in Multiple Cell Types in the Developing Mouse Retina
Fuerst, P. G., Bruce, F. M., Tian, M., Wei, W., Elstrott, J., Feller, M. B., Erskine, L., Singer, J. H., & Burgess, R. W. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.027 · Cited by 229 · cited 1×
“melanogaster DSCAM, both mouse homologues play a part in self-avoidanc”
BackgroundSpatial control of branching within dendritic arbors by dynein-dependent transport of Rab5-endosomes
Satoh, D., Sato, D., Tsuyama, T., Saito, M., Ohkura, H., Rolls, M. M., Ishikawa, F., & Uemura, T. (2008) · Nature Cell Biology · doi:10.1038/ncb1776 · Cited by 210
Dscam-Mediated Cell Recognition Regulates Neural Circuit Formation
Hattori, D., Millard, S. S., Wojtowicz, W. M., & Zipursky, S. L. (2008) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.24.110707.175250 · Cited by 205 · cited 1×
“DSCAMs also have a role in circuit formation that is discussed in several recent review”
BackgroundNanos and Pumilio are essential for dendrite morphogenesis in Drosophila peripheral neurons.
Ye, B., Petritsch, C., Clark, I. E., Gavis, E. R., Jan, L., & Jan, Y. (2004) · Current Biology · doi:10.1016/j.cub.2004.01.052 · Cited by 205
Self-citationDrosophila Lis1 is required for neuroblast proliferation, dendritic elaboration and axonal transport
Liu, Z., Steward, R., & Luo, L. (2000) · Nature Cell Biology · doi:10.1038/35041011 · Cited by 203
Wang, J., Zugates, C. T., Liang, I. H., Lee, C.-H. J., & Lee, T. (2002) · Neuron · doi:10.1016/s0896-6273(02)00570-6 · Cited by 202 · cited 1×
“melanogaster neurons including mushroom body neuron”
Walsh, C. A., Morrow, E. M., & Rubenstein, J. L. R. (2008) · Cell · doi:10.1016/j.cell.2008.10.015 · Cited by 198
The tumour suppressor Hippo acts with the NDR kinases in dendritic tiling and maintenance.
Emoto, K., Parrish, J. Z., Jan, L. Y., & Jan, Y.-N. (2006) · Nature · doi:10.1038/nature05090 · Cited by 194 · cited 1×
“Moreover, trans-heterozygous flies carrying one mutant copy of a PcG gene and one mutant copy of a Hippo core complex gene display the same dendrite phenotype: the dendrites initially grow and tile normally, but the dendritic fields are not maintained, leading to progressive loss of dendrite branches and large gaps in…”
BackgroundSelf-citationParrish, J. Z., Kim, M. D., Jan, L. Y., & Jan, Y. N. (2006) · Genes & Development · doi:10.1101/gad.1391006 · Cited by 192
Self-citationA Centrosomal Cdc20-APC Pathway Controls Dendrite Morphogenesis in Postmitotic Neurons
Kim, A. H., Puram, S. V., Bilimoria, P. M., Ikeuchi, Y., Keough, S., Wong, M., Rowitch, D. H., & Bonni, A. (2009) · Cell · doi:10.1016/j.cell.2008.11.050 · Cited by 190
Jinushi-Nakao, S., Arvind, R., Amikura, R. M., Kinameri, E., Liu, A. W., & Moore, A. W. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.031 · Cited by 189
Dscam and DSCAM: complex genes in simple animals, complex animals yet simple genesPreprint
Schmucker, D., & Chen, B. (2009) · Genes & Development · doi:10.1101/gad.1752909 · Cited by 188 · cited 1×
“DSCAMs also have a role in circuit formation that is discussed in several recent review”
BackgroundRegulation of Dendritic Branching and Spine Maturation by Semaphorin3A-Fyn Signaling
Morita, A., Yamashita, N., Sasaki, Y., Uchida, Y., Nakajima, O., Nakamura, F., Yagi, T., Taniguchi, M., Usui, H., Katoh‐Semba, R., et al. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5453-05.2006 · Cited by 178 · cited 1×
“For example, the secreted ligand SEMA3A promotes dendrite branching and spine maturation in mouse cortical neuron”
BackgroundDendritic patterning by Dscam and synaptic partner matching in the Drosophila antennal lobe
Zhu, H., Hummel, T., Clemens, J. C., Berdnik, D., Zipursky, S. L., & Luo, L. (2006) · Nature Neuroscience · doi:10.1038/nn1652 · Cited by 175
Embryonic Origins of a Motor System: Motor Dendrites Form a Myotopic Map in Drosophila
Landgraf, M., Jeffrey, V., Fujioka, M., Jaynes, J. B., & Bate, M. (2003) · PLoS Biology · doi:10.1371/journal.pbio.0000041 · Cited by 173
Dijkhuizen, P., & Ghosh, A. (2005) · Journal of Neurobiology · doi:10.1002/neu.20100 · Cited by 171
Uncoupling Dendrite Growth and Patterning: Single-Cell Knockout Analysis of NMDA Receptor 2B
Espinosa, J. S., Wheeler, D. G., Tsien, R. W., & Luo, L. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.006 · Cited by 171
Komiyama, T., Sweeney, L. B., Schuldiner, O., García, K. C., & Luo, L. (2007) · Cell · doi:10.1016/j.cell.2006.12.028 · Cited by 170 · cited 1×
“melanogaster antennal lobe, Semaphorin 1A ( SEMA1A ) is expressed in a graded fashion along the dendrites of projection neurons and functions as a receptor for an as yet unknown ligand that targets these dendrites to the appropriate glomerul”
BackgroundLissencephaly and LIS1: insights into the molecular mechanisms of neuronal migration and development
Wynshaw-Boris, A. J. (2007) · Clinical Genetics · doi:10.1111/j.1399-0004.2007.00888.x · Cited by 169
Lin, B., Wang, S. W., & Masland, R. H. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.002 · Cited by 167 · cited 1×
“Nonetheless, the remaining neurons are regularly spaced and normal dendrite size is maintained in the absence of dendrite–dendrite contact of neurons of the same type, suggesting that homotypic repulsion is not required for tilin”
BackgroundParrish, J. Z., Xu, P., Kim, C. C., Jan, L. Y., & Jan, Y. N. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.006 · Cited by 167 · cited 1×
“This is followed by dendritic scaling in later larval stages, to match dendrite growth precisely with larval body growth — a tripling in body length over only 3 day”
BackgroundSelf-citationDSCAM functions as a netrin receptor in commissural axon pathfinding
Liu, G., Li, W., Wang, L., Kar, A. N., Guan, K., Rao, Y., & Wu, J. Y. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811083106 · Cited by 166
Polarity and intracellular compartmentalization of Drosophila neurons
Rolls, M. M., Satoh, D., Clyne, P. J., Henner, A. L., Uemura, T., & Doe, C. Q. (2007) · Neural Development · doi:10.1186/1749-8104-2-7 · Cited by 163
Sagasti, A., Guido, M. R., Raible, D. W., & Schier, A. F. (2005) · Current Biology · doi:10.1016/j.cub.2005.03.048 · Cited by 162
Dendritic stability in the adult olfactory bulb
Mizrahi, A., & Katz, L. C. (2003) · Nature Neuroscience · doi:10.1038/nn1133 · Cited by 161 · cited 1×
“Extended time-lapse analyses of mouse cortical neurons have revealed that, following a period of juvenile plasticity during which neurons establish normal dendritic fields, dendrites become stable with most neurons maintaining their dendritic fields for the remainder of their lifespa”
BackgroundFrom Lineage to Wiring Specificity
Komiyama, T., Johnson, W. A., Luo, L., & Jefferis, G. S. X. E. (2003) · Cell · doi:10.1016/s0092-8674(03)00030-8 · Cited by 155
Secretory trafficking in neuronal dendrites
Horton, A. C., & Ehlers, M. (2004) · Nature Cell Biology · doi:10.1038/ncb0704-585 · Cited by 154 · cited 1×
“melanogaster dendritic arborization neurons and cultured hippocampal neurons, Golgi outposts reside in dendrites but not in axons and are often found at branch points of dendritic arbor”
BackgroundTransmitting on actin: synaptic control of dendritic architecture
Schubert, V., & Dotti, C. G. (2007) · Journal of Cell Science · doi:10.1242/jcs.03337 · Cited by 151
Developmental disruptions in neural connectivity in the pathophysiology of schizophrenia
Karlsgodt, K. H., Sun, D., Jimenez, A. M., Lutkenhoff, E. S., Willhite, R., van Erp, T. G. M., & Cannon, T. D. (2008) · Development and Psychopathology · doi:10.1017/s095457940800062x · Cited by 149
Sugimura, K., Yamamoto, M., Niwa, R., Satoh, D., Goto, S., Taniguchi, M., Hayashi, S., & Uemura, T. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-09-03752.2003 · Cited by 147 · cited 1×
“Furthermore, dendrites of different neuronal types can cover the same region (coexistence”
BackgroundSweeney, L. B., Couto, A., Chou, Y.-H., Berdnik, D., Dickson, B. J., Luo, L., & Komiyama, T. (2007) · Neuron · doi:10.1016/j.neuron.2006.12.022 · Cited by 147
Huang, X., Powell‐Coffman, J. A., & Jin, Y. (2004) · Development · doi:10.1242/dev.00959 · Cited by 145
Dscam2 mediates axonal tiling in the Drosophila visual system
Millard, S. S., Flanagan, J. J., Pappu, K. S., Wu, W., & Zipursky, S. L. (2007) · Nature · doi:10.1038/nature05855 · Cited by 145
Activity-Independent Regulation of Dendrite Patterning by Postsynaptic Density Protein PSD-95
Charych, E. I., Akum, B. F., Goldberg, J. S., Jörnsten, R. J., Rongo, C., Zheng, J. Q., & Firestein, B. L. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2379-06.2006 · Cited by 141 · cited 1×
“Postsynaptic density protein 95 (PSD95), a scaffold protein that contains multiple PDZ domains and is localized at the postsynaptic density (PSD), acts in a neuronal activity-independent manner and suppresses dendrite branching locally, possibly by altering microtubule organizatio”
BackgroundHippocampal 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 140 · cited 1×
“In heterozygous LIS1-mutant mice, dendrites of heterotopic pyramidal neurons in the hippocampus show reduced dendrite length and branching compared with those of wild-type mic”
BackgroundSmall GTPase Cdc42 Is Required for Multiple Aspects of Dendritic Morphogenesis
Scott, E. K., Reuter, J. E., & Luo, L. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03118.2003 · Cited by 134
A Cost–Benefit Analysis of Neuronal Morphology
Wen, Q., & Chklovskii, D. B. (2008) · Journal of Neurophysiology · doi:10.1152/jn.00280.2007 · Cited by 129 · cited 1×
“Physiological requirements of dendrite patterns A balance between the metabolic costs of dendrite elaboration and the need to cover the receptive field presumably determines the size and shape of dendrite”
BackgroundKim, M. D., Jan, L. Y., & Jan, Y. N. (2006) · Genes & Development · doi:10.1101/gad.1459706 · Cited by 129 · cited 1×
“melanogaster homologue of the mammalian aryl hydrocarbon (dioxin) receptor (AHR), Spineless , is expressed in all four classes of dendritic arborization neurons and is essential for the diversification of their dendrite pattern”
BackgroundSelf-citationHeritability of Changes in Brain Volume Over Time in Twin Pairs Discordant for Schizophrenia
Brans, R. G. H., van Haren, N. E. M., van Baal, G. C. M., Schnack, H. G., Kahn, R. S., & Pol, H. E. H. (2008) · Archives of General Psychiatry · doi:10.1001/archpsyc.65.11.1259 · Cited by 129
Dscam guides embryonic axons by Netrin-dependent and -independent functions
Andrews, G. L., Tanglao, S., Farmer, W. T., Morin, S., Brotman, S. J., Berberoglu, M. A., Price, H., Fernandez, G. C. J., Mastick, G. S., Charron, F., et al. (2008) · Development · doi:10.1242/dev.023739 · Cited by 128
Mechanosensory neurite termination and tiling depend on SAX-2 and the SAX-1 kinase.
Gallegos, M. E., & Bargmann, C. I. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.021 · Cited by 124 · cited 1×
“Interestingly, SAX-1 and SAX-2 — which are the homologues of TRC and FRY, respectivel”
BackgroundOlson, E. C., Kim, S., & Walsh, C. A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3000-05.2006 · Cited by 123 · cited 1×
“In early cortical development, coordination of radial migration of mammalian pyramidal neurons is dependent on the Rho family of small GTPases, with the leading process becoming the apical dendrit”
BackgroundSfakianos, M. K., Eisman, A. S., Gourley, S. L., Bradley, W. D., Scheetz, A. J., Settleman, J. E., Taylor, J. R., Greer, C. A., Williamson, A., & Koleske, A. J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0793-07.2007 · Cited by 123
Vessey, J. P., Macchi, P., Stein, J. M., Mikl, M., Hawker, K. N., Vogelsang, P., Wieczorek, K., Vendra, G., Riefler, J., Tübing, F., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804583105 · Cited by 123
Convergent CaMK and RacGEF signals control dendritic structure and function
Penzes, P., Cahill, M. E., Jones, K. A., & Srivastava, D. P. (2008) · Trends in Cell Biology · doi:10.1016/j.tcb.2008.07.002 · Cited by 123
Cytoplasmic and mitochondrial protein translation in axonal and dendritic terminal arborization
Chihara, T., Luginbuhl, D. J., & Luo, L. (2007) · Nature Neuroscience · doi:10.1038/nn1910 · Cited by 118 · cited 1×
“In addition to the cellular machinery of dendrite growth discussed above (including the secretory pathway, endocytic pathway and cytoskeletal elements), local regulation of translation also has a role in controlling dendritic arborizatio”
BackgroundThe Coiled-Coil Protein Shrub Controls Neuronal Morphogenesis in Drosophila
Sweeney, N. T., Brenman, J. E., Jan, Y. N., & Gao, F. (2006) · Current Biology · doi:10.1016/j.cub.2006.03.067 · Cited by 118
Self-citationA glimmer of light for neuropsychiatric disorders
Hyman, S. E. (2008) · Nature · doi:10.1038/nature07454 · Cited by 117
Molecules and mechanisms of dendrite development in Drosophila
Corty, M. M., Matthews, B. J., & Grueber, W. B. (2009) · Development · doi:10.1242/dev.014423 · Cited by 116 · cited 1×
“melanogaster larval peripheral nervous system (PNS) acquire their distinct dendrite morpholog”
BackgroundPeng, Y., He, S., Marie, H., Zeng, S.-Y., Ma, J., Tan, Z.-J., Lee, S. Y., Malenka, R. C., & Yu, X. (2009) · Neuron · doi:10.1016/j.neuron.2008.11.015 · Cited by 111 · cited 1×
“In addition, the non-canonical Wnt pathway involving catenins and Rac may promote dendrite growth and branchin”
BackgroundRhoA Regulates Dendrite Branching in Hippocampal Neurons by Decreasing Cypin Protein Levels
Chen, H., & Firestein, B. L. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0872-07.2007 · Cited by 110
Transient neurites of retinal horizontal cells exhibit columnar tiling via homotypic interactions
Huckfeldt, R. M., Schubert, T., Morgan, J., Godinho, L., Cristo, G. D., Huang, Z. J., & Wong, R. (2008) · Nature Neuroscience · doi:10.1038/nn.2236 · Cited by 107 · cited 1×
“Indeed, imaging of the developing mouse retina reveals that the horizontal cells elaborate transient neurites that tile through homotypic interactio”
BackgroundSugimura, K., Satoh, D., Estes, P. A., Crews, S. T., & Uemura, T. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.016 · Cited by 105
Li, W., Wang, F., Menut, L., & Gao, F. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.040 · Cited by 100
Intrinsic neuronal regulation of axon and dendrite growth
Goldberg, J. L. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.08.012 · Cited by 99
A mosaic genetic screen for genes necessary forDrosophilamushroom body neuronal morphogenesis
Reuter, J. E., Nardine, T. M., Penton, A. L., Billuart, P., Scott, E. K., Usui, T., Uemura, T., & Luo, L. (2003) · Development · doi:10.1242/dev.00319 · Cited by 97
Quitsch, A., Berhörster, K., Liew, C. W., Richter, D., & Kreienkamp, H.-J. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2699-04.2005 · Cited by 95 · cited 1×
“This pathway is modulated by the postsynaptic protein Shan”
Li, H.-L., Huang, B. S., Vishwasrao, H. D., Sutedja, N. A., Chen, W., Jin, I., Hawkins, R. D., Bailey, C. H., & Kandel, E. R. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.010 · Cited by 90 · cited 1×
“and trans-synaptic interactions involved in synapse remodelling in Aplysia californica”
BackgroundHattori, Y., Sugimura, K., & Uemura, T. (2007) · Genes to Cells · doi:10.1111/j.1365-2443.2007.01107.x · Cited by 85
The RNA binding protein CPEB regulates dendrite morphogenesis and neuronal circuit assembly in vivo
Bestman, J. E., & Cline, H. T. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806296105 · Cited by 81 · cited 1×
“In addition, the cytoplasmic polyadenylation element binding protein, which has been shown to have a role in mRNA trafficking and translation regulation, is implicated in experience-dependent dendrite growth in the developing frog visual syste”
BackgroundControl of multidendritic neuron differentiation in Drosophila: The role of Collier
Crozatier, M., & Vincent, A. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2007.12.030 · Cited by 81
Mauss, A. S., Tripodi, M., Evers, J. F., & Landgraf, M. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000200 · Cited by 80 · cited 1×
“melanogaster motor neurons do not seem to rely on homotypic repulsion for their placement; these dendrites map myotopically along the antero-posterior axis and the medio-lateral axis, directed by guidance cues and their respective receptors such as Slit–Robo and Netrin–Frazzled for dendritic targetin”
BackgroundRemodeling dendrites during insect metamorphosis
Williams, D. W., & Truman, J. W. (2005) · Journal of Neurobiology · doi:10.1002/neu.20151 · Cited by 76 · cited 1×
“Moreover, larval class I dendritic arborization neurons extend secondary dendrites mostly to one side of the primary dendrite; these neurons remodel their dendrites during metamorphosis to adopt more symmetrical and complex patterns in the adult fl”
BackgroundParrish, J. Z., Emoto, K., Jan, L. Y., & Jan, Y. N. (2007) · Genes & Development · doi:10.1101/gad.1514507 · Cited by 76 · cited 1×
“Mutation of PcG genes produces phenotypes of impaired dendrite maintenanc”
BackgroundSelf-citationIntrinsic Control of Precise Dendritic Targeting by an Ensemble of Transcription Factors
Komiyama, T., & Luo, L. (2007) · Current Biology · doi:10.1016/j.cub.2006.11.067 · Cited by 73 · cited 1×
“melanogaster olfactory system and controls the targeting of their dendrite”
BackgroundKoike-Kumagai, M., Yasunaga, K.-I., Morikawa, R., Kanamori, T., & Emoto, K. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.312 · Cited by 72 · cited 1×
“TORC2 components associate physically with the TRC protein and their respective genes interact, suggesting that these proteins act in the same pathway that regulates tilin”
BackgroundSpatial Regulation of nanos Is Required for Its Function in Dendrite Morphogenesis
Brechbiel, J. L., & Gavis, E. R. (2008) · Current Biology · doi:10.1016/j.cub.2008.04.033 · Cited by 70
The origin recognition core complex regulates dendrite and spine development in postmitotic neurons
Huang, Z. D., Zang, K., & Reichardt, L. F. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200505075 · Cited by 65 · cited 1×
“, as well as the origin recognition complex (ORC) that regulates dendrite branching and spine formatio”
BackgroundSlit and Robo control the development of dendrites inDrosophilaCNS
Furrer, M.-P., Vasenkova, I. A., Kamiyama, D., Rosado, Y., & Chiba, A. (2007) · Development · doi:10.1242/dev.02882 · Cited by 62 · cited 1×
“melanogaster , the Robo receptor and its ligand, Slit, which is a secreted protein, promote dendrite formation of the motor neurons RP3 and aC”
BackgroundPatterning and organization of motor neuron dendrites in the Drosophila larva
Kim, M. D., Wen, Y., & Jan, Y. N. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.09.041 · Cited by 61 · cited 1×
“melanogaster motor neurons do not seem to rely on homotypic repulsion for their placement; these dendrites map myotopically along the antero-posterior axis and the medio-lateral axis, directed by guidance cues and their respective receptors such as Slit–Robo and Netrin–Frazzled for dendritic targetin”
BackgroundSelf-citationBrierley, D. J., Blanc, E., Reddy, O. V., VijayRaghavan, K., & Williams, D. W. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000199 · Cited by 61 · cited 1×
“melanogaster motor neurons do not seem to rely on homotypic repulsion for their placement; these dendrites map myotopically along the antero-posterior axis and the medio-lateral axis, directed by guidance cues and their respective receptors such as Slit–Robo and Netrin–Frazzled for dendritic targetin”
BackgroundRho GTPases and Phosphoinositide 3-Kinase Organize Formation of Branched Dendrites
Leemhuis, J., Boutillier, S., Barth, H., Feuerstein, T. J., Brock, C., Nürnberg, B., Aktories, K., & Meyer, D. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m307066200 · Cited by 59
Dscam-mediated repulsion controls tiling and self-avoidance
Millard, S. S., & Zipursky, S. L. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.05.005 · Cited by 56
Slit and Robo regulate dendrite branching and elongation of space-filling neurons in Drosophila
Dimitrova, S., Reissaus, A., & Tavosanis, G. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.08.028 · Cited by 50 · cited 1×
“as well as dendrite branching of the space-filling class IV dendritic arborization neurons, without affecting class I dendritic arborization neurons ( Box 2 ), as revealed by mutants that lack Rob”
BackgroundGan, W., & Macagno, E. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-05-03243.1995 · Cited by 49
General design principle for scalable neural circuits in a vertebrate retina
Lee, S., & Stevens, C. F. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705469104 · Cited by 45 · cited 1×
“Between these extremes is the intriguing example of how RGCs adjust to growth in the goldfis”
BackgroundActin Filament-Stabilizing Protein Tropomyosin Regulates the Size of Dendritic Fields
Li, W.-J., & Gao, F. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-15-06171.2003 · Cited by 40
ネズミのスタウフェン1に対する機能消失対立遺伝子は,樹状突起のStaufen1‐RNP配送や樹状突起棘の形態形成の障害を誘導する
John, P. V., Paolo, M., Joel, M. S., Martin, M., Kelvin, N. H., Petra, V., Krzysztof, W., Vendra, G., Riefler, J., Fabian, T., et al. (2008) · Cited by 36
The role of cytoplasmic dynein in the human brain developmental disease lissencephaly
Vallee, R. B., Faulkner, N. E., & Tai, C. (2000) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/s0167-4889(00)00011-2 · Cited by 34
Adhesion molecules in establishing retinal circuitry
Fuerst, P. G., & Burgess, R. W. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.07.013 · Cited by 27 · cited 1×
“DSCAMs also have a role in circuit formation that is discussed in several recent review”
BackgroundCompetition during innervation of embryonic amphibian head skin
Kitson, D. L., & Roberts, A. (1983) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1983.0025 · Cited by 26 · cited 1×
“, the sensory arbors that innervate the skin of the fro”
BackgroundCardno, A. G., & Gottesman, I. I. (2000) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(200021)97:1
Flagged first, then by citations
Research works printed but not linked: 2
- Bestman, J., Silva, J. S. D. & Cline, H. T. in Dendrites (Eds G. Stuart, N. Spruston & M. Häusser) 69–94 (Oxford University Press, Oxford, 2008).
- Polleux, F. & Ghosh, A. in Dendrites (Eds G. Stuart, N. Spruston & M. Häusser) 95–115 (Oxford University Press, Oxford, 2008).
Cited by
Sorted by citations
Gao, S., Zhou, M., Wang, Y., Cheng, J., Yachi, H., & Wang, J. (2018) · IEEE Transactions on Neural Networks and Learning Systems · doi:10.1109/tnnls.2018.2846646 · Cited by 708
“Besides, a slightly morphological difference can lead to the notable functional discrepancy, playing a role in filters to determine the types of signals that single neurons receive and the way used to integrate the signals [27].”
BackgroundFunctional architecture of the retina: Development and disease
Hoon, M., Okawa, H., Santina, L. D., & Wong, R. (2014) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2014.06.003 · Cited by 628
“The molecular mechanisms that regulate the tiling of bipolar cell arbors are unknown, but studies elucidating the signaling mechanisms that drosophila sensory neurons use to populate the larval body wall may be instructive (Emoto et al., 2004; Jan and Jan, 2010).”
BackgroundThe single dendritic branch as a fundamental functional unit in the nervous system
Branco, T., & Häusser, M. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.07.009 · Cited by 355
“One interesting aspect of such local control of dendritic growth is that a highly compartmentalized neuron will tend to grow in an even more compartmentalized way given that growth signals will automatically be kept local [72].”
Fieblinger, T., Graves, S. M., Sebel, L. E., Alcacer, C., Plotkin, J. L., Gertler, T. S., Chan, C. S., Heiman, M., Greengard, P., Cenci, M. A., et al. (2014) · Nature Communications · doi:10.1038/ncomms6316 · Cited by 304
Precise temporal regulation of alternative splicing during neural development
Weyn‐Vanhentenryck, S. M., Feng, H., Ustianenko, D., Duffié, R., Yan, Q., Jacko, M., Martinez, J. C., Goodwin, M., Zhang, X., Hengst, U., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-04559-0 · Cited by 272
“…neurons mature through a prolonged and sophisticated process that involves dramatic morphological and functional changes in individual neurons as well as formation of synaptic connections between neurons to build intricate neural circuits (Barnes and Polleux 2009; Jan and Jan 2010; Rasband 2010).”
Background
Metadata
- Authors
- Jan, Y.-N., & Jan, L. Y.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Jan, Yuh-Nung
- Venue
- Nature Reviews Neuroscience
- Published
- 2010-05
- Volume
- 11
- Issue
- 5
- Pages
- 316-328
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- PMC
- PMC3079328
- OpenAlex
- W2065943966
- Cited by
- 693
- References
- 162
- Citations by year
- 2026: 15 · 2025: 41 · 2024: 24 · 2023: 29 · 2022: 33 · 2021: 41 · 2020: 71 · 2019: 41 · 2018: 45 · 2017: 49 · 2016: 52 · 2015: 38 · 2014: 58 · 2013: 53 · 2012: 53
- FWCI
- 4.49
- Type
- journal article
- Language
- en
- Update notices
- erratum (2010-06-01)
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health
- National Institute of Mental Health (R01MH084234)
- National Institute of Neurological Disorders and Stroke (R37NS040929)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Keywords
- dendritic branching, dendrite morphogenesis, dendritic morphology, Drosophila melanogaster, transcription factors, ligand-receptor interactions, signaling pathways, local translation, cytoskeleton, endosomes, autism spectrum disorder, neurodevelopmental disorders, neural circuits
- MeSH terms
- Animals, Axons, Dendrites, Humans, Models, Neurological, Morphogenesis, Neurons, Signal Transduction
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