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Tiling of theDrosophilaepidermis by multidendritic sensory neurons
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-9861(19980126)390:4<470::aid-cne2>3.0.co;2-yopenalex-snapshot
Dendritic field development of retinal ganglion cells in the cat following neonatal damage to visual cortex: Evidence for cell class specific interactions
inferredcites →https://doi.org/10.1002/(sici)1096-9861(19990201)404:1<127::aid-cne10>3.0.co;2-mopenalex-snapshot
Development and organization of a nitric- oxide-sensitive peripheral neural plexus in larvae of the moth,Manduca sexta
inferredcites →https://doi.org/10.1002/(sici)1097-4695(199804)35:1<53::aid-neu5>3.0.co;2-aopenalex-snapshot
A detached branch stops being recognized as self by other branches of a neuron
inferredcites →https://doi.org/10.1002/1096-9861(20000911)425:1<34::aid-cne4>3.3.co;2-7openalex-snapshot
Central projections of Drosophila sensory neurons in the transition from embryo to larva
inferredcites →https://doi.org/10.1002/1097-4695(200010)45:1<47::aid-neu5>3.0.co;2-copenalex-snapshot
Possible role of the receptor protein tyrosine phosphatase HmLAR2 in interbranch repulsion in a leech embryonic cell
inferredcites →https://doi.org/10.1002/cne.1385openalex-snapshot
Tiling of the body wall by multidendritic sensory neurons in Manduca sexta
inferredcites →https://doi.org/10.1002/cne.902900203openalex-snapshot
Modality‐specific axonal projections in the CNS of the flies Phormia and Drosophila
inferredcites →https://doi.org/10.1002/jez.1400990302openalex-snapshot
The reception of mechanical and thermal stimuli by caterpillars
inferredcites →https://doi.org/10.1002/neu.1048openalex-snapshot
Cell‐type specific dendritic contacts between retinal ganglion cells during development
inferredcites →https://doi.org/10.1006/bbrc.1998.8183openalex-snapshot
A New Member of the Amiloride-Sensitive Sodium Channel Family inDrosophila melanogasterPeripheral Nervous System
inferredcites →https://doi.org/10.1007/bf00402027openalex-snapshot
Morphological differentiation of the embryonic peripheral neurons in Drosophila
inferredcites →https://doi.org/10.1016/0092-8674(84)90069-2openalex-snapshot
Neuronal development in the drosophila retina: Monoclonal antibodies as molecular probes
inferredcites →https://doi.org/10.1016/0092-8674(93)90358-wopenalex-snapshot
atonal is a proneural gene that directs chordotonal organ formation in the Drosophila peripheral nervous system
inferredcites →https://doi.org/10.1016/0896-6273(89)90112-8openalex-snapshot
Neurogenesis of the peripheral nervous system in Drosophila embryos: DNA replication patterns and cell lineages
inferredcites →https://doi.org/10.1016/s0092-8674(00)80046-xopenalex-snapshot
Flamingo, a Seven-Pass Transmembrane Cadherin, Regulates Planar Cell Polarity under the Control of Frizzled
inferredcites →https://doi.org/10.1016/s0896-6273(00)00088-xopenalex-snapshot
Control of Dendritic Field Formation in Drosophila
inferredcites →https://doi.org/10.1016/s0896-6273(00)80478-xopenalex-snapshot
Extreme Diversity among Amacrine Cells: Implications for Function
inferredcites →https://doi.org/10.1016/s0896-6273(00)80701-1openalex-snapshot
Mosaic Analysis with a Repressible Cell Marker for Studies of Gene Function in Neuronal Morphogenesis
inferredcites →https://doi.org/10.1016/s0896-6273(00)80871-5openalex-snapshot
The Proneural Gene amos Promotes Multiple Dendritic Neuron Formation in the Drosophila Peripheral Nervous System
inferredcites →https://doi.org/10.1016/s0896-6273(00)81169-1openalex-snapshot
Drosophila Futsch/22C10 Is a MAP1B-like Protein Required for Dendritic and Axonal Development
inferredcites →https://doi.org/10.1016/s0925-4773(01)00375-6openalex-snapshot
The selector gene cut represses a neural cell fate that is specified independently of the Achaete-Scute-Complex and atonal
inferredcites →https://doi.org/10.1016/s1534-5807(01)00072-7openalex-snapshot
Sequoia, a Tramtrack-Related Zinc Finger Protein, Functions as a Pan-Neural Regulator for Dendrite and Axon Morphogenesis in Drosophila
inferredcites →https://doi.org/10.1038/292344a0openalex-snapshot
Dendritic territories of cat retinal ganglion cells
inferredcites →https://doi.org/10.1038/297683a0openalex-snapshot
Evidence for dendritic competition in the developing retina
inferredcites →https://doi.org/10.1038/nn0901-877openalex-snapshot
The fundamental plan of the retina
inferredcites →https://doi.org/10.1073/pnas.92.9.4002openalex-snapshot
Spatial organization of retinal information about the direction of image motion.
inferredcites →https://doi.org/10.1083/jcb.140.1.143openalex-snapshot
Ripped Pocket and Pickpocket, Novel Drosophila DEG/ENaC Subunits Expressed in Early Development and in Mechanosensory Neurons
inferredcites →https://doi.org/10.1098/rstb.1988.0090openalex-snapshot
The organization of mechanosensory neuropiles in locust thoracic ganglia
inferredcites →https://doi.org/10.1101/gad.1.3.297openalex-snapshot
Independent subpatterns of sense organs require independent genes of the achaete-scute complex in Drosophila larvae
inferredcites →https://doi.org/10.1101/gad.13.19.2549openalex-snapshot
Genes regulating dendritic outgrowth, branching, and routing in Drosophila
inferredcites →https://doi.org/10.1101/gad.4.8.1322openalex-snapshot
Patterns of expression of cut, a protein required for external sensory organ development in wild-type and cut mutant Drosophila embryos.
inferredcites →https://doi.org/10.1113/jphysiol.1976.sp011642openalex-snapshot
Physiological properties and receptive fields of mechanosensory neurones in the head ganglion of the leech: comparison with homologous cells in segmental ganglia.
inferredcites →https://doi.org/10.1152/physrev.1991.71.2.447openalex-snapshot
Functional architecture of the mammalian retina
inferredcites →https://doi.org/10.1242/dev.106.3.589openalex-snapshot
Exclusionary dendritic interactions in the retina of the goldfish
inferredcites →https://doi.org/10.1242/dev.121.9.2923openalex-snapshot
Origin and specification of type II sensory neurons in Drosophila
inferredcites →https://doi.org/10.1242/dev.128.5.631openalex-snapshot
Lineage, cell polarity and inscuteable function in the peripheral nervous system of the Drosophila embryo
inferredcites →https://doi.org/10.1242/jeb.204.3.457openalex-snapshot
Defensive Responses of Larval Manduca Sexta and Their Sensitization by Noxious Stimuli In the Laboratory and Field
inferredcites →https://doi.org/10.1523/jneurosci.03-12-02474.1983openalex-snapshot
Formation of the receptive fields of leech mechanosensory neurons during embryonic development
inferredcites →https://doi.org/10.1523/jneurosci.05-03-00768.1985openalex-snapshot
Developmental arborization of sensory neurons in the leech Haementeria ghilianii. II. Experimentally induced variations in the branching pattern
inferredcites →https://doi.org/10.1523/jneurosci.15-03-01755.1995openalex-snapshot
Central projections of sensory neurons in the Drosophila embryo correlate with sensory modality, soma position, and proneural gene function
inferredcites →https://doi.org/10.1523/jneurosci.15-05-03243.1995openalex-snapshot
Interactions between segmental homologs and between isoneuronal branches guide the formation of sensory terminal fields
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Dscam-mediated repulsion controls tiling and self-avoidance
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Signaling mechanisms that coordinate the development and maintenance of dendritic fields
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nanos and pumilio Are Essential for Dendrite Morphogenesis in Drosophila Peripheral Neurons
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Spatial Regulation of nanos Is Required for Its Function in Dendrite Morphogenesis
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Cytokine Signaling Mediates UV-Induced Nociceptive Sensitization in Drosophila Larvae
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Bicaudal-D Regulates Fragile X Mental Retardation Protein Levels, Motility, and Function during Neuronal Morphogenesis
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Directed Microtubule Growth, +TIPs, and Kinesin-2 Are Required for Uniform Microtubule Polarity in Dendrites
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Dscam1-Mediated Self-Avoidance Counters Netrin-Dependent Targeting of Dendrites in Drosophila
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Hedgehog Signaling Regulates Nociceptive Sensitization
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Dendritic Patterning: Three-Dimensional Position Determines Dendritic Avoidance Capability
inferred← citeshttps://doi.org/10.1016/j.cub.2012.09.019openalex-snapshot
Dendritic Filopodia, Ripped Pocket, NOMPC, and NMDARs Contribute to the Sense of Touch in Drosophila Larvae
inferred← citeshttps://doi.org/10.1016/j.cub.2014.03.041openalex-snapshot
Trim9 Regulates Activity-Dependent Fine-Scale Topography in Drosophila
inferred← citeshttps://doi.org/10.1016/j.cub.2015.04.016openalex-snapshot
Role of the Subesophageal Zone in Sensorimotor Control of Orientation in Drosophila Larva
inferred← citeshttps://doi.org/10.1016/j.cub.2016.09.038openalex-snapshot
The TRP Channels Pkd2, NompC, and Trpm Act in Cold-Sensing Neurons to Mediate Unique Aversive Behaviors to Noxious Cold in Drosophila
inferred← citeshttps://doi.org/10.1016/j.cub.2017.06.068openalex-snapshot
Neural Circuitry that Evokes Escape Behavior upon Activation of Nociceptive Sensory Neurons in Drosophila Larvae
inferred← citeshttps://doi.org/10.1016/j.cub.2017.07.031openalex-snapshot
Nociceptive Circuits: Can’t Escape Detection
inferred← citeshttps://doi.org/10.1016/j.cub.2019.01.060openalex-snapshot
Characterization of Proprioceptive System Dynamics in Behaving Drosophila Larvae Using High-Speed Volumetric Microscopy
inferred← citeshttps://doi.org/10.1016/j.cub.2019.02.004openalex-snapshot
Coordinated Movement: Watching Proprioception Unfold
inferred← citeshttps://doi.org/10.1016/j.cub.2019.02.025openalex-snapshot
Direction Selectivity in Drosophila Proprioceptors Requires the Mechanosensory Channel Tmc
inferred← citeshttps://doi.org/10.1016/j.cub.2019.03.050openalex-snapshot
Epidermis-Derived L1CAM Homolog Neuroglian Mediates Dendrite Enclosure and Blocks Heteroneuronal Dendrite Bundling
inferred← citeshttps://doi.org/10.1016/j.cub.2020.10.054openalex-snapshot
Deterministic and Stochastic Rules of Branching Govern Dendrite Morphogenesis of Sensory Neurons
inferred← citeshttps://doi.org/10.1016/j.cub.2021.10.069openalex-snapshot
A neuropeptidergic circuit gates selective escape behavior of Drosophila larvae
inferred← citeshttps://doi.org/10.1016/j.cub.2022.05.030openalex-snapshot
Self-avoidance alone does not explain the function of Dscam1 in mushroom body axonal wiring
inferred← citeshttps://doi.org/10.1016/j.cub.2023.05.043openalex-snapshot
Comparative connectomics and escape behavior in larvae of closely related Drosophila species
inferred← citeshttps://doi.org/10.1016/j.cub.2026.09.030openalex-snapshot
Cold sensing by a glutamate receptor drives avoidance behavior in Drosophila larvae
inferred← citeshttps://doi.org/10.1016/j.devcel.2004.07.007openalex-snapshot
Regulation of Dendritic Maintenance and Growth by a Mammalian 7-Pass Transmembrane Cadherin
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.02.010openalex-snapshot
Dendrite Reshaping of Adult Drosophila Sensory Neurons Requires Matrix Metalloproteinase-Mediated Modification of the Basement Membranes
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.10.024openalex-snapshot
Sensory-Neuron Subtype-Specific Transcriptional Programs Controlling Dendrite Morphogenesis: Genome-wide Analysis of Abrupt and Knot/Collier
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.06.019openalex-snapshot
Fish Scales Dictate the Pattern of Adult Skin Innervation and Vascularization
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.10.008openalex-snapshot
Parallel Processing of Two Mechanosensory Modalities by a Single Neuron in C. elegans
inferred← citeshttps://doi.org/10.1016/j.exphem.2014.06.002openalex-snapshot
Drosophila as a model for the two myeloid blood cell systems in vertebrates
inferred← citeshttps://doi.org/10.1016/j.expneurol.2022.114198openalex-snapshot
Intrinsic regulation of axon regeneration after spinal cord injury: Recent advances and remaining challenges
inferred← citeshttps://doi.org/10.1016/j.febslet.2014.02.010openalex-snapshot
Control of neuronal morphology and connectivity: Emerging developmental roles for gap junctional proteins
inferred← citeshttps://doi.org/10.1016/j.gendis.2022.11.009openalex-snapshot
The organization and function of the Golgi apparatus in dendrite development and neurological disorders
inferred← citeshttps://doi.org/10.1016/j.gene.2020.144473openalex-snapshot
The cytoplasmic polyadenylation element binding protein (CPEB), Orb, is important for dendrite development and neuron fate specification in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.ibmb.2011.05.008openalex-snapshot
Human down syndrome cell adhesion molecules (DSCAMs) are functionally conserved with Drosophila Dscam[TM1] isoforms in controlling neurodevelopment
inferred← citeshttps://doi.org/10.1016/j.ijdevneu.2003.12.008openalex-snapshot
Maturation of astrocyte morphology and the establishment of astrocyte domains during postnatal hippocampal development
inferred← citeshttps://doi.org/10.1016/j.isci.2020.101865openalex-snapshot
Distinct Relations of Microtubules and Actin Filaments with Dendritic Architecture
inferred← citeshttps://doi.org/10.1016/j.isci.2021.103536openalex-snapshot
Ataxin-2 is essential for cytoskeletal dynamics and neurodevelopment in Drosophila
inferred← citeshttps://doi.org/10.1016/j.jbc.2023.105265openalex-snapshot
Phenotypic analysis with trans-recombination–based genetic mosaic models
inferred← citeshttps://doi.org/10.1016/j.jgg.2019.03.010openalex-snapshot
Die in pieces: How Drosophila sheds light on neurite degeneration and clearance
inferred← citeshttps://doi.org/10.1016/j.mcn.2007.04.001openalex-snapshot
A sensory feedback circuit coordinates muscle activity in Drosophila
inferred← citeshttps://doi.org/10.1016/j.mcn.2010.06.001openalex-snapshot
SIDL interacts with the dendritic targeting motif of Shal (Kv4) K+ channels in Drosophila
inferred← citeshttps://doi.org/10.1016/j.mcn.2011.05.002openalex-snapshot
Nmnat exerts neuroprotective effects in dendrites and axons
inferred← citeshttps://doi.org/10.1016/j.mcn.2012.11.008openalex-snapshot
The role of autophagy in Nmnat-mediated protection against hypoxia-induced dendrite degeneration
inferred← citeshttps://doi.org/10.1016/j.mod.2004.04.001openalex-snapshot
Slit-Robo signalling prevents sensory cells from crossing the midline in Drosophila
inferred← citeshttps://doi.org/10.1016/j.neulet.2015.04.033openalex-snapshot
NOMPC-dependent mechanotransduction shapes the dendrite of proprioceptive neurons
inferred← citeshttps://doi.org/10.1016/j.neures.2018.09.015openalex-snapshot
Stages and transitions in dendrite arbor differentiation
inferred← citeshttps://doi.org/10.1016/j.neuron.2004.08.002openalex-snapshot
Retinal Ganglion Cell Type, Size, and Spacing Can Be Specified Independent of Homotypic Dendritic Contacts
inferred← citeshttps://doi.org/10.1016/j.neuron.2004.08.016openalex-snapshot
Development of Morphological Diversity of Dendrites in Drosophila by the BTB-Zinc Finger Protein Abrupt
inferred← citeshttps://doi.org/10.1016/j.neuron.2004.08.040openalex-snapshot
BTB/POZ-Zinc Finger Protein Abrupt Suppresses Dendritic Branching in a Neuronal Subtype-Specific and Dosage-Dependent Manner
inferred← citeshttps://doi.org/10.1016/j.neuron.2004.09.021openalex-snapshot
Mechanosensory Neurite Termination and Tiling Depend on SAX-2 and the SAX-1 Kinase
inferred← citeshttps://doi.org/10.1016/j.neuron.2007.03.029openalex-snapshot
Drosophila Sensory Neurons Require Dscam for Dendritic Self-Avoidance and Proper Dendritic Field Organization
inferred← citeshttps://doi.org/10.1016/j.neuron.2007.04.013openalex-snapshot
Homophilic Dscam Interactions Control Complex Dendrite Morphogenesis
inferred← citeshttps://doi.org/10.1016/j.neuron.2007.10.031openalex-snapshot
Knot/Collier and Cut Control Different Aspects of Dendrite Cytoskeleton and Synergize to Define Final Arbor Shape
inferred← citeshttps://doi.org/10.1016/j.neuron.2008.01.007openalex-snapshot
The Cadherin Flamingo Mediates Level-Dependent Interactions that Guide Photoreceptor Target Choice in Drosophila
inferred← citeshttps://doi.org/10.1016/j.neuron.2009.08.006openalex-snapshot
The microRNA bantam Functions in Epithelial Cells to Regulate Scaling Growth of Dendrite Arbors in Drosophila Sensory Neurons
inferred← citeshttps://doi.org/10.1016/j.neuron.2010.07.004openalex-snapshot
The Role of the TRP Channel NompC in Drosophila Larval and Adult Locomotion
inferred← citeshttps://doi.org/10.1016/j.neuron.2011.06.026openalex-snapshot
Control of Neuronal Morphology by the Atypical Cadherin Fat3
inferred← citeshttps://doi.org/10.1016/j.neuron.2011.08.028openalex-snapshot
Nak Regulates Localization of Clathrin Sites in Higher-Order Dendrites to Promote Local Dendrite Growth
inferred← citeshttps://doi.org/10.1016/j.neuron.2011.10.033openalex-snapshot
Integrins Establish Dendrite-Substrate Relationships that Promote Dendritic Self-Avoidance and Patterning in Drosophila Sensory Neurons
inferred← citeshttps://doi.org/10.1016/j.neuron.2011.10.036openalex-snapshot
Integrins Regulate Repulsion-Mediated Dendritic Patterning of Drosophila Sensory Neurons by Restricting Dendrites in a 2D Space
inferred← citeshttps://doi.org/10.1016/j.neuron.2012.01.028openalex-snapshot
γ-Protocadherins Control Cortical Dendrite Arborization by Regulating the Activity of a FAK/PKC/MARCKS Signaling Pathway
inferred← citeshttps://doi.org/10.1016/j.neuron.2012.02.029openalex-snapshot
Complementary Chimeric Isoforms Reveal Dscam1 Binding Specificity In Vivo
inferred← citeshttps://doi.org/10.1016/j.neuron.2012.10.008openalex-snapshot
Golgi Outposts Shape Dendrite Morphology by Functioning as Sites of Acentrosomal Microtubule Nucleation in Neurons
inferred← citeshttps://doi.org/10.1016/j.neuron.2013.05.020openalex-snapshot
Dscam Expression Levels Determine Presynaptic Arbor Sizes in Drosophila Sensory Neurons
inferred← citeshttps://doi.org/10.1016/j.neuron.2014.02.016openalex-snapshot
Interplay of Cell-Autonomous and Nonautonomous Mechanisms Tailors Synaptic Connectivity of Converging Axons In Vivo
inferred← citeshttps://doi.org/10.1016/j.neuron.2016.01.020openalex-snapshot
Epidermis-Derived Semaphorin Promotes Dendrite Self-Avoidance by Regulating Dendrite-Substrate Adhesion in Drosophila Sensory Neurons
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2024.102635openalex-snapshot
Calcium plays an essential role in early-stage dendrite injury detection and regeneration
inferred← citeshttps://doi.org/10.1016/j.semcdb.2022.02.015openalex-snapshot
Molecular mechanisms regulating the spatial configuration of neurites
inferred← citeshttps://doi.org/10.1016/j.tcb.2020.07.004openalex-snapshot
Golgi Outposts Nucleate Microtubules in Cells with Specialized Shapes
inferred← citeshttps://doi.org/10.1016/j.tig.2017.10.002openalex-snapshot
Keeping Neurons Young and Foxy: FoxOs Promote Neuronal Plasticity
inferred← citeshttps://doi.org/10.1016/j.tins.2011.07.004openalex-snapshot
How does morphology relate to function in sensory arbors?
inferred← citeshttps://doi.org/10.1016/j.tins.2011.11.003openalex-snapshot
Seeing the light: photobehavior in fruit fly larvae
inferred← citeshttps://doi.org/10.1016/j.ydbio.2004.01.032openalex-snapshot
A hidden program in Drosophila peripheral neurogenesis revealed: fundamental principles underlying sensory organ diversity
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.09.054openalex-snapshot
The rodent Four-jointed ortholog Fjx1 regulates dendrite extension
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.12.030openalex-snapshot
Control of multidendritic neuron differentiation in Drosophila: The role of Collier
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.03.038openalex-snapshot
Branch architecture of the fly larval abdominal serotonergic neurons
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.07.003openalex-snapshot
Sensory mechanisms controlling the timing of larval developmental and behavioral transitions require the Drosophila DEG/ENaC subunit, Pickpocket1
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.08.028openalex-snapshot
Slit and Robo regulate dendrite branching and elongation of space-filling neurons in Drosophila
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.12.026openalex-snapshot
The atypical cadherin Flamingo is required for sensory axon advance beyond intermediate target cells
inferred← citeshttps://doi.org/10.1016/j.ydbio.2009.09.041openalex-snapshot
Patterning and organization of motor neuron dendrites in the Drosophila larva
inferred← citeshttps://doi.org/10.1016/j.ydbio.2010.07.004openalex-snapshot
Developmental timing of a sensory-mediated larval surfacing behavior correlates with cessation of feeding and determination of final adult size
inferred← citeshttps://doi.org/10.1016/j.ydbio.2011.07.032openalex-snapshot
The core planar cell polarity gene prickle interacts with flamingo to promote sensory axon advance in the Drosophila embryo
inferred← citeshttps://doi.org/10.1016/j.ydbio.2014.07.002openalex-snapshot
Developmental shaping of dendritic arbors in Drosophila relies on tightly regulated intra-neuronal activity of protein kinase A (PKA)
inferred← citeshttps://doi.org/10.1016/j.ydbio.2016.08.018openalex-snapshot
FoxO regulates microtubule dynamics and polarity to promote dendrite branching in Drosophila sensory neurons
inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.12.009openalex-snapshot
Glycerophospholipids – Emerging players in neuronal dendrite branching and outgrowth
inferred← citeshttps://doi.org/10.1016/j.ydbio.2020.07.006openalex-snapshot
Neurons survive simultaneous injury to axons and dendrites and regrow both types of processes in vivo
inferred← citeshttps://doi.org/10.1016/j.ydbio.2022.03.009openalex-snapshot
Microtubule polarity is instructive for many aspects of neuronal polarity
inferred← citeshttps://doi.org/10.1016/j.ydbio.2022.05.014openalex-snapshot
Dendrite regeneration in the vertebrate spinal cord
inferred← citeshttps://doi.org/10.1016/j.ydbio.2022.09.005openalex-snapshot
The exocyst complex is required for developmental and regenerative neurite growth in vivo
inferred← citeshttps://doi.org/10.1016/j.ydbio.2023.03.001openalex-snapshot
Dendrite regeneration mediates functional recovery after complete dendrite removal
inferred← citeshttps://doi.org/10.1016/s0012-1606(03)00215-xopenalex-snapshot
Charting the Drosophila neuropile: a strategy for the standardised characterisation of genetically amenable neurites
inferred← citeshttps://doi.org/10.1016/s0091-679x(03)01011-2openalex-snapshot
Techniques to Dissect Cellular and Subcellular Function in the Drosophila Nervous System
inferred← citeshttps://doi.org/10.1016/s0092-8674(03)00160-0openalex-snapshot
Different Levels of the Homeodomain Protein Cut Regulate Distinct Dendrite Branching Patterns of Drosophila Multidendritic Neurons
inferred← citeshttps://doi.org/10.1016/s0092-8674(03)00272-1openalex-snapshot
painless, a Drosophila Gene Essential for Nociception
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