Integration of chemosensory pathways in the Drosophila second-order olfactory centers.

By N. Tanaka, T. Awasaki, T. Shimada, Kei Ito. 2004

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In Biomaterials

Citations in the corpus

The neuronal architecture of the mushroom body provides a logic for associative learning (2014, background): “, 2009)— comprise small groups containing from one to 20 neurons (Tanaka et al., 2004; Tanaka et al., 2008, 2012; Yu et al., 2010).”
The Mushroom Body of Adult Drosophila Characterized by GAL4 Drivers (2009, background): “However, in practice, it seems unlikely that even 200 cells cover all microglomeruli in the calyx, since each subtype has spatial preference of dendritic terminals (Jefferis et al., 2007; Lin et al., 2007; Tanaka et al., 2004).”
Functional analysis of a higher olfactory center, the lateral horn (2012, background): “…and clustering in the projections of genetically labeled PNs in the LH (Tanaka et al., 2004; Jefferis et al., 2007; Lin et al., 2007; Kazama and Wilson, 2009), but whether dendrites of LHNs are restricted to these clusters remains controversial (Tanaka et al., 2004; Jefferis et al., 2007).”
Generating sparse and selective third-order responses in the olfactory system of the fly (2010, background): “The lateral horn is believed to be important in generating innate behaviors (6), including those elicited by pheromones (7).”
Parallel Pathways for Cross-Modal Memory Retrieval in Drosophila (2013, background): “…may be achieved indirectly via other regions (e.g., the ventrolateral protocerebrum) that receive projection neurons from different modalities (Tanaka et al., 2004; Kamikouchi et al., 2006; Otsuna and Ito, 2006) or via synchronized activity between modality-specific nuclei (van Swinderen and…”
A map of olfactory representation in the Drosophila mushroom body. (2007, unknown): “The spatial distribution of PN axon branching patterns is highly stereotyped in the LH but less clear in the MB calyx where stereotypic projections may exist in three roughly defined calycal zones (Marin et al., 2002; Wong et al., 2002; Tanaka et al., 2004).”
Olfactory information processing in Drosophila. (2009, unknown): “Projection neuron input to the lateral horn is highly spatially stereotyped across animals [20,23,105,106], and the dendrites of a few lateral horn output neurons have been mapped to restricted and reproducible subregions of the lateral horn [23,106].”
Synaptic organization in the adult Drosophila mushroom body calyx (2009, background): “We concentrated on the microglomerular synaptic complexes and now confirm that dendrites of Kenyon cell subpopulations are reliably found at defined positions in the calyx (Strausfeld et al., 2003; Tanaka et al., 2004), where they are allocated to distinct populations of microglomeruli.”
Neuronal assemblies of the Drosophila mushroom body (2008, methodology): “To visualize the labeled cells, we crossed these GAL4 strains with a line carrying two reporter genes: UAS-mCD8::GFP and UAS-GFP S65T (T10; Tanaka et al., 2004).”
Molecular architecture of smell and taste in Drosophila. (2007, background): “To appreciate the level of integration in these higher olfactory centers, the connectivity between PNs and third-order olfactory neurons was assessed (Tanaka et al. 2004).”
Testing odor response stereotypy in the Drosophila mushroom body. (2008, unknown): “More recent results suggest some broad ‘‘zonal’’ stereotypy, both for PN axons and for KC dendritic fields in the MB calyx (Jefferis et al., 2007; Lin et al., 2007; Tanaka et al., 2004; Zhu et al., 2003).”
Drosophila olfactory memory: single genes to complex neural circuits (2007, background): “In addition, two reports have detailed intrinsic lateral horn neurons that arborize in lateral horn strata that overlap with the PN input zone”
Comprehensive Maps of Drosophila Higher Olfactory Centers: Spatially Segregated Fruit and Pheromone Representation (2007, unknown): “Six Gal4 lines have been reported that may label LHNs (Tanaka et al., 2004).”