Spatial representation of the glomerular map in the Drosophila protocerebrum.

By A. Wong, Jing W. Wang, R. Axel. 2002

586 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Endocrine and Autonomic Systems, Sensory Systems

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Citations in the corpus

Mushroom body output neurons encode valence and guide memory-based action selection in Drosophila (2014, methodology): “In Drosophila, olfactory information is delivered to the MB by projection neurons from each of ∼50 antennal lobe glomeruli (Marin et al., 2002; Wong et al., 2002; Jefferis et al., 2007; Lin et al., 2007; Vosshall and Stocker, 2007; Yu et al., 2010).”
Recognition (2003, neutral): “Most PNs innervate a single glomerulus (Jefferis et al., 2007; Marin et al., 2002; Wong et al., 2002), while mitral/tufted cells project to the primary olfactory cortex (Price & Powell, 1970).”
The neuronal architecture of the mushroom body provides a logic for associative learning (2014, background): “Most antennal lobe projection neurons (PNs) extend dendrites to a single glomerulus and project axons that bifurcate to innervate two brain regions, the lateral horn and the MB (Stocker et al., 1990; Wong et al., 2002; Jefferis et al., 2007).”
A connectome of a learning and memory center in the adult Drosophila brain (2017, background): “…projection neurons of olfactory and other modalities including visual, gustatory and thermal (Vogt et al., 2016; Kirkhart and Scott, 2015; Yagi et al., 2016; Caron et al., 2013; Stocker et al., 1990; Wong et al., 2002; Strausfeld, 1976; Tanaka et al., 2004; Liu et al., 2015; Frank et al., 2015).”
Functional analysis of a higher olfactory center, the lateral horn (2012, result): “Consistent with this proposal, anatomical studies in Drosophila showed stereotypical clustering of PN arborizations in the LH (Marin et al., 2002; Wong et al., 2002; Tanaka et al., 2004).”
Generating sparse and selective third-order responses in the olfactory system of the fly (2010, background): “PN projections to lateral horn neurons (LHNs) are spatially stereotyped (8, 9) and clustered (10), suggesting that circuits in this region may be “hardwired” for the detection of specific odors that elicit innate behavioral responses.”
Genetic dissection of neural circuits. (2008, unknown): “, 2002) or Flp-out (Wong et al., 2002), a large collection of individually labeled 2 order olfactory PNs were sorted into classes based on their dendritic innervation of 1 of 50 glomeruli in the fly antennal lobe.”
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].”
Olfactory memory formation in Drosophila: from molecular to systems neuroscience. (2005, background): “Generally, the ∼180 PNs extend dendrites into a single antennal lobe glomerulus and convey olfactory information to the mushroom bodies (MBs) and to the lateral horn (LH) (Figures 1 & 2; Jefferis et al. 2001, Marin et al. 2002, Wong et al. 2002).”
The Q System: A Repressible Binary System for Transgene Expression, Lineage Tracing and Mosaic Analysis (2010, unknown): “…integration into the attP2 locus (Groth et al., 2004). pUAST > stop > mCD8-GFP The widely used FLP-Out reporter, UAS > CD2,y+ > mCD8-GFP (Wong et al., 2002) contains non-optimal FRT sites (‘ > ’ represents FRT), which were chosen in order to increase the percentage of small FLP-out…”
Two-photon calcium imaging reveals an odor-evoked map of activity in the fly brain. (2003, background): “…neurons within a cluster is not spareflected by defined spatial patterns of activity, first in the antennal lobe and ultimately in higher olfactory centially stereotyped (Jefferis et al., 2001; Marin et al., 2002; Wong et al., 2002), and it is therefore difficult to identify ters in the brain.”