Molecular, anatomical, and functional organization of the Drosophila olfactory system.
By Africa Couto, Mattias Alenius, Barry J. Dickson. Current Biology, 2005
988 citations recorded by the source corpus.
Subfields: Cellular and Molecular Neuroscience, Immunology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/d950af25d0023f3240aac789e2ad5e6c0e5c0002
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cellular and Molecular Neuroscience
- S. Waddell
- Hiromu Tanimoto
- Richard Benton
- Andrew C. Lin
- Wolf Huetteroth
- Leslie B. Vosshall
- N. Tanaka
- Johannes Felsenberg
In Immunology
- Hiromu Tanimoto
- Wolf Huetteroth
- S. Waddell
- E. Perisse
- Andrew C. Lin
- Johannes Felsenberg
- R. Stocker
- D. Owald
In Molecular Biology
- Kei Ito
- Keita Endo
- Richard Benton
- Gregory S. X. E. Jefferis
- Liqun Luo
- S. Waddell
- Torsten Rohlfing
- Stephan Saalfeld
Citations in the corpus
- A predicted sex pheromone receptor of codling moth Cydia pomonella detects the plant volatile pear ester (2014, background): “Indeed, closely related ORs with high sequence similarity are often expressed in OSNs that project to neighboring glomeruli in the AL (Couto et al., 2005; Masse et al., 2009; Ramdya and Benton, 2010; Cande et al., 2013).”
- Insect olfaction and the evolution of receptor tuning (2015, background): “Electrophysiological recordings from OSNs expressing IRs in the bristletail Lepismachilis ysignata using 36 stimuli at a high concentration (10−2 dilutions) showed a broader tuning as compared to the response of the IRs in D. melanogaster (Missbach et al., 2014).”
- Non-Canonical Odor Coding in the Mosquito (2020, background): “(Couto et al., 2005; Fishilevich and Vosshall, 2005; Tanaka et al., 2012) including a recent count of 54 (Grabe et al.”
- Genetic and functional subdivision of the Drosophila antennal lobe. (2005, background): “A related paper in the same issue of the journal [ 1 ] observed the same axonal-targeting phenotype for an independently generated Or67d-Gal4 transgene, but concluded that VA2 targeting was due to ectopic expression of the reporter in a second class of olfactory neurons.”
- Complementary Function and Integrated Wiring of the Evolutionarily Distinct Drosophila Olfactory Subsystems (2011, methodology): “Glomeruli receiving exclusively ipsilateral input, including the V glomerulus innervated by GR21a/GR63a neurons (Stocker et al., 1983; Scott et al., 2001; Couto et al., 2005; Jones et al., 2007; Kwon et al., 2007), are also grouped together in a posterior–ventral portion of the lobe (Fig.”
- Dopamine activity in projection neurons regulates short‐lasting olfactory approach memory in Drosophila (2022, background): “The ALs are composed of glomeruli, and each glomerulus consists of a cluster of synapses that receive input from sensory receptor neurons expressing a specific olfactory receptor (Couto et al., 2005; Laissue & Vosshall, 2008).”
- A Complete Developmental Sequence of a Drosophila Neuronal Lineage as Revealed by Twin-Spot MARCM (2010, background): “Following the trajectories of PNs that connect with distinct ORNs has started to unravel how different olfactory inputs might be processed differentially to govern diverse organismal behaviors [35].”
- Comprehensive Maps of Drosophila Higher Olfactory Centers: Spatially Segregated Fruit and Pheromone Representation (2007, positive): “Biological Correlates of Higher Olfactory Center Organization Recent progress in Drosophila olfaction has established a nearly complete map of the projections of ORNs expressing specific odorant receptors to the identified glomeruli of the antennal lobe (Couto et al., 2005; Fishilevich and Vosshall,”
- A conserved dedicated olfactory circuit for detecting harmful microbes in Drosophila. (2012, positive): “(E) Mean increase in free intracellular Ca2+ concentration [Ca2+]i in CHO cells expressing Orco and Or33a or nontransfected CHO cells after the application of saline (control), geosmin (50 mM), and VUAA1 (100 mM).”
- Neuronal assemblies of the Drosophila mushroom body (2008, background): “The AL consists of about 50 glomeruli, each of which receives input from a specific type of ORNs (Laissure et al., 1999; Vosshall et al., 2000; Couto et al., 2005; Fishilevich and Vosshall, 2005).”
- Activity of Defined Mushroom Body Output Neurons Underlies Learned Olfactory Behavior in Drosophila (2015, background): “Axons fromOSNs expressing the same receptor converge onto the same glomerulus in each antennal lobe (Vos- shall, 2000; Gao et al., 2000; Couto et al., 2005; Fishilevich and Vosshall, 2005), where their activity is relayed to excitatory and inhibitory projection neurons (Olsen et al., 2010;…”
- Drosophila olfactory memory: single genes to complex neural circuits (2007, background): “Exhaustive studies have determined that OSNs expressing the same olfactory receptor project to the same glomerulus among the ∼50 glomeruli in the antennal lob”
- Testing odor response stereotypy in the Drosophila mushroom body. (2008, neutral): “The glomeruli are in turn distributed in consistent spatial patterns in which neighborhood relationships are conserved across individuals (Couto et al., 2005; Dobritsa et al., 2003; Fishilevich and Vosshall, 2005; Laissue et al., 1999; Mombaerts et al., 1996; Ressler et al., 1994; Vassar et al., 199”
- Homeostatic matching and nonlinear amplification at identified central synapses. (2008, neutral): “In general, antennal lobe glomeruli vary widely in size, and the size of each glomerulus is stereotyped across individuals (Couto et al., 2005; Fishilevich and Vosshall, 2005; Laissue et al., 1999).”