Or83b encodes a broadly expressed odorant receptor essential for Drosophila olfaction.

By M. Larsson, A. Domingos, Walton D. Jones, M. E. Chiappe, Hubert Amrein, Leslie B. Vosshall. Neuron, 2004

1,328 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Genetics, Insect Science

View Paper: https://www.semanticscholar.org/paper/e79ee1d0765acff27894021627dd49fa678f5cd9

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

1. Richard Benton
2. S. Waddell
3. Glenn C. Turner
4. Leslie B. Vosshall
5. Kei Ito
6. Gregory S. X. E. Jefferis
7. N. Tanaka
8. Keita Endo

In Genetics

1. Leslie B. Vosshall
2. S. Waddell
3. Richard Benton
4. Glenn C. Turner
5. Kei Ito
6. N. Tanaka
7. Keita Endo
8. Gregory S. X. E. Jefferis

In Insect Science

1. Leslie B. Vosshall
2. Richard Benton
3. Gregory S. X. E. Jefferis
4. Glenn C. Turner
5. Kei Ito
6. N. Tanaka
7. R. Stocker
8. Silke Sachse

Citations in the corpus

• Organization of antennal lobe‐associated neurons in adult Drosophila melanogaster brain (2012, background): “…and send projections to one of about 50 glomeruli in the AL (Stocker, 1994; Laissue et al., 1999; Clyne et al., 1999; Gao and Chess, 1999; Vosshall et al., 2000; Scott et al., 2001; Stortkuhl and Kettler, 2001; Wetzel et al., 2001; Larsson et al., 2004; Benton et al., 2009; Silbering et al., 2011).”
• Non-Canonical Odor Coding in the Mosquito (2020, methodology): “Coordinated co-expression of chemosensory receptors in the maxillary palp We have documented extensive chemosensory co-receptor co-expression, but to form functional odorant-sensitive IR or OR complexes, olfactory sensory neurons must express both co-receptors and ligand-sensitive receptors (Abuin e”
• Uncovering the novel characteristics of Asian honey bee, Apis cerana, by whole genome sequencing (2015, background): “Insects have a number of variable Ors, which form a chaperone with olfactory receptor co-receptor (Orco) in vivo [82-85].”
• Molecular, anatomical, and functional organization of the Drosophila olfactory system. (2005, neutral): “Only six ORN classes express more than one receptor (excluding the widely expressed Or83b [8], which heterodimerizes with other odorant receptors but is not functional by itself [ 37 , 38]; as well as the low levels of some additional Or or Gr genes in some neurons).”
• Atypical Membrane Topology and Heteromeric Function of Drosophila Odorant Receptors In Vivo (2006, methodology): “Diego, California, United States), mouse a-KDEL 1:100 (Stressgen Biotechnologies, Victoria, British Columbia, Canada), rabbit a-OR83b (EC2) 1:5000 [22], mouse a-OR83b (IC2) 1:100 (University of Texas Southwestern Medical Center Program for Genomic Applications, Dallas, Texas, United States), rabbit ”
• The evolution of animal chemosensory receptor gene repertoires: roles of chance and necessity (2008, background): “The active receptor complex is formed by the heterodimerization of a member of the OR family with the ubiquitously expressed receptor Or83b”
• Evolution of insect olfaction. (2011, neutral): “In contrast to the ORs of vertebrates, the insect ORs form heteromeric complexes typically composed of a single ligand-binding OR (Stö rtkuhl and Kettler, 2001; Dobritsa et al., 2003, but see Goldman et al., 2005) and the OR coreceptor Orco (Vosshall et al., 2000; Larsson et al., 2004).”
• Olfactory information processing in Drosophila. (2009, neutral): “in most olfactory receptor neurons, where it is required for odour responses [11].”