Coding of odors by a receptor repertoire.

By E. Hallem, John R. Carlson. Cell, 2006

1,255 citations recorded by the source corpus.

Subfields: Biomedical Engineering, Cellular and Molecular Neuroscience, Sensory Systems

View Paper: https://www.semanticscholar.org/paper/4421ff5640e334d2613ed5a578a45400e24c055a

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In Biomedical Engineering

In Cellular and Molecular Neuroscience

In Sensory Systems

Citations in the corpus

A predicted sex pheromone receptor of codling moth Cydia pomonella detects the plant volatile pear ester (2014, background): “The OR repertoire of Drosophila has been studied exhaustively (Hallem et al., 2004; Kreher et al., 2005; Hallem and Carlson, 2006) and current research aims at other insect groups.”
Dimensionality reduction for large-scale neural recordings (2014, methodology): “Dimensionality reduction has been used for data visualization and hypothesis generation in various brain areas, including the motor cortex 36,42,52,53 , hippocampus 54 , frontal cortex 55 , auditory cortex 56 , prefrontal cortex 57 , striatal cortex 58 and the olfactory system 59 .”
Activity of Defined Mushroom Body Output Neurons Underlies Learned Olfactory Behavior in Drosophila (2015, background): “The tuning of each OSN type is determined by the expression of a single odorant receptor gene (Dobritsa et al., 2003; Hallem and Carlson, 2004, 2006; Vosshall, 2000).”
Organization of antennal lobe‐associated neurons in adult Drosophila melanogaster brain (2012, background): “Recent genetic techniques have revealed the odor response profile of each type of olfactory receptor and projection patterns of OSNs expressing a given receptor (Hallem et al., 2004; Couto et al., 2005; Fishilevich and Vosshall, 2005; Hallem and Carlson, 2006; Silbering et al., 2011).”
Olfactory representations by Drosophila mushroom body neurons. (2008, methodology): “5), we adjusted our stimulus protocol to match that in the study of Hallem and Carlson (2006) in which OSN responses have been most thoroughly characterized to date.”
Divisive normalization in olfactory population codes (2010, methodology): “Based on a previous study (Hallem and Carlson, 2006), we identified four likely private odors and their cognate ORN types (Table S1).”
Comprehensive Maps of Drosophila Higher Olfactory Centers: Spatially Segregated Fruit and Pheromone Representation (2007, neutral): “We have combined this with physiological data from Hallem and Carlson (2006) to simulate putative ''odor activation maps''.”
Molecular architecture of smell and taste in Drosophila. (2007, methodology): “(d ) A possible chemotopic arrangement of glomeruli in the AL, such that glomeruli activated by similar odors cluster in the AL, remains a point of controversy (Couto et al. 2005, Fishilevich & Vosshall 2005, Hallem & Carlson 2006).”
Olfactory information processing in Drosophila. (2009, neutral): “Given the need to detect many more than 50 odorants, most olfactory receptor neurons respond to a broad range of odorants [36], a characteristic shared with mammals (for example, [37]).”
Non-Canonical Odor Coding in the Mosquito (2020, background): “Certain odors repress OR activity relative to baseline in Drosophila melanogaster (Hallem and Carlson, 2006; Yao et al., 2005) and it is possible that multiple receptors housed in a single neuron could be a source of blend-specific repression.”
Cellular-resolution population imaging reveals robust sparse coding in the Drosophila Mushroom Body (2011, methodology): “Our ability to track population-level responses reveals that this experience-dependent process can generate concentration-invariant levels of response in the MB. Sparse MB responses to natural and artificial multimolecular odors Our panel of monomolecular odors was chosen to activate a diverse set o”