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1 on of gap-junctions between PCB and the hook sensillum.
2 gOR profile within a single labial olfactory sensillum.
3 e dendrites project to the distal end of the sensillum.
4 nd widely distributed of these is the hooded sensillum.
5 ins can be coexpressed in the same gustatory sensillum.
6  sensillum, the hair sensillum, and the knob sensillum.
7 ese differentiated characteristics give each sensillum a unique identity and potentially endow the co
8 or the response of the other ORN within that sensillum, ac3A.
9 al segments: the papilla sensillum, the hair sensillum, and the knob sensillum.
10 at the choices made by neighboring ORNs of a sensillum are coordinated via the asymmetric segregation
11 ne the repertoire of receptor genes for each sensillum by analyzing GAL4 driver lines of Ir, Gr, Ppk,
12 e coexpressed, indicating that an individual sensillum can contain more than one odorant-binding prot
13 rate that the two neurons within one type of sensillum can function independently.
14 rons (ORNs) housed in the same sensory hair (sensillum) can inhibit each other non-synaptically.
15  neurons, which observe a pairing rule: each sensillum combines neurons of two particular classes, th
16 osterior cells, P(9-11).p, comprise the hook sensillum competence group (HCG) with three potential fa
17 he cpA outer dendrite is embedded within the sensillum cuticle, potentially improving access to envir
18 required for odorant transport and that this sensillum does not require an abundant Obp.
19 ection of food aversion combined with single-sensillum electrophysiology to test whether the mouthpar
20 xillary palps in these two species by single-sensillum electrophysiology.
21 ned dominant trait and resides in changes in sensillum function.
22 d that when one functional type of olfactory sensillum in Drosophila was depleted of its sole abundan
23 ese results support the idea that the hooded sensillum is a singular and biologically important sensi
24 ures-including extracellular vacuoles within sensillum lumen, intricate dendritic branching, mitochon
25 rant-binding protein (OBP76a) present in the sensillum lymph bathing trichoid olfactory neuron dendri
26  by carrier proteins through the hydrophilic sensillum lymph in the antennae toward their membrane re
27              After transport across the bulk sensillum lymph into the lower pH area near the dendriti
28 olutions at the physiological pH of the bulk sensillum lymph near pH 6.5 show only BmorPBP(A), and in
29 eted from nonneuronal support cells into the sensillum lymph that bathes the olfactory neurons within
30 eromones and other semiochemicals across the sensillum lymph to the olfactory receptors (ORs) within
31  antiserum to SNMP infused directly into the sensillum lymph, we show that SNMP function is required
32 ble to degradation by enzymes present in the sensillum lymph.
33 nding affinity can only be bound in the bulk sensillum lymph.
34 d with direct delivery of pheromone into the sensillum milieu.
35 riads within the maxillary-palp capitate-peg-sensillum population.
36 functionally characterized them using single sensillum recording (SSR).
37  sensilla to 104 human odorants using single sensillum recording and characterized the electro-physio
38 n of action potentials is observed by single sensillum recordings and mixing these odorants with humi
39                  Electrophysiological single sensillum recordings demonstrated that the wall-pore sen
40                                       Single sensillum recordings from Orco-expressing Ir25a mutant a
41 with the selected sensitive line, and single sensillum recordings identified DEET-sensitive sensilla
42 t responses in electroantennogram and single sensillum recordings in adult Drosophila melanogaster an
43                                       Single-sensillum recordings showed that the BmorOR1-expressing
44    Electroantennogram experiments and single-sensillum recordings supported this hypothesis: antennae
45                                 Using single-sensillum recordings, we find that group housing increas
46 erforming heterologous expression and single-sensillum recordings, we show that odorant receptor (Or3
47                                 Using single-sensillum recordings, we systematically investigate the
48         Our findings suggest that each taste sensillum represents a discrete, functional unit express
49 simplex workers and identified the olfactory sensillum responding to neocembrene, thus likely express
50                                   Decreasing sensillum responsiveness to cuticular hydrocarbons could
51 high sensitivity might lead to plasticity in sensillum responsiveness.
52 thoracic and abdominal segments: the papilla sensillum, the hair sensillum, and the knob sensillum.
53                                          One sensillum type contains four ORNs and the others contain
54                         The map identifies a sensillum type that contains a single abundant Obp, Obp2
55      Recordings were made from an identified sensillum (type II), and the Jensen-Shannon divergence (
56                                          The sensillum types are intermingled on the surface of the p
57 o found an endogenous receptor in one of the sensillum types on Drosophila antenna that responds to b
58                            All of six tested sensillum types responded robustly to odors of widely di
59 itochondria enrichment in select ORNs, novel sensillum types, and empty sensilla containing no neuron
60 o particular classes, thereby yielding three sensillum types.
61 ptake of bombykol at the pore endings in the sensillum wall, whereas compounds with lower binding aff
62 e examined setae with features of the hooded sensillum, which is a class of bimodal chemomechanosensi
63 is examined in detail for the neurons of one sensillum, which were found to differ in their relative
64 R genes are expressed in several neurons per sensillum, while IR56d expression is restricted to sweet