ライフサイエンスコーパス: sensillum

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1 gOR profile within a single labial olfactory sensillum.

2 e dendrites project to the distal end of the sensillum.

3 nd widely distributed of these is the hooded sensillum.

4 ins can be coexpressed in the same gustatory sensillum.

5 on of gap-junctions between PCB and the hook sensillum.

6 ese differentiated characteristics give each sensillum a unique identity and potentially endow the co

7 or the response of the other ORN within that sensillum, ac3A.

8 at the choices made by neighboring ORNs of a sensillum are coordinated via the asymmetric segregation

9 ne the repertoire of receptor genes for each sensillum by analyzing GAL4 driver lines of Ir, Gr, Ppk,

10 e coexpressed, indicating that an individual sensillum can contain more than one odorant-binding prot

11 rate that the two neurons within one type of sensillum can function independently.

12 neurons, which observe a pairing rule: each sensillum combines neurons of two particular classes, th

13 osterior cells, P(9-11).p, comprise the hook sensillum competence group (HCG) with three potential fa

14 required for odorant transport and that this sensillum does not require an abundant Obp.

15 ned dominant trait and resides in changes in sensillum function.

16 ese results support the idea that the hooded sensillum is a singular and biologically important sensi

17 rant-binding protein (OBP76a) present in the sensillum lymph bathing trichoid olfactory neuron dendri

18 by carrier proteins through the hydrophilic sensillum lymph in the antennae toward their membrane re

19 After transport across the bulk sensillum lymph into the lower pH area near the dendriti

20 olutions at the physiological pH of the bulk sensillum lymph near pH 6.5 show only BmorPBP(A), and in

21 eted from nonneuronal support cells into the sensillum lymph that bathes the olfactory neurons within

22 eromones and other semiochemicals across the sensillum lymph to the olfactory receptors (ORs) within

23 antiserum to SNMP infused directly into the sensillum lymph, we show that SNMP function is required

24 ble to degradation by enzymes present in the sensillum lymph.

25 nding affinity can only be bound in the bulk sensillum lymph.

26 d with direct delivery of pheromone into the sensillum milieu.

27 riads within the maxillary-palp capitate-peg-sensillum population.

28 sensilla to 104 human odorants using single sensillum recording and characterized the electro-physio

29 with the selected sensitive line, and single sensillum recordings identified DEET-sensitive sensilla

30 Single-sensillum recordings showed that the BmorOR1-expressing

31 Electroantennogram experiments and single-sensillum recordings supported this hypothesis: antennae

32 Using single-sensillum recordings, we systematically investigate the

33 Our findings suggest that each taste sensillum represents a discrete, functional unit express

34 Decreasing sensillum responsiveness to cuticular hydrocarbons could

35 high sensitivity might lead to plasticity in sensillum responsiveness.

36 One sensillum type contains four ORNs and the others contain

37 The map identifies a sensillum type that contains a single abundant Obp, Obp2

38 Recordings were made from an identified sensillum (type II), and the Jensen-Shannon divergence (

39 The sensillum types are intermingled on the surface of the p

40 o found an endogenous receptor in one of the sensillum types on Drosophila antenna that responds to b

41 o particular classes, thereby yielding three sensillum types.

42 ptake of bombykol at the pore endings in the sensillum wall, whereas compounds with lower binding aff

43 e examined setae with features of the hooded sensillum, which is a class of bimodal chemomechanosensi

44 is examined in detail for the neurons of one sensillum, which were found to differ in their relative

45 R genes are expressed in several neurons per sensillum, while IR56d expression is restricted to sweet

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