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1 efining a form of contact-dependent, aquatic chemosensation.
2 ctive and chemorepulsive neurons compromises chemosensation.
3  Caenorhabditis elegans memory formation and chemosensation.
4 it, papilla and knob sensilla act in contact chemosensation.
5 orm a Na(+)-sensitive channel mediating salt chemosensation.
6 defects associated with mechanosensation and chemosensation.
7 or that functions specifically in salt taste chemosensation.
8 nel function in the regulation of C. elegans chemosensation.
9 y neurons that are not normally required for chemosensation.
10 phisms contribute to individual variation in chemosensation.
11 some fresh approaches to classic problems in chemosensation.
12 h the adaptive and non-adaptive evolution of chemosensation.
13 resentation of anticipatory and consummatory chemosensation.
14 nels or raphe neurons in central respiratory chemosensation.
15 there is no evidence that opsins function in chemosensation.
16  elegans arrestin-1 (arr-1) does not disrupt chemosensation.
17 t role for RGS proteins in the regulation of chemosensation.
18 ry modalities, such as vision, audition, and chemosensation.
19 action, osmosensation, mechanosensation, and chemosensation.
20 multiple egl-4-regulated pathways, including chemosensation.
21 ted in a coordination mutant and involved in chemosensation.
22 e and many other species, strongly relies on chemosensation.
23 aluable model for studying the mechanisms of chemosensation.
24 luble molecules to mediate contact-dependent chemosensation.
25  mtm-10 functions in AWC neurons to preserve chemosensation after pathogen infection.
26 ions of vagal and spinal afferent neurons to chemosensation and chemonociception.
27 ved huge expansions of genes associated with chemosensation and detoxification compared with speciali
28 data, we annotated the genes associated with chemosensation and found a reduced gene repertoire compo
29       Nervous systems are endowed with rapid chemosensation and intercellular signaling by ligand-gat
30  somatosensation, including thermosensation, chemosensation and nociception.
31        Our study reveals roles for opsins in chemosensation and raise questions concerning the origin
32 ein-coupled receptors that mediate olfactory chemosensation and serve as chemosensors in other tissue
33  a resolution device, with specific focus on chemosensation and the olfactory system, is of appeal.
34  proposed to form a transduction channel for chemosensation and thermosensation, and tax-2 activity i
35  grooves thought to aid in thermoregulation, chemosensation, and even hunting.
36 scular biology, immunology, insulin release, chemosensation, and others.
37 ensory functions, such as phototransduction, chemosensation, and thermosensation, in many species fro
38                    Phenotypic differences in chemosensation are well documented and influence food ch
39 e recently been made in understanding insect chemosensation at the molecular and cellular levels.
40 in adult sensory neurons profoundly disrupts chemosensation, based on both behavioral analysis and Ca
41 s respond to many chemosensory cues, but how chemosensation contributes to host seeking and intra-hos
42                     Here, we investigate how chemosensation drives host seeking and activation in ski
43       Eight domains were included (distorted chemosensation, emotional, food and meals, social, hygie
44  and chemesthesis), here also referred to as chemosensation, enables animals to find high-value foods
45 ore rhythmogenic microcircuits to O2-related chemosensation for the first time.
46       In recent years, however, the field of chemosensation has benefited from new methods and techni
47 sodium-sensitive channel required for sodium chemosensation in C. elegans, but its specific role rema
48 this coding strategy is a general feature of chemosensation in C. elegans, we imaged calcium response
49  G protein signaling (RGS) protein, restores chemosensation in Ce-grk-2 mutants.
50 3a together are sufficient for olfactory CO2-chemosensation in Drosophila.
51    Our results suggest an important role for chemosensation in iL3 host seeking and infectivity and p
52 the workshop: 1) refining methods to measure chemosensation in large cohort studies and validating me
53                  We find that the quality of chemosensation in lower dimensions is controlled by doma
54  that P2Y1 modulates heat responsiveness and chemosensation in muscle afferents to play a key role in
55  of general importance to both modalities of chemosensation in other insects.
56 nd demonstrate the essential role of contact chemosensation in the early courtship steps of mate sele
57                   To interrogate the role of chemosensation in the migration of larval worms, arthrop
58                                              Chemosensation in the nervous system of the nematode Cae
59 g an important starting point to investigate chemosensation in this class.
60 bstances as medicines, yet the importance of chemosensation in this process is poorly understood.
61 utrition, and health sciences to explore how chemosensation influences dietary choice and health.
62                                      Contact chemosensation is required for several behaviors that pr
63 ing a conserved role in thermoregulation and chemosensation, is required for this specialized host-se
64 ression, little is known about their role in chemosensation, largely due to the lack of available mut
65  of carbon dioxide, suggesting that aberrant chemosensation may underlie anxiety disorders associated
66 si that express OBPs are required for normal chemosensation mediated through the leg, as ablation of
67 h aligns with their proposed role in contact chemosensation of CHCs.
68 FAR1) and GPR120 have been implicated in the chemosensation of dietary fats.
69 oline receptors to mediate contact-dependent chemosensation of insoluble molecules that do not readil
70                            Here we show that chemosensation of phenazines produced by pathogenic Pseu
71 is required for some forms of olfaction, for chemosensation of salts, and for thermosensation.
72 of extracellular nucleotides cilia-dependent chemosensation of the nucleotides inhibited migration an
73 types of sensory neurons are responsible for chemosensation, olfaction, and mechanosensation.
74                     In contrast to mammalian chemosensation or Drosophila olfaction, which are initia
75 l types that are not associated with contact chemosensation raising the possibility that these protei
76        This study significantly extended the chemosensation-related gene profiles (particularly, OBPs
77  measures that reflect perception of complex chemosensations relevant to dietary choice; 2) character
78 is-specific genes possess predicted roles in chemosensation, reproduction, adaptation to specific die
79 regimes, we found that genes associated with chemosensation responded rapidly to the elimination of s
80 Here we present a theory of the precision of chemosensation that covers bounded domains of any dimens
81 n one well-known example of gastrointestinal chemosensation (the "incretin effect"), it is known that
82 ucleotide-gated channel that is required for chemosensation, thermosensation and normal axon outgrowt
83 tify genes and small molecules that modulate chemosensation, thermosensation, and mechanosensation.
84 y of male flies to detect females by contact chemosensation through the pheromone-sensing ion channel
85                                     We found chemosensation to be strongly predictive of therapeutic
86 ly, Drosophila melanogaster, rely on contact chemosensation to detect nutrient-rich foods, to avoid c
87           Insect survival depends on contact chemosensation to sense and avoid consuming plant-derive
88  causing defects in locomotion, feeding, and chemosensation when mutated.