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1 ents toward preferred temperatures (positive thermotaxis).
2 ficiently steep to elicit readily detectable thermotaxis.
3 ryophilic drive) precedes Tc tracking during thermotaxis.
4 s cPKC, is essential for a complex behavior, thermotaxis.
5 s emerges in distinct motor responses during thermotaxis.
6 anglion (DOG) that are required for positive thermotaxis.
7 s are shared among pH-taxis, chemotaxis, and thermotaxis.
8 , a pathway that has been recently linked to thermotaxis.
9 rosophila gustatory receptor is required for thermotaxis.
10 slugs are highly defective in phototaxis and thermotaxis.
11 e down temperature gradients during negative thermotaxis.
12 icate dTRPA1-expressing neurons in mediating thermotaxis.
13 eurons are also implicated in chemotaxis and thermotaxis.
14  ability to sustain forward movements during thermotaxis.
15 nction as highly sensitive thermosensors for thermotaxis.
16 hicle") which closely approximates basic fly thermotaxis.
17 minates the strategy behind larval zebrafish thermotaxis.
18 l is present in spermatozoa and required for thermotaxis.
19              pkc-2 gene disruption abrogated thermotaxis; a PKC-2 transgene, driven by endogenous pkc
20 Our results suggest that sensory systems for thermotaxis and chemotaxis may converge on a common beha
21 te that human scent acts critically to guide thermotaxis and host selection by this prolific malaria
22  groundbreaking development in the form of a thermotaxis and rheotaxis microfluidic (TRMC) device des
23 ed by mutating Ser(311) or Ser(322), disrupt thermotaxis and suppress PKC-2-dependent cryophilic migr
24 e elucidate the basic rules of Aedes aegypti thermotaxis and test the function of candidate thermorec
25 ove up temperature gradients during positive thermotaxis and to move down temperature gradients durin
26 p a detailed, quantitative map of C. elegans thermotaxis and use these data to derive a computational
27 ncluding bacterial chemotaxis, pH taxis, and thermotaxis), and it also leads to predictions that can
28 ermotaxis, (b) that retinal is essential for thermotaxis, and (c) that tri-cis retinal isomer uniquel
29 ain and by actions such as eating, drinking, thermotaxis, and predator escape.
30                       Currently, chemotaxis, thermotaxis, and rheotaxis have not been definitively es
31 and computational mechanisms responsible for thermotaxis are distinct in these organisms.
32                                           In thermotaxis assays of temperature gradient and two-tempe
33  (a) that opsins are thermosensors for sperm thermotaxis, (b) that retinal is essential for thermotax
34 we show that feeding state alters C. elegans thermotaxis behavior by engaging a modulatory circuit wh
35 xt-specific behavioral strategies underlying thermotaxis behavior in C. elegans.
36 iven by endogenous pkc-2 promoters, restored thermotaxis behavior in pkc-2(-/-) animals.
37  that disrupts vesicle clustering and animal thermotaxis behavior when expressed in a single neuron i
38 erneurons to override and disrupt AFD-driven thermotaxis behavior.
39 uits, and molecular networks responsible for thermotaxis behavior.
40 ind that C. elegans exhibits robust negative thermotaxis bias under conditions of varying T(c) and te
41   The Drosophila melanogaster larva performs thermotaxis by biasing stochastic turning decisions on t
42                          Disrupting positive thermotaxis by inactivating cold-sensitive neurons in th
43                We propose dTRPA1 may control thermotaxis by sensing environmental temperature.
44 tate does not alter the activity of the core thermotaxis circuit comprised of AFD thermosensory and A
45   This computational analysis indicates that thermotaxis enables animals to avoid temperatures at whi
46 desiccation and enabling transport (negative thermotaxis) from hazardous environments (like heat).
47               A candidate neural network for thermotaxis in C. elegans has been identified, but the b
48 l (TRP) family ion channel, is essential for thermotaxis in Drosophila.
49          Finally, characterization of larval thermotaxis in individuals reveals a bimodal distributio
50 required for this specialized host-selective thermotaxis in mosquitoes.
51 D causes a near-total loss of phototaxis and thermotaxis in mutant aggregates, without obvious effect
52                       We quantify C. elegans thermotaxis in response to various conditioning temperat
53 AWC and AIA, respectively, restores negative thermotaxis in starved animals.
54 ional migration is not a result of bacterial thermotaxis in the classical sense, because the steepnes
55 hese data to derive a computational model of thermotaxis in the soil, a natural environment of C. ele
56                      We discover that larval thermotaxis involves a larger repertoire of strategies t
57 manipulation of PKC-2 activity revealed that thermotaxis is controlled by cooperative PKC-2-mediated
58                                              Thermotaxis is important for animal survival, but the mo
59                    TRPA1-dependent tuning of thermotaxis is likely critical for mosquitoes host-seeki
60                                         This thermotaxis learning behavior associates paired stimuli,
61 mutants, indicating that crh-1 is crucial in thermotaxis memory in these mutants.
62 Our observations demonstrate that a negative thermotaxis navigational strategy can be generated via d
63  whose activity gates the output of the core thermotaxis network.
64 cially designed microfluidic device to study thermotaxis of Escherichia coli in a broad range of ther
65 ition, the loss of crh-1/CREB suppressed the thermotaxis phenotypes of rcan-1 and tax-6 mutants, indi
66                        Our data suggest that thermotaxis relies upon neurons and molecules distinct f
67 r different conditions to execute a negative thermotaxis strategy.
68                 On the other hand, bacterial thermotaxis, the directed migration of bacteria in a gra
69 ermal gradients, Caenorhabditis elegans uses thermotaxis to bias its movement along the direction of
70                   This role for rhodopsin in thermotaxis toward 18 degrees C was light-independent.
71 erature (T(c)), C. elegans exhibits negative thermotaxis toward colder temperatures using a biased ra
72 , and display diel vertical migration (i.e., thermotaxis) up to warmer waters (when present) during t
73                                              Thermotaxis was restored after replenishment of vitamin
74 cursor of retinal) resulted in loss of sperm thermotaxis, without affecting motility and the physiolo