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1 ents toward preferred temperatures (positive thermotaxis).
2 s are shared among pH-taxis, chemotaxis, and thermotaxis.
3 , a pathway that has been recently linked to thermotaxis.
4 rosophila gustatory receptor is required for thermotaxis.
5 ryophilic drive) precedes Tc tracking during thermotaxis.
6 slugs are highly defective in phototaxis and thermotaxis.
7 e down temperature gradients during negative thermotaxis.
8 s cPKC, is essential for a complex behavior, thermotaxis.
9 icate dTRPA1-expressing neurons in mediating thermotaxis.
10 eurons are also implicated in chemotaxis and thermotaxis.
11 s emerges in distinct motor responses during thermotaxis.
12 anglion (DOG) that are required for positive thermotaxis.
14 Our results suggest that sensory systems for thermotaxis and chemotaxis may converge on a common beha
15 ed by mutating Ser(311) or Ser(322), disrupt thermotaxis and suppress PKC-2-dependent cryophilic migr
16 e elucidate the basic rules of Aedes aegypti thermotaxis and test the function of candidate thermorec
17 ove up temperature gradients during positive thermotaxis and to move down temperature gradients durin
18 p a detailed, quantitative map of C. elegans thermotaxis and use these data to derive a computational
19 ncluding bacterial chemotaxis, pH taxis, and thermotaxis), and it also leads to predictions that can
24 that disrupts vesicle clustering and animal thermotaxis behavior when expressed in a single neuron i
26 ind that C. elegans exhibits robust negative thermotaxis bias under conditions of varying T(c) and te
27 The Drosophila melanogaster larva performs thermotaxis by biasing stochastic turning decisions on t
30 This computational analysis indicates that thermotaxis enables animals to avoid temperatures at whi
34 D causes a near-total loss of phototaxis and thermotaxis in mutant aggregates, without obvious effect
35 ional migration is not a result of bacterial thermotaxis in the classical sense, because the steepnes
36 hese data to derive a computational model of thermotaxis in the soil, a natural environment of C. ele
38 manipulation of PKC-2 activity revealed that thermotaxis is controlled by cooperative PKC-2-mediated
43 Our observations demonstrate that a negative thermotaxis navigational strategy can be generated via d
44 ition, the loss of crh-1/CREB suppressed the thermotaxis phenotypes of rcan-1 and tax-6 mutants, indi
47 ermal gradients, Caenorhabditis elegans uses thermotaxis to bias its movement along the direction of
49 erature (T(c)), C. elegans exhibits negative thermotaxis toward colder temperatures using a biased ra
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