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1 ototaxis (consequently, they were negatively phototactic).
2 ions in which wild-type cells are positively phototactic.
3  produce measurable carotenoids or to become phototactic.
4                     Analysis of E. gracilis' phototactic accumulation dynamics over a broad range of
5 ociated with either photophobic responses or phototactic accumulation of live cells.
6           In a control experiment, the known phototactic alga Chlamydamonas reinhardtii was shown to
7                    Rhodopsin photosensors of phototactic algae act as light-gated cation channels whe
8          Normal Dictyostelium aggregates are phototactic and thermotactic, moving towards sources of
9 ermissenda exhibited persistent increases in phototactic behavior after EU training.
10 domonas reinhardtii that had defects in both phototactic behavior and flagellar motility were identif
11               Modifications of Hermissenda's phototactic behavior by compound pairings of light, scal
12 mities, photoreceptor patterning defect, and phototactic behavior defect, indicating that these defec
13 mal phenotypes of cell cycle, cell size, and phototactic behavior exhibited substantial genetic varia
14                       The observed change in phototactic behavior observed in these studies suggests
15 ed orfamide A, protegencin thus prevents the phototactic behavior of C. reinhardtii A mutant of P. pr
16                                The increased phototactic behavior of EU animals was paralleled by sel
17                                          The phototactic behavior of individual cells of the cyanobac
18 modated fraction (WAF) of fresh crude oil on phototactic behavior of the calanoid copepod Calanus fin
19 xposure significantly increased the positive phototactic behavior of the copepods after 24 h exposure
20                         Adult mutants lacked phototactic behavior, and the off-transient component of
21 defects in photoreceptor cell patterning and phototactic behavior.
22  generation of testable hypotheses regarding phototactic behavior.
23  of the 1alpha Dhc in flagellar motility and phototactic behavior.
24 ble the f dynein complex and did not exhibit phototactic behavior.
25 e explain the swimming mechanism and predict phototactic behavior.
26 or both Dm8's spatial opponency and animals' phototactic behavior.
27 ibit some variation in their respective mean phototactic behaviors; however, it is not clear to what
28  required for the control of chemotactic and phototactic behaviour of both swim and swarm cells.
29 orts, cya1 and sycrp1 mutants are motile and phototactic but are impaired in one particular phase of
30               Go-opsin1 knockout larvae were phototactic but showed reduced efficiency of phototaxis
31 we consider only local interactions of these phototactic cells in order to mathematically model this
32 dynamic particle system modeling interacting phototactic cells.
33 ow that the emergent spatial organization of phototactic communities requires modification of the sub
34                      UV is a well-documented phototactic cue for adult Drosophila, but it is an avers
35 d by an associated pigment cell, providing a phototactic cue.
36 hototaxis-like swims, even in the absence of phototactic cues.
37                            Surprisingly, the phototactic efficiency has a minimum at a well-defined n
38 upports real-time interaction with swarms of phototactic Euglena cells hosted on a cloud laboratory.
39                      Optogenetics allows for phototactic guidance, steering, and turning maneuvers.
40 cators of the presence of photosynthetic and phototactic microbes in aquatic environments as early as
41                                 The proposed phototactic model captures the temporal dynamics of both
42 rst quantitative study of the long timescale phototactic motility of Chlamydomonas at both single cel
43 on components that coordinate gravitaxis and phototactic motility.
44  are consistent with experimentally observed phototactic motion.
45  evidence that type IV pili are required for phototactic movement in certain cyanobacteria and sugges
46                  We have recently shown that phototactic movement in the unicellular cyanobacterium S
47                                              Phototactic movement of the cyanobacterium Synechocystis
48               Most notably, this mutant lost phototactic movement with a concomitant loss of pili, wh
49  Inactivation of these pilA genes eliminated phototactic movement, though some pili were still presen
50  sp. strain PCC 6803 that exhibited aberrant phototactic movement.
51 d with the wild type, a permanently negative phototactic mutant required higher light intensities to
52                           Several negatively phototactic mutants mapped to the tax1 locus, which cont
53 is a light-sensitive organelle important for phototactic orientation of the alga.
54  white-dependent serotonin as suppressors of phototactic personality.
55 ue-light helmchromes, potentially underlying phototactic/photophobic and other behaviors toward speci
56                             Here, we present phototactic/phototherapeutic nanomotors where biodegrada
57 enomenology is well captured by modeling the phototactic response as a density-dependent torque actin
58 ight photoreceptor, implicated in a negative phototactic response in Ectothiorhodospira halophila, th
59 an efficient exposure to light, and that the phototactic response is modulated over typical timescale
60 gests that the high-frequency migration is a phototactic response to absolute light level.
61 ve yellow protein that ultimately mediates a phototactic response to blue light in certain purple bac
62                            A weakly negative phototactic response was also observed in the spectral r
63  spatial and population heterogeneity in its phototactic response.
64 of its photocycle, S(373), and an attractant phototactic response.
65 n less than a second, generating a repellent phototactic response.
66                                          All phototactic responses are mediated by the same set of se
67 haracterized and reexamined the motility and phototactic responses of Synechocystis sp. adenylyl cycl
68                   Both positive and negative phototactic responses were abolished in all che mutants,
69  an important component in the adaptation of phototactic sensitivity in Chlamydomonas.
70 h positive and negative phototaxis only when phototactic sensitivity is modeled by a generalized "rec
71                               Changes in the phototactic sign were accompanied by alterations in the
72                  Our results reveal that the phototactic strategy adopted by these microorganisms lea
73     The results suggest that potentiation of phototactic suppression by compound conditioning involve
74 r conditioning or sensory preconditioning of phototactic suppression was observed, indicating that wi
75  In general, the scallop extract potentiated phototactic suppression.
76 lecular and covalent networks reminiscent of phototactic swimming in living systems.
77 Nostoc punctiforme hormogonia are positively phototactic to white light over a wide range of intensit
78 trically between the two flagella to achieve phototactic turning.
79 pilT2 mutants are motile, but are negatively phototactic under conditions in which wild-type cells ar