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2 vision in Caulobacter normally yields larger stalked and smaller swarmer daughters, we observe a loss
3 rol system drives progression of the coupled stalked and swarmer cell cycles of the bacterium Cauloba
8 describe the larval adhesive systems in the stalked barnacle, Octolasmis angulata and the findings d
12 er 1 interneurons, such as neurogliaform and stalked-bouton cells; the latter two groups showing no d
13 xonal distributions; rosehip, neurogliaform, stalked-bouton, layer 2-3 innervating and a pool of othe
14 analysis of growth and morphogenesis in the stalked budding alphaproteobacterium Hyphomonas neptuniu
15 ton as a key regulator of cell growth in the stalked budding alphaproteobacterium Hyphomonas neptuniu
18 division yields dissimilar daughter cells: a stalked cell and a swarmer cell that assembles several p
21 distinct cell types at each cell division: a stalked cell competent for DNA replication, and a swarme
23 roteolytically turned over during swarmer-to-stalked cell differentiation, coinciding with the loss o
24 is temporally separated from the swarmer-to-stalked cell differentiation, which is normally coincide
29 ivision to yield a motile swarmer cell and a stalked cell in the gram-negative bacterium Caulobacter
30 he morphological change from swarmer cell to stalked cell is a result of changes of function of two b
31 orms, the holdfast structure at the tip of a stalked cell is crucial for mediating the initial attach
34 hat there was a block in both the swarmer-to-stalked cell polar differentiation program and the initi
38 urs at the chromosomal origin located at the stalked cell pole, coincident with the initiation of DNA
39 ted CpdR accumulates and is localized to the stalked cell pole, where it enables ClpXP localization a
42 l types at each cell division: (i) a sessile stalked cell that can initiate DNA replication immediate
46 sis as cells enter S-phase at the swarmer-to-stalked cell transition and in the stalked portion of th
47 cleared by proteolysis during the swarmer-to-stalked cell transition as usual, but DNA replication in
48 ation of several dna genes at the swarmer to stalked cell transition occurs in response to cell cycle
49 ne, podJ, is expressed during the swarmer-to-stalked cell transition of the Caulobacter crescentus ce
52 th several genes expressed at the swarmer-to-stalked cell transition; while another appears to be con
55 es from 13 min in swarmer cells to 55 min in stalked cell types, confirming cell type-specific degrad
58 des asymmetrically into a swarmer cell and a stalked cell, a process that is governed by the imbalanc
59 mer cell for the impending transition into a stalked cell, a transition that is sparked by the abrupt
60 re induced at the transition from swarmer to stalked cell, coincident with the initiation of DNA repl
61 n differentiation of the swarmer cell into a stalked cell, full length PodJ is synthesized and locali
62 SpmX stimulates DivK phosphorylation in the stalked cell, unphosphorylated DivK in the swarmer cell
76 the preceding stage of the cell cycle (the "stalked" cell), DivL is localized uniformly along the ce
78 monstrates that disruption of the swarmer-to-stalked-cell developmental sequence does not affect the
79 mutants, which are blocked in the swarmer-to-stalked-cell transition and form flagellated, nonmotile
80 po IV genes is induced during the swarmer-to-stalked-cell transition when cells prepare for initiatio
81 e regulation of PodJ phase separation by the stalked-cell-pole scaffold protein SpmX is revealed.
83 While the holdfast was readily detectable in stalked cells and at the stalked poles of predivisional
84 before the swarmer cells differentiate into stalked cells and the intracellular concentration of Fts
86 ivision in which FtsZ and FtsA are stable in stalked cells but degraded in the non-replicative swarme
88 rol of available CcrM in progeny swarmer and stalked cells serves to protect the hemimethylated state
92 y after the initiation of DNA replication in stalked cells, one of the origins moves to the opposite
93 concentration and the ratio of nonstalked to stalked cells, over a range of flow rates and found that
94 at their concentration is low in swarmer and stalked cells, peaks in pre-divisional cells, and then d
96 the proportion was greater than 50% because stalked cells, with their shorter reproductive cycle tim
105 warmer-to-stalked cell transition and in the stalked compartment of the predivisional cell, CtrA is l
106 icate that cidaroid sea urchins feed on live stalked crinoids, leaving distinct bite marks on their s
107 ibia, which follows the underlying form of a stalked, cup-shaped, calcitic skeleton, with six radiall
109 e results in its specific inheritance in the stalked daughter cell where it phosphorylates DivK.
110 e that the functionally distinct swarmer and stalked daughter cells produced by the model alpha-prote
112 ort neurological remains associated with the stalked eyes and "anterior sclerite" in the (middle Camb
114 ylindrical slug transforms into an immotile, stalked fruiting body and the constituent cells change f
116 y cavity contents acquired from the capitate-stalked glandular trichomes by glass microcapillaries, a
118 to ensure that CtrA is degraded only in the stalked half of the predivisional cell, perhaps by local
121 little is known about the link between being stalked or obtaining a restraining order and risk of car
124 ines: the ClpXP degradation machinery at the stalked pole and the flagellar basal body at the swarmer
126 the cell fate-determining kinase DivJ at the stalked pole in Caulobacter, in cousins such as Asticcac
133 adily detectable in stalked cells and at the stalked poles of predivisional cells, we were unable to
134 warmer-to-stalked cell transition and in the stalked portion of the asymmetric predivisional cell.
135 transcriptional regulator molecules from the stalked portion of the predivisional cell is a controlli
136 Upon asymmetric cell division, swarmer and stalked progeny cells employ distinct mechanisms to cont
139 e nature of sea pen distribution relative to stalked sponges (Hyalonema sp.), suggesting occurrence o
141 form distribution throughout the swarmer and stalked stages of the cell cycle but more highly cluster
144 form of PleC is essential for the swarmer-to-stalked transition and to prevent premature development
145 osphate (polyP), that inhibit the swarmer-to-stalked transition in both complex and glucose-exhausted