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1  terminates within the tight junction of the amphid.
2  ring, as well as a major sensory organ, the amphid.
3 lled by sensory neurons in sensilla known as amphids.
4 is examined, with particular emphasis on the amphids.
5 , SRB-6, which is expressed in five types of amphid and phasmid chemosensory neurons.
6 or maintenance of cilia and dendrites in the amphid and phasmid ciliated sensory neurons.
7 GFP reporter indicates that the cilia of the amphid and phasmid dendritic endings are foreshortened.
8  amphid sensilla, DYF-6::GFP is expressed in amphid and phasmid neurons.
9 loss of ccpp-1 causes progressive defects in amphid and phasmid sensory cilia, suggesting that CCPP-1
10 rt-term foraging mode decisions, mediated by amphid and pre-motor interneurons, as well as the long-t
11 trate that the glial cells of the C. elegans amphid apparatus serve as odorant receptor cells and reg
12 hat localizes to the luminal surfaces of the amphid channel and other C. elegans tubes.
13 tially redundant manner to build full-length amphid channel cilia but are completely redundant for bu
14                                           In amphid channel cilia, nphp-4 mutations cause B tubule de
15 r, the morphological elaborations of several amphid cilia are different between them, most notably in
16 systems for ventral guidance of axons in the amphid commissure, a major route of axon entry into the
17             Our previous studies showed that amphid compartment size is controlled by opposing activi
18                          During development, amphid dendrites extend by attaching to the nose via DYF
19                Thus, unlike other dendrites, amphid dendritic tips are positioned by DEX-1 and DYF-7
20                          The degeneration in amphid function corresponds with a failure of the glial-
21             ACD-1 is expressed in C. elegans amphid glia and functions with neuronal DEG/ENaC channel
22 reen aimed at identifying genes required for amphid glia remodeling.
23  of such neurons, we examined the C. elegans amphid, in which dendrites protrude through a glial chan
24 th CeKinesin-II and CeOsm-3 are expressed in amphid, inner labial, and phasmid chemosensory neurons.
25 wiring diagram of amphid sensory neurons and amphid interneurons in P. pacificus and found striking p
26 ression of SSU-1 protein in only the two ASJ amphid interneurons is sufficient to restore the wild ty
27                            Here, we identify amphid interneurons that integrate pheromone cues and pr
28                                         Each amphid is innervated by 13 neurons, and the dendritic pr
29                        The morphology of the amphids is discussed primarily in the context of the cha
30             While daf-6 mutants display only amphid lumen defects, animals defective for both daf-6 a
31                              We propose that amphid lumen morphogenesis is coordinated by neuron-deri
32 ression in various cell types, including the amphid neuron sheath and excretory cells.
33 rprets environmental signals relayed through amphid neurons and actively inhibits dauer formation dur
34                           Here, we show that amphid neurons and glia exhibit epithelial properties, i
35                                          The amphid neurons first assemble into a multicellular roset
36 mily in both phasmid neurons in the tail and amphid neurons in the head supports the conclusion that
37 f five head neuron pairs, three of which are amphid neurons involved in dauer formation.
38 pon food availability, ILC-17.1 signaling by amphid neurons promotes glucose utilization and suppress
39 analysis indicates a progressive loss in the amphid neurons' ability to fill with lipophilic dyes as
40 but in ciliated sensory neurons of the head (amphid neurons) and the tail in hermaphrodites (phasmid
41 pressed in certain chemosensory neurons (ASI amphid neurons) throughout development and is also expre
42 ioral studies, here we report that a pair of amphid neurons, ASI, is activated by nutrition and regul
43 ake, we have assigned homologies between the amphid neurons, their first-layer interneurons, and seve
44 n additional sensory neuron not found in the amphid of C. elegans and propose homology with the C. el
45                                         Each amphid of H. contortus is innervated by 12 neurons.
46  The anterior sensory anatomy (not including amphids) of the nematode Aphelenchus avenae (Tylenchomor
47 hat ALR-1 is required for maintenance of the amphid organ structure throughout larval development.
48 sensory organ of Caenorhabditis elegans, the amphid, provides a powerful setting for studying glial c
49                                              Amphid sensilla are the primary olfactory, chemoreceptiv
50 roscopy, we reconstructed the anatomy of the amphid sensilla in the more distantly related nematode,
51 cates that dyf-6 functions in neurons of the amphid sensilla, DYF-6::GFP is expressed in amphid and p
52 orhabditis elegans aristaless orthologue, in amphid sensory function.
53      Moreover, our studies revealed that the amphid sensory neuron ASJ is involved in mediating the i
54          CAI-1 is detected by the C. elegans amphid sensory neuron AWC(ON).
55  that disrupts the structure and function of amphid sensory neurons also disrupts electrosensory beha
56  We established a synaptic wiring diagram of amphid sensory neurons and amphid interneurons in P. pac
57  body wall muscles during embryogenesis, and amphid sensory neurons and pharyngeal neurons in adults.
58  of immobilized worms, we show that specific amphid sensory neurons are sensitive to the direction an
59 d metabolism and reproductive physiology.(4) Amphid sensory neurons feed into both rapid chemotactic
60 ing intracellular calcium dynamics among the amphid sensory neurons of immobilized worms, we show tha
61  ablation of the AWC(ON) cell, but not other amphid sensory neurons, abolished chemoattraction to CAI
62 ons, CHE-12 expression is restricted to some amphid sensory neurons, suggesting a specific role in th
63 ion to indole ascarosides depends on the ASK amphid sensory neurons.
64                          We find that in the amphid sensory organ of Caenorhabditis elegans, differen
65 lled dauer, in which glia and neurons of the amphid sensory organ remodel.
66  show that lumen formation in the C. elegans amphid sensory organ requires the gene daf-6.
67 e cell adhesion processes in maintaining the amphid sensory organs.
68 e regulation, we used Caenorhabditis elegans amphid sheath (AMsh) glia as a model and show that a con
69 the confines of a compartment defined by the amphid sheath (AMsh) glial cell that envelops these endi
70                     In the sense-organ glia, amphid sheath (AMsh), this causes progressive fibroblast
71 rescent pH imaging and RNA sequencing of the amphid sheath glia of Caenorhabditis elegans to reveal a
72 e describe our discovery that the C. elegans amphid sheath glia regulate intracellular pH via HCO3 (-
73 o HCO3 (-) and mediates HCO3 (-) uptake into amphid sheath glia.
74                 Here, we demonstrate how the Amphid Single Cilium J (ASJ) chemosensory neurons, known
75 nergistic, and that two types of neuron, the amphid single-ciliated sensory neuron type K (ASK) and t
76 corresponds with a failure of the glial-like amphid socket cell to maintain its specific cell shape a
77  Consistent with ALR-1 expression within the amphid socket cell, our results indicate a cell autonomo
78 cts expression in the motor neurone PDA, the amphid socket cells and the spermatheca; pC directs expr
79                                              Amphid structure is broadly conserved in number and arra
80 ns in a C. elegans sensory organ, called the amphid, undergo a collective dendrite extension to form
81 ompletely redundant for building full-length amphid wing (AWC) cilia.