ライフサイエンスコーパス: amphid

1 terminates within the tight junction of the amphid.

2 lled by sensory neurons in sensilla known as amphids.

3 is examined, with particular emphasis on the amphids.

4 , SRB-6, which is expressed in five types of amphid and phasmid chemosensory neurons.

5 or maintenance of cilia and dendrites in the amphid and phasmid ciliated sensory neurons.

6 GFP reporter indicates that the cilia of the amphid and phasmid dendritic endings are foreshortened.

7 amphid sensilla, DYF-6::GFP is expressed in amphid and phasmid neurons.

8 loss of ccpp-1 causes progressive defects in amphid and phasmid sensory cilia, suggesting that CCPP-1

9 hat localizes to the luminal surfaces of the amphid channel and other C. elegans tubes.

10 tially redundant manner to build full-length amphid channel cilia but are completely redundant for bu

11 In amphid channel cilia, nphp-4 mutations cause B tubule de

12 systems for ventral guidance of axons in the amphid commissure, a major route of axon entry into the

13 Our previous studies showed that amphid compartment size is controlled by opposing activi

14 Thus, unlike other dendrites, amphid dendritic tips are positioned by DEX-1 and DYF-7

15 The degeneration in amphid function corresponds with a failure of the glial-

16 ACD-1 is expressed in C. elegans amphid glia and functions with neuronal DEG/ENaC channel

17 reen aimed at identifying genes required for amphid glia remodeling.

18 th CeKinesin-II and CeOsm-3 are expressed in amphid, inner labial, and phasmid chemosensory neurons.

19 ression of SSU-1 protein in only the two ASJ amphid interneurons is sufficient to restore the wild ty

20 Each amphid is innervated by 13 neurons, and the dendritic pr

21 The morphology of the amphids is discussed primarily in the context of the cha

22 While daf-6 mutants display only amphid lumen defects, animals defective for both daf-6 a

23 We propose that amphid lumen morphogenesis is coordinated by neuron-deri

24 ression in various cell types, including the amphid neuron sheath and excretory cells.

25 rprets environmental signals relayed through amphid neurons and actively inhibits dauer formation dur

26 mily in both phasmid neurons in the tail and amphid neurons in the head supports the conclusion that

27 f five head neuron pairs, three of which are amphid neurons involved in dauer formation.

28 analysis indicates a progressive loss in the amphid neurons' ability to fill with lipophilic dyes as

29 but in ciliated sensory neurons of the head (amphid neurons) and the tail in hermaphrodites (phasmid

30 pressed in certain chemosensory neurons (ASI amphid neurons) throughout development and is also expre

31 ioral studies, here we report that a pair of amphid neurons, ASI, is activated by nutrition and regul

32 n additional sensory neuron not found in the amphid of C. elegans and propose homology with the C. el

33 Each amphid of H. contortus is innervated by 12 neurons.

34 The anterior sensory anatomy (not including amphids) of the nematode Aphelenchus avenae (Tylenchomor

35 hat ALR-1 is required for maintenance of the amphid organ structure throughout larval development.

36 sensory organ of Caenorhabditis elegans, the amphid, provides a powerful setting for studying glial c

37 Amphid sensilla are the primary olfactory, chemoreceptiv

38 roscopy, we reconstructed the anatomy of the amphid sensilla in the more distantly related nematode,

39 cates that dyf-6 functions in neurons of the amphid sensilla, DYF-6::GFP is expressed in amphid and p

40 orhabditis elegans aristaless orthologue, in amphid sensory function.

41 CAI-1 is detected by the C. elegans amphid sensory neuron AWC(ON).

42 that disrupts the structure and function of amphid sensory neurons also disrupts electrosensory beha

43 body wall muscles during embryogenesis, and amphid sensory neurons and pharyngeal neurons in adults.

44 of immobilized worms, we show that specific amphid sensory neurons are sensitive to the direction an

45 ing intracellular calcium dynamics among the amphid sensory neurons of immobilized worms, we show tha

46 ablation of the AWC(ON) cell, but not other amphid sensory neurons, abolished chemoattraction to CAI

47 ons, CHE-12 expression is restricted to some amphid sensory neurons, suggesting a specific role in th

48 ion to indole ascarosides depends on the ASK amphid sensory neurons.

49 lled dauer, in which glia and neurons of the amphid sensory organ remodel.

50 show that lumen formation in the C. elegans amphid sensory organ requires the gene daf-6.

51 e cell adhesion processes in maintaining the amphid sensory organs.

52 the confines of a compartment defined by the amphid sheath (AMsh) glial cell that envelops these endi

53 rescent pH imaging and RNA sequencing of the amphid sheath glia of Caenorhabditis elegans to reveal a

54 e describe our discovery that the C. elegans amphid sheath glia regulate intracellular pH via HCO3 (-

55 o HCO3 (-) and mediates HCO3 (-) uptake into amphid sheath glia.

56 nergistic, and that two types of neuron, the amphid single-ciliated sensory neuron type K (ASK) and t

57 corresponds with a failure of the glial-like amphid socket cell to maintain its specific cell shape a

58 Consistent with ALR-1 expression within the amphid socket cell, our results indicate a cell autonomo

59 cts expression in the motor neurone PDA, the amphid socket cells and the spermatheca; pC directs expr

60 Amphid structure is broadly conserved in number and arra

61 ompletely redundant for building full-length amphid wing (AWC) cilia.