ライフサイエンスコーパス: sensory cilia

1 shared components with motile or specialized sensory cilia.

2 on intraflagellar transport in photoreceptor sensory cilia.

3 actor essential for G protein trafficking in sensory cilia.

4 mize the functional properties of C. elegans sensory cilia.

5 plays an essential role in some, but not all sensory cilia.

6 Most studies of BBS have focused on primary, sensory cilia.

7 e and the microtubular axoneme of motile and sensory cilia.

8 , as well as genes required for formation of sensory cilia.

9 tial for the construction and maintenance of sensory cilia.

10 r male mating behaviors and are localized to sensory cilia.

11 nd or maintain cilia and flagella, including sensory cilia.

12 cellular membranes while another is found in sensory cilia.

13 se neurons, CePPEF is highly enriched in the sensory cilia.

14 ide, all move at the same rate in C. elegans sensory cilia.

15 ct is necessary for the assembly of a set of sensory cilia.

16 ultrastructural development of male-specific sensory cilia.

17 all eukaryotic motile flagella and nonmotile sensory cilia.

18 agged Odr-10 protein is localized to the AWA sensory cilia.

19 he development and maintenance of motile and sensory cilia [4].

20 nctional, tagged NOMPB protein is located in sensory cilia and around basal bodies.

21 UF protein may localize translation near the sensory cilia and cell body.

22 o result in defects in the ultrastructure of sensory cilia and defects in chemosensory and mechanosen

23 Tax-2::GFP fusion protein is present both in sensory cilia and in sensory axons.

24 Sensory cilia and intraflagellar transport (IFT), a path

25 Previous work has indicated that sensory cilia and polycystin-2 (Pkd2), a cation channel,

26 2, tagged OCR-2 and OSM-9 proteins reside in sensory cilia and promote each other's localization to c

27 bly, maintenance, and function of motile and sensory cilia, and, consequently, this process underlies

28 Sensory cilia are assembled by intraflagellar transport

29 Sensory cilia are populated by a select group of signali

30 luding processes and dendritic endings where sensory cilia are situated.

31 , centrioles fail to form the TZ, precluding sensory cilia assembly, and no ciliary membrane cap asso

32 A class of mutants with deformed sensory cilia at their dendrite endings have extra axon

33 og of IFT88, is required for the assembly of sensory cilia but not for the extension or function of t

34 rade motor, kinesin-II, and its cargo within sensory cilia, but not within dendrites.

35 ) kinesin-2 motors are required to establish sensory cilia by intraflagellar transport (IFT) where KI

36 ows through two distinct ion channels on the sensory cilia: Ca2+ influx through a cyclic nucleotide-g

37 omain-dependent tubulin-binding activity for sensory cilia development.

38 Many primary sensory cilia exhibit unique architectures that are crit

39 ion factor (TF) daf-19 null mutant lacks all sensory cilia, fails to express many ciliogenic genes, a

40 ndrome (JBTS), is required for photoreceptor sensory cilia formation and the development of photorece

41 pression levels correlate with the extent of sensory cilia growth and branching patterns.

42 ensory receptors, and mutants with defective sensory cilia have impaired sensory perception.

43 pe the morphology and protein composition of sensory cilia in C. elegans.

44 intraflagellar transport prevent assembly of sensory cilia in Drosophila, leaving the fly deaf and un

45 ree-dimensional structures of fifty of sixty sensory cilia in the C. elegans adult hermaphrodite at h

46 ese end in double processes, resulting in 13 sensory cilia in the channel.

47 yogenesis, including the formation of motile sensory cilia in the pronephros.

48 To study Ttc26 function in sensory cilia in vivo, we utilized a zebrafish vertebrat

49 chment of rhodopsin within rod photoreceptor sensory cilia, inhibited enrichment of the somatostatin

50 that expression of the shared components of sensory cilia is activated by daf-19, whereas cell-type-

51 norhabditis elegans result in defects in the sensory cilia located on the dendritic processes of sens

52 e photoreceptor cells are highly specialized sensory cilia made up of hundreds of membrane discs stac

53 nitial but incomplete description of diverse sensory cilia morphologies in C. elegans.

54 the structural integrity of microtubules in sensory cilia of a multicellular, living animal.

55 In sensory cilia of Caenorhabditis elegans male-specific ne

56 mary cilia of mammalian kidney epithelia and sensory cilia of Caenorhabditis elegans neurons, polycys

57 m/s by intraflagellar transport (IFT) within sensory cilia of chemosensory neurons of living Caenorha

58 whether the IFT complex is conserved in the sensory cilia of photo-receptors, we investigated protei

59 Sensory cilia of photoreceptors regulate phototransducti

60 elegans sensory neurons and localize to the sensory cilia of these cells.

61 We show that the sensory cilia of these neurons are malformed and the neu

62 The diversity of sensory cilia on Caenorhabditis elegans neurons allows t

63 tors and signaling proteins are localized to sensory cilia on olfactory dendrites.

64 we show that mutations that cause defects in sensory cilia or their support cells, or in sensory sign

65 ent over epithelial surfaces, while primary (sensory) cilia play roles in cellular signalling.

66 y analyzing the composition of photoreceptor sensory cilia (PSC) in Rpgr(ko) retina.

67 cystins LOV-1 and PKD-2 act in male-specific sensory cilia required for response and vulva-location m

68 -specific manner contributes to diversity in sensory cilia structure and might allow dynamic remodeli

69 Specialized sensory cilia such as retinal photoreceptors and olfacto

70 vely investigated for nonmotile cilia or for sensory cilia such as vertebrate photoreceptors.

71 es progressive defects in amphid and phasmid sensory cilia, suggesting that CCPP-1 activity is requir

72 hough IFT proteins are present in cells with sensory cilia, the organization of IFT protein complexes

73 Often called sensory cilia, they are thought to receive chemical and

74 ciliary transmembrane proteins in different sensory cilia types.

75 e leftward flow that is detected by immotile sensory cilia, which transduce flow into downstream asym

76 e nematode Caenorhabditis elegans depends on sensory cilia, whose assembly and maintenance requires t