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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 d signaling protein transport in specialized sensory cilia.
5 mize the functional properties of C. elegans sensory cilia.
6 plays an essential role in some, but not all sensory cilia.
7 Most studies of BBS have focused on primary, sensory cilia.
8 e and the microtubular axoneme of motile and sensory cilia.
9 , as well as genes required for formation of sensory cilia.
10 tial for the construction and maintenance of sensory cilia.
11 r male mating behaviors and are localized to sensory cilia.
12 nd or maintain cilia and flagella, including sensory cilia.
13 cellular membranes while another is found in sensory cilia.
14 se neurons, CePPEF is highly enriched in the sensory cilia.
15 ide, all move at the same rate in C. elegans sensory cilia.
16 ct is necessary for the assembly of a set of sensory cilia.
17 ultrastructural development of male-specific sensory cilia.
18 all eukaryotic motile flagella and nonmotile sensory cilia.
19 agged Odr-10 protein is localized to the AWA sensory cilia.
20 CA) in Caenorhabditis elegans that disrupted sensory cilia.
21 he development and maintenance of motile and sensory cilia [4].
22 nctional, tagged NOMPB protein is located in sensory cilia and around basal bodies.
23 UF protein may localize translation near the sensory cilia and cell body.
24 o result in defects in the ultrastructure of sensory cilia and defects in chemosensory and mechanosen
25 Tax-2::GFP fusion protein is present both in sensory cilia and in sensory axons.
26                                              Sensory cilia and intraflagellar transport (IFT), a path
27  presence of APP in motile and in non-motile sensory cilia and its potential implication for ciliogen
28             Previous work has indicated that sensory cilia and polycystin-2 (Pkd2), a cation channel,
29 2, tagged OCR-2 and OSM-9 proteins reside in sensory cilia and promote each other's localization to c
30 mal region is enriched for tanycytes bearing sensory cilia and receptors implicated in metabolic sens
31 bly, maintenance, and function of motile and sensory cilia, and, consequently, this process underlies
32                                              Sensory cilia are assembled by intraflagellar transport
33                                              Sensory cilia are populated by a select group of signali
34 luding processes and dendritic endings where sensory cilia are situated.
35 , centrioles fail to form the TZ, precluding sensory cilia assembly, and no ciliary membrane cap asso
36             A class of mutants with deformed sensory cilia at their dendrite endings have extra axon
37 og of IFT88, is required for the assembly of sensory cilia but not for the extension or function of t
38 rade motor, kinesin-II, and its cargo within sensory cilia, but not within dendrites.
39 ) kinesin-2 motors are required to establish sensory cilia by intraflagellar transport (IFT) where KI
40 ows through two distinct ion channels on the sensory cilia: Ca2+ influx through a cyclic nucleotide-g
41 omain-dependent tubulin-binding activity for sensory cilia development.
42                                 Many primary sensory cilia exhibit unique architectures that are crit
43 ion factor (TF) daf-19 null mutant lacks all sensory cilia, fails to express many ciliogenic genes, a
44 ndrome (JBTS), is required for photoreceptor sensory cilia formation and the development of photorece
45 pression levels correlate with the extent of sensory cilia growth and branching patterns.
46 e in terms of sensitivity and whether motile sensory cilia have a further advantage.
47 ensory receptors, and mutants with defective sensory cilia have impaired sensory perception.
48 pe the morphology and protein composition of sensory cilia in C. elegans.
49 intraflagellar transport prevent assembly of sensory cilia in Drosophila, leaving the fly deaf and un
50 ree-dimensional structures of fifty of sixty sensory cilia in the C. elegans adult hermaphrodite at h
51 ese end in double processes, resulting in 13 sensory cilia in the channel.
52 yogenesis, including the formation of motile sensory cilia in the pronephros.
53                   To study Ttc26 function in sensory cilia in vivo, we utilized a zebrafish vertebrat
54 chment of rhodopsin within rod photoreceptor sensory cilia, inhibited enrichment of the somatostatin
55  that expression of the shared components of sensory cilia is activated by daf-19, whereas cell-type-
56 norhabditis elegans result in defects in the sensory cilia located on the dendritic processes of sens
57 e photoreceptor cells are highly specialized sensory cilia made up of hundreds of membrane discs stac
58 nitial but incomplete description of diverse sensory cilia morphologies in C. elegans.
59  the structural integrity of microtubules in sensory cilia of a multicellular, living animal.
60                                           In sensory cilia of Caenorhabditis elegans male-specific ne
61 1 mechanotransduction channel complex in the sensory cilia of Caenorhabditis elegans mechanoreceptor
62 mary cilia of mammalian kidney epithelia and sensory cilia of Caenorhabditis elegans neurons, polycys
63 m/s by intraflagellar transport (IFT) within sensory cilia of chemosensory neurons of living Caenorha
64  whether the IFT complex is conserved in the sensory cilia of photo-receptors, we investigated protei
65                                              Sensory cilia of photoreceptors regulate phototransducti
66  elegans sensory neurons and localize to the sensory cilia of these cells.
67                             We show that the sensory cilia of these neurons are malformed and the neu
68                             The diversity of sensory cilia on Caenorhabditis elegans neurons allows t
69 tors and signaling proteins are localized to sensory cilia on olfactory dendrites.
70 we show that mutations that cause defects in sensory cilia or their support cells, or in sensory sign
71 ent over epithelial surfaces, while primary (sensory) cilia play roles in cellular signalling.
72 y analyzing the composition of photoreceptor sensory cilia (PSC) in Rpgr(ko) retina.
73 cystins LOV-1 and PKD-2 act in male-specific sensory cilia required for response and vulva-location m
74 ng C. elegans animals, we find that neuronal sensory cilia shed TRP polycystin-2 channel PKD-2::GFP-c
75            Quantitative phenotypic assays of sensory cilia structure and function (neuronal dye filli
76 -specific manner contributes to diversity in sensory cilia structure and might allow dynamic remodeli
77                                  Specialized sensory cilia such as retinal photoreceptors and olfacto
78 vely investigated for nonmotile cilia or for sensory cilia such as vertebrate photoreceptors.
79 es progressive defects in amphid and phasmid sensory cilia, suggesting that CCPP-1 activity is requir
80 and cone photoreceptor cells are specialized sensory cilia that contain hundreds of opsin-loaded stac
81 hough IFT proteins are present in cells with sensory cilia, the organization of IFT protein complexes
82    It is also an emerging model for studying sensory cilia, the production of high-value bioproducts,
83                                 Often called sensory cilia, they are thought to receive chemical and
84  ciliary transmembrane proteins in different sensory cilia types.
85 e leftward flow that is detected by immotile sensory cilia, which transduce flow into downstream asym
86 e nematode Caenorhabditis elegans depends on sensory cilia, whose assembly and maintenance requires t