ライフサイエンスコーパス: olfactory cilia

1 ized, implicating AP-1 in protein sorting to olfactory cilia.

2 presence of adenylyl cyclases 2, 3, and 4 in olfactory cilia.

3 ants, despite the presence of AC2 and AC4 in olfactory cilia.

4 y rapid exchange of the solution bathing the olfactory cilia.

5 e no significant diffusional barriers inside olfactory cilia.

6 cient of 2.7 +/- 0.2.10(-6) cm2 s-1 for frog olfactory cilia.

7 te odorant signal transduction in vertebrate olfactory cilia.

8 ted ability to regulate morphogenesis of the olfactory cilia.

9 tors to the type 3 adenylyl cyclase (AC3) in olfactory cilia.

10 the mechanisms of protein sorting/entry into olfactory cilia.

11 properties of Ca2+ transients in individual olfactory cilia and implicate CNG channels as a major pa

12 mouse CETN2 regulates protein trafficking of olfactory cilia and participates in specifying planar po

13 s required for motility of presumptive 9 + 2 olfactory cilia and, unexpectedly, 9 + 0 neural cilia.

14 ed mechanism for Ca2+ homeostasis within the olfactory cilia, and are consistent with the notion that

15 Frog olfactory cilia are 25-200 microm in length, so the spat

16 en repurposed for the biogenesis of immotile olfactory cilia, as well as for the development of the O

17 Olfactory cilia contain the known components of olfactor

18 nd [Formula: see text] in the small space of olfactory cilia during an odorant response.

19 cyclic nucleotide concentrations within the olfactory cilia during prolonged odour stimulation.

20 Although olfactory cilia dysfunction can cause anosmia, how their

21 A single mouse can produce enough olfactory cilia for up to 4000 384-well assay wells, and

22 gate odor-induced Ca2+ changes in individual olfactory cilia from salamander using the Ca2+ indicator

23 mical sensing in small compartments, such as olfactory cilia, insect antennae, or even synaptic bouto

24 refore, the diffusion coefficient of cAMP in olfactory cilia is an important factor in the transducti

25 activity by PEA was significantly greater in olfactory cilia isolated from PEA-imprinted salmon compa

26 Absence of CETN2 leads to olfactory cilia loss, impaired ciliary trafficking of ol

27 for sensory signaling-dependent reshaping of olfactory cilia morphology.

28 and display subtle morphological defects of olfactory cilia only.

29 A brief exposure of mouse olfactory cilia or primary olfactory neurons to odorants

30 However, because of the small size of the olfactory cilia, the existence and properties of such Ca

31 llular organelles in the sub-micron diameter olfactory cilia, this finding indicates that the IP(3) r

32 ory cilia such as retinal photoreceptors and olfactory cilia use diverse ion channels.

33 In keeping with the immotile nature of olfactory cilia, we observed that ciliary motility genes

34 To begin to understand Ca2+ signaling in olfactory cilia, we used high-resolution imaging techniq

35 ned and showed a reduced beat amplitude, and olfactory cilia were absent in mutants.

36 PDE2 and GC-D are both expressed in olfactory cilia where odorant signaling is initiated; ho

37 III are expressed almost exclusively in the olfactory cilia whereas PDE4A is present only in the cel

38 elevations have not been demonstrated in the olfactory cilia, which are the site of primary odor tran