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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
18 gate odor-induced Ca2+ changes in individual olfactory cilia from salamander using the Ca2+ indicator
19 mical sensing in small compartments, such as olfactory cilia, insect antennae, or even synaptic bouto
20 refore, the diffusion coefficient of cAMP in olfactory cilia is an important factor in the transducti
21 activity by PEA was significantly greater in olfactory cilia isolated from PEA-imprinted salmon compa
25 However, because of the small size of the olfactory cilia, the existence and properties of such Ca
26 llular organelles in the sub-micron diameter olfactory cilia, this finding indicates that the IP(3) r
28 To begin to understand Ca2+ signaling in olfactory cilia, we used high-resolution imaging techniq
31 III are expressed almost exclusively in the olfactory cilia whereas PDE4A is present only in the cel
32 elevations have not been demonstrated in the olfactory cilia, which are the site of primary odor tran
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