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1 an be activated in plants by disruption of a cyclic nucleotide-gated ion channel.
2 irectly engaging hyperpolarization-activated cyclic nucleotide-gated ion channels.
3 epend entirely on Ca2+ entry through ciliary cyclic nucleotide-gated ion channels.
4 ensory transduction in the VNO might involve cyclic nucleotide-gated ion channels.
6 ttention will be given to the involvement of cyclic nucleotide-gated ion channels and Ca(2+) sensors.
7 function of BAG neurons requires TAX-2/TAX-4 cyclic nucleotide-gated ion channels and the receptor-ty
10 a G-protein-coupled mechanism and involves a cyclic nucleotide-gated ion channel as in the nasal olfa
11 2 mutation as a 3-kb deletion that fuses two cyclic nucleotide-gated ion channel (ATCNGC)-encoding ge
12 l studies were conducted on the cloned plant cyclic nucleotide-gated ion channels AtCNGC2 and AtCNGC1
13 Real-time measurements of cAMP using mutant cyclic nucleotide-gated ion channel biosensors, pharmaco
16 the structure-function relationship of plant cyclic nucleotide-gated ion channels (CNGCs), we identif
19 IH, a sea urchin hyperpolarization-activated cyclic nucleotide-gated ion channel (HCN), has a dual ef
20 ing heart rate (HR) involves activation of a cyclic nucleotide-gated ion channel (HCN4) by beta-adren
21 n and vertical migrations required the TAX-4 cyclic nucleotide-gated ion channel in the AFD sensory n
22 irectly activated by cAMP (EPAC), as well as cyclic nucleotide-gated ion channels in certain tissues.
24 xcised, inside-out membrane patch containing cyclic nucleotide-gated ion channels is used as a biosen
25 DND1 encodes the same protein as AtCNGC2, a cyclic nucleotide-gated ion channel of previously unknow
26 rexpression of a hyperpolarization-activated cyclic nucleotide-gated ion channel rescues the muscle p
27 ed by the gcy genes, and two presently known cyclic nucleotide-gated ion channel subunits, encoded by
28 have examined domain interactions in the rod cyclic nucleotide-gated ion channel using both physiolog
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