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1 re-forming subunit of the rapidly activating delayed rectifier potassium channel.
2 e (HERG) that encodes the rapidly activating delayed rectifier potassium channel.
3 ith KVLQT1 to form the slow component of the delayed rectifier potassium channel.
4 side chains which influence binding to brain delayed rectifier potassium channels.
5 ferentiation and the accompanying changes in delayed rectifier potassium channel activity.
6 rteriosus involves the coordinated action of delayed rectifier potassium channels and voltage-gated c
7 currents (primarily through rapid and slowed delayed rectifier potassium channels) and that block of
8                    This also depends on slow delayed-rectifier potassium channels, and preferred thet
9                                  Kv2 family "delayed-rectifier" potassium channels are widely express
10 d neurotransmitter/neuromodulator receptors, delayed-rectifier potassium channels, calcium-dependent
11 a-go-go-related gene (HERG), which encodes a delayed-rectifier potassium channel, cause the disease i
12 al features of inactivation of the rat Kv2.1 delayed rectifier potassium channel, expressed in Xenopu
13 el, Isk-related family, member 1 (KCNE1) the delayed rectifier potassium channel I(Ks).
14 d gene (hERG) encodes the rapidly activating delayed rectifier potassium channel (I(Kr)) which plays
15 re-forming subunit of the rapidly activating delayed rectifier potassium channel (IKr), which is impo
16 re-forming subunit of the rapidly activating delayed rectifier potassium channel (IKr).
17  the alpha subunit of the rapidly activating delayed rectifier potassium channel (IKr).
18                             The cardiac slow delayed rectifier potassium channel (IKs), comprised of
19 tions in the gene encoding the voltage-gated delayed rectifier potassium channel Kv1.1 as underlying
20 ate and thereby suppress the activity of the delayed rectifier potassium channel Kv1.2.
21 oltage-induced activation of the human brain delayed rectifier potassium channel, Kv1.1.
22 ions in the function and localization of the delayed-rectifier potassium channel, Kv2.1.
23 achea correae, inhibits Kv1.3, a Shaker-type delayed rectifier potassium channel present in human T l
24                             Gene transfer of delayed rectifier potassium channels represents a novel
25 assium 2.1 (Kv2.1) channels are the dominant delayed rectifier potassium channels responsible for act
26    The Kv2.1 gene encodes a highly conserved delayed rectifier potassium channel that is widely expre
27               HERG encodes the cardiac rapid delayed rectifier potassium channel that mediates repola
28 ongation of the action potential by block of delayed rectifier potassium channels would be expected t

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