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1 inactivation caused by the "ball" peptide in voltage-dependent K+ channels.
2 matched closely the nodal presence of these voltage-dependent K+ channels.
3 + channels, Ca(2+)-activated K+ channels and voltage-dependent K+ channels.
4 c densities that clusters NMDA receptors and voltage-dependent K+ channels.
5 l types: ATP-sensitive, Ca(2+)-regulated and voltage-dependent K(+) channels.
6 on with peptide toxins that target different voltage-dependent K(+) channels.
7 Patch-clamp techniques were used to survey voltage-dependent K+ channel activities in different cel
8 ever, we were able to identify four types of voltage-dependent K(+) channels and we categorized them
11 Regulation by voltage is similar to that in voltage-dependent K+ channels, arising from positively c
12 Here, we report that guard cells utilize voltage-dependent K+ channels as targets of the osmosens
20 We have analysed by electron microscopy a voltage-dependent K(+) channel from Aeropyrum pernix (Kv
21 tarantula venom voltage-sensor toxins on the voltage-dependent K+ channel from Aeropyrum pernix (KvAP
23 of a variety of antiproliferative agents on voltage-dependent K+ channel function in cortical oligod
24 ontrols the membrane expression of the human voltage-dependent K(+) channel human ether-a-go-go-relat
25 to establish the basic gating mechanisms of voltage-dependent K(+) channels, implying prior independ
27 the major somatodendritic delayed rectifier voltage-dependent K+ channel in central neurons, is regu
28 lcium-dependent potassium (BK-type) Ca2+ and voltage-dependent K+ channels in chromaffin cells exhibi
30 died the role of Kv1.4, a presynaptic A-type voltage-dependent K+ channel, in both memory and LTP.
32 rprisingly large effect on the function of a voltage-dependent K(+) channel, including its pharmacolo
34 variety of conditions that the function of a voltage-dependent K+ channel is dependent on the negativ
35 and (ii) cell depolarization and blockage of voltage-dependent K+ channels is likely to be the trigge
36 with the recent proposal that the sensor in voltage-dependent K+ channels is located at the membrane
37 structural basis for the activation gate of voltage-dependent K+ channels is not known, but indirect
38 ctively decreases 4-aminopyridine sensitive, voltage-dependent K(+) channel (K(v)) currents by approx
40 STRACT: Large-conductance KCa (BK) and other voltage-dependent K(+) channels (Kv) are highly expresse
41 ance Ca(2+) -activated K(+) channel (BK) and voltage-dependent K(+) channels (Kv) on [Ca(2+) ]i respo
42 test directly the hypothesis that different voltage-dependent K+ channel (Kv channel) alpha subunits
48 d phospholipid interface of the VSD from the voltage-dependent K(+) channel KvAP (prokaryotic Kv from
50 KOR sequence to the crystal structure of the voltage-dependent K+ channel KvAP from Aeropyrum pernix
51 al structure and dynamics of the prokaryotic voltage-dependent K+ channel (KvAP) at 0 millivolts, usi
52 tretch of eight residues that are similar in voltage-dependent K+ channels, Kvs, and this stretch is
55 This rise in [Ca2+]i causes inhibition of voltage-dependent K+ channels (possibly Kv1.5), membrane
59 2 clonal cell line expresses an O2-sensitive voltage-dependent K+ channel similar to that recorded in
61 Mutations in the K(V)7.2 gene encoding for voltage-dependent K(+) channel subunits cause neonatal e
64 mbrane depolarizes, but in contrast to other voltage-dependent K(+) channels, they also open when int
65 f channel opening on membrane voltage allows voltage-dependent K+ channels to turn on almost like a s
66 The structure of the cytoplasmic assembly of voltage-dependent K+ channels was solved by x-ray crysta
68 he IfastAHP is predominantly attributable to voltage-dependent K+ channels, whereas Ca2+-dependent an
69 ere we describe the structure of a chimaeric voltage-dependent K+ channel, which we call the 'paddle-
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