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1 ation, the sporophyte dries from the outside inwardly and continues to do so after guard cells die an
2  regions, however with the open state facing inwardly and the closed state facing outwardly.
3  transmembrane cargo can be sequestered into inwardly budding vesicles for degradation, or can exit t
4 s thaliana) plasma membrane Ca(2+)-permeable inwardly conducting ion channel impairs HR and that this
5 ear-UV photon drives the complex back to the inwardly connected conformer in the repellent signaling
6  by approximately 1.5 units from that of the inwardly connected conformer.
7 auses a Schiff base connectivity switch from inwardly connected to outwardly connected states in the
8      Throughout reversion, MreB localized to inwardly curved regions of the cell, and fluorescent cel
9                                    pUL31 can inwardly deform membranes by oligomerizing on their inne
10 cause it is spontaneous, self-generated, and inwardly directed (inner thoughts).
11                        The likelihood of the inwardly directed arrangement increases when Glu177 resi
12 ntaining electron-rich aromatic walls and an inwardly directed carboxylic acid displayed the necessar
13                      A deep cavitand with an inwardly directed carboxylic acid function reacts with s
14 zed by a synthetic cavitand receptor with an inwardly directed carboxylic acid function.
15 tion of a substrate, SERT and DAT display an inwardly directed current comprised of a peak and a stea
16 around the guest species; presents them with inwardly directed functionality; and provides a generall
17 esicles, melibiose efflux is inhibited by an inwardly directed gradient of Na(+) or Li(+) and stimula
18 esence of H(+) or Na(+) and stimulated by an inwardly directed Na(+) gradient.
19 ransport of chemically diverse ligands to an inwardly directed proton electrochemical gradient.
20 rotein- and energy-dependent pathway for the inwardly directed transbilayer movement of lipids other
21 ward transport of di- or tripeptides with an inwardly directed transport of protons.
22 ins, and distinct from previous undefined or inwardly facing arms.
23 to alternate between "outwardly facing" and "inwardly facing" conformations of the transmembrane subs
24                         Guard cells collapse inwardly, increase in surface area, and remain perched o
25 o the outwardly located periplasmic side and inwardly located cytoplasmic side.
26 sporter: the changes from an outwardly to an inwardly open conformation during the transport cycle us
27 e whether current conducted by KACh channels inwardly or outwardly rectifies.
28      Globally, the reaction from many was to inwardly - or publicly - scream.
29       These networks are believed to support inwardly oriented attention and inhibit bottom-up sensor
30                     In general, uracils with inwardly oriented backbones farther away from the dyad c
31 ackbones is 2-10-fold higher than those with inwardly oriented backbones.
32             Because we previously found that inwardly permeating Na ions facilitate dissociation of t
33 ally coordinated to water molecules and five inwardly pointing backbone phosphates.
34                     Each end cap includes an inwardly projecting tubular section, which prevents dc f
35 er concentration of cGMP and manifests as an inwardly rectified, K+-specific current with a 10.8 pS u
36 ely by Ca(2+), but the SK current (I(SK)) is inwardly rectified.
37 ed K(+) channel (KACh) conducts current that inwardly rectifies when activated by some ligands (such
38 ether their macroscopic current outwardly or inwardly rectifies, whereby rectification refers to a ch
39 h that GABABR activation shifts from opening inwardly rectifiying potassium channels (Kir/GIRK) to in
40 ents here, functional voltage-gated (Kv) and inwardly rectifying (Kir) K(+) channel remodeling was ex
41 e concurrent inhibition of barium-sensitive, inwardly rectifying (Kir) potassium channels and activat
42           We investigated the development of inwardly rectifying AMPA receptor-mediated currents and
43 ious results, whole-cell recordings revealed inwardly rectifying AMPAR EPSCs, a hallmark of CP-AMPARs
44                              The current was inwardly rectifying and inhibited by Ba(2+) (10 mum) and
45 clic monophosphate showed the presence of an inwardly rectifying and TRAM-34-sensitive K(+) channel i
46                 We identified the underlying inwardly rectifying Ca(2+)-dependent I(CRAC) (Ca(2+) rel
47                                              Inwardly rectifying Ca(2+)-permeable AMPA receptors medi
48 -expressed with STIM1, Orai1 induced a large inwardly rectifying Ca(2+)-selective current with Ca(2+)
49 d orai-1 cDNAs in HEK293 cells induces large inwardly rectifying cation currents activated by ER Ca(2
50 [sulfonylurea receptor (SUR) 1 and potassium inwardly rectifying channel (Kir) 6.1] were expressed se
51 3, member 13 of subfamily J of the potassium inwardly rectifying channel family in all affected indiv
52  activity, but does not alter activity of K+ inwardly rectifying channels (ROMK channels).
53  in neurons and glia, where they form strong inwardly rectifying channels.
54      CLC-2 is a hyperpolarization-activated, inwardly rectifying chloride channel.
55  Like human CFTR, ovine CFTR formed a weakly inwardly rectifying Cl(-) channel regulated by PKA-depen
56  of multiple Kir2 family paralogues, and the inwardly rectifying conductance contributes to the regul
57 izing mutants in the same loop express large inwardly rectifying CRAC current, and two of these exhib
58 ) and (I362T+A419P) generated a constitutive inwardly rectifying current that suggests a sensitivity
59 I-AMPARs as evidenced by polyamine-dependent inwardly rectifying current-voltage (I-V) relationships,
60  0.1 versus 1.2 +/- 0.1 nA at -160 mV) or in inwardly rectifying current-voltage relationships.
61 ve varitint-waddler hair cells as a distinct inwardly rectifying current.
62  potassium (ROMK) channel is a member of the inwardly rectifying family of potassium (Kir, Kir1.1) ch
63 hus the SNr receives direct projections from inwardly rectifying gamma-aminobutyric acid (GABA)-ergic
64 a(2+) (CRAC)-like current while retaining an inwardly rectifying I-V characteristic.
65                             In many tissues, inwardly rectifying K channels such as the renal outer m
66 is a critical determinant of G-protein-gated inwardly rectifying K(+) (GIRK) channel activation and u
67 G(i/o) proteins to promote G protein-coupled inwardly rectifying K(+) (GIRK) channel activation.
68 omplexes from Gi/o-gated G protein-regulated inwardly rectifying K(+) (GIRK) channels and delayed GIR
69 ing cascade that activates G-protein-coupled inwardly rectifying K(+) (GIRK) channels and small condu
70 Here we demonstrate that G protein-regulated inwardly rectifying K(+) (GIRK) channels can operate as
71 ate a shared pool of cardiac G protein-gated inwardly rectifying K(+) (GIRK) channels in SAN cells fr
72 hibitory signaling involving G-protein-gated inwardly rectifying K(+) (Girk) channels in VTA DA neuro
73          The presence of G protein-activated inwardly rectifying K(+) (GIRK) channels near excitatory
74                          G protein-activated inwardly rectifying K(+) (GIRK) channels regulate neuron
75 , including that mediated by G protein-gated inwardly rectifying K(+) (GIRK) channels, has been impli
76 nhibit neurons by activating G protein-gated inwardly rectifying K(+) (GIRK) channels, thereby modera
77 s reflects the activation of G protein-gated inwardly rectifying K(+) (GIRK) channels.
78                              G protein-gated inwardly rectifying K(+) (Girk/K(IR)3) channels mediate
79                              G-protein-gated inwardly rectifying K(+) (GIRK/Kir3) channel activation
80                              G protein-gated inwardly rectifying K(+) (GIRK/Kir3) channels mediate th
81 ve small molecule agonist of G-protein-gated inwardly rectifying K(+) (GIRK/Kir3) channels.
82               Once released, K(+) stimulates inwardly rectifying K(+) (K(IR) ) channels on the vascul
83 nished, suggesting a defect in smooth muscle inwardly rectifying K(+) (KIR) channel function.
84 ified in mouse macrophages: Ba(2+)-sensitive inwardly rectifying K(+) (Kir) channels and 4-aminopyrid
85                                    ABSTRACT: Inwardly rectifying K(+) (Kir) channels are known to be
86                                              Inwardly rectifying K(+) (Kir) channels are known to be
87  shown that capillary endothelial cell (cEC) inwardly rectifying K(+) (Kir) channels can sense neuron
88                                              Inwardly rectifying K(+) (Kir) channels set the resting
89                                              Inwardly rectifying K(+) (Kir) channels, serving as natu
90 uced excitation is mediated by inhibition of inwardly rectifying K(+) (Kir) channels.
91  increase in membrane cholesterol suppresses inwardly rectifying K(+) (Kir2) channels that are respon
92                      KEY POINTS: Endothelial inwardly rectifying K(+) (Kir2.1) channels regulate flow
93                                  Endothelial inwardly rectifying K(+) (Kir2.1) channels regulate flow
94 2 receptors activates atrial G protein-gated inwardly rectifying K(+) (Kir3) channels via the betagam
95 6-/-)) rats; Kcnj16 encodes the pH-sensitive inwardly rectifying K(+) 5.1 (Kir5.1) channel.
96 hannels are present in the lumen or when the inwardly rectifying K(+) channel blocker BaCl(2) is pres
97 perpolarization, increased G-protein-coupled inwardly rectifying K(+) channel current, and attenuated
98 rant localization, and enhanced block of the inwardly rectifying K(+) channel Kir2.1, compared with t
99 18, which encodes a skeletal muscle-specific inwardly rectifying K(+) channel Kir2.6, were reported i
100 etic neuralgia through downregulation of the inwardly rectifying K(+) channel Kir4.1 in satellite gli
101 ia development through downregulation of the inwardly rectifying K(+) channel Kir4.1 in satellite gli
102       Knockdown of the KCNJ15 gene (encoding inwardly rectifying K(+) channel Kir4.2) specifically ab
103 age-gated potassium channel (Kv), as well as inwardly rectifying K(+) channel remodeling, were invest
104  activation of the GIRK (G-protein activated inwardly rectifying K(+) channel).
105 t DNA sequencing of KCNJ10, which encodes an inwardly rectifying K(+) channel, identifies previously
106 at the CaR interacts with and inactivates an inwardly rectifying K(+) channel, Kir4.1, which is expre
107 naptic inhibition in the brain by activating inwardly rectifying K(+) channels (GIRKs) and inhibiting
108 amus through activation of G-protein-coupled inwardly rectifying K(+) channels (GIRKs).
109 most circumstances, outward currents through inwardly rectifying K(+) channels are reduced at more de
110 e that this inhibition requires one of three inwardly rectifying K(+) channels encoded by the C. eleg
111 lial cell Ca(2+)-activated K(+) channels and inwardly rectifying K(+) channels in arterial myocytes.
112 ABA(B)) receptors from their G-protein-gated inwardly rectifying K(+) channels in hypothalamic neuron
113  Comparison of high-resolution structures of inwardly rectifying K(+) channels suggests a model for a
114                        BaCl(2), a blocker of inwardly rectifying K(+) channels, also inhibited AITC-i
115            Ethanol activates G protein-gated inwardly rectifying K(+) channels, but the molecular mec
116 neurons in this region via inhibition of the inwardly rectifying K(+) channels.
117 nductance KCa1.1, Kv1.2/1.3, Kv7.4, hERG, or inwardly rectifying K(+) channels.
118 t investigations in this unexplored class of inwardly rectifying K(+) channels.
119 urine colonic muscles express genes encoding inwardly rectifying K(+) channels.
120 man resistance arteries is also regulated by inwardly rectifying K(+) channels.
121  does not act via either G-protein-activated inwardly rectifying K(+) conductance (G(IRK)) or hyperpo
122 y is that ICC express the Ba(2+) -sensitive, inwardly rectifying K(+) conductance in colonic muscles.
123 tence of I(OMMKi), a novel voltage-dependent inwardly rectifying K(+) conductance located in the OMM.
124 onic muscles, expressed a Ba(2+) -sensitive, inwardly rectifying K(+) conductance.
125 we pinpointed the lack of the Kir2.1-encoded inwardly rectifying K(+) current (I(K1)) as the single m
126                       There was little or no inwardly rectifying K(+) current (I(K1)) in the ED11 atr
127 kephalin (DAMGO) and endomorphin-2 activated inwardly rectifying K(+) current in a concentration-depe
128 ized fashion mainly by a G-protein-activated inwardly rectifying K(+) current.
129  by increased PIP(2)-gated G-protein coupled inwardly rectifying K(+) currents as well.
130 ation of G proteins, and G protein-activated inwardly rectifying K(+) currents.
131 R)-mediated activation of G-protein-coupled, inwardly rectifying K(+) currents.
132 tor-mediated activation of G-protein-coupled inwardly rectifying K(+)-like currents.
133 istent with opening of a G protein-regulated inwardly rectifying K+ (GIRK) channel.
134                                              Inwardly rectifying K+ (Kir) channels are responsible fo
135  (KATP) is formed by the association of four inwardly rectifying K+ channel (Kir6.x) pore subunits wi
136  reduction in GABABR-dependent activation of inwardly rectifying K+ channel currents.
137 e frequency, increased GIRK (G-protein-gated inwardly rectifying K+ channel) current, and attenuated
138                          G protein-activated inwardly rectifying K+ channels (GIRK) generate slow inh
139  however, it requires synaptic activation of inwardly rectifying KARs and release of Ca(2+) from stor
140 hannels are heteromultimeric complexes of an inwardly rectifying Kir channel (Kir6.x) and sulfonylure
141          In this, they more closely resemble inwardly rectifying Kir6.2 potassium channels than the m
142 had depolarized resting potentials due to an inwardly rectifying leak conductance formed by the mutan
143 s, including the hyperpolarization-activated inwardly rectifying non-specific cation current (I(h)),
144 polarized potential (e.g. cells with a large inwardly rectifying or Ca(2+)-activated K(+) current), a
145 onstant inhibitory action of ATP on the K(+) inwardly rectifying pore.
146 that alcohol activation of a G-protein-gated inwardly rectifying potassium (GIRK or Kir3) channel is
147 lular pathways that regulate G protein-gated inwardly rectifying potassium (GIRK or Kir3) channels ar
148                          G protein-activated inwardly rectifying potassium (GIRK or Kir3) channels ar
149 etween GPCRs, G proteins and G protein-gated inwardly rectifying potassium (GIRK or Kir3) channels.
150  REM sleep; likewise, with G-protein-coupled inwardly rectifying potassium (GIRK) channel blockade.
151     Tertiapin Q (TPQ), a G protein-dependent inwardly rectifying potassium (GIRK) channel inhibitor,
152              For example, in excitable cells inwardly rectifying potassium (GIRK) channels are activa
153                              G protein-gated inwardly rectifying potassium (GIRK) channels are critic
154 iously, we demonstrated that G-protein-gated inwardly rectifying potassium (GIRK) channels are expres
155                              G protein-gated inwardly rectifying potassium (GIRK) channels are import
156                            G-protein-coupled inwardly rectifying potassium (GIRK) channels contribute
157 the effect of cholesterol on G protein-gated inwardly rectifying potassium (GIRK) channels expressed
158 onist baclofen to activate G protein-coupled inwardly rectifying potassium (GIRK) channels in hypotha
159 rnalization of M(2)R and G-protein-activated inwardly rectifying potassium (GIRK) channels in neurona
160 s revealed the expression of G protein-gated inwardly rectifying potassium (GIRK) channels in these c
161 latonin receptors activate G-protein-coupled inwardly rectifying potassium (GIRK) channels in Xenopus
162                Activation of G protein-gated inwardly rectifying potassium (GIRK) channels leads to a
163                          G protein-activated inwardly rectifying potassium (GIRK) channels mediate sl
164 jor subunits of neuronal G protein-activated inwardly rectifying potassium (GIRK) channels that media
165 eurons by avidin-mediated cross-linking, and inwardly rectifying potassium (GIRK) channels were used
166 d a photochromic opener of G protein-coupled inwardly rectifying potassium (GIRK) channels, termed CL
167                              G-protein-gated inwardly rectifying potassium (GIRK) channels, which hel
168 rons through activation of G-protein-coupled inwardly rectifying potassium (GIRK) channels.
169 ) virally overexpressing G-protein-activated inwardly rectifying potassium (GIRK) channels.
170 Cl2 , characteristics of a G protein-coupled inwardly rectifying potassium (GIRK) conductance.
171 and D2L receptor-dependent G protein-coupled inwardly rectifying potassium (GIRK) currents.
172 oltage clamp, Dyn-A opened G-protein-coupled inwardly rectifying potassium (GIRK)-like channels on PO
173                        The G-protein coupled inwardly rectifying potassium (GIRK, or Kir3) channels a
174 ted by GABA(B) receptors and G protein-gated inwardly rectifying potassium (GIRK/Kir(3)) channels, ho
175                              G protein-gated inwardly rectifying potassium (GIRK/Kir3) channels media
176 es D2-receptors on MSNs, G protein activated inwardly rectifying potassium (GIRK2; Kir 3.2) channels
177                              G-protein-gated inwardly rectifying potassium (GIRK; also known as Kir3)
178                           Here, we show that inwardly rectifying potassium (Irk) channels regulate re
179                              G protein-gated inwardly rectifying potassium (K(+)) (Girk/Kir3) channel
180              We tested whether activation of inwardly rectifying potassium (K(IR) ) channels underlie
181 traction is due in part to the activation of inwardly rectifying potassium (K(IR) ) channels.
182 raction is mediated in part by activation of inwardly rectifying potassium (K(IR) ) channels.
183                                     Although inwardly rectifying potassium (K(IR)) channels are known
184  via the activation of Na(+)/K(+)-ATPase and inwardly rectifying potassium (K(IR)) channels in humans
185 e antiviral immune response by ATP-sensitive inwardly rectifying potassium (KATP) channels.
186 nted during exercise following inhibition of inwardly rectifying potassium (KIR ) channels and Na(+)
187 ilatation that is dependent on activation of inwardly rectifying potassium (KIR ) channels, with a mo
188                    Nearly all members of the inwardly rectifying potassium (Kir) channel family share
189 ics simulations containing >100 copies of an inwardly rectifying potassium (Kir) channel which forms
190 in human sequence databases) that encodes an inwardly rectifying potassium (Kir) channel, Kir2.6.
191 ypothesized that RH occurs via activation of inwardly rectifying potassium (KIR) channels and Na(+)/K
192 llular polyamines are endogenous blockers of inwardly rectifying potassium (Kir) channels and underli
193                                              Inwardly rectifying potassium (Kir) channels are charact
194                                              Inwardly rectifying potassium (Kir) channels are gated b
195                                              Inwardly rectifying potassium (Kir) channels form gates
196             Control of surface expression of inwardly rectifying potassium (Kir) channels is importan
197                                              Inwardly rectifying potassium (Kir) channels play an imp
198                                              Inwardly rectifying potassium (Kir) channels regulate mu
199                                              Inwardly rectifying potassium (Kir) channels were the fi
200 annels are prokaryotic homologs of mammalian inwardly rectifying potassium (Kir) channels, and recent
201                        Cholesterol modulates inwardly rectifying potassium (Kir) channels.
202 sphate (PIP(2)) is an activator of mammalian inwardly rectifying potassium (Kir) channels.
203 ive potassium channels, most consistent with inwardly rectifying potassium (Kir) channels.
204 , we show that the voltage dependence of the inwardly rectifying potassium (KIR) conductance activate
205 ular complexes with neuronal G protein-gated inwardly rectifying potassium (Kir3 or GIRK) channels.
206            Expression of this photoinducible inwardly rectifying potassium (PIRK) channel in rat hipp
207                                          The inwardly rectifying potassium 3.2 (Kir3.2) channel is fo
208 crystallization conditions for a prokaryotic inwardly rectifying potassium channel (>130 different co
209 xpressing rat MOR1 as well G protein-coupled inwardly rectifying potassium channel (GIRK) channel sub
210 ce that reversed at -93 mV, indicative of an inwardly rectifying potassium channel (GIRK) mechanism.
211  KOR-induced tyrosine phosphorylation of the inwardly rectifying potassium channel (GIRK) subunit Kir
212 -MSN hyperexcitability mediated by decreased inwardly rectifying potassium channel (IRK) function.
213 nal excitability through co-expression of an inwardly rectifying potassium channel (Kir2.1).
214 r-mediated activation of G-protein-activated inwardly rectifying potassium channel (Kir3.X) (GIRK) co
215  multimeric protein complex composed of four inwardly rectifying potassium channel (Kir6.2) and four
216 mutations in KCNJ6 (GIRK2), which encodes an inwardly rectifying potassium channel and maps to the Do
217 ings of ligand activated G-protein-activated inwardly rectifying potassium channel currents in mouse
218  mutation in the gene encoding the G-protein inwardly rectifying potassium channel Girk2, exhibits a
219  specific amino acid mutations in the Kir2.1 inwardly rectifying potassium channel have been found to
220 Mutations that disrupt function of the human inwardly rectifying potassium channel KIR2.1 are associa
221 use visual system to ectopically express the inwardly rectifying potassium channel Kir2.1 in individu
222 us activity due to the overexpression of the inwardly rectifying potassium channel Kir2.1 in the olfa
223 n of a photoreactive Uaa into the pore of an inwardly rectifying potassium channel Kir2.1.
224 iesterase (PDE) 1C, and PDE9A; and channels: inwardly rectifying potassium channel Kir2.4, transient
225  mediated via the G protein-coupled receptor inwardly rectifying potassium channel Kir3.Our findings
226                                              Inwardly rectifying potassium channel Kir4.1 is critical
227                     Whether the basolateral, inwardly rectifying potassium channel Kir4.1/Kir5.1 (a h
228 stal convoluted tubule (DCT), comprising the inwardly rectifying potassium channel Kir4.1/Kir5.1 hete
229                                          The inwardly rectifying potassium channel Kir4.2 is sensitiv
230                                          The inwardly rectifying potassium channel Kir6.2 assembles w
231                                          The inwardly rectifying potassium channel Kir6.2 is the pore
232 ng the sulfonylurea receptor 1 (SUR1) or the inwardly rectifying potassium channel Kir6.2, respective
233  P(a) < 0.08), as well as with ATP-sensitive inwardly rectifying potassium channel subunit Kir6.2 (KC
234 t of Gbetagamma on GIRK (G protein activated inwardly rectifying potassium channel) activation.
235 TA neurons, NK receptor activation closes an inwardly rectifying potassium channel, and moreover inhi
236 l, cytoplasmic domain of the G-protein-gated inwardly rectifying potassium channel, K(ir)3.1 facilita
237 yperexcitable due to reduced function of the inwardly rectifying potassium channel, Kir2.
238 ned by mutations in a novel gene encoding an inwardly rectifying potassium channel, Kir2.6.
239                  The KCNJ13 gene encodes the inwardly rectifying potassium channel, Kir7.1.
240 igand-induced coupling of MC4R to closure of inwardly rectifying potassium channel, Kir7.1.
241 larke et al. now present 11 structures of an inwardly rectifying potassium channel, providing evidenc
242 ptor-mediated opening of a G-protein-coupled inwardly rectifying potassium channel.
243 d postsynaptic activation of G-protein-gated inwardly rectifying potassium channels (GIRKs) electroph
244 ought to determine whether G protein-coupled inwardly rectifying potassium channels (GIRKs) modulate
245 ty of effectors, including G-protein-coupled inwardly rectifying potassium channels (GIRKs)(1,2).
246 ave investigated the role of G-protein-gated inwardly rectifying potassium channels (GIRKs), a recent
247 trimers to interact with G-protein regulated inwardly rectifying potassium channels (GIRKs), and we s
248 nd specific members of the G-protein-coupled inwardly rectifying potassium channels (GirKs).
249 rated by the activation of G-protein-coupled inwardly rectifying potassium channels (GIRKs).
250 ated vasodilatation occurs via activation of inwardly rectifying potassium channels (KIR ), and synth
251  consequent upon loss or reduced function of inwardly rectifying potassium channels affecting various
252 ha(i/o)-coupled receptors, G protein-coupled inwardly rectifying potassium channels and adenylate cyc
253  We tested the hypothesis that activation of inwardly rectifying potassium channels and the sodium-po
254                                     Strongly inwardly rectifying potassium channels are blocked by in
255                                Regulation of inwardly rectifying potassium channels by intracellular
256 hloroquine and related compounds can inhibit inwardly rectifying potassium channels by multiple poten
257                                              Inwardly rectifying potassium channels enforce tight con
258 ore, whether Cav-1 regulates the function of inwardly rectifying potassium channels Kir2.1 that play
259 r and its downstream GIRK (G protein-coupled inwardly rectifying potassium channels) channels (IK,Ado
260 -THCs enable CB1-mediated optical control of inwardly rectifying potassium channels, as well as adeny
261 er L-glutamate or expressing G-protein-gated inwardly rectifying potassium channels, hepatic lineage
262 oding Trpv4, Aqp4, and the Kir4.1 subunit of inwardly rectifying potassium channels.
263  through the activation of G-protein-coupled inwardly rectifying potassium channels.
264 In the striatum, light delivery activated an inwardly rectifying potassium conductance and biased rot
265 iated by the mGlu2 subtype that activates an inwardly rectifying potassium conductance in the dendrit
266 ine-mediated activation of G protein-coupled inwardly rectifying potassium conductance was measured u
267 ing to the activation of a G protein-coupled inwardly rectifying potassium conductance.
268 tion (61%) of KF neurons by activation of an inwardly rectifying potassium conductance.
269 es have postulated an important role for the inwardly rectifying potassium current (I(K1)) in control
270 wo critical ionic current mechanisms are the inwardly rectifying potassium current (I(K1)), which is
271  sarcoplasmic reticulum Ca2+ concentrations, inwardly rectifying potassium current (IK1) density, and
272  excitability through inhibition of a tonic, inwardly rectifying potassium current (K(IR) ).
273          The activation of G protein-coupled inwardly rectifying potassium current was measured using
274 ors by (1) activation of a G protein-coupled inwardly rectifying potassium current, (2) inhibition of
275 potential from resting value, mediated by an inwardly rectifying potassium current, resulting in redu
276 types of TH neuron through G-protein coupled inwardly rectifying potassium currents mediated by delta
277 nist baclofen both elicited increases of the inwardly rectifying potassium currents that could be blo
278                              G protein-gated inwardly rectifying potassium ion (GIRK/Kir3) channels,
279 he Kir7.1 subunit that acts as a tetrameric, inwardly rectifying potassium ion channel in the retinal
280 ltage-dependent inward rectification of Kir (inwardly rectifying potassium) channels arises from bloc
281 receptor desensitization from a linear to an inwardly rectifying shape, in contrast to their heterome
282  currents in primary hippocampal neurons are inwardly rectifying upon desensitization.
283  by submicromolar concentrations of 5-HT, is inwardly rectifying with a reversal potential near the e
284 he current-voltage relationship was slightly inwardly rectifying with a reversal potential of -52 +/-
285 ons from refractory and late SE animals were inwardly rectifying, and philanthotoxin-sensitive; simil
286 itions are associated with shifts from CI to inwardly rectifying, GluA2-lacking, Ca(2+)-permeable (CP
287  of capsaicin-induced mEPSCs, from linear to inwardly rectifying, indicating an increased prevalence
288                We conclude that TRPML1 is an inwardly rectifying, proton-impermeable, Ca(2+) and Fe(2
289  and TRPML3 to be measured and identified as inwardly rectifying, proton-impermeant, Ca(2+)-permeant
290                                              Inwardly rectifying, voltage-gated, two-pore domain, and
291 ontrast to WT TASK3 channels, the current is inwardly rectifying.
292                              G-protein-gated inwardly-rectifying K(+) (GIRK) channels are targets of
293 g from GABAB receptor to the G protein-gated Inwardly-rectifying K+ (GIRK) channels.
294 potassium, which are largely mediated by the inwardly-rectifying potassium channel Kir4.1, and to tak
295 -targeted CaMKII directly phosphorylates the inwardly-rectifying potassium channel, Kir6.2 (alpha sub
296 e desensitization of the G protein-activated inwardly-rectifying potassium current evoked by receptor
297  of each individual cell protruding from the inwardly regressive arm of the cell-cell interface, and
298 l periphery from where activation propagates inwardly through Ca(2+)-induced Ca2+ release (CICR) from
299 anule cell precursors, whose progeny migrate inwardly to form the internal granule cell layer.
300 pecks may represent lipofuscin translocating inwardly within cones.

 
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