ライフサイエンスコーパス: receptor subunit

1 832407) in GRIK1, encoding the kainate GluK1 receptor subunit.

2 xpression of the GluK5 high-affinity kainate receptor subunit.

3 rotein kinase C (PKC) phosphorylation of the receptor subunit.

4 ion of the muscle-specific GluRIIA glutamate receptor subunit.

5 identified as a potent ligand for this NMDA receptor subunit.

6 scripts including one encoding NR2A, an NMDA receptor subunit.

7 (LIF), signal via the common GP130 cytokine receptor subunit.

8 d in the low pH treatment, including a GABAA receptor subunit.

9 mologous segments from the rat GluK2 kainate receptor subunit.

10 te, located at the interface of two adjacent receptor subunits.

11 ocated at the interface between two adjacent receptor subunits.

12 e complementary genetically modified GABA(A) receptor subunits.

13 terodimerization of the IL-2Rbeta and gammac receptor subunits.

14 ns showed relatively low expression of GABAA receptor subunits.

15 eto2 at these structurally discrete sites on receptor subunits.

16 ls and to other neurons that coexpress these receptor subunits.

17 as exemplified by deficiency of IL-10 or its receptor subunits.

18 tenin-1-mediated dendritic transport of NMDA receptor subunits.

19 eptor (AMPAR) and GluN1 N-methyl-D-aspartate receptor subunits.

20 by reducing proteasomal degradation of GluA1 receptor subunits.

21 and through AMPA and kainate-like glutamate receptor subunits.

22 expression of AMPAR and N-methyl-D-aspartate receptor subunits.

23 UR2 and GLUR3) and GABAA (GABAA1 and GABAA2) receptor subunits.

24 nriched for specific nicotinic acetylcholine receptor subunits.

25 naling were identified, including four GABAA receptor subunits.

26 enzymes with variable substrate-adaptor and -receptor subunits.

27 wed over 70-fold selectivity over other NMDA receptor subunits.

28 12 families) via its interaction with shared receptor subunits.

29 in the relative expression of NMDA glutamate receptor subunits.

30 surface expression of GluA1- and GluA2-AMPA receptor subunits.

31 oprecipitates with both GluA1 and GluA2 AMPA receptor subunits.

32 functional expression of both human GABA(B) receptor subunits.

33 ately 5 mum, along with GluA1 and GluA2 AMPA receptor subunits.

34 unbiased capture of five alpha or beta GABAA receptor subunits.

35 tor expression and a decrease in GluN2B NMDA receptor subunits.

36 MDA receptors (NMDARs) in PSD via GluN2-type receptor subunits.

37 We studied GABAB receptor subunit 1 (GABAB1) splicing in alcoholic postmo

38 an increase of synaptic AMPA-type glutamate receptor subunit 1 (GluA1), there is a delay in GluA1 in

39 mpetition for IFN-alpha2A binding to the IFN receptor subunit 1 (IFNAR1) and do not involve inhibitin

40 protein causes the degradation of type I IFN receptor subunit 1 (IFNAR1).

41 cells from wild-type (WT) or IFN-alpha/beta receptor subunit 1 knockout (IFNAR1(-/-)) mice into RAG(

42 h its receptor IFNAR1 (interferon alpha/beta receptor subunit 1) is vital for host-protective anti-vi

43 receptor delta and gamma-aminobutyric acid B receptor subunit 1; their differential methylation was a

44 osphorylation of N-methyl-D aspartate (NMDA) receptor subunit 2 (GluN2) that is critical for neuropla

45 ve inhibiting IFN-alpha2A binding to the IFN receptor subunit 2 (IFNAR2).

46 using the N-terminal 150 residues of kainate receptor subunit 2 (KA2) to the recently discovered high

47 that DNE reduced the expression of glutamate receptor subunits 2 and 3 (GluR2/3) in the XIIMN and the

48 cted down-regulation of N-methyl-D-aspartate receptor subunits 2A and 2B (GluN2A and GluN2B) in the m

49 ted by a reduction of the expression of NMDA receptors subunit 2A and 2B.

50 my (T286A) or binding to NMDA-type glutamate receptor subunit 2B (GluN2B; formerly NR2B; I205K).

51 tic proteins, including N-methyl-d-aspartate receptor subunit 2B (NR2B) and PSD-95.

52 s the mechanism of KIF17 binding to the NMDA receptor subunit 2B (NR2B).

53 Since the discovery of the glutamate NMDA receptor subunit 3A (GluN3A), the functional role of thi

54 In addition, we find that all three receptor subunits accumulate rapidly within a subpopulat

55 te fusion protein composed of yeast adhesion receptor subunit Aga2, selection and counterselection su

56 nnels, CaM kinase kinase, and the GluA2 AMPA receptor subunit, akin to a homeostatic process.

57 trol and especially identify the IL-27/IL-27 receptor subunit alpha (IL-27RA) axis as a predictor of

58 explained by their higher expression of IL-2 receptor subunit alpha (IL-2Ralpha) and gamma chain and

59 apolipoprotein E and nicotinic acetylcholine receptor subunit alpha 5 genes are associated with lifes

60 c4, Ampd3, Trim63 (MuRF1), and acetylcholine receptor subunit alpha1 (Chrna1).

61 rincipal neurons were found to express GABAA receptor subunits alpha1 , alpha3 , beta2/3 , gamma2 , a

62 However, GABAA receptor subunits alpha1 and gamma2 were upregulated, an

63 Here, the expression of GABAA receptor subunits alpha1, alpha2, alpha3, alpha5, beta2,

64 w cells (calbindin and cholinergic nicotinic receptor subunit alpha2 [Chrna2]), two general markers f

65 Genes encoding the nicotinic acetylcholine receptor subunits alpha2 and beta4 are transcribed in th

66 utative trafficking sequences in two GABA(A) receptor subunits: alpha4 and delta.

67 line receptors that contain alpha7 nicotinic receptor subunits (alpha7-nAChRs).

68 e lacking platelets or the platelet integrin receptor subunit alphaIIb established that the survival

69 ion of Neto1 and 2 with pore-forming kainate receptor subunits also increases the duration of bursts

70 Sharing of receptor subunits among different cytokine receptor comp

71 s a paradoxical enhancement in membrane AMPA receptor subunits, AMPA responsiveness, and the motivati

72 e encodes the alpha5 nicotinic acetylcholine receptor subunit, an "accessory" subunit of pentameric n

73 n-6 (IL-6) and IL-27 signal through a shared receptor subunit and employ the same downstream STAT tra

74 ed cell-surface expression of the GluR2 AMPA receptor subunit and increased intracellular Ca(2+) sign

75 The postsynaptic gamma2-GABA(A)-receptor subunit and the presynaptic vesicular inhibitor

76 nregulation and internalization of glutamate receptor subunits and alterations of the dendritic spine

77 the spider Cupiennius salei have 15 Cys-loop receptor subunits and an acetylcholine-binding protein (

78 Transcripts of NMDA receptor subunits and GABAergic interneuron markers, as

79 dition to expected components including GABA receptor subunits and gephyrin, several novel proteins w

80 e assessed by measuring N-methyl-D-aspartate receptor subunits and glutamic acid decarboxylase, 67 kD

81 Glur2/3 AMPA receptor subunits and postsynaptic GABABR1b receptor sub

82 reased mRNA expression of NR1- and NR2B-NMDA-receptor subunits and prevented ischemia-induced reducti

83 lexity in the mutual regulation of the TRC40 receptor subunits and raise the question as to the role

84 ession analysis revealed upregulation of IL6 receptor subunits and signal transducers CD126 and GP130

85 ng the levels of N-methyl-D-aspartate (NMDA) receptor subunits and the HSA21 proteins amyloid beta (A

86 the functions of individual IL-27 and IL-27 receptor subunits and the role of IL-27 in dictating the

87 We observed that NMDA receptor subunits and their transcripts are increased in

88 ociated with delayed expression of glutamate receptor subunits and transporters.

89 th AMPA (GluA1) and NMDA (GluN2A and GluN2B) receptor subunits, and a reduction in the glutamate tran

90 s of 7 of the most commonly expressed GABA-A receptor subunits, and both GABA-B receptor subunits, in

91 Our results reveal a novel GABA(A) receptor subunit- and input-specific form of inhibitory

92 eto1 and Neto2, which impact KAR gating in a receptor subunit- and Neto isoform-specific manner.

93 Receptor subunits are arranged in a 1-2-1-2 fashion, dem

94 variants of several nicotinic acetylcholine receptor subunits are associated with nicotine dependenc

95 in the absence of filamin, type-A glutamate receptor subunits are lacking at the postsynapse, while

96 A disadvantage is that the different receptor subunits are not identified.

97 ly up-regulated while post synaptic GABABR1b receptor subunits are significantly down regulated.

98 GABA alpha1 receptor subunits are significantly down-regulated in la

99 and VI the GluR2/3 and presynaptic GABABR1a receptor subunits are significantly up-regulated, while

100 receptor subunits and postsynaptic GABABR1b receptor subunits are up and down regulated respectively

101 omic analyses and identified several GABA(A) receptor subunits as possible candidates.

102 t DL and DC express very high levels of NMDA receptor subunits as well as CaMKIIalpha, a key downstre

103 We found that the minor receptor subunit, ASGR2, is not required for effective i

104 The alpha9 and alpha10 cholinergic nicotinic receptor subunits assemble to form the receptor that med

105 ncrease in phosphorylation of the AMPA GluA1 receptor subunit at serine 831 (S831), a CaMKII site, al

106 enhanced ability to increase glutamate AMPA receptor subunits at the cell surface of wild type neuro

107 3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor subunits at the putative time of memory restabi

108 ine in the transcript encoding the glutamate receptor subunit B, glutamate receptor ionotropic AMPA 2

109 ene encoding the GluN2A N-methyl-d-aspartate receptor subunit being most often affected.

110 f patients and treatment with IL-1 and IL-12 receptor subunit beta 1 (Rb1) antibodies may also be use

111 - and GluA2-containing AMPARs, regardless of receptor subunit binding specificity, through increased

112 nteracts with the bone morphogenetic protein receptor subunits BMPR1a and BMPR1b.

113 entified in many ionotropic glutamate (iGlu) receptor subunits, but which of these sites are GPCR tar

114 ta suggest that expression of GM-CSF and its receptor subunits by colon tumors may be a useful marker

115 depended on the ectopic expression of GM-CSF receptor subunits by tumors.

116 Receptor subunits can exist in surface-bound or soluble

117 f neuronal GT1-7 cells with an NR1-NR2a NMDA receptor subunit cassette specifically targeting mitocho

118 and function of the nicotinic acetylcholine receptor subunit cluster of alpha3, alpha5, and beta4.

119 utamatergic transmission and changes in AMPA receptor subunit composition at 72 h postsurgery.

120 lates with a change in glutamate and glycine receptor subunit composition quantified via mRNA levels.

121 agonist is heavily dependent upon the GABAA receptor subunit composition underpinning tonic inhibiti

122 iderable alignment of synaptic AMPA and NMDA receptor subunit composition within specific subtypes of

123 ive zones and altered postsynaptic glutamate receptor subunit composition, coinciding with a reductio

124 Met) mice, suggesting a modification of NMDA receptor subunit composition.

125 very likely resulting from changes in GABAA receptor subunit composition.

126 icity, demonstrating its reliance on GABA(A) receptor subunit composition.

127 he cell type studied, their respective GABAA receptor subunit compositions, and critically, on the am

128 for glycinergic and glutamatergic ionotropic receptor subunits, confirming a switch from Glyalpha2 to

129 NMDA receptor subunits containing the GluN2B C-terminal are m

130 ayer 5; we found increased numbers of alpha1 receptor subunit-containing GABAergic synapses detected

131 istinct interneuron types have similar GABAA receptor subunit content.

132 ata indicate that the GluN2B and GluN2D NMDA receptor subunits contribute to synaptic activity in the

133 ceptor to both Glu and IVM, and improved the receptor subunits' cooperativity.

134 leukemias (B-ALLs) overexpress the cytokine receptor subunit CRLF2, which may confer a poor prognosi

135 (B-ALL) with rearrangements of the cytokine receptor subunit cytokine receptor-like factor 2 (CRLF2)

136 ) blockade or genetic deletion of the GB(1a) receptor subunit disrupts homeostatic regulation of syna

137 ressing reduced levels of the essential NMDA receptor subunit dNR1 also showed reduced ethanol tolera

138 The addition of the beta1a dihydropyridine receptor subunit enhanced FRET to the II-III loop, thus

139 e-protective EPO receptor, comprising an EPO receptor subunit (EPOR) and the common beta-chain (CD131

140 ant disorder with mutations reported for all receptor subunits except gamma.

141 pliced, flip and flop variants of GluA1 AMPA receptor subunit exhibit no functional difference in hom

142 Using truncated and mutated NMDA receptor subunits expressed in heterologous cells, we fo

143 gh a chromatin-mediated suppression of GABAA receptor subunit expression and inhibitory tone on NAc n

144 Differences in GABAA receptor subunit expression between the human and rodent

145 Furthermore, reducing nicotinic ACh receptor subunit expression in MBONs compromises odor-ev

146 rotein 130 (gp130) is the signal transducing receptor subunit for cytokines of the interleukin-6 (IL-

147 pentameric GABAA receptors require multiple receptor subunits for their synaptic localization in bas

148 including the expression switch of the NMDA receptor subunits from 2B to 2A, which is dependent on b

149 inhibition is marked by a switch in glycine receptor subunits from neonatal to adult form around the

150 al staining intensity for all positive GABAA receptor subunits from the dorsolateral pole to ventrome

151 ositive for a gamma-aminobutyric acid (GABA) receptor subunit (GABAA Ralpha1 ), and that a synaptic r

152 Further, expression of an important GABAA receptor subunit, GABAAR alpha1, was significantly atten

153 of CHOP prevented heterodimerization of the receptor subunits GABAB1 and GABAB2 and subsequent forwa

154 short splicing variants in addition to GABAB receptor subunit GABAB1a, the longest known major transc

155 e inhibitory gamma-amino butyric acid alpha2 receptor subunit (GABRA2) gene.

156 r nucleases (TALENs) to target interleukin-2 receptor subunit gamma (IL2RG) in pronuclear stage marmo

157 in-interacting domain of GABA type A (GABAA) receptor subunit gamma2 (TAT-GABAgamma2) and muscimol, a

158 s variant rs16969968 in the alpha5 nicotinic receptor subunit gene (CHRNA5) is the strongest genetic

159 ediate early genes Fos and FosB and the NMDA receptor subunit gene Grin2a in only Fos-positive neuron

160 ants, and those variants, as in GluA2-4 AMPA receptor subunits, generally show different properties.

161 Mutations in GABAA receptor subunit genes are frequently associated with ep

162 sense variants in the integrin alphaIIbbeta3 receptor subunit genes ITGA2B and ITGB3 identified by wh

163 ating synaptic transmission, including GABAA receptor subunit genes.

164 the "photoswitch-ready" version of a GABA(A) receptor subunit genomically replaces its wild-type coun

165 in the common gamma (gammac) chain cytokine receptor subunit give rise to severe combined immunodefi

166 -hydroxy-5-methyl-4-isoxazolepropionic acid) receptor subunit GluA1 C terminus (Ser818, Ser831, Thr84

167 r phosphorylation of the AMPA-type glutamate receptor subunit GluA1 on Ser-845 by PKA and for synapti

168 ly, NMDA-induced internalization of the AMPA receptor subunit GluA1 was impaired in LRP1-deficient ne

169 ated region of Gria1, which encodes the AMPA receptor subunit GluA1, to pull down miRNAs binding to i

170 hydroxy-5-methyl-4-isoxazole propionic acid) receptor subunit GluA1.

171 sities of synapse-sized clusters of the AMPA receptor subunit GluA1.

172 droxy-5-methyl-4-isoxazole propionate (AMPA) receptor subunits GluA1 and GluA2 in prefrontal neurons.

173 lectively upregulated synthesis of glutamate receptor subunits GluA1 and GluA2, facilitating AMPA rec

174 lted in increased surface expression of AMPA receptor subunits GluA1 and GluA2.

175 -fold), GluK1b (5-fold), as well as the AMPA receptor subunit GluA1i (5-fold).

176 , trpv1, chrm4, and syt6), of which the AMPA receptor subunit GluA2 is a top hit.

177 ed surface levels of the AMPA-type glutamate receptor subunit GluA2, an effect that is due to diminis

178 2 may be mediated by the AMPA-type glutamate receptor subunit GluA2, which can become associated with

179 . (2017) reveal a critical role for the AMPA receptor subunit GluA3 in cerebellar synaptic plasticity

180 The AMPA-receptor subunit GluA4 is expressed transiently in CA1 p

181 on PV interneurons are dependent on the AMPA receptor subunit GluA4, which is regulated by presynapti

182 mpal neurons, we discovered that the kainate receptor subunit GluK2 and the auxiliary subunit Neto2 s

183 ex and the transmembrane M3 helix of kainate receptor subunit GluK2.

184 PFC that include ERK/MAP kinase and the NMDA receptor subunits, GluN1 and GluN2B.

185 ressing recombinant NMDA family of glutamate receptor subunits, GluN1/GluN2A, we found that NPA has a

186 , we found that one of these positions, NMDA receptor subunit, GluN2A(F636), can strongly regulate et

187 inase II (CaMKII) to the NMDA-type glutamate receptor subunit GluN2B is an important control mechanis

188 sphatase (STEP) are known to target the NMDA receptor subunit GluN2B on tyrosine 1472, which is a cri

189 of Grin2b (encoding the NMDA-type glutamate receptor subunit GluN2B) or DS-restricted GluN2B antagon

190 3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor subunit GluR1, GABABR1, and GABABR2 levels, whe

191 g the functional expression of the glutamate receptor subunits GluR2 and NR2B in brain.

192 3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor subunit GluR4.

193 al treatment with antisense directed to IL-6 receptor subunit gp130 (gp130), but not to tumor necrosi

194 r1), Bdnf and its receptor (Trkb), glutamate receptor subunits (Gria1, Gria3, Grm1), and epigenetic e

195 substitution (p.A636T) occurs in a glutamate receptor subunit, GRIA1.

196 the homologous but distinct mouse glutamate receptor subunit Grid2 is associated with Lurcher ataxia

197 t-term habituation in mice lacking the NMDAR receptor subunit Grin2a (which also shows association to

198 y number variation studies [3-7], fewer GABA receptor subunits have been observed in the post-mortem

199 ngle gene coding for a high-affinity kainate receptor subunit (i.e., grik4) in a limited area of the

200 IFN-alpha/beta or IFN-I) signals through two receptor subunits, IFNAR1 and IFNAR2, to orchestrate ste

201 cropatterning of the type I interferon (IFN) receptor subunit IFNAR2 fused to the HaloTag was achieve

202 riptional silencing of the unique IFN-lambda receptor subunit (IFNLR1) in a cell-type-specific manner

203 ional assays have identified residues of the receptor subunit IL-1Rrp2 needed for cytokine recognitio

204 unctions even though both signal through the receptor subunit IL-2Rbeta and the common gamma-chain (g

205 in M receptor beta and the cytokine-specific receptor subunit IL-31Ralpha, of which there are several

206 tibodies against IL-13 or the IL-4 and IL-13 receptor subunit IL-4Ralpha, as well as an antibody agai

207 Upregulation of IL-13, its receptor subunits IL-13Ralpha1 and IL-13Ralpha2, and sha

208 al epithelial cells (IEC) express both IL-27 receptor subunits IL-27RA and gp130.

209 Our results showed that Il25 and its receptor subunit, Il17rb, were upregulated during a prim

210 oxed CNTFRalpha mice depletes this essential receptor subunit in a large subset of motor neurons (and

211 plex by interacting with the DCAF1 substrate receptor subunit in a Vpx-dependent manner.

212 nclude that GluK1 is the predominant kainate receptor subunit in cb1 and cb3 Off bipolar cells.

213 rons using targeted deletion of the NR1 NMDA receptor subunit in dopamine neurons.

214 ment or specific deletion of beta2 nicotinic receptor subunits in dopamine neurons mitigates aberrant

215 To identify the role of individual receptor subunits in ethanol-induced behaviors, we devel

216 ochemical staining data for AMPA and GABAA/B receptor subunits in the area 3b cortex of adult squirre

217 t ATP-gated ion channels assembled from P2X2 receptor subunits in the cochlea are necessary for the d

218 xtensive hydrophobic interfaces between AMPA receptor subunits in the ion channel.

219 Accordingly, inhibition of Grin2c NMDA receptor subunits in the NAcore reduced aversion-resista

220 xpressed with Agam/Orco (odorant receptor co-receptor subunit) in Xenopus oocytes and assayed by two-

221 in schizophrenia of CHRNA7, the gene for the receptor subunit, in the neurobiology of deficits in att

222 ed GABA-A receptor subunits, and both GABA-B receptor subunits, in these same mice following saline (

223 e we report that the GluK1 and GluK2 kainate receptor subunits interact with the spectrin-actin bindi

224 iple factors including assembly of different receptor subunits, interaction with auxiliary subunits,

225 structural differences in binding subsites, receptor subunit interfaces, or transmembrane regions.

226 g to propofol-selective binding within GABAA receptor subunit interfaces, with stable hydrogen bonds

227 ased hippocampal expression of the GABAB(1b) receptor subunit is associated with a depression-like ph

228 ken together, the data suggest that GABAB(1) receptor subunit isoforms differentially regulate the de

229 Fibrinogen receptor subunits Itga2b (alphaIIb) and Itgb3 (beta3) mR

230 , we trained wild-type and alpha-9 nicotinic receptor subunit knock-out (KO) mice, which lack choline

231 Using multiple cytokine and cytokine receptor subunit knockout mice, we demonstrate that stem

232 GRIA4 encodes an AMPA receptor subunit known as GluR4, which is found on excit

233 A multitude of 18 iGluR receptor subunits, many of which are diversified by spli

234 that CRF1 neurons exhibit an alpha1 GABA(A) receptor subunit-mediated tonic conductance that is driv

235 NrCAM formed a complex in brain with Sema3F receptor subunits Neuropilin-2 (Npn-2) and PlexinA3 (Ple

236 ns of mRNA and protein of the principal GABA receptor subunits normally present in the temporal corte

237 antibodies (AB) against N-methyl-D-aspartate receptor subunit NR1 (NMDAR1) are highly seroprevalent i

238 te transporter VGLUT2 or the obligatory NMDA receptor subunit NR1 promoted axon survival in experimen

239 eroprevalence (~10%) of N-methyl-D-aspartate-receptor subunit-NR1 (NMDAR1) autoantibodies (AB) in hea

240 Furthermore, the cAMP effector PKA, the NMDA receptor subunits NR2A and -B, as well as PSD95, were te

241 toxicity, as the N-methyl-d-aspartate (NMDA) receptor subunit NR2B was up-regulated in the cultures.

242 re we show that the F-box protein FBXL2 (the receptor subunit of one of 69 human SCF (SKP1, CUL1, F-b

243 -binding CXXHX16H motif on the sulphonylurea receptor subunit of the channel, and mutagenesis togethe

244 130 (gp130) is the common signal-transducing receptor subunit of the interleukin-6 (IL-6) family, whi

245 enes is GRIK4, a gene coding for a glutamate receptor subunit of the kainate type.

246 thickness and an upregulation of GluA3 AMPA receptor subunits on bushy cells.

247 ce implicates gamma-aminobutyric acid type A receptor subunits on chromosome 15q12 as candidate genes

248 membrane protein translocase but not the two receptor subunits, one of which is essential for protein

249 ng that is mimicked by activating lesions in receptor subunits or downstream mediators as well as abe

250 The IL-27 cytokine and soluble receptor subunits p28 and EBI3 can be secreted independe

251 e cytokine subunit p19 and the soluble alpha receptor subunit p40, binds to a receptor complex consis

252 R-induced cocaine seeking and synaptic GluA1 receptor subunit phosphorylation was explored.

253 fly antennal tissue and identified IR8a as a receptor subunit physically associated with IR64a by mas

254 rs (USERs) that allow activation of a single receptor subunit population sensitized to extremely low

255 r targeted-ABPP and observed a lack of GABAA receptor subunit protection.

256 ns were found to be colocalized with GABA(A) receptor subunit protein gamma2.

257 ion increases the surface expression of AMPA receptor subunits, providing insight to the mechanism by

258 pha1 , alpha3 , beta2/3 , gamma2 , and GABAB receptor subunits R1 and R2.

259 p(-/-) neurons as the alpha1 to alpha2 GABAA receptor subunit ratio was increased.

260 compression, the pattern of AMPA and GABAA/B receptor subunits remain significantly altered in a laye

261 p-regulated, while the postsynaptic GABABR1b receptor subunits remain significantly down-regulated.

262 mploy small diffusible molecules and involve receptor subunits resembling highly conserved G-protein

263 Based upon (3)H incorporation into receptor subunits resolved by SDS-PAGE, there was etomid

264 uitinated in cells, especially the ubiquitin receptor subunit, Rpn13.

265 reduction in the expression of distinct NMDA receptor subunits selectively in identified mesolimbic D

266 tion demonstrates striking interfacial GABAA receptor subunit selectivity in the native milieu, sugge

267 ction of differential N-glycan processing or receptor subunit selectivity.

268 also known as GluRA or GluR1) AMPA glutamate receptor subunit, shows genome-wide association to schiz

269 Coexpression of mutant and WT P2X(2) receptor subunits significantly reduced ATP-activated me

270 Here we investigate the input and GABA(A) receptor subunit specificity of inhibitory synaptic plas

271 ng proteins (including the high-affinity IgE receptor subunits, spleen tyrosine kinase, and phospholi

272 pregulated the expression of IL-33 and IL-25 receptor subunits (ST2 and IL-17RA).

273 se states, the contribution of specific NMDA receptor subunits still remains to be elucidated.

274 However, the inability to assess receptor subunit stoichiometry in situ has hampered effo

275 xchange protein (Band 3), asialoglycoprotein receptor subunits, sucrase-isomaltase, the erythropoieti

276 -forming subunit (Kir6.1) and a sulfonylurea receptor subunit (SUR2B).

277 lon tumors that overexpressed GM-CSF and its receptor subunits survived at least 5 years after diagno

278 e null for the P2RX2 gene (encoding the P2X2 receptor subunit), sustained 85-dB noise failed to elici

279 ssociated with expression of the sweet taste receptor subunit, Tas1r2.

280 (BLA) revealed an increase in the GluA1 AMPA receptor subunit that correlated with SEFL.

281 This targeting of a receptor subunit that is common to all members of an oth

282 ntegrin alpha(3) is a transmembrane integrin receptor subunit that mediates signals between the cells

283 th mice deficient in GluK1 and GluK2 kainate receptor subunits to assess the role of GluK1 kainate re

284 3, dynorphin-B, and phosphorylated glutamate receptor subunit, type 1 expression.

285 ide important insight into the role of GABAA receptor subunit under- or overexpression in disease sta

286 expression and phosphorylation of glutamate receptor subunits underlie the alterations in LTP and th

287 amma molecule (gammac) is a shared signaling receptor subunit used by six gammac-cytokines.

288 This requires bridging receptor subunits via covalent attachment of 4,4'-bis(ma

289 rformed, and subcellular expression of GABAA receptor subunits was analyzed semiquantitatively.

290 3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor subunits was impaired in the GluD1 knockout mic

291 stably expressing different combinations of receptor subunits, was developed.

292 gamma-Aminobutyric acid type A receptor subunits were coexpressed in non-neuronal cells

293 gene expression levels of glutamate and GABA receptor subunits were compared between sedentary and ph

294 and signaling in cells in which both hIL-12 receptor subunits were functionally deleted.

295 gene expressions of AMPA and NMDA glutamate receptor subunits were markedly increased after cisplati

296 uning and switch in the N-methyl-D-aspartate receptor subunit, which are relevant to autism and other

297 ng advantage of various agonists binding the receptor subunits with different affinities and rate con

298 ising number of mutations found in glutamate receptor subunits, with the GRIN2A gene encoding the Glu

299 beta2/3 , and gamma2 ) and GABAB (R1 and R2) receptor subunits within the normal human STN.

300 We then show that GluN1 and GluA1 receptor subunits within these neuronal subpopulations m