ライフサイエンスコーパス: receptor gene

1 inside gene GABRB2 and GRIA1 (AMPA subunit 1 receptor gene).

2 ed knockdown of CNR1 (the cannabinoid type 1 receptor gene).

3 uated the methylation status of the androgen receptor gene.

4 ogenitor cells harboring a transgenic T-cell receptor gene.

5 lutamine encoding CAG repeat of the androgen receptor gene.

6 gpr126, an adhesion class G protein-coupled receptor gene.

7 ine repeat in the first exon in the androgen receptor gene.

8 urons (OSNs) that express a specific odorant receptor gene.

9 e first event targeted the promoter of a V1R receptor gene.

10 r virus (EBV) positive, with germline T-cell receptor gene.

11 c trait mediated by the TAS2R38 bitter taste receptor gene.

12 dults due to polymorphisms in a bitter taste receptor gene.

13 ecule and results in the assembly of antigen receptor genes.

14 ted with inherited variations near glutamate receptor genes.

15 ted in rodenticide resistance, and olfactory receptor genes.

16 ler surviving mammals with more bitter taste receptor genes.

17 of 34 GAL4-lines of individual chemosensory receptor genes.

18 IR family, which includes all HLA-C-specific receptor genes.

19 enes to generate the mature forms of antigen receptor genes.

20 a critical role in the expression of odorant receptor genes.

21 ability to assemble a diverse set of antigen receptor genes.

22 ng GAL4 driver lines of Ir, Gr, Ppk, and Trp receptor genes.

23 r gene allele from a large family of odorant receptor genes.

24 pre-T cells that actively rearrange antigen receptor genes.

25 g an ancient coevolution between peptide and receptor genes.

26 ilar to the animal NOD1 receptor-like immune receptor genes.

27 of GIBBERELLIN-INSENSITIVE DWARF1 (GID1) GA receptor genes.

28 Thus, miR-99b targets TNF-alpha and TNFRSF-4 receptor genes.

29 CR target genes including multiple chemokine receptor genes.

30 gene family clades, as well as their cognate receptor genes.

31 reduced chromatin accessibility on IFN-gamma receptor genes.

32 e, a novel antisense gene to three olfactory receptor genes.

33 ereby affecting the expression levels of ABA receptor genes.

34 erated species-specific sets of bitter taste receptor genes.

35 infection is independent of known arenavirus receptor genes.

36 ome complement and mutations in the androgen-receptor gene, a mutation in the gene encoding estrogen

37 nt activating mutation affecting the activin receptor gene ACVR1 in 20% of DIPGs.

38 single nucleotide polymorphism in the PACAP receptor gene ADCYAP1R1, adenylate cyclase activating po

39 is pivotal to activate the beta1-adrenergic receptor gene (Adrb1) and downstream targets including U

40 The beta2-adrenergic receptor gene (ADRB2) contains a common, non-synonymous

41 Genetic variation in the beta-2 adrenergic receptor gene (ADRB2) has been implicated in asthma seve

42 sensory neuron expresses one single odorant receptor gene allele from a large family of odorant rece

43 ysis of rearranged immunoglobulin and T-cell receptor genes (allele-specific oligonucleotide [ASO]-PC

44 termined the positions of homologous odorant receptor gene alleles in relation to different nuclear c

45 These two receptor genes along with CsPYL1 were cloned and express

46 enetic variation of the cholinergic nicotine receptor gene, alpha-7 subunit (CHRNA7) has been shown t

47 eta-glucuronidase fusions with the MtCRE1 CK receptor gene and a CK response reporter (TWO COMPONENT

48 common variants of the TAS2R31 bitter taste receptor gene and to NNS intake.

49 sequence variants in nicotine acetylcholine receptor genes and at other loci.

50 signaling by binding to the chromatin of ABA receptor genes and by maintaining low levels of acetylat

51 e Mphi precursors have non-rearranged B-cell receptor genes and coexpress myeloid (GR1, CD11b, and CD

52 9 causes upregulation of abscisic acid (ABA) receptor genes and hypersensitivity of ABA-responsive ge

53 icient to suppress the expression of odorant receptor genes and likely acts through histone methylati

54 colocalization of mu-opioid and kappa-opioid receptor genes and OT genes at the OT-releasing sites in

55 erozygosity hotspots, enriched for olfactory receptor genes and other genes with high levels of ances

56 luding four involving new kinase or cytokine receptor genes and seven involving new partners for prev

57 m this extensive meta-analysis of five GABAA receptor genes and substance abuse support their involve

58 lities, given the staged expression of taste receptor genes and taste transduction elements in cultur

59 used on the expression profiles of olfactory receptor genes and transcription factors-the two main cl

60 riptional activator of the G-protein-coupled receptor gene Aplnr, the expression of which is uniquely

61 among humans, polymorphisms in the melatonin receptor gene are associated with insulin resistance.

62 he two homologous alleles of a given odorant receptor gene are frequently segregated to separate comp

63 The assembly and expression of mouse Ag receptor genes are controlled by a collection of cis-act

64 Zebrafish chemosensory receptor genes are expressed across a large dynamic rang

65 tural killer (NK) cell receptors, and CD8 co-receptor genes are found on non-MHC chromosomes, with so

66 We construct a map of the TO, in which the receptor genes are mapped to neurons of individual sensi

67 The expression levels of the receptor genes are only transiently induced by auxin, su

68 enomic "hot spots" encoding NLR plant immune receptor genes are recurrently responsible for hybrid ne

69 ant receptor is chosen for expression, other receptor genes are suppressed by a negative feedback mec

70 s are downregulated and the GA catabolic and receptor genes are upregulated in the nfl mutant compare

71 Opioid peptide genes, compared with their receptor genes, are transcribed at much greater absolute

72 mmaRIIIa-pSyk up-regulated several toll-like receptor genes as well as the HMGB1 and MyD88 gene trans

73 Co-option of RAG1 and RAG2 for antigen receptor gene assembly by V(D)J recombination was a cruc

74 pening DNA hairpins generated during antigen receptor gene assembly from variable (V), diversity (D),

75 Antigen receptor gene assembly proceeds through DNA DSB intermed

76 d to contribute to the regulation of antigen receptor gene assembly via V(D)J recombination.

77 ates DNA double strand breaks during antigen receptor gene assembly, an essential process for B- and

78 J recombination intermediates during antigen receptor gene assembly.

79 scend hazardous intermediates during antigen receptor gene assembly.

80 maintaining genome integrity during antigen receptor gene assembly.

81 ariation and variation in the vasopressin 1a receptor gene (Avpr1a) in bonobos.

82 ere is a strong history of mutations in GABA receptor genes being involved in neurologic diseases, pa

83 ons in the bone morphogenetic protein type 2 receptor gene (BMPR2), but how these promote pulmonary v

84 liferation and transcription of basal lamina receptor genes, both necessary for radial sorting of axo

85 uring iron starvation, as is common for iron receptor genes, but that expression of the bfrD and bfrE

86 Interestingly, the Arabidopsis thaliana AHK4 receptor gene can functionally replace Lhk1 in mediating

87 demonstrate that splice variants of a single receptor gene can regulate strikingly different behavior

88 fashion, and that individual main olfactory receptor genes can contribute substantially to odour per

89 amage-/pathogen-associated molecular pattern receptor genes capable of inducing type I IFN were upreg

90 zation and establishment of single olfactory receptor gene choice.

91 The alpha7 nicotinic acetylcholine receptor gene (CHRNA7) is linked to schizophrenia.

92 g the null mutation for the alpha7 nicotinic receptor gene (Chrna7).

93 were observed at the chromosome 15 nicotinic receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) previously

94 functional variation (rs2023239) in the CB1 receptor gene (CNR1) that may moderate CB1 receptor dens

95 ed, those with a variant at the serotonin 2A receptor gene contribute more than those without it.

96 The degree to which individual receptor genes contribute to odour perception is unclear

97 ordingly, reduction in the levels of the EGF receptor gene contributes to the activation of Esrrb.

98 and glands, and expression of TLR7 and DDX58 receptor genes correlated with upregulation of type I IF

99 n p.R782G in the Colony-Stimulating Factor 1 Receptor gene (CSF1R).

100 in the granulocyte colony-stimulating factor receptor gene CSF3R, which signals through JAK-STAT prot

101 mutations in the colony-stimulating factor 3 receptor gene (CSF3R) in CNL patients.

102 -modifying protein-1 (RAMP-1) and calcitonin receptor gene (CT-R) expression in striatum [coexpressio

103 A SNP (rs17601612) in the dopamine D2 receptor gene (DRD2) was significantly associated with s

104 rs2283265 and rs1076560, in the dopamine D2 receptor gene (DRD2) were found to be significantly asso

105 V(D)J recombination assembles Ag receptor genes during lymphocyte development.

106 (VDJ recombination) that acts on the surface receptor gene each time a new immune cell is created fro

107 In many GBMs, the EGF receptor gene (EGFR) is amplified and may be truncated t

108 reater prevalence of epidermal growth factor receptor gene (EGFR) mutations in adenocarcinomas among

109 Five additional growth factor receptor genes (EGFR, FGFR1, IGF1R, LIFR, and NGFR) also

110 ations in TGFbeta/bone morphogenetic protein receptor genes, ENG, encoding endoglin (HHT1), or ACVRL1

111 nancies may also be possible through antigen receptor gene engineering.

112 fferent rearrangements of the erythropoietin receptor gene EPOR in Philadelphia chromosome-like (Ph-l

113 ar three of the four epidermal growth factor receptor genes (ERBB2/HER2, ERBB3/HER3 and ERBB4/HER4) a

114 current rearrangements between the oestrogen receptor gene ESR1 and its neighbour CCDC170, which are

115 and newly acquired mutations in the estrogen receptor gene (ESR1), PIK3CA gene, and fibroblast growth

116 10) chemotactic chemokines and ccr1 and ccr5 receptor genes, evaluated by reverse transcription-quant

117 rsification of structurally distinct antigen receptor genes evolved independently in jawless and jawe

118 ypically expresses one, or very few, sensory receptor genes, excluding all others.

119 p, expression of glucocorticoid and androgen receptor genes explained the most variance in these age-

120 well as changes in the repertoire of antigen receptor genes expressed by these cells.

121 Variable numbers of taste 2 receptor genes expressed in the gustatory end organs ena

122 fic neuronal circuits and reveal local taste receptor gene expression in the gustatory ganglia and th

123 Leptin-mediated leptin/leptin-receptor gene expression likely amplifies leptin signali

124 pathway activity, which upregulated insulin receptor gene expression to promote insulin sensitivity.

125 ght control and glucose sensitivity, and EPO receptor gene expression was reduced in wild-type female

126 not induce compensatory changes in glutamate receptor gene expression, they cause a decrease in inhib

127 ired A6 cell and tadpole kidney type III IFN receptor gene expression.

128 xplained by the FV3 impairment of IFN-lambda receptor gene expression.

129 nisms mediating repression of glucocorticoid receptor gene expression.

130 Olfactory receptor gene families are significantly expanded in pan

131 ave expanded annotations of the chemosensory receptor gene families, and provide first-time transcrip

132 air is likely effected by expansion of other receptor gene families.

133 ve assignment of odor responses to olfactory receptor gene families.

134 Members of the low-density lipoprotein (LDL) receptor gene family have a diverse set of biological fu

135 The insect olfactory receptor gene family is absent from S. maritima, and olf

136 etic variants in the nicotinic acetylcholine receptor gene family jointly contribute to subclinical a

137 enes are a small, highly conserved olfactory receptor gene family of only six genes, whose direct ort

138 SorCS2 is a member of the Vps10p-domain receptor gene family receptors with critical roles in th

139 t association of the nicotinic acetylcholine receptor gene family with both intima-media thickness an

140 erexpressed microRNA393 to silence the auxin receptor gene family, and these roots were hyposensitive

141 and suppression of the rest of the olfactory receptor gene family, thereby locking in the expression

142 ression patterns of the Drosophila serotonin receptor gene family.

143 ), PIK3CA gene, and fibroblast growth factor receptor gene (FGFR2), among others.

144 Further, we determine the repertoire of receptor genes for each sensillum by analyzing GAL4 driv

145 We use variation in 33 SNPs for the receptor genes for six well-known social neuropeptides i

146 known, but we have recently identified a Wnt receptor gene, Frizzled6 (Fzd6), that is mutated in a hu

147 identities by typically expressing a single receptor gene from a large genomic repertoire.

148 pying genetic haploinsufficiency for the Fsh receptor gene Fshr.

149 med a meta-analysis of variants in the GABAA receptor genes (GABRB2, GABRA6, GABRA1, and GABRG2 on ch

150 e thereof, we challenged mice lacking the GH receptor gene (Ghr(-/-), a model for GH resistance) by c

151 To understand the role of the three GA receptor genes (GID1A, GID1B and GID1C) in Arabidopsis d

152 nonymous SNP, rs34144324, was in a glutamate receptor gene (GRID2, P = 8.65 x 10(-6) [OR 3.46] and P

153 na1c exon 7, and also exclusion of both NMDA receptor gene Grin1 exon 4, and Enah exon 12, all consis

154 ble mutant mouse lines lacking the glutamate receptor genes Grin1 or Gria1 in either DA transporter (

155 Further, CNVs mapped to glutamate receptor genes (GRM1, GRM5, GRM7 and GRM8) have been imp

156 -number variants affecting the host invasion receptor genes GYPA and GYPB We find that a nearby assoc

157 the Lotus histidine kinase1 (Lhk1) cytokinin receptor gene has shown that it is required and also suf

158 CHRNA7, the alpha7-nicotinic acetylcholine receptor gene, has been associated with schizophrenia, a

159 cid (GABA), in this putative imbalance: GABA receptor genes have been associated with autism in linka

160 ologic control by sequencing viruses, T cell receptor genes, HIV integration sites, and cellular tran

161 n transporter gene (SLC6A4) and serotonin 2A receptor gene (HTR2A) predict contributions to the publi

162 ) (rs201253747) c.*61 T > C within the 5-HT4 receptor gene HTR4 to be predominantly present in diarrh

163 hRNA-mediated screen of the 48 human nuclear receptor genes identified multiple candidates likely to

164 tations in the cytosolic double-stranded RNA receptor gene IFIH1 (also called MDA5) cause a spectrum

165 -of-function mutations in the interleukin-21 receptor gene (IL21R; c.G602T, p.Arg201Leu and c.240_245

166 Loss-of-function variants of the IL23-receptor gene (IL23R) protect against IBD, and, in anima

167 de polymorphism (rs11209026G>A) of the IL-23 receptor gene (IL23R) protects against psoriasis.

168 Functional variants in the interleukin-6 receptor gene (IL6R) are associated with asthma risk.

169 A conditional knockout (cKO) of the androgen receptor gene in PM cells resulted in male infertility.

170 lso named GPR48), the only G-protein-coupled receptor gene in the human chromosome 11p12-11p14.4 frag

171 The recent discovery of a conserved octenol receptor gene in the strictly nectar-feeding elephant mo

172 es are intermingled with all other olfactory receptor genes in a single sensory surface.

173 ocess of secondary rearrangements of antigen receptor genes in autoreactive lymphocytes-is a well-est

174 Inactivation of chitin-receptor genes in Ljlys6, Mtlyk9, and Mtlyr4 mutants eli

175 riants and mutations have been found in GABA receptor genes in patients with autism, schizophrenia, a

176 icles; RT-PCR analysis identified 3 relevant receptor genes in scalp follicles in vivo.

177 we propose the use of ectopic expression of receptor genes in suitable plant cells like Nicotiana be

178 by the cortex and the expression of ethylene receptor genes in the seed.

179 of cannabinoid, dopamine, and glutamatergic receptor genes in the striatum, a key component of the n

180 also found extensive expansion of olfactory receptor genes in these turtles.

181 methylation to maintain the silenced odorant receptor genes in transcriptionally inactive heterochrom

182 The variable domains of Ig and T-cell receptor genes in vertebrates are assembled from gene fr

183 le cells somatically rearrange their antigen receptor genes [in a process called variable-diversity-j

184 sts a fundamental role for TNFSF15, a T-cell receptor gene involved in T-cell maturation, in the path

185 D1), and IGF1R (insulin-like growth factor 1 receptor) genes involved in proliferation and antiapopto

186 tion requires the function of the Ionotropic Receptor genes IR25a, IR76b and IR56d.

187 The HVEM (TNFRSF14) receptor gene is among the most frequently mutated genes

188 valent genetic polymorphism among the opioid receptor genes is also considered.

189 Expression of ETH and ETH receptor genes is in turn dependent on ecdysone (20E).

190 ated DCS cells by using the diphtheria-toxin receptor gene knocked into the murine Reg4 locus.

191 Mice with global IL-1 receptor gene knockout or central IL-6 receptor knockdow

192 monoclonal antibody or tumor necrosis factor receptor gene knockout, reduced inflammation and retinal

193 ective inactivation of KIR3DL and activating receptor genes leaves a functional cohort of one inhibit

194 l: 1.14, 3.55, 9 studies, I(2) = 0%), leptin receptor gene (LEPR) polymorphism rs1137100 (odds ratio

195 Conformation of antigen receptor gene loci spatially juxtaposes rearranging gene

196 are moderated by variation at the mu-opioid receptor gene locus (OPRM1).

197 eration in the expression of Notch ligand or receptor genes, loss of function of jam1a led to loss of

198 e rescued by reducing the dose of the Wnt co-receptor genes Lrp5 and Lrp6, or by inactivating the gen

199 nine common polymorphisms in melanocortin-1 receptor gene (MC1R).

200 cus on indoor tanning and the melanocortin 1 receptor gene, MC1R.

201 The genetic variants near the Melanocortin-4 receptor gene (MC4R), a key protein regulating energy ba

202 is assumed that the orthologous bitter taste receptor genes mediate the recognition of bitter toxins

203 gle-nucleotide polymorphism at the vitamin D receptor gene met our corrected significance threshold o

204 , we explain the concept of chimeric antigen receptor gene-modified T cells, describe the extant resu

205 rtheless, a number of cytokine and chemokine receptor genes, most notably CCR8, were upregulated in t

206 e activating mutations in the thrombopoietin receptor gene (MPL).

207 expression controlled by a beta1-adrenergic receptor gene network.

208 ant, X-linked mutants in the nuclear hormone receptor gene nhr-40 that are haploinsufficient.

209 pigenetic modification of the glucocorticoid receptor gene (NR3C1) are related to the risk of post-tr

210 ignatures of selection on the glucocorticoid receptor gene (Nr3c1) in African starlings that inhabit

211 recurrent fusions involving the neurotrophin receptor genes NTRK1, NTRK2 and NTRK3 in 40% of NBS-HGGs

212 at assembles the B- and T-lymphocyte antigen receptor genes of jawed vertebrates.

213 quired for the assembly of the Ig and T-cell receptor genes of the immune system.

214 Here we show that the olfactory receptor gene Olfr78 is highly and selectively expressed

215 rons expressed only one of the ~1000 odorant receptor genes (Olfrs) available, and at a high level.

216 Among opioid receptor genes, one polymorphism is much more frequent i

217 reen fluorescent protein (eGFP) into the NOP receptor gene (Oprl1) and producing mice expressing a fu

218 ive 3' alternative splicing of the mu opioid receptor gene OPRM1 creates multiple C-terminal splice v

219 de polymorphism (SNP) in the human mu-opioid receptor gene (OPRM1 A118G) has been widely studied for

220 two copies of the G allele of the mu-opioid receptor gene (OPRM1 A118G) may have higher receptor bin

221 the sole targeted deletion of the mu opioid receptor gene (Oprm1) alters the brain connectome in liv

222 sm (rs1799971, Asn40Asp) of the micro-opioid receptor gene (OPRM1) is associated with the risk of rel

223 gle nucleotide polymorphism in the mu-opioid receptor gene (OPRM1), A118G (Asn40Asp), may moderate na

224 cleotide polymorphism (SNP) in the mu-opioid receptor gene (OPRM1), A118G, and psychophysical respons

225 olymorphism (SNP rs1799971) in the mu-opioid receptor gene, OPRM1, has been much studied in relation

226 The mu-opioid receptor gene, OPRM1, undergoes extensive alternative pr

227 response, the most robust being the oxytocin receptor gene OXTR, for which we observed a correspondin

228 Several common alleles in the oxytocin receptor gene (OXTR) are associated with altered brain f

229 f a common variant (rs53576) in the oxytocin receptor gene (OXTR) has been associated with protective

230 The oxytocin receptor gene (OXTR) has been studied as a risk factor f

231 The oxytocin receptor gene (OXTR) polymorphism rs53576, which has fig

232 s receptor, which is encoded by the oxytocin receptor gene (OXTR).

233 ssing tdTomato under the control of the P2X4 receptor gene (P2rx4).

234 up-regulating the negative immune regulator receptor genes Pdcd1, Lag3, Ctla4, Tigit, and Btla, ther

235 r cytokine proteins and cytokine or cytokine receptor gene polymorphisms in smallpox vaccine-induced

236 Mutations in odorant receptor genes predict olfactory perception of common co

237 e an unusually diverse repertoire of NK cell receptor genes predicted to encode receptors that recogn

238 A rhodopsin receptor gene previously associated with pyrethroid resi

239 to a heterozygous mutation in the prolactin receptor gene, PRLR, resulting in an amino acid change f

240 ger RNA under the control of the D1 dopamine receptor gene promoter (mGluR5(KD-D1)) were tested in a

241 association of Reptin with the progesterone receptor gene promoter is concomitant with changes in H3

242 pigenetic modification of the glucocorticoid receptor gene promoter is linked to interindividual and

243 s co-expressed with the phytosulfokine (PSK) receptor genes PSKR1 and PSKR2 in Arabidopsis thaliana.

244 Tight control of antigen-receptor gene rearrangement is required to preserve geno

245 superfamily gene member, initiating antigen receptor gene rearrangement via the RAG recombinase in a

246 d CD4 and CD8 coreceptors, underwent antigen receptor gene rearrangement, and demonstrated functional

247 defects in genes required for T- and B-cell receptor gene rearrangement.

248 concomitant loss of RAG1/2-mediated antigen receptor gene rearrangement.

249 try, examination of blood smears, and T cell receptor gene rearrangements), and performed muscle immu

250 tes examination of immunoglobulin and T cell receptor gene rearrangements, and initial studies using

251 ut of a possible approximately 1,000 odorant receptor genes, reflecting an exquisite mode of gene reg

252 signaling by deletion of the TGFbeta type II receptor gene relieves a restraint on tumorigenesis.

253 eir proliferation and survival and alters Ag receptor gene repertoires for largely undefined reasons.

254 between functional olfactory and vomeronasal receptor gene repertoires in the cat and dog genomes, wi

255 hrough cross-mammal analyses of bitter taste receptor gene repertoires.

256 ets from 5-HT synthesis genes to transmitter receptor genes required for afferent modulation of 5-HT

257 le-nucleotide polymorphisms in the vitamin D receptor gene, requiring P < .002 (0.05 divided by 30 ge

258 Transcriptional profile of ABA receptor genes revealed a different induction in respons

259 itative next generation sequencing of T-cell receptor genes revealed distinct oligoclonal CD4(+) and

260 of all 61 SNPs in 7 nicotinic acetylcholine receptor genes revealed significant association of the n

261 a mutation in the beta-adrenergic octopamine receptor gene (RmbetaAOR).

262 , a brain-derived neurotrophic factor (BDNF) receptor gene, rs1211166, P = 1.04E-06] in the Phase IV

263 cle weakness, and mutations in the ryanodine receptor gene (RYR1) represent the most frequent cause o

264 ATIONALE: Mutations in the cardiac Ryanodine Receptor gene (RYR2) cause dominant catecholaminergic po

265 Most odorant and ionotropic receptor genes seemed to be expressed in all libraries.

266 ccination (as defined by their unique T cell receptor gene sequence) and by tracking clones that ente

267 s imply that future studies investigating D2 receptor genes should covary for genetic ancestry or stu

268 changes, modulation of a chemokine/chemokine receptor gene signature, and activation of the pleiotrop

269 we demonstrate in the zebrafish that odorant receptor gene silencing is dependent on receptor activit

270 al transduction mechanism subserving odorant receptor gene silencing remains obscure, however.

271 differences in polymorphisms of two oxytocin receptor gene SNPs, rs53576 and rs2254298, in four popul

272 ciated genes, such as MAP70-5 and CLASP, and receptor genes, such as HERK1 and WAK1, were changed in

273 They both bind to the promoter of the immune receptor gene SUPRESSOR OF npr1-1, CONSTITUTIVE 1 (SNC1)

274 ceptor DCAR (dendritic cell immunoactivating receptor; gene symbol Clec4b1) is a direct receptor for

275 rating that Klf13 is a direct glucocorticoid receptor gene target.

276 Alleles of the receptor gene TAS2R38 are responsible in part for the va

277 the thymus where they rearrange their T-cell receptor genes (TCR) and undergo selection on the basis

278 zygous missense mutations in either TGF-beta receptor gene (TGFBR1 or TGFBR2), which are predicted to

279 wn that the deletion of the TGF-beta type II receptor gene (Tgfbr2) expression in myeloid cells is as

280 on, T835M (rs137875858), in the UNC5C netrin receptor gene that segregated with disease in an autosom

281 No variants of the commonly studied GABA receptor genes that have been associated with substance

282 genomes contain pairs of orthologous bitter receptor genes that have been conserved throughout evolu

283 Diverse repertoires of antigen-receptor genes that result from combinatorial splicing o

284 erential methylation in two neurotransmitter receptor genes, the gamma-Aminobutyric acid-A receptor d

285 w recent clinical trials of TILs and antigen receptor gene therapy for advanced cancers.

286 murine T cell receptor and chimeric antigen receptor gene therapy models.

287 he pursuit of immunotherapies such as T cell receptor gene therapy or adoptive transfer, may be more

288 s the transcription of the foxA ferrioxamine receptor gene through the extracytoplasmic function sigm

289 ndogenous ligand (PDF) signaling or rhythmic receptor gene transcription.

290 tissues resulted in down-regulation of auxin receptor genes (transport inhibitor response1 and auxin-

291 Olfactory receptor genes, upstream effectors of the MAPK signaling

292 le of all KIR family genes and C-type lectin receptor genes using RNA sequencing on NKTCL cases (n =

293 prevalence of type 2 diabetes by APOB vs LDL receptor gene was 1.91% vs 1.33% (OR, 0.65 [95% CI, 0.48

294 present study, mRNA expression of all 6 LPA receptor genes was detected in murine aortic VSMCs, with

295 ne segments of the rearranged immunoglobulin receptor genes were amplified and sequenced from pretrea

296 us contains a small family of four cytokinin receptor genes, which all respond to M. loti infection.

297 genetic variants in the MC1R (melanocortin 1 receptor) gene, which determines skin and hair color, ar

298 he analogous residue in the Grid2 (glutamate receptor) gene, which is mutated in the mouse neurobehav

299 tor antagonist or knocking down the ecdysone receptor gene with RNAi resulted in an increased product

300 of 61 tag SNPs in 7 nicotinic acetylcholine receptor genes with subclinical atherosclerosis, as meas