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

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

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

6 uated the methylation status of the androgen receptor gene.

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

8 gly exacerbated by the loss of another GID1b receptor gene.

9 ained the recent variation in this pheromone receptor gene.

10 associates with the single active olfactory receptor gene.

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

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

13 e distinct gene segments to assemble antigen-receptor genes.

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

15 reduced chromatin accessibility on IFN-gamma receptor genes.

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

17 ereby affecting the expression levels of ABA receptor genes.

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

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

20 ted with inherited variations near glutamate receptor genes.

21 ted in rodenticide resistance, and olfactory receptor genes.

22 ler surviving mammals with more bitter taste receptor genes.

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

24 similar to that observed for other olfactory receptor genes.

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

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

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

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

29 ticated transposase, for assembly of antigen receptor genes.

30 ly and diversification of lymphocyte antigen receptor genes.

31 to stimulate transcription of acetylcholine receptor genes.

32 I and class II HLA, B-cell receptor, and Fc receptor genes.

33 infection is independent of known arenavirus receptor genes.

34 dispensable genes was enriched in olfactory receptor genes (41 genes).

35 sterone, intercalated cell mineralocorticoid receptor gene ablation directly reduced pendrin's relati

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

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

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

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

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

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

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

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

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

45 The 125 dispensable nonolfactory receptor genes also displayed a relaxation of selective

46 ssess the most diverse repertoire of NK cell receptor genes among all mammals studied to date.

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 ones through paired sequencing of the T cell receptor genes and high-dimensional single-cell spatial

53 9 causes upregulation of abscisic acid (ABA) receptor genes and hypersensitivity of ABA-responsive ge

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

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

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

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

58 ranscriptional changes in multiple glutamate receptor genes and strong upregulation of genes coding f

59 demethylase can induce derepression of NOTCH receptor genes and subsequent activation of the NOTCH pa

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

61 s known to suppress the expression of immune receptor genes and to positively regulate stomatal closu

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

63 the expression of ethylene biosynthesis and receptor genes, and the synergistic interactions of OPDA

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

65 m a CAG repeat expansion within the androgen receptor gene (AR).

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

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

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

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

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

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

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

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

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

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

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

77 scend hazardous intermediates during antigen receptor gene assembly.

78 maintaining genome integrity during antigen receptor gene assembly.

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

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

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

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

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

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

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

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

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

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

89 s and their progenitors shows that olfactory receptor gene clusters from 18 chromosomes make specific

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

91 at a niche-associated variation in pheromone receptor genes contributes to natural differences in phe

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

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

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

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

96 larly affected by mutations in the chemokine receptor gene, cxcr4b, suggesting it is a potential Neur

97 thood by targeting the netrin-1 guidance cue receptor gene Dcc in the medial prefrontal cortex (mPFC)

98 fied mutations of the axon guidance molecule receptor gene, DCC, present an opportunity to investigat

99 Receptor gene deletion reduced tsetse infection, identif

100 The 41 dispensable olfactory receptor genes displayed a relaxation of selective const

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

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

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

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

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

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

107 ithin the NK complex and killer cell Ig-like receptor genes encoded within the leukocyte receptor com

108 Killer cell receptor genes encoded within the NK complex and killer

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

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

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

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

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

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

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

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

117 creted miRNAs in the regulation of glutamate receptor gene expression and their relevance for schizop

118 ry stimuli do no impact cerebral adiponectin receptor gene expression in mouse.

119 Thus, FUS regulates acetylcholine receptor gene expression in subsynaptic myonuclei, and m

120 ing GLP-1 receptor, preproglucagon or amylin-receptor gene expression in the DVC.

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

122 l-DOPA-induced activation, and >100 neuronal receptor gene expression maps based on transcriptional d

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

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

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

126 receptor antagonist and increased adenosine receptor gene expression.

127 tnatal tactile stimulation on glucocorticoid receptor gene expression.

128 Olfactory receptor gene families are significantly expanded in pan

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

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

131 In conclusion, all members of the opioid receptor gene family express circRNAs, with Oprm1 circRN

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

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

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

135 ression patterns of the Drosophila serotonin receptor gene family.

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

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

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

139 pying genetic haploinsufficiency for the Fsh receptor gene Fshr.

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

141 mRNAs (linRNA), mouse, rat, and human opioid receptor genes generate exonic circRNA isoforms.

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

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

144 revealed genetic interactions with the Notch receptor gene glp-1 that influenced development and embr

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

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

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

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

149 creased expression of metabotropic glutamate receptor gene Grm5.

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

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

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

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

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

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

156 236757, P = 4.99 x 10(-8)) in the interferon receptor gene IFNAR2.

157 beta upregulates the expression of the IL-33 receptor gene Il1rl1 (encoding IL-1 receptor-like 1, als

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

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

160 ntified a mutation in the beta(1)-adrenergic receptor gene in humans who require fewer hours of sleep

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

162 blockade and knockdown of the melanocortin-4 receptor gene in the DMV abolish this stimulation-induce

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

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

165 the functional diversification of olfactory receptor genes in a bird lineage that relies extensively

166 tion assembles and diversifies Ig and T cell receptor genes in developing B and T lymphocytes.

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

168 by all of the rearranged antibody and T cell receptor genes in one person-the 'genome' of the adaptiv

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

170 ion profile of gonadotropin subunit and GnRH receptor genes in rat pituitary in vitro and in vivo to

171 we sequence recombined and expressed B cell receptor genes in several individuals to determine the s

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

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

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

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

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

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

178 membrane (TM) domains of the mouse mu-opioid receptor gene, in enhancing expression of the full-lengt

179 In addition, we observed that other opioid receptor genes including delta, kappa, and nociceptin re

180 neth cells in mice, using a diphtheria toxin receptor gene inserted into the P-lysozyme locus, does n

181 tations in both alleles of the human insulin receptor gene (INSR) cause extreme insulin resistance (I

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

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

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

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

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

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

188 tations in the LDL (low-density lipoprotein) receptor gene (LDLR) cause elevated levels of LDL choles

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

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

191 Conformation of antigen receptor gene loci spatially juxtaposes rearranging gene

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

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

194 Germline variants in the melanocortin 1 receptor gene (MC1R) might increase the risk of childhoo

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

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

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

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

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

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

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

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

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

204 Allelic differences in the human mu opioid receptor gene, notably the A118G single nucleotide polym

205 n mammals, methylation of the glucocorticoid receptor gene Nr3c1 has been implicated as mediator of l

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

207 ced expression of the CREB-regulated nuclear receptor gene Nr4a2 is selectively impaired in aged rats

208 euroticism, and a locus overlapping the BDNF receptor gene, NTRK2.

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

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

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

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

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

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

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

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

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

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

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

220 The mu-opioid receptor gene, OPRM1, undergoes extensive alternative sp

221 ous missense common variant in the olfactory receptor gene OR2AG2 that segregated with a risk haploty

222 mbly reveals the duplication of an olfactory receptor gene (OR3), which we demonstrate enhances the a

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

224 ariations of the oxytocin and/or vasopressin receptor genes OXTR and AVPR1A, respectively.

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

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

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

228 neurons in the PFC that express the oxytocin receptor gene (Oxtr) impairs the ability to distinguish

229 Epigenetic modification to the oxytocin receptor gene (OXTR) in ASD could be an informative biom

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

231 ith Cre-recombinase directed to the oxytocin receptor gene (Oxtr), we revealed that oxytocin receptor

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

236 genes including delta, kappa, and nociceptin receptor genes produced similar circRNAs.

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

238 r (DeltaE9-10) combined with loss of the SHH receptor gene Ptch1 resulted in fully penetrant medullob

239 chain reaction-based investigation of T-cell receptor gene rearrangement to detect clonality.

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

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

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

243 ve PCR analysis of immunoglobulin and T-cell receptor gene rearrangements.

244 iate this transition and suppressing antigen receptor gene recombination, ensuring that only one prod

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

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

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

248 insect lineages, most notably the ants, have receptor gene repertoires many times larger than D. mela

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

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

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

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

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

254 Mutations in the skeletal muscle ryanodine receptor gene (RYR1) can cause susceptibility to maligna

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

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

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

258 phila melanogaster, OSNs expressing specific receptor genes send stereotyped projections to one or tw

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

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

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

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

263 VEGF ligand and receptor genes, specifically genes relevant to FLT4 and

264 n deletions that impair duplicated pheromone receptor genes (srg-36 and srg-37), which were previousl

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

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

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

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

269 In addition, we find that the sweet receptor gene TAS1R2, which has been proven to be a pseu

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

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

272 se A (PKA), protein kinase C (PKC), and AMPA receptor genes that play a pivotal role in memory functi

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

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

275 bolishing somatic diversification of antigen receptor genes, the hallmark of canonical adaptive immun

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

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

278 kground of high genetic diversity of NK cell receptor genes, this KLRA allele fixation points to fund

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

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

281 sitive neurons and abundance of chemosensory receptor gene transcripts in the maxillary palp.

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

283 The mu-opioid receptor gene undergoes extensive alternative splicing t

284 Olfactory receptor genes, upstream effectors of the MAPK signaling

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

286 However, we found very few olfactory receptor genes, very few trace amine-associated receptor

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

288 ighly expressed in the slug brain, while the receptor gene was expressed at lower levels in general w

289 de-binding, leucine-rich repeat (NLR) immune receptor gene was isolated using mutagenesis and R gene

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

291 Expression of ten VEGF ligand and receptor genes was quantified using RNA sequencing of pr

292 -brain transcriptional data of >100 neuronal receptor genes, we found that both interventions specifi

293 Two splicing variants of the receptor gene were functionally expressed and tested for

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

295 y in the amygdala, but none of the serotonin receptor genes, were predictive of interindividual diffe

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 more, we isolated a number of cognate T cell receptor genes with tumor reactivity.