ライフサイエンスコーパス: expression pattern

1 interplay reveals a geometry-dependent gene-expression pattern.

2 d the light-dependent regulation of the CKI1 expression pattern.

3 pregulated in human cancers, exhibiting a co-expression pattern.

4 ifferently for gene structure, sequence, and expression pattern.

5 show that iPSCs retain a donor-specific gene expression pattern.

6 pective promoter sequences support this gene-expression pattern.

7 rphogenesis, and dynamic spatiotemporal gene expression patterns.

8 y effectively 'freezing in' the in vivo gene expression patterns.

9 ional and translational fusions show similar expression patterns.

10 morphophysiological responses based on gene expression patterns.

11 large number of LexA driver lines with known expression patterns.

12 , GATA-2-6, with distinct and/or overlapping expression patterns.

13 ions but reset leukemic DNA methylation/gene expression patterns.

14 cence morphology result from shifts in their expression patterns.

15 s, electrophysiological properties, and gene-expression patterns.

16 th typical mutational, cytogenetic, and gene expression patterns.

17 esources and identifies sex- and age-related expression patterns.

18 ton, reduced the chromosome instability gene expression patterns.

19 ses six LAZY genes having spatially distinct expression patterns.

20 located on autosomes and exhibit male-biased expression patterns [6].

21 icient to explain all aspects of the complex expression patterns acquired by a receptor family that s

22 is known about the variation of neuropeptide expression patterns across closely related species in in

23 chniques are limited to only exploiting gene expression patterns across multiple tissues either in a

24 but these orthologues did not show parallel expression patterns across species more than expected by

25 d major differences in the immune checkpoint expression patterns across tumor types and individual tu

26 This gene expression pattern agrees with uncoupled rates of trait

27 This expression pattern aligns well with RNA-seq data, but co

28 vivo can be hard to predict based on target expression pattern alone.

29 The present work compares the expression patterns among cochlear type II afferents of

30 We compared gene expression patterns among primary human gastric cells, u

31 traspecies conservation and describing their expression patterns among several organs/tissues and str

32 Results demonstrated variation of gene expression patterns among species and a strong correlati

33 ults were well correlated with the same gene expression pattern analysed in the thyroid tissue of the

34 r was created for functional rescue, protein expression pattern analysis, and to distinguish between

35 xpression of SPZ1 exhibited a tumor-specific expression pattern and a high correlation with patients'

36 report that SCARF-1 shows a highly localised expression pattern and co-localised with endothelial mar

37 insights into the role that changes in gene expression pattern and epigenetic mechanisms contribute

38 tingly, not much is known about the specific expression pattern and function of the individual activa

39 Here, for the first time we unravel the expression pattern and functional significance of Wnt5a

40 and pattern, with consequent impact on dand5 expression pattern and left-right (L-R) axis establishme

41 The expression pattern and localization of Vimentin confirme

42 To provide further insight into the Hoxa5 expression pattern and potential functions in the brain,

43 The function of the gene, its expression pattern and subcellular localization were cha

44 d with increased chromosome instability gene expression patterns and aneuploidy.

45 nals from the microenvironment regulate gene expression patterns and cell behavior.

46 ted sequences can encode genes with specific expression patterns and development-related functions, w

47 in regions, but exhibit strikingly different expression patterns and developmental dynamics.

48 Here, we analyzed ecdysone-related gene expression patterns and found that they were consistent

49 ve been described, each with distinct tissue expression patterns and functions.

50 ed from these areas, attending to their gene expression patterns and histogenesis.

51 ng number of questions that remain about NGF expression patterns and NGF's various functions and inte

52 samples were collected and analyzed for gene expression patterns and phosphorylation of signaling pro

53 potential pharmacological targets, yet their expression patterns and physiological functions remain c

54 We report that RFRP-3 immunofluorescence expression patterns and RFRP-3/GnRH cross-talk are large

55 In summary, our studies identify distinct expression patterns and roles in synaptic plasticity for

56 markers because of their cell type-specific expression patterns and stability in peripheral blood.

57 a foundation for detailed analysis of miRNA expression patterns and transcriptional control regions.

58 utaneous infections in mice and exhibit gene expression patterns and virulences distinct from those o

59 rent understanding of betaCA tissue-specific expression patterns and what controls them are reviewed,

60 ldren with asthma would induce specific gene expression patterns and whether such patterns were assoc

61 ion of a set of CRMs known to drive a common expression pattern, and assign that pattern to other CRM

62 as to investigate the receptor pharmacology, expression pattern, and in vivo function of ELA peptides

63 arbonate transporter with a brain-restricted expression pattern, and variant rs16846053 affects a put

64 haracterization of phenotypes including gene expression patterns, and generation of human disease mod

65 27A) mice had increased CIN25 and CIN70 gene expression patterns, aneuploidy, and defects in mitosis.

66 The diversity of opsins and their retinal expression patterns appear greatest for animals that exp

67 Precise gene expression patterns are established by transcription fac

68 ing and alterations in Ca(2+)-dependent gene expression patterns are pivotal characteristics of faili

69 atients with pure DCIS have a different gene expression pattern as compared to patients with DCIS and

70 oss the entire cortex, consistent with their expression patterns as described in macaques.

71 The expression patterns assist interpretation of the essenti

72 evated TLR9 and PAX5, but not BLIMP1 (a gene-expression pattern associated with mature follicular B c

73 Neutrophil activity and gene expression patterns associated with cartilage damage wer

74 Gene expression patterns associated with chromosome instabili

75 Ifnb in wild-type B cells and distinct gene expression patterns associated with endogenous IFN-beta.

76 ns between HNF4A and microbiota promote gene expression patterns associated with human inflammatory b

77 sion, we identified tissue-specific microRNA expression patterns associated with several kidney patho

78 rning methods can be trained to use the gene expression patterns associated with the text-derived lab

79 f such differential histone modification and expression patterns at MAC-/OC-specific genes.

80 rvised learning algorithm that predicts gene expression patterns based on enriched sequence features.

81 we identified 51 lincRNAs with differential expression patterns between embryonic and adult hearts,

82 Comparisons of gene expression patterns between retained transcription facto

83 sequencing revealed distinct gene and miRNA expression patterns between the sole -7 and non -7 AML c

84 or the lack of Rpl10, which exhibits a broad expression pattern but is subject to MSCI during spermat

85 ogs, TaVIT1 and TaVIT2, which have different expression patterns but are both low in the endosperm.

86 genes under one condition have different co-expression patterns compared with another.

87 with the CMG helicase component SLD5, and an expression pattern confined to actively dividing cells.

88 rly stages of this symbiosis, including gene expression patterns consistent with biochemical stresses

89 resulted in differences in gene function and expression patterns, contributing to differences in flow

90 The expression pattern corresponded to the normoxic animals,

91 The dynamic gene expression pattern data reveal clear sex-related charact

92 of the RBM28 cDNA sequence and profiled its expression patterns detecting a negative correlation (R

93 act at transcribed enhancers to dictate gene expression patterns determining growth outcomes, includi

94 The observed RSV-induced gene expression patterns did not differ significantly in NP s

95 cells demonstrated an adhesion macromolecule expression pattern distinct from Hodgkin and Reed-Sternb

96 hange in microcirculation inflammation, gene expression patterns, DSA levels, or kidney function.

97 served matricellular protein with a distinct expression pattern during development and disease.

98 et of miRNAs that exhibited an age-dependent expression pattern during wound closure was identified,

99 udy aimed to clarify HIF1alpha and HIF2alpha expression patterns during cytotrophoblast differentiati

100 3 regulatory system in finely balancing gene expression patterns during H. schachtii parasitism of Ar

101 However, little is known about their expression patterns during human infections.

102 ures of breast cancer (based on complex gene expression patterns) enabled identification of several i

103 This indicates that E- and P-cadherin expression patterns evolved differently between chick an

104 trees is roughly reflected by similarity of expression pattern for most HLA-A and -C loci.

105 ng filamentous cyanobacteria and the similar expression patterns for hmpF and hmpD imply that HmpF is

106 s approach, we uncovered complex overlapping expression patterns for hundreds of molecules involved i

107 leaf domains of the tcp mutants show changed expression patterns for many photosynthesis-related gene

108 neurons differed markedly from that the gene expression patterns found previously using whole DRG tis

109 of the metatranscriptomes showed correlated expression patterns helping to elucidate how metabolic i

110 s a choline transporter-like protein with an expression pattern highly correlated with auxin distribu

111 We clustered the genes by temporal expression pattern, identified transcription factor bind

112 macologic studies, together with analysis of expression patterns, identified GPR120 on F4/80(+)/CD11b

113 ways are highly enriched in all non-additive expression pattern in endosperm, while cytokinine biosyn

114 ated that Ebf3 and Meis2 showed a restricted expression pattern in female VMP and prostate mesenchyme

115 s functionally conserved, driving a specific expression pattern in lignifying vascular tissues.

116 We identified a gene expression pattern in rectal tissues of patients with UC

117 tance for proper brain function, its overall expression pattern in the mammalian brain at the resolut

118 that OsbHLH068 and AtbHLH112 share a similar expression pattern in transgenic Arabidopsis during the

119 ography to rapidly image brain-specific gene expression patterns in 3D at cellular resolution.

120 and their neighborhoods correlated with gene expression patterns in a predictable manner.

121 Because of their genome-wide expression patterns in a variety of tissues and their ti

122 ONS_00028686, which exhibit cardiac-enriched expression patterns in adult heart.

123 suggesting organ-specific hardwiring of NLR expression patterns in anticipation of distinct challeng

124 KFB(CHS) exhibits developmental expression patterns in Arabidopsis leaves, stems, and si

125 ring method was used to identify immune gene expression patterns in blood over time points (before NA

126 pigenetic modifications in pathological gene expression patterns in CCC patients' myocardium.

127 oinformatic and qPCR analysis, different miR expression patterns in colon cancer versus non tumour ce

128 Here, we use gene expression patterns in combination with weighted gene co

129 Here, we examine global gene expression patterns in corals and their intracellular al

130 urther integrated our inferred GRN with gene expression patterns in different seed compartments and a

131 Expression analysis reveals both diverse expression patterns in different soybean tissues and pre

132 ted distinct and recognizable spatiotemporal-expression patterns in human brains and laminar-expressi

133 Examination of expression patterns in human heart tissues indicates a c

134 Moreover, we identified distinctive gene expression patterns in human urine as potential biomarke

135 We compared global gene expression patterns in livers from wildtype, Gcn2 (-/-),

136 were no fundamental differences in the gene expression patterns in multibacillary and paucibacillary

137 junum in rhesus macaques, revealing distinct expression patterns in naive and memory subsets.

138 al blood leukocyte levels/responses and gene expression patterns in nasal cells were largely concorda

139 TCH 1, NOTCH2, and NOTCH3 and resulting gene expression patterns in parental and NOTCH1-expressing C2

140 e syndrome and in characterising the protein expression patterns in plasma and bronchoalveolar lavage

141 action array to analyze messenger RNA (mRNA) expression patterns in rectal mucosal samples from 138 t

142 amics that gives rise to heterogeneous Nanog expression patterns in reporter cell lines that are not

143 ropeptides, were selected according to their expression patterns in small and unique subsets of neuro

144 The comparison of gene expression patterns in the embryonic brain of mouse and

145 that SOHLH1 and SOHLH2 demonstrate distinct expression patterns in the embryonic ovary and interact

146 tailed and thus complete picture of survivin expression patterns in the gastrointestinal tract, we us

147 Accordingly, we identified miRNA expression patterns in the normal human colonic SC niche

148 ed this model and revealed differential mRNA expression patterns in these tissues.

149 Yet, opsin repertoires and expression patterns in this group of fishes are poorly d

150 powerful methodology to quantify global gene expression patterns in various contexts from single cell

151 forms displayed a strong correlation in gene expression patterns, including a strong induction of inn

152 reestablished leukemic DNA methylation/gene expression patterns, including an aberrant MLL signature

153 lagin biosynthesis were identified and their expression patterns indicated that gallic acid synthesis

154 Cell subtype prediction using messenger RNA expression patterns indicated that NK-cell populations i

155 dicine paradigm, wherein a biomarker or gene expression pattern indicates a patient's likelihood of r

156 This biphasic expression pattern indicates the active requirement of t

157 ted with distinctive organellar features and expression patterns indicative of cellular stress.

158 ealed that heterologous symbionts induced an expression pattern intermediate between the typical symb

159 Surprisingly, a relatively constrained gene expression pattern is observed in brain compared with ot

160 adaptive immune response as defined by mRNA expression pattern is reproducible and sufficient to pre

161 Thus, the means by which the interphase expression pattern is transduced to daughter cells have

162 hosphoribosyltransferase also displayed gene expression patterns linked to mitochondrial dysfunction

163 help discover tumor subtype specific gene co-expression patterns (modules) that are significantly enr

164 mmune signaling pathways and maintained gene expression patterns normally decreased by castration.

165 ons of these moieties were in line with gene expression patterns observed during wing imaginal disc d

166 e similarities contrast with the unique gene expression patterns observed in sporozoites isolated fro

167 The expression patterns obtained using our method were conco

168 mining the TCM, we quantified changes in the expression pattern of 804 proteins in nCPC-derived TCM a

169 summary, we provide novel insights into the expression pattern of C3aR in mice.

170 The restricted expression pattern of CD22 on B cells and most B cell ly

171 gans males exhibit an altered, male-specific expression pattern of daf-7 in the ASJ sensory neuron pa

172 amily GTPase 1 (DIRAS1) gene with an altered expression pattern of DIRAS1 protein in the affected bra

173 region of DUO1 (ROD1), which replicates the expression pattern of DUO1 in Arabidopsis (Arabidopsis t

174 findings are that (i) TAL TJs show a mosaic expression pattern of either cldn10b or cldn3/cldn16/cld

175 k as a model, we found a precise and dynamic expression pattern of fibroblast growth factor 8 (Fgf8)

176 This region-specific expression pattern of genes, such as synaptogenic modula

177 A key finding is the unique expression pattern of growth hormone (Gh) and prolactin

178 tion between the Eda haplotype block and the expression pattern of key immune system genes.

179 Comparison of the expression pattern of Ki-67, a protein that acts as a ce

180 by mass cytometry revealed a highly similar expression pattern of killer inhibitory receptors and ot

181 We studied the neural gene expression pattern of LIMK-1, cofilin-1, and beta-actin

182 rthermore, the linkage of LSD1 to an altered expression pattern of lung-lineage specific transcriptio

183 We identified the expression pattern of mERbeta2 in mouse tissues and asse

184 We investigated the expression pattern of Pcdh19 and Ncdh in limbic structur

185 let prior distribution to capture the common expression pattern of replicates from the same condition

186 Our results showed that the expression pattern of ribosome-associated mRNA profiles

187 engineered knockin reporter mouse to map the expression pattern of the Gpr182 during development and

188 The RNA expression pattern of the NCAN gene in human tissues was

189 ied out to identify and analyze differential expression pattern of tomato membrane bound NAC transcri

190 The expression pattern of Zt6 and potent toxicity towards mi

191 We integrated data on expression patterns of 123 genes and the model for end-s

192 determined and compared inhibitory receptor expression patterns of 2B4, CTLA-4, LAG-3, PD-1, and Tim

193 The expression patterns of 917 recurrently deregulated lncRN

194 yocyte differentiation, we analyzed the gene expression patterns of 96 developmental genes at single-

195 -2 expression in S. stercoralis, we observed expression patterns of a transgene construct encoding gr

196 Here, we investigated the expression patterns of all of the GalNAc-Ts in colon can

197 anged periodically, as also reflected in the expression patterns of an RA-responsive gene, STRA8; RA

198 We analyzed the expression patterns of AqJAG in various tissues and deve

199 In conclusion, there are similarities in the expression patterns of ArPPLNP1 and ArPPLNP2 but our dat

200 The expression patterns of beat and side genes suggest that

201 Most expression patterns of both cadherins remain constant wi

202 genome-wide nuclear DNA methylation and gene expression patterns of brain tissue.

203 The expression patterns of Cgrpalpha and Th formed opposing

204 ng RNA sequencing (RNA-Seq), we compared the expression patterns of circular RNAs in proliferating (e

205 study found a clear correlation between the expression patterns of CorTFL1 and CorAP1 and the inflor

206 We compared the spatiotemporal expression patterns of CorTFL1, CorAP1 and CorLFY in six

207 we performed a comprehensive analysis of the expression patterns of dystrophin isoforms across human

208 genes are assigned based on tissue-specific expression patterns of flanking genes.

209 atomically distinct structures; however, the expression patterns of genes across hundreds of brain st

210 ng of the conservation and divergence of the expression patterns of genes between plant species is li

211 The tissue-specific expression patterns of homeobox genes suggested roles in

212 how that each MED12 mutations cause specific expression patterns of JUN, FOS and EGR1 immediate early

213 Here, we unveil the visual opsin expression patterns of juvenile starry flounder (Platich

214 e complemented by cell division profiles and expression patterns of key genes, including invected and

215 The expression patterns of known and putative SSP genes base

216 and-specific RNA-sequencing, we profiled the expression patterns of lincRNAs in Arabidopsis, rice and

217 Analyses of expression patterns of LN chains in the human limbal nic

218 ancer cell lines generally recapitulated the expression patterns of matched primary cells, their isom

219 Furthermore, similar cellular expression patterns of MET in the brainstem of both the

220 ealed tissue-specific and hormone-responsive expression patterns of MeTCP genes.

221 hese caste differences, we compared the gene expression patterns of MGs from queens, queenright worke

222 The Cancer Genome Atlas to elucidate how the expression patterns of mRNAs are shaped by regulatory no

223 found an unexpectedly high variation in the expression patterns of neuropeptides across species.

224 We show novel actions of RvE1 and expression patterns of neutrophil receptors in type 2 di

225 of miR-211 in melanocytes was shown to alter expression patterns of newly identified target genes, an

226 rophages with knockdown of NR1D1 had altered expression patterns of NLRP3, compared to macrophages th

227 We demonstrated that expression patterns of opioid genes highly correlate wit

228 ngs, we used a microarray to investigate the expression patterns of other pyknon-containing genomic l

229 The expression patterns of S100beta and glial fibrillary aci

230 Transcriptional expression patterns of several genes were consistent wit

231 Profiling the expression patterns of small nucleolar RNAs (snoRNAs) in

232 Profiling the expression patterns of snoRNAs is the initial step in de

233 antly, this phenomenon explains the aberrant expression patterns of some cancer driver genes, potenti

234 Moreover, we investigated the expression patterns of the conserved lncRNAs at differen

235 xperimentally investigating and manipulating expression patterns of the human renin gene in a native

236 The comparative expression patterns of these genes, critical for pallial

237 cing of lupus patient blood revealed similar expression patterns of these same pathways.

238 he developing mouse and human ENS, we mapped expression patterns of transcription and signaling facto

239 efined) physiological functions and cellular expression patterns of TSPO in health and disease.

240 The cellular expression patterns of uPA and uPAR were characterized b

241 previously reported in wheat, both in shared expression patterns of wheat homologs of Brachypodium ge

242 ionship between personal expression and gene expression, patterns of natural language use may provide

243 vely remove unwanted cells from a Split GAL4 expression pattern or to subtract neurons of interest fr

244 transcriptional activity, generating diverse expression patterns over time that partition into distin

245 ctures of the limbic system with overlapping expression patterns particularly within regions of the a

246 galactosidase for high-resolution mapping of expression patterns post-mortem.

247 a temperature-dependent, sexually dimorphic expression pattern, preceding gonadal sex differentiatio

248 es as well as a small set of key genes whose expression patterns reflect these relationships.

249 cells in vitro, and possessed a unique gene expression pattern related to Tfh and Th2 cells.

250 atinum drugs, in large part by altering gene expression patterns related to DNA repair and immune act

251 Changes in gene expression patterns represent an essential source of evo

252 The zQ175 mouse model recapitulates the expression pattern seen in humans with HD and may have v

253 elationships among miRNA duplications, novel expression patterns, sequence change, and the acquisitio

254 IFNlambdas) or type III IFNs share homology, expression patterns, signaling cascades, and antiviral f

255 cted cells displayed a plasma cell-like gene expression pattern similar to PELs.

256 eta-catenin) resulted in organoids with gene expression patterns similar to developing human duodenum

257 Gene expression patterns specific for maturation were mimicke

258 Phylogenetic inference and different gene expression patterns support functional divergence of the

259 rophil subsets and a novel monoallelic CD177 expression pattern that does not follow classical random

260 B, I80 and I86) showed a lifespan trajectory expression pattern that is anticorrelated with the expre

261 due to their antigenic properties and unique expression pattern that is primary restricted to germ ce

262 that FIS2 and MEA have reproductive-specific expression patterns that are correlated and derived from

263 (STAT) proteins, leads to inappropriate gene expression patterns that can promote tumor initiation an

264 Transcriptomics identified expression patterns that explain PD duplication, includi

265 h the goal of investigating changes in miRNA expression patterns that might contribute to resistance.

266 an ordered set of biological processes with expression patterns that showed sequential reversal foll

267 diversification, and non-spidroin genes with expression patterns that suggest roles in silk productio

268 t the network settles into attractors, or TF expression patterns, that correlate with NE or ML phenot

269 Together with their distinct gene expression patterns, this differential accumulation of t

270 enes are perturbed in T2D and have a similar expression pattern to that of dedifferentiated islets.

271 We investigated T-cell gene expression patterns to determine the mechanisms by which

272 elation analysis are then used to compare 3D expression patterns, to automatically detect all statist

273 tant to identify groups of genes with common expression patterns under certain conditions.

274 found that MeTCPs showed similar or distinct expression patterns under cold and/or drought stress, su

275 vide a high-quality resource of altered gene expression patterns under severe OXPHOS deficiency compa

276 to be responsible for alterations in Nkx3.1 expression patterns under various physiological conditio

277 quencing analyses revealed differential gene expression patterns unique to infiltrating and resident

278 In addition, abrB gene expression patterns varied significantly between codY-nu

279 Finally, an opposite expression pattern was observed for TrkC-miR2 and the AP

280 Given the n1-src expression pattern, we investigated a possible role for

281 In comparisons of EAC gene expression patterns, we associated high expression of ER

282 ecause of their dramatically different brain expression patterns, we studied similarities and differe

283 Predicted expression patterns were 73-98% accurate, predicted assi

284 ged genes, three clades showing differential expression patterns were constructed to identify genes a

285 age colony-stimulating factor-receptor-alpha expression patterns were examined by flow cytometric and

286 Cytokines, chemokines, and gene expression patterns were measured by flow cytometry and

287 only 17% of the remaining genotype-specific expression patterns were not changed by water deficit.

288 ptive (IC-associated) and constitutive PD-L1 expression patterns were observed.

289 We also found that clag3 expression patterns were reset during transmission stage

290 on-making is the ability to generate bimodal expression patterns where 2 alternate expression states

291 nalysis indicated a unique monoallelic CD177 expression pattern, where the offspring stably transcrib

292 l pituitaries exhibited similar sst2/sst5/D2 expression patterns, wherein BIM-23A760 inhibited the ex

293 y inducing an early myogenesis -related gene expression pattern which includes myogenin and Myf5 up-r

294 iscern between protein isoforms according to expression patterns, which is most significant in light

295 ity involves a precise orchestration of gene expression patterns whose transcriptional regulators hav

296 n SPARC knockout myoblasts reveals a changed expression pattern with dominance of gamma-actin.

297 We correlated expression patterns with the presence of immune cell inf

298 th other human calpains, CAPN14 has a unique expression pattern, with the highest levels in the upper

299 ls and found significant differences in gene-expression patterns, with activation of genes involved i

300 -DCB and 4'-OH-2,5-DCB resulted in different expression patterns, with the former leading to enrichme