ライフサイエンスコーパス: spatial expression

1 early have distinct patterns of temporal and spatial expression.

2 re precisely regulated in their temporal and spatial expression.

3 se orthologue of ELOVL4 and its temporal and spatial expression.

4 e genes that show no or little divergence in spatial expression.

5 ay analysis was consistent with the observed spatial expression.

6 omplex ways with enhancers to direct correct spatial expression.

7 be important in regulating its temporal and spatial expression.

8 istinct, despite their partially overlapping spatial expression.

9 oter, and both genes overlap in temporal and spatial expression.

10 d by their distinct patterns of temporal and spatial expression.

11 Spatial expression analysis using in situ hybridization

12 he NR2E3 function, we performed temporal and spatial expression analysis, yeast two-hybrid screening,

13 e CRS also mediates proper developmental and spatial expression and behavioral rescue, we used the CR

14 ato XET gene, LeXET2, that shows a different spatial expression and diametrically opposite pattern of

15 ecific expression, suggesting a link between spatial expression and imprinting.

16 Spatial expression and repression, and the changing rate

17 distinct region within LST-1 determines its spatial expression and size of the GSC pool.

18 role of ARPs in plants, we have examined the spatial expression and subcellular distribution of two h

19 lization based on their distinct patterns of spatial expression and the inability of LAX sequences to

20 The present study compares the temporal-spatial expression and tissue localization of the rat ep

21 Changes in spatial expression are associated with the evolution of

22 the sequence level basis for control of alx1 spatial expression by the double negative gate GRN archi

23 gylocentrotus purpuratus, and show how their spatial expression changes dynamically during developmen

24 The abundance of spatial expression data in recent years has led to the m

25 A particularly rich source of spatial expression data is the Allen Brain Atlas (ABA),

26 The availability of high-throughput spatial expression data opens the door to methods that c

27 Here, we describe the in vivo spatial expression distribution, properties, and structu

28 nt of mechanisms regulating the temporal and spatial expression domain of the C-function genes.

29 Once established, spatial expression domains and cell fates are fixed and

30 First, genetic markers reveal distinct spatial expression domains and subdomains along the long

31 of Zelda influences both the timing and the spatial expression domains for most of the genes control

32 sed among the digits of amniote limbs; their spatial expression domains, however, vary between specie

33 individual cell can be precisely mapped into spatial expression domains.

34 the mechanisms that control its temporal and spatial expression during development.

35 evel resulting in strict tissue-specific and spatial expression during embryonic development.

36 We report the spatial expression during larval development of the five

37 er, little is known about their temporal and spatial expression during seed development and upon germ

38 vivo, however, with a variable temporal and spatial expression during spirochete infection in mice a

39 Our results allowed us to determine spatial expression foci for each expressed gene in the g

40 press PLETHORA (PLT) genes, regulating their spatial expression gradient.

41 he primate neocortex, dozens of genes showed spatial expression gradients among interneurons of the s

42 1-4 have been deleted, we find temporal and spatial expression, identical to wild-type, from a previ

43 The temporal and spatial expression in brain of the mRNAs for the pleiotr

44 d significant alteration in the temporal and spatial expression in endometrial epithelial cells.

45 work for Hoxa2, responsible for temporal and spatial expression in hindbrain development.

46 emonstrates similar patterns of temporal and spatial expression in human and sheep, but these differ

47 s well as a distinct pattern of temporal and spatial expression in the brain, suggesting the critical

48 For spatial expression in the endoderm, one particular pair

49 at the correct stage but showed an incorrect spatial expression in the majority of blastocysts.

50 moter contains elements required for correct spatial expression in the primary mesenchyme cells of an

51 onjugate molecules whose proper temporal and spatial expression is important at all stages of neurode

52 Interestingly, variability in spatial expression is not random; rather, transgene acti

53 enes, including Hox genes whose temporal and spatial expression is tightly regulated to guide pattern

54 functions of which are required for correct spatial expression late in embryogenesis.

55 tissues, and diversity in their temporal and spatial expression likely corresponds to diversity in fu

56 al V1 inhibitory interneurons, for which the spatial expression of 19 transcription factors has been

57 These sequences can drive correct temporal-spatial expression of a GFP reporter gene in transgenic

58 in thymocytes and orchestrates temporal and spatial expression of a large number of genes in the T-c

59 ng actin cytoskeleton through changes in the spatial expression of actin regulatory proteins.

60 d greater correspondence in the temporal and spatial expression of alpha3 and beta4 subunit mRNAs eme

61 ic mice recapitulated the known temporal and spatial expression of alpha9 AChR.

62 orphology are influenced by the temporal and spatial expression of ameloblastin and may implicate the

63 The temporal and spatial expression of both Srg1 and hr is characteristic

64 Analysis of temporal and spatial expression of c-Jun, phospho-c-Jun, and Etv5/ERM

65 s developed using grid column units, and the spatial expression of calculation parameters based on th

66 injury models, we examined the temporal and spatial expression of CCL2 and CCR2 in Mmp12(-/-) and wi

67 Understanding the temporal and spatial expression of CD8+ T cell antigens such as Cap1

68 We propose that temporal and spatial expression of chemokines are crucial factors, co

69 Here, we map the temporal and spatial expression of CHL1 and assess functional roles o

70 hanges in youth are correlated with cortical spatial expression of CNV genes in neurotypical adults.

71 that organ boundary specification by correct spatial expression of CUC genes requires STM mobility in

72 Our data show that LPA induced temporal and spatial expression of Cyr61, which promptly accumulated

73 t the regulatory effects of gap genes on the spatial expression of disco, disco-r, and tsh during Dro

74 the molecular mechanism of the temporal and spatial expression of dor and the roles of the delta-opi

75 Such distinct temporal and spatial expression of dor during development suggests a

76 pecific probes have been used to analyse the spatial expression of each individual member of the blt1

77 erged from D. melanogaster by about 100 Myr, spatial expression of emc, h and sr is conserved at the

78 FAC1 expression paralleled the temporal and spatial expression of eN-CAM following ERC lesion.

79 interactions that, together, achieve precise spatial expression of endo-mesoderm fates in C. elegans

80 ional processing, shedding, and temporal and spatial expression of endogenous fibrocystin at the cell

81 examined in avian embryos and related to the spatial expression of genes implicated in early cardioge

82 e identify an organization principle for the spatial expression of genes in animal tissues, which can

83 We reconstruct the spatial expression of genes in mammalian liver and intes

84 nalisation is responsible for regulating the spatial expression of genes in the underlying mesenchyme

85 The temporal and spatial expression of genes is controlled by promoters a

86 nistic hypotheses; yet information about the spatial expression of genes may be equally useful in int

87 , leading to differences in the temporal and spatial expression of genes or in the coding region of t

88 en made possible by changes in the timing or spatial expression of genes regulating development.

89 y sequences responsible for the temporal and spatial expression of genes regulating embryonic develop

90 specialized root nodules involves an altered spatial expression of genes that are otherwise induced s

91 Together, they regulate the temporal and spatial expression of GL2 and TTG2, which are considered

92 and HLH-1) that are crucial for the temporal-spatial expression of hlh-1 and proper myogenesis.

93 erall, we establish that, by controlling the spatial expression of Hox genes in the posterior limb an

94 inding proteins are likely to be involved in spatial expression of Hoxa5 during development.

95 m, we find the virus corresponds to distinct spatial expression of interferon response genes demonstr

96 The temporal and spatial expression of IPP-5 is consistent with its propo

97 is problem, we have studied the temporal and spatial expression of key genes known to orchestrate bra

98 spite cell cycle defects and cell death, the spatial expression of key limb patterning genes was main

99 to spinal cord lesions, and the temporal and spatial expression of KSPGs was examined using the 5D4 m

100 er fusions in transgenic roots establish the spatial expression of LATD/NIP in primary root, lateral

101 In Caulobacter crescentus, the temporal and spatial expression of late flagellar genes is regulated

102 The temporal and spatial expression of LMI1 supports a role in meristem i

103 Regulation of the precise temporal and spatial expression of Mash1 is thus likely to be importa

104 , the factors that regulate the temporal and spatial expression of Math1 within the cochlea are unkno

105 in injury and reveal a distinct temporal and spatial expression of MCP-1 in cells believed to be neur

106 Spatial expression of MIM is enriched in the anterior ne

107 Despite its known function, the temporal and spatial expression of miR-430 remains unclear.

108 end of the promoter is important for proper spatial expression of MsENOD40 in nodules and also for N

109 ightly coupled to ensure strict temporal and spatial expression of nascent proteins.

110 The temporal and spatial expression of netrin 1, netrin 4, and Unc5b gene

111 the endocardium, defined by the temporal and spatial expression of Nfatc1 during heart valve developm

112 region, and this corresponded with a higher spatial expression of nrd4, a key marker of neurogenesis

113 l ectoderm territory, are needed for correct spatial expression of oral and aboral ectoderm-specific

114 The temporal and spatial expression of PaFTL1 and PaFTL2 largely compleme

115 g requirements are not essential for correct spatial expression of phas during embryogenesis.

116 nsively investigated and is due to a precise spatial expression of proneural genes.

117 Here we report that the complex temporal and spatial expression of Ptf1a is controlled by at least th

118 The spatial expression of RAS enzymes was determined by immu

119 ind that QKY is required for the appropriate spatial expression of several epidermal cell fate regula

120 Furthermore, the spatial expression of several transcripts is expanded in

121 Here, we examined the temporal and spatial expression of Shroom3 in the mammalian kidney.

122 in development, and this is reflected by the spatial expression of signalling molecules such as Fgf8

123 Here, we analyzed the spatial expression of SL RNAs in the planarian flatworm

124 cess that relies on the precise temporal and spatial expression of specific genes in germ cells and i

125 surge and is controlled by the temporal and spatial expression of specific genes.

126 s was employed to determine the temporal and spatial expression of Stat3 and Ascl1a proteins followin

127 Here we demonstrate that Plzf regulates the spatial expression of the AbdB HoxD gene complex by bind

128 nts and trans-acting repressors that control spatial expression of the Abdominal-A (ABD-A) homeotic p

129 on, we found differences in the temporal and spatial expression of the alpha-, gamma-, and delta-zein

130 ith MPN, we determined that the differential spatial expression of the chemokine CXCL4/platelet facto

131 zation of F-actin and MTs through changes in spatial expression of the corresponding actin and MT reg

132 his gene in human and mouse retina, although spatial expression of the CRX gene appears to be conserv

133 g >400 bp to bring about proper temporal and spatial expression of the dev operon, resembling the reg

134 All of our data suggest that the spatial expression of the dpy-7 cuticle collagen gene is

135 but consistent with distinctive temporal and spatial expression of the EDA-A2 isoform, are likely req

136 lineages and regulation of the temporal and spatial expression of the growth hormone, prolactin (PRL

137 is study is to characterize the temporal and spatial expression of the mouse Pramel1 gene, and to det

138 ciated with changes in both the temporal and spatial expression of the proneural genes achaete (ac) a

139 ization is likely important to ensure strict spatial expression of the protein.

140 ous Pdx1 gene to ensure correct temporal and spatial expression of the regulatable transactivator.

141 l processing of the peptide and temporal and spatial expression of the transcript.

142 mRNA expression were similar to GPCR101, the spatial expression of the two mRNA species was different

143 The spatial expression of the two rat intestinal alkaline ph

144 The temporal and spatial expression of these 'mesoderm' genes suggests th

145 l mechanisms correlate with the temporal and spatial expression of these factors and may provide a me

146 The complexity of the spatial expression of these genes on the notum increased

147 lda, contribute to the accurate temporal and spatial expression of these miRNAs, which are known to f

148 The aggregate spatial expression of these regulators is not sufficient

149 SMR1 are due to differences in temporal and spatial expression of these two genes in Arabidopsis tis

150 Here, the temporal and spatial expression of these ZO-1 isoforms has been inves

151 Spatial expression of this GFP expression construct is s

152 d connectivity maps overlapped with the AHBA spatial expression of three gene clusters: (i) neuronal

153 However, the temporal and spatial expression of THSD7A and its biologic function f

154 nt is coordinately regulated by temporal and spatial expression of transcription factors, such as the

155 The correct spatial expression of two Drosophila bithorax complex (B

156 e been clarified by numerous observations on spatial expression of various genes, and by elegant line

157 Precise temporal and spatial expression of VEGF-A is required for vascular pa

158 illary plexus, and regulate the temporal and spatial expression of Vegfa.

159 signals prevents the incorrect temporal and spatial expression of virulence factors during cholera p

160 ne regulatory network encode the coordinated spatial expression of Wnt and Notch signaling as they sw

161 Taken together, our results suggest that the spatial expression of Wnt ligands within the dental epit

162 A comparison of the spatial expression of WRKY75 and the localization of the

163 e first characterization of the temporal and spatial expressions of the alpha 2A-AR, alpha 2B-AR, and

164 These findings reflect distinct temporal and spatial expressions of TSP1 and TSP2 in the healing woun

165 ry sequences that control their temporal and spatial expression or different functional protein domai

166 stages, which shows a gene's progression of spatial expression over developmental time.

167 implicated in cementogenesis, their precise spatial expression pattern and molecular role are not cl

168 stages (time) of embryos in images capturing spatial expression pattern are annotated manually, which

169 rotein sequence divergence and divergence of spatial expression pattern are initially coupled.

170 irects GUS activity in the same temporal and spatial expression pattern as the APETALA3 RNA and prote

171 orl meristem in female and male flowers, its spatial expression pattern became sex-specific as reprod

172 the embryonic shoot apical meristem, and its spatial expression pattern changes rapidly with cytokini

173 d mammalian homeobox gene whose temporal and spatial expression pattern during limb development sugge

174 rentiation and demonstrates the temporal and spatial expression pattern during skeletal development.

175 xperimentally observed 'all-or-nothing' LAX3 spatial expression pattern in cortical cells containing

176 d both genes share a restricted temporal and spatial expression pattern in normal renal precursors.

177 The temporal and spatial expression pattern of dpr10 correlates with musc

178 The spatial expression pattern of HMP2 was determined by bot

179 In the present study,we analyze the spatial expression pattern of human duplicate gene pairs

180 We show that the spatial expression pattern of MIR395 transcripts in the

181 The spatial expression pattern of MMP-2, -3, -9 and MT1-MMP

182 MMP functions in the retina, we studied the spatial expression pattern of MMP-2, -3, -9 and MT1-MMP

183 ded that study by examining the temporal and spatial expression pattern of neuroD in the embryonic an

184 The temporal-spatial expression pattern of Nmyc, but not other Myc fa

185 rejection are dependent on the temporal and spatial expression pattern of NOS2 during both forms of

186 Here, we describe the spatial expression pattern of Notch pathway components i

187 tablishing the method as a tool to determine spatial expression pattern of sequences obtained from ge

188 gene activation, but it also determines the spatial expression pattern of target genes within the de

189 resent study was to examine the temporal and spatial expression pattern of the chick CNTFRalpha prote

190 The temporal and spatial expression pattern of the Drosophila Cyp306a1 ho

191 The temporal and spatial expression pattern of the human transgene mirror

192 egulatory mechanism that drives this precise spatial expression pattern of the nocturnin gene.

193 To study the spatial expression pattern of these microRNAs and the ef

194 The temporal and spatial expression pattern of this protein, taken togeth

195 The temporal and spatial expression pattern of Xanx-4 suggests it may hav

196 The ovine CFTR gene has a temporal and spatial expression pattern that is very similar to that

197 examine the relationship of the temporal and spatial expression pattern to the clinical manifestation

198 Spatial expression pattern was determined by whole mount

199 f the flower, in an overlapping temporal and spatial expression pattern with the C-function and SEP-l

200 uplicate genes that show rapid divergence in spatial expression pattern with the functions of those d

201 ng an array of mouse strains to modulate the spatial expression pattern, temporal profile, and magnit

202 d that each exhibits a distinct temporal and spatial expression pattern.

203 ebrafish, the two genes exhibited a distinct spatial expression pattern.

204 g a differential effect on Shh, defining its spatial expression pattern.

205 the gene showed an interesting temporal and spatial expression pattern: it had no or a low expressio

206 Their torus-like spatial expression patterns and gene regulatory analysis

207 rium between two Notch ligands with distinct spatial expression patterns and opposing functional role

208 h anatomical ontology terms by analyzing the spatial expression patterns and their textual descriptio

209 functions in vivo because their temporal and spatial expression patterns are different.

210 uch lower than those of YY1, but the overall spatial expression patterns are similar to those of Mbtp

211 dual PPK genes showing distinct temporal and spatial expression patterns as development progressed.

212 retations of similarities and differences in spatial expression patterns challenging, particularly wh

213 r mammalian orthologs, and have temporal and spatial expression patterns consistent with previous in

214 -associated and confirmed their temporal and spatial expression patterns during the hair-growth cycle

215 regulatory regions that confer temporal and spatial expression patterns for the uncharacterized gene

216 Images containing spatial expression patterns illuminate the roles of diff

217 expression patterns during embryogenesis and spatial expression patterns in adult animals.

218 dehydrogenase (MDH) isozymes have different spatial expression patterns in certain fishes: one is ex

219 essed by the adult human lens, defines their spatial expression patterns in lens epithelia and fibers

220 Identifying genes that display spatial expression patterns in spatially resolved transc

221 n a data set of over 30 enhancers regulating spatial expression patterns in the blastoderm-stage Dros

222 , it is of central importance to capture the spatial expression patterns in the brain.

223 We investigated the temporal and spatial expression patterns in the CNS of nine MMP genes

224 strate overlapping but distinct temporal and spatial expression patterns in the Drosophila embryo, an

225 anscriptional activity, as well as different spatial expression patterns in the intestinal epithelium

226 Currently, genome-wide atlas of spatial expression patterns in the mouse brain has been

227 and sections we delineated the temporal and spatial expression patterns in the neural tube, trunk sk

228 Analyses of temporal and spatial expression patterns indicated that the duplicate

229 r temporal phases, which together with their spatial expression patterns leads to a model of the regu

230 We found that the combined spatial expression patterns of 170 neuron-specific trans

231 applied in situ hybridization to analyze the spatial expression patterns of 49 genes encoding well-kn

232 idge relating transcriptome to activity: the spatial expression patterns of a few genes predict regio

233 The temporal and spatial expression patterns of AtACX3 during development

234 strate a direct role for PNY in defining the spatial expression patterns of boundary genes and the si

235 The spatial expression patterns of cFN and alpha9beta1 are d

236 eceptors on T cell subsets, the temporal and spatial expression patterns of chemokines in vivo and th

237 ctions between GID1s and DELLAs, we analyzed spatial expression patterns of four DELLA genes that hav

238 e used as a predictive tool in analyzing the spatial expression patterns of genes and it has led to t

239 a statistical method, SPARK, for identifying spatial expression patterns of genes in data generated f

240 se (GUS) reporter gene, and the temporal and spatial expression patterns of GUS activity were examine

241 scription factor 4 (KLF4), we determined the spatial expression patterns of KLF4 and K19 in relations

242 The ability to regulate the temporal and spatial expression patterns of lipoproteins throughout i

243 We now show temporal and spatial expression patterns of lmx1b and its potential b

244 In this study, we analyzed the temporal and spatial expression patterns of mibp1 mRNA in developing

245 potential targets of miRNAs, elucidating the spatial expression patterns of miRNAs is necessary to id

246 observations, together with the temporal and spatial expression patterns of Mixer and Milk, lead us t

247 tive stress, we have examined the levels and spatial expression patterns of MsrA in the human lens an

248 The identities and spatial expression patterns of MsrB1, -B2, and -B3 trans

249 The transport properties and spatial expression patterns of MtPT4 are consistent with

250 situ hybridization, we examined temporal and spatial expression patterns of neuroligin (NLGN) and neu

251 Temporal and spatial expression patterns of PEDF were analyzed by in

252 The different temporal but similar spatial expression patterns of phototransduction protein

253 rogression prostate cancer, the temporal and spatial expression patterns of platelet endothelial cell

254 The temporal and spatial expression patterns of Sim2 in these skeletal el

255 Spatial expression patterns of skeletal muscle-specific

256 The spatial expression patterns of substance P and proenkeph

257 The spatial expression patterns of the cyclophilin B isoform

258 To investigate the temporal and spatial expression patterns of the gene (lat ) encoding

259 promoters of the homologs drove temporal and spatial expression patterns of the GUS reporter gene in

260 The spatial expression patterns of the Hox genes illuminate

261 MtPT1, we have analysed the accumulation and spatial expression patterns of the MtPT1 transporter.

262 zation experiments revealed the temporal and spatial expression patterns of these genes during early

263 The temporal and spatial expression patterns of three 1-aminocyclopropane

264 We analyzed temporal and spatial expression patterns of three per-reporter fusion

265 Analysis of the spatial expression patterns of two mycorrhiza-induced ge

266 Spatial expression patterns of vitronectin receptor subu

267 scovery of miRNAs with specific temporal and spatial expression patterns revealed a hidden layer of p

268 b gene family exhibit different temporal and spatial expression patterns suggesting a distinctive fun

269 Decorin and biglycan exhibited overlapping spatial expression patterns throughout the corneal strom

270 y generating surrogate datasets with similar spatial expression patterns using a Monte Carlo swap sam

271 te biomineralisation genes revealed discrete spatial expression patterns within the mantle tissue, hi

272 and GhCesA2-D(T) shared common temporal and spatial expression patterns, and they were highly and pr

273 Consistent with their spatial expression patterns, membrane location and desig

274 oots with partially overlapping but distinct spatial expression patterns, responses to Pi and express

275 proteinase inhibitor proteins, with distinct spatial expression patterns, were isolated and character

276 be developed to properly normalize and model spatial expression patterns.

277 for the tight control of their temporal and spatial expression patterns.

278 ast majority of these genes have appropriate spatial expression patterns.

279 structural properties and developmental and spatial expression patterns.

280 inducible gene expression and directs unique spatial expression patterns.

281 e they show precisely regulated temporal and spatial expression patterns.

282 sed destabilized reporter genes to determine spatial expression patterns.

283 are due to their differences in temporal and spatial expression patterns.

284 ning NMDA receptors are present that vary in spatial expression, perhaps indicating distinct physiolo

285 GGT2 exhibited narrow temporal and spatial expression primarily in immature trichomes, deve

286 We compare the spatial expression profile determined in this study with

287 Spatial expression profiles of astrocyte- and oligodendr

288 ory molecules in terms of their temporal and spatial expression profiles, their effects of T and B ce

289 ip telocytes as regulators of the epithelial spatial expression programs along the villus axis.

290 Besides displaying organ, developmental, and spatial expression properties that are strikingly up-reg

291 his correlation between genomic location and spatial expression provides unique insights about the re

292 Spatial expression studies found similar levels of expre

293 XKaiso's spatial expression was defined via in situ hybridization

294 ry elements that control DSP-PP temporal and spatial expression, we constructed a -5 kb upstream regi

295 highly expressed chemokine, its temporal and spatial expression were determined in the present study.

296 Quantitative and spatial expression were examined with Western blot analy

297 Trx1 and Trx2 quantitative and spatial expression were examined with Western blot and i

298 RNA and protein levels and we compared their spatial expression with the onset of calcification.

299 However, each gene has a distinct spatial expression within the epididymis and different r

300 enetic regulatory mechanisms controlling Dlx spatial expression within the visceral arches have not y