ライフサイエンスコーパス: control region

1 whale shark mitogenome had a slightly longer control region.

2 g genes, two rRNA genes, 22 tRNA genes and a control region.

3 cross the beta-globin gene cluster and locus control region.

4 hin each lesion and a corresponding adjacent control region.

5 ectly associating with the beta-globin locus control region.

6 the control of the B-specific nondisjunction control region.

7 -regulatory elements, namely the Hoxd Global Control Region.

8 hylation at the germ-line-derived imprinting control region.

9 of the CTCF-binding sites in the imprinting control region.

10 pt that is embedded within the major latency control region.

11 ctional CTCF binding sites in the imprinting control region.

12 enes, two ribosomal RNA (rRNA) genes and one control region.

13 molecular analyses of the beta-globin locus control region.

14 pulation size coupled with saturation at the control region.

15 volution differ between cytochrome b and the control region.

16 tion, and in the primary visual cortex, as a control region.

17 which forms a displacement (D-) loop in the control region.

18 on through its modification of the Th2 locus control region.

19 5 bp, and contains the expected 37 genes and control region.

20 the replication origin (Rep-P) and the locus control region.

21 ave been confirmed to function as imprinting control regions.

22 synchrony were not found in several proximal control regions.

23 ell as postcentral gyrus and global cerebrum control regions.

24 d promoters that extend beyond known imprint control regions.

25 s II), and microvessels (CD31) in plaque and control regions.

26 or cingulate cortex, two important cognitive control regions.

27 analysis in early visual areas as well as in control regions.

28 e ultrasound treatment compared to untreated control regions.

29 A methylation of the H19 and Gtl2 imprinting control regions.

30 ications from target loci, without affecting control regions.

31 e the boundaries of several known imprinting control regions.

32 on of EBNA 3C association with cellular-gene control regions.

33 , promoters, insulators, silencers and locus control regions.

34 methylation of their corresponding imprinted control regions.

35 mmon feature of vertebrate mitochondrial DNA control regions.

36 lculate metabolic rate in frontotemporal and control regions.

37 mtDNA genome, incorporating both coding and control regions.

38 a finch telencephalon, overlapping with song control regions.

39 ted by shared DNA elements called Imprinting Control Regions.

40 g promoters, enhancers, insulators and locus-control regions.

41 iRNA expression patterns and transcriptional control regions.

42 eption of certain loci, including imprinting control regions.

43 duced recombination rate compared to matched control regions.

44 nct methylation patterns at their imprinting control regions.

45 e regulation by determining accessibility of control regions.

46 2 cis-expression quantitative trait loci and control regions.

47 ion (TMS) of the RLPFC versus two prefrontal control regions.

48 tional systems and later developing top-down control regions.

49 side of these regions, in the noncoding mRNA control regions.

50 The intergenic control region 1 (IGCR1) in the V(H)-to-D intergenic reg

51 ination regulatory region, termed intergenic control region 1 (IGCR1), which lies between the V(H) an

52 IGCR1 (intergenic control region 1), the DQ52 promoter/enhancer, and the i

53 herian mammals so far examined, with a locus control region 1.54 kb upstream.

54 the DNA methylation status of the imprinting control region 2 (ICR2), which is commonly hypomethylate

55 We used 344 mitochondrial control region (717 bp) sequences from the finless porpo

56 ree unlinked genetic loci: the mitochondrial control region, a gene associated with yellow skin color

57 he HS2 sequence within the beta-globin locus control region, a major regulator of globin expression.

58 together, the Ikzf1 enhancers provided locus control region activity, allowing reporter expression in

59 eus of the arcopallium (RA), a cortical song control region analogous to human layer 5 primary motor

60 We analysed 530 bp of mitochondrial control region and 12 microsatellite loci from 94 indivi

61 We examined mitochondrial DNA in the control region and ATP6 in 28 mole rats from basalt and

62 KLF2 binding to HS2 of the beta-globin locus control region and enhanced -globin mRNA production by t

63 ucleosome occupancy in the beta-globin locus control region and gamma-globin gene.

64 tial proximity between the beta-globin locus control region and gene and for transcription activation

65 hylogeographic dataset for the mitochondrial control region and generated additional data from nine p

66 cidate a long-sought Igh V(D)J recombination control region and indicate a new role for the generally

67 ome identify positions -69 to -35 as the key control region and indicate that an activator protein mo

68 rs is the discovery of the beta-globin locus control region and several associated transcription fact

69 utilized CRISPR/Cas9 to target the noncoding control region and the late gene open reading frame of t

70 e the rate of nucleotide substitution in the control region and to better understand the interplay of

71 s of gene rearrangement, duplications of the control region and tRNA mutations.

72 nced a ~ 300 bp portion of the mitochondrial control region and ~ 5 Mbp of the nuclear genome.

73 malian-conserved genomic regions relative to control regions and interpreted this as due to lineage-s

74 e who were better able to recruit prefrontal control regions and modulate amygdala reactivity during

75 on the cause and effect relationship between control regions and perceptual processing.

76 low levels of diversity in the mitochondrial control region, and few clear phylogeographic patterns w

77 ein complexes that bind at beta-globin locus control region, and purified and characterized the funct

78 2 kb of these ERVs' integration sites and in control regions, and analyzed them using Functional Data

79 Rearrangements in the archetype noncoding control region are necessary for neurovirulence.

80 upport prior findings showing that cognitive control regions are at times more active during mind wan

81 Duplicated control regions are found in the Aeolothripidae and the

82 5F transcript variant 2, and PEG3 imprinting control regions are not methylated in the macaque germli

83 In sum, classic homeostatic control regions are sufficient but not individually nece

84 unoreactivity for TH was higher in the vocal control region Area X compared to the surrounding MSt (m

85 nd following tRNS to either IFC or an active control region (area V5/MT).

86 bin genes, and also to the beta-globin locus control region, as demonstrated by ChIP assays with mous

87 ariant at nucleotide pair 16184-16193 of the control region, as well as a resistant group consisting

88 fMRI study, we aimed to identify generalized control regions associated with sustained attention usin

89 nomic regions (target loci) in comparison to control regions (background loci) using standard enrichm

90 , but it did not increase KLF2 mRNA or locus control region binding above levels seen with normal dif

91 o in ADC-rCBV ROIs was compared with that in control regions by using analysis of variance.

92 abnormalities in distinct respiratory neural control regions can be initiated by prolonged hypoxia ex

93 found that mtDNA variants in the coding and control regions can have combined effects influencing di

94 n complex (chromosome 1q21.3), the Th2 locus control region (chromosome 5q31.1), and the major histoc

95 at this domain is regulated by an imprinting control region consisting of two distinct elements, the

96 introns and only one sizeable noncoding, or control, region containing key cis-elements for its repl

97 rns also have been observed in mitochondrial control region data in Finland, which contrasts with the

98 but the chronological resolution of existing control-region data is poor, and an East Indonesian orig

99 Activation in certain executive control regions decreased with age until adolescence, an

100 arboring deletions of promoters or the locus control region demonstrates that these sequences are not

101 influencing recruitment of frontal cortical control regions depending on specific task demands.

102 of H19 (H19-DMR), serving as the imprinting control region, determines the reciprocal expression of

103 racts known to connect cortical sensorimotor control regions dictates the functional influence of sle

104 We sequenced mitochondrial control region DNA from 122 modern and 22 ancient chicke

105 To test this premise, we amplified a 449 bp control region DNA sequence from the mitochondrial genom

106 types from 402 samples and 565 mitochondrial control region DNA sequences (including mitochondrial se

107 Microsatellite and mitochondrial (control region) DNA markers provided mixed evidence for

108 the inhibition of TPJ by dorsal attentional control regions during top-down serial visual search.

109 exhibited increased activation in executive control regions (e.g., dorsolateral prefrontal and supra

110 eg stimulation from the periaqueductal gray, control regions (e.g., white matter) or the control time

111 -control-related neural activity in classic 'control' regions (eg, dorsolateral prefrontal cortex and

112 ith the beta-globin gene, but not with locus control region element HS2, and led to reduced transcrip

113 onal relevant polymorphism in the TH 2 locus control region, equivalent to RHS7 in mice, affects DNA

114 romatin becomes equalized and how imprinting control regions escape from this reprogramming is largel

115 SNPs tagging a locus control region for IL4 and IL13 were associated with an

116 In mice, this region harbors a locus control region for nearby TH 2 cytokines, which is chara

117 to several sites within the immediate early control region for ORF50 and to more distal 5' sites tha

118 Compared with paired control regions, GA precursor regions at 2, 3, and 4 yea

119 Moreover, we show that the global control region (GCR) long-range enhancer spatially coloc

120 gion 2 (DMR2) of IGF2 and the H19 imprinting control region (H19 ICR) compared with term infants over

121 r general understanding of mitochondrial DNA control region heteroplasmy and provide additional empir

122 14.5 (eight dams and 58 fetuses; imprinting control region ICR strain) and 17.5 (21 dams and 158 fet

123 cted at CTCF sites in the IGF2/H19 imprinted control region (ICR) as well as other genomic CTCF sites

124 ized DNA demethylation at the H19 imprinting control region (ICR) induced by 5-AzaCdR, reduced IGF2,

125 d hypomethylation at the IGF2-H19 imprinting control region (ICR) result in reciprocal changes in IGF

126 e-specific DNA methylation at the imprinting control region (ICR), but the underlying mechanism remai

127 regulator region encompassing the imprinting control region (ICR), concomitant with increased DNA met

128 mouse line lacking this potential imprinting control region (ICR).

129 ed by a differentially methylated imprinting control region (ICR).

130 cluding the paternally methylated imprinting control region (ICR).

131 ive methylation of CpG islands at imprinting control regions (ICR) determines the monoparental expres

132 methylated cytosines that act at imprinting control regions (ICRs) and meiotic genes (stage II).

133 CpG islands within these regions, imprinting control regions (ICRs) and secondary differentially meth

134 sis successfully identifies known imprinting control regions (ICRs) as well as some novel differentia

135 cluding significant demethylation of imprint control regions (ICRs) associated with increased mRNA ex

136 imprinted genes are regulated by imprinting control regions (ICRs) characterized by DNA methylation

137 the origins of imprinting, binds imprinting control regions (ICRs) in mice and humans.

138 Differential DNA methylation at imprinted control regions (ICRs) is established in gametes and, al

139 Additionally, all the known imprinting control regions (ICRs) were classified into germ-line or

140 ably, H4R3me2s is mono-allelic at imprinting control regions (ICRs), at which it marks the same paren

141 These genes are regulated by imprinting control regions (ICRs), cis-regulatory elements that exh

142 maintenance of DNA methylation at imprinting control regions (ICRs), revealing an allele-specific bin

143 genomic imprinting in mammals are imprinting control regions (ICRs), which are the discrete genetic e

144 llele-specific DNA methylation at imprinting control regions (ICRs).

145 by differentially DNA methylated imprinting control regions (ICRs).

146 ific regulatory elements known as imprinting control regions (ICRs).

147 ave eluded consensus, with various executive control regions implicated in different studies.

148 ial haplogroup and the mtDNA sequence of the control region in 859 subjects with diabetes and 1,151 n

149 may be the result of hypervariability in the control region in gray and humpback whales but, in minke

150 richment at the H-DNA region compared with a control region in human cells.

151 -, epsilon- and gamma-globin genes and locus control region in KLF1(-/-) embryos, correlating with re

152 ilar to Brg1, to the mouse beta-globin locus control region in MEL cells.

153 he area of new-onset GA and one size-matched control region in the same eye were segmented separately

154 connectivity between language and cognitive control regions in bilinguals who learned their two lang

155 NA methylation memory at multiple imprinting control regions in early mouse embryos and embryonic ste

156 ng relevant top-down pathways from cognitive control regions in medial prefrontal cortex (mPFC).

157 increased activation of prefrontal cognitive-control regions in older adults, compared with younger a

158 acquisition of DNA methylation at imprinted control regions in oocytes.

159 i in their brains which corresponded to song control regions in other songbirds.

160 A greater engagement of inhibitory control regions in response to food cues as well as a gr

161 Greater hyperactivation in executive control regions in the T1D group was correlated with imp

162 the stability of G-quadruplexes in the mtDNA control region, influencing the balance between transcri

163 histone methyltransferase to the imprinting control regions, inhibiting production of an activating

164 berrant acquisition of H3K4me3 at imprinting control regions instead of DNA methylation.

165 nstrate that a cell type-specific regulatory control region is a credible target for creating loss-of

166 The majority of the control region is made up of a large tandem-repeat regio

167 The PWS imprinting control region is the promoter for a one megabase patern

168 We conclude that grammar of gene control regions is pervasively used in the patterning of

169 ge interaction between the beta-globin locus control region (LCR) and active globin genes, and althou

170 In erythroid cells, the locus control region (LCR) and beta-globin promoter form a chr

171 ge interaction between the beta-globin locus control region (LCR) and gene in adult mouse erythroid c

172 ctor Nipped-B-like (Nipbl) bind to the locus control region (LCR) at the CTCF insulator and distal en

173 E6, E7, E1, E2 and E4) and a non-coding long control region (LCR) between L1 and E6.

174 gene (hGH-N) is regulated by a distal locus control region (LCR) composed of five deoxyribonuclease

175 In erythroid cells, the locus control region (LCR) contacts beta-type globin genes in

176 ime increased the binding of Pol II at locus control region (LCR) element HS2, suggesting that Pol II

177 nd their expression is controlled by a locus control region (LCR) embedded within this locus.

178 Locus control region (LCR) functions define cellular identity

179 ndem Maf recognition element (MARE) in locus control region (LCR) hypersensitive site 2 (HS2) reveals

180 uous with the previously described TH2 locus control region (LCR) in the mouse.

181 The beta-globin locus control region (LCR) is necessary for high-level beta-gl

182 le donors showed that the L/M enhancer locus control region (LCR) loops with either the L or M promot

183 e sites (HSs) of the human beta-globin locus control region (LCR) may function as part of an LCR holo

184 The long control region (LCR) of human papillomavirus (HPV) regul

185 To study the influence of a locus control region (LCR) on the expression of a highly chara

186 pillomavirus E2 protein can silence the long control region (LCR) promoter that controls viral E6 and

187 8;E2C-dependent repression of the viral long control region (LCR) promoter.

188 equired for looping of the beta-globin locus control region (LCR) to the active beta-globin promoter.

189 hromatin structure that juxtaposes the locus control region (LCR) with downstream globin genes.

190 r of the beta-globin locus, called the locus control region (LCR), dynamically interacts with the dev

191 BCL11A binds the upstream locus control region (LCR), epsilon-globin, and the intergenic

192 A conserved regulatory element, the locus control region (LCR), was revealed by analyzing DNase I

193 obin genes is regulated by the distant locus control region (LCR), which is brought into direct gene

194 e (hGH) locus is regulated by a distal locus control region (LCR), which is required in cis for the p

195 x, and MeCP1, which are members of the locus control region (LCR)-associated remodeling complex (LARC

196 ough embryogenesis by a multicomponent locus control region (LCR).

197 ne under the control of a reduced-size locus-control region (LCR).

198 s, including promoter, enhancer, and a locus control region (LCR).

199 nta by distinct components of a remote locus control region (LCR).

200 diator and cohesin to establishment of locus control region (LCR)/beta-globin proximity.

201 fetal globin genes from the enhancer (locus control region [LCR]).

202 Locus control regions (LCRs) are cis-acting gene regulatory el

203 Locus control regions (LCRs) comprise sets of DNA elements cap

204 nd V) and placental (HSIII, IV, and V) locus control regions (LCRs).

205 ex and right fusiform gyrus and sources in a control region (left V1) yielded successful classificati

206 as administered over the left vlPFC versus a control region, left somatosensory cortex, concurrently

207 l capacities and suggest that some executive control regions may buttress immature networks as error

208 ochondrial genome, such as the mitochondrial control region (MCR), are under-represented in the nucle

209 24 h nonfasting glucose levels in imprinting control region mice on a high fat diet with diet-induced

210 cies variation between the mitochondrial DNA control region (mtDNA CR) and cytochrome c oxidase I (CO

211 tion on the mechanisms contributing to mtDNA control region mutation and evolution.

212 t commonly observed correlated with reported control region mutational hotspots.

213 from nine populations for the mitochondrial control region (n = 302) and for eleven nuclear microsat

214 and HIVSGD-2, both containing the noncoding control region (NCCR) architecture OPQPQQS, were assesse

215 cultures is regulated by the viral noncoding control region (NCCR) comprising the core origin and fla

216 irus generally harbors reorganized noncoding control region (NCCR) DNA interspersed on the viral geno

217 leukoencephalopathy (PML)-derived noncoding control region (NCCR) sequences permitted greater early

218 enced multiple isolates of the JCV noncoding control region (NCCR), VP1 capsid coding region, and the

219 early region, a late region, and a noncoding control region (NCCR).

220 murine locus, neither the beta-globin locus control region nor the gene promoters were required for

221 from the amygdala (N=19) or from a parietal control region not involved in emotional processing (N=1

222 is relevant for eye movements, but not in a control region (occipital cortex).

223 the signal that is transmitted to the kinase control region of Aer.

224 germinal center B cells, centered on a locus control region of Bcl6.

225 The methylation pattern of the imprinting control region of chromosome 11p15.5 and ABCC8 promoter

226 c process of reorganization of the noncoding control region of JC polyomavirus in vivo, mainly in CSF

227 ation within the promoter and the imprinting control region of MEG3 gene in meningiomas.

228 The hypothalamus is the central homeostatic control region of the brain and, therefore, highly influ

229 dorsolateral prefrontal cortex, an executive-control region of the brain, and the salience network co

230 hibited the transcription driven by the long control region of the HPV genome.

231 The RNA of these R-loops maps to the control region of the mitochondrial DNA and is complemen

232 ose-dependent association of the GR with the control region of the mitochondrial genome.

233 m repeats (STRs), Y-chromosomal STRs and the control region of the mitochondrial genome.

234 In the current study, the imprinting control region of the mouse Peg3 domain was deleted to t

235 an extensive analysis of the cis-regulatory control regions of a battery of pan-neuronal C. elegans

236 hese findings link CTCF and cohesin with the control regions of a subset of imprinted genes, supporti

237 istones surrounding SRF-binding sites in the control regions of cardiac and smooth muscle genes throu

238 Both the coding and control regions of mitochondrial DNA (mtDNA) play roles

239 The cis-regulatory control regions of other ASE-expressed genes also contai

240 ver, displayed hypomethylation of imprinting control regions of select imprinted genes and a global r

241 Resequencing of the coding and control regions of TG and SLA did not disclose putative

242 According to the results, the Imprinting Control Regions of the PEG3, MEST and GNAS domains are i

243 tion experiments show that Mit1 binds to the control regions of the previously known regulators of ps

244 und to innervate the central brain and motor control regions of the thoracic ganglion.

245 achining (ablation) is utilized to introduce controlled regions of sp(2) carbon into a high quality p

246 The ICR (Imprinting Control Region) of the Peg3 (Paternally Expressed Gene 3

247 s the impact of virtually resecting putative control regions on synchronization in a validated model

248 tary changes on CFP, versus two of 29 (6.9%) control regions (P < 0.001).

249 ctivity on SDOCT, versus seven of 39 (17.9%) control regions (P < 0.001).

250 The pluripotency control regions (PluCRs) are defined as genomic regions

251 An A1d1a control region polymorphism predicted to influence trans

252 ntrol over adolescence, while motor response control regions provide early-maturing foundational capa

253 Furthermore, the arcopallial song control regions RA (nucleus robustus arcopallialis) and

254 eposition, brain activation in the cognitive control region reaches a maximum with lower control dema

255 mtDNA have been detected when analyzing the control region; recurrent mutations, however, tend to bl

256 ensitivity site (RHS)6 and RHS7 of the locus control region relative to AP-1 sites surrounding type-2

257 Cntnap2 protein is enriched in several song control regions relative to surrounding tissues, particu

258 ptional control, such as enhancers and locus-control regions, represent major sites of extragenic non

259 tails mediated by a capacity-limited frontal control region, resulting in impaired recollection.

260 rowth curves of activation in motor response control regions revealed no changes with age, although i

261 traploid genotypes which harbor the apomixis control region(s).

262 gulator Sox2 and its essential enhancer Sox2 Control Region (SCR) in living embryonic stem cells (ESC

263 made the first identification of a stability control region (SCR), residues 97-118, in the Tm sequenc

264 tor systems, top-down modulation helps motor-control regions "select" movement patterns.

265 It can alter a critical noncoding control region sequence and potentially facilitate use o

266 In the control region, sequence analysis found one repetitive u

267 mtDNAs were assayed by PCR-RFLP analysis and control region sequencing, and the nonrecombining portio

268 lemented in certain cases with mitochondrial control region sequencing.

269 No control region showed an APOE effect.

270 Control regions showed no associations.

271 are often tissue-specific and overlap locus control regions, suggesting that they are important chro

272 er increases in hyperactivation of executive control regions (T1D: r = 0.284, 95% CI 0.08 to 0.46, p

273 m between -123 to -156 kb, termed the T cell control region (TCCR).

274 nding site mutations at the Igf2-H19 imprint control region that abolishes CTCF insulator activity, r

275 latory elements located within the noncoding control region that control early gene expression and mi

276 s on 15q11-q13 is regulated by an imprinting control region that is maternally methylated and silence

277 as performed, with emphasis on the noncoding control region, the major capsid protein gene VP1, and t

278 of active retrotransposons and to imprinting control regions, the two major regulatory sequences cont

279 n adaptive control, whereas stimulation of a control region-the primary motor cortex-had no effect on

280 ic mutational motifs (in both the coding and control regions), these haplotypes could be easily used

281 is and site-directed mutagenesis of the atxA control region to demonstrate that atxA transcription fr

282 The only known pathway from song control regions to dopaminergic neurons involves a proje

283 ltransferases are targeted to the imprinting control regions to initiate and maintain DNA methylation

284 nals in visuotopic coordinates from parietal control regions to sensory regions in humans.

285 op-down influences from frontal and parietal control regions to visual occipital cortex in visuospati

286 urther mutagenesis narrowed this endocytosis-controlling region to four residues conforming to a YXXP

287 d with more open chromatin at the HPV16 long control region, together with greater loading of chromat

288 n of a GC-specific, highly interactive locus control region upstream of Bcl6 abrogated GC formation i

289 bosomal RNA and 22 transfer RNA genes, and a control region varying in sizes.

290 The TBR of a noncalcified control region was also calculated.

291 The TBR of the control region was not significantly different from that

292 r retinotopic activity in these higher level control regions was synchronous with retinotopic activit

293 length heteroplasmy in the mitochondrial DNA control region were compiled and analyzed from over 5,00

294 selected a priori: 15 experimental and five control regions were included.

295 als H3K4me2 enrichment at the Zac1 imprinted control region when transcription is ablated, establishi

296 nal constraints heavily recruited prefrontal control regions, whereas natural, voluntary switching di

297 region is an additional principal imprinting control region, which directs Gnas methylation and there

298 AT/TA](24) and [A/T](19-28), compared with a control region with minimal secondary structure.

299 Th2 cytokine locus in particular in a locus control region within the DNA repair gene RAD50, contain

300 gion around individual ODS and corresponding control region without ODS in the same eye.