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

12 ctional CTCF binding sites in the imprinting control region.

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

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

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

16 pulation size coupled with saturation at the control region.

17 volution differ between cytochrome b and the control region.

18 5 bp, and contains the expected 37 genes and control region.

19 alian c-myc promoter and H19/Igf2 imprinting control region.

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

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

22 or cingulate cortex, two important cognitive control regions.

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

24 iRNA expression patterns and transcriptional control regions.

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

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

27 ications from target loci, without affecting control regions.

28 e the boundaries of several known imprinting control regions.

29 eption of certain loci, including imprinting control regions.

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

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

32 duced recombination rate compared to matched control regions.

33 nct methylation patterns at their imprinting 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 that YtxR interacted with the yopE and yopH control regions.

40 e regulation by determining accessibility of control regions.

41 2 cis-expression quantitative trait loci and control regions.

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

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

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

45 ave been confirmed to function as imprinting control regions.

46 synchrony were not found in several proximal control regions.

47 ted by shared DNA elements called Imprinting Control Regions.

48 ell as postcentral gyrus and global cerebrum control regions.

49 d promoters that extend beyond known imprint 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 ctions occur between the IGF2/H19 imprinting control region-1 (ICR1) and ICR2, a region which regulat

55 phism, rs35136575, in the downstream hepatic control region 2 (HCR-2) was associated with LDL-C in Ca

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

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

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

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

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

66 -specific loop between the beta-globin locus control region and the downstream beta major promoter, d

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

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

69 nts - particularly enhancers, but also locus control regions and insulators - have been defined by sp

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

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

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

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

74 We also present improved rates for the mtDNA control region, and the first comprehensive estimates of

75 h the suite of genes encoding tRNA(Gln), the control region, and tRNA(Ile) located downstream of the

76 2 kb of these ERVs' integration sites and in control regions, and analyzed them using Functional Data

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

78 , in P. opilio, some genes near the putative control region are rearranged, with the suite of genes e

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

80 5F transcript variant 2, and PEG3 imprinting control regions are not methylated in the macaque germli

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

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

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

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

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

86 e identified for the first time, a stability control region between residues 97 and 118.

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

88 nucleotide polymorphisms (SNPs) in the mtDNA control region by direct sequencing.

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

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

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

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

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

94 Using paired cytochrome b and control region data across individuals, we show that the

95 ght the complexity of making inferences from control region data alone and suggest that applying simp

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

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

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

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

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

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

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

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

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

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

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

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

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

109 association of RNA polymerase II with locus control region element HS2 and with the beta-globin gene

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

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

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

113 erved GC-rich motifs in conserved Area II, a control region essential to islet beta cell-enriched exp

114 ble than expected given the diversity in the control region for gray and humpback whales, even after

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

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

120 The 2.4-kb H19 imprinting control region (H19ICR) is required to establish parent-

121 A major latency control region has been identified upstream of the diver

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

123 14.5 (eight dams and 58 fetuses; imprinting control region ICR strain) and 17.5 (21 dams and 158 fet

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

125 methylated maternal allele of the imprinting control region (ICR) in the Igf2/H19 imprinting domain a

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

127 several kilobases upstream of the imprinting control region (ICR) of the domain, from a promoter regi

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

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

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

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

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

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

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

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

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

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

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

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

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

141 cally at discrete elements termed imprinting control regions (ICRs) with their parental origin in gam

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

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

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

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

146 riched in the inactive alleles of Imprinting Control Regions (ICRs).

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

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

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

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

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

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

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

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

160 tly more on nocebo regions compared with the control regions in which no expectancy/conditioning mani

161 imer pairs that amplify targets in the mtDNA control region, including the hypervariable regions typi

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

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

164 s studies have shown that this major latency control region is occupied by the cellular chromatin bou

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

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

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

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

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

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

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

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

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

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

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

176 erythroid cells derived from WT/Delta locus control region (LCR) heterozygous mice reveals no signif

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

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

179 The beta-globin locus control region (LCR) is able to enhance the expression o

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

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

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

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

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

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

186 8;E2C-dependent repression of the viral long control region (LCR) promoter.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

205 erage rate of nucleotide substitution in the control region may be on average 2.6 times higher than p

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

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

208 24 h nonfasting glucose levels in imprinting control region mice on a high fat diet with diet-induced

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

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

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

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

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

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

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

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

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

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

219 t (i) two of them are potential heavy-strand control regions (O(H)) for regulating replication and/or

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

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

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

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

224 that both lesions map to the cis-regulatory control region of cog-1 and affect a phylogenetically co

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

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

227 ic importance of a T414G mutation within the control region of mtDNA, previously shown to accumulate

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

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

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

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

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

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

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

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

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

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

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

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

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

246 how that Tax1BP1 and E2 localize to the long control region on the BPV1 genome.

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

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

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

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

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

256 The rapidly evolving mitochondrial control region remains an important source of informatio

257 etic and geographic patterns of variation of control region repeat sequence and number in a nonparasi

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

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

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

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

265 In this study, we analysed mitochondrial control region sequences of 625 individuals to assess si

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

267 lemented in certain cases with mitochondrial control region sequencing.

268 No control region showed an APOE effect.

269 Control regions showed no associations.

270 AMD retinas exhibited increased mtDNA control region SNPs compared to normal retinas.

271 The control region SNPs T16126C and A73G, commonly found in

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

296 variant H2A.Z colocalize on transcriptional control regions, whether H2A.Z directly affects remodele

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.