ライフサイエンスコーパス: upstream

1 stream and a predicted antiterminator (licT) upstream.

2 ent downstream, additional H2A.Z accumulates upstream.

3 earrangement and impede scanning any further upstream(5).

4 n sites (ESs) where VSG genes are flanked by upstream 70 bp repeats and downstream telomeric repeats.

5 PARP1 coordinates BER and relies on the upstream 8-oxoguanine-DNA glycosylase (OGG1) to recognis

6 the G-protein coupled receptor, GPR119] and upstream (a fatty acid translocase, CD36) signaling targ

7 Upstream activation factor (UAF) is a multifunctional tr

8 or 2 C (MEF2C) transcription factor as a key upstream activator of Myoc whose gain of function signif

9 en made from efforts that characterize their upstream activators, assembly of signaling complexes, an

10 notably amplified by virtual emissions from upstream activities that contribute 33-68% to their tota

11 We find that Rme1 binds upstream and activates the expression of genes that are

12 t information to be further utilized in both upstream and downstream analyses.

13 We find that coupling between upstream and downstream bifurcations can lead to chaos;

14 to longer duration of disconnection between upstream and downstream habitats, a consequence of incre

15 CD2AP and PI3K are both upstream and downstream of actin polymerization.

16 itous discoveries of translated ORFs encoded upstream and downstream of annotated ORFs, from alternat

17 cluding increased sense-strand transcription upstream and downstream of genes, increased antisense tr

18 tranded 3' ends, which require microhomology upstream and downstream of the DSB.

19 cement, at 11 sites along the Colorado River upstream and downstream of the WWTP and analyzed for in

20 is essential during their production in both upstream and downstream processes.

21 progress has been made in understanding the upstream and downstream regulators of canonical PINK1/pa

22 Gene associations were linked to upstream and downstream regulators using connectivity ma

23 ircuit that can be used in future studies of upstream and downstream sensory processing.

24 TCRbeta loci contain 30 Vbeta gene segments upstream and in the same transcriptional orientation as

25 esults demonstrate significant fragmentation upstream and inside the TIMS tunnel that corresponds to

26 mmonly utilized leak detection method in the upstream and midstream sectors of the U.S. natural gas i

27 a bistable mechanism between LFA-1-mediated upstream and VLA-4-mediated downstream phenotypes.

28 lowed by wild salmon captured upstream (wild-upstream) and wild-salmon captured downstream (wild-down

29 The functional pathway, upstream, and network analyses revealed both unique and

30 DNA binding; both half sites can be extended upstream, and these are typically not of equal strength

31 d regional memory while chronicling previous upstream antigen experiences.

32 e outcome of a match/non-match decision from upstream areas.

33 agating, hyperpolarizing signal that dilates upstream arterioles to rapidly increase local blood flow

34 e vessels, functioning at the mercy of their upstream arterioles, into independent contractile units

35 temperate-region effluent-dominated stream (upstream, at, and progressively downstream from effluent

36 We noted that the upstream attenuator hairpin activity is also functionall

37 Whether upstream autonomic signaling pathways responsible for ra

38 ery, wherein receptor-mediated clustering of upstream autophagy factors drives continued autophagosom

39 main, bypassing the requirement of canonical upstream autophagy machinery.

40 ates ~90 degrees and is perpendicular to the upstream base pair planes.

41 hes are developed and assessed in this work: upstream-based permitting (i.e., environmental outcomes

42 th detectable rDNA are active, as defined by upstream binding factor loading.

43 ol I and the architectural chromatin protein Upstream Binding Transcription Factor (UBF) reveals a ra

44 This upstream biochemical circuit is further wired with a dow

45 ons received afferent inputs from a range of upstream brain regions as well as hypothalamic nuclei.

46 n of exonic stem-loop structures immediately upstream (but not downstream) of the introns regulate al

47 s experiments in P. putida, we uncovered an 'upstream' cascade of three consecutive transcription fac

48 a recombination centre-based J(H), RAG scans upstream chromatin via loop extrusion, potentially media

49 uction via the transcriptional regulation of upstream clade-III MAP3Ks, particularly MAP3K14.

50 Source populations for sponges in the upstream closure are likely in adjacent waters of the Ca

51 glia-specific mechanism of RICD involving an upstream complement cascade component, C1q.

52 n mice-to determine whether a glia-specific, upstream complement cascade contributes to RICD.

53 ESCRT-I is the most upstream complex and bridges the system to HIV-1 Gag in

54 ts support a model in which integrins are an upstream component of the mechanosensory cellular appara

55 on of RhoA and the coordination of different upstream components in its regulation have not been well

56 In the absence of these upstream components, NPHP3 is redistributed within cilia

57 .e., environmental outcomes as a function of upstream conditions) and means-based permitting (i.e., p

58 tion is allowed) regardless of the uncertain upstream conditions.

59 avl4 isoform-specific translation depends on upstream control by another RBP, Celf1.

60 We posit that the extent of upstream damage to mammalian plasma membranes, calibrate

61 Upon deflection of distal upstream DNA over the RNA polymerase zinc-binding domain

62 ase, trapping and locally unwinding proximal upstream DNA.

63 Although the main upstream effectors that regulate its activity have been

64 ts of GHGs, SO(2), and NO(x) from direct and upstream effects.

65 nicate a negative feedback signal-correction upstream electrically.

66 luidic channel and is easily integrated with upstream electronic, hydrodynamic, or other focusing uni

67 For Pol I, UAF binds to a specific upstream element in the ribosomal DNA (rDNA) promoter an

68 al emissions (volatile chemical products and upstream emissions) are emerging as important sources of

69 ol biosynthesis, only inhibition of the most upstream enzyme, EBP, led to cancer cell death via deple

70 rs or calculations before surgery (so-called upstream errors) were the second most common cause of su

71 However, upstream errors, originating in the clinic or office bef

72 ne deformation and facilitate ILV formation: Upstream ESCRT-driven budding does not require ATP consu

73 ells with a mathematical model, we show that upstream ESCRT-induced alteration of the Gaussian bendin

74 ished function in ILV formation, the role of upstream ESCRTs (0 to II) in membrane shape remodeling i

75 Multiple upstream events activate the pathway, but how each contr

76 The upstream exonic loops of the test substrate promoted rec

77 metal depletion and human toxicity caused by upstream extraction and manufacturing linked to technolo

78 by raising the intravascular pressure in the upstream feeding arteriole and promoting its rupture at

79 we show that RNA decay mechanisms involving upstream frameshift 1 (UPF1), including nonsense-mediate

80 Diminished river loads measured upstream from the coast, however, should not be assumed

81 h pharmaceuticals only sporadically detected upstream from the effluent.

82 Consistently, we find deoxyadenosine upstream from the most abundant genomic rCMPs and rGMPs.

83 mbrane integration of a transmembrane domain upstream from the ribosomal slip site generates a force

84 ibrated, pressure-driven changes in diameter upstream from the valve.

85 lls, with initiation of replication from the upstream genome copy.

86 A proposed model is that upstream, highly interconnected regulatory ASD gene muta

87 arcoma, driving growth and survival when the upstream Hippo tumor suppressor pathway is silenced, but

88 dbrain regions and is innervated by discrete upstream hypothalamic sites.

89 y professionals will need to be more engaged upstream in the technology design process and provide le

90 The upstream inducers of Ctgf, such as Yap, etc, are well-kn

91 The L2 might function as an upstream integration center enabling faster movement dec

92 virus infection results in reduced levels of upstream intermediaries (called IKKs) that are needed fo

93 MDV U(S)3 thus acts as an upstream kinase of the CREB signaling pathway to regulat

94 d to NF-kappaB are in fact mediated by these upstream kinases by novel mechanisms.

95 genes pho1, pho84 and tgp1 are repressed by upstream lncRNAs and are sensitive to changes in lncRNA

96 in phosphate-rich medium by transcription of upstream lncRNAs that interferes with activation of the

97 t KO mice accumulated high concentrations of upstream lysine metabolites including Delta1-piperideine

98 Ks) MPK3 and MPK6 by wounding depends on the upstream MAPK kinases MKK4 and MKK5 but is independent o

99 at EGC tuning was sparser, not broader, than upstream MCs.

100 But the upstream mechanism by which it modulates holotransferrin

101 After considering a variety of upstream medical or behavioral risk factors, the group i

102 or the first time how rapid (100-450 m/year) upstream migration of 5-to-30 m high knickpoints can con

103 The Upstream module outputs were fitted to kinetic data on c

104 Likewise, expression of upstream monolignol biosynthetic genes was increased in

105 lation efficiency checkpoint that integrates upstream mRNA signals to activate anaerobic metabolism.

106 venues for future therapeutic strategies for upstream mutations in cancer, such as in EGFR.

107 iring, tripeptide motifs, positively charged upstream nascent chain residues, and cognate tRNA concen

108 acre outdoor facility that closely resembles upstream natural gas field operations.

109 results suggest a novel role for RAB23 as an upstream negative regulator of both FGFR and canonical H

110 nt states are maintained in the brain, which upstream networks drive state transitions and how state-

111 olling tick salivary glands (SGs) are direct upstream neural signaling pathways arising from the tick

112 Reconstructing 821 upstream neurons reveals input selectivity, supporting t

113 ve consistent expression levels by buffering upstream noise through a separation of transcription fac

114 vum) and wheat (Triticum aestivum), was just upstream of a minimal promoter and that none of these fo

115 our variants (but none of them individually) upstream of a reporter induced a decrease in reporter si

116 pendent manner, arguing that Nodal acts both upstream of and in parallel with PCP during gastrulation

117 s with unimpaired cognition on chromosome 18 upstream of ATP8B1 (index single nucleotide polymorphism

118 We outline the role of ROS in signalling upstream of autophagy initiation, by increased gene expr

119 matic amino acid biosynthesis (SA) pathways (upstream of BNA2), which produce tryptophan (the Bna2p s

120 our results suggest that BRCA1 may function upstream of BRCA2 in the stalled fork repair pathway.

121 bits classical and lectin pathway activation upstream of C3 activation.

122 at SINE1 and SINE2 act downstream of ABA but upstream of Ca(2+) and F-actin.

123 ase, affects responses to axon guidance cues upstream of cdk5, specifically, to Sema3a.

124 tion of a ferroptosis-inducing signal occurs upstream of cell rupture and involves the spreading of a

125 , NEUROD1) emerged as key regulators, acting upstream of core components of the fly's molecular machi

126 therefore suggest that UBP12 and UBP13 work upstream of DA1, DAR1 and DAR2 to restrict their proteas

127 ng factor-bound elements (CBEs) within IGCR1 upstream of Ds impede RAG scanning(3-5); however, their

128 autocrine FGF21 expressed by adipocytes and upstream of endocrine FGF21 expressed by hepatocytes.

129 les map to a set of sensory neurons that act upstream of fat regulation as well as of central sleep-c

130 1 is a regulator of Fe homeostasis that acts upstream of FIT in concert with ILR3 and its closest hom

131 BAP2L is an essential SG nucleator that acts upstream of G3BP1 and 2 and facilitates G3BP1 core forma

132 x TF GAGA1 contributes to stamen development upstream of GhCYC3 Our data demonstrate how interactions

133 rescued the limb defects, thus placing Tbx5 upstream of Hh-signaling in limb defects.

134 dentify the PIP5K family as novel regulators upstream of Hippo signaling, and uncover the importance

135 R interference screen, we identified factors upstream of HRI: OMA1, a mitochondrial stress-activated

136 Construction of obstacles upstream of hydraulic structures is a common method of t

137 emature termination of host gene transcripts upstream of iCGIs is closely correlated with the level o

138 The TGF-beta ligand DAF-7 likely acts upstream of IIS and links feeding to odr-10 only in male

139 In a metaanalysis, we found that a variant upstream of IL12A (rs17753641) is strongly associated wi

140 emonstrate that spindle checkpoint genes act upstream of Isc1, and their deletion phenocopies that of

141 rs45471499, P(combined) = 1.15 x 10(-9)) and upstream of LRP2BP (rs4317244, P(combined) = 4.17 x 10(-

142 ce of Rspo2, suggesting that Rspo2 functions upstream of Mek1.

143 o populations of inhibitory neurons that lie upstream of neurons in the periaqueductal gray (PAG) tha

144 , and report a novel uORF frameshift variant upstream of NF2 in neurofibromatosis.

145 cluster with super enhancer characteristics upstream of Nppb.

146 RNA Shine-Dalgarno (SD) sequences positioned upstream of open reading frames facilitate translation i

147 tself a short AT-tract, resides 5 base pairs upstream of otherwise cryptic -10 elements.

148 s by activating a calcium-mitochondrial axis upstream of PGC-1alpha transcriptional upregulation, rec

149 eam of the RGF1-RGI ligand-receptor pair and upstream of PLT1/PLT2 to modulate the stem cell populati

150 id backbone and sterol biosynthesis pathways upstream of pregnenolone synthesis was coordinately down

151 ignals and their reciprocal interaction were upstream of proximal tubule YAP activation in diabetic k

152 isoform that is activated by MCP-1 and acts upstream of Pyk2 in primary monocytes.

153 188 functions in centriole duplication at or upstream of Sas6 loading.

154 , we provide genetic evidence that NPVF acts upstream of serotonin in the RN to maintain normal sleep

155 rs5855544, upstream of SLC51A, was associated with higher levels of

156 ng pregnancy, with the lead SNP located 15kB upstream of SLC5A2, a target of antidiabetic drugs.

157 r, these findings place Rho-actin and NAD(+) upstream of spheroid formation and may suggest that othe

158 We show that A-rich sequences upstream of start codons promote initiation.

159 ors are closely clustered in genomic regions upstream of target genes, defining cis-regulatory module

160 vealed that LM11A-31 likely acts principally upstream of tau phosphorylation, and has effects prevent

161 ker-specific REs were identified up to 1 Mbp upstream of TBX3 in a region close to MED13L harboring v

162 d common genomic variants in the gene desert upstream of TBX3 in cardiac conduction velocity.

163 of how the ~90 kDa TOP1 protein is processed upstream of TDP1.

164 sed towards selecting start codons that were upstream of the actual start.

165 ry similar sequence, located ~60 nucleotides upstream of the atpI initiation codon, was also found in

166 target genes suggesting that PTPRF functions upstream of the beta-catenin destruction complex.

167 COM1 acts upstream of the boundary gene Liguleless1 and confers me

168 originates in the mitochondria and operates upstream of the CRL2(VHL) ligase complex.

169 cxcr4b through an E-box cluster located just upstream of the cxcr4b transcription start site.

170 sion, specifically interacting with a region upstream of the DDIT4L gene and changing the chromatin a

171 tion through inhibition of DHTKD1, an enzyme upstream of the defective glutaryl-CoA dehydrogenase, ha

172 tes all potential in-frame initiation codons upstream of the DNA binding domain.

173 at presynaptic terminals of the hippocampus upstream of the exocytic machinery.

174 on as a repressor of photoperiodic flowering upstream of the floral activators OsMADS14 and Hd3a, thr

175 ific variability of sequences from the U5 to upstream of the gag gene start codon of diverse HIV-1 st

176 rs present in photosystem I subunits, acting upstream of the high-chlorophyll fluorescence 101 (HCF10

177 e-a receptor, anaplastic lymphoma kinase, is upstream of the HLH regulatory protein, Id2a, and of the

178 We have identified an enhancer ~5 kb upstream of the IFNK gene driving its expression in kera

179 ng interspersed element-1 (LINE-1) insertion upstream of the IMPG2 gene.

180 essential meiotic transcription factor Ndt80 upstream of the integration site, thereby tightly linkin

181 e, HIV-1 infection activates LTR12C elements upstream of the interferon-inducible genes GBP2 and GBP5

182 sufficient for conferring mechanosensitivity upstream of the junctional complex and integrins.

183 control via energy balance sensing, which is upstream of the known genetic networks for branching and

184 cell growth and intracellular stress signals upstream of the mammalian target of rapamycin complex 1

185 the sRNA SgrS through a binding interaction upstream of the manY SD.

186 precocious' lncRNA 3'-processing/termination upstream of the mRNA promoters.

187 This SNP is 29 426-bp upstream of the nearest gene EOMES and in LD with additi

188 point 6955C->T mutation in the Notch2 locus upstream of the PEST domain, and we termed this model No

189 SsrB promotes phoP transcription by binding upstream of the phoP promoter.

190 r that these CREs, located at -44 and -35 kb upstream of the promoter, have strong cell-type-selectiv

191 Upstream of the RIPK3-MLKL necroptotic machinery lies RI

192 is often modulated by enhancer-like elements upstream of the SD, sRNA-mediated enhancer silencing cou

193 ere we report that promoter sequence changes upstream of the site of transcription initiation similar

194 at DRT111 controls splicing of ABI3 and acts upstream of the splicing factor SUPPRESSOR OF ABI3-ABI5.

195 ading and the presence of a subdominant peak upstream of the transcription start site.

196 While most kinases upstream of the yeast histone methylation enzymes remain

197 l inhibitors or genetic knockdown of enzymes upstream of their target PTM sites.

198 ndability within nucleosome-depleted regions upstream of transcription start sites (TSSs).

199 Upstream of USP30, the E3 ligase March5 ubiquitinates mi

200 ental myelination by transiently controlling upstream OPC differentiation but not downstream oligoden

201 In this work, we demonstrate that an upstream open reading frame (uORF) present in the 5' unt

202 NLA1 promoter region was found to contain an upstream open reading frame that is required for Pi-resp

203 Upstream open reading frames (uORFs) are known to contro

204 Upstream open reading frames (uORFs) are tissue-specific

205 We observed thousands of AUG-initiated upstream open reading frames (uORFs) that are a major co

206 The LLT RNA contains multiple upstream open reading frames that can inhibit translatio

207 We find multiple microproteins encoded in upstream open reading frames, which form stable complexe

208 However, very little is known about the upstream or downstream factors that underlie YBX1's regu

209 Second, we find that over-expression of an upstream or downstream gene by a fusion-mediated reposit

210 of this study was to compare downstream and upstream oral P2Y(12) inhibitors administration strategi

211 of new open reading frames (ORFs), including upstream ORFs (uORFs) and internal ORFs (iORFs), generat

212 enhancing translation of specific mRNAs with upstream ORFs (uORFs) situated in their 5'-leader region

213 These ORFs include upstream ORFs that are likely to have a regulatory role,

214 of the electrophysiological function of the upstream primary auditory receptors is warranted to unde

215 sponsible for the emissions generated in the upstream processes (allocation).

216 o LC11 confirmed the model conjectures about upstream processing.

217 occurs when the act of transcription from an upstream promoter suppresses utilization of a co-oriente

218 An upstream promoter, P (oah) , controls the constitutive t

219 xed Lineage Kinase Domain-Like (MLKL) by the upstream protein kinase RIPK3 is a hallmark of pathway a

220 of a specialised repair complex required for upstream proteolysis of TOP1ccs and their subsequent res

221 ons in the expression of direct and specific upstream Rap1 activators and inhibitors.

222 , natural step-pools and cascades in steeper upstream reaches.

223 river mutation in the Galphaq subunit or the upstream receptor.

224 We address the poorly understood upstream regulation of SPL/NZZ in ovules, showing that t

225 Transcriptional networks and upstream regulator analyses showed FOXA3, HNF4alpha, NR1

226 By leveraging causal network and upstream regulator analysis, we identified several candi

227 epigenome map, and a knockout of a predicted upstream regulator disrupts normal regeneration, validat

228 responsive to nutrient stress, including the upstream regulator KLF15, aminoacid catabolizing enzymes

229 f ATC and suggest that ASH1L, along with its upstream regulator miR-200b-3p and its downstream mediat

230 In bioinformatics analysis of upstream regulator networks, the Cxcl8 pathway exhibited

231 , we identify the ABL2 tyrosine kinase as an upstream regulator of HSF1 protein expression and show t

232 res a bidirectional promoter with MAP3K4, an upstream regulator of the MAPK signaling pathway, and re

233 updosing detected minimal changes to pathway/upstream regulator profiles despite 32.5% symptom reduct

234 overed cell-type heterogeneity and predicted upstream regulator proteins that mediate cell survival,

235 y, we used RT-qPCR, RNA sequencing, pathway, upstream regulator, and histological analyses to demonst

236 Suppression of phc1 or its upstream regulator, p53, rescues the loss of both Notch

237 the expression of miRNA-485, as a PGC1alpha upstream regulator.

238 , NF-kappaB, complement, IL-6 signaling) and upstream regulators (INFgamma, IL-1beta, NF-kappaB, MYD8

239 These data were analyzed to predict upstream regulators and affected signaling pathways foll

240 Because shared upstream regulators can ensure correlated gene expressio

241 retaining the pattern of gene expression and upstream regulators characteristic of each species.

242 However, no upstream regulators of ankyrin-G at synapses are known.

243 Here, we identified upstream regulators of GhCYC3, a gene that specifies ray

244 AM-1 expression, and decreased expression of upstream regulators of KLF2 (ERK5 and MEF2).

245 describe upstream regulators of mTORC1 activity which promote pal

246 diovascular side effects because they target upstream regulators of muscle contraction.

247 Although multiple upstream regulators of RhoA have been identified, the te

248 H), pyroglutamylated RFamide, and luqin, all upstream regulators of sexual reproduction.

249 Early transcriptomic changes and predicted upstream regulators that were found in all three procedu

250 tical role in modulating levels of KLF2, its upstream regulators, and its downstream target molecules

251 ences in the expression or function of their upstream regulators, providing insights into the genetic

252 compared with curated data sets to identify upstream regulators.

253 sponses at the level of genes, pathways, and upstream regulators.

254 ) was used to identify enriched pathways and upstream regulators.Measurements and Main Results: Respo

255 pression levels of microRNA-155 and PU.1 (as upstream regulatory axis of FcepsilonRI) and transcripti

256 The transcriptional programs and upstream regulatory events operating in different subpop

257 estor of plants, fungi, and animals, but the upstream regulatory mechanisms and downstream effectors

258 However, upstream regulatory mechanisms for Cdc42 activity in pod

259 arts, demonstrating deep conservation of its upstream regulatory network.

260 ationship between transcriptional states and upstream regulatory programs determining different cell

261 We cloned and analysed selected upstream regulatory regions of IRE1a and IRE1b, which re

262 sing on predicting and preventing modifiable upstream risk factors associated with stroke, but there

263 Together, these data uncover TDRD7's novel upstream role in elevation of stress-responsive chaperon

264 tions that force nonoptimal modifications to upstream sample preparation steps, limit the throughput

265 er, the specific cell death pathways and key upstream sensors activated in the context of Candida and

266 wever, some of these barriers should prevent upstream shifts for a considerable number of species, re

267 ing seems to be especially prevalent amongst upstream short ORFs located in the 5' mRNA leaders, and

268 However, the upstream signaling and the downstream targets of cAMP in

269 ate publicly available databases to identify upstream signaling events and novel therapeutic targets.

270 hepatocellular carcinogenesis (HCC), but the upstream signaling events remain poorly defined.

271 However, the upstream signaling events that instigate CCF formation r

272 en calcium/calmodulin-dependent pathways and upstream signaling of Ras in the ISO-specific context.

273 acity or phenoloxidase activation, or at the upstream signaling pathways that regulate these immune e

274 TFs can operate outside the confine of their upstream signaling.

275 some hotspots were on arterial roads with an upstream signalized intersection and positive road grade

276 r, the precise mechanism of how NF2 mediates upstream signals to regulate the Hippo pathway is not cl

277 MKKs), MKK1/2/3/7/9 are required to transmit upstream signals to two MPKs, MPK3/4, to mediate compati

278 ne-replete conditions by transcription of an upstream SRG1 lncRNA that traverses the SER3 promoter an

279 e of this viral strategy: the acquisition of upstream start codons from host-derived sequences and su

280 stigated S838/T841 dual phosphorylation, its upstream stimulus, and downstream functional output.

281 (Downstream Versus Upstream Strategy for the Administration of P2Y(12) Rece

282 the superiority of the downstream versus the upstream strategy on the combination of efficacy and saf

283 article presents a framework of a potential upstream stroke prevention program with evidence-based i

284 clinicians and health systems with effective upstream stroke prevention strategies that encourage sca

285 ous sclerosis 1 (Tsc1) gene which encodes an upstream suppressor of mTORC1.

286 vide the identification and visualization of upstream TF binding motifs in InDel-containing enhancers

287 promoters indicates that the PIC scans from upstream to downstream to identify TSSs.

288 rganic C contents and storage decreased from upstream to downstream, likely due to primarily changes

289 nsive enhancers (RREs), including an element upstream to inhibin beta A (inhba), a known effector of

290 reases beta-catenin occupancy at a site 4 kb upstream to Lef1.

291 ichiometry of the SHR-SCR complex as well as upstream transcriptional regulation of SHR and SCR.

292 pre-mRNAs on the forward strand and promoter upstream transcripts (PROMPTs) on the reverse strand.

293 We show that most overlapping upstream transcripts use poly(A) sites within the first

294 ribed as a consequence of their proximity to upstream TSSs on the opposite strand.

295 Small ORFs in 5' UTRs (upstream (u)ORFs) often repress translation of the canon

296 roduce mature alphabeta T cells that express upstream Vbeta peptides in surface TCRs and carry Trbv31

297 or silencing and DNMT3B was identified as an upstream viral genome CpG methylation initiator.

298 Upstream, we highlight IRF4 and its complexes with SPI1

299 experience, followed by wild salmon captured upstream (wild-upstream) and wild-salmon captured downst

300 activity, and therefore predict response to upstream Wnt inhibitors in cancers without microsatellit