ライフサイエンスコーパス: clip

1 oncentration using liquid intake by paper (P-CLIP).

2 ication and high-throughput sequencing (HITS-CLIP).

3 after crosslinking and immunoprecipitation (CLIP).

4 d by cross-linking immunoprecipitation (HITS-CLIP).

5 ed crosslinking and immunoprecipitation (PAR-CLIP).

6 idate protein-RNA interactions in vivo (RESA-CLIP).

7 essed by intramembrane-cleaving proteases (I-CLiPs).

8 e term chemically induced liver progenitors (CLiPs).

9 n peptide (CLIP) region, nor does it present CLIP.

10 that these stubs are substrates for three I-CLiPs.

11 omatic sidewall, have the shape of molecular clips.

12 ants to mentally replay short sound or video clips.

13 s but is also processed by three different I-CLiPs.

14 rnover numbers may be a general feature of I-CLiPs.

15 hose determined recently for rhomboid-type I-CLiPs.

16 ther with sutures, staples, adhesive glue or clips.

17 s marked by endoscopically placed radiopaque clips.

18 e like human behaviors depicted in the movie clips.

19 h1's functions in telomeric silencing and H3 clipping.

20 raniotomy for meningioma removal or aneurysm clipping.

21 sing endovascular treatment or microsurgical clipping.

22 establish the supposed superior efficacy of clipping.

23 show that the MT plus-end-associated protein CLIP-170 binds tightly to formins to accelerate actin fi

24 Furthermore, we observed mDia1 dimers and CLIP-170 dimers cotracking growing filament ends for sev

25 Instead, both CLIP-190 and CLIP-170 form F-actin-dependent patches in growth cones,

26 at neither Drosophila CLIP-190 nor mammalian CLIP-170 is a prominent MT plus end tracker in neurons,

27 tivity requires interactions between EB1 and CLIP-170 plus end-tracking protein (+TIP) family members

28 These activities of CLIP-170 were required in primary neurons for normal den

29 ein 1 (EB1), cytoplasmic linker protein 170 (CLIP-170), and dynactin-1 (DCTN1) to initiate retrograde

30 ization is dependent on other +TIPs, EB1 and CLIP-170, but in the leading edge of the cell, CLASPs di

31 dynamics co-reconstitution system to observe CLIP-170-mDia1 complexes being recruited to growing MT e

32 CLIP-170-mDia1 complexes promoted actin polymerization ~

33 ed number of cargoes absolutely dependent on CLIP-170-mediated capture to initiate transport in prima

34 tions with four other +TIPs, we propose that CLIP-190 and -170 are not essential axon extension regul

35 Instead, both CLIP-190 and CLIP-170 form F-actin-dependent patches in

36 owever, we show here that neither Drosophila CLIP-190 nor mammalian CLIP-170 is a prominent MT plus e

37 in culture failed to reveal axonal roles for CLIP-190, even in double-mutant combinations with four o

38 ) and Goldblatt hypertensive (two kidney one clip; 2K1C) rats.

39 oss-Linking and Isolation by Pull-Down (Chem-CLIP), a small-molecule RNA target validation approach,

40 PAR-CLIP, a CLIP-seq protocol, derives a transcriptome wide

41 Combined RNA sequencing, qRT-PCR, CLIP-ADAR1, and pri-let-7 mutagenesis data suggest that

42 Here we use discriminative learning on AGO CLIP and CLASH interactions to train a novel miRNA targe

43 95% CI 1.05-9.3), and necessity to perform a clip and drop procedure (aOR 30, 95% CI 3.9-237) were as

44 e, we produce data with multiple variants of CLIP and evaluate the data with various computational me

45 t of three distinct versions: HITS-CLIP, PAR-CLIP and iCLIP.

46 e Zinc Finger Protein 598 (ZNF598) using PAR-CLIP and revealed that it cross-links to tRNAs, mRNAs an

47 Here we identified Msi2 targets with HITS-CLIP and revealed that Msi2 primarily recognizes mRNA 3'

48 ctor-specific profiles, common artifacts for CLIP and RNA-centric perspectives on RBP activity.

49 nctions, using NOVA1 and NOVA2 specific HITS-CLIP and RNA-seq data from mouse cortex lacking either N

50 2/56 (3.6% (1.0%-12.1%)) patients allocated clipping and coiling, respectively.

51 omain of Ctp1 is required for both efficient clipping and resection of DSBs by MRN and these activiti

52 terials produced and the number of newspaper clips and bulletins published in support of polio eradic

53 events by showing people several short video clips and then asking them to recall these clips, either

54 ed crosslinking and immunoprecipitation (PAR-CLIP) and anti-m(6)A immunoprecipitation (MeRIP) approac

55 e we used cross-linking immunoprecipitation (CLIP) and ligation of miRNA-target chimeras on the Argon

56 CB concentrations in sediment, biota lipids (Clip) and porewater measured with passive samplers were

57 d Cross-Linking and Immunoprecipitation (PAR-CLIP) and RNA sequencing.

58 gnition of an unexpected finding (a surgical clip) and subjective depth perception (using a Likert sc

59 po11-oligonucleotide complexes from 5' ends (clipping) and their resection to generate invasive 3'-en

60 mpares favorably to other methods, including CLIP, and we have identified RBP targets from as little

61 4% (4.5%-22.2%)) patients allocated surgical clipping, and 10/56 (17.9% (10.0%-29.8%)) patients alloc

62 lude vein cutting, trenching, girdling, leaf clipping, and application of fluids from exocrine glands

63 We used the HITS-CLIP approach to perform a genome-wide identification of

64 uch as RNA IP (RIP) and crosslinking and IP (CLIP) are key starting points for evaluating the molecul

65 indings introduce tryptase-catalyzed histone clipping as a novel epigenetic regulatory mechanism, whi

66 CLIP-associated proteins CLASPs are mammalian microtubul

67 the structural basis of HLA-DQ2.5's unusual CLIP association characteristics, better insight into th

68 ted in 5 patients with placement of a single clip at the A2-P2 segments of the mitral valve.

69 that these syndromes are caused by a lack of clipping at DSB ends that require repair.

70 ecipitation (doubled and halved), and annual clipping at the end of growing seasons in a mixed-grass

71 with the neural pattern distance between two clips at encoding in the right entorhinal cortex.

72 CLIP-based methods, which measure protein-RNA binding in

73 ive lipid-normalized bioaccumulation metrics Clip, Biota sediment accumulation factor (BSAF), Bioaccu

74 multiple S. pombe ctp1 mutants deficient in clipping but proficient in resection during meiosis.

75 ndovascular coiling than after neurosurgical clipping, but the risk was small and the probability of

76 HEJ) protein, indicating that Ctp1-dependent clipping by MRN is required for Ku removal from DNA ends

77 Axillary lymph nodes marked with a clip can be localized and selectively removed to accompl

78 A clip can be placed to designate lymph nodes with documen

79 CLiPs can differentiate into both MHs and biliary epithe

80 fMRI while they viewed two versions of movie clips (colored, achromatic) of five different object cla

81 teristics, better insight into the HLA-DQ2.5.CLIP complex structures is required.

82 Enhanced CLIP confirms RNA binding activity and identifies transc

83 ng a 4F quadripolar catheter or an alligator-clip-connected angioplasty wire.

84 hy of the specimen to confirm removal of the clip-containing lymph node and seed.

85 Preoperative targeting of the clip-containing lymph node under ultrasonographic guidan

86 In 4 of the 5 patients (80%), the clip-containing lymph node was one of the SLNs.

87 motherapy; all had disease identified in the clip-containing lymph node.

88 Confirmation of the removal of the clip-containing lymph node.

89 SLN dissection in addition to removal of the clip-containing lymph node.

90 The ability to add selective removal of the clip-containing lymph nodes to SLN dissection may identi

91 of lymph nodes known to contain metastases (clip-containing nodes) as well as sentinel lymph nodes (

92 class-II-associated invariant chain peptide (CLIP) content.

93 ponse of GPP compared to ER, indicating that clipping could potentially be an effective land practice

94 t 2 examined whether learning faces in video clips could generalise more effectively to a new view.

95 Subsequent content analysis of video clips created from this response profile confirmed this

96 We adapted UV CLIP (cross-linking immunoprecipitation) to accurately l

97 Here, we employed CLIP (cross-linking immunoprecipitation)-seq datasets fo

98 for flexible, streamlined and comprehensive CLIP data analysis.

99 tistical and computational framework for PAR-CLIP data analysis.

100 atics pipelines for handling the genome-wide CLIP data have also been developed.

101 urately resolves miRNA interactions from AGO CLIP data than previous methods.

102 We use published PAR-CLIP data to demonstrate the advantages of our approach,

103 tein binding sites at high resolution in PAR-CLIP data.

104 the in-house Ago2-dataset and on an Ago2-PAR-CLIP dataset in human stem cells.

105 mount of common backgrounds present in a PAR-CLIP dataset, and we provide the user the option to use

106 fied from Tarbase 6.0 and confirmed with PAR-CLIP dataset.

107 coclip, on four publicly available Ago2-HITS-CLIP datasets and one unpublished in-house Ago2-dataset

108 We used the proposed strategy in 30 PAR-CLIP datasets from nine proteins.

109 ify the presence of common background in PAR-CLIP datasets is not yet available.

110 re that reflects its presence in several PAR-CLIP datasets.

111 backgrounds which are present in several PAR-CLIP datasets.

112 utants that were reported to be specifically clipping deficient.

113 The mutants tested, like ctp1Delta, were clipping-deficient by both genetic and physical assays-.

114 cture while subjects watched identical video clips designed to induce different arousal levels.

115 As described herein, DMF-IP and P-CLIP-DMF-IP are rapid, automated, and multiplexed method

116 Clip domain serine protease homologs (SPHs) are positive

117 demonstrated for faces learnt through video clips, dynamic facial expression did not create better t

118 y of errors committed by others during movie clips (e.g., figure skaters falling down and persons beh

119 We have developed an enhanced CLIP (eCLIP) protocol that decreases requisite amplifica

120 o clips and then asking them to recall these clips, either aloud (Experiment 1) or silently while in

121 In addition, we found that clipping enhanced NEE due to a stronger positive respons

122 essing of amyloid precursor protein (APP) by clipping enzymes (beta- and gamma-secretases).

123 Several variants of CLIP exist, which require different computational approa

124 iRNAs, we analyze multiple datasets from PAR-CLIP experiments in conjunction with RNA-Seq data.

125 t data compendium to date, which includes 31 CLIP experiments on 19 RBPs involved in splicing (such a

126 g and crosslinking immunoprecipitation (HITS-CLIP) experiments of human Argonaute (AGO) during HCV in

127 For example, the CLIP family of +TIPs are known MT polymerization promote

128 UV cross-linking and immunoprecipitation (CLIP), followed by high-throughput sequencing, is a powe

129 We identified 389 artifact-free EEG clips following behavioral assessments.

130 , decellularized, and mounted in specialized clips for seeding and culture.

131 d how much time had elapsed between pairs of clips from the story.

132 e of the intramembrane-cleaving proteases (I-CLiPs), gamma-secretase, is also intimately implicated i

133 he results show that faces learnt from video clips generalised effectively to a new expression with e

134 dency in the coiling group compared with the clipping group, but the medium-term results showed the i

135 sed to assess bioaccumulation, in the order: Clip > BSAF > BPAF > BAF, and were nonsignificant for BA

136 tal structural analyses have revealed that I-CLiPs harbor their active sites buried deeply in the mem

137 The resulting clipped herceptin-Ex-4 fusion protein is more potent in

138 The clipped herceptin-Ex-4 has an extended plasma half-life

139 IF4A3 using individual-nucleotide resolution CLIP (iCLIP), employing either UV-C or photoactivatable

140 t (UV) crosslinking and immunoprecipitation (CLIP) identifies the sites on RNAs that are in direct co

141 s who underwent transcatheter mitral leaflet clip in 2015 were similar to patients from 2013 to 2014,

142 The standard connection works as a clip in order to support the paper in between.

143 CLiPs in long-term culture did not lose their proliferat

144 Placing clips in nodes with biopsy-confirmed metastasis before i

145 sham CSD (n = 9) 5 weeks after renal artery clipping, in comparison with normal Wistar rats (n = 5).

146 ormalization of bleeding after a severe tail clip injury in these mice.

147 g blocks, two CoTPyP units and four arene-Ru clips, into a cofacial motif previously demonstrated wit

148 ovascular embolization, prostheses, surgical clips, intraorbital and other medical implants, etc.

149 PAR-CLIP is a recently developed Next Generation Sequencing-

150 Continuous liquid interface production (CLIP) is an alternative approach to AM that capitalizes

151 ther integrated systems (BCLC, HKLC, MESIAH, CLIP, JIS).

152 MDCK epithelial cells, we used the SNAP and CLIP labeling systems to fluorescently tag temporally de

153 d anterior communicating artery aneurysms by clip ligation (n = 14) or coiling (n = 9).

154 In cases with a clip placed in the node, the clip location at surgery (SLN or ALND) was evaluated.

155 th cN1 disease and at least 2 SLNs resected, clip location was confirmed in 141 cases.

156 R were end-diastolic dimension, MR severity, clip location, and case volume.

157 to r(CGG)(exp) in cellulo as shown with Chem-CLIP-Map, an approach to map small molecule binding site

158 CLEAR-CLIP mapped approximately 130,000 endogenous miRNA-targe

159 y cut within the binding sites, the original CLIP method is less capable of identifying the longer bi

160 Analysis of EBV PAR-CLIP miRNA targetome data sets combined with pathway ana

161 ly targeted in the RISC, indicating that PAR-CLIP more accurately defines meaningful targeting intera

162 Unlike glycoluril-based dimers, these clips neither dimerize nor accept any organic guests, du

163 of node-positive disease with removal of the clipped node during SLN surgery reduces the FNR of SLN s

164 t a clip placed (n = 355) and in those where clipped node location was not confirmed at surgery (n =

165 Adding evaluation of the clipped node reduced the FNR to 1.4% (95% CI, 0.03 to 7.

166 de at initial diagnosis with confirmation of clipped node resection at surgery.

167 The clipped node revealed metastases in 115 patients, result

168 and evaluation of resected specimens for the clipped node should be considered when conducting SLN su

169 ng TAD had SLND and selective removal of the clipped node using iodine-125 seed localization.

170 nt axillary surgery and the pathology of the clipped node was compared with other nodes.

171 In 34 (24.1%) cases where the clipped node was in the ALND specimen, the FNR was 19.0%

172 The clipped node was not retrieved as an SLN in 23% (31 of 1

173 In 107 (75.9%) patients where the clipped node was within the SLN specimen, the FNR was 6.

174 six with negative SLNs but metastasis in the clipped node.

175 an FNR of 4.2% (95% CI, 1.4 to 9.5) for the clipped node.

176 al was to determine if pathologic changes in clipped nodes reflect the status of the nodal basin and

177 D) and selective localization and removal of clipped nodes, improves the false-negative rate (FNR) co

178 trand breaks (DSBs) requires endonucleolytic clipping of Rec12(Spo11)-oligonucleotides from 5' DNA en

179 Video clips of 39 resultant avatars were rated for dance quali

180 s were scanned with fMRI while viewing movie clips of faces, bodies, and objects before and after tra

181 , over two sessions, while viewing 3 s video clips of moving faces, bodies, and objects.

182 by UV crosslinking and immunoprecipitation (CLIP) of ribonucleoprotein complexes is critical to unde

183 e, we used crosslinking immunoprecipitation (CLIP) of the Argonaute (AGO) proteins to characterize st

184 The fact that BAF, that is, normalization of Clip on porewater concentration, largely removed all eff

185 ) or a portable gamma-camera (GC; Vitom GC), clip-on brackets were designed and printed in 3-dimensio

186 ) or a portable gamma-camera (GC; Vitom GC), clip-on brackets were designed and printed in 3-dimensio

187 Attaching a flat metal clip onto the tragus produced LLTS (20 Hz) in the right

188 We randomly allocated clipping or coiling to patients with one or more 3-25 mm

189 e randomly allocated to either neurosurgical clipping or endovascular coiling after a subarachnoid ha

190 Surgical clipping or endovascular coiling of UIAs did not show di

191 ave traditionally been treated with surgical clipping or endovascular coiling techniques.

192 racranial aneurysm with either neurosurgical clipping or endovascular coiling.

193 es that were either presented in short video clips or still images.

194 development of three distinct versions: HITS-CLIP, PAR-CLIP and iCLIP.

195 s a whole soft-clipping read rather than its clipped part to the target sequence, a segment of the re

196 r peak detection programs, namely CIMS, PIPE-CLIP, Piranha and Pyicoclip, on four publicly available

197 In cases without a clip placed (n = 355) and in those where clipped node lo

198 s of fine-needle aspiration biopsy who had a clip placed in the lymph node targeted for biopsy from D

199 In cases with a clip placed in the node, the clip location at surgery (S

200 ith biopsy-confirmed nodal metastases with a clip placed in the sampled node was performed.

201 Clip placement at diagnosis of node-positive disease wit

202 Clip placement in the biopsy-proven node at diagnosis an

203 One proposed method to decrease the FNR is clip placement in the positive node at initial diagnosis

204 participants to perceive subsequently viewed clips played at standard speed as too fast, so playback

205 The PAR-CLIP procedure induces specific base transitions that or

206 power of bioorthogonal tethering to SNAP and CLIP protein tags to create a family of light-gated meta

207 However, current CLIP protocols are technically demanding and yield low-c

208 The rotaxanes were prepared by a templated clipping reaction and an X-ray crystal structure shows t

209 It aligns a whole soft-clipping read rather than its clipped part to the target

210 It also analyzes soft-clipped reads from alignment to detect insertions accura

211 tains a region of strong similarity with the clip region of the known portal proteins.

212 t of AdV proteins and compared them with the clip region of the portal proteins of bacteriophages phi

213 y by transiently binding DP(84Gly) via a non-CLIP region(s) in a pH-sensitive manner.

214 class II-associated invariant chain peptide (CLIP) region, nor does it present CLIP.

215 HITS-CLIP revealed hundreds of robust Argonaute (Ago) binding

216 -DM sensitivity is the likely reason for the CLIP-rich phenotype of HLA-DQ2.5.

217 to RNA bisulfite sequencing, m(1)A-Seq, Par-CLIP, RIP-Seq, etc.

218 age (respective C indexes of 0.64 and 0.73), CLIP score (0.68 and 0.75), JIS stage (0.67 and 0.70), M

219 We used a combined AGO2 RIP-seq and AGO2 PAR-CLIP-seq (photoactivatable-ribonucleoside-enhanced cross

220 We present CLAM (CLIP-seq Analysis of Multi-mapped reads).

221 CLIP-seq analysis revealed that APOBEC3H preferentially

222 interactions and RNA modification sites from CLIP-seq and RIP-seq data, and reveals the significant c

223 ssociated RBPs, FUS and TDP-43, we integrate CLIP-seq and RNA Bind-N-Seq technologies, and show that

224 methods for identifying RBP targets, such as CLIP-seq and RNAcompete, usually suffer from the false n

225 We show that CLIP-seq data contains clear secondary structure signals

226 tions can greatly improve motif discovery on CLIP-seq data.

227 e corresponding binding targets of RBPs from CLIP-seq data.

228 Through testing on the real CLIP-seq datasets, we have demonstrated that our deep le

229 In a CLIP-seq experiment, we find that EWS-FLI1 RNA-binding m

230 ill be widely applied to analyze large-scale CLIP-seq experimental data and can provide a practically

231 ut protein-RNA interaction data generated by CLIP-seq has provided an unprecedented depth of access t

232 Using our method, we generated CLIP-Seq libraries from nuclear RNA that had been UV-cro

233 fic properties of RBP binding sites, and the CLIP-seq methods, provide additional information not usu

234 immunoprecipitation followed by sequencing (CLIP-seq or RIP-seq) allows transcriptome-wide discovery

235 PAR-CLIP, a CLIP-seq protocol, derives a transcriptome wide set of b

236 desorption/ionization mass spectrometry and CLIP-Seq sequencing, we determined the peptide and oligo

237 ed those regulations inferred by ChIP-Seq or CLIP-Seq to construct the GRN formed by TFs, miRNAs, and

238 s a myriad of techniques such as RNA-Seq and CLIP-Seq to identify splicing regulators and their putat

239 We used CLIP-seq to obtain a comprehensive assessment of DDX3X b

240 crosslinking/immunoprecipitation-sequencing (CLIP-seq) analysis of mouse cells and tissues to disting

241 aute immunoprecipitation and sequencing (Ago CLIP-seq) and represented 3 of the 13 tissues, indicatin

242 ross-linking immunoprecipitation sequencing (CLIP-seq) experiments.

243 slinking immunoprecipitation and sequencing (CLIP-seq) identify RNAs that interact directly with CsrA

244 Cross-Linked ImmunoPrecipitation sequencing (CLIP-seq) to reduce the false-positive rate.

245 oprecipitation coupled with deep sequencing (CLIP-seq) we identify a set of genes involved in synapti

246 on associated to high-throughput sequencing (CLIP-seq).

247 of the necessary follow-up data analysis for CLIP-seq, both to refine the exact locations of RBP bind

248 t leverages transfer learning to incorporate CLIP-Seq, knockdown and over expression experiments, whi

249 Using AGO2 RIP-seq and PAR-CLIP-seq, we show that the DNA damage-induced increase i

250 AGO2 cross-linking sites identified via PAR-CLIP-seq.

251 LAM, we applied it to a wide range of public CLIP-seq/RIP-seq datasets involving numerous splicing fa

252 As CLIP-seq/RIP-seq reads are short, existing computational

253 Recent technologies like AGO CLIP sequencing and CLASH enable direct transcriptome-wi

254 eproducibly identified in two published FMRP CLIP sequencing datasets.

255 linking immunoprecipitation (Argonaute [Ago]-CLIP) sequencing in miR-122 knockout and control mouse l

256 hes, LexisNexis archival databases, and news clipping services) and USA Triathlon (USAT) records.

257 the transcript level while intensity of the CLIP signal, number of RNA-Binding domains, location of

258 synthate allocation to the grain by spikelet clipping significantly increased white root biomass and

259 oach using genetically encoded chemical tags CLIP, SNAP, Halo, and TMP for tissue labeling; this resu

260 SWAN also uses soft-clip/split read remapping to supplement the likelihood a

261 Here we report a modified AGO HITS-CLIP strategy termed CLEAR (covalent ligation of endogen

262 regurgitation using the transcatheter mitral clip system.

263 n rat models of sensory deprivation (whisker clipping, tail suspension, casting).

264 In this review, we discuss the genome-wide CLIP technology and focus on bioinformatics analysis.

265 f layerless and monolithic fabrication using CLIP technology.

266 with high-throughput sequencing (genome-wide CLIP) technology has recently enabled the investigation

267 Thirty-six adults viewed video clips that showed another individual yawning and, in sep

268 Clipping, the interaction of clipping with warming, and

269 ur and six and without stratification, to be clipped to standard oximeters (patients treated with oxy

270 oupled with high-throughput sequencing (HITS-CLIP) to generate the first transcriptome-wide map of mi

271 oss-Linking and Isolation by Pull Down (Chem-CLIP) to study the cellular selectivity and the on- and

272 riments (variety, mutant study, and spikelet clipping) to examine the impacts of rice plant photosynt

273 low-serum media without proteolytic damage (clipping) to the V3 region.

274 The CLIP Tool Kit (CTK) aims at providing a set of tools for

275 In each heart, single-clip treatments involved grasping leaflet pairs in the m

276 Two-clip treatments were then performed considering all poss

277 e detector/data system is saturated, causing clipping/truncation of the signal, or (c) the detector s

278 with an equimolar mixture of Pd(NO3)2 and a clip-type donor (L2) yielded a template-free multicompon

279 One clip was implanted in 61.4% of patients.

280 A clip was placed at initial node biopsy in 203 patients.

281 Annual clipping was used to mimic hay harvest.

282 esence or absence of clinical signs on video clips was high (>/=89%), with interobserver concordance

283 ed by crosslinking immunoprecipitation (HITS-CLIP), we identified the vRNA binding profiles of NP for

284 ed crosslinking and immunoprecipitation (PAR-CLIP), we isolated RNAs associated with Argonaute 2 in t

285 Using HITS-CLIP, we map HuR and miRNA binding sites on human 3' UTR

286 Peaks identified by HITS-CLIP were verified as true NP binding sites based on ins

287 79%) of 835 patients allocated neurosurgical clipping were alive (odds ratio [OR] 1.35, 95% CI 1.06-1

288 70 (78%) patients treated with neurosurgical clipping were independent (modified Rankin scale score 0

289 between warming, altered precipitation, and clipping were observed.

290 contest, additional held-out unlabelled data clips were provided to the top 10 participants and they

291 In both experiments, actively rehearsed clips were remembered in far greater detail than unrehea

292 eir hepatic differentiation ability, and rat CLiPs were shown to extensively repopulate chronically i

293 thogonal x-rays with matching of 4 implanted clips were used for positioning.

294 bered in far greater detail than unrehearsed clips when tested a week later.

295 ligation of endogenous Argonaute-bound RNAs)-CLIP, which enriches miRNAs ligated to their endogenous

296 lar Ctp1 C-terminal portion is essential for clipping, while the N-terminal portion is sufficient for

297 number of binding sites overlapping with PAR-CLIP with maximum F-Score of 0.337.

298 Clipping, the interaction of clipping with warming, and warming-induced changes in so

299 he subjects watched laughter-inducing comedy clips with their close friends for 30 min.

300 rticipants as 10-min interictal and preictal clips, with approximately half of the 60 GB data bundle