ライフサイエンスコーパス: map

1 ting cardiomyocytes provides a functional 3D map of active ECC couplons (on average, 17,000 per myocy

2 acrosection images yields high resolution 3D maps of multiple tumor microenvironment components and b

3 A map of a neuronal circuit in a marine worm reveals how s

4 MS imaging mass spectrometry, we generated a map of small molecules differentially expressed in the D

5 We reconstruct a map-like knowledge structure directly from a hippocampal

6 Such a map helps rationalizing the transport properties of the

7 uring developmental ontogeny, we conducted a mapping experiment using Euphrates poplar (Populus euphr

8 We also construct a mapping of the vertex model into the Chimera architectur

9 imultaneously in the two signals to create a mapping of the particle position to resistive pulse ampl

10 ty of current vendor-provided thoracic MR-AC maps and further investigated the reproducibility of the

11 In total, 90 MR-AC maps were evaluated visually for quality and the occurre

12 Accurate mapping of the composition and structure of minerals and

13 more patients showed at least one BML on ADC maps (98%, 95 of 97 patients) than on FS PD-weighted TSE

14 We also mapped phage 9 g DNA packaging (pac) site containing two

15 97 traumatic brain injury patients were also mapped at the grey matter-white matter boundary.

16 Fluorescence in situ hybridization analysis mapped the EPSPS gene to pericentromeric regions of two

17 Proteomic analysis mapped structural microheterogeneity of signal peptide c

18 ncestry in simulations and produces ancestry maps that agree with published results and global ancest

19 structurally annotate relevant features and map them to biochemical pathways is hampering the full e

20 ivity profiles of cellular zDHHC enzymes and mapped molecular determinants governing this selectivity

21 This framework enables connectivity and mapping projects in individual laboratories and across i

22 uch a dataset as follows: (i) extracting and mapping the stained manifold in each stack into a single

23 Measuring and mapping single platelet forces are desired in both resea

24 unlocking the potential of metamaterials and mapping a new direction for the large-area, cost-efficie

25 In contrast, antigenic maps derived from human postvaccination sera with only t

26 This indicates that global areal maps cannot fully account for orientation information in

27 precise, robust, or scalable for association mapping to be conducted for specific cell wall polymers.

28 pic plasticity in a maize nested association mapping (US-NAM) population grown in multiple environmen

29 ased approach for estimating the attenuation map in the presence of metallic implants, to be used for

30 The initial estimate of the attenuation map was obtained using the MR Dixon method currently ava

31 from these intrasubject repeated attenuation maps.

32 Splice site usage has been mapped exhaustively across different species, cell types

33 tion about their structural defects has been mapped to the HCM phenotype.

34 receptive fields of these neurons have been mapped, allowing us to investigate how well they can sup

35 to characterize the consequences of bifacial maps in the thalamocortical system.

36 hemispheres and assembled 104 complete body maps, revealed by cytochrome-oxidase activity in layer 4

37 lation, which could be developed in to brain mapping applications, but also serves as a potential dru

38 nucleus accumbens shell measured using brain mapping analyses of immediate-early gene expression and

39 Our tool further created browsable maps of a 3D microbiome/metabolome reconstruction map on

40 By mapping changes in enhancer landscape and transcription

41 By mapping the cell cycle in detail, we show that directly

42 network analysis of high-throughput data by mapping the data onto a biological networks such as prot

43 of the visual system of Drosophila larvae by mapping the synaptic wiring diagram and neurotransmitter

44 redict potential phosphorylation switches by mapping phosphorylation sites to protein-protein interac

45 rchical trees of chromosomal domains in Hi-C maps, stratified through their reciprocal physical insul

46 the handling by NCLX of calcium exchange can map to neural circuit patterning and axon guidance decis

47 A new technique called CUT&RUN can map the distribution of proteins on the genome with high

48 SIMS) as a label-free approach to chemically map small molecules in aggregated and single Escherichia

49 ide, tunable, all-optical functional circuit mapping that captures supra- and subthreshold depolariza

50 enuation on VNCa images by using color-coded maps and performed a quantitative analysis of CT numbers

51 otgun metagenomic reads of known composition map onto well-curated reference protein sequences and th

52 ollectively, this is the first comprehensive map of TSSs in B. burgdorferi and characterization of pr

53 l, our study provides the most comprehensive map of MEIs to date spanning chimpanzees, ancient homini

54 However, the lack of a comprehensive mapping of WGDs within a major plant clade has led to un

55 Our comprehensive maps of cis-acting hippocampal meQTLs and eQTLs provide

56 by an approach of "differential-conductance mapping", which allows us to suppress quantum correction

57 Using a connectivity map, we identified prostaglandin E1 (PGE1) as a small mo

58 cted a three-dimensional global connectivity map of promoters and enhancers, revealing transcription-

59 ndrites, therefore the neuronal connectivity map not only depicts the underlying anatomy, but also ha

60 l profiling studies such as the connectivity map and library of integrated network-based cellular sig

61 isual examination of the chromosomal contact map, however, it is clear that the organization of the d

62 l state is a major predictor of Hi-C contact maps in several eukaryotes tested, including C. elegans

63 results indicate that chromosomal contacts' maps could uncover functionally and clinically related g

64 tial preference of neurons into a continuous map of the space swept out by the whiskers.

65 ganisational principles governing continuous maps may extend to the implicit encoding of discrete, no

66 Two readers correlated mapped lesions with reports of prospectively read MP MR

67 s plasticity occurs at the level of cortical maps and individual neurons in the auditory cortex of aw

68 d step, we selectively expanded this curated map with database knowledge.

69 precise genetic null mutant to definitively map its amorphic phenotypes.

70 manual synapse annotation for large densely mapped connectomes.

71 ng impact on the quality of electron-density maps.

72 parts or hinge-regions into cryo-EM density maps.

73 Electrical impedance tomography-derived maps might become clinically feasible and relevant, bein

74 Electrical impedance tomography-derived maps of pressure-volume curve shapes allow to detect reg

75 Identity-by-descent mapping using empirical estimates of identity-by-descent

76 in vivo lineage tracing to define a detailed map of the postnatal olfactory epithelium, revealing cel

77 rovides the first comprehensive and detailed map of the catecholaminergic structures in the brain of

78 We establish detailed maps for subtelomere gap regions in the human reference

79 of an estuary identified in pre-development maps.

80 dy demonstrates that 3D electron diffraction mapping is a powerful tool for the cross-sectional strai

81 formational analysis, and NOE-based distance mapping between sugar and protein revealed that Manalpha

82 However, MS-based disulfide mapping is challenged when multiple disulfide bonds are

83 To compile DMH maps for the autonomic cold defense and for the cold-see

84 ise for efficient spectrum imaging, low-dose mapping of beam-sensitive specimens, trace element analy

85 ysiological properties of CI channels during mapping with the IntellaMap Orion basket and the Rhythmi

86 The AAR derived from ECV maps (threshold of >33) demonstrated good agreement with

87 Here, we effectively map part of the folding pathway for the model large mult

88 1 in rice, can be accurately and efficiently mapped using an innovative strategy consisting of multip

89 ures into cryo-electron microscopy (cryo-EM) maps is a major challenge, as the moderate resolution ma

90 esolution cryo electron microscopy (cryo-EM) maps of wild type CPMV containing RNA-2, and of naturall

91 Of 6889 endocardial-epicardial mapping point pairs, 547 (8%) pairs with distance <10 mm

92 Epitope mapping was performed by pepscan analysis, site-directed

93 e determined by a novel CD154 T cell epitope mapping assay.

94 oscopy is extensively used to obtain epitope maps of ligands binding to protein receptors, thereby re

95 1E2 also resulted in identifying the epitope maps of diverse mAbs and the disulfide connectivity unde

96 li and provide a time-resolved response eQTL map.

97 d are quite consistent with the experimental map.

98 B1(+) field and variable flip angle (FA) mapping were included in the dynamic contrast-enhanced b

99 Moreover, fate-mapping experiments revealed that the timing of SOX2 exp

100 In this study, fate-mapping mice were used to assess the stability of Treg f

101 Fine mapping analysis by integration with genome-wide express

102 Here we establish, through fine mapping, genome sequencing, genetic complementation, and

103 gulatory regions in transgenic mice and fine-mapped separate enhancers controlling expression in join

104 This grain length effect was fine-mapped to a 4.3 cM interval.

105 Association and fine-mapping analyses identified a protein-coding variant, rs

106 We apply fine-mapping analysis to dissect associations in the human le

107 annotation data, fastPAINTOR increases fine-mapping resolution relative to existing methods.

108 saturating in situ mutagenesis permits fine-mapping of function across genomic segments.

109 al variant(s), a variety of statistical fine-mapping methods have been proposed to prioritize variant

110 m x 100 m) regional (10,000 km(2)) CH4 flux map of the Mackenzie Delta, Canada, based on airborne CH

111 logical data, cheminformatics approaches for mapping the extracted chemical names into chemical struc

112 his represents an important step forward for mapping genes involved in complex diseases.

113 e developed a novel analytical framework for mapping and testing the distribution of these QTL.

114 lack of simple, high-throughput methods for mapping the transcriptomes of subcellular compartments.

115 A protocol for mapping amino-acid sequences to coarse-grained beads ena

116 e found that local eQTL were more frequently mapped to adjacent genes, displaying a mode of expressio

117 it minimizes false positives resulting from mapping errors and other technology specific artifacts i

118 Furthermore, mapping these projections allows us to identify the fibe

119 project has patched the hole in the genetic map of Eurasia: we demonstrated complexity of genetic st

120 pen1-1 genetic background as well as genetic mapping and characterization of the Arabidopsis nonhost

121 Using a combination of genetic mapping approaches, we show that the white recessive all

122 ondestructive modalities to provide a global mapping of the stratigraphy, information that is crucial

123 significant challenge of traditional glycan mapping techniques is that they do not provide site-spec

124 and variant data for every strain, and a GWA mapping portal for studying natural variation in C. eleg

125 The scoring matrix is represented as a heat map reflecting the potential interface regions in both q

126 n of seven patients followed by homozygosity mapping and linkage analysis were performed.

127 Using homozygosity mapping, array CGH, and exome sequencing, we uncovered b

128 Conclusion Serial multiparametric MR imaging mapping can be used to evaluate cartilage beyond mere st

129 Raman spectra were acquired in mapping mode from multiple spots on a bloodstain to acco

130 y motor (M1) cortices play a central role in mapping sensation to movement.

131 echniques were used to generate BC incidence maps in Hangzhou.

132 Near-infrared mapping reveals the relative humidity within prominent d

133 xpensive methods for INTACT, T-DNA insertion mapping, and profiling of the complete nuclear transcrip

134 ng MARGI, we produced RNA-genome interaction maps for human embryonic stem cells (ESCs) and human emb

135 , we identified a highly reproducible jigsaw map of dysferlin fragments protected from digestion.

136 Through linkage mapping we assign these variants to a particular rDNA cl

137 We also construct de novo linkage maps on 7-12x whole-genome data on the Red postman butte

138 en dominant loci and recovering true linkage maps of 6 dominant loci in coupling and unknown linkage

139 New techniques for lymphatic mapping attempt to further simplify the procedure.

140 We found that M1 maps of the amputated limb in TMSR patients were similar

141 or merge a complete linkage dominant marker maps.

142 Contrast material maps clearly differentiated the distributions, with gado

143 a 7.8 A resolution cryo-electron microscopy map of a Mediator-RNA polymerase II holoenzyme reveals t

144 cently reported 9-A cryo-electron microscopy map of the Tetrahymena telomerase holoenzyme has provide

145 Disrupting synapses and motor maps by infusions of anisomycin (ANI) into anatomically

146 Obtaining the full MS/MS map for fragments and precursors of complex mixtures wit

147 eveal large differences regardless of the mu-map used.

148 r an oncogenomics paradox, whereby mutations mapping to the same domain evoke opposing drug susceptib

149 ions were used to construct a social network map that showed each participant's ties to other partici

150 Second, lesion network mapping was used to identify brain regions functionally

151 ocessing requires proper alignment of neural maps throughout the brain.

152 primary reason for the appearance of neural maps, which we link to a known phase transition in an Is

153 data from the literature to show that neural maps appear as the number of neurons in visual cortex in

154 iliac crests and in vivo sentinel lymph node mapping were performed during open standard oncological

155 of indocyanine green and sentinel-lymph-node mapping followed by pelvic lymphadenectomy with or witho

156 Sentinel-lymph-node mapping with complete pelvic lymphadenectomy was done in

157 , were included as part of the assessment of mapping and in the safety analysis in an intention-to-tr

158 med digit that implements a novel measure of mapping ambiguity to discover interchromosomal SVs from

159 (GCIB-SIMS) has shown the full potential of mapping intact lipids in biological systems with better

160 tervention (injection of dye), regardless of mapping result, were included as part of the assessment

161 of genomic analysis due to the resolution of mapping algorithms.

162 this technique provides an effective way of mapping the EM field or the local density of states with

163 zens of scaffolds encompassing more than one mapped gene were identified.

164 ing process critically depends on an ongoing mapping between the representations and the objects in t

165 Interestingly, orientation preference (OP) maps in the visual cortex are found in carnivores, ungul

166 Optical mapping is a technique for capturing fluorescent signal

167 Optical mapping of perfused hearts confirmed slowed conduction o

168 -time sequencing and high-resolution optical mapping.

169 Starting with the 3D genome organization map of LCL, we constructed a comprehensive EBV regulome

170 PCA and Kohonen self-organizing maps showed the formation of groups, corresponding to th

171 expression analyses based on self-organizing maps with sequence-based transcription factor binding pr

172 stimation of tumor load and tissue-of-origin mapping in the circulating cell-free DNA of 59 patients

173 formed comprehensive anatomical input-output mapping.

174 sfies (i), and by using a pre-drawn overview map of metabolism based on the Roche map satisfies (ii)

175 ion-level analyses in statistical parametric mapping.

176 arge vessels, on imager-generated parametric maps to measure hepatic PDFF.

177 MAM is a peptide mapping method utilizing mass spectrometry to detect and

178 etry, ion mobility, and quantitative peptide mapping.

179 were identified (median 2; quartiles 1-3 per map), although this represented LR in only n=7 out of 50

180 es, our approach first measures haloed phase maps of the sample.

181 The collection of mutant-phenotype mapping provides a framework for engineering AMPAR gatin

182 It is our hope that the use of phenotypic maps such as these will further the understanding of gen

183 ) to produce a de novo whole-genome physical map.

184 We precisely map RNA-programmed DNA methylation to targeted CpG sites

185 quantitative mass spectrometry, we precisely mapped key residues involved in substrate recognition an

186 reating a comprehensive NUDIX enzyme profile map, which will prove fundamental to understanding their

187 e an important methodology for proteogenomic mapping by providing evidence for the existence of prote

188 In practice, the regular approaches for QTL mapping analysis may be adopted for metabolites-phenotyp

189 acid and 2, 3-hydroxypropanoic acid).Two QTL mapping approaches were carried out using SNP markers on

190 A quantitative trait (QTL) mapping approach was applied and successfully identified

191 We used this method to quantitatively map the intracellular fate of micelles of a recombinant

192 sonance imaging to quantify iron through R2* map at 24-72 h and at 1-year follow-up.

193 Liver R2* mapping is often degraded by the low signal-to-noise rat

194 Purpose To create a radiogenomic map linking computed tomographic (CT) image features and

195 A radiogenomic map was created with 32 statistically significant correl

196 Ambiguous read mapping is modeled as a multinomial distribution, and am

197 ruction of individual haplotypes using reads mapped to a reference genome sequence.

198 of a 3D microbiome/metabolome reconstruction map on a radiological image of a human lung and forms an

199 detail our selection criteria for reference maps, which clarify why the work of Schepaschenko et al

200 ime points, we found a hypomethylated region mapping to Iqgap2 (IQ motif-containing GTPase activating

201 uencing (NGS) to generate genome-wide repair maps.

202 the first genome-wide, base pair-resolution map of 6mA in Tetrahymena by applying single-molecule re

203 Hence, high resolution mapping of transcriptional repression reveals complex an

204 , and beta-galactosidase for high-resolution mapping of expression patterns post-mortem.

205 Single-nucleotide-resolution mapping of m(6)A coupled with ribosome profiling reveals

206 Resulting maps of annual daytime NO, NO2, and black carbon at 30 m

207 rn of alpha coherence across the retinotopic map in V4 matches many of the properties of receptive fi

208 Spatial receptive fields (RFs) mapped using melanopsin-isolating stimuli had ON centers

209 We developed risk maps for autochthonous CHIKV transmission in Canada unde

210 Our revised road map emphazises close parallels of terminal mTEC developm

211 However, a robust map of immune-related gene networks in circulating human

212 verview map of metabolism based on the Roche map satisfies (ii) and comes close to satisfying (iii).

213 We found that rs31746 mapped to a long-range neuron-specific enhancer element

214 Here, we report large-scale mapping of the branchpoints from deep sequencing data in

215 Nevertheless, sequences mapping to spliced mRNAs were identified within HEK293T

216 cipal Component Analysis to build similarity maps in the molecular descriptor and spectral domains.

217 ing for MNase-seq, DNase hypersensitive site mapping, site annotation and motif identification for DN

218 Cdc55 and Igo/ENSA, and phosphorylation site mapping and mutagenesis indicate that phosphorylation of

219 le pockets of p53 are identified via solvent mapping to aid future drug discovery studies.

220 ry of consecutive patients undergoing source mapping for AF.

221 We propose that momentum-space mapping of the second-order non-linear structure factor

222 onses in single spines, we provide a spatial map of synaptic calcium signals along dendritic arbors o

223 ion and the neurons there encode the spatial map of the environment.

224 r movement-integration in generating spatial maps.

225 ld-type mice was supported by stable spatial maps and robust remapping of place fields toward the goa

226 ic range can accurately detect and spatially map pressure profiles.

227 on Analysis in Yeast (SATAY) allows one-step mapping of all genetic loci in which transposons can ins

228 By comparison with strain maps of the developing skeleton, we identify canonical W

229 Seismic surveys map the seabed using intense, low-frequency sound signal

230 The viral determinants of Lv2 susceptibility mapped to the HIV-2 envelope (Env) and capsid (CA).

231 sed-and structural connectome-lesion symptom mapping approach, since cortical dysfunction after strok

232 Here we have systematically mapped and compared cleavage and polyadenylation sites (

233 We systematically mapped infants' categorical recognition memory for hue o

234 d modified look-locker inversion recovery T1 mapping differentiates reversible and irreversible myoca

235 -1.6 to 1.3) and AAR derived from native T1 maps (bias=1; 95% CI, -0.37 to 2.4).

236 fying the AAR following AMI, which unlike T2-mapping, is not affected by IPC.

237 ove intraoperative neurophysiological target mapping during electrode implantation.

238 Several Myo7a deafness mutants that map to the surface of MF2 disrupt harmonin binding, reve

239 variations in gut microbial activities that mapped onto tacrine-induced transaminitis.

240 Here, we describe the map-based cloning of the Ms2 gene and show that Ms2 conf

241 ture of the segment and local quality of the map.

242 Recent advances in the mapping of biochemical traits have been reported in Loli

243 Here, we report the mapping of two hedonic hotspots in cortex, where mu opio

244 nce for translocations in at least 36 of the maps was found.

245 Moreover, the intervals they mapped to harbored few metabolism-associated genes, sugg

246 Based on this mapping, neighboring neurons showed markedly different a

247 We then compared trajectories through maps both with and without high-order epistasis.

248 Lead CpGs at PTPN6/PHB2, ANKRD11, and TNRC18 map to active enhancers in kidney cortex.

249 To map the critical determinant, Ser5 mutants bearing C-ter

250 ) to identify the substrates directly and to map the phosphorylation site(s) of plant symbiotic recep

251 tures (e.g. shape, orientation, etc.) and to map them into our own peripersonal space.

252 rotron X-ray nanofluorescence was applied to map the trace element distributions in selected areas of

253 d a mass spectrometry (MS)-based approach to map the complete glycosylation profile at every site in

254 We apply this framework to map different global climate regimes and identify where

255 ting, disulfide trapping, and mutagenesis to map the structures of ACKR3:CXCL12 and ACKR3:small-molec

256 s to infer a strongly supported phylogeny to map major morphological and molecular transitions in din

257 presents a validated lipidomics platform to map the fecal lipidome, which integrates unique informat

258 pe, but hitherto it has not been possible to map vibrational modes directly in a single nanostructure

259 ate the capability of the miniature probe to map the biomechanical properties in phantom and human ca

260 chromatographic tandem mass spectrometry to map phosphorylation sites to the otherwise divergent ami

261 chnologies allows us, for the first time, to map the physical 3D structure of previously inaccessible

262 ieve 55-fold genome coverage, allowing us to map autonomous promoter activity genome-wide in K562 cel

263 Phase retrieval methods allow us to map the internal spin structure of the skyrmion core, id

264 ecific polymerase chain reaction was used to map the neoplastic clone in 20 adults with LCH, ECD, and

265 s on phenotypes, we developed an approach to mapping structural variants that segregate in a populati

266 g frequency preferences across tonotopically mapped auditory cortex spatially correlate with R1-estim

267 t time of axon outgrowth directs topographic mapping without affecting hox5 expression.

268 how that hox5 expression directs topographic mapping without affecting time of axon outgrowth and tha

269 projection fields to provide a topographical map of this dual dysregulation and explore potential cel

270 the pre-surgical deterministic tractography map for each subject.

271 he post-operative probabilistic tractography map to the pre-surgical deterministic tractography map f

272 Transcripts mapping to these genomes increased from <0.3% of total m

273 ns were performed by building a transmission map, completed by genotyping Pneumocystis isolates and b

274 Here we performed TSS mapping of the translatome following energy stress.

275 This updating process relies on a unique mapping between each VWM representation and an actual ob

276 Using map-based cloning we positioned the her2 mutation to the

277 ars, and construct a comprehensive variation map to provide genomic insights into the divergence and

278 Here we report an apple genome variation map generated through genome sequencing of 117 diverse a

279 r-225 and Thr-227, matching previous in vivo-mapped phosphorylation sites.

280 allowing simultaneous optical pacing and Vm mapping.

281 xide, and their transcriptional activity was mapped to genomes from cells on the electrode surface an

282 n CDC Frontier and ICCV 96029, this gene was mapped to the site of a quantitative trait locus on Ca5

283 We map three cytosine variants and two adenine variants.

284 In addition, we map a region of NEMO (residues 112-150) in its coiled-co

285 near population receptive field modeling, we map and characterize the topographic organization of sev

286 Next, we map the cell states within each species and also between

287 We mapped forest cover, modeled regional precipitation, and

288 In this study, we mapped and characterized epitopes on DENV4 recognized by

289 st majority (81%) of meiotic crossovers were mapped to less than 5 kb.

290 hundred ninety-six salivary metabolites were mapped into 49 metabolic pathways and connected with hum

291 g correlations among allocation metrics were mapped, and loci related to nitrogen uptake and floral o

292 of serum immunoreactivities toward ZnT8 were mapped to its transmembrane domain that is accessible to

293 ent the first quantitative human genome-wide map of DNA lesions induced by ultraviolet (UV) radiation

294 aturation mutagenesis revealed a genome-wide map of the genetic determinants of plant root colonizati

295 lls thus provides an extensive proteome-wide map of protein ligandability and facilitates the coordin

296 Using a transcriptome-wide map of m(6)Am we find that m(6)Am-initiated transcripts

297 hmU, we develop a method for the genome-wide mapping of 5hmU-modified loci based on a chemical taggin

298 hepatocyte-like cells (HLCs) for genome-wide mapping of expression quantitative trait loci (eQTLs) an

299 At both time points the genome-wide mapping reveals that there is significant co-occupancy o

300 floral organ development were located within mapped quantitative trait loci.