ライフサイエンスコーパス: probing

1 ed by primer extension (SHAPE) RNA structure probing.

2 an those recommended for reliable structural probing.

3 within cells, as determined by intracellular probing.

4 ters including probing depth and bleeding on probing.

5 s between in silico prediction and structure probing.

6 ing, cryo-electron microscopy and structural probing (16) .

7 Probing 372 single nucleotide polymorphisms (SNPs) in 63

8 Probing a custom-designed proteome microarray with sera

9 materials, which offer a novel platform for probing a distinct type of spin-Fermion interaction.

10 comb spectroscopy to shorter wavelengths by probing a transition frequency in a trapped Mg+ ion usin

11 rprisingly, a widely used small molecule for probing aggregation reactions, thioflavin T (ThT), was f

12 frared laser pulses through atmospheric air, probing air dispersion in the 3.6-4.2-mum wavelength ran

13 g and processing information, and ultimately probing and controlling behaviour at the quantum level.

14 associated with increased extent bleeding on probing and levels of microorganisms Porphyromonas gingi

15 This approach provides an opportunity for probing and manipulating cellular functions that cannot

16 antly improves experimental capabilities for probing and manipulating exciton dynamics of atomically

17 the broader use of 2-aza-Cope reactivity for probing and manipulating FA biology.

18 these events through dimethyl sulfate (DMS) probing and mutational profiling.

19 tools, both small molecule and genetic, for probing and perturbing the assembly of the Corynebacteri

20 at induction minus baseline) for bleeding on probing and probing depth (PD), the patients were separa

21 , including full-mouth, six-site periodontal probing, and attachment loss assessment.

22 pid progress in RNA structure determination, probing, and biophysical studies, the past decade has se

23 clinical attachment level (CAL), bleeding on probing, and plaque index were measured, and subgingival

24 unoprecipitation, fluorescein isothiocyanate-probing, and surface plasmon resonance analysis.

25 This is important for tailoring, probing, and understanding spin and electron dynamics in

26 fferent delivery platforms for intracellular probing as well as novel MB designs for detecting a vari

27 the limitations of current methodologies for probing auxin.

28 ed 3D and 2D motion analysis to quantify the probing behavior of the fruit-fly parasitoid Diachasmimo

29 Here, we propose a novel technique for probing biomolecular structure based on the changes in p

30 dontitis, and the combination of bleeding on probing (BOP) and clinical attachment loss (CAL) was est

31 es were percentage of teeth with bleeding on probing (BOP) and combination of BOP and attachment loss

32 ith probing depth (PD) >4 mm and bleeding on probing (BOP) at 12 months post-therapy.

33 clinical attachment level (CAL), bleeding on probing (BOP), and plaque index were measured at four si

34 g depth (PD), plaque index (PI), bleeding on probing (BOP), mucosal redness (MR), suppuration (SUP),

35 index (PI), gingival index (GI), bleeding on probing (BOP), PD, gingival crevicular fluid (GCF) volum

36 Full-mouth plaque index (PI), bleeding on probing (BOP), probing depth (PD) >/=4 mm, and clinical

37 Periodontal examinations of bleeding on probing (BOP), probing depth (PD), and clinical attachme

38 g pocket depth (PD) >/=5 mm with bleeding on probing (BOP).

39 ket during PMT with a history of bleeding on probing (BOP).

40 probing depth (PD) >/=5 mm with bleeding on probing (BOP).

41 que index; 2) gingival index; 3) bleeding on probing (BOP); 4) probing depth; and 5) attachment loss

42 index [PI], gingival index [GI], bleeding on probing [BOP], and clinical attachment level) and photog

43 e parameters (plaque index [PI], bleeding on probing [BOP], and probing depth [PD] >/=4 mm) and crest

44 in evenly spaced nucleosomes, which requires probing both sides of the nucleosome, yet the way remode

45 at BEN mapping may provide a useful tool for probing brain mechanisms related to smoking.

46 esearch to move from its original domain, of probing bulk media, to imaging biological tissues and si

47 optogenetics, has created new frontiers for probing causal dependencies in neural and behavioral sta

48 equencing offers a promising opportunity for probing cell types mediating specific behavioral functio

49 l-defined initiation of interactions enables probing cellular responses from the very onset, permitti

50 the method offers a possibility of directly probing charge-density distributions at interfaces betwe

51 ciated with deficits in performance on tasks probing cognitive control (Stroop task) and working memo

52 Structure probing coupled with high-throughput sequencing could re

53 ew complementary approaches - stable isotope probing coupled with nanoscale secondary ion mass spectr

54 earcher to easily locate, view, and retrieve probing data for a given RNA molecule.

55 In 110 adults, pretreatment probing data identified 486 sextants with PSR scores of

56 increased GCF-IL-1beta levels, and extent of probing depth >/=4 mm (P </=0.05).

57 laque index (PI), bleeding on probing (BOP), probing depth (PD) >/=4 mm, and clinical attachment loss

58 defined as radiographic bone loss of > 2 mm, probing depth (PD) >/=5 mm with bleeding on probing (BOP

59 one infrabony defect >/=3 mm in depth with a probing depth (PD) >/=6 mm were randomly treated with EM

60 tential predictors of at least one site with probing depth (PD) >4 mm and bleeding on probing (BOP) a

61 Probing depth (PD) and bleeding on probing were measured

62 egistration at six sites per tooth including probing depth (PD) and clinical attachment level (CAL).

63 cation as well as continuous measurements of probing depth (PD) and clinical attachment loss (AL).

64 therapy has been shown to reduce periodontal probing depth (PD) and local inflammatory mediators in g

65 Fourteen patients having sites with residual probing depth (PD) of at least 5 mm and 2 mm loss of cli

66 Greater mean probing depth (PD) reduction and greater mean gain in re

67 eta-analyses were performed for defect fill, probing depth (PD) reduction, and clinical attachment le

68 single-mask, randomized, controlled study if probing depth (PD) was </=3 mm and attachment loss was <

69 er 6 months were: 1) gingival index (GI), 2) probing depth (PD), 3) clinical attachment level (CAL),

70 l examinations of bleeding on probing (BOP), probing depth (PD), and clinical attachment level (CAL)

71 us bleeding index (mSBI), plaque index (PI), probing depth (PD), and clinical attachment level (CAL).

72 (PI), modified sulcus bleeding index (mSBI), probing depth (PD), and clinical attachment level (CAL).

73 (PI), modified sulcus bleeding index (mSBI), probing depth (PD), clinical attachment level (CAL), and

74 Probing depth (PD), clinical attachment level (CAL), and

75 Periodontal parameters including probing depth (PD), clinical attachment level (CAL), ble

76 At baseline, probing depth (PD), clinical attachment level (CAL), ble

77 included width of keratinized tissue (KTw), probing depth (PD), clinical attachment level (CAL), cli

78 Clinical and radiologic parameters such as probing depth (PD), clinical attachment level (CAL), IBD

79 linical and radiologic parameters, including probing depth (PD), clinical attachment level (CAL), IBD

80 re evaluated: gingival bleeding index (GBI), probing depth (PD), myeloperoxidase (MPO) activity, alve

81 clinical analyses were carried out including probing depth (PD), plaque index (PI), bleeding on probi

82 re analyzed, and clinical parameters such as probing depth (PD), relative clinical attachment level (

83 laque index, modified sulcus bleeding index, probing depth (PD), relative vertical attachment level (

84 minus baseline) for bleeding on probing and probing depth (PD), the patients were separated into hig

85 EGF-A, and TNF-alpha levels with periodontal probing depth (PD).

86 cal documentation included the following: 1) probing depth (PD); 2) keratinized tissue width (KT); 3)

87 index; 2) modified sulcus bleeding index; 3) probing depth (PD); 4) relative clinical attachment leve

88 e index [PI], bleeding on probing [BOP], and probing depth [PD] >/=4 mm) and crestal bone loss (CBL)

89 at three representative sites, one healthy (probing depth [PD] </=3 mm) and two diseased (PD >/=6 mm

90 ing index [PBI]); and 3) periodontal status (probing depth [PD], attachment loss [AL]).

91 Clinical data (probing depth [PD], plaque index [PI], gingival index [G

92 omplete examinations (plaque/gingival index, probing depth [PD], vertical clinical attachment level [

93 nation; and 5) clinical parameters including probing depth and bleeding on probing.

94 ials should be analyzed according to initial probing depth and characteristics of the treated sites,

95 Probing depth and clinical attachment loss (AL) were rec

96 ever, the CLM group presented lower means of probing depth for pockets >/=7 mm at 6 months (4.0 +/- 1

97 s the first to use photoacoustic imaging for probing depth measurements with potential implications t

98 tool for periodontal examinations, including probing depth measurements, but is limited by systematic

99 The outcome measure was improvement in probing depth of >/=2 mm.

100 ddition to a significant attachment gain and probing depth reduction, adjunctive use of a CTG to a bu

101 mplete periodontal examination consisting of probing depth, bleeding on probing, tooth mobility, ging

102 dontal status was assessed by measurement of probing depth, clinical attachment level, and extent and

103 Recession height, probing depth, clinical attachment level, and keratinize

104 Samples were obtained first, with probing depth, clinical attachment level, bleeding on pr

105 dontal clinical parameters recorded included probing depth, clinical attachment level, plaque index,

106 periodontal parameters: bleeding on probing, probing depth, clinical attachment loss, and plaque inde

107 ival index; 3) bleeding on probing (BOP); 4) probing depth; and 5) attachment loss (AL).

108 ed plaque accumulation, bleeding on probing, probing depths (PDs), and clinical attachment loss.

109 l attachment levels (CALs; primary outcome), probing depths (PDs), plaque, and BOP also were recorded

110 ere treated with the contrast agent, and the probing depths were measured with novel photoacoustic im

111 sound for high-spatial resolution imaging of probing depths.

112 strating a change of >/=1 mm, and changes in probing depths.

113 PSCs have become an important tool for probing developmental questions, while differentiated ce

114 K, was investigated using DNA-Stable Isotope Probing (DNA-SIP).

115 mensional diffusion to search for telomeres, probing each telomere thousands of times each S-phase bu

116 iquitin ligases proved remarkably useful for probing enzyme mechanism and modulating E3 activities in

117 yloid assembly, we performed single-molecule probing experiments to measure interactions between hair

118 nd potential of transcriptome-wide structure probing experiments.

119 synthesized and examined in vitro by in-line probing for the formation of G-quadruplex structures.

120 hlighting the potential of TAL effectors for probing fundamental aspects of plant transcription.

121 ubstrate binding, representing an example of probing gas-amide binding interactions by such experimen

122 in vivo RNA proximity ligation method toward probing global sRNA interactions with their targets in P

123 Our results highlight the importance of probing how mechanochemistry functions in vivo.

124 visual system has become a premier model for probing how neural diversity is generated during develop

125 illustrate the usefulness of nanomechanical probing in nanolayer/nanolayer or nanolayer/substrate in

126 Mouse genetics combined with pharmacological probing in vivo and in vitro demonstrate that MMP-2 exte

127 Probing initial interactions at the interface of hybrid

128 me, would enable high-density nanomechanical probing inside materials.

129 uptake in the sarcoplasmic reticulum, and by probing its dynamical activation upon phosphorylation.

130 oscopy and first-principles calculations for probing Li-ion intercalation in zero-strain electrodes,

131 y, structural priming is a valuable tool for probing linguistic representation.

132 By combining electrical probing measurements, atomic force microscopy (AFM), and

133 xperiments and aid in interpreting the SHAPE probing measurements.

134 tential of (1)H HR-MAS as a rapid method for probing metabolomic profiles and compositional changes d

135 ChemModSeq, a high-throughput RNA structure probing method, to quantitatively measure changes in RNA

136 Using a high-throughput RNA structure probing method, we provide nucleotide resolution insight

137 be newly developed genome-wide RNA structure-probing methods and synthesize the information emerging

138 High-throughput RNA structure chemical probing methods generate millions of sequencing reads to

139 oscopy, or in vivo crosslinking and chemical probing methods.

140 small-molecule compounds to mitochondria for probing mitochondria function, as diagnostic tools and p

141 nsitivity and potential of this technique in probing molecular excitations and photochemistry.

142 tages, which include a high selectivity when probing molecule-surface interactions, the possibility o

143 ule-surface interactions, the possibility of probing molecules at low concentrations due to the stron

144 om 600 cm(-1) to 4500 cm(-1), sufficient for probing most vibrational Raman transitions.

145 our system guides a patient through an exact probing motion that precisely matches the palpation moti

146 report that LSPR sensors are also capable of probing nanoscale ( approximately 1 nm) variations in th

147 s, show the high potential of these dyes for probing nanoscale membrane heterogeneity.

148 course of development.SIGNIFICANCE STATEMENT Probing naturally occurring reciprocal copy number varia

149 xosome and virus detection and analysis, and probing nucleic acid conformations and binding interacti

150 n contrast, real-time control allows dynamic probing of biological systems with perturbations that ar

151 arge dating based on direct, non-destructive probing of chronometric information.

152 The successful probing of differences in chromatin compaction suggests

153 e soft X-ray regime above 200 eV, permit the probing of electronic excitation, chemical state, and at

154 analysis technology enables high-throughput probing of many protein-lipid interactions among blood-c

155 rogen-vacancy (NV) color centers enables the probing of nanoscale ensembles down to approximately 30

156 Optical trapping allows noninvasive probing of piconewton forces and thus emerged as a promi

157 In addition to rejection, probing of T and B cell fate in vivo provides insights i

158 This method, called RNA sequential probing of targets (SPOTs), provides an accurate, flexib

159 surface phenomena, which has restricted the probing of the dynamic volumetric domain morphology in o

160 In-line probing of the full-length T-box combined with molecular

161 tative high-resolution chromatin mapping and probing of the local chromatin environment.

162 In this work, the direct probing of the polarization charge at the nanoscale is d

163 bsequent momentum- and spin-resolved in situ probing of the SOC band structure and eigenstates.

164 Mechanical probing of transverse sections of M x giganteus stems an

165 The on-chip glycan modification and probing (on-chip GMAP) method provides a platform for an

166 inity of a chemical series by systematically probing one of its exit vectors is a medicinal chemistry

167 antages that can reduce sensitivity, such as probing only a small percentage of the nanoprobes presen

168 icted for topological crystalline insulators.Probing optical and transport properties of the surface

169 This strategy could be used for probing other aspects of the photoreactivity of the H-cl

170 bREC and probing parameters were assessed at presurgery and 6 mon

171 Probing path-dependent rheological changes constitutes a

172 nd has emerged as the preferred modality for probing peripheral nerves.

173 epth, clinical attachment level, bleeding on probing, plaque index scores, and keratinized tissue wid

174 Probing plasma from 500 subjects with a smaller subset o

175 percentage of sites (0%, <30%, >/=30%) with probing pocket depth (PD) >/=4 mm, and NAFLD status was

176 defined as radiographic bone loss of >2 mm, probing pocket depth (PD) >/=5 mm with bleeding on probi

177 clinical periodontal parameters: bleeding on probing, probing depth, clinical attachment loss, and pl

178 ed included plaque accumulation, bleeding on probing, probing depths (PDs), and clinical attachment l

179 spectroscopy offers temporal resolution for probing processes in the femto- and picosecond regimes.

180 ion strategies for applications ranging from probing protein function to antibody-drug conjugates and

181 In this context, methods for probing protein-protein interfaces at atomic resolution

182 s (sPREs) proved to be a powerful method for probing protein-protein interfaces in large complexes in

183 ) for deriving protein 3D structures and for probing protein/protein interactions has largely increas

184 g transmission electron microscopy and X-ray probing proved the presence of <110> Sr columns located

185 spectroscopy, coupled with deuterium isotope probing (Raman-DIP), provides a culture-independent and

186 ch, so called Raman Deuterium Stable Isotope Probing (Raman-DIP), was developed to identify AMR bacte

187 via Raman spectroscopy based stable isotope probing (Raman-SIP) using a single and double labeling a

188 structurally mapping their TMT reactions and probing relative stabilities of metalated fluoroaromatic

189 ng reward anticipation, and a go/no-go task, probing response inhibition, on two occasions, in the pr

190 performed the monetary incentive delay task, probing reward anticipation, and a go/no-go task, probin

191 used as the input, highlighting the value of probing signaling networks at intermediate nodes to deco

192 this proof-of-concept study, stable isotope probing (SIP) was used to identify microorganisms from a

193 DNA stable isotope probing (SIP) was used to identify the bacterial guilds

194 ology and should be generally applicable for probing size-related genotype-phenotype relationships.

195 Here, we demonstrate the feasibility of probing specific water-protein chemical exchange in memb

196 In part, this is because probing spindle mechanics in live cells is difficult.

197 xes, which we validate biochemically, and by probing structurally predicted, disruptive, genetic vari

198 Directly probing structure dynamics at metal/oxide interfaces has

199 d with PDE6 represents an effective tool for probing structure-function relationships of AIPL1 and re

200 ate) (ABTS) and 17beta-estradiol (E2) as the probing substrates.

201 tural modeling, as supported by experimental probing, suggested that resulting intraluminal hydrogen

202 te pairs, qRT-PCR and in vitro RNA structure probing supported both shared expression and shared stru

203 timulation of SOs is an easy-to-use tool for probing SWS functions, and might also bear the potential

204 e and recent variant and provide a means for probing T-cell receptor cross-reactivity.

205 Existing research probing task-related reconfiguration of brain network st

206 A wide range of molecular probing technologies involving real-time polymerase chai

207 Here, we introduce a method for probing the absolute concentrations of proteins, RNA and

208 d nanoparticle growth in aqueous solution by probing the acoustic vibrations with four-wave mixing.

209 Thus, by probing the actions of microbial beta-glucuronidases, an

210 s from colloidal SERS were more sensitive in probing the aggregation of AuNS-SCARB2 for detecting the

211 Probing the array with several glycan-binding proteins u

212 not only provides an important platform for probing the atomic-level understanding of the fundamenta

213 Studies probing the basis of this link have been contradictory r

214 y isogenic virus-free lines enabling studies probing the biological role of trypanosomatid viruses.

215 viding, to our knowledge, a new platform for probing the biomechanics of red blood cells.

216 first study describing ToF-SIMS imaging for probing the brain-wide accumulation of supplemented Li i

217 een used in mendelian randomisation analyses probing the causal association between obesity and its m

218 ion (EBS) complements neural measurements by probing the causal relationship between brain and percep

219 se of tissues by stripping antibodies and re-probing the cerebellum.

220 port the development of molecular assays for probing the characteristics of a disease.

221 tes with optical tweezers and simultaneously probing the chromophore with fluorescence.

222 p FRET anisotropy imaging and demonstrate by probing the dynamics of NMDA receptor ion channel and ki

223 ty suggests that caution should be used when probing the effect of myoVin-1 on myosin-5-dependent tra

224 ll lacking due to the difficulty of directly probing the electrochemical interface.

225 nt a promising material platform for in-situ probing the electrochemical processes, and could open up

226 offer a convenient, contactless approach to probing the electronic properties of low-dimensional cha

227 An important consideration when probing the function of any neuron is to uncover the sou

228 of the family, together with analogues, for probing the functional role of the pseudaminic acids and

229 Tn-Seq is an experimental method for probing the functions of genes through construction of c

230 Probing the genome-wide mechanisms by which this occurs,

231 ming self-assembly chemistries and processes.Probing the growth pathways of quasicrystalline material

232 y by SERS and LSPR scattering are useful for probing the identity and structure of the surface specie

233 stic mass and heat transport in the process, probing the impact of various membrane parameters and sy

234 Probing the importance of CD38 further, we created HL-60

235 a mesoscopic TiO2 film, we have succeeded in probing the influence of electrochemical bias on the cha

236 By probing the infrared spectroscopic signatures and cataly

237 ured to expose particular surface sites, but probing the intrinsic activity of these sites is often b

238 hereby the transient states, while optically probing the level of molecular assembly by Forster reson

239 While advances have been made in probing the magnetic properties of d-shell impurities on

240 pinning potential at the junction and allow probing the magnetization locally.

241 d small- and wide-angle X-ray scattering for probing the material ordering on the micrometer scale, a

242 ditionally lays a foundation for experiments probing the mechanics of individual channels.

243 ynamic method should be especially useful in probing the mechanisms of transporters with available st

244 Probing the mechanistic details of their operation at th

245 activation, serving as a valuable system for probing the mechanistic features of Mn C-H bond activati

246 ere we move beyond transport measurements by probing the microwave response of a magnetised disk of C

247 Probing the oculomotor circuits with these decision-irre

248 Here, we introduce a method for probing the optical properties of two-dimensional materi

249 Probing the origin of binary black hole mergers will be

250 Unfortunately, present-day methods for probing the performance of third-order nonlinear optical

251 We demonstrate a method for probing the properties of 2D materials via nanometer-sca

252 Probing the receptor for ubiquitination using biolumines

253 DX/MS thus represents a promising avenue for probing the relationship between enzyme dynamics and cat

254 By probing the relationship of construct size and induction

255 Hi1a is a powerful pharmacological tool for probing the role of ASIC1a in acid-mediated neuronal inj

256 gment-based drug discovery campaign involves probing the SAR around one or more fragment hits.

257 By probing the sensitivity of each nucleotide in oncomiR-1

258 cience, including competitive advantages for probing the shape properties of adsorbed, nanoscale biol

259 derstand this process, techniques capable of probing the solvated state are consequently required.

260 on and design of future experiments aimed at probing the spontaneous knotting of biopolymers.

261 o develop relevant supramolecular chemistry, probing the strong affinity of the inner and outer faces

262 tility of ion mobility mass spectrometry for probing the structure and dynamics of heterogeneous prot

263 ing patient data is an effective approach to probing the structure/function relationship of NMDARs.

264 Their small size offers the possibility of probing the superfluid on scales comparable to, and belo

265 high-pressure muon-spin rotation experiments probing the temperature-dependent magnetic penetration d

266 Recent experimental progress in probing the thermopower (Seebeck effect) of molecular ju

267 Probing the time evolution of the electronic and structu

268 microscopy, and finite-element modeling for probing the tooth's mechanical properties, spatially res

269 ted, this study emphasizes the importance of probing the toxicity of ENM mixtures under environmental

270 come among the most promising strategies for probing the underpinnings of human health and disease.

271 The ionization state is determined by probing the vibrational signatures of the carboxylic aci

272 mputational study of 134 different quinones, probing their 1 e(-) reduction potentials, pKa values, a

273 lexibility of ncRNA provides a challenge for probing their complex 3D conformational landscape, both

274 e, this is the most relevant environment for probing their function.

275 However, probing their functions at the cellular level typically

276 tailored for characterizing biomaterials and probing their interactions with biological tissues.

277 lasmonic molecules of varying complexity and probing them at the individual plasmonic molecule level,

278 derstand intrinsic defects in materials, but probing them collectively over large area remains nontri

279 dy, primarily due to technical challenges in probing these materials in situ.

280 Probing these systems on a microscopic level with single

281 tions on the low microsecond time scale when probing these types of interactions.

282 s the applicability of Raman spectroscopy to probing thin, highly diffusely scattering layers such as

283 Instrumentation for probing this interface is limited.

284 Probing this quantity could provide insight into materia

285 lume are homogeneous and constant during the probing time.

286 measurements and single-cell stable isotope probing to demonstrate that ANME in deep-sea sediments c

287 t becomes necessary to ensure that such cell-probing tools do not themselves harm cells through compl

288 ion consisting of probing depth, bleeding on probing, tooth mobility, gingival index, and plaque inde

289 in this area because of their advantages in probing transcriptional and posttranscriptional control

290 upport the use of human neuronal systems for probing transcriptional responses to physiological stimu

291 Further, it is capable of probing very small changes in conformation, making it co

292 nvolved experimental techniques with similar probing volumes, whereas the potential of utilizing tech

293 o-dimensional (1)H-(13)C correlation spectra probing water (1)H polarization transfer to the peptide

294 f bound water and provide a new approach for probing water interactions with lignocellulose materials

295 There exists very little experimental data probing WDM states at the atomic level to test current m

296 ylation by primer extension (SHAPE) chemical probing, we show that splicing yields distinct local 5'-

297 er cent) probability, indicating that we are probing well within the reionization epoch of the Univer

298 Probing depth (PD) and bleeding on probing were measured at six sites per tooth.

299 bits an extraordinary lifestyle, and further probing will answer exciting basic microbiological and c

300 Stable isotope probing with 99% (13) C-CO2 was applied to trace (13) C-