ライフサイエンスコーパス: scramble

1 is function on ANO1, which normally does not scramble.

2 d treated with miR-24 inhibitor or inhibitor scramble.

3 ent noise modulation segments was temporally scrambled.

4 cyclic products are directionally uniform or scrambled.

5 mutant mice, in which neural positioning is scrambled.

6 impaired Ca(2+)-triggered phosphatidylserine scrambling.

7 insertion of loxPsym sites to enable genome scrambling.

8 een shown to be involved in Ca(2+)-dependent scrambling.

9 they are scramblases or channels regulating scrambling.

10 cyclophilin D/TMEM16F-dependent phospholipid scrambling.

11 , including Bronsted acid-catalyzed C-F/Co-C scrambling.

12 ndrome with deficient Ca(2+)-dependent lipid scrambling.

13 usly involves both Ni-H moieties without H/D scrambling.

14 nels and regulators of membrane phospholipid scrambling.

15 brane-protein interactions involved in lipid scrambling.

16 ff' = 0 [0 to 25]%, 'On' = 69 [53 to 100]%, 'Scrambled' = 28 [13 to 63]%; Friedman Chi-squared test s

17 Off' = 0 [0 to 50]%, 'On' = 69 [67 to 95]%, 'Scrambled' = 59 [42 to 95]%; Friedman Chi-squared test s

18 c with 1 except that the targeting region is scrambled (a YI-YI motif, see text), showed that 1 is co

19 We present 'Scramble': a new C implementation of SAM, BAM and CRAM f

20 tion solutions of serum and nonamyloidogenic scrambled Abeta(42-1) peptides.

21 ly members but less so in those with reduced scrambling ability.

22 ridic hydrogen (delta = -28.3 ppm) that also scrambles across the Sn(9) cluster.

23 de that scramblases exhibit Ca(2+)-dependent scrambling activity by aggregation of protein.

24 The lipid scrambling activity of protein extracts and purified scr

25 that the addition of PRD to hPLSCR2 restored scrambling activity, and deletion of PRD in hPLSCR1 (Del

26 SCR2 showed Ca(2+)-dependent aggregation and scrambling activity, whereas hPLSCR2 and DeltaPRD-hPLSCR

27 ghput gene synthesis, here we report a codon-scrambling algorithm that enables the PCR-based gene syn

28 A scrambled alphaA-crystallin peptide produced no such eff

29 lly expressed proteins upon OTA treatment in scrambled and ASK1 knockdown cells, respectively.

30 and the rate of endocytosis observed in both scrambled and ClC-5 knockdown cells were not significant

31 ectivities is a necessity to avoid disulfide scrambled and incorrectly folded forms in the final prod

32 served regions of its primary structure were scrambled and the mutations were tested for the RD3 abil

33 Deuterium scrambling and DFT calculations suggest a stepwise elect

34 This species is capable of H2/D2 scrambling and hydrogenating alkenes at room temperature

35 Deuterium scrambling and kinetic studies offer valuable facts for

36 ), provides steric protection against ligand scrambling and metal complex oligomerization and electro

37 mmalian TMEM16F, mediates simultaneous lipid scrambling and nonspecific ion transport.

38 n inverse kinetic isotope effect, fast H2/D2 scrambling and slow alkene isomerizations pointing to an

39 ase fragment ion isomers related to sequence scrambling and the underlying fragmentation mechanism, w

40 hat range from ion transport to phospholipid scrambling and to regulating other ion channels.

41 d key amino acids necessary for phospholipid scrambling and validated the idea that ions permeate TME

42 membrane induced by oxidative stress, lipid scrambling, and artificial cell aging modulate the cell

43 sin to metarhodopsin II are not required for scrambling, and that the lipid translocation pathway eit

44 d, to determine the extent of disulfide bond scrambling, and to understand why scrambling occurs, we

45 randomizing effects from vibrational energy scrambling are avoided, and excitation-energy specific r

46 We show the utility of SCRaMbLE as a novel method of combinatorial mutagenesis,

47 eptide, we show that UVPD occurs without H/D scrambling as the peptide probe accurately retains its s

48 lisinopril (100 mg/kg/d), PBS (control), or scrambled ASO (66 mg/kg/wk) for 10 wk, followed by tissu

49 onucleotides (ASOs) to knockdown Mogat1 or a scrambled ASO control for 12 weeks while remaining on di

50 Interestingly, typical regiochemical scrambling associated with the C-H activation was furthe

51 zing a (2)H-labeled silolane probe; complete scrambling at the silicon center was observed, consisten

52 ed Cu(I)Cu(II) pair; the Cu(II), however, is scrambled between the two locations within the dicopper

53 observed both while viewing coherent versus scrambled biological motion, and while listening to happ

54 Synteny analysis uncovered localized but scrambled blocks of genes in putative orthologous relati

55 ndom (CSR) background, before every point is scrambled by its localization precision.

56 Interestingly, also a scrambled CBX3 version with preserved CpG-sites retained

57 cell lines (A549 and H1437) as compared with scramble cells.

58 developed elaborate eccentricities, such as scrambled coding regions, nonstandard genetic codes, and

59 rization-sensitive OCT imaging, polarization-scrambling columns were found at the level of the RPE.

60 aluated in cells transfected with miR-29b or scramble control and treated with TGFbeta2, and the expr

61 with the single-knockdown and short hairpin scramble control groups.

62 se oligodeoxynucleotides targeting Notch3 or scramble control oligodeoxynucleotides in wild-type mice

63 obscurin short hairpin RNA (shRNA), but not scramble control shRNA, exhibit increased primary tumor

64 work (HTM) cells transfected with miR-29b or scramble control.

65 and 61% (all p<0.001), respectively, versus scrambled control and decreased COL1A1 protein by 60% (p

66 o be in the Cdc42/ciliogenesis pathway and a scrambled control morpholino showed no phenotypic effect

67 both cell types were blunted compared with a scrambled control peptide.

68 randomized to receive anti-miR-21 (KD21) or scrambled control sequence (Scr21) injections into the l

69 mals received a comparable vector encoding a scrambled control short hairpin RNA (control vector).

70 tide depletion in adult rats, CART shRNAs or scrambled control shRNAs were administered bilaterally i

71 ent regions of the rat AQP8 molecule or with scrambled control siRNA.

72 HFs with lipofectamine and CDH3-specific or scrambled control siRNAs.

73 tilized synthetic peptides for EA, EB, and a scrambled control to examine cellular responses.

74 CI, 0.30-0.36]; P = .02; mean for miR-34b vs scrambled control, 0.31 RLU [95% CI, 0.30-0.32]; P = .01

75 ase (mean luciferase activity for miR-34a vs scrambled control, 0.33 RLU [95% CI, 0.30-0.36]; P = .02

76 0.30-0.32]; P = .01; and mean for miR-34c vs scrambled control, 0.35 RLU [95% CI, 0.33-0.37]; P = .02

77 periments indicate that NoxA1ds, but not its scrambled control, binds Nox1.

78 ased baseline Tshb mRNA levels compared with scrambled control, but surprisingly had no affect on the

79 rostate cancer cell xenografts compared with scrambled controls, suggesting HIP1R is a key functional

80 scale constrictions on similar timescales as scrambled controls.

81 oron-dipyrromethene (IYIY-I2-BODIPY) and its scrambled counterpart YIYI-I2-BODIPY have been prepared.

82 unmodified or lesion-containing CRE, but not scrambled CRE or scrambled CRE with a G/U mispair, resul

83 ion-containing CRE, but not scrambled CRE or scrambled CRE with a G/U mispair, resulted in increased

84 Gly(6)-Gln(7) residues or by random sequence scrambling demonstrated a crucial role for this structur

85 V1 by natural images presented during a face/scramble discrimination task.

86 ration of the lack of a significant level of scrambled disulfide bonds are critical to ensure the app

87 disulfide linkage and the ability to detect scrambled disulfide bonds from a single experiment with

88 method capable of detecting both native and scrambled disulfide bonds has been established.

89 le and lysozyme and by the detection of four scrambled disulfide bonds in the IgG1 molecule.

90 misfolded proteins for the determination of scrambled disulfide linkages.

91 cularly useful for the identification of the scrambled disulfides.

92 mes more efficiently than controls including scrambled-DNA modified MSCs.

93 ium-labeling studies indicate that deuterium scrambling does not take place in this sp(2) -sp(3) cros

94 Peptide sequence scrambling during mass spectrometry-based gas-phase frag

95 r use in RT-PCR diagnostics: we encapsulated scrambled Ebola RNA sequences inside of tobacco mosaic v

96 owder reached 1g, it was replaced with 8g of scrambled egg, after then subsequent doses were increase

97 e top-down routine does not trigger hydrogen scrambling either during the electrospray ionization pro

98 nformation was maintained in one SF band but scrambled elsewhere.

99 urements appear to be unaffected by hydrogen scrambling, even when high collisional energies are util

100 The scrambling experiment has given hybrid macrocycles in yi

101 of the reaction were further confirmed by a scrambling experiment, involving pillar[5]arene and per-

102 Scrambling experiments and theoretical modeling support

103 to be reversible, consistent with deuterium-scrambling experiments.

104 modulate the firing rate of neurons to phase-scrambled face stimuli in any recording region.

105 inferior temporal (IT) cortex to intact and scrambled faces that were filtered to selectively preser

106 , whereas face responsivity (neutral faces > scrambled faces) and face selectivity (neutral faces > n

107 longitudinally the responsiveness to faces, scrambled faces, and objects in macaque inferotemporal c

108 ldren while viewing happy, fear, neutral, or scrambled faces.

109 Specificity tests reveal that BR scrambles fluorescent analogues of common phospholipids

110 A scrambled form of beta1a490-508 peptide was used as nega

111 bserved in the native CTX III, and 10 in its scrambled form, X-CTX III.

112 d that the peak was related to the disulfide scrambled forms and was isobaric with the correctly fold

113 g step, misfolded proteins such as disulfide scrambled forms can be formed, and purification steps ar

114 e complex, 5, was obtained through deuterium scrambling from eta(2)-D(2) in 2-d(2) into the methyl gr

115 the genetics by removing or recoding genes, scrambling gene order and replacing all non-coding DNA w

116 SCRaMbLE generates genome diversity in designated region

117 and modification by loxP-mediated evolution (SCRaMbLE) generates combinatorial genomic diversity thro

118 ncrypted genome architecture contains >3,500 scrambled genes, as well as >800 predicted germline-limi

119 duplication and an alternative processing of scrambled genes.

120 This genome assembly provides a draft of a scrambled genome and a powerful model for studies of gen

121 ng disorder caused by defective phospholipid scrambling, has been associated with mutations in the TM

122 Due to disulfide scrambling highlighted with the reduction approaches, ox

123 onses to point-light displays of coherent vs scrambled human motion.

124 face-selective response is absent for phase-scrambled images and therefore not due to low-level info

125 en category correlations for both intact and scrambled images demonstrating distinct patterns of resp

126 Participants then viewed intact and scrambled images from different object categories (bottl

127 e spatial patterns of response to intact and scrambled images from different object categories.

128 se were more distinct for intact compared to scrambled images in V3, but not in V1 or V2.

129 rithms are utilized to convert the spatially scrambled images into fluorescent images and video.

130 Our rationale for using scrambled images is that they contain the same low-level

131 However, the difference between intact and scrambled images was smaller in V3 compared to V1 and V2

132 ons are consistent with the lack of isotopic scrambling in C(16)O-(18)O(2)-(16)O(2) reactions, and wi

133 cyclization pattern due to the lack of label scrambling in double crossover experiments.

134 The absence of hydrogen scrambling in the gas phase prior to ion dissociation is

135 njected with EETI 2.5F proteins containing a scrambled integrin-binding sequence, demonstrating the i

136 e interaural level differences but presented scrambled interaural time differences with vocoded speec

137 for the two peptides, without any disulfide scrambling interference.

138 Here we show that scrambling is a constitutive activity of rhodopsin, dist

139 is asymmetry by ATP-independent phospholipid scrambling is important in cellular signaling, but its m

140 rometric conditions where gas-phase hydrogen scrambling is negligible.

141 A major consequence of Ca(2+)-dependent scrambling is the release of extracellular vesicles that

142 compare native cytotoxin 3 (CTX III) and its scrambled isomer, another category of protein mixture, f

143 cterized by cell shrinkage and cell membrane scrambling leading to phosphatidylserine (PS) externaliz

144 beta2-adrenergic and adenosine A2A receptors scramble lipids, suggesting that rhodopsin-like G protei

145 The mechanism by which opsin scrambles lipids is unknown.

146 rovide a possible mechanism for phospholipid scrambling mediated by PLSCRs and the importance of PRD

147 hat target Foxp3 and IL-17, respectively, or scrambled miR (mock) or inhibitors confirmed that these

148 ats were then treated with miR-133a mimic or scrambled miRNA.

149 oint inactivation of beta- and gamma-catenin scrambles motor neuron settling position in the spinal c

150 more reliable for the intact movie than the scrambled movie, indicating that these regions accumulat

151 rom movies containing other objects and from scrambled movies (ordinate-level categorization).

152 neous low-level properties of the intact and scrambled movies.

153 signals from individuals watching intact and scrambled movies.

154 number, and blood vessel density compared to scrambled, negative control peptides.

155 In contrast, neurons transfected with a scrambled nontargeting siRNA were indistinguishable from

156 ect classes (faces, scenes, bodies, objects, scrambled objects).

157 y respond more to intact objects compared to scrambled objects.

158 lfide bond scrambling, and to understand why scrambling occurs, we determined the disulfide bond prof

159 tion of brain Galphai(2) proteins, but not a scrambled ODN, abolished the renal sympathoinhibitory re

160 In scrambled ODN-treated rats, chronic changes in dietary s

161 ducts of deuterated retinol showed a lack of scrambling of a putative allylic radical at C-3 and C-4.

162 Rapid scrambling of axial chirality of allenyl acetates in the

163 Scrambling of halide ions between chlorofluoropyridines

164 The scrambling of halogens at the zinc carbenoid led to the

165 ements - result in a cancer genome that is a scrambling of intervals, or "blocks" of the germline gen

166 onversion of carbene and alkyne leads to the scrambling of labels over both alkynyl (sp) carbons.

167 10,000 phospholipids per protein per second) scrambling of phospholipid probes.

168 e protein, is known to mediate bidirectional scrambling of phospholipids in a Ca(2+)-dependent manner

169 Scrambling of the chromosome in a heterozygous diploid r

170 include poor pharmacodynamics and potential scrambling of the disulfide bonds in vivo.

171 serve as channels facilitating the movement (scrambling) of phospholipids between leaflets of the mem

172 tubule cell lines compared with wild-type or scrambled oligonucleotide-treated cells, respectively.

173 ble for peptides that are prone to disulfide scrambling or are unstable in solution with partly reduc

174 d to be neutral, since gene order is largely scrambled over evolutionary time.

175 gns and providing a new way to determine the scrambling patterns, which could be applied for those se

176 n, TAT-CBD3, but not CBD3 without TAT or TAT-scramble peptide, inhibited increases in cytosolic Ca(2+

177 espectively, whereas the third analogue is a scrambled peptide (Mel-SCR) that contains the amino acid

178 The ability of TAT-C24WT but not a scrambled peptide (TAT-C24Scr) to block the CaMKIIalpha-

179 membrane-delineated cAMP (tau=251+/-51 s for scrambled peptide control vs. 399+/-79 s for Ht31).

180 In vitro, compared to scrambled peptide controls, HNGF6A increased GSIS in iso

181 cross-linking, in contrast to Pep1-E396A and scrambled peptide controls.

182 dified controls or those with inclusion of a scrambled peptide domain.

183 RK motif, as an Alanine-Alanine variant or a scrambled peptide fails to reactivate plasticity.

184 We used a scrambled peptide for control.

185 ls (n = 12) were evenly split into pHBSP and scrambled peptide groups and injected daily (10 mug/kg p

186 GFR-dependent cancer cell lines, whereas the scrambled peptide is inactive.

187 actions by comparing adhesion sequences with scrambled peptide sequences.

188 inst bacterial virulence mechanisms, while a scrambled peptide showed no bactericidal activity.

189 pHBSP or scrambled peptide treatment did not alter hematocrit.

190 the presence of EGF, Disruptin, but not the scrambled peptide, inhibits EGFR dimerization and causes

191 n mutant mice injected with either saline or scrambled peptide.

192 -mer alphaA- or alphaB-crystallin-derived or scrambled peptides.

193 onclude that an engineered opsin monomer can scramble phospholipids, and that the lipid-exposed face

194 ight-sensitive photoreceptor compartment and scramble phospholipids.

195 Phospholipid scrambling (PLS) is a ubiquitous cellular mechanism invo

196 This response was weaker with a scrambled PMAP-36, relating to its lower antimicrobial a

197 multigram scale-up route for highly soluble 'scrambled' porous cages prepared from a mixture of comme

198 We also show that the codon-scrambling problem is analogous to the well-known travel

199 changes based on their specific polarization-scrambling qualities.

200 whereas no tumor uptake was observed with a scrambled radiolabeled peptide (64)Cu-NO2A-GSG-DRD-RWSWW

201 est that the mixed dinuclear Pd(III) complex scrambles readily to give the two Pd(III) homodimers [Ac

202 tch are predictive of enhancer activity; (3) scrambling repressor motifs leads to aberrant reporter e

203 he design of negative controls by permitting scrambling, reversing, complementing or introducing mult

204 HSP27 short interfering RNA (siRNA) but not scrambled RNA disrupted this association and reduced the

205 her the SGLT1 short hairpin RNA (shRNA) or a scrambled RNA sequence.

206 e.g. OnRS/miR-124, OnRS/GFP-siRNA, OnRS/Neg (scrambled RNA) and OnRS/MGA (malachite green aptamer)) w

207 ats compared with the rats injected with the scrambled RNA.

208 ing constructs: RCASBP(B)-RFP, RCASBP(B)-RFP-scrambled RNAi, or RCASBP(B)-RFP-GluA2 RNAi.

209 It catalyzes reduced RNase oxidation and scrambled RNase isomerization and insulin reduction and

210 ling responses were seen in the polarization-scrambling RPE layer, ranging from hyperproliferation to

211 hat the plasma membrane cell fate regulator, SCRAMBLED (SCM), is mislocalized in ugt80B1 mutants, und

212 ere identified by contrasting sentences with scrambled sentences, revealing a bilateral temporal lobe

213 th lentiviruses that expressed miR-26a1 or a scrambled sequence (control); proliferation and colony f

214 rgeting catenin beta 1 (CTNNB1; CTNNB1-LNP), scrambled sequence (Scr-LNP), or phosphate-buffered sali

215 plementary target sequence exceeds that of a scrambled sequence by nearly 3 orders of magnitude.

216 n reverse micelles, while an analogue with a scrambled sequence does not.

217 Mutation of the motif to a scrambled sequence resulted in complete loss of nuclear

218 eas controls were treated with a nonspecific scrambled sequence small interfering RNA.

219 Studies with D-amino acid and scrambled sequence versions of htt(NT) suggest that inhi

220 1, we overexpressed precursor miR-181c (or a scrambled sequence) in primary cultures of neonatal rat

221 t, which we call Disruptin; and one with the scrambled sequence.

222 nterference targeting of the gene Dcdc2 or a scrambled sequence.

223 cterial lung burden than mice treated with a scrambled-sequence PPMO or phosphate-buffered saline.

224 either IGCR1 CBE1 or CBE2 was replaced with scrambled sequences that do not bind CTCF.

225 The 'Scrambled' setting consisted of a random, scattered sign

226 t with the prosthesis in the 'On', 'Off' or 'Scrambled' setting presented in a randomised order.

227 Isotope scrambling shows that intramolecular rearrangement of cy

228 d with eIF5A shRNA was compared with that of scramble shRNA-transduced counterpart by the iTRAQ metho

229 aH2AX by H2O2 treatment (20 mum) subsided in scrambled shRNA but exacerbated in SelH shRNA MRC-5 cell

230 d after pretreatment with anti-Gli1 shRNA or scrambled shRNA control.

231 utathione level was lower in SelH shRNA than scrambled shRNA HeLa cells, and the H2O2-induced cell de

232 more polarized compared with cells in which scrambled shRNA is expressed.

233 migrate faster than the ones expressing the scrambled shRNA on a collagen I gel (two-dimensional) al

234 pression did not change in similarly treated scrambled shRNA transgenic kidneys, and we observed no C

235 ity behavior and matrix adhesion assembly to scrambled shRNA treated control keratinocytes.

236 c mice that express stanniocalcin-1 shRNA or scrambled shRNA upon removal of a floxed reporter (phosp

237 lk1 knockouts, as well as with a fraction of scrambled shRNAs, suggesting a sequence-dependent but no

238 Phospholipid scrambling significantly alters the physical properties

239 onalized nanoparticles loaded with siCD98 or scrambled siRNA (control) via gavage.

240 was reduced in CVB3 S100A8 knockdown versus scrambled siRNA CVB3 cells.

241 A similarly delivered amplicon for scrambled siRNA did not inhibit TLR4 or MCP-1 expression

242 e vectors did not alter sucrose intake and a scrambled siRNA vector was negative.

243 a simple random permutation of the sequence (scrambled siRNA).

244 ession in Sp1-silenced NHKs as compared with scrambled siRNA-silenced cells.

245 Sp1-silenced keratinocytes as compared with scrambled siRNA-silenced keratinocytes.

246 with BCMO1 small interfering RNA (siRNA) or scrambled siRNA.

247 24 +/- 4% max vs. 34 +/- 5% max) relative to scrambled-siRNA rabbits.

248 Scrambled siRNAs and empty lentiviral vectors were used

249 When tested in the original assay, the scrambled siRNAs showed significantly reduced activity i

250 ff, and with the system on but with randomly scrambled spatial information.

251 ter performance with normal rather than with scrambled spatial information.

252 Every SCRaMbLE strain was unique, validating the capability of

253 Deep sequencing of 64 synIXR SCRaMbLE strains revealed 156 deletions, 89 inversions,

254 H/D scrambling studies indicate that this Ag(I) complex can

255 ied TMEM16-channel homologues do not mediate scrambling, suggesting that the family diverged into cha

256 irs) or up to 2,104 "SD" mutations (randomly scrambled synonymous codons).

257 act maps to detect rearrangements induced in SCRaMbLE (synthetic chromosome rearrangement and modific

258 By both complementation assays and SCRaMbLE (synthetic chromosome rearrangement and modific

259 ically, we created a series of truncated and scrambled tau constructs and characterized the size and

260 Neural responses were higher for scrambled than intact images in all regions.

261 ssion of these factors and, thereby, lineage scrambling that is disconnected from TCR restriction by

262 rgy internal isomerization pathway which can scramble the D and H atom labels.

263 (-) lead to incorrect conclusions since they scramble the deuterium label).

264 ly underlie oncogenic transformation and can scramble the genome.

265 ctions in disordered media are well-known to scramble the information content of light by complex but

266 ttering, in which multiple scattering events scramble the recorded electron diffraction intensities s

267 Alkyne metathesis is expected to scramble the relative orientation of adjacent ester grou

268 ty to recover dynamical information, and can scramble the sequence of events.

269 We have scrambled the first six amino acids of this segment of t

270 dex distribution of biological tissue, which scrambles the incident light and destroys the optical fo

271 Proteasomal targeting was verified by either scrambling the mODC-PEST motif, or via proteasomal inhib

272 Scrambling the sequence of Lnk2 is inconsequential on ac

273 n of an object at a particular location, but scrambling the timing of the spikes over one whisking cy

274 mplications of Ca(2+)-dependent phospholipid scrambling, the extracellular vesicles associated with t

275 -react with other amyloidogenic proteins and scrambling their grafted sequences eliminates antibody r

276 Scrambling these six amino acids markedly reduces EGFR s

277 The increase in polarization-scrambling tissue over the course of 3 months indicates

278 ain was unique, validating the capability of SCRaMbLE to explore a diverse space of genomes.

279 ents, regulators, and dialysis organizations scramble to keep up with the frequent release of wide-ra

280 We applied SCRaMbLE to yeast synthetic chromosome arm synIXR (43 re

281 Adapting videos that were scrambled to remove recognizable human figures or cohere

282 Hep3B alpha3-positive, but not wild-type and scramble transfected, cells acquired protection by soraf

283 feration of ECs that occurred within 24 h in scrambled-transfected controls.

284 nd cellular senescence markers compared with scrambled treated controls.

285 g only two heavy chains, generated much less scrambling under the same heat-stressed conditions.

286 is difficult because spatial information is scrambled upon propagation.

287 ll proliferation compared with mock and pSV (scrambled vector) treatments, as determined by 5-bromo-2

288 al-life auditory narrative and to temporally scrambled versions of the narrative.

289 Pictures of faces and houses, scrambled versions of these pictures, and pictures of bu

290 ly support the mechanism of peptide sequence scrambling via b ion cyclization, and provide the first

291 range of nonvocal control sounds, including scrambled voices, environmental noises, and animal cries

292 CO scrambling was observed using (13)C labeled CO, and exch

293 The preferred sites of scrambling were identified, such as the intrachain disul

294 butene cis-trans isomerization and H(2)/D(2) scrambling were shown to be catalyzed by MoS(2) and WS(2

295 Mosaicization and scrambling were used to produce degraded versions of the

296 teins and via TMEM16F-dependent phospholipid scrambling with an assistant role of mPTP formation.

297 cterized by cell shrinkage and cell membrane scrambling with phosphatidylserine (PS) exposure.

298 In vitro, ZIP and scrambled ZIP inhibited PKM-zeta, PKC-iota and PKC-zeta

299 ort that ZIP as well as its inactive analog, scrambled ZIP, induced a dose-dependent increase in spon

300 ort that ZIP as well as its inactive analog, scrambled ZIP, induced a dose-dependent increase in spon