ライフサイエンスコーパス: scramble

1 deuterium labels along the peptide (hydrogen scrambling).

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

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

4 ent noise modulation segments was temporally scrambled.

5 mutant mice, in which neural positioning is scrambled.

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

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

8 nels and regulators of membrane phospholipid scrambling.

9 brane-protein interactions involved in lipid scrambling.

10 insertion of loxPsym sites to enable genome scrambling.

11 ions (i.e., b/y ions) exhibit extensive H/D scrambling.

12 obular conformation and suppressed disulfide scrambling.

13 4) ions from ubiquitin exhibit extensive H/D scrambling.

14 rane expansion in parallel with phospholipid scrambling.

15 elationship between ion conduction and lipid scrambling.

16 bation time; it is accompanied by fast lipid scrambling.

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

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

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

20 One of the most radical is SCRaMbLE, a system of inducible in vivo deletion and rea

21 imental LLPS data on the wild-type, a charge-scrambled, a phenylalanine-to-alanine (FtoA), and an arg

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

23 Mutations in the pore reduce scrambling activity and yield markedly smaller autophago

24 Cells lacking TMEM16F-dependent lipid scrambling activity are deficient in generation of extra

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

26 Our study further implicates TMEM16K lipid scrambling activity in endosomal sorting at these sites.

27 The lipid scrambling activity of protein extracts and purified scr

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

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

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

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

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

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

34 require both TMEM16F-dependent phospholipid scrambling and calcium influx, as a kinetic assay to inv

35 Deuterium scrambling and DFT calculations suggest a stepwise elect

36 and EGCG on inhibiting TMEM16F phospholipid scrambling and discourage the use of these polyphenols a

37 Scrambling and entanglement can reconcile seemingly unre

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

39 Deuterium scrambling and kinetic studies offer valuable facts for

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

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

42 o not generally discriminate between quantum scrambling and ordinary decoherence.

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

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

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

46 ing for their interdependency in relation to scrambling and transmission efficiency.

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

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

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

50 into a single peak over time, suggestive of scrambling, and the effect of the channel on the transbi

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

52 Two separate grading sets consisting of scrambled, anonymized SS-OCTA and FA images were created

53 e stage, an absence of corneal epithelium, a scrambled appearance of the anterior stroma and a hetero

54 icrobial attack), can help misconstrue lipid scrambling as the action of proteins or peptides, when i

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

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

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

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

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

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

61 servations are likely the result of isotopic scrambling between transiently produced carbonyl-contain

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

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

64 a path to experimental use FOTOCs to explore scrambling, bounds on quantum information processing and

65 ional assays showing severely impaired lipid scrambling, but robust channel activity by L302A.

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

67 maller autophagosomes, indicating that lipid scrambling by ATG9A is essential for membrane expansion.

68 SCRaMbLE can yield strains with improved biosynthetic ph

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

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

71 H(2)(18)O) exhibited significant (16)O/(18)O scrambling, characteristic of a redox mechanism.

72 lated primary auditory neurons to generate a scrambled cochleotopic projection.

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

74 owing intact-face previews compared with the scrambled condition.

75 The fast-scrambling conjecture is that the time to thoroughly mix

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

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

78 tering oxygen consumption rate compared with scramble control.

79 tering oxygen consumption rate compared with scramble control.

80 erated by CRISPR-based gene editing compared scramble control.

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

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

83 nd non-polypoid lesions by comparison with a scrambled control peptide.

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

85 al and histological endpoints, compared with scrambled control-treated IL-15 transgenic CTCL mice.

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

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

88 The C4S-binding peptides, but not their scrambled counterparts, when added to cultures of mouse

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

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

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

92 Complete assignments of native and scrambled disulfide linkages of insulin, alpha-lactalbum

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

94 ically, we removed 62 genes of which 45 were scrambled due to misassembly in the reference.

95 ly, a/x and c/z ions have also undergone H/D scrambling due to UV-induced heating of the precursor io

96 considered as a competition in which neurons scramble during a critical selection period for integrat

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

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

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

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

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

102 s (FOTOCs) can elucidate connections between scrambling, entanglement, ergodicity and quantum chaos (

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

104 The scrambling experiment has given hybrid macrocycles in yi

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

106 Scrambling experiments and theoretical modeling support

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

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

109 oveated face under three preview conditions: scrambled face, incongruent face (different identity fro

110 f one's own face, another female face, and a scrambled face.

111 ter a congruent-face preview compared with a scrambled-face preview.

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

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

114 ircuit that provides a positive test for the scrambling features of a given unitary process(5,6).

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

116 a detailed investigation of the level of H/D scrambling for all fragment ion types upon UVPD of the p

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

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

119 Using this rule, we were able to reduce scrambling from 75% to below 5% on average using the hig

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

121 SCRaMbLE generates genome diversity in designated region

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

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

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

125 t, providing an unambiguous test for whether scrambling has occurred, while simultaneously measuring

126 mesityl-borenium cation, which isotopically scrambles HD.

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

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

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

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

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

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

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

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

135 n response to scenes and faces compared with scrambled images was measured.

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

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

138 -irradiation of ubiquitin did not induce H/D scrambling in the nonfragmented precursor ion population

139 ormations resemble their counterparts of the scrambling-incompetent anion channel mTMEM16A, yet with

140 t, and enable us to experimentally bound the scrambling-induced decay of the corresponding OTOC measu

141 ane permeabilization, blebbing, phospholipid scrambling, inflammasome activation, and IL-1beta releas

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

143 m CO(2) and that electrochemical nanocrystal scrambling is an avenue toward creating such catalysts.

144 e direct experimental measurement of quantum scrambling is difficult, owing to the exponential comple

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

146 Quantum scrambling is the dispersal of local information into ma

147 Scrambling is the process by which information stored in

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

149 One way to characterize quantum scrambling is to measure an out-of-time-ordered correlat

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

151 of buckling modes that reorient the head and scramble its extensile trajectory.

152 rdioprotective as GLP-1 and was abolished by scrambling its amino acid sequence.

153 83%), TNFA (by 77%), and PI3 (by 65%) versus scrambled L-SNA and vehicle controls (all P < 0.001).

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

155 orrelation function (OTOC); however, because scrambling leads to their decay, OTOCs do not generally

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

157 The mechanism by which opsin scrambles lipids is unknown.

158 direct experimental evidence of an isotopic scrambling mechanism.

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

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

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

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

163 This implies that lipid scrambling must be considered a possible mode of action

164 ion, we designed a series of linker sequence scrambling mutants to suppress potential complex interpl

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

166 containing bodies, faces, objects, scenes or scrambled objects, and static pictures from the beginnin

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

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

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

170 measurements after lipid exchange and after scrambling of asymmetry.

171 Rapid scrambling of axial chirality of allenyl acetates in the

172 Scrambling of halide ions between chlorofluoropyridines

173 Detergent-induced lipid scrambling of liposomes mimicking the charge asymmetry o

174 10,000 phospholipids per protein per second) scrambling of phospholipid probes.

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

176 Scrambling of the chromosome in a heterozygous diploid r

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

178 ndicator for the occurrence of extensive H/D scrambling of the precursor ion population.

179 ias-induced rapid fusion or "electrochemical scrambling" of Cu NPs creates disordered structures intr

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

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

182 parison with Match oligonucleotides, (111)In-Scramble or (111)In-Mismatch oligonucleotides demonstrat

183 th high potency, which was not observed with Scramble or Mismatch oligonucleotides.

184 complementary (Match) and noncomplementary (Scramble or Mismatch) to hTR were conjugated to diethyle

185 in levels in MC3T3-E1 cells transfected with scrambled or protein kinase B (Akt) small interfering RN

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

187 TA and EGCG do not inhibit the phospholipid-scrambling or ion conduction activities of the dual-func

188 d then presented a novel set of objects in a scrambled order.

189 in NAT1-modified cell lines compared to the Scrambled parental cell line.

190 zed by profound epigenetic changes including scrambled patterns of DNA methylation, deregulated histo

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

192 We used a scrambled peptide for control.

193 t surgery, the Cx43 mimetic peptide Gap27 or scrambled peptide, were administered via osmotic minipum

194 -dependent and saturable manner, whereas the scrambled peptides showed highly reduced or no binding t

195 ing our scattering experiments, we identify 'scrambles' (periods of time in which no pairwise binarie

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

197 ight-sensitive photoreceptor compartment and scramble phospholipids.

198 Here we find that ATG9A scrambles phospholipids of membranes in vitro.

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

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

201 Now, vertex-functionalized amorphous scrambled porous organic cages (ASPOCs) have been utiliz

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

203 mbly behavior in a predictable manner, while scrambling primary sequence has little effect on PrLD as

204 fragment ion types upon UVPD of the peptide scrambling probe P1 (HHHHHHIIKIIK) using an Orbitrap tri

205 bling-sensitive quadruply charged P1 peptide scrambling probe resulting in a minor 33% transmission l

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

207 s thus a concentration window in which lipid scrambling proceeds without leakage.

208 We engineer quantum scrambling processes through a tunable three-qubit unita

209 It scrambles relationships between individuals: encrypted g

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

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

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

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

214 s one- and two-base mismatches (1MM, 2MM) or scrambled (SCR) sequences was highlighted and the applic

215 ectivity towards one base mismatch (1-MM) or scrambled (SCR) sequences was obtained.

216 75% to below 5% on average using the highly scrambling-sensitive quadruply charged P1 peptide scramb

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

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

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

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

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

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

223 culature) than control DPSCs transduced with scrambled sequences.

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

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

226 ls observed in wild-type mice receiving AAV8-scrambled short hairpin RNA (shSCR).

227 To minimize H/D scrambling, short UV-irradiation time and high gas press

228 Isotope scrambling shows that intramolecular rearrangement of cy

229 ced diabetic C57BL/6 mice were injected with scramble shRNA and PRR shRNA and followed for a period o

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

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

232 mination in the zebrafish eye as compared to scrambled shRNA control (p = 0.0005).

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

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

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

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

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

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

239 Phospholipid scrambling significantly alters the physical properties

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

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

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

243 cted by TNF-alpha, whereas NPSCs loaded with scrambled siRNA do not cause the predicted changes.

244 24 +/- 4% max vs. 34 +/- 5% max) relative to scrambled-siRNA rabbits.

245 Scrambled siRNAs and empty lentiviral vectors were used

246 , Il17c, S100a7, Pi3, Krt16, and Tnfa versus scrambled spherical nucleic acid (Scr SNA) controls.

247 situ, and in situ analyses reveals that the scrambled state exhibits several structural signatures:

248 Every SCRaMbLE strain was unique, validating the capability of

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

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

251 the Pd(0) pathway, as evident from deuterium scrambling studies that could reveal differentiating pro

252 ng to transient or, in the case of apoptotic scrambling, sustained collapse of membrane asymmetry.

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

254 syntenic homolog because of local indels or scrambled synteny.

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

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

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

258 ials to 3 Hz alternations between intact and scrambled text comprised of letters of varying size.

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

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

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

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

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

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

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

266 Shortening or scrambling the IDRs in both subunits ablates MMR in vivo

267 A related, detergent-based protocol for scrambling the lipid asymmetry of liposomes and maybe ce

268 Scrambling the sequence of Lnk2 is inconsequential on ac

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

270 transmembrane flip-flop of lipids and thus "scramble" this asymmetry.

271 ystems at infinite temperature, bounding the scrambling time by a finite decay time of local quantum

272 tary circuits, we propose that a logarithmic scrambling time can be achieved in most quantum systems

273 h infinite Lyapunov exponent but logarithmic scrambling time.

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

275 positive results is partly attributable to a scramble to find simple solutions for complex problems t

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

277 Here, we use SCRaMbLE to optimise yeast strains engineered to produce

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

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

280 icrocephaly and other birth defects, we have scrambled to understand how.

281 g different tpy "heads" and thiolate "tails" scrambles to afford up to 10 ternary assemblies via two

282 scribe an optimization strategy for reducing scrambling to a negligible level while minimizing the im

283 HN(SiMe(3))(2), followed by silyloxy ligand scrambling, to form 1 and the U(VI) bis(silsesquioxane)

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

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

286 nd cellular senescence markers compared with scrambled treated controls.

287 is difficult because spatial information is scrambled upon propagation.

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

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

290 al form and the other with a partially phase-scrambled visual form, were completely irrelevant to the

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

292 employed in this key step, no conformational scrambling was observed during the asymmetric synthesis

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

294 As a measure of lipid scrambling, we used differential scanning calorimetry to

295 quantum chaos is not universally related to scrambling: We construct random few-body circuits with i

296 embrane suffice for virtually complete lipid scrambling, whereas leakage remains below 10% for up to

297 and suggest methods to experimentally study scrambling with as many as 100 sparsely connected quantu

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

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