ライフサイエンスコーパス: dissociation

1 tion using the Multidimensional Inventory of Dissociation.

2 limited number of steps prior to stalling or dissociation.

3 utions but is resistant to thermally induced dissociation.

4 ing a chemically defined medium without cell dissociation.

5 agmentation via low energy collision-induced dissociation.

6 erhangs and magnifying the energy barrier to dissociation.

7 and accurately via one-step radical-induced dissociation.

8 ree Cys residues, avoiding nonspecific metal dissociation.

9 BPs in the gas phase using collision-induced dissociation.

10 em mass spectrometry using collision-induced dissociation.

11 are always slower than that of MHCI-peptide dissociation.

12 of the additional energy required for water dissociation.

13 l kingdoms of life may partially unfold upon dissociation.

14 s to quantify the evidence for and against a dissociation.

15 al changes ranging from unfolding to subunit dissociation.

16 and binding/flow cytometry; fast association/dissociation (~2 min)] revealed 26 as a useful molecular

17 here as assessed by a very high incidence of dissociations across various language task-induced asymm

18 droxylated TiO(2) surface increased the H(2) dissociation activation barrier by ~0.2 eV, in good agre

19 and showed that subsequent RNA cleavage and dissociation acts as an 'off-switch' for the cyclase act

20 illuminated how RNA binding specificity and dissociation after cleavage can be balanced to permit tu

21 s issues with RNA unfolding and nanoparticle dissociation after high-density drug loading.

22 models achieved moderate ability to estimate dissociation, after controlling for childhood trauma and

23 s needed to explore the relationship between dissociation and antidepressant response at the molecula

24 Raman scattering to monitor individual bond-dissociation and bond-formation events occurring locally

25 arge and energy transfer, as well as exciton dissociation and charge recombination.

26 Endocardial-epicardial dissociation and focal breakthroughs in humans with atri

27 Since Wigner predicted the dissociation and metallization of solid hydrogen at mega

28 This study aimed to determine whether dissociation and reconstitution of rat fetal testis tiss

29 trogen as active sites, achieving dihydrogen dissociation and subsequent transformation of oxygenates

30 a multi-role reagent to effect quantitative dissociation and subsequently catalyze covalent bond rea

31 Therefore, both heavy-light chain dissociation and the deconjugation of the warhead will a

32 s for carbon dioxide activation and hydrogen dissociation and their cooperative action converted CO(2

33 to participate in the recognition, chaperone dissociation and unfolding of exported T3SS proteins.

34 ly correlated with pre-seizure self-reported dissociation, and local brief electrical stimulation of

35 circular DNA (cccDNA), to characterize this dissociation, and virological outcomes.

36 ful in a range of pericyclic reactions, bond dissociations, and isomerizations, but they have several

37 To test this claim, we used a dissociation approach that allowed us to evaluate exogen

38 We defined endocardial-epicardial dissociation as phase difference of >=20 ms between pair

39 , releasing its internal strain, induces the dissociation, as was previously proposed, but as a "latc

40 dergo hydrogenation to methanol than the C-O dissociation associated with hydrocarbon formation.

41 ed fragmentation rather than electron-driven dissociation because glycan-retaining peptide fragments

42 a substantial delay in the antibody-antigen dissociation behavior.

43 We identified a dissociation between 2-5 Hz and 5-9 Hz theta oscillation

44 Understanding sex-specific differences and dissociation between baseline cardiovascular risk and su

45 modal events, our findings show a functional dissociation between early encoding processes that engag

46 Our results show evidence for a dissociation between experience and reportability, where

47 The dissociation between increased pTau and APP in different

48 alpha power time courses revealed a temporal dissociation between item and associative memory in hipp

49 Causal evidence for a double dissociation between LOC and OPA in representing objects

50 s revealed unambiguous evidence for a double dissociation between LOC and OPA: relative to vertex sti

51 attributable primarily to a reduced rate of dissociation between miRNA-AGO complexes and their dual-

52 eating neural control of behavior requires a dissociation between stimulus valence and stimulus-drive

53 In particular, the dissociation between the degree of hypoxemia and Crs was

54 Dissociation between the output of the circadian clock a

55 However, there was a clear dissociation between the two rhythms in V4 that became a

56 Finally, the dissociation between upper and lower respiratory tract r

57 P aeruginosa-induced dissociation between VE-cadherin and beta-catenin, but i

58 increase the vulnerability of the D-loop to dissociation by helicases, thereby promoting ectopic tel

59 EID) was compared to collisionally activated dissociation (CAD) on a series of agrochemicals.

60 olated, and subjected to collision-activated dissociation (CAD; MS(2) experiments).

61 ronments with position-dependent association-dissociation, caused by, for example, spatial gradients

62 ate radical, whereas reactions following the dissociation channel localize most of their kinetic ener

63 d electron spectroscopy giving access to the dissociation channels as well as their energetics.

64 Modeling of the gas-phase structures and dissociation chemistry of these triply charged analyte i

65 nal dissociation (HCD) and collision-induced dissociation (CID) are employed to provide complementary

66 of tandem-TIMS results in collision-induced dissociation (CID) of avidin tetramers into compact mono

67 Collision-induced dissociation (CID) of MALDI-generated ozonide ions (with

68 Collision-induced dissociation (CID) of the resulting demethylated PC prod

69 IV-1 MA binds cooperatively to the PM with a dissociation coefficient of K(d) ~16 muM and Hill coeffi

70 y, thereby quantifying the alphabeta-tubulin dissociation constant (8.48 +/- 1.22 nM) and its tighten

71 binders to this membrane protein, one with a dissociation constant (K(D) ) as low as 0.8 nm We furthe

72 Using MS, we determined the dissociation constant (K(d) ) for the SvWhiD-sigma(HrdB)

73 egion of OLE RNA, including stem P13, with a dissociation constant (K(D) ) of ~700 pm Analyses with m

74 Strongest binding, with an equilibrium dissociation constant (K(D) = 32 nM) close to values pre

75 emoval of the compound; 3) binds to tubulin [dissociation constant (K(d)) 0.4 +/- 0.1 muM] and inhibi

76 ide sensor binds strongly to the UlaG with a dissociation constant (K(d)) = 0.5 nM.

77 eap1) engages KEAP1 with nanomolar affinity (dissociation constant (K(d)) = 114 nM) and disrupts the

78 The peptide matrix lowered the dissociation constant (K(D)) by two orders of magnitude

79 vealed a high affinity toward glucose with a dissociation constant (K(d)) of 3 x 10(-8) M whereas the

80 binds to ATP with higher affinity than P2K1 (dissociation constant [K (d)] = 44.47 +/- 15.73 nm).

81 Zr]Zr-DFO-N-suc-muS110, targeting mouse CD3 (dissociation constant [K(D)], 2.9 nM) and mouse epitheli

82 ensor which responds to beta-carotene with a dissociation constant of 2.2 muM.

83 A TTR/Abeta(1-42) (1:1) complex with a dissociation constant of K(d) = 0.94 muM is formed; with

84 is of the monomer/dimer equilibria reveals a dissociation constant of K(d) =0.14+/-0.03 muM, indicati

85 iated with the partition coefficient and the dissociation constant of the acid, as well as to the con

86 ming a PS-Zn(2+) complex with an equilibrium dissociation constant of ~100 muM.

87 s the scFv antibody with a K(D) (equilibrium dissociation constant) of 46 nM.

88 s) binds ssDNA containing N6mA, with a 10 nM dissociation constant.

89 Equilibrium dissociation constants (K(d)) for each coagulation facto

90 Dissociation constants (pK(a)) and log P values were mea

91 peptide sequences for which the experimental dissociation constants of binding to the well-characteri

92 ders specific to carbonic anhydrase II, with dissociation constants ranging between 6 muM and 14 nM.

93 and temperature-induced shifts in the oxygen dissociation curve.

94 ) of free molecules was higher than that for dissociation (d) of the stable complex ( [Formula: see t

95 ed temperatures (prior to temperatures where dissociation dominates).

96 We demonstrate that the dissociation dynamics of adamantane dications takes plac

97 light chains of mAbs using electron capture dissociation (ECD) and 157 nm ultraviolet photodissociat

98 gnetostatic cell to perform electron capture dissociation (ECD) within a quadrupole/ion mobility/time

99 ectromagnetostatic cell for electron capture dissociation (ECD).

100 uctural characterization by electron-induced dissociation (EID) was compared to collisionally activat

101 nduced reaction cascades, ligand binding and dissociation, electron transfer, enzymatic reactions, an

102 tates toward substrates with modest O-H bond dissociation energies (e.g., 4-substitued-2,6-di-tert-bu

103 OEEFs also affect bond-dissociation energies and dissociation modes (covalent v

104 In general, higher dissociation energies imply longer DNA dwell times of th

105 mainly attributed to the higher bond (N-Cl) dissociation energy (BDE) of NH(2)Cl than NHCl(2).

106 lectivity favoring C-H bonds with lower bond dissociation energy as well as a wide range of functiona

107 en atom transfer reactions in which the bond-dissociation energy is the thermodynamic driving force.

108 Bond dissociation enthalpies (BDEs) of organic molecules play

109 The dissociation equilibrium constant of the beta-clamp is o

110 standard SPS workflow, an electron-transfer dissociation (ETD) MS2 was performed and analyzed in the

111 metry (HDX-MS) followed by electron-transfer dissociation (ETD), chemical cross-linking, and molecula

112 electron-transfer/higher-energy collisional dissociation (EThcD) and 213 nm ultraviolet photodissoci

113 ed electron-transfer/higher-energy collision dissociation (EThcD) mass spectrometry.

114 re, in this review, we present values of ion dissociation for ILs and IL solutions (aqueous and nonaq

115 ificantly less thermally stable, having bond dissociation free energies that are over 50 kJ/mol below

116 calculated to have an exceptionally low bond dissociation free energy (BDFE(C-H) ~ 29 kcal mol(-1) an

117 neration of an alkoxy radical utilizing bond-dissociation free energy (BDFE) as the thermodynamic dri

118 reduction potential and pK(a), the O-H bond dissociation free energy (BDFE) of hydroperoxide species

119 use-release and a transient genome-wide NELF dissociation from chromatin, unexpectedly, independent o

120 ificant steady-state currents during UBP-310 dissociation from GluK1 homotetramers, indicating that a

121 de the unique opportunity to investigate ion dissociation from infinite dilution in the solvent to a

122 e allows for a complete mapping of molecular dissociation from photoexcitation to photoproducts.

123 namic coactivation patterns, and its partial dissociation from respiration effects during task states

124 function in transcription and implicate CAK dissociation from TFIIH as essential for kinase activati

125 t the coupled steps of phosphate release and dissociation from the microtubule become more similar fo

126 ral element determining the macrolides' slow dissociation from the ribosome and likely accounts for t

127 perones in the bacterial cytoplasm after the dissociation from their exported proteins.

128 This dissociation has largely been explored by contrasting vi

129 uding NiO, that offer active sites for water dissociation have been extensively investigated.

130 ntensity above air photoionization and photo-dissociation have demonstrated excitation and confinemen

131 Higher-energy collisional dissociation (HCD) and collision-induced dissociation (C

132 ling, oxonium ions from higher-energy C-trap dissociation (HCD) fragmentation of alpha2,3-sailoglycop

133 t ions for further higher energy collisional dissociation (HCD) fragmentation with the resulting MS3

134 aches for predicting high-energy collisional dissociation (HCD) spectra are limited to predict the in

135 RNA hydrolysate by higher-energy collisional dissociation (HCD)-based fingerprints and isotope labeli

136 mpared to those of higher-energy collisional dissociation (HCD).

137 We demonstrate this double dissociation in 129 male humans using eye-tracking, pupi

138 itself, which triggers rapid MAKR2 membrane dissociation in a TMK1-dependent manner.

139 ances in state-trace analysis to assess this dissociation in an attentional/experiential blink paradi

140 A possible explanation for this dissociation in DP could be that the deficit originates

141 The most common way to estimate ion dissociation in ILs and IL solutions is by comparing the

142 water molecules for accelerated Volmer H-OH dissociation in neutral and alkaline HER.

143 potential alternative to collision-activated dissociation in tandem mass spectrometry (MS(2)) experim

144 ecisions in the inferior frontal gyrus and a dissociation in the anterior prefrontal cortex and anter

145 of the visual motion pathway to demonstrate dissociation in the fMRI response magnitude between adja

146 enhanced only by wild-type D2R, signifying a dissociation in the mechanisms that underlie distinct D2

147 These findings identify a double dissociation in the roles for different VP cell types an

148 indings and show the role of ligand-receptor dissociation in the selectivity of the weak multivalent

149 plasma membrane-associated protein, Rho GDP-dissociation inhibitor 2 [ARHGDIB], Rho guanine nucleoti

150 Rho and Rab subfamilies, guanine nucleotide dissociation inhibitors (GDIs).

151 t 8-10 NO molecules per cluster, resulted in dissociation into the separate proteins.

152 Infrared multiphoton dissociation (IRMPD) has been used in mass spectrometry

153 exploiting resonant infrared multiple photon dissociation (IRMPD), has been applied for the identific

154 riverine DOM using infrared multiple photon dissociation (IRMPD).

155 tonated species [1-LH](+), from which ligand dissociation is facile, generating [2-LH](+).

156 Signal-induced dissociation is initiated by autoubiquitylation of Met30

157 erature does not support the conclusion that dissociation is necessary for antidepressant response to

158 Notably, the dissociation is prevalent across a number of node-centri

159 Interestingly, different dissociation kinetic behaviors of the product molecules

160 gas hydrates as well as their formation and dissociation kinetics and then reviews the fast-growing

161 t demonstration on the chemically-controlled dissociation kinetics of antibody-antigen pairs by the u

162 Polyphasic stopped-flow association and dissociation kinetics support the existence of at least

163 e redox-dependent switch with 70-fold faster dissociation kinetics than streptavidin.

164 Analysis of virus dissociation kinetics using the Bell model revealed mean

165 tability of the complex, the association and dissociation kinetics, and the microviscosity, which gov

166 association of the ATP-bound form but faster dissociation leading to less stable Rad50 dimer.

167 hesis that SC formation provokes DSB protein dissociation, leading in turn to loss of a DSB competent

168 plenial cortex layer 5 neurons recapitulated dissociation-like behavioural effects.

169 Here we establish such a dissociation-like state in mice, induced by precisely-do

170 es profile each cell separately after tissue dissociation, losing information on cell-cell interactio

171 ngs shows significant Endocardial-epicardial dissociation marked temporal heterogeneity, discordant a

172 ed molecular HNO(3) have focused on the acid dissociation mechanism.

173 s also affect bond-dissociation energies and dissociation modes (covalent vs ionic), as well as alter

174 Negative electron transfer dissociation (NETD) has proven valuable in sequencing ol

175 ng cascade based on a new antagonist-induced dissociation NMR assay, called the weak-AIDA-NMR.

176 st rapid dissociation of H(2), while no such dissociation occurs on diabatic HE states.

177 ms of anxiety, depression, and peritraumatic dissociation (odds ratio of 0.58 [95% confidence interva

178 e, we study the reversible, pressure-induced dissociation of a natural protein nanocage, E. coli bact

179 riming the protein for fusion activation and dissociation of ACE2-bound S1 monomers.

180 ide a neural explanation for the behavioural dissociation of acoustic and visual speech comprehension

181 The reversible association/dissociation of an incoming peptide and overall growth k

182 therefore, we asked whether NAP promotes the dissociation of ankyrin-G and L1.

183 ior temporal sulcus (STS), we found a double dissociation of areas processing facial expression and t

184 cin contraction: tail fibres trigger lateral dissociation of baseplate triplexes; the dissociation th

185 excitons, including inverted regimes for the dissociation of both states.

186 (2)O on DLC electrodes was attributed to the dissociation of C-O bonds at the DLC surface.

187 ization of the CA lattice leads to premature dissociation of CA from viral cores, which exposes the v

188 ilization of the CA lattice led to premature dissociation of CA from vRNPs in target cells, which was

189 Removal of oleate led to dissociation of CCTalpha from the NE and increased phosp

190 CD36 formed a complex with IRbeta and dissociation of CD36/Fyn complex or inhibition of Fyn on

191 These findings explain the rapid dissociation of certain substrates from BiP observed in

192 ed that their activation is preceded by fast dissociation of Cic from the regulatory DNA.

193 HeLa cells, whereas it was required for the dissociation of cohesin from chromatin as cells transit

194 pletion of CTCF leads to the almost complete dissociation of cohesin from sites at which they colocal

195 Conversely, Nek2 knockout led to incomplete dissociation of DAs and cilia in mitosis.

196 The local dissociation of ECM ligands creates an ECM ligand gradie

197 get (Elongation factor G [EF-G]) and promote dissociation of EF-G from FA-stalled ribosome complexes.

198 om of CIs, and (ii) a following unimolecular dissociation of EHP.

199 erase II (Pol II)-associated RNA by XRN2 and dissociation of elongating Pol II.

200 We discovered a strong dissociation of fMRI response magnitude between region M

201 , our previous work demonstrated a post-LVAD dissociation of glycolysis and oxidative-phosphorylation

202 min resulted in the degradation of Arl1 and dissociation of GRIP domain-containing proteins Golgin-9

203 ions on the diabatic CT states suggest rapid dissociation of H(2), while no such dissociation occurs

204 d at the inlet temperature used for complete dissociation of HNO(3) and NH(4)NO(3), suggesting that t

205 col was optimized, resulting in irreversible dissociation of human antibodies-Ara h 6 immune complex,

206 scopy, we monitor the temporal formation and dissociation of hundreds of functional protein complexes

207 of the L1 cytoplasmic domain, leading to the dissociation of L1 from ankyrin-G and the spectrin-actin

208 ributed to a two-stage process that involves dissociation of molecular hydrogen at catalytically acti

209 aB signaling and tumor growth, whereas later dissociation of MTA2/NuRD complex from the promoter of N

210 flux blockade, and simultaneously caused the dissociation of mTOR from the surface of lysosomes leadi

211 eurovascular coupling involves a tau-induced dissociation of neuronal nitric oxide synthase (nNOS) fr

212 Second, E449K accelerates the dissociation of non-productively bound complexes and ina

213 dies show that this complex is stable toward dissociation of oxygen but reacts with simple nucleophil

214 subsequently rephosphorylated to facilitate dissociation of p53 from promoters and inactivate p53-me

215 erichia coli, revealing partially reversible dissociation of ParB foci and concomitant nucleoid conde

216 een HIV Tat and LINC00313 contributed to the dissociation of PRC2 from LINC00313 and the disinhibitio

217 However, 1,25(OH)(2)-D(3) induced dissociation of PU.1 and YY1 from the FCER1A promotor, e

218 Final dissociation of RG from DNA results in rewinding of the

219 nd impaired Pparg activation, leading to the dissociation of steatosis, inflammation, and fibrosis in

220 This causes dissociation of tau from and subsequent destabilization

221 zation is thought to be reversible, with the dissociation of the 100S complexes enabling ribosome rec

222 ve cooperativity can be attributed to faster dissociation of the 1:2 complex.

223 of regulation: by increasing the energy for dissociation of the activator-DNA complex or decreasing

224 Dissociation of the AGPCR fragments stimulates G protein

225 The collision-induced dissociation of the charge-inverted complex cations lead

226 gh levels of non-iron metals likely triggers dissociation of the complex.

227 A knockout mouse model allows dissociation of the coordination between cell types, wit

228 processive synthesis by Rev1 and facilitate dissociation of the DNA product from the enzyme.

229 notype); and in vitro, R55G-R57E accelerated dissociation of the eIF2.GTP.Met-tRNAi ternary complex (

230 ha)-acetylation at Thr-2 of EsxA facilitates dissociation of the EsxA:B heterodimer required for EsxA

231 2 at the pThr(607)-Pro motif, leading to the dissociation of the Kv4.2-DPP6 complex.

232 However, mechanisms governing dissociation of the Myo2-Vac17-Vac8 complex are not well

233 -limiting step of the transport cycle is the dissociation of the nucleotide-binding-domain dimer, whi

234 he structure and triggering hybridization or dissociation of the overhangs via changes in solution io

235 nd SCAP by sterol levels is critical for the dissociation of the SCAP-SREBP complex from the endoplas

236 2-Pyridone-assisted dissociation of the trimeric palladium acetate [Pd(3)(OA

237 showed muscle twitches during sleep and the dissociation of theta activity and muscle atonia.

238 However, dissociation of tissue results in loss of information ab

239 re, by analyzing in vitro helicase activity, dissociation of UPF1 from purified mRNPs, and transcript

240 clear physical picture of photoinduced H(2) dissociation on Au clusters, which has important implica

241 reactions is still not clear, even for H(2) dissociation on metal nanoparticles.

242 ies provides a low energy pathway for ligand dissociation, opening the needed coordination site.

243 the base peak of the spectrum and no further dissociation or fragmentation was observed.

244 and Cu(II) , as well as their resistance to dissociation or inactivation under cytosolically relevan

245 overy of roaming as an alternative molecular dissociation pathway in formaldehyde (H(2)CO), it has be

246 rdered dimeric intermediates along the dimer dissociation pathway.

247 lary sizes displayed similar surface-induced dissociation patterns at similar activation energies.

248 lting curve was specific presenting a single dissociation peak (T(melting) = 88.7 degrees C).

249 dely exploited, the accompanying low rate of dissociation prevents its use in many applications where

250 K1 homotetramers, indicating that antagonist dissociation proceeds in a nonuniform and cooperativity-

251 A novel radical dissociation process is presented, and electron capture

252 bonate group, which initiated a free radical dissociation process.

253 ean recoil distance (3.2 angstrom) of its Br dissociation product, as compared with the markedly long

254 The low yield of dissociation products from the aromatic PhBr was attribu

255 e anti-bonding state, in which recoil of the dissociation products occurred due to C.Br repulsion alo

256 tion for fixed wavelength IRMPD exploited in dissociation protocols of peptides and proteins.

257 the presence of GTP (3.69 +/- 0.65 nM), at a dissociation rate >10(-2) s(-1).

258 s such as the rupture length (chi(beta)) and dissociation rate (k(off)) are extracted using the model

259 simulations, we find that the lower membrane dissociation rate (k(off)) of Rok at the tissue boundary

260 , with K(i)* = 0.13 muM, and an atypical low dissociation rate (residence time tau = 205 min).

261 ivalent effects, with a significantly slower dissociation rate and 4-24-fold higher potency compared

262 ed for both AMT and RMT in the S31N, but the dissociation rate constant (k(2)) is dramatically increa

263 chanism of the parent ferrocene, leading the dissociation rate constant to increase by several orders

264 s (TCs) at the ribosomal A-site enhances the dissociation rate of such TCs from their L7/L12 tethers.

265 latory nascent peptides, determines the slow dissociation rate of the extended macrolides from the ri

266 and with the aptamer but does not impact its dissociation rate, suggesting an S(N)1-like mechanism wh

267 ffinity for ACE2 was reduced due to a faster dissociation rate.

268 r massively identifying the odorant-receptor dissociation rates of relevance to flies.

269 time scales in the prototypical formaldehyde dissociation reaction.

270 The proton from acid dissociation reacts with the halochromic chemical compou

271 Thus, the entire ligand dissociation-recombination cycle in MbNO is a spin cross

272 from the transition state (TS) of the dimer dissociation reveal that the final outcome depends on re

273 c analysis of reductively triggered chloride dissociation, revealing that chloride loss is 1000 times

274 This dissociation reveals a hierarchical, two-stage process.

275 This double dissociation reveals that crowding disrupts certain comb

276 and sensitivity of a brain-based measure of dissociation severity.

277 structures and reports from surface-induced dissociation (SID); (3) avidin oligomers are best descri

278 savings will require methods that allow such dissociations.SIGNIFICANCE STATEMENT Latent motor memori

279 rate of association was faster than that of dissociation since the activation Gibbs free energy (Del

280 Upon gastruloid dissociation, single cells reseeded onto micro-discs wer

281 Using paired collision- and electron-based dissociation spectra, O-Pair Search identifies O-glycope

282 The initial association and dissociation steps do not require ATP hydrolysis, but su

283 hosphate release, GTP binding, and G protein dissociation studies revealed much slower rates for G pr

284 This double dissociation suggests a differential development of face

285 This neural dissociation suggests two systems for reasoning about ot

286 ons derived from the application of multiple dissociation techniques and/or multiple precursor ions w

287 ral dissociation of baseplate triplexes; the dissociation then initiates a cascade of events leading

288 main interactions, but also engage in domain dissociation to allosterically invoke a downstream effec

289 HG, allowing binding affinities and rates of dissociation to be obtained.

290 R,R)-((iPr) DuPhos)Co(CO)(2) Cl underwent CO dissociation to form (R,R)-((iPr) DuPhos)Co(CO)Cl.

291 used to restrict the mechanism of ferrocene dissociation to proceed through ligand 'peeling', as opp

292 ne intermediate is diverted from arylnitrene dissociation toward heterolytic ring opening with the ar

293 n of phosphopeptides by infrared multiphoton dissociation two-dimensional mass spectrometry (IRMPD 2D

294 ed for continuous measures of trauma-related dissociation using the Multidimensional Inventory of Dis

295 ms of anxiety, depression, and peritraumatic dissociation was 50.4%, 30.4%, and 32%, respectively, wi

296 Electron-induced C-Br bond dissociation was found to be a single-electron process f

297 Endocardial-epicardial dissociation was seen in 50.3% of phase maps with signif

298 ing the task states; because of such partial dissociation, we assume that GSCORR could not be equated

299 two configurations is affected by water self-dissociation, which can only be described properly by FP

300 the protein assembly also favorably accrues dissociation yields.