ライフサイエンスコーパス: dissociation

1 tandem mass spectrometry (electron transfer dissociation).

2 phorylation of Cdc55 contributes to Igo/ENSA dissociation.

3 ns were measured and they displayed a strong dissociation.

4 d closed states of Tiam1 contributes to Rac1 dissociation.

5 substrates and fostering their pre-incision dissociation.

6 n TAZ1 that increases the rate of HIF-1alpha dissociation.

7 nergetics, and dynamics of O2 adsorption and dissociation.

8 mophore followed by light-independent strand dissociation.

9 g energy distributions and their coupling to dissociation.

10 eactive properties of cluster-mediated ionic dissociation.

11 he inhibitor ubiquitin aldehyde slowed their dissociation.

12 ns and the kinetics of sugar association and dissociation.

13 hot states (>6.0 eV) that lead to molecular dissociation.

14 ons can occur both with and without oligomer dissociation.

15 exciton binding energy and promotes exciton dissociation.

16 nt manner and ultimately promotes outer coat dissociation.

17 io)phenyl]acetic acid upon collision induced dissociation.

18 grated two-stage device with minimal cluster dissociation, 99% recovery of large clusters, cell viabi

19 We find the ground-state dissociation activation energy to be 4.74 eV/N2, with Fe

20 The reverse reactions, namely adduct dissociation and benzoxazine recovery, were successfully

21 cts directly in catalysis without any ligand dissociation and DFT calculations indicate a concerted n

22 nce of sulfoxides at 10.6 mum, for selective dissociation and discovery of S-sulfonated peptides.

23 lantic bottom water forced rapid gas hydrate dissociation and enhanced methane emissions during the p

24 n of EZH2 by PARP1 then induces PRC2 complex dissociation and EZH2 downregulation, which in turn redu

25 P56) mouse hearts were isolated by enzymatic dissociation and fluorescence-activated cell sorting at

26 sis confirmed the NEIL1 mediated PCNA trimer dissociation and formation of a 1:1:1 NEIL1-DNA-PCNA(mon

27 plain unlikely chemical processes, involving dissociation and formation of multiple chemical bonds, o

28 Our data suggest that oligomer dissociation and increased flexibility of the dimer cont

29 Although ribosomal subunit dissociation and nascent peptide degradation are well-un

30 h (sNucDrop-seq), which is free of enzymatic dissociation and nucleus sorting.

31 gests that nucleotide binding stimulates PPi dissociation and occurs before polymerase translocation.

32 heme iron and O2 , resulting in increased O2 dissociation and reduced O2 affinity at high E degrees '

33 Finally, slow drug-target dissociation and slow diffusion out of cells act to prol

34 re heat treatment led to increases in casein dissociation and the concentrations of kappa-casein and

35 ure to the complex causes its time-dependent dissociation and the loss of both DHO and ATC activities

36 found that GS domain phosphorylation, FKBP12 dissociation, and disease mutations all destabilize a D3

37 gion and chain directionality assist product dissociation, and that isoprenoid stepping ensures short

38 The mechanism and dynamics of O2 dissociation are also reviewed, including the importance

39 collisional scattering and collision-induced dissociation are expected to underlie much of the ion lo

40 r applications that require efficient ligand dissociation, as well as for those that require minimal

41 silica nanoparticles is achieved via vesicle dissociation at room temperature; moreover, the rate of

42 een excited states may effectively lower the dissociation barrier to 1.33 eV.

43 In addition, they suggest a dissociation between aberrant internetwork connectivity

44 These results highlight a dissociation between deficit-driven reward seeking and r

45 resentational similarity analysis revealed a dissociation between dorsal and ventral LOTC.

46 We also demonstrate a dissociation between FFR-related cortical activity from

47 e FCIC proxy in mixed communities, including dissociation between rates of lysogeny and FCIC values.

48 This functional dissociation between the BNST and amygdala is however co

49 Given the functional dissociation between the language and MD networks, their

50 +), ex-Th17 and iTreg cells demonstrates the dissociation between the metabolic fitness and the suppr

51 op signal task, we found a functional double dissociation between the right ventrolateral prefrontal

52 We demonstrate a dissociation between this FFR-f0-sensitive response in t

53 These findings show dissociations between both the computational mechanisms

54 Electroencephalography revealed spectral dissociations between somatic and visual effects, and hi

55 found that single kinesins undergo premature dissociation, but not preferential pausing, at the annea

56 The collision-activated dissociation (CAD) fragmentation patterns (obtained in M

57 strong coupling between internal energy and dissociation chemistry, such non-Boltzmann effects can i

58 pectra (MS/MS) obtained by collision induced dissociation (CID) and 351 nm ultraviolet photodissociat

59 lation window, followed by collision-induced dissociation (CID) at 1.5 keV in a collision cell filled

60 online mobility separated collision-induced dissociation (CID) followed by high resolution mass spec

61 as the dominant feature of collision-induced dissociation (CID) fragmentation, but targeted analysis

62 Collision-induced dissociation (CID) of these cationic modified lipids ena

63 phorylated peptides during collision-induced dissociation (CID), a data dependent neutral-loss-trigge

64 fragmentation techniques: collision-induced dissociation (CID), beam-type CID (HCD), electron-transf

65 incorporation pattern upon collision-induced dissociation (CID).

66 In addition, electron-transfer dissociation combined with higher energy collision disso

67 hibitory concentration (PSMA) of 15 nM and a dissociation constant (HSA) of 11.2 muM, cleared from th

68 es on ERK2, and we obtain an estimate of the dissociation constant (Kd ) for this interaction of 8 mu

69 the soluble beta-1,3-glucan laminarin with a dissociation constant (Kd ) of approximately 26 mum and

70 rmation of each heterooligomer has a similar dissociation constant (Kd) and free energy of associatio

71 mon resonance (SPR) to determine the binding dissociation constant (off-rate, kd) for compounds bindi

72 y, theoretical results indicate aqueous acid dissociation constant (pKa) values of 1.5 +/- 1 for NH3C

73 otein complexes, allowing us to detect their dissociation constant and stoichiometry directly inside

74 The dissociation constant between CEA protein and anti-CEA w

75 The dissociation constant for CysK:CdiA-CT (K d 11 nM) is

76 used to successfully measure an equilibrium dissociation constant for Zn(2+) and human serum albumin

77 Association constant kon, dissociation constant koff, and binding potential (kon/k

78 Counterintuitively, dissociation constant measurements show a stabilization

79 bound to phosphorylated beta-catenin with a dissociation constant of 0.28 mum, and although both the

80 lized aptamer for thrombin was raised with a dissociation constant of 1.6 nM.

81 strongest binding to a hemagglutinin trimer (dissociation constant of 1.6 x 10(-7) M) and afforded th

82 (18)F-FHNP had a dissociation constant of 2 nM and maximum binding capaci

83 of 18 fmol/10(6) cells, and (18)F-FES had a dissociation constant of 3 nM and maximum binding capaci

84 NSAH binds to hRRM1 with an apparent dissociation constant of 37 microM, and steady-state kin

85 ctin domain of LecRK-I.8 binds NAD(+) with a dissociation constant of 436.5 +/- 104.8 nM, although mu

86 The low value of equilibrium dissociation constant or affinity unit (KD) showed high

87 CPR(ox)/CYP2C9 complexes have a much higher dissociation constant than CPR(2-)/CYP2C9 or CPR(4-)/CYP

88 raction was 0.2%; thus, the tracer's in vivo dissociation constant was estimated to be 55 pM.

89 o binding characteristics of (213)Bi-IMP288 (dissociation constant, 0.45 +/- 0.20 nM) to TF2-pretarge

90 lls were similar to those of (177)Lu-IMP288 (dissociation constant, 0.53 +/- 0.12 nM).

91 Results:(111)In-DTPA-anti-PD-L1 (dissociation constant, 0.6 +/- 0.1 nM) demonstrated incr

92 -saturation to estimate the tracer's in vivo dissociation constant, nondisplaceable volume of distrib

93 form a one-to-one complex with a micromolar dissociation constant.

94 inhibitors 10 and chemical probe VH298, with dissociation constants <100 nM, which induced marked HIF

95 ate with the trends of nonheme-metal-binding dissociation constants (35, 22, and 9 muM) closely, sugg

96 ed more than 20 synbodies with low nanomolar dissociation constants (KD < 10 nM) for GII.4 VLP.

97 ents revealed tight binding to McpX(PR) with dissociation constants (Kd ) in the nanomolar range for

98 entally measured bond lifetimes (1/koff) and dissociation constants (Kd = koff/kon), determined by me

99 resolution binding curves from which precise dissociation constants (Kd) for protein-peptide interact

100 and specificity to both beta-LG A and B with dissociation constants (Kds) of 82 and 80nM, respectivel

101 lls via low-affinity anti-human IgE Abs with dissociation constants in the 10(-6) to 10(-8) M range.

102 n of M w with loading concentration revealed dissociation constants in the range 25-75 muM, commensur

103 pair of Ca(2+) binding sites with identical dissociation constants of 5.03 muM, (ii) a Ca(2+)-depend

104 Because the dissociation constants of the dimer and tetramer are ver

105 makes weak binding (micromolar to millimolar dissociation constants) difficult to quantify under biol

106 by the substrate/product concentrations and dissociation constants, and can follow either a ping-pon

107 orms in distinct pockets with low millimolar dissociation constants.

108 te analogues of PNP bind with picomolar (pm) dissociation constants.

109 biology tools especially in determination of dissociation constants.

110 ermined by energy-resolved collision-induced dissociation cross-section experiments, models the net s

111 single cells and/or cause cluster damage or dissociation during processing.

112 d membranes with very high affinity and slow dissociation dynamics.

113 ltiphoton decay (IRMPD) and electron capture dissociation (ECD) as fragmentation techniques, and D-al

114 The unique nature of electron capture dissociation (ECD) for cleaving protein backbone bonds w

115 agment types produced in electron detachment dissociation (EDD), negative electron transfer dissociat

116 ed ion ETD (AI-ETD), significantly increases dissociation efficiency resulting in improved overall pe

117 activation method, 30 eV electron ionization dissociation (EID), for the top-down MS characterization

118 d coupling partners with relatively low bond dissociation energies (BDE) such as dicumyl peroxide, he

119 radical species was quantified through bond dissociation energies and relative rotational energy bar

120 ns characterized by relatively high C-H bond dissociation energies.

121 The O-H bond dissociation energy of the Fe(II)-OH2 complex was estima

122 Very low N-H bond dissociation enthalpies, ranging from 65 (Fe-C identical

123 t obstacles: lack of sensitivity due to high dissociation equilibrium constant KD and non-specificity

124 , and shape of macromolecular complexes with dissociation equilibrium constants from picomolar to mic

125 study, we present direct evidence for water dissociation equilibrium on rutile-TiO2(110) by combinin

126 Electron-transfer dissociation (ETD) analysis indicates the presence of K4

127 nalysis of MS1 pairs using electron transfer dissociation (ETD) markedly reduced adduct loss.

128 IR photoactivation during electron transfer dissociation (ETD) reactions, i.e., activated ion ETD (A

129 on of multi-point HR-HRPF, electron-transfer dissociation (ETD) tandem MS (MS/MS) acquisition, measur

130 ne disulfide bond, we used electron transfer dissociation (ETD) to partially dissociate disulfide bon

131 rsors could be achieved by electron-transfer dissociation (ETD) with increased supplemental activatio

132 lision dissociation (HCD), electron-transfer dissociation (ETD), and electron-transfer combined with

133 CID), beam-type CID (HCD), electron-transfer dissociation (ETD), and the combinations ETciD and EThcD

134 iation combined with higher energy collision dissociation (EThcD) provides exceptional data-rich MS/M

135 ansfer combined with higher-energy collision dissociation (EThcD), for characterization of middle-ran

136 lly relevant timescales, and whether binding/dissociation events are involved in coupling electron tr

137 Collision induced dissociation experiments and Kendrick mass defect analys

138 d species validated by high-energy collision dissociation experiments.

139 sally conserved GTPase (HflX) as a bona fide dissociation factor of the S. aureus 100S ribosome.

140 f FAIMS-selected in source collision induced dissociation (FISCID) yields fragmentation of ions, whic

141 ldiazoacetate ester for arylpropargyl cation dissociation followed by recombination through cation ad

142 dependence of the reflectance data yields a dissociation fraction of 65 +/- 15%, supporting theoreti

143 rmed in the rate-determining step has a bond dissociation free energy (BDFE) of approximately 32 kcal

144 ol, which corresponds to a 6-kcal/mol higher dissociation free energy barrier.

145 beled Galphai1 subunits (exhibiting impaired dissociation from activated GPCRs) showed that 2PPM is c

146 ween mCpG sites along the DNA as well as the dissociation from DNA, acting like an anchor that restri

147 he activation of ICAM-1 leads to VE-cadherin dissociation from ICAM-1 and VE-cadherin association wit

148 hyperaccuracy and (for D215L) accelerated TC dissociation from reconstituted PICs.

149 cridines increase the rate of [(3)H]prazosin dissociation from the alpha1A- and alpha1B-adrenergic re

150 amidal side effects (EPS) due to their rapid dissociation from the dopamine D2 receptor.

151 ates from degradation by promoting substrate dissociation from the proteasome prior to the commitment

152 death signaling complexes by mediating RIP1 dissociation from TNF receptor 1.

153 de bonds followed by high-energy collisional dissociation (HCD) to determine disulfide linkages.

154 echniques, including higher-energy collision dissociation (HCD), electron-transfer dissociation (ETD)

155 We observed no dissociation in pupil responses when timing equivalent n

156 de bond reduction and alpha/beta heterodimer dissociation in the cytosol.

157 ew empirical studies with children showing a dissociation in the origins of and developmental change

158 These findings indicate a distinct temporal dissociation in the physiological role of the CB and M1

159 oirs rather than warming-induced gas hydrate dissociation in this shallow water seep site.

160 At high doses, staple dissociation increases which causes structural disintegr

161 exponentially accelerated Thy-1/alphavbeta3 dissociation, indicating slip bond behavior.

162 e each flanked by genes encoding Rho guanine-dissociation inhibitors (GDI), known regulators of RhoGT

163 SESN proteins function as guanine nucleotide dissociation inhibitors (GDIs) for RAGA/B, and interact

164 s, Gbetagamma, effectors, guanine nucleotide dissociation inhibitors (GDIs), GTPase-activating protei

165 ly alkaline buffer led to their quantitative dissociation into low molecular weight oligomers ( appro

166 Its dissociation into monomers leads to the formation of fib

167 ate-induced v-ATPase inhibition involved its dissociation into two parts: the cytosolic V1 and the in

168 Dissociation is a complex, ubiquitous construct in psych

169 f organosolv on cellulose surfaces, physical dissociation is not enhanced.

170 We demonstrate that ubiquinol-10 dissociation is not rate determining and deduce that ubi

171 d reaction turnover is limited by the duplex dissociation kinetics beyond probes longer than a 6-mer

172 ucial interactions for both the affinity and dissociation kinetics of this family of ligands.

173 monitor fast blinking of an organic dye, the dissociation kinetics of very short DNA and conformation

174 Analysis of single-molecule dissociation kinetics reveals that TFIID interacts with

175 Channel dissociation kinetics show even stronger dependence, wit

176 time of this state depend on the E-site tRNA dissociation kinetics, which may vary among tRNA species

177 B2R with fast association (kon) and moderate dissociation (koff) kinetics.

178 mplex dissociates after DNA damage, and this dissociation may be ataxia telangiectasia mutated-depend

179 e of short-chain quinones, for which product dissociation may become rate limiting.

180 es key information to understand the exciton dissociation mechanism and to design nanostructures for

181 the results together point to a heterolytic dissociation mechanism of H2 over ceria, leading to eith

182 hat removal of RPA occurs via an association-dissociation mechanism where HARP does not remain associ

183 nt ions, in turn shedding light on gas-phase dissociation mechanisms of glycosidic linkages.

184 Here, we describe a dissociation method that uses a protease with high activ

185 tool-use manipulation produced the opposite dissociation, modifying the boundaries of PPS, but leavi

186 ssociation (EDD), negative electron transfer dissociation (NETD), or extreme UV photodissociation (XU

187 the differences in reversibility of tetramer dissociation observed for wild-type GFP-Mrr and a cataly

188 culations suggest that the reaction involves dissociation of a phosphorus centered radical (stabilize

189 whereupon conformational changes result in a dissociation of a subset of the major capsid protein L1

190 The ATPase activity controls dissociation of an MVH complex containing PIWI proteins,

191 econd transmembrane site (TM2) that inhibits dissociation of anesthetic from the TM1 site and is cons

192 We present a new LFA design that probes the dissociation of aptamers from the surface of gold nanopa

193 The sluggish dissociation of bactericidal macrolides correlates with

194 e large diffusion potential generated by the dissociation of carbonic acid, colloidal particles move

195 BPh3 prevents the dissociation of CN(-), leading to a less rigid kappa(2)-

196 utophagy genes, including Tfeb, resulting in dissociation of CRTC2, LSD1-mediated demethylation of ge

197 ange within the RRE that persists even after dissociation of DDX1.

198 (FP) spectroscopy, kinetically resolves the dissociation of detergents from membrane proteins and pr

199 ARP1, while excess APE1 also facilitated the dissociation of DNA-bound PARP1.

200 that proteins in solution can accelerate the dissociation of DNA-bound proteins.

201 n rates but also on the rates of binding and dissociation of effectors containing phosphotyrosine-dep

202 icant changes in mRNP composition, marked by dissociation of eIF4G and PABP, and by recruitment of DD

203 sequence together with the hairpin promotes dissociation of futile EF-G and thus causes multiple EF-

204 Seafloor methane release due to the thermal dissociation of gas hydrates is pervasive across the con

205 nto a copper(I) hydride formed by reversible dissociation of HBpin from the copper dihydridoborate sp

206 and IV, leading to a transient unfolding and dissociation of helix H that becomes more prominent at h

207 recruitment of Crf1p, followed by concerted dissociation of Hmo1p and Tor1p.

208 pathway along the detached interface and the dissociation of hydrogen-vacancy complexes are critical

209 multiple subunits of the complex, as well as dissociation of Igo/ENSA.

210 o highly curled membranes with a concomitant dissociation of membrane curvature-generating proteins.

211 the presence of methyl farnesoate stimulates dissociation of Met multimers with subsequent associatio

212 ermafrost on shallow continental shelves and dissociation of methane hydrate on upper continental slo

213 (less than 3% visible transmittance) due to dissociation of methylamine.

214 th embedded membrane proteins to confirm the dissociation of MSP prior to desolvation.

215 excited-state potential energy surfaces for dissociation of N2 on an Fe-doped Au(111) surface.

216 rom the physical and chemical absorption and dissociation of O2 , especially at tellurium vacancy sit

217 Y658 phosphorylation induces dissociation of p120ctn, which allows binding of the pol

218 This novel functional dissociation of pain processing within the insula togeth

219 lyzed oxidation of PerR by H2O2 leads to the dissociation of PerR from DNA.

220 ontribution of London dispersion to the bond dissociation of proton-bound dimers, both in the gas pha

221 ong these: oxygen evolving activity, partial dissociation of PsbV, regulation of dimerization, downsi

222 ransport, chaperoning the assembly site, and dissociation of ribosomal proteins from karyopherins.

223 possibly responsible for the unconventional dissociation of S-S bond under visible light.

224 ell surface and directly measure binding and dissociation of signalling molecules from early endosome

225 iated acetylation of TACC1, which results in dissociation of TACC1 from retinoic acid response elemen

226 eteroarene carbanion to the silyl ether, and dissociation of tert-butoxide from silicon lead to the s

227 e increased translation downtime due to slow dissociation of the antibiotic may damage cells beyond t

228 This leads to dissociation of the antibody from the electrode surface,

229 Our data suggest that Wnt-induced dissociation of the Axin/GSK3 complex allows SIAH to int

230 mechanism of thermally induced unfolding and dissociation of the Crcen-HsPrp40Ap complex using two-di

231 Furthermore, the chromatin association/dissociation of the DDB2-AGO1 complex is under the contr

232 er amines at the expense of a more difficult dissociation of the dimeric species.

233 A slippery sequence also helps dissociation of the EF-G by providing alternative base-p

234 electron-deficient H atom and the subsequent dissociation of the electron-rich HO-H bond via H transf

235 trate reactions may result from an increased dissociation of the final complexes.

236 eatment with glucocorticoids resulted in the dissociation of the GR-MDFIC complex.

237 oloenzyme synthesizing DNA and stimulate the dissociation of the holoenzyme to trigger polymerase rec

238 hat vary with experimental conditions, where dissociation of the K409R parental Ab into half-Ab contr

239 e DFT calculations the reaction proceeds via dissociation of the metal-bound complex of the azirinium

240 Dissociation of the native transthyretin (TTR) tetramer

241 transfer, ATP hydrolysis, release of Pi, and dissociation of the oxidized, MgADP-bound Fe protein fro

242 tomic force microscopy also demonstrated the dissociation of the PCNA homotrimer in the presence of N

243 The color change resulting from the dissociation of the self-assembled monolayer (SAM) was d

244 allowing subsequent RQC reactions including dissociation of the stalled ribosome into subunits.Sever

245 uct of a pH-based mechanism that induces the dissociation of the Vps34 class III phosphatidylinositol

246 g experiments, support a mechanism involving dissociation of the ynoate from a catalytically dormant

247 oncentrations of either QNB or NMS slow down dissociation of their radiolabeled species from all five

248 blocked, and repair was associated with the dissociation of these complexes.

249 Concurrently, resistance exercise led to the dissociation of TSC2 from Rheb and increased in the co-l

250 Here, we report that dissociation of UNC5C and polymerized TUBB3, the highly

251 impedes its internalization, suggesting that dissociation of Vangl2 from Celsr1 is a prerequisite for

252 Significant dissociation of vasomotor and metabolic levodopa respons

253 ry (DSC) data for the peaks corresponding to dissociation of water (calorimetric effect of 536Jg(-1)

254 The photocatalytic O-H dissociation of water absorbed on a rutile TiO2(110) sur

255 idal arenes and colloidenes, the spontaneous dissociation of which is achieved with precision and sta

256 Preferential dissociation on the single-molecule level has the potent

257 y is executed to further promote the exciton dissociation or light harvesting ability of these PHJs v

258 (1.2 mg/kg, i.p.) or vehicle in association, dissociation, or absence of an RW.

259 f both surface and bulk Ce-H species upon H2 dissociation over ceria via in situ inelastic neutron sc

260 challenge, we have implemented ozone-induced dissociation (OzID) in-line with LC, IMS, and high resol

261 xperiments showed that DMSO could modify the dissociation pathway of CYP142A1, while CIU revealed the

262 ther this alters a purely physical cellulose dissociation pathway.

263 th high or medium confidence scores have ion dissociation patterns consistent with the xMSannotator a

264 on during both the aggregation phase and the dissociation phase.

265 ments was thought to result from gas hydrate dissociation, possibly triggered by anthropogenic ocean

266 s to promote all the elementary steps of the dissociation process and subsequent hydrogen migration,

267 ssisting role of a water molecule in its own dissociation process on a metal oxide.

268 We therefore optimized the hair cell dissociation protocol in order to isolate mature type I

269 , W50Pra]Ts1 for Nav with high affinity, low dissociation rate and reduced toxicity while retaining t

270 Conversely, the dissociation rate constants of the ternary complexes var

271 -Boltzmann effects can influence the overall dissociation rate in the gas.

272 Using steady-state approximations, the dissociation rate of PS in cavitating bubble systems was

273 ated an exponential dependence of the unit's dissociation rate on the force delivered to the rotor.

274 lecular interactions and increases GPIbalpha dissociation rate.

275 effects of SRI-compounds on cocaine-mediated dissociation rate.

276 association rates to the D2 receptor, while dissociation rates correlate with prolactin elevation.

277 D2 receptors and integrates association and dissociation rates to calculate the net rate of reversal

278 n through alteration of both association and dissociation rates.

279 al parameters that determine association and dissociation rates.

280 /(3)pipi* excited state in 2 promotes ligand dissociation, representing a new manner to effect photoi

281 We therefore speculated that the dissociation requires a conformational change in the int

282 nd most affective disorders also showed mean dissociation scores >15.

283 The largest mean dissociation scores were found in dissociative disorders

284 Although spontaneous (i.e., competitor-free) dissociation shows a strong salt dependence, we find tha

285 x mass spectrometry studies, surface-induced dissociation (SID) has been successfully applied in quad

286 Despite this dissociation, the two mechanisms likely depend on common

287 were accompanied by HDAC4/Ubc9/Rad51 complex dissociation through inhibiting nuclear translocation.

288 of the instrumental time resolution and the dissociation time of a ligand and protein which limits t

289 First, we extract the association and dissociation times from data for various genomic distanc

290 l loss signals obtained by collision-induced dissociation to a user-defined white list of fatty acid

291 and quantify the kinetics of association and dissociation to ascertain the conformational selectivity

292 miting step from MoFe protein and Fe protein dissociation to release of Pi Because the Fe protein can

293 o a disulfide with a neighboring cysteine or dissociation upon reduction of Fe(3+)- to Fe(2+)-heme, d

294 Cognitive motor dissociation was identified in four patients, including

295 Higher-order cortex motor dissociation was identified in two additional patients.

296 ssion sites, these cycles of association and dissociation were correlated with relative lateral displ

297 a consistent radical-initiated mechanism of dissociation, which shares similarities with fragment ty

298 interface and undergoes readily O-H and C-H dissociations with the aid of interfacial oxygen, which

299 9-dioctylfluorene) backbone promotes exciton dissociation within the poly(N-decanyl-2,7-carbazole-alt

300 , whereas filament twisting enhances cofilin dissociation without compromising filament integrity.