ライフサイエンスコーパス: exchange

1 -induced opening of Hsp70 to allow substrate exchange.

2 arch into plant physiological traits and gas exchange.

3 drophilic core, which also showed fast water exchange.

4 f the gel, which is reduced using the buffer exchange.

5 or the effects of ventilator settings on gas exchange.

6 y that seemed to be more pronounced with IOL exchange.

7 g from net nitrate uptake to nitrate/nitrite exchange.

8 equency of genes acquired by horizontal gene exchange.

9 ndered water-insoluble through reverse anion exchange.

10 noncrossovers (NCOs), via nonreciprocal DNA exchange.

11 trate coordination via proton-coupled ligand exchange.

12 is position impaired GEF-mediated nucleotide exchange.

13 reabsorption, therefore reducing Na(+)/K(+) exchange.

14 as not historically been limited to monetary exchange.

15 PORB mutant proteins with defined Cys-->Ala exchanges.

16 meiosis I, which also results in chromosomal exchanges.

17 ents, 3.2%), inflammation (2 patients with 3 exchanges, 1.9%).

18 tures), these samples showed reduced Fe atom exchange (9-30% at pH 7) and inhibited secondary mineral

19 Full exchange activity is realized with a single SWR1 complex

20 centaur (BCNT), is essential for the histone exchange activity of SWR, whereas an acidic region at th

21 Adenine nucleotide translocase (ANT) exchanges ADP/ATP through the mitochondrial inner membra

22 ection (SSC) and the Autism Genetic Resource Exchange (AGRE) cohorts of children with autism spectrum

23 The enamine exchange allows for a rapid and modular synthesis of var

24 at temperatures above 80 K, when an isotope exchange allows the preferential adsorption of heavy iso

25 ures, can be caused by quasi-periodic energy-exchange among magnetic fields, Rossby waves and differe

26 predictor of instantaneous net ecosystem CO2 exchange and 3) functional diversity of leaf N concentra

27 Bacteria can exchange and acquire new genetic material from other org

28 nsider the dynamic nature of whole-plant gas exchange and how it represents much more than the sum of

29 model, allowing for free fluid and cellular exchange and microsphere retrieval during release.

30 h continuous measurements of respiratory gas exchange and noninvasive (rebreathing) hemodynamic data.

31 The method utilizes both ion exchange and normal phase chromatography to generate fra

32 uired TTP respond to a combination of plasma exchange and rituximab, but some die or acquire irrevers

33 X-ray fibre diffraction, hydrogen-deuterium exchange and solid-state NMR studies map the beta-formin

34 framework (MOF) activation involving solvent exchange and solvent evacuation are reported.

35 al barrier around the seed through which gas exchange and the passage of water are prevented.

36 material mimics enable highly enhanced mass exchange and transfer in liquid-solid, gas-solid and ele

37 lation are properly interpreted by comparing exchange and Zeeman energy terms.

38 le differences in their GTP-binding, GDP/GTP-exchange, and GTP-hydrolysis activities, but the extent

39 rests dominate global terrestrial carbon (C) exchange, and recent droughts in the Amazon Basin have c

40 asurements of leaf water potential, leaf gas exchange, and root hydraulic conductance attested that,

41 haeological evidence that points to cultural exchange, and thus possible admixture, between hunter-ga

42 to decreased lung compliance, disrupted gas exchange, and ultimately respiratory failure and death.

43 Stickler syndrome, and 1 patient with an IOL exchange at 8 months postoperatively.

44 Ion exchange at charged solid-liquid interfaces is central t

45 rting the role for NCX-9 in handling calcium exchange at the mitochondrion.

46 ction profile, while mutants with S residues exchanged at 255 and 279/282 did not.

47 However, mutants with S residues exchanged at positions 365, 368, and 373 exhibited a sig

48 Despite substantial reductions in leaf gas exchange, barley plants with significantly reduced stoma

49 ing a new platform for understanding ancient exchange based on actual material transfers, both in the

50 s the key assumption that gA monomers do not exchange between bilayers.

51 acted effectively due to the direct electron exchange between heme of ADH and modified AuNPs.

52 ensed-phase reaction, where catalytic proton exchange between intermediate(s) and solvent (Bronsted-L

53 T) experiments previously revealed a dynamic exchange between partially closed and open conformations

54 To date information exchange between patients and nurses has not been explor

55 and this heterogeneity arises from sequence exchange between strains as well as from spontaneous mut

56 n the climate system as it regulates the gas exchange between the biosphere and the atmosphere.

57 Here we confirm the conservative energy exchange between the electromagnetic field fluctuations

58 Lipid exchange between the endoplasmic reticulum (ER) and pero

59 nts one of the major mechanisms driving mass exchange between the mantle and the Earth's surface, and

60 A comprehensive interface exchange between the TCR alpha/beta constant domain pair

61 relative diversity, and the level of genetic exchange between them.

62 itophorous vacuole and allows vesicles to be exchanged between parasites.

63 maximize larval connectivity, thus allowing exchanges between populations and recolonization after l

64 Simulations show frequent exchanges between terminal aquo groups and adsorbed wate

65 Here, we report the control of the exchange bias (EB) in single-phase manganite thin films

66 Moreover, the exchange bias field (HEX) started to appear at T 40 K an

67 are behind the resulting large value of the exchange bias field and its good thermal stability.

68 gion and explain the experimentally observed exchange bias.

69 Rearing animals in open-exchange cages permits the release of organic wastes, so

70 thermodilution (femoral blood flow) with net exchange calculated via the Fick principle.

71 ity by which the handling by NCLX of calcium exchange can map to neural circuit patterning and axon g

72 robial population capable of horizontal gene exchange can result in genome surfing, a mechanism that

73 nophore-based polymeric films of defined ion-exchange capacity have recently emerged as a promising a

74 thin-layer ionophore-based films with cation-exchange capacity read out with cyclic voltammetry.

75 e utilized to elute [(18)F]fluoride from ion exchange cartridges.

76 were quantified using high-performance anion exchange chromatography (HPAEC) with pulsed amperometric

77 f foulant deposition during multimode cation exchange chromatography based purification of human seru

78 We used ion exchange chromatography to separate free and complexed z

79 e present work a fast, reliable and safe Ion Exchange Chromatography-Pulsed Amperometry Detection (IC

80 ilver-ion) UHPLC column from a strong cation exchange column for (2)D, coupled with UV and LC1MS2 det

81 ical IDP, samples multiple discrete, rapidly exchanging conformational states.

82 Using hydrogen-deuterium exchange coupled to mass spectrometry, combined with in

83 Here, using hydrogen-deuterium exchange coupled with MS (HDX-MS), we probed the RcnR st

84 roism techniques, we demonstrate a collinear exchange coupling between an epitaxial antiferromagnet,

85 We show that the exchange coupling between two spin centres is increased

86 er kinetics and as much as five-times higher exchange current densities, in comparison to their spont

87 ever, the details of the PITP-mediated lipid exchange cycle remain entirely obscure.

88 d five key insights into the PITPalpha lipid exchange cycle: (i) interaction of PITPalpha with the me

89 Given the availability of two tracer exchange data sets that explore pH and particle size eff

90 he Labrador Sea, intense winter air-sea heat exchange drives the formation of deep waters and the sur

91 transition metals (Fe, Cu, Mn, and Zn) were exchanged during incubation at 37 degrees C.

92 lacking the beta2 sliding clamp), is rapidly exchanged during processive DNA replication.

93 microdisk resonator and a fiber taper which exchange energies at two distinct regions.

94 ist at which the singlet-triplet energy gap (exchange energy) is close to zero, so that rapid interco

95 Unlike other systems with low exchange energy, substantial oscillator strength is sust

96 g the largest total energy intake and energy exchange enhanced the effect of free sugars on total and

97 We describe the use of thioester exchange equilibria to measure the propensities of amino

98 could still perform electrogenic Na(+)/H(+) exchange even in the absence of a protonatable residue a

99 However, hydrogen/deuterium exchange experiments confirm the second harmonic generat

100 ides using variable-temperature (VT) NMR and exchange (EXSY) spectroscopy experiments.

101 find that Bem1 directly augments the guanine exchange factor (GEF) activity of Cdc24.

102 NCE STATEMENT Ric-8b is a guanine nucleotide exchange factor (GEF) expressed in the olfactory epithel

103 ase that functions as a guanosine nucleotide exchange factor (GEF) for ARL3-GDP.

104 (leukemia-associated Rho guanine nucleotide exchange factor (GEF)), PDZ-RhoGEF, and p115RhoGEF augme

105 re, we demonstrate that the Hsp70 nucleotide exchange factor Bag1 promotes hERG degradation by the ub

106 ng Scrib from its complex with the Rac/Cdc42 exchange factor betaPIX and decreasing the activity of t

107 uiting its activator, the guanine nucleotide exchange factor GEF-H1.

108 Active nuclear import of Ran exchange factor RCC1 is mediated by importin alpha3.

109 lear transport of the Ran guanine nucleotide exchange factor RCC1.

110 The chaperone protein and guanine nucleotide exchange factor SmgGDS (RAP1GDS1) is a key promoter of c

111 The Rac1 guanine nucleotide exchange factor Tiam1 mediates an OGD-induced increase i

112 inase (PI3K) and the Rac1 guanine nucleotide exchange factor Tiam1.

113 explains how KaiA, by acting as a nucleotide exchange factor, can stimulate phosphorylation of KaiC,

114 previously identified the guanine nucleotide exchange factor, RAPGEF5.

115 rones, an Hsp40 (J-protein) and a nucleotide exchange factor.

116 a GTPase activating protein and a nucleotide exchange factor.

117 he SH3BP5 family of Rab11 guanine nucleotide exchange factors (GEFs).

118 RasGRPs are guanine nucleotide exchange factors that are specific for Ras or Rap, and a

119 an be stimulated by two different nucleotide exchange factors, Sil1 and Lhs1.

120 ways, involving ubiquitin ligases and GTPase exchange factors/GTPase-activating proteins (GEF/GAP).

121 ndoreduplication and development of nutrient exchange/feeding sites include manipulation centered on

122 yer WSe2, utilizing the interfacial magnetic exchange field (MEF) from a ferromagnetic EuS substrate.

123 rom unconventional natural gas extraction in exchange for consolidated state-level regulatory authori

124 m to reward senior PIs with research time in exchange for less funding, this may reverse a decades-lo

125 rom the soil bacterium Mesorhizobium loti in exchange for photosynthate.

126 e study undermines centralized narratives of exchange for this period, offering a new platform for un

127 in colloidal CsPbBr3 NCs, whereby Pb(2+) is exchanged for several isovalent cations, resulting in do

128 Prostheses were exchanged for the following reasons - fractures (5 patie

129 external redox partner, rather than cofactor exchange, for multiple turnover.

130 This process is triggered by an anion exchange from 1[SO4] to 1[BF4].

131 conductor Li2Mg2P3O9N was synthesized by ion exchange from a Na2Mg2P3O9N precursor.

132 , we demonstrate the measurement of chemical exchange from a single aliquot of a ligand hyperpolarize

133 ctive barrier and tightly controls the fluid exchange from the circulation to the surrounding tissues

134 five orders of magnitude longer than typical exchange gate times, and exceeding the longest coherence

135 ntify the response of tropical net biosphere exchange, gross primary production, biomass burning, and

136 oup and -3.8 +/- 6.4 mm Hg (P < .001) in the Exchange group (group difference: P = .05).

137 ME (n = 4), and redislocation (n = 1) in the exchange group.

138 Hydrogen-deuterium exchange (HDX) coupled with mass spectrometry (HDXMS) is

139 sible surface area and by hydrogen-deuterium exchange (HDX) experiments.

140 Hydrogen/deuterium exchange (HDX) mass spectrometry (MS) reports on backbon

141 eled projections of biosphere-atmosphere CO2 exchange in a changing climate.

142 present a method that allows partial cation exchange in colloidal CsPbBr3 NCs, whereby Pb(2+) is exc

143 lyses are poorly constrained by measured CO2 exchange in drylands.

144 ion exchanger 1 (AE1) mediates Cl(-)/HCO3(-) exchange in erythrocytes and kidney intercalated cells w

145 facilitates rapid transbilayer phospholipid exchange in liposomes.

146 ses DNA breaks and elevates sister chromatid exchange in mammalian cells.

147 terials offer possibilities for passive heat exchange in stretchable electronics and bioinspired robo

148 cal with the first, except for an amino acid exchange in the stalk region abolishing the N-linked gly

149 n structuring alliances, we examine material exchanges in northwest Argentina (part of the south-cent

150 Even if the final product of the exchange, in both cases, was rock-salt PbSe nanocrystals

151 E effect to modulations of the strong double-exchange interaction between conducting electron spins a

152 The exchange interaction, J, between two spin centres is a c

153 tibonding molecular orbitals relative to the exchange interactions between electrons in these orbital

154 pically evaluate in-depth the intramolecular exchange interactions in this type of probe.

155 Mn(III)2 ferromagnetic and antiferromagnetic exchange interactions, and the resultant spin vector ali

156 dly quenches the quantum dots through cation exchange (ionic etching), and facilitates renal clearanc

157 rategy, dimethylation-deuteration and oxygen-exchange IPTL (diDO-IPTL), for high-precision, broad-cov

158 Inhibition of Ras nucleotide exchange is a promising new approach but better understa

159 hemical processes that underlie plant carbon exchange is common across different plant types, but tha

160 ments show that direct, anhydrous Cs(+)-K(+) exchange is kinetically viable and leads to the formatio

161 geometry upon hydrogen-to-deuterium isotope exchange is obtained from a comparison of experimental a

162 This exchange is possible because of the segmented nature of

163 attained separation performance with buffer exchange is relevant to detection of currently unmeasura

164 Correction for H-D exchange is required for accurate assessment of biologic

165 the IgG4 isotype can undergo in vivo Fab arm exchange leading to bispecific antibody and off-target e

166 e information provided by hydrogen/deuterium exchange mass spectrometry (HDX-MS) in the protein thera

167 Here, we show how hydrogen/deuterium-exchange mass spectrometry (HDX-MS) provides detailed in

168 rehensive mutagenesis and hydrogen deuterium exchange mass spectrometry (HDX-MS) to identify critical

169 mplementary approaches of hydrogen/deuterium exchange mass spectrometry (HDX-MS), fast photochemical

170 in explicit water, complemented by hydrogen exchange mass spectrometry (HDX/MS).

171 pproach of cross-linking, hydrogen-deuterium exchange mass spectrometry (MS), electron microscopy, mu

172 PA:nanobody complexes and hydrogen-deuterium exchange mass spectrometry revealed molecular insights a

173 PDE8), monitored by amide hydrogen-deuterium exchange mass spectrometry, we show progressive disrupti

174 of biochemical assays and hydrogen-deuterium exchange mass spectrometry.

175 directed mutagenesis, and hydrogen/deuterium exchange-mass spectrometry.

176 splant center participation in paired kidney exchanges may increase sex equity in LDKT.

177 ound that Rv2466c uses a monothiol-disulfide exchange mechanism to reduce S-mycothiolated mixed disul

178 ree electrode system with Nafion as a proton exchange membrane (PEM).

179 e, we demonstrate a versatile partial cation exchange method to fabricate lamellar Ag-CoSe2 nanobelts

180 ue mouse model, called Mitochondrial Nuclear eXchange mice, that contain the nuclear DNA from one inb

181 , releasers (amphetamines, which promote the exchange mode), and more recently, discovered partial su

182 Amphetamines trigger the exchange mode, leading to substrate efflux.

183 ations that affect GTP hydrolysis or GTP/GDP exchange modified this localization.

184 nergy perturbation (FEP) coupled with lambda-exchange molecular dynamics method to calculate the bind

185 equilibrium unfolding and hydrogen/deuterium exchange monitored by mass spectrometry indicated that a

186 is, resonance Raman (RR), hydrogen-deuterium exchange MS (HDX-MS) methods, and molecular dynamics (MD

187 Hydrogen-deuterium exchange MS revealed that membrane-resident HRas, but no

188 also to restore one gene by another allelic exchange mutation leading to the restoration of transcri

189 ese, when added as an additive to the proton exchange Nafion membrane, provide significant enhancemen

190 ctivity in the atrial-specific Na(+) /Ca(2+) exchange (NCX) knockout (KO) mouse, a model of cellular

191 ggest that EVs may be a general mechanism to exchange non-specialized genetic cargo between bacterial

192 However, how ubiquinone/ubiquinol exchange occurs on catalytically relevant timescales, an

193 lled single-crystal to single-crystal linker exchange of 2-methylimidazole in ZIF-8 membrane grains w

194 erformed in a standardized fashion including exchange of a disc of full-thickness recipient cornea (u

195 , which can most likely be attributed to the exchange of a methyl group.

196 ve accomplished this goal by prohibiting the exchange of an organ for "valuable consideration," which

197 The exchange of bone marrow between wild-type and MAP3K14(al

198 results document regulated nucleocytoplasmic exchange of C3G in response to physiological stimuli and

199 rate that the intercalation is driven by the exchange of charge between the host [Co6Te8(P(n)Pr3)6][C

200 ocysts, is postulated to depend on metabolic exchange of electrons, carbon, and fixed nitrogen.

201 First, we demonstrated the exchange of gA between 1,2-dierucoyl-sn-glycero-3-phosph

202 between epidermal cells that facilitates the exchange of gases between the chamber containing the pho

203 ymine starvation and overcome it through the exchange of genetic material.

204 The circulation and exchange of goods and resources at various scales have l

205 Although exchange of interlayer K(+) for Cs(+) is nearly thermody

206 On top of the very large exchange of knowledge, all companies involved synergisti

207 Our process involved the exchange of less hydrophilic trifluoromethanesulfonate a

208 nd its cognate SNARE proteins mainly support exchange of lipids but not cytoplasmic content between c

209 opening a gap in the disk and preventing the exchange of material between the two reservoirs.

210 One of its most important functions is the exchange of metabolites between the photoreceptors and R

211 transport (0-2 kt yr(-1)) and via diffusive exchange of methane dissolving in the surface mixed laye

212 ed plant organ (i.e., root nodule) where the exchange of nutrients between host and endosymbiont occu

213 sea data from the same region suggest little exchange of Operational Taxonomic Units (OTUs) between d

214 t, 3D design files in STEP (Standard for the Exchange of Product model data) and STL (Standard Tessel

215 ost reputation, or to retaliate, through the exchange of ratings.

216 In contrast, exchange of Ribeye between other ribbons via the cell's

217 Exchange of the 1,3-COD ligand by PMe3 led to [Si(II)(Xa

218 molecule spectroscopy (CoSMoS) to follow the exchange of the E. coli replicative DNA polymerase Pol I

219 We show that the exchange of the physicochemical conditions in the entire

220 ious work has shown that TNTs facilitate the exchange of viral or prion proteins from infected to nai

221 he physiological control on the simultaneous exchange of water and carbon dioxide in terrestrial ecos

222 Exchanges of chemical cues are likely to occur not only

223 Exchanges of matrix contents are essential to the mainte

224 e functionally interchangeable, and separate exchanges of the stem and loop portions were likewise we

225 Slow host-guest exchange on the NMR time scale enabled the characterizat

226 STD-NMR experiments did not show NAD or NADH exchange on the NMR timescale.

227 tacts, has left important aspects of ancient exchange open to speculation.

228 to consideration the long-term effect on gas exchange over time.

229 obal estimate of microbial loads and air-sea exchanges over the tropical and subtropical oceans based

230 tion that the organization has to the kidney exchange paired recipient, the naming of alternative rec

231 However, vegetation gas exchange parameters derived from EC data are subject to

232 of Osm1 and fumarate completes the disulfide exchange pathway that results in Tim13 oxidation.

233 g nanocrystals has a strong influence on the exchange pathway.

234 ed by the inability to interpret the complex exchange patterns in relation to protein structure.

235 ntific understanding, and top-down knowledge exchange patterns.

236 efining feature of PITPs is their ability to exchange phosphatidylinositol (PtdIns) molecules between

237 plants and arbuscular mycorrhizal (AM) fungi exchange photosynthetically fixed carbon for soil nutrie

238 retrospectively analyze the effect of plasma exchange (PLEX; yes = PLEX(+) , no = PLEX(-) ) and stero

239 To improve understanding of ancient exchange practices and their potential role in structuri

240 We report a method based on ion-exchange preconcentration and HPLC/mass spectrometry to

241 rose bengal and sulforhodamine B by a ligand-exchange procedure.

242 Moreover, an anion exchange process on both CaAl LDHs was followed by in si

243 Applying the exchange process to nanotubes presorted by surfactant-ba

244 able organic radicals involved in reversible exchange processes as functional paramagnetic probes.

245 In parallel, activation of the exchange protein directly activated by cAMP (Epac) provo

246 icipation of the cGMP/PKG and cAMP/PKA/Epac (exchange protein directly activated by cAMP) directly ac

247 and cAMP/PKA, and inhibition of increase in exchange protein directly activated by cAMP1 (Epac1).

248 t of RAD51, which encodes the central strand exchange protein in yeast required for conservative HR.

249 he unique capability of post-synthesis anion exchange providing facile tunability of the optical prop

250 pm to 62000 ppm, mainly as a function of air exchange rate and occupancy.

251 the discrepancy by measuring the chromophore exchange rate of the bound 11-cis-retinal chromophore wi

252 Furthermore, the respiratory exchange rate was significantly lower in LERKO mice than

253 mined from titration experiments, and proton-exchange rates are measured at pH 5 and pH 7.

254 dy and quantitatively assess a wide range of exchange rates, from 35 to more than 5000 s(-1) .

255 A weak correlation was found among hydrogen exchange rates, hydrogen bonding energies, and amino aci

256 bility, backbone dynamics, or amide hydrogen exchange rates.

257 peptides, are involved in disulfide-dithiol exchange reaction, resulting in formation of adventitiou

258 valuate the optimality of putative metabolic exchange reactions between heterocysts and vegetative ce

259 ures and used as the host material in cation exchange reactions with Pb(2+) ions.

260 heterostructures, formed upon partial cation exchange reactions, is intimately connected not only to

261 the dihydrogen complexes, as well as isotope exchange reactions, provide evidence for proposed ionic

262 lease monomeric RRM2 through thiol-disulfide exchange reactions.

263 Plasma exchange reduces levels of B7 in sera from patients with

264 rates of subsurface/atmospheric natural gas exchange remain uncertain.

265 orption onto a commercially available cation exchange resin.

266 exed zinc, and identified appropriate cation exchange resins for the individual systems.

267 uclei via signal amplification by reversible exchange (SABRE) was investigated under conditions of he

268 Solvent assisted linker exchange (SALE) and de novo synthesis of mixed-linker ZI

269 Our 13C- and 1H-chemical exchange saturation transfer (CEST) experiments previous

270 ntitation and imaging of pH through chemical exchange saturation transfer (CEST).

271 Here we combine (15)N and (1)H dark-state exchange saturation transfer (DEST), relaxation, and che

272 show that this approach, which we term guest exchange saturation transfer (GEST), allows the use of a

273 ridges containing materials for strong anion exchange (SAX) chromatography increased yield and identi

274 Adiabatically prepared chemical exchange-sensitive spin-lock imaging was performed with

275 er Pu capacity than the resin with fewer ion-exchange sites per unit mass.

276 When infants and adults communicate, they exchange social signals of availability and communicativ

277 ate a quantitative site-specific-Acyl-Biotin-Exchange (ssABE) method that allowed the identification

278 using several techniques, including leaf gas exchange, stable isotope discrimination, and eddy covari

279 s the most probable candidate for the slowly exchanging substrate water in the S0 state.

280 Lattice parameter changes during ion exchange suggest that the reaction proceeds through a Na

281 drophobic core showed extremely slow solvent exchange, suggesting the trimer formed by this region is

282 oadcasters' property rights, the goods to be exchanged, the quantities to be traded, the computationa

283 ribe here the first use of thiosemicarbazone exchange to form dynamic combinatorial libraries.

284 ons by mass spectrometry, titration, and H/D exchange) to the regional level by incorporating enzymat

285 ition (CDI) is a mechanism by which bacteria exchange toxins via direct cell-to-cell contact.

286 he van der Waals density functional with C09 exchange (vdW-DF-C09), which has been applied to describ

287 The sampler-tissue exchange was isotropic, and PRC were shown to be good in

288 Guest exchange was slow on the NMR time scale, while tumbling

289 ide uptake on bauxite -primarily through ion-exchange- was strongly pH-dependent, with highest remova

290 tions for inferences in leaf hydraulics, gas exchange, water use, and isotope physiology.

291 FA+ ions will facilitate the intramolecular exchange with FA+ ions, thereby enabling the formation o

292 agents prepared in situ by halogen/magnesium exchange with i-PrMgCl, or aryllithium reagents prepared

293 reagents prepared in situ by bromine/lithium exchange with n-BuLi are compatible with the reaction co

294 through the tissue and lateral diffusion and exchange with skin appendages is presented.

295 thesis and respiration, hydrospheric isotope exchange with water, and stratospheric photochemistry.

296 Luminescent zeolites exchanged with two distinct and interacted emissive ions

297 y moving marmosets engaged in conversational exchanges with a visually occluded virtual marmoset.

298 from the replisome during DNA synthesis and exchanges with free copies from solution.

299 The elements of information exchange within a recognised model of shared decision-ma

300 cloth, and biochar, for long-range electron exchange without the need for e-pili.