ライフサイエンスコーパス: exchange

1 s on the surface of plants that regulate gas exchange.

2 nctionally monovalent as a result of Fab-arm exchange.

3 (+63%) the activation energy of 3HM subunit exchange.

4 ersistent PARP1 foci without affecting PARP1 exchange.

5 ring cells in support of lateral information exchange.

6 o and emissivity) and land-atmosphere energy exchange.

7 hloride (Na/Cl) ratios resulting from cation exchange.

8 rylation of TSC2, which is essential for TSC exchange.

9 roups that are underwritten by symbolic gift exchange.

10 re coinage metal family by means of galvanic exchange.

11 inding pocket and alters the kinetics of GTP exchange.

12 lectively - as a variety of representational exchange.

13 bases remain labeled without detectable back-exchange.

14 der collective instances of representational exchange.

15 he interpersonal aspects of representational exchange.

16 culicine larvae respire via atmospheric gas exchange.

17 II) chain that exhibits anisotropic magnetic exchange.

18 cytosolic region that regulate NADPH/NADP(+) exchange.

19 the cardiovascular system to accomplish gas exchange.

20 et of symptoms and modular components can be exchanged.

21 of the face-processing system during social exchanges.

22 alpha(s) and Galpha(q) Unlike the nucleotide-exchange acceleration observed for Galpha(i), DAPLE inhi

23 ordination of leaf hydraulic traits with gas exchange across closely-related species adapted to varyi

24 FC) is thought to afford dynamic information exchange across task-relevant neural ensembles.

25 store depletion is mediated by Na(+)/Ca(2+) exchange across the ER membrane induced by Na(+) influx

26 geable ligand, and that phosphatidylinositol-exchange activity is resuscitated in heme binding-defici

27 ane nucleus to target the guanine nucleotide exchange activity of DOCK5, which is essential for bone

28 that attracts TF molecules in a promiscuous exchange among myriads of intermediate affinity binding

29 The electron and proton exchange among PEDOT, PSS, and the molecular de-dopants

30 remain unclear, as they do for long-distance exchanges among African foragers more broadly.

31 These findings and gas exchange analyses of quintuple/sextuple ABA receptor mut

32 tosynthesis in grasses, we examined leaf gas exchange, anatomy and ultrastructure, and tissue localiz

33 model that accounts for the observed isotope exchange and catalytic effect of Fe(II).

34 er, CIU still lacks in automation for buffer exchange and data acquisition, precluding its wide adopt

35 king of lipids to neighboring glia for lipid exchange and disposal of potentially lipotoxic metabolit

36 ere, we extend this work by studying isotope exchange and dissolution with lepidocrocite (Lp) and goe

37 ing stable carbon isotope analysis, leaf gas exchange and eddy covariance (EC) fluxes.

38 ify temporal coordination between DSB strand exchange and homolog pairing as a critical determinant f

39 d binocular circuit in layer 2/3 by cellular exchange and not by refining the original circuit.

40 nergistic manner to facilitate both the Mn-I exchange and the C-C bond-forming steps.

41 Net cerebral glucose/lactate exchange, and biomarkers of oxidative and inflammatory s

42 d mesophyll development for optimal leaf gas exchange, and that both genetic and physiological factor

43 ed by HDX-MS experiments and by the model of exchange are sufficient to recover correctly weighted st

44 bonds that can also be reversed, cleaved or exchanged are the subject of so-called dynamic covalent

45 lding blocks and/or under conditions of slow exchange, as kinetic traps and nonequilibrium product di

46 2) and is highly active for hydrogen isotope exchange at (hetero)aromatic hydrocarbons under mild con

47 y adopts the known open and closed states in exchange at 4 us.

48 cules that are continuously recruited to and exchanging at DNA lesions due to attenuated XRCC1-LIG3 r

49 mpering metadynamics and temperature-replica exchange atomistic molecular dynamics simulations of dif

50 e timing of reproduction can inhibit genetic exchange between closely related species; however, these

51 The genetic exchange between homologous chromosomes plays a major ro

52 When (57)Fe(II) was added first, isotope exchange between surface and solution could be observed

53 uronal assemblies, a hallmark of information exchange between the HPC and mPFC for memory transfer/co

54 It relies on the slow exchange between the invisible antigen-mAb complex and t

55 sting internalized metabolites and metabolic exchange between the two cell types.

56 ee form, the protein undergoes a microsecond exchange between two states, one of which is predisposed

57 lf-organize, by assuming that information is exchanged between adjacent cells only, under the guidanc

58 Robust estimates of CO(2) budget, CO(2) exchanged between the atmosphere and terrestrial biosphe

59 s, giving rise to spin-glass behavior and an exchange bias.

60 to its magnetic texture leads to a strongly exchange biased anomalous Hall effect.

61 rd formats, including the Biological Pathway Exchange (BioPAX) language and the Proteomics Standards

62 does not result in simple metathetic ligand exchange but entails disproportionation with formation o

63 at mediates respiratory oxygen transport and exchange by cooperatively binding oxygen with moderate a

64 into the Community Atmosphere Biosphere Land Exchange (CABLE) land surface model.

65 onding and the ease with which hydrogen-bond exchange can occur (either through a classical over-the-

66 e and caused only slight changes in electron exchange capacities of dissolved and sorbed HA fractions

67 found only for anionic PFASs, whereas cation exchange capacity had an approximate positive correlatio

68 heduled hemodialysis treatment via the newly exchanged catheter.The patient denied trauma prior to th

69 bacteria use outer membrane vesiculation to exchange cell surface components, thereby increasing sur

70 ectrophiles that undergo sulfur(VI) fluoride exchange chemistry.

71 torial combination in reversed phase and ion exchange chromatography (RPLC and IEC) modes are generat

72 Here we apply pH gradient cation exchange chromatography and microfluidic capillary elect

73 Size-exclusion and ion-exchange chromatography were used to fractionate various

74 High-performance anion-exchange chromatography-pulse amperometric detector perf

75 ydrolysis followed by High Performance Anion Exchange Chromatography-Pulsed Amperometric Detection an

76 le in the absence of peptide and can readily exchange cognate peptides.

77 ble filter, orthogonal reversed-phase/cation-exchange columns (RP/IEX-HPLC), UV/vis detector, and a R

78 An ion-exchange-HPLC (with anion and cation exchange columns) and an ICPMS/MS system were used to st

79 Hydrogen-deuterium exchange combined with mass spectrometry (HDX-MS) is a w

80 om an agent-based stochastic model of market exchange, combining all expenditure modes (basic food, o

81 mmunicates with other cellular structures by exchanging content and information and by establishing m

82 Hydrogen-Deuterium eXchange coupled to Mass Spectrometry (HDX-MS) is now co

83 inetic studies involving H/D and (13)C/(12)C exchange, coupled with operando infrared spectroscopy an

84 As a result of strong metal-ligand exchange coupling between the Fe(II) center and ligand,

85 e ferroelectricity, i.e. modification of the exchange coupling.

86 nces, they do affect the distribution of the exchange couplings in these biradicals.

87 orption capacities of strong and weak cation exchange cryogels were found to be 188.3 and 79.7 mg/g c

88 atively test model against multiple leaf gas-exchange datasets.

89 s and either stimulate or inhibit nucleotide exchange depending on the G-protein subtype.

90 tion of a desolvation device, that is, a gas-exchange device (GED), can improve the detection efficie

91 aemoglobin had no worsening of pulmonary gas exchange during hypoxic exercise but had greater lactate

92 AS), may cause compromise of respiratory gas exchange during sleep, related to transient upper airway

93 Here, a combination of hydrogen-deuterium exchange, electron paramagnetic resonance, and NMR spect

94 Here we demonstrate that, in regions of high exchange energy density, skyrmions may exhibit such extr

95 Protein variants with exchanged epitope residues confirmed the antibody-bindin

96 lly, delta(13) C was not correlated with gas-exchange estimates of WUE(i) under short- and long-term

97 nd galactose (Gal) derived by systematically exchanging every hydroxyl group by a fluorine atom, we d

98 saturation transfer, and hydrogen-deuterium exchange experiments show that the variant exists in a m

99 , through steady state and transient isotope exchange experiments, H(2)O cofeed measurements, and den

100 non-crossovers to crossover-specific strand exchange, explaining Mph1's apparent anti-crossover func

101 structure and stability, guanine nucleotide exchange factor (GEF) and GTPase-activating protein (GAP

102 ion of a single gene, Rap guanine nucleotide exchange factor 3 (Rapgef3), was strongly up-regulated i

103 he essential subunits for guanine nucleotide exchange factor activity for Rab1 GTPase.

104 in turn sequesters the eIF2-specific guanine exchange factor eIF2B to block eIF2 recycling, thereby h

105 MAPK pathway, and VAV1, a guanine nucleotide exchange factor for Rho family GTPases that also activat

106 y bound to HSPA1L, and the Hsp110 nucleotide-exchange factor HSPH2 preferred HSPA1A.

107 tional association of nascent RAB13 with the exchange factor RABIF.

108 The RAS exchange factor RASGRP1 is frequently overexpressed in T

109 GBF1 encodes a guanine-nucleotide exchange factor that facilitates the activation of membe

110 hat recruits Ras-specific guanine nucleotide exchange factor, Son of Sevenless 1 (SOS1), to the plasm

111 ue enables the linking of guanine nucleotide exchange factor-induced Eu(3+)-GTP association to RAS, m

112 rate patterns by coupling guanine nucleotide exchange factors (GEF) to effectors, generating a positi

113 ptic Ras homologous (Rho) guanine nucleotide exchange factors (GEFs) Kalirin and Trio have emerged as

114 teraction with activating guanine nucleotide exchange factors (GEFs) or receptor tyrosine kinase-medi

115 rolled by 145 multidomain guanine nucleotide exchange factors (RhoGEFs) and GTPase-activating protein

116 assay, BioID, to identify guanine nucleotide exchange factors that activate Cdc42 in immortalized hum

117 nterfacial CrI(3) layer, while the proximity exchange field is highly sensitive to the layered magnet

118 rates and other nutrients to the bacteria in exchange for fixed nitrogen.

119 d a protocol allowing for efficient chemical exchange for hundreds of C. elegans embryos simultaneous

120 ds succinate, which is exported by DcuABC in exchange for L-aspartate and L-malate.

121 erol-binding protein and related proteins in exchange for other lipids and sterols, which places Sac1

122 The P-fluoro substituent is exchanged for hydride by treatment with DIBAL-H, generat

123 -Ru(III) Cl(4) ](-) with simultaneous ligand exchange from Cl(-) to CO.

124 , to enable fine-mapping of sister chromatid exchanges, germline inversion and to support global hapl

125 Cross-peak development due to chemical exchange has been seen previously for semiquinones in ES

126 Hydrogen/Deuterium Exchange (HDX) coupled with Mass Spectrometry (HDX-MS) i

127 Hydrogen-deuterium exchange (HDX-MS) mapped onto a full structural model of

128 An ion-exchange-HPLC (with anion and cation exchange columns) a

129 handoffs significantly improved information exchange in 2 mixed surgical ICUs, with a concomitant in

130 dox catalysis enables C-H activation and H/D exchange in a number of additional substrates with favor

131 on activation the crystals can undergo guest exchange in a single-crystal-to-single-crystal transform

132 ed promoter activation assay to study signal exchange in and out of the 200 nm cytoplasmic pole-organ

133 nolysis and the extent of hydrogen-deuterium exchange in local secondary structures of A1 within mult

134 a is used for 3D array partitioning and data exchange in parallel.

135 is an effective intervention to improve gas exchange in patients with severe acute respiratory distr

136 nodes of MUV-10(Ca) enables controlled metal exchange in soft positions for the generation of heterom

137 rstand the involvement of glymphatic CSF-ISF exchange in tau pathology.

138 ine, thereby triggering protamine-to-histone exchange in the fertilized oocyte.

139 hree S-haplotypes revealed potential genetic exchange in the flanking regions of SLF genes, resulting

140 Activation energies for bond exchange in the solid state are lower for networks incor

141 oach to improve modeling of carbon and water exchange in tropical forests.

142 e protonated phosphate groups are fully back-exchanged in the source, while the exchanged nucleobases

143 rt of the spinwave spectrum dominated by the exchange interaction.

144 and dopant placement on the Heisenberg spin exchange interaction.

145 tion in the spin-up channel, strengthens the exchange interactions and increases the Curie temperatur

146 Higher-order exchange interactions and quantum effects are widely kno

147 It is found that biquadratic exchange interactions are essential to quantitatively de

148 in, valley and mini-valley) can be lifted by exchange interactions below 1 K.

149 (up to 231 +/- 21), which implies huge sp-d exchange interactions in 2D monolayer regimes, leading t

150 Classical Monte Carlo simulations based on exchange interactions inferred from [Formula: see text]-

151 c Gd(2)CCl caused by attenuating interatomic exchange interactions, consistent with theoretical calcu

152 helicoidal textures stabilized by competing exchange interactions.

153 lent chemistry based on siloxane equilibrium exchange into the LCE to enable processing (director ali

154 of enzyme activity based on thiol-disulfide exchange is a regulatory mechanism in which the protein

155 o a more mechanistic prediction of plant gas exchange is challenging because of the diversity of biol

156 actions (e.g. anion deintercalation or anion-exchange) is extremely challenging as these low-temperat

157 The procedure requires that lipid-detergent exchange kinetics are in the fast exchange regime in ord

158 Quantifying the exchange kinetics for analytes relative to the exchange

159 change kinetics for analytes relative to the exchange kinetics of the standards results in greater ac

160 Although using hydrogen-deuterium exchange kinetics with MS (HDX-MS) to interrogate the hi

161 ptions including a top load (low volume) and exchange (large volume) infusion of a tense quaternary s

162 ts that are efficient near the acidic proton-exchange layer with those efficient near the alkaline hy

163 those efficient near the alkaline hydroxide-exchange layer, we demonstrate a BPM driving WD with ove

164 tent to which leaf and plant morphology, gas exchange, leaf and stem hydraulics and growth rates have

165 by reducing sequence coverage, by averaging exchange levels over longer peptide segments, or by inco

166 e seasonal assessment of photosynthesis (gas exchange, limitations to partitioning, photochemistry an

167 PITPs) provide cues for membrane identity by exchanging lipophilic substrates, ultimately governing m

168 ng calorimetry (DSC), and hydrogen-deuterium exchange mass spectrometry (H/D exchange MS), to charact

169 Hydrogen/deuterium exchange mass spectrometry (HDX-MS) of complexes I and I

170 lished through the use of hydrogen-deuterium exchange mass spectrometry (HDX-MS).

171 s spectrometry (LTMS) and hydrogen-deuterium exchange mass spectrometry (HXMS) are applied to wild-ty

172 Hydrogen/deuterium exchange mass spectrometry and mutagenesis studies revea

173 Hydrogen-deuterium exchange mass spectrometry was used to map their mutual

174 n this study, we employed hydrogen-deuterium exchange-mass spectrometry (HDX-MS) to investigate how F

175 Measuring WUE(i) by gas exchange measurements is laborious and time consuming an

176 between the monomers as well as into monomer exchange mechanisms and dynamics, which have a crucial i

177 potential as a direct consequence of genetic exchange mechanisms such as horizontal gene transfer and

178 In a mainstream proton exchange membrane (PEM) fuel cell, platinum-group-metal

179 aline media is critical for developing anion exchange membrane electrolyzers.

180 eed to address the high-cost issue of proton-exchange membrane fuel cell (PEMFC) technologies, partic

181 rolytes, which was further studied in proton-exchange membrane fuel cells with encouraging performanc

182 This work provides proton exchange membrane fuel cells with enhanced power perform

183 it highly promising in economical hydroxide exchange membrane fuel cells.

184 by a 100 to 800 nm thick layer of the proton exchange membrane Nafion.

185 s is one of the major requirements in proton-exchange-membrane water electrolyzers.

186 construct metallo-polyelectrolytes as anion-exchange membranes in solid-state alkaline fuel cells.

187 re alternate electrode materials, use of ion exchange membranes, and development of other sensor comp

188 rward NMR approach termed hydrogen/deuterium exchange memory (HDXMEM).

189 The developed lipid exchange method was then used to remove phosphatidylseri

190 sorbent materials: two commercial weak anion-exchange mixed-mode sorbents (Strata X-AW and Oasis WAX)

191 h factor stimulation, the guanine-nucleotide exchange modulator dissociates Galphai*betagamma trimers

192 Hydrogen/deuterium exchange monitored by NMR can be used to map epitopes on

193 We used hydrogen-deuterium exchange MS to map the binding interface of the evasin P

194 en-deuterium exchange mass spectrometry (H/D exchange MS), to characterize the global and peptide-lev

195 broadening at the exciton level results from exchange narrowing of strong static disorder found for i

196 nvironmental stresses and modulating the gas exchange necessary for photosynthesis.

197 Hunter-gatherer exchange networks dampen subsistence and reproductive ri

198 al pore size and porosity to water and CO(2) exchange (New Phytol., 168, 2005, 275).

199 ully back-exchanged in the source, while the exchanged nucleobases remain labeled without detectable

200 They describe how representational exchange occurs not only by post hoc rationalization but

201 evidence of a shared host, in which genetic exchange occurs.

202 bolism elucidates frequent cross-compartment exchange of a standing pool of amino acids which is used

203 ments have been implicated in enrichment and exchange of antibiotic resistance genes and bacteria.

204 organic cages, we studied the formation and exchange of both dialdehydes and triamines of two differ

205 balance the charge deficit generated by the exchange of Ca(2+).

206 , for easy tailoring of conditions or facile exchange of catalysts and reactions.

207 Deepened snow increased the net ecosystem exchange of CO(2) (NEE) and reduced intra- and inter-ann

208 rmed immunological synapses which facilitate exchange of crucial biochemical information and are crit

209 osome segregation and enables the reciprocal exchange of DNA segments between homologous chromosomes(

210 olic interactions, such as cross-feeding and exchange of electron acceptors and small molecules, that

211 The exchange of genetic information between parental chromos

212 Meiotic recombination enables reciprocal exchange of genetic information between parental chromos

213 een less focus on how networks influence the exchange of genetic variation.

214 They involve bipartite cooperation via the exchange of goods or services between actors of differen

215 The paternal genome undergoes a massive exchange of histone with protamine for compaction into s

216 he global erasure of DNA methylation and the exchange of histones with protamines(1,2).

217 this barrier and promote release by stepwise exchange of hydrogen bonds.

218 Previous studies have analyzed this exchange of information by assuming that all agents shar

219 To our knowledge, this represents the first exchange of its kind in the United States.

220 The exchange of knowledge across different areas and discipl

221 nnections (plasmodesmata) facilitating rapid exchange of metabolites and signal molecules, plant cell

222 nalize the absolute templating, the complete exchange of metals in a template, of group 11 clusters a

223 nt ternary complex formation, and (iii) fast exchange of monomers by competitive substitution, which

224 Postsynthetic ligand exchange of native oleate capping ligands for NHCs resul

225 upled exchangers, CLCs uniquely catalyze the exchange of oppositely charged ions (Cl(-) for H(+)).

226 tissue and cell level, regulating local mass exchange of oxygen and nutrient-rich blood.

227 The kinetics of transport showed that exchange of S-components is part of the transport mechan

228 In addition, exchange of the dialysis catheter via guidewire was perf

229 t COVID-19 ICUs, 28 patients required urgent exchange of their ETT.

230 out) of 5 mm, indicating that ClC-5-mediated exchange of two Cl(-) out for one H(+) in is not permiss

231 cellular communication is the production and exchange of various types of extracellular vesicle (EV).

232 During this process, the exchange of Vps24 for Did2 induces a tilt in the polymer

233 ayer and an underlying deeper layer, and the exchange of water between these layers was calculated us

234 at content and barystatic changes due to the exchange of water mass between land and ocean.

235 However, performing efficient reagent exchange on chip for large numbers of embryos remains a

236 ed for Galpha(i), DAPLE inhibited nucleotide exchange on Galpha(s) and Galpha(q) These findings indic

237 emented using 1,2-ethanedithiol (EDT) ligand exchange on top of the CQD active layer.

238 or MgSO(4) did not affect CO(2) /H(2) O gas exchange or stomatal conductance significantly, indicati

239 asured evapotranspiration and carbon dioxide exchange over and under an oak savanna and over an annua

240 Annual CH(4) exchanges over the natural forest (9.1 +/- 0.9 g CH(4) m

241 This study compared the performance of exchange plus treatment against treatment alone by model

242 ct, therefore, combined use of ballast water exchange plus treatment has been suggested to provide gr

243 findings demonstrate that selective isotope exchange potentially opens new opportunities for tuning

244 The ligand-exchange process was found to be mediated by a proton-sh

245 These exchange processes can operate in tandem such that the s

246 Fe-Mn- and sulfate-reduction and cation-exchange processes may mobilize polonium from mineral su

247 ild thermal annealing treatment after ligand exchange processing (referred to as "LE-TA") triggered b

248 ytes showed deviations in their standardized exchange profiles that are attributed to field heating a

249 The exchange protein activated by cAMP (EPAC) is a promising

250 ts the 3'-ended strand and loads RecA strand-exchange protein onto it.

251 Exchange proteins directly activated by cAMP (EPAC) play

252 Unexpectedly, we found that PARP1 exchanges rapidly at DNA damage sites even in the presen

253 s a single, integral inner-sphere water that exchanges rapidly on the NMR timescale.

254 of the sinigrin hydrolysis, the AITC surface exchange rate and the AITC fat solubility, an overall pi

255 tion transfer NMR experiments to measure the exchange rate constant (k(ex)) of the imino protons in t

256 Differences in H/D exchange rates and analyses of mAb reactivity to homolog

257 useful mechanistic insights into the monomer exchange rates and free energy of interactions between t

258 metabolism, such as lower total respiratory exchange rates and higher hepatic oxidative capacity.

259 These enhancements depend on the exchange rates between the amides and the water, thereby

260 nular from non-annular lipids based on their exchange rates in solution.

261 We analysed VO(2max), respiratory exchange ratio and test duration to determine an optimal

262 WT ClC-5 had a 2Cl(-)/H(+) exchange ratio at a V(h) of +40 mV with a [Cl(-)](out) o

263 CD38 then performs a base-exchange reaction with the donor NA group deriving from

264 ty, we design a CRISPR-array-mediated primer-exchange-reaction-based biochemical circuit cascade, whi

265 -detergent exchange kinetics are in the fast exchange regime in order to follow linear and nonlinear

266 ain (5.6% for morphine) due to greater water exchange relative to channel flow.

267 ombination and recombinase-mediated cassette exchange (RMCE) reactions in mammalian cell cultures.

268 Signal amplification by reversible exchange (SABRE) is a hyperpolarization technique that u

269 que known as hyperpolarized (129)Xe chemical exchange saturation transfer (hyper-CEST).

270 NMR relaxation dispersion, chemical exchange saturation transfer, and hydrogen-deuterium exc

271 omatography (HILIC), strong cation and anion exchange (SCX, SAX), and mixed-mode separations.

272 To shed light on this issue, we exchanged selected amino acid residues in a highly conse

273 Using a modified gas exchange setup, we measured the effects of diffuse light

274 in 3 patients undergoing PPV with gas-fluid exchange (SF(6) or C(3)F(8)).

275 interactions, which is supported by replica-exchange simulations for the Grb2-SOS1 complex models.

276 Many organisms exchange small RNAs (sRNAs) during their interactions, t

277 The natural ability of plants to exchange small RNAs with invading eukaryotic organisms c

278 Exchange-split energy gaps of J and 3J separate a single

279 cal ESR frequencies because, unlike NMR, the exchanging states yield ESR signals that are not resolve

280 We recently introduced sulfur-triazole exchange (SuTEx) chemistry to demonstrate the triazole a

281 Model simulations reveae metabolic exchanges that sustain the heterotrophs in minimal media

282 a-organothiol interactions could be tuned by exchanging the potassium surface ions for copper ions.

283 opment and subsequent bidirectional nutrient exchange, the root cortical cells undergo substantial tr

284 ld engage eIF2alpha during active nucleotide exchange, thereby discouraging both binding events.

285 cantly affect the rate of the supramolecular exchanges, they were found to control (1) the kinetics o

286 urfactants affect heat, energy, and momentum exchange through altered size distribution and concentra

287 (HGT), including conjugation and cytoplasmic exchange through nanotubes.

288 aim of this study was to evaluate if plasma exchange, through the removal of circulating mediators,

289 ase, we found a gradual recovery of leaf gas exchange to 50% to 60% of control values.

290 Paired blood exchange tracked the fate of monocytes recruited to the

291 acture next to a contaminated rock matrix by exchanging uncontaminated groundwater, unamended or lact

292 They can be exchanged, varied, and selected between individuals in a

293 tial application of superhydrophilic lithium exchanged vermiculite as a thin coating layer on microfi

294 The lithium-exchanged vermiculite laminate is found to provide a sup

295 The net CO(2) exchange was generally more moisture limited in the bore

296 the late Pleistocene ice ages, surface-deep exchange was somehow weakened in the Southern Ocean's An

297 globulin + rituximab with or without plasma exchange were tested for total IgG and IgG1-4 by ELISA,

298 molecules between the layers allows for ion exchange with 3d and 5f metal cations.

299 with newly synthesized protein that does not exchange with NPCs even after mitotic NPC breakdown.

300 found to control (1) the kinetics of ligand exchange, with bulkier thiolates causing dramatic rate r