戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 steep gradients in solute concentrations and redox potential.
2 ing Cd(II) as this metal has a more negative redox potential.
3 s complex displayed a lower and irreversible redox potential.
4  for free and Brine Releasable (BR) VSCs and redox potential.
5 , and pheomelanin possesses a more oxidative redox potential.
6 of matrix superoxide/H2O2 production at this redox potential.
7 heir flexibility in tuning the Fe(3+)/Fe(2+) redox potential.
8 cathepsins through modulation of the lumenal redox potential.
9 ts oxidation level into large changes in its redox potential.
10 ified susceptible neurons by their increased redox potential.
11 esidues in the gamma subunit influence thiol redox potential.
12 ata to calculate their Gibbs free energy and redox potential.
13 gical agents modulating mitochondrial pH and redox potential.
14 , the concentrations of ions, the pH and the redox potential.
15 (-1) s(-1), respectively, and correlate with redox potentials.
16 olor changes, is achieved by tuning external redox potentials.
17 itu determination of reduced ZnO nanocrystal redox potentials.
18 l straddle the water oxidation and reduction redox potentials.
19 d water, with respect to vacuum and to water redox potentials.
20 nment between the solid band edges and water redox potentials.
21 presence of Sec is not tied to unusually low redox potentials.
22 while allowing sensitivity to drugs with low redox potentials.
23 3)6(3+) and Fe(CN)6(3-), which have resolved redox potentials.
24  aid in the detection of molecules with high redox potentials.
25 resulting catalysts, when exposed to extreme redox potentials.
26 l radicals, as well as their electrochemical redox potentials.
27 bit relatively low solubility and inadequate redox potentials.
28 duce multiple bonds without unreasonably low redox potentials.
29 ommunity compete for hydrogen in soil at low redox potentials.
30 n CH3CN), multiple electron transfers at low redox potentials (-1.7 and -1.9 V versus Ag/Ag(+)), and
31   OleTJE heme iron has an unusually positive redox potential (-103 mV versus normal hydrogen electrod
32 ed similar affinities for Cu(2+) (12-31 nM), redox potentials (242 and 251 mV), and electron paramagn
33 d the relationship between mitochondrial pH, redox potential, [2Fe-2S] clusters and Fech activity, we
34 st specific capacity (3861 mAh/g) and lowest redox potential (-3.04 V vs standard hydrogen electrode)
35 egulatory disulfide bond with a low midpoint redox potential (-335 mV at pH 7.9).
36            From the pH dependency of the GOx redox potential, a pK(a) of 7.2 has been determined for
37 ysis to a shift in the distal [Fe4S4](2+/1+) redox potential, a previously experimentally inaccessibl
38 rategies the most important properties, i.e. redox potentials, absorption and emission maxima or fluo
39 pplied potentials are believed to affect the redox potential across the cell membrane and disrupt red
40                                  The altered redox potentials allowed us furthermore to experimentall
41                           Heterogeneities in redox potentials among NPs not visible in bulk electroch
42        The calculated values of the relative redox potential and (31)P NMR chemical shifts of corresp
43  thereby anodically shifting the metal ion's redox potential and (ii) optimizes the bond strength bet
44 py, and 3) nicotinamide adenine dinucleotide redox potential and adenosine triphosphate/adenosine dip
45 studies elucidate the contributions of metal redox potential and ammonia acidity to this effect.
46 sing roGFP2 and HyPer showed a rapid loss of redox potential and an increase in H2O2 of mitochondrial
47 ant exhibited a reductive shift in mycothiol redox potential and compromised stress response.
48 mannii DsbA (AbDsbA) enzyme has an oxidizing redox potential and dithiol oxidase activity.
49 s(V) under abiotic conditions, even with low redox potential and high Fe(II) content (4.5 mM).
50 drenocortical cell line resulted in impaired redox potential and increased reactive oxygen species (R
51              Here, we identified cytoplasmic redox potential and intracellular redox sensor, WhiB4, a
52 ated with an oxidising shift in the GSSG/GSH redox potential and is inhibited by the antioxidants ebs
53 rin electron density, which affects cofactor redox potential and ligand affinity.
54 alysis and established relationships between redox potential and O2-adsorption strength, we conclude
55 of redox polymers with variation possible in redox potential and physicochemical properties.
56 igration, while soil characteristics such as redox potential and surface salinity developed later in
57          Correlation between the AOA and the redox potential and the biological activity of the tococ
58 erenol (0.1 muM) decreased the mitochondrial redox potential and the ratio of reduced to oxidated glu
59 e result of a clear correlation between heme redox potential and the strength of electronic coupling
60 he modified ATP synthase has a more reducing redox potential and thus remains predominantly oxidized
61  is thought to be crucial for maintenance of redox potential and vitality of the cell but is poorly u
62 as-phase ionization energies to the solution redox potentials and chemical behavior.
63                                              Redox potentials and current intensities of Cu(II)-conta
64 st-principles calculations of proton-coupled redox potentials and magnetizations reveal that the Ni-o
65 lustrate structural effects on their various redox potentials and on the p Ka values of the correspon
66 ring photodoping, allowing correlation of NC redox potentials and reduction levels.
67 APBA; however, the binding did not alter the redox potentials and the apparent diffusivities of ions.
68 lems caused by energy mismatch between water redox potentials and the band edges of hematite and many
69 s between these binding modes modulate the Q redox potentials and the rate of electron transfer (eT)
70 ation by peak cU(aq), we reanalyzed measured redox potentials and total concentrations of aqueous ura
71 omposition, (iii) reducing agent, (iv) metal redox potential, and (v) addition of surfactants for con
72 lts for the number of electrons transferred, redox potential, and diffusion coefficient are in good a
73 e from this system feature very high pH, low redox potential, and low ionic concentrations, making it
74 timuli, e.g. light, temperature, metal ions, redox potential, and mechanical stress.
75 ity, defects in neuronal function, decreased redox potential, and reduced numbers of presynaptic mito
76          Severe changes in the environmental redox potential, and resulting alterations in the oxidat
77 and the effect of sorbent concentration, pH, redox potential, and the sulphite and iron content of th
78 be converted into each other by changing the redox potential, and this redox switch caused a major al
79 tudies of the ground electronic state (GES), redox potentials, and C-H amination of [Rh2(II,III)(O2CC
80  Cu(II) as these metals have relatively high redox potentials, and microbial electrolysis cells for r
81 PeT + w) values from experimentally measured redox potentials, and validate the voltage sensitivities
82 , between the pro-oxidant parameters and the redox potentials, antioxidant capacities and lipophilici
83 ) ), this Mn-oxide is predicted to show high redox potentials ( approximately 4.2 V vs Na/Na(+) ) wit
84                              pH, enzyme, and redox potential are the most frequently used biological
85 ors in standard hydrogenases, although their redox potentials are higher.
86 ve as the reservoir for electrons, but their redox potentials are tuned by the choice of ligand at Mn
87 ations indicate that both UQ and MQ have low redox potentials around -260 and -230 mV, respectively,
88                              The role of the redox potential as a factor contributing to the NO-gener
89                         Our study highlights redox potential as a pivotal factor that could serve as
90 ed to be a consequence of increased cellular redox potential as judged by an elevated ratio of oxidiz
91 e NAD(+) or NADH at about the same operating redox potential as the NADH/NAD(+) pool and comprise the
92 ives with carboxylic acids can improve their redox potential as well as their charge capacity.
93 o has a significant impact on Co(III)-Co(IV) redox potential, as revealed by the change in the lithiu
94 refore not necessarily be explained by lower redox potentials, as has often been claimed.
95 hondrial metabolic potential and an abnormal redox potential, associated with reduced nicotinamide ad
96                      A comparison of the SAM redox potential at a fixed surfactant concentration of i
97 king at physiological or neutral pH, the GOx redox potentials at pH 7.4 and pH 7.0 are of main intere
98  the redox couple, the OCP deviates from the redox potential because of additional background half re
99  are less sensitive to viologens, which have redox potentials below -350 mV.
100 hors show that cobalt moieties have a higher redox potential, bind oxygen more weakly and are less ac
101  for measuring the intracellular glutathione redox potential by direct and quantitative measurement o
102 polymers (Os-EDPs) with specifically adapted redox potential by means of chemical co-deposition.
103                                  Theoretical redox potential calculations clearly indicate that the r
104  cannot be explained in terms of distance or redox potential change between donor and acceptor but in
105 tion state of the polymer, in the absence of redox potential change, resulting in increased emission.
106 terrestrial environments subject to periodic redox potential changes such as peatlands, marshes, and
107 pecies within this group, we identified that redox potential changes with diet and is the main factor
108 This is similar to isolated catalyst 2, with redox potentials comparable to the [-Ru(b)-OH(2)](2+) si
109                                          The redox potential decreases as the number of bound Li atom
110               Determination of the effective redox potential demonstrates that coordination of water
111 dicate that Cu+ and Cu2+ isotherms exhibit a redox potential-dependent intersection point.
112 en spectroscopically characterized and their redox potentials, determined by cyclic voltametry, revea
113 ties, i.e., its (electro)chemical stability, redox potential, diffusion coefficient and the influence
114               This indicates a difference in redox potential distribution of the redox-active functio
115 stic conductance, determine the shift in the redox potential due to mechanical stretching of the meta
116  to a reordering in the anionic and cationic redox potentials during cycling.
117 ents of photon capture, electron fluxes, and redox potentials during photosynthesis cause reactive ox
118 gnificant effects on the oligomerization and redox potential (E degrees ') of the enzyme.
119 20H2), a stronger reductant with a mid-point redox potential (E'0) of -360 mV; E'0 of NAD(P)H is -320
120        roGFP2, a reporter of the glutathione redox potential (E(GSH)), was used to monitor EGSH in cu
121 roGFP-based specific bioprobe of glutathione redox potential (E(GSH); Grx1-roGFP2) and measured subce
122  end of the basin, anomalies in water column redox potential (E(h)) were detected close to the seaflo
123       Our genomic analysis suggests that the redox potential effect stems from a reduced number of an
124  allow the quantification of the glutathione redox potential (EGSH) in the cytoplasm and the mitochon
125 is not expected to be stable at the measured redox potentials (Eh) in our experiments.
126 tammetry, where several parameters including redox potential, electron transfer rate, and surface cov
127       Using a genetic biosensor of mycothiol redox potential (EMSH), we demonstrated that a modest de
128  I (NADH:ubiquinone oxidoreductase) uses the redox potential energy from NADH oxidation by ubiquinone
129  tailored to be responsive to pH variations, redox potential, enzymatic activation, thermal gradients
130                               The calculated redox potentials excellently correlate with the experime
131 e examples reveals that solvent, spin state, redox potential, external co-reductants, and ligand arch
132 n-SOD, interacts with Cu(2+), which provides redox potential for catalytic removal of O2[Symbol: see
133 ely 1 nM; from the experimentally determined redox potential for CBP21-Cu(2+) of 275 mV using a therm
134                                     Measured redox potential for glucose oxidation was lower than 0 V
135 ated Cu(II) ATSM-F3 displays the appropriate redox potential for selective accumulation in hypoxic ce
136 ere measured that reveal that changes in the redox potential for the Cu(III)/Cu(II) couple are only p
137 e (UME) and its application to determine the redox potential for the deoxygenation of ZnO.
138 n historically discarded due to the negative redox potential for the NO,H+/HNO couple.
139 he strong oxidant diamide, implying that the redox potential for the thiol/disulphide transition in g
140                The two enzymes had a similar redox potential for their regulatory redox-active disulf
141 ot only to a much broader range of available redox potentials for the resulting phenanthro[9,10-d]imi
142                                   Individual redox potentials give rise to a free energy profile for
143 compounds have been examined, and reversible redox potentials have been compared with results obtaine
144               In this work, we calculate the redox potential in a series of Ir and Ru complexes beari
145 hepatic NAD(+)/NADH ratios 3-fold, oxidizing redox potential in liver but not skeletal muscle.
146 -lactam resistance (e.g. beta-lactamase) and redox potential in Mtb.
147 hile either the macrophyte or SMFC increased redox potential in sediments, redox potentials near the
148 ted potent antiproliferative activity having redox potentials in a range accessible to biological red
149 sing the pKa values and Ni(II/I) and Ni(I/0) redox potentials in a thermochemical cycle, the free ene
150 "sets" signaling at distinct, nonoverlapping redox potentials in support of multiplexing and error co
151 o [4Fe-4S] clusters adjacent to the Cbl have redox potentials in the range expected for Cbl reduction
152                                         With redox potentials in the range of 336-413 mV chlordecone
153 oredoxin)-based buffers regulate the ambient redox potentials in the various intracellular compartmen
154 al expansion" (i.e., a further separation of redox potentials) in single-pyridinium EPs (4, 5), where
155 xplicit solvation into account and show that redox potentials increase over the whole range of forces
156 risons reveal that for C-terminal motifs the redox potentials increased between 20-25 mV when the sel
157     A comparison of calculated acidities and redox potentials indicates that pyridinium cations behav
158 d 4-chlorobenzonitrile, having two different redox potentials indicates that the reaction does not in
159 ce in driving force is opposite the trend in redox potentials, indicating that basicity is a key fact
160              When the differences in monomer redox-potential induced by the environment are small (as
161                                              Redox potential is of key importance in the control and
162 uch surface bound Fe(II) species in terms of redox potential is still missing.
163 sors, which however do not allow quantifying redox potentials, lack specificity, and the possibility
164 edox states, precise control of a molecule's redox potential, leading to a single output voltage in a
165 se complexes, the phosphonate groups provide redox-potential leveling through charge compensation and
166 nformation and oxidation state in catalysis, redox potential modulation of the metal site, and cataly
167 SMFC increased redox potential in sediments, redox potentials near the anode (approximately 6 cm dept
168         The binding of PBA to ARS shifts its redox potential negatively.
169 vious approaches to measuring the biological redox potential noninvasively in real time are limited t
170          Cyclic voltammetry reveals a record redox potential of -1.70 V vs. saturated calomel electro
171                 The disulfide has a standard redox potential of -261 mV and is efficiently reduced by
172            The disulfide bond has a standard redox potential of -301 mV and is stoichiometrically red
173                                          The redox potential of -P-S-Cl is thus higher than that of G
174 ca 3.2 m in the anolyte and a relatively low redox potential of 2.2 V vs. Li(+) /Li.
175 logical effects are consistent with the high redox potential of 5-Me-PCA, which distinguishes it from
176 eveals that a mechanical force can shift the redox potential of a molecule, change its redox state, a
177 he position of the wave is determined by the redox potential of a redox relay when intramolecular ele
178  NMR further reveal that C91 has the highest redox potential of all cysteines in MAL.
179   AHSP binding also dramatically reduces the redox potential of alpha-subunits, from +40 to -78 mV in
180 , through a mechanism that also involved the redox potential of catechins to maintain l-5-MTHF in its
181                      Furthermore, the higher redox potential of copper and the enhanced weakening of
182 lly favorable reaction, with a less negative redox potential of CoxB (E'0 = -231 mV) as compared with
183                                          The redox potential of CuB is expected, and found by density
184          It was demonstrated that the formal redox potential of direct electron transfer between elec
185                             In addition, the redox potential of DsbP (-161 mV) is more reducing than
186                                          The redox potential of Dtrx (-181 mV) is significantly less
187 We provide information on how changes in the redox potential of either reaction partner significantly
188 lla oneidensis could potentially control the redox potential of environments relevant to the geologic
189                                          The redox potential of Eu(3+/2+) shifts to more positive pot
190 ion in M. oryzae, we measured the amount and redox potential of glutathione (E(GSH)), as the major cy
191                                 However, the redox potential of iron also contributes to its toxicity
192 ve to HbA is consistent with the much higher redox potential of LtHb.
193 DeltaEm_b can be markedly increased, and the redox potential of one of the hemes can stay above the l
194 ulted in higher oxidative shift in mycothiol redox potential of PknG mutant compared with the wild ty
195  which is much higher than the thermodynamic redox potential of SmI2(H2O)n determined by electrochemi
196 s of L2 results in significant shifts in the redox potential of the [2Fe-2S] cluster and orders of ma
197 dentified based on the Bronsted basicity and redox potential of the active site, explaining the chang
198  electronics, where careful attention to the redox potential of the backbone relative to the organic
199 uctive half-reaction and have determined the redox potential of the bound flavin to be -123 +/- 7 mV.
200  proposed manner in which CobA increases the redox potential of the cob(II)alamin/cob(I)alamin couple
201 and might play a key role in adjusting a low redox potential of the FADH(*)/FAD pair required for fer
202 Fc(+) and adsorbed Fe(II) increases with the redox potential of the ferrocene derivative, as expected
203 undamental parameters were obtained: (i) the redox potential of the haem-containing centre of the enz
204  NAD(+), total NAD contents, and NAD(+)/NADH redox potential of the healthy human brain were revealed
205 tions at these residues are sensitive to the redox potential of the internal solution, providing evid
206     The charge separation is directed by the redox potential of the involved bases and thus controlle
207 ined in terms of the large difference in the redox potential of the isolated subunits.
208 shell control the catalytic activity via the redox potential of the metal oxide and of the OCl(-).
209                             The pH dependent redox potential of the oxidoreductase glucose oxidase (G
210                                          The redox potential of the quinone/semiquinone couple of fla
211 the 'OFF' state, and show that the mid-point redox potential of the redox switch affords it sensitivi
212  group to a histidine nitrogen positions the redox potential of the tyrosine between those of P680(*+
213 d to confirm that the membrane potential and redox potential of the ubiquinone pool could be measured
214 ectron transfer reactions, yet the effective redox potential of these powerful reductants has not bee
215                                     The high redox potential of this catalyst system is achieved by a
216             The variation of optical gap and redox potentials of 1-4 does not correlate with the numb
217 thalpies, free energies of reaction, and the redox potentials of Ar-X/Ar-H couples, were investigated
218                                   Changes in redox potentials of cardiac myocytes are linked to sever
219        A potentiometric method for measuring redox potentials of colloidal semiconductor nanocrystals
220 en shown to have a significant effect on the redox potentials of compounds such as 1,4-dinitrobenzene
221 ey to rechargeability lies in exploiting the redox potentials of Cu to reversibly intercalate into th
222 t was then calculated from the difference in redox potentials of cytochrome c and ubiquinone pool usi
223 nd an excited fluorophore is governed by the redox potentials of each moiety according to a Rehm-Well
224  of (III,II) and (II,II) species and similar redox potentials of iron and manganese sites.
225                                 The measured redox potentials of MK-2 differed in three organic solve
226                                          The redox potentials of oxygenated nitrogen compounds predic
227 can be explained by differences in predicted redox potentials of PSII electron acceptors that control
228 erns the motifs' reactivity, we measured the redox potentials of Sec-containing motifs and their corr
229            The Li-binding thermodynamics and redox potentials of seven different quinone derivatives
230 olecular dynamics simulations to compute the redox potentials of the 10 hemes of MtrF in aqueous solu
231                                          The redox potentials of the [SrMn3O4] and [CaMn3O4] clusters
232 terconversion of succinate and fumarate, the redox potentials of the biologically available ubiquinon
233  into how the intervening protein matrix and redox potentials of the electron donor and acceptor dete
234     Further, DFT-based investigations of the redox potentials of the Li-bound quinone derivatives pro
235 erent acidities of the M-H bonds and overall redox potentials of the molecules.
236 ive force while simultaneously measuring the redox potentials of the NADH/NAD(+) and ubiquinol/ubiqui
237 s of the form 3H(Phl(R)).2F(-) modulates the redox potentials of the parent phlorin.
238 fine-tuning of the electronic properties and redox potentials of the photocatalyst in both the excite
239 ndependent of material and controlled by the redox potentials of the photogenerated charge carriers,
240 l selection by LOX and the adjustment of the redox potentials of their protein-bound catalytic metals
241                          The optical gap and redox potentials of these copolymers were fine-tuned by
242                                          The redox potentials of these ligands are controlled by func
243                   The absorption spectra and redox potentials of these molecules can be modulated by
244                 Other methods for tuning the redox potentials of these unusual reagents are desired.
245 aluated the dependency of a disulfide bond's redox potential on a pulling force applied along the sys
246 dency of the reduction mechanism and the GOx redox potential on the presence of halides, especially o
247 nstant, regardless of the proteins' in vitro redox potentials or their putative positions in the aero
248 based on differences in redox reversibility, redox potential, or both.
249 tumor microenvironment like low pH, elevated redox potential, over-expressed enzymes and hyperthermia
250          Versatile peroxidase (VP) is a high redox-potential peroxidase of biotechnological interest
251 NN up to 172 cm(-1)), decreases the Fe(0)-N2 redox potential, polarizes the N-N bond, and enables -N
252         Higher radiation doses increased the redox potential, promoted the lipid oxidation and elevat
253 y designed to target different areas of this redox potential range and are monitored by surface-enhan
254 f -470 to +130 mV vs NHE, which includes the redox potential range occupied by cells in a state of ox
255 racellular nanosensors to cover a much wider redox potential range of -470 to +130 mV vs NHE, which i
256 re synthesized and the respective Ru(II/III) redox potentials (ranging from DeltaE = +0.46 to +1.04 V
257 ere, we tested whether cytosolic NADH/NAD(+) redox potential regulates NCX activity in adult cardiomy
258                                          The redox potentials revealed lower values for the electron-
259 d organs can be ischemic, the measurement of redox potential (RP) in blood serum reflects the prooxid
260  2 (TRPM2) channel is known to be a cellular redox potential sensor that provides an important pathwa
261  which reports at a distinct, nonoverlapping redox potential, serving as a drift-correcting reference
262 to the bioreactor, that is, by maintaining a redox potential set-point value, appeared to be ineffect
263 lculated affinity change associated with the redox potential shift observed for [4Fe4S] cluster prote
264  Ga(Sbx)N1-x are found to straddle the water redox potentials showing excellent suitability for solar
265 old constitute reference electrodes having a redox potential similar to that of Ag/AgCl in physiologi
266                  In turn, Atox1, which has a redox potential similar to that of glutaredoxin, becomes
267                                              Redox potentials span a 400-mV range (+349 mV vs. standa
268 show that slow oscillations in mitochondrial redox potential stimulated by 10 mm glucose are in phase
269 he same exposed Trp-164 responsible for high redox potential substrate oxidation (as shown by activit
270 coli, the enzymes were shown to oxidize high redox potential substrates, but not Mn(2+).
271 ed to differentiate species with overlapping redox potentials, such as dopamine/Fe(CN)6(3-) and ferro
272 ristic sigmoid plots when represented versus redox potential suggesting that all changes are the resu
273                                    Trends in redox potentials suggests that other unsymmetrically sub
274 trongly affected by the nitroxyl/oxoammonium redox potential than by steric effects.
275 mation of a single disulfide bond with a low redox potential that can be efficiently reduced by the N
276  a [4Fe-4S] cluster and exhibits a DNA-bound redox potential that is physiologically relevant.
277 lytes) with the necessary combination of (1) redox potentials that exceed the potential limits of wat
278 ctroscopic determination of the one-electron redox potentials that have been difficult to establish v
279                                       At the redox potential, the conductance changes abruptly as the
280      Binding of ligands to iron modifies its redox potential, thereby permitting iron to transfer ele
281 ion of free radicals from energy stored in a redox potential through a 2e(-)/1H(+) transfer process,
282 m of NCX regulation by cytosolic NADH/NAD(+) redox potential through a ROS-generating NADH-driven fla
283 obial metabolism markedly reduces gut pH and redox potential through the production of short-chain fa
284 he Mn(IV) at site 1 is necessary to tune the redox potential to a value similar to that of the tyrosi
285  forces to be likely to tune the disulfide's redox potentials to an extent similar to the tuning with
286 stors, the electrical/optical "dual-function redox-potential transistors", which is solution processa
287 tive to glycation, albumin concentration, or redox potential, unlike other methods to quantify HSA-bo
288 jury, and in situ mapping of the hepatic GSH redox potential using a redox-sensitive green fluorescen
289 sed dyes by nine ferrocene derivatives whose redox potentials vary by 0.85 V, resulting in 54 differe
290  receptor, Aer, monitors cellular oxygen and redox potential via FAD bound to a cytosolic PAS domain.
291 on of glycolytic ATP production and cellular redox potential via HDAC3-mediated PGK1 deacetylation.
292                    Surprisingly, the midwave redox potential was positively shifted with respect to t
293  catalytic activity were maintained, and its redox potential was reduced modestly by 20 mV possibly d
294 a variety of aryl halides, and, owing to its redox potential, was found to be the first organic donor
295                             Their Fe(III/II) redox potentials were all within the range accessible to
296  O2 exceptional availability and high O2/H2O redox potential, which may in particular allow highly en
297  and do not follow the trend in one-electron redox potentials, which appear to dominate HAT reactivit
298 eads to a non-Nernstian variation of the SAM redox potential with concentration.
299  the entropic and enthalpic contributions to redox potentials with Q and with the identity and hydrop
300 nt enzymes to ROS scavenging and glutathione redox potential within each intracellular compartment.

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top