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1 o NAD(+) (nicotinamide adenine dinucleotide, oxidized form).
2 at can be fully reversed by reduction of the oxidized form.
3 es with stabilization of the polymer's fully oxidized form.
4 avin cofactor, maintains Cys352-Cys355 in an oxidized form.
5 ores and impaired generation of GSH from its oxidized form.
6 d with little effect on the structure of the oxidized form.
7 F required 8-9 electrons to fully reduce the oxidized form.
8  a dsbD null mutant, DsbC accumulates in the oxidized form.
9 ent with the higher folding stability of the oxidized form.
10 thode which returns the Prussian blue to its oxidized form.
11 ubstrate inhibition by APS compared with the oxidized form.
12  proteins are released from Mia40 in a fully oxidized form.
13 bisretinoid pigments of lipofuscin and their oxidized forms.
14  dihydropterins but not by the corresponding oxidized forms.
15 rm two intramolecular disulfide bonds in the oxidized forms.
16 f circulating glutathione in its reduced and oxidized forms.
17 were often present in the cytosol as several oxidized forms.
18 lthough fewer fibrils were observed with the oxidized forms.
19 ixed-valence compounds in their one-electron oxidized forms.
20  and HDL-associated apoA1 in both native and oxidized forms.
21 idates unexpectedly possess in the activated oxidized form a Pd(III) center bound to a ferrocene core
22               PKG1alpha can also be directly oxidized, forming a disulfide bond between homodimer sub
23 leotides, two of the cysteines of RNR become oxidized, forming a disulfide bond.
24                                In the active oxidized form, a nuclear export signal (NES) in the carb
25 etylation, phosphorylation, deamidation, and oxidized forms, a total of 8106 modified peptides could
26 e stress on cellular DNA, is readily further oxidized forming adducts with nucleophiles.
27 bines exceptional long-term stability in its oxidized form and a record-breaking intrinsic capacity o
28  a shift of thioredoxin-1 redox state to the oxidized form and activation of the p38/c-Jun NH(2)-term
29 C. albicans, SOD5 is secreted in a disulfide-oxidized form and apo-pools of secreted SOD5 can readily
30            In these cells, it occurred in an oxidized form and was not reducible by DTT.
31 nthesis from carbohydrates, recycling of the oxidized forms and degradation.
32 -beta is at least the more active of the two oxidized forms and may be the only active form.
33 e to NAD (nicotinamide adenine dinucleotide, oxidized form) and NADH, and it is unclear how CR relays
34  cycling of ETF, or simple conversion to the oxidized form, and (ii) mutagenesis of Arg-alpha237.
35  larger in pristine graphane compared to its oxidized forms, and at room temperature, it is on the or
36 es, such as 5-methylcytosine ((5m)C) and its oxidized forms, are implicated in important epigenetic r
37 al nitrogen from the atmosphere into a fixed oxidized form (as nitrate) is represented in the nitroge
38                                       In its oxidized form, B-VKQ is non-emissive, while upon reducti
39 ies was nearly completely CEST-silent in the oxidized form but was "turned on" upon reduction with be
40                                NI is a fully oxidized form, but its spectral features are very differ
41            H4B was found recyclable from its oxidized form by dihydrofolate reductase (DHFR) in sever
42 th a slow off-rate which, in the case of the oxidized form, can influence the kinetics of P(+) reduct
43 e cofactor that, in its as-isolated resting (oxidized) form, can be conclusively described as a ferri
44 dipyrrocorphin (Co(II)-precorrin-2), and the oxidized form, Co(III) 2,7-dimethyl-isobacterioclorin (C
45 e scales in the reduced form relative to the oxidized form, consistent with a more rigid oxidized pro
46 ron-transfer annihilation of the reduced and oxidized forms, consists of a single peak with maximum e
47 ron-transfer annihilation of the reduced and oxidized forms, consists of a single peak with maximum e
48  steps subsequent to formation of the highly oxidized forms could not be fully characterized.
49 teine and methionine and their corresponding oxidized forms cystine and methionine sulfoxide are pres
50 anisms, rodents were gavaged with Asc or its oxidized form dehydroascorbic acid (DHA), and plasma Asc
51 ll lines can only transport vitamin C in the oxidized form (dehydroascorbic acid) in vitro; however,
52 vestigated the transport of vitamin C in its oxidized form (dehydroascorbic acid) via GLUT1 into eryt
53                         Ascorbic acid or its oxidized form (dehydroascorbic acid) was administered in
54 penetrate the blood-brain barrier (BBB), its oxidized form, dehydroascorbic acid (DHA), enters the br
55 e compound was 21 mM with 84% present in the oxidized form (determined by electron paramagnetic reson
56 annulenoid macrocycle and its [38]annulenoid oxidized form display residual macrocyclic ring currents
57 lly, good-quality signal of dopamine and its oxidized form, dopamine o-quinone, was obtained using 10
58 rd soils is transported offsite in dissolved oxidized forms during dormant season rainstorms.
59  of the lipoyl groups in the E2 60mer to the oxidized form (E2(ox)) greatly reduced k(cat) and the K(
60  FAD cofactor in these proteins is its fully oxidized form, FADox.
61 vented by 5-MTHF and BH(4), but not by their oxidized forms folic acid and 7,8-dihydrobiopterin.
62 ction of reduced glutathione (GSH), over its oxidized form (GSSG), and glutathione reductase (GR) in
63 xidation of reduced glutathione (GSH) to its oxidized form (GSSG).
64                                          The oxidized form has also been investigated by resonance Ra
65  Cys(5)-Cys(20), and Cys(10)-Cys(30)) in the oxidized form (HD5(ox)).
66          Recycling of ascorbic acid from its oxidized forms helps to maintain the vitamin in human er
67 ation are sources of Hg to the Arctic in its oxidized form (Hg(ii)).
68 of stable three-dimensional structure in the oxidized form.Hsp33 provides an example of a redox signa
69 d, ascorbic acid can be regenerated from its oxidized form in a reaction catalyzed by dehydroascorbat
70 robacter cloacae has been determined for the oxidized form in separate complexes with benzoate and ac
71                                          The oxidized form in the absence of zinc is active, while th
72 that are reduced in solution appear in their oxidized form in their ESI mass spectra.
73  Finally, native PRL-1 is crystallized in an oxidized form in which a disulfide is formed between the
74  two nonaggregating forms of the peptide, an oxidized form in which both methionine residues are oxid
75 o the structure of other PDZ domains, and an oxidized form in which the ligand-binding site is distor
76 and ascorbic acid occur predominately in the oxidized forms in the QC.
77 alytic cycle (starting from reduction of the oxidized form) including proton uptake coupled to reduct
78 rine and several protoberberine alkaloids to oxidized forms, including (RS)-canadine to berberine.
79 L1 and NPAS2:BMAL1 heterodimers, whereas the oxidized forms inhibit.
80 centrations of baicalein, and especially its oxidized forms, inhibit the formation of alpha-synuclein
81 eory analyses collectively indicate that the oxidized form is best regarded as a Cu(I)-aminyl radical
82 -containing proteins where enrichment of the oxidized form is required.
83                                         This oxidized form is then able to promote disulfide bond for
84 a global protein fold similar to that of the oxidized form is, by contrast, resistant in losing its c
85 cessive enzymatic conversion of (5m)C to its oxidized forms is carried out by the ten-eleven transloc
86          This difference between reduced and oxidized forms is expected to apply to D-ribose, D-ribos
87          Recycling of ascorbic acid from its oxidized forms is required to maintain intracellular sto
88  polymer nanosensor material is in partially oxidized form-it is bearing positive charges and its emi
89 02 microM) but binds much more weakly to the oxidized form (Kd = 3.1 microM).
90 orm; recent reports have suggested that this oxidized form might promote disulfide bond formation in
91 rosine in the N- or C-terminus, were rapidly oxidized forming multimer units within thirty minutes.
92                                 NADH and its oxidized form NAD(+) have a central role in energy metab
93 olecules, FMN and FAD, in five redox states--oxidized form, neutral and anionic semiquinones, and neu
94 ed form of 17-AAG is differentiated from its oxidized form not only by the higher affinity for Hsp90
95                    Folic acid is a synthetic oxidized form not significantly found in fresh natural f
96                                    The fully oxidized form, obtained by the addition of K(3)(Fe(CN)(6
97 ly, the (MGD)(3)Fe(3+) complex, which is the oxidized form of (MGD)(2)Fe(2+), was formed; 3) the rate
98         5-hydroxymethylcytosine (5 hmC), the oxidized form of 5-methylcytosine (5 mC), is a base modi
99 probably resulted in the accumulation of the oxidized form of 6-CHQ.
100 oligonucleotide show that both 8-oxoA and an oxidized form of 8-oxoA direct insertion of dTMP by Kf e
101                   However, the corresponding oxidized form of 8-oxoA primarily shows correct insertio
102 n of a base during DNA synthesis opposite an oxidized form of 8-oxoG was investigated in vitro.
103            These results demonstrate that an oxidized form of 8-oxoG, possibly guanidinohydantoin, ma
104 he high-resolution solution structure of the oxidized form of a chimeric human and Escherichia coli t
105 Y3 is also redox-regulated, and the inactive oxidized form of AtAMY3 could be reactivated by reduced
106                                          The oxidized form of ATM is a disulfide-cross-linked dimer,
107    The results implicate participation of an oxidized form of Au (such as a Au(I) thiolate, Au(I)-SR)
108 th cholesterol but not 4-cholesten-3-one, an oxidized form of cholesterol, restored MIP-1 beta bindin
109 ree samples and the elemental composition of oxidized form of Clark I and/or II was confirmed by LC-H
110 stead blocks activity by reducing the active oxidized form of cyclo-oxygenase to an inactive form.
111 ne-sulfenic acid (Cys-SOH) structure for the oxidized form of Cys42; the presence of this redox cente
112 e scaffold of Noggin contains a cystine (the oxidized form of cysteine) knot topology similar to that
113 or E75 in the mutant) is deprotonated in the oxidized form of cytochrome bo(3) and is protonated upon
114 the heme oxoferryl takes place, yielding the oxidized form of cytochrome oxidase (heme a3 Fe3+ and Cu
115 -6-isopropyl-p-benzoquinone (DBMIB), and the oxidized form of DBMIB, but not its reduced form, decrea
116 ee essential redox states of the enzyme: the oxidized form of DmTrxR (Eox), the 2-electron-reduced fo
117  the spontaneous oxidation of DOPAC, and the oxidized form of DOPAC (the quinone) is responsible for
118 ABA in alpha1beta2 receptors, while both the oxidized form of DTT and glutathione (GSSG) caused small
119        This fluorescence is generated by the oxidized form of flavoprotein and is a measure of metabo
120 cements were observed in the presence of the oxidized form of glutathione (GSSG), except in the prese
121 d older leaves yellowed early, and GSSG, the oxidized form of glutathione, accumulated in the apoplas
122  the formation of glutathione disulfide, the oxidized form of glutathione.
123             Graphene oxide (GO), which is an oxidized form of graphene, has a mixed structure consist
124 ducing accumulation of both 8-oxoguanine, an oxidized form of guanine, in mtDNA and intracellular Abe
125  with cellular thiols to form a two-electron oxidized form of hawkinsin.
126 nt (Isd) proteins to capture and extract the oxidized form of heme (hemin) from Hb, IsdH and IsdB.
127                     All inhibitors bound the oxidized form of human enzyme with affinity slightly hig
128 ur findings indicate that Trx recognizes the oxidized form of its target proteins with exquisite sele
129 pendent oxidoreductase, directly reduces the oxidized form of MtAhpE, through a protein mixed disulfi
130 at CuZ degrees is the catalytically relevant oxidized form of N2OR.
131 ugh covalent transfer of ADP-ribose from the oxidized form of nicotinamide adenine dinucleotide (NAD(
132                We show that NHDs are NAD(+) (oxidized form of nicotinamide adenine dinucleotide) bind
133 ylase activity that is dependent on NAD (the oxidized form of nicotinamide adenine dinucleotide).
134 ne in a pathway in the synthesis of NAD, the oxidized form of nicotinamide adenine dinucleotide).
135 al transduction protein GlnK, but not to the oxidized form of NifL.
136 amino group of lysine) at C5 of a 2-electron oxidized form of OG is proposed.
137                                          The oxidized form of one of the chromophores is sufficiently
138            Here we provide evidence that the oxidized form of OxyR [OxyR(ox)] also represses agn43 tr
139 opment of agents that covalently capture the oxidized form of PTP1B generated in cells during insulin
140 that partitions onto GroEL is the reversibly oxidized form of rhodanese.
141                             In contrast, the oxidized form of Rv2466c displays an "open" conformation
142 reductive half-reaction (reduced flavin with oxidized form of substrate), and the dienolate following
143 In addition, 7,8-dihydrobiopterin levels, an oxidized form of tetrahydrobiopterin, were decreased and
144                             Furthermore, the oxidized form of the 6-hydroxychromane could be reduced
145 aling the three-dimensional structure of the oxidized form of the [2Fe-2S] ferredoxin from Trichomona
146 ty Mn is photooxidized (possibly by YD*, the oxidized form of the alternative PSII donor) with a KM =
147                    Finally, the two-electron oxidized form of the apo-MoFe protein could be reduced t
148 tion is first order both in Ce(IV) and in an oxidized form of the assembly.
149       When excess oxidant was used, a highly oxidized form of the blue dimer [4,5] was spectroscopica
150 uman PheOH (hPheOH), cocrystallized with the oxidized form of the cofactor (7,8-dihydro-L-biopterin,
151 e, and two additional electrons to return an oxidized form of the cofactor back to the reduced, O(2)-
152 lfonate, PFOS(-)) as doping ion by which the oxidized form of the ECP becomes hydrophobic.
153 nverts slowly to the spectrum of the resting oxidized form of the enzyme (Eox).
154                               The reversibly oxidized form of the enzyme (PTP1B-OX) is inactive and u
155  an additional molecule of H2O2 binds to the oxidized form of the enzyme and forms compound P, simila
156 n of the native intermediate (NI), the fully oxidized form of the enzyme formed immediately after O-O
157 pears to be the catalytically relevant fully oxidized form of the enzyme, and its role in catalysis i
158 (-1) and is the catalytically relevant fully oxidized form of the enzyme, rather than the resting sta
159 the exclusive interaction of 3H4PTT with the oxidized form of the enzyme.
160 ut not C25S with DHA was consistent with the oxidized form of the enzyme.
161 chemistry actually originates from the fully oxidized form of the flavin cofactor.
162 e that this stereochemistry destabilizes the oxidized form of the heme.
163 ift is easily observed in the spectrum of an oxidized form of the heterogeneous PEGylated protein.
164 aving NI as the catalytically relevant fully oxidized form of the MCO active site.
165           Recent work has suggested that the oxidized form of the methionine at position 213 (Met213)
166      This observation applies to the cyclic, oxidized form of the N_loop but not to the linear, reduc
167 riptions of the Cu(M) and Cu(H) sites in the oxidized form of the noncoupled binuclear copper protein
168 de EPR signal indicative of the two-electron oxidized form of the P cluster (P2+).
169 r-fold pore, these data also reveal that the oxidized form of the protein has a symmetrical ferroxida
170 donor side and by a reduced stability of the oxidized form of the redox-active Tyr residue, YD, in th
171 sis; therefore, 4-CP effectively reduces the oxidized form of the surface bound dye.
172 een defined by crystallography, is the fully oxidized form of the TNC in catalytic turnover.
173                                          The oxidized form of the TOR FATC domain is well structured
174 electron paramagnetic resonance results, the oxidized form of the triple mutant shows a high ratio of
175 cid (AA) intracellularly by transporting the oxidized form of the vitamin, dehydroascorbic acid (DHA)
176 nsporters of the GLUT type can transport the oxidized form of the vitamin, dehydroascorbic acid, but
177                                          The oxidized form of the Yap1 redox domain (Yap1-RD) fragmen
178 hat the backbones of the active sites of the oxidized form of these enzymes may have unusual conforma
179 pidly reduces Fe(III) and Cu(II) in both the oxidized form of this functional model and in CcO itself
180 -phosphate (PLP), the phosphorylated and the oxidized form of vitamin B6 is an organic cofactor.
181  capacity of melanoma cells to transport the oxidized form of vitamin C reflects the increased expres
182 sports hexoses and dehydroascorbic acid, the oxidized form of vitamin C, and interacts with several m
183 ent of [1-(13)C] dehydroascorbate [DHA], the oxidized form of Vitamin C, as an endogenous redox senso
184 d [1-(13)C]dehydroascorbate ((13)C-DHA), the oxidized form of vitamin C, as an MR probe.
185 his effect is due to increased uptake of the oxidized form of vitamin C, dehydroascorbate (DHA), via
186                            We found that the oxidized form of vitamin C, dehydroascorbic acid (DHA),
187                             In contrast, the oxidized form of vitamin C, dehydroascorbic acid (oxidiz
188 esent study shows that dehydroascorbate, the oxidized form of vitamin C, stimulates the antioxidant d
189  from glucose to dehydroascorbate (DHA), the oxidized form of vitamin C.
190 eral ALS-linked SOD1 variants, as well as an oxidized form of WT SOD1, supporting the notion that a s
191 n the activity of xanthine oxidase (XO), the oxidized form of xanthine dehydrogenase, resulting in th
192 mass spectrometry analysis revealed that the oxidized form of Yap1p contains two disulfide bonds betw
193       DFT studies of the ion pairing between oxidized forms of 1 and 2 and anions imply that the loca
194 f [1(gamma-SiW10O36)2](10-) suggest that the oxidized forms of 1 can act as active catalysts for alco
195 lectrochemical studies show that reduced and oxidized forms of 1, 2, 4, and 5 are donor-acceptor syst
196 e been synthesized by using cobaltocene, and oxidized forms of 1, [(TPyA)CoIII(CAn)CoIII(TPyA)]z+ [z=
197 ological advances in mapping and tracing the oxidized forms of 5mC allow further dissection of their
198  how cells deal with the recently identified oxidized forms of 5mdC: 5-hydroxymethyl-2'deoxycytidine
199                                  The various oxidized forms of all complexes were generated and chara
200 ofuscin pigment all-trans-retinal dimer, and oxidized forms of all-trans-retinal dimer.
201 nate was also performed with the reduced and oxidized forms of an indium alkoxide complex.
202 not increase their ubiquitinylation, yet the oxidized forms of both proteins are preferentially degra
203 rmined crystal structures of the reduced and oxidized forms of CymR revealed that Cys-25 is oxidized
204 es of the reduced (at 2.15 A resolution) and oxidized forms of cytochrome c oxidase from Rhodobacter
205 iched in the heavier Hg isotopes relative to oxidized forms of emitted Hg.
206 al cells, as defined by the ratios of GSH to oxidized forms of glutathione and S-adenosylmethionine t
207                                       In the oxidized forms of graphane, the electronic excitations c
208                                          Two oxidized forms of HP are observed with an occupancy rati
209  by a fast, one-step procedure) and peroxide-oxidized forms of human ceruloplasmin.
210  Consequences of the administration of these oxidized forms of human serum albumin to critically ill
211 and without hematite addition) suggests that oxidized forms of iron, naturally present in the sedimen
212  ligands for CD36 and mediate recognition of oxidized forms of LDL by CD36 on macrophages.
213                 Recent findings suggest that oxidized forms of LDL interact with innate immune recept
214 arlier studies of aPL that were specific for oxidized forms of LDL, FB1 cross-reacted with both nativ
215 with CD36, mediating recognition of multiple oxidized forms of LDL.
216 D36 plays an important role in the uptake of oxidized forms of low density lipoprotein (LDL) and cont
217 s an important role in binding and uptake of oxidized forms of low-density lipoprotein (LDL), foam ce
218 y responsible for the removal from plasma of oxidized forms of low-density lipoprotein (LDL).
219 ves 5-formylcytosine and 5-carboxylcytosine, oxidized forms of mC produced by Tet enzymes.
220 rostatic interactions needed to excise these oxidized forms of mC.
221 ses 5-formylcytosine and 5-carboxylcytosine, oxidized forms of mC.
222                                              Oxidized forms of methionine residues in proteins can be
223 formerly YncA) GNAT in the detoxification of oxidized forms of methionine, including methionine sulfo
224  mechanism used by S. enterica to respond to oxidized forms of methionine, which MddA detoxifies by a
225 able to discriminate between the reduced and oxidized forms of NADP independently of its catalytic ac
226 favorably reducing ratios of the reduced and oxidized forms of nicotinamide adenine dinucleotide phos
227 igher affinity of cyanide for reduced versus oxidized forms of nitrite reductase is immediately revea
228  amines, ammonia, and hydroxylamine; and (c) oxidized forms of nitrogen such as the nitroxyl anion, t
229 es both the greenhouse gas nitrous oxide and oxidized forms of nitrogen used by phytoplankton and oth
230 d from the disposed waste effluents, and (2) oxidized forms of Pu sorb less to sediments than reduced
231 patial resolution the reactivity of the more oxidized forms of Pu(V,VI) within Opalinus Clay (OPA) ro
232                                 We show that oxidized forms of quinone electron carriers act as direc
233                                    Native or oxidized forms of rBet v 1 did not induce the production
234 gly vulnerable to oxidation, and we identify oxidized forms of RPA that are associated with impaired
235 thiolate(2-)) that relate to the reduced and oxidized forms of sulfite oxidase (SO).
236 four sequential oxidations; the sequentially oxidized forms of the catalytic site are called the S st
237 es that can regenerate either the reduced or oxidized forms of the cofactor.
238 are produced using the fully reduced and the oxidized forms of the copolymer, respectively.
239                                        Three oxidized forms of the enzyme, designated 'redox cycled',
240 protonation state of D75 for the reduced and oxidized forms of the enzyme, using a combined site-dire
241 m; (b) the concentration ratio of neutral to oxidized forms of the host polymer ([P(n)]/[P(ox)]); and
242 tronic and optical properties of neutral and oxidized forms of the ladder structures were conducted.
243                     However, the reduced and oxidized forms of the mutants revealed significant diffe
244                             The sequentially oxidized forms of the OEC are referred to as the S(n) st
245              Biopterin and pterin, the fully oxidized forms of the pterin molecule, fail to block per
246 iffusion coefficient of both the reduced and oxidized forms of the redox-active species being detecte
247             In the present study we generate oxidized forms of the truncation mutant, K18, which cont
248 a protocol for the separation of reduced and oxidized forms of the tumor suppressor protein p53.
249 ate oxygen from water; the five sequentially oxidized forms of the water splitting complex are known
250 e ground-state co-conformations of the fully oxidized forms of these [2]rotaxanes.
251   Our evidence supports a model in which the oxidized forms of these thioredoxins directly catalyze d
252 e cellular reduction of disulfides and other oxidized forms of thiols was clarified.
253  same proportion, leading to accumulation of oxidized forms of thioredoxin, while 1 and 1-QM were sca
254 rized: TPB and TPCH represent two dissimilar oxidized forms of tmdp dimers; TPCH was less oxidized bu
255 significant spin density in the one-electron oxidized forms of triarylamines.
256 -dehydroascorbic acid (DHA), the reduced and oxidized forms of vitamin C, respectively, and evaluate
257 equilibria between free, metal-complexed and oxidized forms of VSCs.
258  in the reduced form, and is released in the oxidized form on LPS stimulation.
259 protein could be reduced to the one-electron oxidized form (P1+) in a reaction that required Fe prote
260  pol X between a reduced (pol X(red)) and an oxidized form (pol X(ox)), confirmed by mass spectrometr
261 uanines, GG and GGG, are known to be readily oxidized, forming radical cations, i.e., hole traps, on
262 ant however, most of thioredoxin 1 is in the oxidized form; recent reports have suggested that this o
263 perior kinetic stability of its one-electron oxidized form relative to other dimeric Rh complexes.
264 e disulfide isomer; stabilization of a fully oxidized form requires ChEL.
265  three TNC Cu's is oxidized, and the resting oxidized form (RO), where all three TNC Cu's are oxidize
266                While most MnSODs rest as the oxidized form, ScMnSOD was isolated in the Mn(2+) oxidat
267                                  The resting oxidized form shows similar features to the resting form
268 meable to FcTMA(+) with less charge than its oxidized form so that the oxidation of FcTMA(+) at the H
269 acellular translocation, with the activated, oxidized form solely located in the cytosol, whereas red
270 al domain is poorly structured in the active oxidized form suggests that the loss of zinc and unfoldi
271 nge the redox potential and/or the pK on the oxidized form support this mechanism.
272                                In the Rieske oxidized form the 5c sites are square pyramidal but tran
273                                       In the oxidized form, the double mutant exhibits an EPR signal
274 miquinone form of ETF is used instead of the oxidized form, the mirror image of the spectral change s
275                           In addition to the oxidized form, the structure of the molybdate-bound form
276 phores arising from the instability of their oxidized forms, the inability of their oxidized forms to
277                                       In its oxidized form, this lipoprotein can stimulate increased
278 s to regenerate the QD ground state from its oxidized form, thus enabling a continuous device operati
279 their oxidized forms, the inability of their oxidized forms to activate a water oxidation catalyst, o
280 ell correlate with the redox states from the oxidized form, to the more rigid semiquinone and to the
281                      These Cys residues were oxidized forming two pairs of intramolecular disulfides,
282 or cycling of green rust between reduced and oxidized forms under redox dynamics similar to those enc
283  its most reduced valence state back to more oxidized forms usable as electron acceptors.
284 uptake, vitamin C enters mitochondria in its oxidized form via Glut1 and protects mitochondria from o
285 vations that vitamin C is transported in its oxidized form via GLUT1.
286    Furthermore, the percentage of GSH in the oxidized form was higher in the chronic alcoholics (9.8%
287 flavocytochrome, and the fluorescence of its oxidized form was monitored.
288 scorbate transport, either in its reduced or oxidized form was not a substrate for dehydroascorbic ac
289 thioredoxin activated NF-kappaB, whereas the oxidized form was without any effect.
290 ry speciation (i.e., elemental and reactive, oxidized forms) were performed during a six week period
291 ential reduction, in contrast to the resting oxidized form which is activated via type 1 Cu at high p
292  single Tyr-Trp cross-link, as well as a 2e- oxidized form which is postulated to be an intermediate
293  under aerobic conditions is a four-electron oxidized form, which is consistent with its function in
294 as postulated to shift the CXXCH motif to an oxidized form, which must be reduced in a Cyc2p-dependen
295 emental mercury (Hg(0)) to more bioavailable oxidized forms, which can then be methylated by biotic a
296 nriches antibodies to epitopes unique to the oxidized form while excluding antibodies that recognize
297 he native intermediate decays to the resting oxidized form with a rate that is too slow to be in the
298 say showed that the reduced wheat eIF4E, the oxidized form with the disulfide, and the Cys-to-serine
299 ed the interaction of wild-type DJ-1 and its oxidized forms with alpha-synuclein.
300  can be cycled between deoxy, oxygenated, or oxidized forms without significant loss of NO.

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