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1 on in JNCL cells could be reversed by Ca(2+) chelation.
2  kinase kinase (MEK) activity through copper chelation.
3 ron-rich media, failed to prosper under iron chelation.
4 erent approaches: click labeling and surface chelation.
5 eatments that may incorporate selective iron chelation.
6 reduction in cardiovascular events with EDTA chelation.
7 genous zinc application and enhanced by zinc chelation.
8 Ca(2+) channels prevented the effect of zinc chelation.
9 ransferrin- and/or lactoferrin-mediated iron chelation.
10 ine kinase or p38 MAPK inhibition or calcium chelation.
11 F during apoptosis and was blocked by Ca(2+) chelation.
12 eloped parkinsonism that was rescued by iron chelation.
13 peripheralization was blocked by calcium ion chelation.
14 ncreased resistance to disruption by calcium chelation.
15  potassium, but not by intracellular calcium chelation.
16 f short half-life, drug resistance, and iron chelation.
17 y either antioxidant supplementation or Ca2+ chelation.
18 hly transfusions plus daily deferasirox iron chelation.
19 increase in the average lifetime upon Ca(2+) chelation.
20 ent cells are particularly sensitive to iron chelation.
21 se (IN) and influenza endonuclease via metal chelation.
22 n conformational rearrangements enable Ca(2+)chelation.
23 n microscopy, which depolymerized after zinc chelation.
24 ntrol of a kinetic anomeric effect and metal chelation.
25 can be significantly improved without copper chelation.
26                         Intracellular Ca(2+) chelation (1,2-bis(o-aminophenoxy)ethane-N,N,N',N'-tetra
27 o, 8%; HR, 0.77 [95% CI, 0.54-1.11]; stroke: chelation, 1.2%; placebo, 1.5%; HR, 0.77 [95% CI, 0.34-1
28  CI, 0.64-1.02]; hospitalization for angina: chelation, 1.6%; placebo, 2.1%; HR, 0.72 [95% CI, 0.35-1
29      All-cause mortality was reduced by EDTA chelation (10% versus 16%; hazard ratio, 0.57; 95% CI, 0
30  CI, 0.34-1.76]; coronary revascularization: chelation, 15%; placebo, 18%; HR, 0.81 [95% CI, 0.64-1.0
31 similar magnitude as its overall effect (MI: chelation, 6%; placebo, 8%; HR, 0.77 [95% CI, 0.54-1.11]
32      There was no effect on total mortality (chelation: 87 deaths [10%]; placebo, 93 deaths [11%]; HR
33 ane was Ca(2+) dependent, as BAPTA-AM Ca(2+) chelation abrogated the response.
34 ound carbonyl groups, thiol groups and metal chelation activities in addition to phenolic, total flav
35 evaluated the effects of molecules with iron chelation activity on neuroblastoma (NB) cell lines.
36 pacity (TEAC), reducing power (RP) and metal chelation activity were used for all fractions.
37 ocytes was inhibited by intracellular Ca(2+) chelation, aggravated by thapsigargin, and unaffected by
38               Although intracellular calcium chelation almost completely blocked the induction of man
39                                      Calcium chelation also abrogated the gossypol-induced increase i
40                           Mitochondrial iron chelation also alleviated CS-induced impairment of MCC,
41                        Intracellular calcium chelation also inhibited EGF-induced activation of signa
42 gly on geometric factors such as sterics and chelation, although also on the hard/soft match with the
43 acrocycle, although the pathway must involve chelation, amidation, macrocyclic ring reduction, lactam
44 tical for the sulfone-metal exchange because chelation anchors the organometallic proximal to the ele
45 orating structural components for both metal chelation and Abeta interaction.
46 ow that this site is essential for magnesium chelation and allosterically regulates Mg(2+) and MgATP(
47                                        Metal chelation and aromatic diacylation resulted in the most
48 e C13-C15 diene, the identification of alpha-chelation and dipole minimization models for diastereose
49 iation-based therapies; nutritional therapy; chelation and heavy metal therapy; and biological and ph
50 ity and selectivity can be increased through chelation and here we theoretically explore the possibil
51 l balanced in the 451 patients randomized to chelation and in the 460 patients randomized to placebo.
52 ble mechanisms of efficacy is through copper chelation and inhibition of an enzyme involved in catech
53                                              Chelation and luminescence sensitization of Tb(3+) allow
54 in the same predictable manner controlled by chelation and negative hyperconjugation.
55               In dichloromethane, reversible chelation and partial displacement of the P,N coordinati
56                       The main step involved chelation and substrate-controlled diastereoselective re
57 tified Cys466 as a key residue for metal ion chelation and to be the core of an oligomerization motif
58 ry, we present a non-toxic strategy for iron chelation and urinary elimination, based on manipulating
59         Structural data, confirming aldehyde chelation, and a proposed mechanism are provided.
60 ne modifications, including oxidation, metal chelation, and inhibitor binding, within a physiological
61 tin, protein kinase C delta inhibitors, iron chelation, and intra-aortic balloon counterpulsation, pe
62 ost required regular blood transfusion, iron chelation, and intravenous immunoglobulin replacement.
63 um, statins, antidiabetic agents, FX06, iron chelation, and ranolazine).
64  voltage-gated channels, is blocked by BAPTA chelation, and recruits intracellular calcium release on
65 mise of an individually tailored approach to chelation, and subsequent reduction in morbidity and mor
66                                  The surface chelation approach proved to be superior in terms of rad
67 owed similar sensitivity to presynaptic Ca2+ chelation as evoked release, arguing for direct triggeri
68                                      Calcium chelation, as well as the blockade of the mitochondrial
69 ir effects on the above factors, using metal chelation assays, antioxidant assays, and assays of Abet
70 N cross-coupling has been developed based on chelation-assisted amidation of readily available aryl b
71           This material is a rare example of chelation-assisted C-H functionalization performed by a
72 ith aryl isocyanates has been achieved via a chelation-assisted cationic ruthenium(II) complex cataly
73 tion mediated by enzymes (PRIME) followed by chelation-assisted copper-catalyzed azide-alkyne cycload
74 erivatized with an alkyne-probe conjugate by chelation-assisted CuAAC in the second step.
75 tation, we report here a palladium-catalyzed chelation-assisted ortho C-H bond olefination of phenyla
76 nitration of aromatic C(sp(2))-H bonds using chelation-assisted removable vicinal diamine directing g
77  9-methylamino-phenalen-1-one (4a), promoted chelation-assisted single electron transfer (SET) proces
78 neugenic activity, and 6) ethanol or calcium chelation attenuates lipoprotein-induced chromosome mis-
79 anism comprising the bidentate ligand-aided, chelation-based C-H functionalization was proposed for t
80 sed mechanism, and graminaceous plants use a chelation-based mechanism.
81 f cyclic esters that is enabled by transient chelation between a directing group and the lanthanide c
82               The frequency and magnitude of chelation between COO(-) pendant groups of PAA and In(3+
83 f colloidal nanoparticles involving strongly chelation between mercury ion and thiol(s) proved by con
84  are the driving force for the difference in chelation between the two adsorbates.
85  the fluoride adduct confirms fluoride anion chelation between the two antimony centers.
86 are facilitated by Et(2)AlCl, presumably via chelation between the two carbonyl groups of the N-formy
87 odulin-kinase II expression, whereas calcium chelation blunted leptin-mediated increases in CYP11B2,
88                                         Iron chelation by excess Ent or Ybt significantly increased L
89                            We show that iron chelation by FQ leads to epigenetic effects through inhi
90 bility of A. fumigatus to zinc and manganese chelation by neutrophil-derived calprotectin.
91 e in control C3H mice, and in response to Cu chelation by penicillamine (PCA) and dietary supplementa
92 y for fluorescence emission on magnesium ion chelation by phosphorylated peptides carrying an artific
93  the alpha-CNP chelate Mg(2+), mimicking the chelation by the beta- and gamma-phosphate oxygens of dN
94       The findings indicate that strong zinc chelation can promote gastric stability and impede intes
95 razilian and Uruguayan herbs had an 80% iron chelation capacity (p<0.001), while the iron chelation c
96         Finally, the correlation between the chelation capacity and ionophore activity is demonstrate
97 ffinity constant determined in SPR and metal chelation capacity determined from UV-visible spectropho
98 chelation capacity (p<0.001), while the iron chelation capacity of the Argentinean herb was lower but
99 O) radical-scavenging activities, ferric ion-chelation capacity, ferric- (FRAP), and phosphomolybdenu
100 tic compounds may also impart significant Pu chelation character to the colloid.
101 lity of transferrin to chelate iron, as iron chelation combined with sodium bicarbonate completely pr
102 site within a Cu(2+)*GTPgammaS or Cu(2+)*GTP chelation complex, and that Cu(2+)*nucleobase interactio
103 droxyl groups forming five- and six-membered chelation complexes with the iodine atom.
104                                          The chelation-controlled arylation reaction of chiral, enant
105 lyzed alcohol CH syn crotylation followed by chelation-controlled carbonyl dienylation.
106             The key step is a regioselective chelation-controlled lithiation of the (Z)-configured br
107 ctive reactions, including an intramolecular chelation-controlled Michael spirocyclization of an N-Cb
108              The key transformations rely on chelation-controlled organometallic additions and a Peta
109                        The process couples a chelation-controlled reduction of the hydrazone with an
110 eaction, as only the E-isomers could undergo chelation-controlled reduction.
111 n the initial stereocenter by means of a 1,3-chelation-controlled Reetz-Keck-type allylation.
112                         Intracellular Ca(2+) chelation decreased VDCC mobility.
113   Twenty children aged </= 5 y who commenced chelation died during the period studied, with lead pois
114                Taking advantage of phosphine chelation, direct evidence for oxidative addition of Csp
115 s: primary extraction using a divalent metal chelation disk followed by anion-exchange chromatography
116                  Moreover, we show that iron chelation disrupts mitochondrial homeostasis and trigger
117 lective fluorescent sensors that operate via chelation enhanced fluorescence (CHEF).
118 nse brightness and fluorescence enhancement (chelation-enhanced fluorescence = 85 for 3 and 92 for 4)
119 nd continuous PLD assay that is based on the chelation-enhanced fluorescence property of 8-hydroxyqui
120 gh an intermolecular H-bonding induced CHEF (chelation-enhanced fluorescence) process, established by
121                                         Iron chelation experiments demonstrate a relocation of the cl
122 rom dentate fast-spiking interneurones, zinc chelation facilitated T-type Ca(2+) currents, increased
123 although some patients may require intensive chelation for a limited duration.
124 have been proposed; one involves direct iron chelation from beta(2), whereas a second involves Y. des
125                                          Pre-chelation geometric mean blood lead levels for children
126 imary end point occurred in 222 (26%) of the chelation group and 261 (30%) of the placebo group (haza
127 nt discontinued infusions (n=38 [16%] in the chelation group and n=41 [15%] in the placebo group) bec
128                           The primary use of chelation has been transfusional iron overload.
129 inding sites of a multivalent receptor (i.e. chelation) has been proven to have a strong impact.
130 , IC50 of 12.5 vs 30 muM for ADP, and Fe(II)-chelation, IC50 of 80 vs >200 muM for ADP (ferrozine ass
131  of PrOF NMR for efficiently analyzing metal chelation, identifying new binding modes, and studying p
132 sphazene bases and Alder's concept of proton chelation in a constrained geometry regime of basic cent
133 ng body of evidence for the benefits of iron chelation in myelodysplasia, pre-stem cell transplantati
134 l trials into the potential benefits of iron chelation in PD.
135 cle H2 macropa was investigated for (225) Ac chelation in targeted alpha therapy (TAT).
136 allenges of cancer, in nitrogen fixation and chelation, in the production of antibiotics, and in coll
137                                       Al(3+) chelation increased absorbance 2-42x and lambdamax great
138                DPPH scavenging and metal ion chelation increased significantly (p<0.05) from 29-40% t
139 udy of the safety and efficacy of EDTA-based chelation infusions in 1708 post-myocardial infarction (
140 M) or intra-endosomal (Rhod-dextran) calcium chelation inhibited SV generation from bulk endosomes, i
141 -1,9'-xanthen]-3(2H)-one (DEMAX) for Al(III) chelation is described herein.
142  stereochemical outcome of the reaction, and chelation is favored over the natural tendency of this t
143 r data suggest that a pH increase and Ca(2+) chelation lead primarily to a loosening of contacts with
144 Depletion of endogenous Hp and Cp via copper chelation leads to the reduction of hBMVEC Fpn protein l
145  stabilization of allenylzinc derivatives by chelation, made possible by the selection of appropriate
146                 Removal of soluble metals by chelation markedly diminished the pulmonary PM-mediated
147           Recent research suggests that EDTA chelation may be a well-tolerated and effective treatmen
148 ased its effectiveness, suggesting that iron chelation may play some role in its antimycobacterial ef
149                                            A chelation mechanism was initially proposed to explain th
150 pported adsorption steps including a citrate chelation method developed to remove >99.9% of the bariu
151 d (64)Cu labeling was obtained by a standard chelation method.
152 mmatory activity of UC and 14 controls using chelation method.
153 The thioenolate is found to bind via di-zinc chelation, mimicking the binding of intermediates in bet
154 dy-based agents, we designed a multimodality chelation (MMC) scaffold which combined a radiometal che
155  dual-labeling approach with a multimodality chelation (MMC) scaffold would minimize steric effects o
156 yridone analogues designed using a two-metal chelation model of the integrase catalytic active site.
157 ive C-H activation was conducted without any chelation moieties.
158 al Ca(2+) increases, whereas luminal calcium chelation (N-(2-hydroxyetheyl)-ethylendiamin-N,N,N'-tria
159 ing of NOTA to a unique cysteine residue and chelation of (18)F-AlF.
160 ctrum centered at 530 nm attributed to metal chelation of 2-OG bound to JBP, a spectroscopic signatur
161  of the metallocavitand involved the initial chelation of a Ru(III) chloride complex by the tpy ligan
162 tants in subunits a and c is inhibited after chelation of Ag(+) and/or Cd(+2) with the substituted su
163                                        Early chelation of blood-derived iron and antioxidant treatmen
164  the amnioserosa during closure, whereas the chelation of Ca(2+) slows closure.
165 f the enzyme pectin methyl-esterase, and the chelation of calcium by pectic acids.
166                                              Chelation of calcium ions by 1,2-bis(2-aminophenoxy)etha
167 is further stabilized by disulfide bonds and chelation of calcium ions.
168  by its cuprous oxidase activity but also by chelation of copper ions before they can enter the cytop
169 acterised as being the most effective in the chelation of copper ions.
170                                    Histamine chelation of copper(I) by a terminal histidine residue i
171 o-surface attachment was blocked by specific chelation of copper.
172 uptake in the fine lateral root tips and (b) chelation of Cr(III) to the cell wall both of which redu
173                                 Furthermore, chelation of cytoplasmic Ca(2+), but not inhibition of p
174        Instead, pharmacological depletion or chelation of Endoplasmic Reticulum (ER) Ca(2+) prevented
175 ola spatulata mechanotoxin 4 (GsMTx-4) or by chelation of extracellular Ca(2+) Thrombus formation was
176 l adhesion, as reducing cadherin binding via chelation of extracellular calcium inhibits chondrocyte
177       Substitution of extracellular Na(+) or chelation of intracellular Ca(2+) abolished both sADP an
178 el inhibitor l-cis-diltiazem, as well as the chelation of intracellular Ca(2+) with BAPTA, or the abs
179 , PS exposure in platelets was suppressed by chelation of intracellular Ca(2+), whereas caspase inhib
180         Removal of extracellular calcium, or chelation of intracellular calcium did not normalize the
181 lockade of voltage-gated calcium channels or chelation of intracellular calcium, but were blocked by
182 the compounds, CPX, were indeed dependent on chelation of intracellular iron and mediated by both G0/
183                                    Moreover, chelation of intracellular zinc alone was sufficient to
184 ETs in neutrophils, thus indicating that the chelation of iron may largely explain their inhibitory e
185 ne that induces apoptosis in cancer cells by chelation of labile inhibitory zinc from procaspase-3.
186 procaspases to their active cleaved forms by chelation of labile zinc ions.
187 th the sieving mechanism of the membrane and chelation of lead with AG macromolecules incorporated in
188 he accumulation of Cd in grains, such as the chelation of light Cd isotopes by thiol-containing pepti
189                               The effects of chelation of metal ions (Mg(2+), Al(3+), Cr(3+), Fe(3+),
190 ature hydroxamate moieties to facilitate the chelation of metal ions in the catalytic center of targe
191 lavour stability: use of antioxidant crowns, chelation of pro-oxidants, and varying plant content in
192                              Whereas in situ chelation of PyED leads to considerable degradation in t
193 is216 were identified as essential for metal-chelation of sirohydrochlorin.
194 s has been synthesized and evaluated for the chelation of Th(4+).
195 uction of N2 under mild conditions, and then chelation of the alkali metal cation uncovers a highly r
196 0 consists of a monomer in which C,N and N,O chelation of the lithium cations generates a system cont
197 to be increased, probably due to compromised chelation of the metals in the stratum corneum of patien
198 DPPH and hydroxyl radicals, as well as metal chelation of the soluble fraction from PS, were higher t
199 rsus hydroxamate inhibitors reveals that the chelation of the zinc ion is slightly different, leading
200 s) (Mg(2+) or Mn(2+)) in its catalytic site: chelation of these metal cofactors is an attractive stra
201           A reduction of oxidative stress by chelation of toxic metals has been proposed as a possibl
202 avenging of reactive oxygen species, and (3) chelation of traces of transition metal ions, which is s
203 -reducing antioxidant power (FRAP) and metal chelation of VH were comparable to those of NH.
204                            In granule cells, chelation of zinc reduced the time window for the integr
205 g of the chip to yield a 3-D support for the chelation of Zn(2+) ions (ZnCl2) and the subsequent immo
206                                              Chelation of Zn(2+) with N,N,N',N'-tetra-2-picolylethyle
207                                              Chelation of Zn(2+) with the membrane-permeable chelator
208 nd Pb(II) by 1f, as determined by FT-IR, and chelation of Zn(II), but not Ca(II), by 1b, as determine
209                           The effect of EDTA chelation on the components of the primary end point oth
210  was achieved by reducing inflammation by Cu chelation or by providing methyl groups.
211                                       Ca(2+) chelation or calpain inhibition prevented SA processing
212 ificantly inhibited by intracellular Ca(2+)i chelation or CaM inhibition.
213 ption of these labile copper stores by acute chelation or genetic knockdown of the CTR1 (copper trans
214                                       Zn(2+) chelation or loading in cells to alter Zn(2+) availabili
215       Patients received 40 infusions of EDTA chelation or placebo.
216 rments in neurite outgrowth caused by Zn(2+) chelation or ZIP12 knockdown.
217                            Accordingly, iron chelation, or overexpression of a truncated AFT1 allele
218 ression, was blocked by postsynaptic calcium chelation, our findings suggest that endogenous NT may a
219 eatment-related difference (mean difference [chelation.placebo] during follow-up, 0.9 [95% confidence
220 mmune response to Ent and Lcn2 requires iron chelation rather than the Ent+Lcn2 complex itself and al
221 lements for Abeta aggregation control, metal chelation, reactive oxygen species (ROS) regulation, and
222 abilization (LMP) that relied on copper (Cu) chelation, reactive oxygen species generation, and incre
223                                However, iron chelation reduced the oxidation rate.
224                                              Chelation reduced the primary composite end point of mor
225 tes and may provide an adjuvant treatment to chelation, reducing myocardial iron uptake.
226  with a history of MI, use of an intravenous chelation regimen with disodium EDTA, compared with plac
227 /day or placebo in addition to their current chelation regimen.
228 an iron overload (for which the role of iron chelation remains debated).
229 Aspergillus fumigatus and found that calcium chelation severely impedes hyphal growth indicating a cr
230                                              Chelation should be considered in patients with iron ove
231  the calcium signal by intracellular calcium chelation significantly reduced epidermal growth factor
232 cation (VO(+2)) through 4-carbonyl-5-hydroxy chelation site in the two luteolin molecule.
233 rference, and identifies potential magnesium chelation sites while characterizing their coordinated r
234                         Both modes of Ca(2+) chelation slow gastric repair.
235 ndomized to receive 40 infusions of a 500-mL chelation solution (3 g of disodium EDTA, 7 g of ascorba
236 010) to 40 infusions ofa multicomponent EDTA chelation solution or placebo.
237 nction as we observed only modest effects of chelation strategies on the growth of these cells in vit
238  evaluated whether addition of amlodipine to chelation strategies would reduce myocardial iron overlo
239  referred to as "nutritional immunity." This chelation strategy ultimately starves invading pathogens
240                        In addition, the zinc chelation strength of the polyphenols was also tested in
241 nvolves various mechanisms, among them metal chelation, studied by UV-visible spectrophotometry.
242 le size regulation were eliminated by Ca(2+) chelation, suggesting a requirement for TRPML1-mediated
243 C inhibition but not by intracellular Ca(2+) chelation, suggesting Ca(2+) independent activation of n
244 eta)-activated kinase 1 (TAK1) or by calcium chelation, suggesting potential linkage to the mitogen-a
245 ch for individuals under chronic transfusion/chelation support therapy is allogeneic stem cell transp
246 ted from the rabbit intestine using the Ca++ chelation technique.
247 to be a highly promising ligand for (225) Ac chelation that will facilitate the clinical development
248                                 After Pb(2+) chelation, the conjugation system of the PDA was perturb
249 overload correlated with lower compliance to chelation therapy (P<0.013).
250  Institutes of Health.funded Trial to Assess Chelation Therapy (TACT) randomized 1708 stablecoronary
251                          The Trial to Assess Chelation Therapy (TACT) showed clinical benefit of an E
252 y reduced cardiac iron more effectively than chelation therapy alone.
253 aken together, these results suggest that Cu-chelation therapy could be repurposed to treat cancers c
254                          The trial to assess chelation therapy demonstrated a significant (P=0.035) 1
255 with a history of myocardial infarction,EDTA chelation therapy did not have a detectable effect on QO
256 ient evidence to indicate the routine use of chelation therapy for all post-myocardial infarction pat
257 not sufficient to support the routine use of chelation therapy for treatment of patients who have had
258              Recent developments in gene and chelation therapy give hope of better prognosis for pati
259                                         EDTA chelation therapy has been in off-label use for the trea
260                           Mitochondrial iron chelation therapy improved colitis and demonstrated an e
261                    After institution of iron chelation therapy in 2010, no child with thalassemia maj
262 etrospective analysis demonstrates that iron chelation therapy is associated with prolonged survival
263  cardiac siderosis, amlodipine combined with chelation therapy reduced cardiac iron more effectively
264 eposits was associated with lower anti-tumor chelation therapy response.
265                          The trial to assess chelation therapy was a $30 million National Institutes
266 derate strength recommendation to begin iron chelation therapy when indicated.
267                                              Chelation therapy with disodium EDTA has been used for m
268 ly positive results of TACT (Trial to Assess Chelation Therapy), and a body of epidemiological data s
269 ent primarily relies on transfusion and iron-chelation therapy, as well as splenectomy in specific ca
270 es an update on advances in the area of iron chelation therapy, including new indications and uses of
271 measures included environmental remediation, chelation therapy, public health education, and control
272 to 2012 after universal availability of iron chelation therapy.
273 t side effects associated with systemic EDTA chelation therapy.
274 last decade has ushered in a new era in iron chelation therapy.
275 = 45 microg/dL, the threshold for initiating chelation therapy.
276   Eight patients had siderosis and underwent chelation therapy.
277 WiTCH) trial compared standard (transfusions/chelation) to alternative (hydroxyurea/phlebotomy) treat
278 l comparing standard treatment (transfusions/chelation) to alternative treatment (hydroxyurea/phlebot
279 7,000 lead poisoned villagers, to facilitate chelation treatment of children </= 5 years old, and to
280 y as feasible without sedation to tailor the chelation treatment.
281  who underwent between one and 15 courses of chelation treatment.
282 trations by 89%, and 2,349 children received chelation treatment.
283  Fe3O4@Al2O3 MNPs through aluminum phosphate chelation under microwave heating within 1.5 min.
284                    We examine the history of chelation up through the report of TACT.
285 es the intention-to-treat comparison of EDTA chelation vs placebo.
286       The antiproliferative effect of copper chelation was enhanced when combined with inhibitors of
287 expression, function, and mitochondrial iron chelation were assessed in a colitis-associated colon ca
288 idation-induced degradable nanogels for iron chelation were rationally designed by simultaneously pol
289 tion of each chain align, facilitating metal chelation when the residues are good ligands such as his
290           Current therapy is based on copper chelation, which decreases the manifestations of liver d
291 osely bound copper that can be attenuated by chelation, which define a labile copper pool.
292 ion to be efficient, probably because of its chelation with cesium ion.
293    While early, presymptomatic detection and chelation with conventional copper-binding molecules ena
294                                              Chelation with disodium calcium edetate lowers blood man
295 ced PI(4,5)P2 hydrolysis, followed by Ca(2+) chelation with excess EGTA.
296 f arsenite species [As(III)] was achieved by chelation with sodium diethyldithiocarbamate (DDTC) foll
297 rize the mechanisms by which Ag(+) or Cd(2+) chelation with the Cys thiolates caused inhibition.
298  by having a hydroxamate group essential for chelation with the zinc ion in the active site of HDAC a
299                                              Chelation with three representative styrenes has been de
300        Similarly, INDF was blocked by Ca(2+) chelation without a block in ICAD cleavage or caspase-3

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