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1 yclohexadiene, 2,4,6-(t)Bu3C6H2OH) to afford ferrous amido product ((Ar)L)Fe(NHAd), and can mediate i
2  7112.2 eV, 6: 7112.4 eV) as compared with a ferrous amine adduct ((Ar)L)FeCl(NH2Ad) (7: 7110.3 eV).
3    NMR studies showed that Fe(2+) from added ferrous ammonium sulfate binds IscX much more avidly tha
4 a color change following the addition of 10% ferrous ammonium sulfate.
5 nds and the secondary coordination sphere in ferrous and ferric complexes.
6                                              Ferrous and ferric forms of both proteins underwent init
7  the slopes of the bands on concentration of ferrous and ferric ions, it was possible to estimate the
8                However, the redox cycling of ferrous and ferric iron in the presence of H2O2, which i
9                        Bacteria harbour both ferrous and ferric iron transporters.
10 d with chloroquine resistance transport both ferrous and ferric iron, albeit with different kinetics.
11 the bis-imidazole model complex and cyt c in ferrous and ferric oxidation states show quantitative di
12 showed that the heme is pentacoordinate when ferrous and in the hydroxide-ligated form when ferric, e
13 dz forest, which is close to a foundry using ferrous and non-ferrous metals could result in a Hg inta
14 hyrin where the pre-equilibria among ferric, ferrous, and ferric-superoxide intermediates have been q
15 sample containing 2-30 mum grains of various ferrous- and ferric-iron containing minerals, including
16          However, authigenic parasymplesite (ferrous arsenate nanophase), exhibiting a threadlike mor
17  as well as nickel and cobalt recovered in a ferrous-based pregnant leach solution (PLS), facilitatin
18 ferrous fumarate in wheat flour in 2002, and ferrous bisglycinate was added to maize flour in 1999 an
19                      When Np(V) was added to ferrous carbonate solution, the subsequent precipitation
20 ising catalytic materials among the reported ferrous catalysts.
21            The existing assays (oxidation of ferrous cation and iodometric assays) cannot be used in
22     We found that NO(*) binds tightly to the ferrous CBS heme, with an apparent Kd </= 0.23 mum.
23 ic reducing activities (p<0.05), but limited ferrous chelating activities.
24 the powders using three model systems (DPPH, ferrous chelating and reducing power).
25 dical scavenging activity and 10-48% for the ferrous-chelating power.
26       The compounds examined include the all-ferrous clusters [ (n) Bu(4)N][((tbs)L)Fe(3)(mu(3)-Cl)]
27  oxidation state containing oxidized Pdx and ferrous CO-bound P450cam, showing that P450cam remains c
28                      We ruptured the bond in ferrous cyt c using an optical laser pulse and monitored
29                                       In its ferrous deoxy form, GLB-33 GD is capable of reversibly b
30 ctivity and regulates appearance of the free ferrous deoxy-NGB, which is the redox active form of the
31                ArsI is a microbial non-heme, ferrous-dependent dioxygenase that transforms toxic meth
32 ght into the mechanism for conversion of the ferrous-dioxygen complex into the reactive ferryl interm
33 the activity of nitrate-reducing bacteria in ferrous environments may provide a direct link between t
34 fying the rhizosphere and reducing ferric to ferrous Fe prior to membrane transport.
35 ultiple redox states, including the divalent ferrous (Fe(2+)) and the trivalent ferric (Fe(3+)) speci
36 ciently interconvert the ferric (Fe(3+)) and ferrous (Fe(2+)) forms of an immobilized NGB showed that
37 ction mutations in the feoAB operon encoding ferrous (Fe(2+)) iron uptake proteins.
38                           In addition to O2, ferrous (Fe(II)) Hb can bind CO.
39 hown to reduce iron from ferric [Fe(III)] to ferrous [Fe(II)] state, but minerals that form during ir
40 c dithienylethene spacer predictably forms a ferrous [Fe2 L3 ](4+) helicate exhibiting spin crossover
41 ems (potassium ferricyanide/ferrocyanide and ferrous/ferric ammonium sulfate) yielded Nernstian slope
42 dissolve major muscle components and convert ferrous/ferric haem proteins to hemichromes with a uniqu
43 not enantiomer-specific and is stimulated by ferrous/ferric ion and reducing agents including L-ascor
44 distributing heme, iron-sulfur clusters, and ferrous/ferric ions to apoproteins remain incompletely d
45 er (CPET) upon reaction of the mixed-valent (ferrous/ferric) protonated 5H(2-) with TEMPO.
46  the effects of spin (high/low) and valence (ferrous/ferric) states on iron partitioning in the deep
47 two populations have shown that the CO-bound ferrous form of the dimeric protein absorbed at 448 nm (
48                                       In its ferrous form, it undergoes ligand release and doming upo
49 O proteins in their physiologically relevant ferrous form.
50 n occurs in clay minerals in both ferric and ferrous forms.
51 utrient powder (MNP) containing a mixture of ferrous fumarate and sodium iron EDTA (FeFum+NaFeEDTA) i
52 5) after iron supplementation (60 mg iron as ferrous fumarate daily).
53  an ineffective fortificant, was replaced by ferrous fumarate in wheat flour in 2002, and ferrous bis
54 lementation with 60 mg of elemental iron (as ferrous fumarate, n = 237 women) or placebo (n = 233) fr
55 stants for the reaction of STAR with several ferrous globins and biomolecules were determined by kine
56                                One tablet of ferrous gluconate (37.5 mg of elemental iron) daily or n
57 ile approach involving a direct pyrolysis of ferrous gluconate and a following removal of free iron,
58 oups of the globin chains: from paramagnetic ferrous Hb to diamagnetic ferrous oxyhemoglobin (oxyHb)
59 iation ( approximately 10-fold) of CO to the ferrous heme at physiological AdoMet concentrations.
60           NO activates sGC by binding to the ferrous heme cofactor; the relative amount of NO with re
61 lve the reaction of oxygen with the NO-bound ferrous heme complex, but the mechanistic details of the
62                   CO or NO(*) binding at the ferrous heme negatively modulates the enzyme activity.
63 nic structures, together with comparisons to ferrous heme proteins and an Fe(IV) oxene model.
64                                          For ferrous heme proteins, doming is associated with the res
65 e coordinated Cys differs for the ferric and ferrous heme species, with Cys binding as a thiolate and
66 nitrite, the second equiv of NO(g) traps the ferrous heme thus formed.
67 ransient absorption spectrum of 4-coordinate ferrous heme to which NO rebinds with a time constant ta
68 etalated with Fe(II) to yield a 4-coordinate ferrous heme-containing compound.
69 ures of discrete [(L)Cu(II)(NO2(-))](+) plus ferrous heme-nitrosyl compounds; when the first NO(g) eq
70 -NO complex (k(d) ), and of oxidation of the ferrous heme-NO complex (k (ox)).
71              The reaction of oxygen with the ferrous heme-NO species is part of a futile cycle that d
72 ng of NO to myoglobin, giving a 6-coordinate ferrous-heme complex, was inferred from the measured Ram
73 lysulfide-carrying hemoglobin derivatives to ferrous hemoglobin, thus completing the methemoglobin-de
74                                              Ferrous hydroxide coprecipitation was used for the preli
75 nt in promoting amino acid formation: Purely ferrous hydroxides did not drive reductive amination but
76 e the magnetite was partially transformed to ferrous hydroxy carbonate (FHC).
77 nal Fe(II) is incorporated into siderite and ferrous hydroxy carbonate, along with magnetite, in ferr
78 ke system, linking increased Fur activity to ferrous import under iron-sufficient conditions.
79 s mechanistic proposal involving exclusively ferrous intermediates and highlight the importance of th
80 xtracellular Cp accelerates the oxidation of ferrous ion bound to FPN.
81 ydrazy (DPPH) radical scavenging activities, ferrous ion chelating abilities and reducing power resul
82 -1-picrylhydrazyl antioxidant activities and ferrous ion chelating activities.
83                                AOs were weak ferrous ion chelators.
84 o the passive-gradient model, the removal of ferrous ion from the site of release sustains the gradie
85           Furthermore, reduction tests using ferrous ion in suspensions of magnetite and maghemite sh
86 against M. tuberculosis is dependent on high ferrous ion levels and reactive oxygen species productio
87 ntinuous photolysis of 7b in the presence of ferrous ion or thiophenol produces good yields of dA, wh
88    Emulsions containing beta-glucan, oil and ferrous ion showed significant viscosity and molecular w
89 racellular environment binds to the oxidized ferrous ion, completing the release process.
90 ging assays: DPPH, hydroxyl and peroxyl; and Ferrous Ion-chelating Ability Assay).
91 ghest antioxidant activity (57.11 mug mL(-1) Ferrous Ion-chelating Ability, 221.46 mug mL(-1) Hydroxy
92 Singlet oxygen quenching, reducing power and ferrous ion-chelating activities of CS were also pronoun
93 radical scavenging activity, reducing power, ferrous ion-chelating and liposome model system).
94 ds carbon monoxide (CO), biliverdin (BV) and ferrous ion.
95 ted to their ABTS(+) scavenging activity and ferrous-ion-chelating capacity.
96 cals (866.9 +/- 10.6 uM TE/g) and to chelate ferrous ions (75 +/- 0.4%) while displaying the second s
97 estigates the impact of redox reactions with ferrous ions (Fe2+) on the colloidal stability of CeO2 N
98 d culture media without iron (M9(-)) or with ferrous ions (M9(Fe(2+))).
99 dominantly in the reduced ferrous state, but ferrous ions alone cannot form polynuclear iron-sulfur c
100 e-4S] clusters through the photooxidation of ferrous ions and the photolysis of organic thiols.
101  were mixed with different concentrations of ferrous ions at pH 1.5.
102                     Here, we report that the ferrous ions in Fe(2+)-exchanged MOF-5 disproportionate
103     Apparent negative-feedback inhibition by ferrous ions is documented at nanomolar concentrations,
104  release of AA, resulting in the increase of ferrous ions through the redox reaction between AA and I
105 f metal ions and chelating abilities against ferrous ions.
106  linoleate 10S-hydroperoxide with hematin or ferrous ions.
107  activity was obtained after metalation with ferrous ions.
108 ates of the Fenton reaction, by assimilating ferrous iron (Fe(2+)) and inducing the decomposition of
109 iron minerals from the metabolism of soluble ferrous iron (Fe(2+)) coupled to the reduction of nitrat
110                Purified soluble FLD oxidizes ferrous iron (Fe(2+)) to incorporate ferric iron (Fe(3+)
111 ulfoxy species (e.g., S2O3(2-), SO4(2-)) and ferrous iron (Fe(2+)) to the solution and also producing
112                                      CO2 and ferrous iron (Fe(2+)) were produced in stoichiometric am
113 e employed a new proxy, carbonate associated ferrous iron (Fe(carb)), to quantify the seafloor oxygen
114                                      Aqueous ferrous iron (Fe(II)) accelerates the transformation of
115 and hydrological processes: the oxidation of ferrous iron (Fe(II)) and the subsequent formation of pa
116  Neutrophilic microbial aerobic oxidation of ferrous iron (Fe(II)) is restricted to pH-circumneutral
117              Investigation of the effects of ferrous iron (Fe(II)) on the ability of aged (iron oxide
118 other minerals formed from added nitrate and ferrous iron (Fe).
119     A chemical pathway involving reaction of ferrous iron (Fe2+) with nitrite (NO2-), an intermediate
120 (7) complex is best described as a high spin ferrous iron (S=2) antiferromagnetically coupled to an N
121 we demonstrate the role of chemolithotrophic ferrous iron [Fe(II)]-oxidizing bacteria in biogeochemic
122                                              Ferrous iron accumulates over adult lifetime in Caenorha
123 ients, however, suggesting that the heme and ferrous iron acquisition pathways of P. aeruginosa are m
124 ansporter-1 (DMT1) mediates the transport of ferrous iron across the apical membrane of enterocytes.
125 c, and superstoichiometric concentrations of ferrous iron and anthrahydroquinone disulfonate within a
126 sults suggest an ordered stepwise binding of ferrous iron and dioxygen to the ferroxidase site in pre
127                            The production of ferrous iron and sulfide in conjunction with rapid oxida
128                        These species oxidize ferrous iron and thereby displace it from many iron-depe
129                                              Ferrous iron associated with iron mineral phases forms h
130 ader cohort of non-redox enzymes that employ ferrous iron atoms as catalytic cofactors.
131 te ferric iron reduction, with the resulting ferrous iron being available to the bacterium for uptake
132        The Fenton reaction, the oxidation of ferrous iron by hydrogen peroxide (H(2)O(2)), is typical
133 e-O2 bonding situation includes in essence a ferrous iron center, minor superoxide character of the n
134 ic iron assay was used to measure ferric and ferrous iron content in the lesions and the healthy myoc
135 empower enzyme function, and also how labile ferrous iron contributes to iron-dependent cell death (f
136 iron deficiency recommend daily provision of ferrous iron divided through the day to increase absorpt
137  supported by the synergistic actions of the ferrous iron efflux transporter, ferroportin (Fpn) and a
138 how that glutathione depletion is coupled to ferrous iron elevation in these animals, and that both o
139                                              Ferrous iron formed during microbial ferric iron reducti
140 bservations suggest that Salmonella acquires ferrous iron from haemophagocytic macrophages.
141                   Their results suggest that ferrous iron functions as an oxygen sink that is modulat
142 t a dose of ~40 kilograys already yields 50% ferrous iron in a heme protein crystal.
143 view recent insights into the role of labile ferrous iron in biology and disease, and describe new th
144 xide overproduction and accumulation of free ferrous iron in mitochondria caused by oxidative damage
145                                  Over 97% of ferrous iron in pH 2.0-2.2 synthetic mine water was oxid
146 he abundance of methylotrophy substrates and ferrous iron in situ, which underlines the essentiality
147 d and tested for their capacities to oxidize ferrous iron in synthetic and actual acid mine drainage
148 nd ferrous soaked crystals revealed only one ferrous iron in the active site occupying site A.
149 ecreased, with lower soil nitrate and higher ferrous iron in the low marsh compared to the mid and hi
150                Incorporating both ferric and ferrous iron in their structures, these oxides if presen
151      Abundant iron oxides and high dissolved ferrous iron indicate iron reduction in the methanogenic
152 e site showed that the oxidative sorption of ferrous iron is an energetically favored process at seve
153 ular, we found that the ability to transport ferrous iron is reduced by the specific polymorphisms ac
154 scopy suggests that substrate binding to the ferrous iron is through the thiol but indicates that eac
155 The reactive oxygen species produced by free ferrous iron lead to increased oxidative stress and cell
156 creased oxidative stress and elevated labile ferrous iron levels.
157                             Experiments with ferrous iron or anthrahydroquinone-2,6-disulfonate (AH2Q
158 tem essential for photoautotrophic growth by ferrous iron oxidation, influences electron uptake.
159 ter adding 48 ferrous iron to apo-PmFTN (two ferrous iron per subunit), and a much slower phase due t
160 um, sodium and total nitrogen, and decreased ferrous iron relative to the dry season (January 2011).
161 ted to be associated with the oral intake of ferrous iron salts (i.e. nausea, vomiting, heartburn, ab
162 mospheric pO(2) sweeps the deep ocean of the ferrous iron substrate for photoferrotrophy.
163 be associated with sulfide phases, including ferrous iron sulfide (FeS), which can sorb or be copreci
164 (II) which involved the surface oxidation of ferrous iron surface complexes ( identical withS(S,W)OFe
165 rified enzyme was activated more strongly by ferrous iron than by other metals, and only this metallo
166 w-temperature hydrothermal vents enriched in ferrous iron that supports extensive microbial mats.
167 ase site, which is saturated after adding 48 ferrous iron to apo-PmFTN (two ferrous iron per subunit)
168 coproporphyrinogen to coproporphyrin, insert ferrous iron to make Fe-coproporphyrin (coproheme), and
169 probe that couples Fenton-type reaction with ferrous iron to subsequent protein labeling via concomit
170 gulator (Fur) has been thought to respond to ferrous iron to transcriptionally regulate genes require
171 Enhanced iron uptake was not observed with a ferrous iron transport mutant.
172                                          The ferrous iron transport system Feo is widely distributed
173                 The strain carrying only the ferrous iron transporter Feo grew well at acidic, but no
174                                          The ferrous iron transporter FeoB is an important factor in
175                                      The Feo ferrous iron transporter is widely distributed among bac
176 e culture medium triggered expression of the ferrous iron transporter LIT1 (Leishmania iron transport
177 ation of the ferric iron reductase LFR1, the ferrous iron transporter LIT1, and the heme transporter
178 train containing an inactivated feoB-encoded ferrous iron transporter results in increased bacterial
179   Deletion of feoB, which encodes a putative ferrous iron transporter, retarded replication of the LV
180 ic import to the more physiological relevant ferrous iron under anaerobic conditions.
181  on siderophore-mediated ferric iron uptake, ferrous iron uptake, or heme uptake at different points
182     When fed with actual mine water, >90% of ferrous iron was oxidized at D values of 0.4 h(-1), and
183                              Both ferric and ferrous iron were found in the mucus, indicating the occ
184        Subsequent oxidation of the mobilized ferrous iron with manganese oxides results in a large st
185 on mediated by chemical species (sulfide and ferrous iron) and the common metal-reducing microbe Shew
186                      The reconstructed FetR (ferrous iron), MntR (manganese), and ZntR (zinc) regulon
187 eme into the bilirubin precursor biliverdin, ferrous iron, and CO during B. pseudomallei infection.
188 e" iron concentration is elevated, Fur binds ferrous iron, and the iron-bound Fur represses the genes
189 deR represses gene expression in response to ferrous iron, and we here demonstrate that SirR (Rv2788)
190 e, forming a strong hexadentate complex with ferrous iron, by three consecutive oxidation steps.
191 in light of the Fenton chemistry promoted by ferrous iron, suggest a new category of therapeutics exh
192 Because dicotyledonous plants only transport ferrous iron, we checked whether embryos were capable of
193                                              Ferrous iron-bearing minerals are important reductants i
194 troduces a new reactivity-based probe of the ferrous iron-dependent interactome and uncovers new targ
195         ALKBH5 is a 2-oxoglutarate (2OG) and ferrous iron-dependent nucleic acid oxygenase (NAOX) tha
196 st a new category of therapeutics exhibiting ferrous iron-dependent pharmacology.
197 e reduction extents and rates during abiotic ferrous iron-induced transformation of six-line ferrihyd
198           In EPR studies of the oxidation of ferrous iron-loaded Dps following DNA photooxidation, a
199 termediates in the DNA-mediated oxidation of ferrous iron-loaded Dps.
200 y characterize the DNA-mediated oxidation of ferrous iron-loaded Dps.
201 ontributions of an individual regulator, the ferrous iron-responsive regulatory element, BqsR, on glo
202 neral surfaces such as silicate radicals and ferrous iron.
203 n specific ATPase most strongly activated by ferrous iron.
204 buted to the oxidation of organic matter and ferrous iron.
205 iron minerals in the presence of nitrate and ferrous iron.
206 ng uptake and degradation of heme to release ferrous iron.
207 h this did not have a negative impact on net ferrous-iron oxidation.
208 invariance of *Trp decay times in ferric and ferrous Mbs raises the question as to whether electron t
209 35 and the 1970s (1980s) due to expanded non-ferrous metal production.
210  is close to a foundry using ferrous and non-ferrous metals could result in a Hg intake that exceeds
211 xygen-evolving electrocatalyst consisting of ferrous metaphosphate on self-supported conductive nicke
212                                              Ferrous myoglobin was oxidized by sulfur trioxide anion
213 ystem does not terminate at this very stable ferrous nitrosyl.
214 cal oxidation of the corresponding high-spin ferrous NO {FeNO}(7) complex.
215 H bonds, but decay via N-O bond homolysis to ferrous or ferric iron hydroxides in the presence of 1,4
216 idoreductase that reduces ferric iron to the ferrous oxidation state, in the Broad Institute Cancer C
217 uction of the iron center from ferric to the ferrous oxidation state.
218  (lipid hydroperoxides) were measured with a ferrous oxidation-xylenol orange (FOX) assay and volatil
219 determination of peroxide value (PV) and the ferrous oxidation-xylenol orange (FOX) method.
220             Those being minute quantities of ferrous oxide, located near regions of increased porosit
221  GRs can be produced from ferric reducing or ferrous oxidizing bacterial activities.
222 hree distinct steps: 1) initial oxidation of ferrous (oxy) to ferryl Hb; 2) autoreduction of the ferr
223  from paramagnetic ferrous Hb to diamagnetic ferrous oxyhemoglobin (oxyHb) with reversibly bound O2,
224 ic porphyrin, [Fe(III)(TPP)](+)(,) forms the ferrous porphyrin, Fe(II)(TPP), which binds O(2) reversi
225  temperature (RT) with a thiyl-radical bound ferrous porphyrin, i.e., its valence tautomer.
226 e stability of heme coordination upon ferric/ferrous redox cycling is a crucial property of the const
227 1-picrylhydrazyl (DPPH) scavenging activity, ferrous reducing antioxidant power (FRAP), total phenoli
228 inding to the haem decreases activity, while ferrous RsbR results in increased activity, suggesting t
229                                          The ferrous salt of 2,5-dihydroxy-terephthalic acid, a metal
230 des values between $1.32 and $145 per ton of ferrous scrap for this material, if recoverable as pure
231 am to be between 0.13 and 0.29 kg per ton of ferrous scrap.
232 eme-free, ferric, and nitric oxide-sensitive ferrous sGC in cells and tissues, we propose that cinaci
233 ave calculated the average Nd content in the ferrous shredder product stream to be between 0.13 and 0
234 uctures derived from anaerobically grown and ferrous soaked crystals revealed only one ferrous iron i
235 n crystals at increasing exposure times to a ferrous solution showed the progressive formation of a t
236             The crystal structure of the all-ferrous species ([(tren) L)2 Fe8 (PMe2 Ph)2 ] (1) displa
237  one-electron oxidation of the corresponding ferrous species [(PyPz)Fe(II)(OH2)2](4+) (2).
238  O/Fe ratio in FeO(2)Hx, iron remains in the ferrous, spin-paired and non-magnetic state at 60-133 GP
239 early Earth was predominantly in the reduced ferrous state, but ferrous ions alone cannot form polynu
240 ric IDO1 and reduce it to the oxygen-binding ferrous state, thus activating IDO1 to maximal turnover
241 he heme porphyrin (porph), turning it to the ferrous state.
242 the substrate/product from the ferric to the ferrous state.
243 r-bound species followed by reduction to the ferrous state.
244 zymes has His/Cys ligation in the ferric and ferrous states and the midpoint potentials (E(m) ) of th
245 alency for the ferric states relative to the ferrous states.
246 taining 5 mg Fe as (57)FeFum+Na(58)FeEDTA or ferrous sulfate ((54)FeSO4).
247 igned to receive a 3-mo course of daily oral ferrous sulfate (2 mg . kg-1 . d-1) either concurrently
248 n-casein complex (3.4%; 1.4%, 5.4%) and from ferrous sulfate (3.9%; 1.7%, 6.1%) were not statisticall
249 /dL (95% CI, 0.4 to 1.6 g/dL; P < .001) with ferrous sulfate (based on a linear mixed model).
250  the iron-casein complex relative to that of ferrous sulfate (control) when given with whole milk in
251                  Two common fortificants are ferrous sulfate (FeSO4) and ferric sodium EDTA (NaFeEDTA
252 ize meal fortified with isotopically labeled ferrous sulfate (FeSO4; study 1) or ferric pyrophosphate
253 ts consumed a test drink with 6 mg (57)Fe as ferrous sulfate and were intravenously infused with 100
254 ths with nutritional iron-deficiency anemia, ferrous sulfate compared with iron polysaccharide comple
255 mg/kg of elemental iron once daily as either ferrous sulfate drops or iron polysaccharide complex dro
256 complete resolution of IDA was higher in the ferrous sulfate group (29% vs 6%; P = .04).
257 arrhea in the iron complex group than in the ferrous sulfate group (58% vs 35%, respectively; P = .04
258  hemoglobin increased from 7.9 to 11.9 g/dL (ferrous sulfate group) vs 7.7 to 11.1 g/dL (iron complex
259  group), 59 completed the trial (28 [70%] in ferrous sulfate group; 31 [78%] in iron polysaccharide c
260 n-casein complex was compared with that from ferrous sulfate in 21 healthy women aged 20-38 y with no
261 s iron bioavailability comparable to that of ferrous sulfate in healthy young women.
262 led, ((57)Fe)-labelled, or ((58)Fe)-labelled ferrous sulfate in iron-depleted (serum ferritin </=25 m
263                                              Ferrous sulfate is the most commonly prescribed oral iro
264  oral administration of aqueous solutions of ferrous sulfate isotopically labeled with (5)(4)Fe, (5)(
265                         Once daily, low-dose ferrous sulfate should be considered for children with n
266 lability value of the iron-casein complex to ferrous sulfate was determined to be 0.87 (-1 SD, +1 SD:
267                     To compare the effect of ferrous sulfate with iron polysaccharide complex on hemo
268 itin level increased from 3.0 to 15.6 ng/mL (ferrous sulfate) vs 2.0 to 7.5 ng/mL (iron complex) over
269 g capacity decreased from 501 to 389 mug/dL (ferrous sulfate) vs 506 to 417 mug/dL (iron complex) (a
270 e of stimulant laxatives and high-dosages of ferrous sulfate, and a significant relationship between
271 L (95% CI, 6.2 to 14.1 ng/mL; P < .001) with ferrous sulfate.
272 er oral supplementation with 2 mg/kg iron as ferrous sulfate.
273 ling, which was blocked by pretreatment with ferrous sulfate.
274  -50 mug/dL [95% CI, -86 to -14 mug/dL] with ferrous sulfate; P < .001).
275 ment groups (n = 10/group) to receive either ferrous sulphate (200 mg capsules containing 65 mg of ir
276 erestingly, the co-administration of GDP and ferrous sulphate (FeSO4) ameliorated the turpentine-indu
277 uestionnaire was most discriminatory between ferrous sulphate and placebo groups were: heartburn, abd
278 E)/g DW and FRAP from 2793.95 to 11393.97 mg ferrous sulphate equivalents (FSE)/g DW.
279  of symptoms reported by participants in the ferrous sulphate group (4.6 +/- 2.0) appeared higher tha
280  of symptoms reported by participants in the ferrous sulphate group (mean +/- SEM = 6.7 +/- 1.7) was
281 s in the first week of the study were in the ferrous sulphate group.
282 reporting one or more symptom(s) were in the ferrous sulphate group.
283 'bound' to milk or peptides compared to free ferrous sulphate in solution.
284 inal side-effects associated with oral iron (ferrous sulphate) supplementation, and would be appropri
285 ot), and premix composition (with or without ferrous sulphate).
286 aldehyde compared to the blank containing no ferrous sulphate.
287 c acid, and 21,606 M(-1) cm(-1) for ammonium ferrous sulphate.
288 89 mug/mL) and FRAP (225.53 mumol equivalent ferrous sulphate/g).
289  of ferric (hydr)oxides and sulfide, forming ferrous-sulphide minerals.
290 er with ferric porphyrins than corresponding ferrous systems, offering strong thermodynamic driving f
291  ((Ar)L)Fe(NAd) reacts with azide yielding a ferrous tetrazido ((Ar)L)Fe(kappa(2)-N4Ad2), undergoes i
292 d stability of ferric thiolate compared with ferrous thiol arises mainly from entropic factors.
293 bstantially higher than in the corresponding ferrous-thiolate CO adducts.
294                                          The ferrous thiyl state is favored by entropy, populates at
295 orbitals resulting in a stabilization of the ferrous-thiyl radical ground state compared to the five-
296 er ferroxidase, ceruloplasmin (Cp), oxidizes ferrous to ferric ion.
297     In contrast, the Fe analogue undergoes a ferrous-to-ferric oxidation state conversion during this
298  feoABC under anaerobic conditions, allowing ferrous transport to increase even though Fur is more ac
299 ription factors Aft1 and Aft2 (activators of ferrous transport) regulate iron homeostasis in Saccharo
300 ty (AOCS), and two colorimetric methods, the ferrous xylenol orange (FOX) and ferric thiocyanate (Int

 
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