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1 f radioactive isotopes like [57Co]- or [14C]-cyanocobalamin.
2 tive decyanation reaction when it encounters cyanocobalamin.
3 , ferritin, from a small biological organic, cyanocobalamin.
4 ication of the corrin ring b-propionamide of cyanocobalamin.
5 respectively, than transcobalamin binding to cyanocobalamin.
6 ding capacity assay and compared to DTPA and cyanocobalamin.
7 the transcobalamin proteins when compared to cyanocobalamin.
8 ot the pdu) operon is repressed by exogenous cyanocobalamin.
9 lcobalamins and the reductive decyanation of cyanocobalamin.
10 cted for valproic acid, isovaleric acid, and cyanocobalamin.
11 de, to transform all forms of cobalamin into cyanocobalamin.
12 ew method is demonstrated in the analysis of cyanocobalamin, a vitamin B12 supplement, and of an eye-
15 ystal structures of human HC in complex with cyanocobalamin and cobinamide at 2.35 and 3.0 A resoluti
17 consists of 1 mg of folic acid and 0.5 mg of cyanocobalamin and the diet that includes grains fortifi
18 protein required for high-affinity uptake of cyanocobalamin and the translocation of E group colicins
19 s performed for measurement of homocysteine, cyanocobalamin, and erythrocyte folate in participants o
20 ridoxine HCl; 50 microg each of d-biotin and cyanocobalamin; and 400 mcg of folate) or placebo for 30
21 g folic acid, 7.2 mg pyridoxine, and 0.02 mg cyanocobalamin), antioxidant vitamins alone (150 mg asco
22 osed cobalamin deficient patients to receive cyanocobalamin as either 1 mg intramuscularly on days 1,
30 Exogenously added transcobalamin II-[57Co]cyanocobalamin bound very poorly (2-5%) to the affected
31 cobalt containing compounds, namely Co(II), cyanocobalamin (CN-Cbl) and hydroxylcobalamin (OH-Cbl),
34 showed that of the four Co(III) derivatives (cyanocobalamin [CN-Cbl], aquocobalamin [H2O-Cbl], adenos
38 B-dependent active transport of vitamin B12 [cyanocobalamin (CNCbl)] across the outer membrane of Esc
39 aimed to investigate the stability of added cyanocobalamin (CNCbl, chemically modified form) and hyd
40 e excited-state photophysics of vitamin B12 (cyanocobalamin, CNCbl) and the related cob(III)alamins,
42 ith tandem mass spectrometry (LC-MS/MS), the cyanocobalamin content was determined as 0.42 +/- 0.09 m
44 ermination of 5'-hydroxy-alpha-ribofuranosyl cyanocobalamin derivatives with solely 1-D (13)C and DEP
45 of how the cyanide group in vitamin B(12) or cyanocobalamin, discovered 60 years ago, is removed, has
46 The same analysis for the negative control, cyanocobalamin, found no association with suicide attemp
48 ive forms of vitamin B12 (adenosylcobalamin, cyanocobalamin, hydroxocobalamin, methylcobalamin) from
50 was to measure the bioavailability of [13C]-cyanocobalamin in humans and to assess the effect of par
54 ut not decyanation activity, suggesting that cyanocobalamin might be therapeutically useful for patie
55 be rescued by the addition of vitamin B(12) (cyanocobalamin) or the lower ligand of cobalamin, 5,6-di
56 patients with known CHD with folic acid and cyanocobalamin over a 10-year period would result in 310
58 ctivities for processing alkylcobalamins and cyanocobalamin, respectively, to a common intermediate t
63 a stable isotope-labeled vitamin B-12, [13C]-cyanocobalamin, using Salmonella enterica by providing [
64 ity, catalyzing the reductive decyanation of cyanocobalamin (vitamin B(12)), and the dealkylation of
65 and its nutritional determinants folate and cyanocobalamin (vitamin B-12) have been shown to affect
68 l compounds such as pyridoxine (vitamin B6), cyanocobalamin (vitamin B12), and apigenin (a plant flav
71 of new force-field parameters developed for cyanocobalamin, we also simulated the substrate-bound fo
72 mocysteine, red blood cell folate, and serum cyanocobalamin were unrelated to ARM in the overall samp
73 % of total B vitamins); B8 (biotin) and B12 (cyanocobalamin) were not detected in lentil samples.
74 btuB RNA was inhibited by Ado-Cbl but not by cyanocobalamin, with half-maximal inhibition around 0.3