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1 mentarity than those of intrinsic factor and transcobalamin.
2 proteins: haptocorrin, intrinsic factor, and transcobalamin.
3 wanted physiologic tissue uptake mediated by transcobalamin.
4 ely 20-25% of circulating cobalamin binds to transcobalamin 2 (TCN2), which is referred to as active
5 erum vitamin B12 into the fractions bound to transcobalamin and haptocorrin: two carrier proteins wit
6 wer and threefold faster, respectively, than transcobalamin binding to cyanocobalamin.
7                                              Transcobalamin binds cyanocobalamin-b-(5-aminopentylamid
8                                              Transcobalamin bound vitamin B12 (holoTC) was not influe
9           The derivative shows no binding to transcobalamin but is recognized by haptocorrin, a prote
10 rphism of the vitamin B-12 transport protein transcobalamin gene (TCN2) (rs1801198; Pro259Arg) is ass
11  been hypothesized that the response of holo-transcobalamin (holo-TC) to oral vitamin B-12 may be use
12 2 associated with the plasma binding protein transcobalamin (holotranscobalamin) have been developed.
13 ation, whereas B12 bound to non-glycosylated transcobalamin (i.e. holoTC) is not affected.
14                                              Transcobalamin II (TC II) receptor is expressed in the a
15 nesis of the 5'-flanking region of the human transcobalamin II (TC II) transfected in human intestina
16                        Cobalamin attached to transcobalamin II (TC II), known as holo-TC II, is the a
17 75G>C) in the vitamin B12 transport protein, transcobalamin II (TCII), has been identified in which p
18 ptor, the transcobalamin II receptor and the transcobalamin II carrier protein.
19 (bp) (-581/-513) fragment derived from human transcobalamin II distal promoter constructed upstream o
20 t for 12 h also resulted in complete loss of transcobalamin II receptor (TC II-R) activity/protein le
21                                              Transcobalamin II receptor (TC II-R) exists as a monomer
22 esses the B12-intrinsic factor receptor, the transcobalamin II receptor and the transcobalamin II car
23  that the analogs could be effective in vivo transcobalamin II receptor imaging agents.
24 dly dividing cells up-regulate the number of transcobalamin II receptors during DNA replication.
25 cobalamin analogs for the purpose of imaging transcobalamin II receptors in malignant and nonmalignan
26 ysteine, methylmalonic acid, and the ligand, transcobalamin II, in their plasma.
27                            Exogenously added transcobalamin II-[57Co]cyanocobalamin bound very poorly
28                                              Transcobalamin II-receptor (TC II-R) contains 10 half-cy
29   Rabbits injected with pure human placental transcobalamin II-receptor (TC II-R) failed to thrive wi
30 ort is mediated by three transport proteins: transcobalamin, intrinsic factor, and haptocorrin (HC).
31 ine the affinity of different cobalamins for transcobalamin, intrinsic factor, and nonintrinsic facto
32 irect binding assay, where recombinant human transcobalamin is conjugated to a biosensor chip, allows
33 n binding, shows that only recombinant human transcobalamin is sensitive to modification of the corri
34 ponse data for cyanocobalamin binding to the transcobalamin protein surface were globally fitted to a
35       In vitro binding of the analogs to the transcobalamin proteins was assessed by the unsaturated
36 respectively, as efficient in binding to the transcobalamin proteins when compared to cyanocobalamin.
37 ulation bound to transcobalamin (TC) via the transcobalamin receptor (TC-R).
38 uptake of cobalamin (Cbl) is mediated by the transcobalamin receptor (TCblR) that binds and internali
39  Gene defects of transcobalamin (TC) and the transcobalamin receptor (TCblR), needed for cellular upt
40               A common genetic polymorphism [transcobalamin (TC) 776C-->G] may affect the function of
41                              Gene defects of transcobalamin (TC) and the transcobalamin receptor (TCb
42                                              Transcobalamin (TC) has been cloned and used for studyin
43                  Second, Cbl bound to plasma transcobalamin (TC) II is taken up from the circulation
44 receptor (TCblR) that binds and internalizes transcobalamin (TC) saturated with Cbl.
45      The membrane receptor TCblR/CD320 binds transcobalamin (TC) saturated with vitamin B12 [cobalami
46 they obtain it from the circulation bound to transcobalamin (TC) via the transcobalamin receptor (TC-
47      The membrane receptor (TCblR/CD320) for transcobalamin (TC)-bound cobalamin (Cbl) facilitates th
48                                          The transcobalamin (TC, TCII) receptor (TCblR) on the plasma
49 in (TC) 776C-->G] may affect the function of transcobalamin, the protein required for vitamin B-12 ce
50                         Like haptocorrin and transcobalamin, the trout cobalamin-binding protein was
51 ment of cobalamin, holotranscobalamin, total transcobalamin, total haptocorrin, and methylmalonic aci
52 C--> G polymorphism on concentrations of the transcobalamin-vitamin B-12 complex (holo-TC) and to det

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