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1 which leads to the induction of ferritin, an iron-binding protein).
2 he levels of frataxin (FXN), a mitochondrial iron binding protein.
3 ity receptors for iron acquisition from host iron-binding proteins.
4 imiting conditions, presumably for essential iron-binding proteins.
5 sparing resulting from reduced synthesis of iron-binding proteins.
6 r findings have for the role of frataxins as iron-binding proteins.
7 a means to remove the hemin from these host iron-binding proteins.
8 rin is a member of the transferrin family of iron-binding proteins.
11 oncurred with potential interactions between iron binding proteins and SARS CoV-2 surface proteins.
12 ike proteins are oxygen-carrying non-heme di-iron binding proteins and their functions have effect on
13 ut the dual effects of NGAL as a siderophore:iron-binding protein and as a growth factor and examines
14 g activity, whereas CyaY becomes a competent iron-binding protein and attenuates the iron-mediated pr
15 have the capacity to scavenge iron from host iron-binding proteins and deliver it to the mycobacteria
16 erculosis by removing this element from host iron-binding proteins and transferring it to desferri-my
17 , exomycobactins, compete for iron with host iron-binding proteins and, together with the iron-regula
20 were found, as well as other mRNAs encoding iron-binding proteins, bringing the total number of regu
21 stasis is typically regulated by cytoplasmic iron binding proteins, but here we describe a signal tra
22 this recessive disorder, is a mitochondrial iron-binding protein, but how its deficiency leads to ne
26 iron transporter gene (CBU1766), a putative iron binding protein-encoding gene (CBU0970), and a cati
27 r region of the Neisseria gonorrhoeae ferric iron binding protein-encoding gene fbpA, determined the
28 tion via either transgenic expression of the iron binding protein ferritin or oral administration of
30 f frataxins, a family of small mitochondrial iron-binding proteins found in organisms ranging from ba
31 Aconitase was found to associate with the iron binding protein frataxin exclusively during reperfu
34 our known cDNAs included ferritin, the major iron-binding protein in cells; HSGSA2R, a full-length cl
39 y to utilize the iron bound by high-affinity iron-binding proteins in the vertebrate host is an impor
40 tic transferrins comprise a class of bilobal iron-binding proteins in which each lobe carries a singl
42 p. are capable of iron utilization from host iron-binding proteins including transferrin and lactofer
43 cquire iron by direct interaction with human iron-binding proteins, including the serum glycoprotein,
44 wn siderophores but can employ host-derived, iron-binding proteins, including transferrin and lactofe
45 ding, the first description of a T. pallidum iron-binding protein, indicates that the syphilis spiroc
47 boratory cultures that ferritin and the main iron-binding proteins involved in photosynthesis and nit
49 ke other members of the transferrin class of iron-binding proteins, is a bilobal structure, the produ
50 ), IgG-binding protein A (Spa), and the heme-iron-binding protein (IsdA) were most abundant in the ag
51 ted rat hepatocytes bind and internalize the iron-binding protein lactoferrin (Lf) by a set of high-a
56 not macrophages, within the CSF express the iron-binding protein lipocalin-2 (LCN2) and its receptor
58 solved in complex with human transferrin, an iron binding protein normally responsible for delivering
61 by reduced activity of frataxin, a conserved iron-binding protein of the mitochondrial matrix, though
62 ia also express outer membrane receptors for iron-binding proteins of the host and extract iron direc
63 generally encode two different types of FutA iron-binding proteins: periplasmic FutA2 ABC transporter
65 Lactoferrin (LF), traditionally known as an iron-binding protein present in high concentrations in m
66 at the syphilis spirochete lacks most of the iron-binding proteins present in many other bacterial pa
67 xpression of frataxin (FXN), a mitochondrial iron-binding protein required for Fe-S cluster assembly.
69 iron load is, perhaps, by the expression of iron-binding proteins, specifically the iron storage pro
71 f satisfying its iron requirement with human iron-binding proteins such as transferrin and lactoferri
72 sion of receptors that are specific for host iron-binding proteins, such as transferrin and lactoferr
73 hosts, because it is largely sequestered by iron-binding proteins, such as transferrin or lactoferri
74 ria gonorrhoeae is capable of utilizing host iron-binding proteins, such as transferrin, lactoferrin,
75 r, recent evidence indicated that IscA is an iron-binding protein that can provide iron for the iron-
76 er, recent studies indicated that IscA is an iron-binding protein that can provide iron for the iron-
79 ning of the human homologs to IscU and NifU, iron-binding proteins that play a critical role in Fe-S
83 reover, increased apical release of the host iron-binding protein transferrin during RSV infection pr
88 olamines binding to the high-affinity ferric-iron-binding proteins transferrin (Tf) and lactoferrin,
89 l gelatinase-associated lipocalin (NGAL), an iron-binding protein up-regulated in response to kidney