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1 ranslation or stability; all IREs bind IRPs (iron regulatory proteins).
2 ated by iron-regulated RNA-binding proteins (iron regulatory proteins).
3 ystem, mediated through effects on the Aft1p iron-regulatory protein.
4 uster, to its apo-form which functions as an iron-regulatory protein.
5 r the physiological actions of this critical iron-regulatory protein.
6 xpression, intracellular oxidant levels, and iron regulatory proteins.
7 een proposed to make direct contact with the iron regulatory proteins.
8 wo homologous cytosolic regulatory proteins, iron regulatory protein 1 (also known as IRP1 and Aco1)
9 ranscriptional control through the action of iron regulatory protein 1 (IRP1) and IRP2 coordinate the
10 -sulfur cluster-dependent interconversion of iron regulatory protein 1 (IRP1) between its RNA binding
17 ve element-binding (IRE-binding) activity of iron regulatory protein 1 (IRP1) was activated, and incr
19 Knockdown of ISCU enhanced the binding of iron regulatory protein 1 (IRP1), a cytosolic Fe-S prote
20 plicated in Fe/S cluster repair of cytosolic iron regulatory protein 1 (IRP1), a key regulator of cel
21 ble of repairing oxidatively damaged Fe-S of iron regulatory protein 1 (IRP1), a master regulator of
22 the mammalian cytosolic aconitase, known as iron regulatory protein 1 (IRP1), led to the characteriz
23 by the binding of two cytoplasmic proteins, iron regulatory protein 1 and 2 (IRP1 and IRP2) to stem
26 omolog, cytoplasmic aconitase, also known as iron regulatory protein 1, a well-recognized RNA-binding
27 osolic aconitase is known to be converted to iron regulatory protein 1, and consistent with this, we
28 a domain not present in the closely related iron regulatory protein 1, and we found that this domain
30 iron-responsive element-binding activity of iron regulatory protein 1, increased protein levels of i
31 anslational regulation of its expression via iron regulatory proteins 1 and 2 (IRP1 and IRP2, respect
36 ependent manner, by enhancing the binding of Iron-Regulatory Protein 1 (IRP1) to a recently reported
37 everal cytosolic Fe/S proteins, for example, iron-regulatory protein 1, a major component of posttran
39 as well as subsequent reoxygenation, on the iron-regulatory proteins 1 and 2 (IRP1 and IRP2) in a ra
41 , while heavy chain ferritin mRNA levels and iron regulatory protein-1 (IRP-1) RNA binding activity w
42 o provide in vitro and in vivo evidence that iron regulatory protein-1 (IRP1) inhibits protoporphyrin
44 dependent manner by promoting the binding of iron regulatory protein-1 (IRP1) to a noncanonical iron
45 aconitase was responsible for activation of iron regulatory protein-1 and increased expression of Tf
47 ked by the antioxidant N-acetyl cysteine and iron regulatory protein-1 siRNA, suggesting involvement
48 n converting cytosolic aconitase (ACO1) into iron regulatory protein-1 to bind iron-responsive elemen
49 ugh disruption of the iron-sulfur complex of iron regulatory protein-1, a translational regulator.
52 se of repressor interaction of APP mRNA with iron-regulatory protein-1 (IRP1) whereas IRP2 controls t
53 protein 1 (also known as IRP1 and Aco1) and iron regulatory protein 2 (also known as IRP2 and Ireb2)
56 eficient cells revealed increased binding of iron regulatory protein 2 (IRP2) and decreased binding o
57 pletion, as indicated by increased levels of iron regulatory protein 2 (IRP2) and/or increased IRE-bi
65 lated tightly in mammalian cells, in part by iron regulatory protein 2 (IRP2), a protein that is degr
66 ate covalently modifies cysteine residues on iron regulatory protein 2 (IRP2), rendering it unable to
69 /6 mice and mice with a targeted deletion of iron regulatory protein 2 (IRP2-/-) that have been repor
70 the expression of transferrin receptor 1 and iron regulatory protein 2 consistent with decreased iron
74 eceptor-interacting protein 1, Hemo-oxidized iron regulatory protein 2 ligase 1 (HOIL-1), HOIL-1-inte
75 he catalytic core component is heme-oxidized iron regulatory protein 2 ubiquitin ligase-1-interacting
76 igase complex that mediates the stability of iron regulatory protein 2, an important posttranscriptio
77 atory protein 1, increased protein levels of iron regulatory protein 2, and resulted in abnormal punc
78 cient erythropoietic tissues of mice lacking iron regulatory protein 2, in iron-deficient murine eryt
79 lated neurodegeneration has been reported in iron regulatory protein 2-deficient (IRP2 -/-) mice coin
81 iron, and to stimulate the expression of the iron regulatory protein-2 (IRP2), which increases the in
85 with relatively higher labile iron pool and iron regulatory protein activity than WT or H63D HFE.
86 ynthesis at the translational level and that iron regulatory proteins appear to differentially affect
88 onal mRNAs whose expression is controlled by iron regulatory proteins, as well as provide insight int
91 RNA using a poly(G) stretch or the mammalian iron regulatory protein bound to the iron responsive ele
93 expression of genes encoding Epo, EpoR, and iron regulatory proteins contributes to defective erythr
94 d cytosolic aconitase of the capacity of the iron regulatory protein controlling the translation of s
95 t excess H-ferritin generated as a result of iron-regulatory protein deactivation sequesters toxic ir
96 te immune protein, has emerged as a critical iron regulatory protein during physiological and inflamm
98 reased intracellular iron levels measured by iron regulatory protein gel-shift assays and ferritin le
102 is analysis revealed that the basal level of iron regulatory protein in growth-arrested cells was 6-f
103 determined iron levels and the expression of iron regulatory proteins in the liver and gut of nonobes
104 [2Fe-2S]-coordinating complexes in vitro and iron-regulatory proteins in fungi, but it is not clear h
105 tin-H, and increased iron-responsive element-iron regulatory protein interaction are also observed in
106 pendent iron signaling via activation of the iron-regulatory protein/iron-responsive element interact
108 nganese (Mn) exposure alters the function of iron regulatory protein (IRP) and increases iron (Fe) co
109 t enhancing ferritin expression by targeting iron regulatory protein (IRP) binding activity reduces c
110 ithelial antigen of the prostate (STEAP) and iron regulatory protein (IRP) families in cancer have pr
113 eimer brain might result from alterations in iron regulatory proteins (IRP) such as IRP-1 and IRP-2,
115 ed its identity to the previously identified iron-regulatory protein (IRP)-like cDNA from Plasmodium
116 ng the IRE, bind specifically to recombinant iron-regulatory proteins (IRP) and to IRP from neuroblas
117 IRE-RNA riboregulators bind specifically to iron-regulatory proteins (IRP) proteins, inhibiting ribo
120 muscle was associated with a decrease in the iron regulatory protein IRP1 and intracellular iron over
130 uctures (iron-responsive elements, IREs) and iron-regulatory proteins (IRP1 and IRP2), controlling ei
132 llular iron homeostasis is controlled by the iron regulatory proteins (IRPs) 1 and 2 that bind cis-re
136 tural group of mRNA-specific sequences, bind iron regulatory proteins (IRPs) differentially and fold
139 h iron regulation by altering the binding of iron regulatory proteins (IRPs) to their response elemen
140 metabolism is mediated by the interaction of iron regulatory proteins (IRPs) with RNA stem-loop seque
142 of cellular iron homeostasis is regulated by iron regulatory proteins (IRPs), which control the expre
143 teractions of iron-sensing proteins known as iron regulatory proteins (IRPs), with transcripts that c
150 involving hypoxia-inducible factor (HIF) and iron-regulatory proteins (IRPs) are responsive to both t
154 erritin mRNA model that is recognized by the iron-regulatory protein repressor, were identified by us
156 by NO into an mRNA binding protein (IRP, or iron-regulatory protein) that regulates iron homeostasis
158 tal muscle cells by promoting the binding of iron regulatory proteins to iron-responsive elements pre
160 ation principally through the interaction of iron regulatory proteins with mRNAs that contain an iron
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