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1 t dependent on cis-acting elements unique to selenoprotein P.
2 was fully dependent on the supplies of Se by selenoprotein P.
3 a constituent of the heparin-binding site of selenoprotein P.
4 cted 57-kDa size of full-length glycosylated selenoprotein P.
5 e protein forms from immunoaffinity-purified selenoprotein P.
6                                              Selenoprotein P, a glycoprotein that contains 10 selenoc
7 associated signal transducer-2 (Trop-2), and Selenoprotein-P, a gene that binds selenium and prevents
8 d liver support the binding of Hg(Sec)(4) to selenoprotein P and biomineralization of Hg(Sec)(4) to c
9                                Nevertheless, selenoprotein P and several other selenoproteins are kno
10                                  Full-length selenoprotein P and three smaller isoforms that have ide
11                             Four isoforms of selenoprotein P are present in rat plasma.
12                                              Selenoprotein P binds to endothelial cells in the rat, a
13                    It was distinguished from selenoprotein P by N-glycosidase assay and by the period
14 , and seventh selenocysteines in full-length selenoprotein P can alternatively serve to terminate tra
15                       To optimize the plasma selenoprotein P concentration in this study, 50 microg S
16 one peroxidase activity was optimized before selenoprotein P concentration was optimized, indicating
17 roxidase activity and in plasma selenium and selenoprotein P concentrations were measured.
18 tive real-time reverse transcription-PCR for Selenoprotein-P demonstrated a similar down-regulation o
19 (a) of which is 7.0, explains the release of selenoprotein P from heparin binding as pH rises above 7
20 peculative and much work on the mechanism of selenoprotein P function lies ahead.
21 single UGA codon and a single SECIS element, selenoprotein P genes encode multiple UGAs and two SECIS
22  have identified evolutionary adaptations in selenoprotein P genes that contribute to the efficiency
23                              The function of selenoprotein P has remained elusive, in part due to the
24 first time the expression of recombinant rat selenoprotein P in a transiently transfected human epith
25  describe for the first time the presence of selenoprotein P in human breast milk.
26                               Measurement of selenoprotein P in human plasma has shown that it is dep
27  property would lead to increased binding of selenoprotein P in tissue regions that have low pH.
28 st, the efficiency of Sec incorporation into selenoprotein P in vitro is approximately 40%, suggestin
29 oteins, glutathione peroxidase (GSHPx-3) and selenoprotein P, in the plasma of patients with cirrhosi
30                                              Selenoprotein P increased significantly in all selenium
31                                              Selenoprotein P is a plasma protein that has oxidant def
32                                       Plasma selenoprotein P is a useful biomarker of status in popul
33                                              Selenoprotein P is an abundant extracellular glycoprotei
34                                              Selenoprotein P is an abundant extracellular glycoprotei
35                                          Rat selenoprotein P is an extracellular glycoprotein of 366
36                            Thus, full-length selenoprotein P is both N- and O-glycosylated.
37 s were reduced by about 75%, suggesting that selenoprotein P is primarily exported from the liver.
38 ration was optimized, indicating that plasma selenoprotein P is the better index of human selenium nu
39                                              Selenoprotein P is unique in that its mRNA encodes 10-12
40              These findings demonstrate that selenoprotein P isoforms of differing peptide lengths ar
41                                              Selenoprotein P knockout mice have very low selenium con
42                                       Plasma selenoprotein P levels were reduced by about 75%, sugges
43 the possibility that the second UGA codon in selenoprotein P mRNA can have alternative functions: cod
44             Third, the two SECIS elements in selenoprotein P mRNA function with differing efficiencie
45  been identified in rat plasma, but only one selenoprotein P mRNA has been characterized.
46 Gla protein, apolipoprotein D precursor, and selenoprotein P precursor).
47                                              Selenoprotein P (Se-P) contains most of the selenium in
48                                              Selenoprotein P (Sel P) is a selenium-rich glycoprotein
49 nd two SECIS elements make the mRNA encoding selenoprotein P (Sel P) unique.
50 ws the order: glutathione peroxidase (GPX) ~ selenoprotein P (SELENOP) > selenocystamine (SeCA) > oth
51  between selenium status [serum selenium and selenoprotein P (SELENOP) concentrations and glutathione
52                               However, human selenoprotein P (SelenoP) has a redox-functioning seleno
53 iosynthesis of the selenium (Se) transporter selenoprotein P (SELENOP) is particularly sensitive to a
54 ted antioxidant selenium-containing protein, selenoprotein P (SELENOP), substantially increased tumor
55 A coding for the selenium transport protein, selenoprotein P (SELENOP), which in vertebrates may cont
56 d begins with the uptake of the Sec carrier, selenoprotein P (SELENOP).
57 ) is bound to the carboxy-terminus domain of selenoprotein P (SelP) which contains 12 Sec residues.
58 traselenolate species, Hg-selenoneine and Hg-selenoprotein P (SelP), each with distinct delta(202)Hg
59 GPx-2), thioredoxin reductase-1 (TrxR-1) and selenoprotein P (SeP) mRNA expression and GPx-1 enzyme a
60 ckdowns of the SEPP1 gene, which encodes the selenoprotein P (SeP) protein, have been shown to increa
61 ed into at least 25 selenoproteins including selenoprotein P (SePP), which transports Se within the b
62                                              Selenoprotein P (Sepp1) and its receptor, apolipoprotein
63 in Se metabolism (Scly(-/-)Sepp1(-/-) mice), selenoprotein P (Sepp1) and Sec lyase (Scly), develop se
64          The liver synthesizes selenium-rich selenoprotein P (SEPP1) and secretes it into the plasma
65                                              Selenoprotein P (Sepp1) contains most of the selenium in
66                                              Selenoprotein P (Sepp1) has two domains with respect to
67  type II diabetes risk, and plasma levels of selenoprotein P (SEPP1) have been positively correlated
68 ciency by curtailing excretion and secreting selenoprotein P (Sepp1) into the plasma at the expense o
69                                              Selenoprotein P (Sepp1) is a plasma and extracellular pr
70                                              Selenoprotein P (Sepp1) is an important protein involved
71                        Among selenoproteins, selenoprotein P (Sepp1) is particularly distinctive due
72             The selenium-rich plasma protein selenoprotein P (Sepp1) is required for maintenance of t
73                                              Selenoprotein P (Sepp1) is taken up by receptor-mediated
74 oprotein S (SelS) production and circulating selenoprotein P (Sepp1) levels are significantly diminis
75  quantification of selenium (Se) included in selenoprotein P (SEPP1), an important biomarker for huma
76 sported from the liver to target tissues via selenoprotein P (SEPP1).
77 logous to regions of deduced sequence of the selenoprotein-P (SPP) family in bovine, rat, and human.
78                             Several forms of selenoprotein P that share the same N-terminal sequence
79 , and recognizing the important functions of selenoprotein P, these results provide important evidenc
80                                              Selenoprotein P turns over rapidly in rat plasma with th
81                      Immunoaffinity-purified selenoprotein P was digested with proteases, and the res
82                                              Selenoprotein P was purified from rat plasma, and the fo
83  and known to be correlated with circulating selenoprotein P, was the biomarker chosen.
84        Based on the histidine-rich nature of selenoprotein P, we have purified the recombinant and en
85 n of lung glutathione peroxidase-1 and liver selenoprotein P were increased in OVA-challenged mice co
86                                              Selenoprotein P, which originates largely in the liver,
87                      The shortest isoform of selenoprotein P, which terminates at residue 244, was an
88               This predicts that full-length selenoprotein P will contain 10 selenocysteine residues.