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PMID |
Sentence |
1 |
1707948
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The characteristics of a panel of anti-gp13 monoclonal antibodies (P28, P17, 14H7, 16E4 and 16H9) were assessed both in vivo and in vitro. 16E4 and P28 showed high levels of complement-mediated neutralization of virus, complement-mediated lysis of virus-infected target cells and passive protection of hamsters.
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2 |
2468160
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SIVagm exhibits the following pattern of major virus proteins: p18, p28, gp45, p64, gp140.
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3 |
10878054
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Of the 18 protein bands analyzed, 8 were found to be significantly different (P<0.05) between the two groups. p93, p34, p31, and p28 occurred with increased frequency in vaccinated dogs, while p58, p37, p35, and p30 occurred more frequently in naturally infected dogs.
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4 |
11122460
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Three of the four mimotopes (p28, p29 and p30) were efficiently recognized in an in vitro radioimmunoassay by the monoclonal antibody and by sera from infected mice and one (p30) induced in vitro proliferation of primed lymphocytes.
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5 |
11483501
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P25 and P28 proteins of the malaria ookinete surface have multiple and partially redundant functions.
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6 |
11483501
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The ookinete surface proteins (P25 and P28) are proven antimalarial transmission-blocking vaccine targets, yet their biological functions are unknown.
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7 |
11483501
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By using single (Sko) and double gene knock-out (Dko) Plasmodium berghei parasites, we show that P25 and P28 share multiple functions during ookinete/oocyst development.
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8 |
11483501
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P25 and P28 are partially redundant in these functions, since the efficiency of ookinete/oocyst development is only mildly compromised in parasites lacking either P25 or P28 (Sko parasites) compared with that of Dko parasites.
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9 |
11483501
|
P25 and P28 proteins of the malaria ookinete surface have multiple and partially redundant functions.
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10 |
11483501
|
The ookinete surface proteins (P25 and P28) are proven antimalarial transmission-blocking vaccine targets, yet their biological functions are unknown.
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11 |
11483501
|
By using single (Sko) and double gene knock-out (Dko) Plasmodium berghei parasites, we show that P25 and P28 share multiple functions during ookinete/oocyst development.
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12 |
11483501
|
P25 and P28 are partially redundant in these functions, since the efficiency of ookinete/oocyst development is only mildly compromised in parasites lacking either P25 or P28 (Sko parasites) compared with that of Dko parasites.
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13 |
11483501
|
P25 and P28 proteins of the malaria ookinete surface have multiple and partially redundant functions.
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14 |
11483501
|
The ookinete surface proteins (P25 and P28) are proven antimalarial transmission-blocking vaccine targets, yet their biological functions are unknown.
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15 |
11483501
|
By using single (Sko) and double gene knock-out (Dko) Plasmodium berghei parasites, we show that P25 and P28 share multiple functions during ookinete/oocyst development.
|
16 |
11483501
|
P25 and P28 are partially redundant in these functions, since the efficiency of ookinete/oocyst development is only mildly compromised in parasites lacking either P25 or P28 (Sko parasites) compared with that of Dko parasites.
|
17 |
11483501
|
P25 and P28 proteins of the malaria ookinete surface have multiple and partially redundant functions.
|
18 |
11483501
|
The ookinete surface proteins (P25 and P28) are proven antimalarial transmission-blocking vaccine targets, yet their biological functions are unknown.
|
19 |
11483501
|
By using single (Sko) and double gene knock-out (Dko) Plasmodium berghei parasites, we show that P25 and P28 share multiple functions during ookinete/oocyst development.
|
20 |
11483501
|
P25 and P28 are partially redundant in these functions, since the efficiency of ookinete/oocyst development is only mildly compromised in parasites lacking either P25 or P28 (Sko parasites) compared with that of Dko parasites.
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21 |
15596852
|
The poxviral RING protein p28 is a ubiquitin ligase that targets ubiquitin to viral replication factories.
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22 |
15596852
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Furthermore, p28 is ubiquitinated in vivo and ubiquitin colocalizes with p28 to virus factories independently of an intact RING domain.
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23 |
15596852
|
The poxviral RING protein p28 is a ubiquitin ligase that targets ubiquitin to viral replication factories.
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24 |
15596852
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Furthermore, p28 is ubiquitinated in vivo and ubiquitin colocalizes with p28 to virus factories independently of an intact RING domain.
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25 |
15733320
|
Do malaria ookinete surface proteins P25 and P28 mediate parasite entry into mosquito midgut epithelial cells?
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26 |
16327807
|
The essential mosquito-stage P25 and P28 proteins from Plasmodium form tile-like triangular prisms.
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27 |
16327807
|
P25 and P28 proteins are essential for Plasmodium parasites to infect mosquitoes and are leading candidates for a transmission-blocking malaria vaccine.
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28 |
16327807
|
The residues forming the triangle are conserved in P25 and P28 from all Plasmodium species.
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29 |
16327807
|
The essential mosquito-stage P25 and P28 proteins from Plasmodium form tile-like triangular prisms.
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30 |
16327807
|
P25 and P28 proteins are essential for Plasmodium parasites to infect mosquitoes and are leading candidates for a transmission-blocking malaria vaccine.
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31 |
16327807
|
The residues forming the triangle are conserved in P25 and P28 from all Plasmodium species.
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32 |
16327807
|
The essential mosquito-stage P25 and P28 proteins from Plasmodium form tile-like triangular prisms.
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33 |
16327807
|
P25 and P28 proteins are essential for Plasmodium parasites to infect mosquitoes and are leading candidates for a transmission-blocking malaria vaccine.
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34 |
16327807
|
The residues forming the triangle are conserved in P25 and P28 from all Plasmodium species.
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35 |
17298856
|
Such responses to p1, p4, p14, p21, p28 and p29 were significantly higher in the eight infected patients and, with the exception of p14, these peptides differed from those found in three HIV-negative controls (p11, p14 and p27).
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36 |
17298856
|
Peptides p1, p28 and p29 are major immunogenic epitopes.
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37 |
17298856
|
Such responses to p1, p4, p14, p21, p28 and p29 were significantly higher in the eight infected patients and, with the exception of p14, these peptides differed from those found in three HIV-negative controls (p11, p14 and p27).
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38 |
17298856
|
Peptides p1, p28 and p29 are major immunogenic epitopes.
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39 |
17517859
|
Nineteen out of 22 OMP-1/P28 family proteins, including P28 (which previously was shown to be surface exposed), were detected in E. chaffeensis cultured in human monocytic leukemia THP-1 cells.
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40 |
17557884
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Plasmodium p25 and p28 surface proteins: potential transmission-blocking vaccines.
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41 |
19032156
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These proteins present on zygotes, ookinetes and young oocysts of Plasmodium are categorized in P25 and P28 families and are well known malaria vaccine candidate proteins.
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42 |
19057932
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A very large C-loop in EGF domain IV is characteristic of the P28 family of ookinete surface proteins.
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43 |
19057932
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Together with P25 proteins, P28 proteins protect the parasite from the harsh proteolytic environment prevailing inside the mosquito midgut.
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44 |
19057932
|
The purpose of this study was to structurally characterise six members of the P28 family of ookinete surface proteins with the help of homology modelling, to compare these proteins in terms of transmission blocking and host parasite interactions, and to analyse phylogenetic relationships within the P28 family and with the P25 family.
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45 |
19057932
|
Our results indicate that all the members of the P28 family studied have four EGF domains arranged in triangular fashion with a very big C loop present in EGF domain IV, which could serve as a diagnostic feature of the P28 family as this loop is absent in the P25 family of ookinete surface proteins.
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46 |
19057932
|
A very large C-loop in EGF domain IV is characteristic of the P28 family of ookinete surface proteins.
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47 |
19057932
|
Together with P25 proteins, P28 proteins protect the parasite from the harsh proteolytic environment prevailing inside the mosquito midgut.
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48 |
19057932
|
The purpose of this study was to structurally characterise six members of the P28 family of ookinete surface proteins with the help of homology modelling, to compare these proteins in terms of transmission blocking and host parasite interactions, and to analyse phylogenetic relationships within the P28 family and with the P25 family.
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49 |
19057932
|
Our results indicate that all the members of the P28 family studied have four EGF domains arranged in triangular fashion with a very big C loop present in EGF domain IV, which could serve as a diagnostic feature of the P28 family as this loop is absent in the P25 family of ookinete surface proteins.
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50 |
19057932
|
A very large C-loop in EGF domain IV is characteristic of the P28 family of ookinete surface proteins.
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51 |
19057932
|
Together with P25 proteins, P28 proteins protect the parasite from the harsh proteolytic environment prevailing inside the mosquito midgut.
|
52 |
19057932
|
The purpose of this study was to structurally characterise six members of the P28 family of ookinete surface proteins with the help of homology modelling, to compare these proteins in terms of transmission blocking and host parasite interactions, and to analyse phylogenetic relationships within the P28 family and with the P25 family.
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53 |
19057932
|
Our results indicate that all the members of the P28 family studied have four EGF domains arranged in triangular fashion with a very big C loop present in EGF domain IV, which could serve as a diagnostic feature of the P28 family as this loop is absent in the P25 family of ookinete surface proteins.
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54 |
19057932
|
A very large C-loop in EGF domain IV is characteristic of the P28 family of ookinete surface proteins.
|
55 |
19057932
|
Together with P25 proteins, P28 proteins protect the parasite from the harsh proteolytic environment prevailing inside the mosquito midgut.
|
56 |
19057932
|
The purpose of this study was to structurally characterise six members of the P28 family of ookinete surface proteins with the help of homology modelling, to compare these proteins in terms of transmission blocking and host parasite interactions, and to analyse phylogenetic relationships within the P28 family and with the P25 family.
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57 |
19057932
|
Our results indicate that all the members of the P28 family studied have four EGF domains arranged in triangular fashion with a very big C loop present in EGF domain IV, which could serve as a diagnostic feature of the P28 family as this loop is absent in the P25 family of ookinete surface proteins.
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58 |
21710262
|
Binding affinity and stability assays in T2 cells showed that two native peptides, p28 and p31, and their analogues (p28-1Y9 V, p31-1Y2L) had more potent binding activity towards HLA-A*0201 molecule.
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59 |
21710262
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The CTLs induced by these four peptides from the peripheral blood mononuclear cells (PBMCs) of HLA-A*02+ healthy donor could lyse MCF-7 breast cancer cells (HLA-A*0201+, PLAC1+) in vitro.
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60 |
23880886
|
DENV-2 subunit proteins fused to CR2 receptor-binding domain (P28)-induces specific and neutralizing antibodies to the Dengue virus in mice.
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61 |
23880886
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Thus, this study aimed to generate DENV-2 recombinant fusion proteins (i.e., rEII*EIII and rEII*EIII/NS1*) either alone or fused to 3 copies of P28, the minimum CR2-binding domain of the complement protein C3d.
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62 |
23880886
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DENV-2 subunit proteins fused to CR2 receptor-binding domain (P28)-induces specific and neutralizing antibodies to the Dengue virus in mice.
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63 |
23880886
|
Thus, this study aimed to generate DENV-2 recombinant fusion proteins (i.e., rEII*EIII and rEII*EIII/NS1*) either alone or fused to 3 copies of P28, the minimum CR2-binding domain of the complement protein C3d.
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