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PMID |
Sentence |
1 |
16517100
|
Identification of a follistatin-related protein from the tick Haemaphysalis longicornis and its effect on tick oviposition.
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2 |
16517100
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A gene encoding a follistatin-related protein (FRP) was obtained by random sequencing from the ovary cDNA library of the tick Haemaphysalis longicornis.
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3 |
16517100
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The sequence shows homology with the follistatin-related protein (FRP), which was thought to play some roles in the negative regulation of cellular growth.
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4 |
16517100
|
The recombinant proteins were found to have binding activity for both activin A and bone morphogenetic protein-2 (BMP-2).
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5 |
16517100
|
Identification of a follistatin-related protein from the tick Haemaphysalis longicornis and its effect on tick oviposition.
|
6 |
16517100
|
A gene encoding a follistatin-related protein (FRP) was obtained by random sequencing from the ovary cDNA library of the tick Haemaphysalis longicornis.
|
7 |
16517100
|
The sequence shows homology with the follistatin-related protein (FRP), which was thought to play some roles in the negative regulation of cellular growth.
|
8 |
16517100
|
The recombinant proteins were found to have binding activity for both activin A and bone morphogenetic protein-2 (BMP-2).
|
9 |
16517100
|
Identification of a follistatin-related protein from the tick Haemaphysalis longicornis and its effect on tick oviposition.
|
10 |
16517100
|
A gene encoding a follistatin-related protein (FRP) was obtained by random sequencing from the ovary cDNA library of the tick Haemaphysalis longicornis.
|
11 |
16517100
|
The sequence shows homology with the follistatin-related protein (FRP), which was thought to play some roles in the negative regulation of cellular growth.
|
12 |
16517100
|
The recombinant proteins were found to have binding activity for both activin A and bone morphogenetic protein-2 (BMP-2).
|
13 |
19553557
|
Lipoprotein lipase and hydrofluoric acid deactivate both bacterial lipoproteins and lipoteichoic acids, but platelet-activating factor-acetylhydrolase degrades only lipoteichoic acids.
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14 |
19553557
|
To identify the Toll-like receptor 2 ligand critically involved in infections with gram-positive bacteria, lipoprotein lipase (LPL) or hydrogen peroxide (H(2)O(2)) is often used to selectively inactivate lipoproteins, and hydrofluoric acid (HF) or platelet-activating factor-acetylhydrolase (PAF-AH) is used to selectively inactivate lipoteichoic acid (LTA).
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15 |
19553557
|
We investigated the reaction specificities by using two synthetic lipoproteins (Pam(3)CSK(4) and FSL-1) and LTAs from pneumococci and staphylococci.
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16 |
19553557
|
Changes in the structures of the two synthetic proteins and the LTAs were monitored by mass spectrometry, and biological activity changes were evaluated by measuring tumor necrosis factor alpha production by mouse macrophage cells (RAW 264.7) following stimulation.
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17 |
19553557
|
PAF-AH inactivated LTA without reducing the biological activities of Pam(3)CSK(4) and FSL-1.
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18 |
19553557
|
Our results indicate that treatment with 1% H(2)O(2) for 6 h at 37 degrees C inactivates Pam(3)CSK(4), FSL-1, and LTA by more than 80%.
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19 |
19553557
|
Although HF, LPL, and H(2)O(2) treatments degrade and inactivate both lipopeptides and LTA, PAF-AH selectively inactivated LTA with no effect on the biological and structural properties of the two lipopeptides.
|
20 |
19553557
|
Lipoprotein lipase and hydrofluoric acid deactivate both bacterial lipoproteins and lipoteichoic acids, but platelet-activating factor-acetylhydrolase degrades only lipoteichoic acids.
|
21 |
19553557
|
To identify the Toll-like receptor 2 ligand critically involved in infections with gram-positive bacteria, lipoprotein lipase (LPL) or hydrogen peroxide (H(2)O(2)) is often used to selectively inactivate lipoproteins, and hydrofluoric acid (HF) or platelet-activating factor-acetylhydrolase (PAF-AH) is used to selectively inactivate lipoteichoic acid (LTA).
|
22 |
19553557
|
We investigated the reaction specificities by using two synthetic lipoproteins (Pam(3)CSK(4) and FSL-1) and LTAs from pneumococci and staphylococci.
|
23 |
19553557
|
Changes in the structures of the two synthetic proteins and the LTAs were monitored by mass spectrometry, and biological activity changes were evaluated by measuring tumor necrosis factor alpha production by mouse macrophage cells (RAW 264.7) following stimulation.
|
24 |
19553557
|
PAF-AH inactivated LTA without reducing the biological activities of Pam(3)CSK(4) and FSL-1.
|
25 |
19553557
|
Our results indicate that treatment with 1% H(2)O(2) for 6 h at 37 degrees C inactivates Pam(3)CSK(4), FSL-1, and LTA by more than 80%.
|
26 |
19553557
|
Although HF, LPL, and H(2)O(2) treatments degrade and inactivate both lipopeptides and LTA, PAF-AH selectively inactivated LTA with no effect on the biological and structural properties of the two lipopeptides.
|
27 |
24743542
|
Whole blood was stimulated for 24 hours and the pro-inflammatory tumor necrosis factor (TNF) and the anti-inflammatory/regulatory interleukin-10 (IL-10) cytokines in culture supernatant were measured by enzyme-linked immunosorbent assay (ELISA).
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28 |
24743542
|
Gabonese children had a lower pro-inflammatory response to poly(I:C) (TLR3 ligand), but a higher pro-inflammatory response to FSL-1 (TLR2/6 ligand), Pam3 (TLR2/1 ligand) and LPS (TLR4 ligand) compared to Dutch children.
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29 |
26174952
|
Here, we show porin differentially regulated splenic marginal zone (MZ) and follicular zone (FO) B cell responses in contrast to other classical TLR2-ligands FSL-1 and Pam3CSK4.
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30 |
26174952
|
The protein up-regulated TLR2 and TLR6 and stimulated the activation and costimulatory molecules on FO B cells skewing the cells toward TLR-dependent type-1 cytokine response.
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31 |
26174952
|
These cells responded to porin by expressing toll-interacting protein (TOLLIP), the TLR2 and -4 signaling inhibitor along with stimulation of the intracellular pathogen recognition receptor NLR caspase recruitment domain containing protein 5 (NLRC5).
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32 |
26174952
|
The CD1d(hi) MZ B cells released IL-10 unequivocally demonstrating regulatory B cell feature.
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33 |
26174952
|
Immunization with porin also resulted in transient IL-10 expression by the CD19(+)CD21(hi) B cells prior to plasma cell formation.
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