Figure 4. Coordinates of the center of the two batteries ventilation holes (per battery pack). These coordinates are given with reference to the S/C coordinate system origin located at the center of the S/C separation plane (X, Y, Z) : A= 1042.425 , -857.5 , -145.75 B= 1042.425 , 857.5 , -145.75 D= -1042.425, -857.5, -145.75 C= -1042.425, 857.5, -145.75 Frequency (MHz) E_Field (dBmV/m) The susceptibility level is at equipment surface. To evaluate the effect of the launcher radiated field on the L/V onto S/C TC receivers, the launcher radiation level at S/C separation plane region must be attenuated by 33 dB to account for the presence of S/C structures and MLI and the location of the TC receivers inside the S/C. INMARSAT-4 radiated emissions (TM emitters OFF)
Figure 4. Permeability evolution as a function of effective pressure of the thermally cracked and unreacted Carnmenellis granite (black curve), and after three fluid-rock interaction experiments. The black curve shows the permeability measured in the unreacted core. The red, green, and blue curves correspond to measurements on the core after it was recovered from experiments 1, 2, and 3, respectively. Inset: Deficit between the initially measured permeability at 10 MPa (grey dotted line) and that measured at the same pressure after the full pressurization/depressurization cycle.
Figure 4. 2 below shows the major existing developments at the surroundings of the Project Area within the Study Area. The heights (in mPD) of the developments are also listed. Project Area 1. Project Area (proposed 110mPD), currently Hong Kong School of Motoring (~9.6mPD) 2. Horizon Plaza (110.5mPD), Electric Tower (118.3mPD) Ap Xxx Xxxx Industrial Estate Station Building (27.6mPD)
Figure 4. .2.3 a) In-situ evidence for some landslides occurring along the hillslopes facing the town of Quindici (Xxxxxxx et al., 2008); b) Shallow flow-type landslides connected to mountain tracks during the May 1998 event.
Figure 4. 2.4 a) Schemes adopted in the numerical analyses performed by Xxxxxxx et al., 2008; b)
Figure 4. Figure 5. Participants
Figure 4. What kind of learning information do you wish to know about your children? (Score, localisation …)? Figure 5: What disabilities should Beaconing provide support for? Figure 6: What could be the main security issues?
Figure 4. Unified Modeling Language (UML): Sequence Diagram. Yellow titles indicate passage of time from left to right. Top layer (User Interface, Server, and Output) match three-tiered system as described in methods section. Second layer indicates phases of the device that the user accesses. The ‘GUI’ is the graphical user interface that displays data input fields, instructions, and a link to the original model. ‘Data Validation’ indicates step in sequence that screens for accurate formatting of data required to run in the formulae. ‘Xxxxxxxx Model’ indicates the copy/pasted code provided by X. Xxxxxxxx. ‘Certainty %’ is a calculation that indicates the percentage certainty that <1% of the population has loiasis at > 20,000 mf/ml. ‘Final Output’ indicates with visual images whether the Xxxxxxxx model determined the village to be > 95% certain that less than 1% of the village has loiasis (Green Thumbs up – or safe to treat ivermectin), or < 95 % (Red Thumbs Down – recommend to test and treat the village). Arrows and white blocks with text beneath yellow titles indicate logical sequence of events as experienced by the user. The illustration utilized xxxxxxxx.xxx for sequence diagram template (accessed April 10, 2017).
Figure 4. At sacrifice, blood and spleen cells were isolated (n=5 per group) and percentages of CD4+ and CD8+ T cells were determined with flow cytometry (A). In addition, CD4+CD62Llow effector T cells and CD4+CD44low62Lhigh naive T cells were determined in the spleen (B). Splenic T cell subsets were determined by staining for CD4 and the transcription factors T-bet (Th1), GATA-3 (Th2), RORγt (Th17) B Naive Effector D and Foxp3 (CD25+ Tregs) (C). The effect of MDSC administration % within CD4+ T cells 15 60 on spleen cell proliferation was 9 50 S.I. T-bet GATA-3 ROR t + Foxp3 CD25 Control MDSCs determined by culturing splenocytes (n=5 per group) in the presence or absence of CD3/CD28 stimulation (D). Proliferation was assessed by the amount of 3H-thymidine incorporation in dividing cells. The proliferation is expressed as stimulation index. ***P<0.001 population of the spleen compared with control mice (Figure 4C). In contrast, Th2 and Treg responses remained unchanged following adoptive transfer of MDSCs. Although adoptive transfer of MDSCs decreased the pool of splenic effector CD4+ T cells and more specifically, decreased Th1 and Th17 cell subsets, we did not observe any difference in splenocyte proliferation of MDSC-treated mice (stimulation index of 49.7±3.6) in comparison with control mice (stimulation index of 51.8±2.0) after stimulation with αCD3/CD28 (Figure 4D). Adoptive transfer of MDSCs also affected B cell responses since MDSC-treated mice had reduced circulating CD19+ B cells (23.7±1.4% vs. 30.3±2.3% in control mice, P<0.05, Figure 5A). More particular, we observed a 30% decrease in circulating B2 cells in MDSC-treated mice (15.2±1.0%) in comparison with control mice (21.6±2.1%, P<0.05, Figure 5B). Furthermore, we found that splenic B cells of MDSC-treated mice proliferated less vigorously (29.5±1.4% CD19+Ki-67+ cells) than B cells of control mice (35.9±1.2% CD19+Ki-67+ cells, P<0.05, Figure 5C). We also determined oxLDL-specific antibodies in serum (Figure 5D) but did not find any difference in MDSC-treated mice in comparison with control mice. A % CD19+ cells C Control MDSCs % Ki-67+ within CD19+ cells % B2 cells OD 450 nm
