Software fixes are distributed in the form of service packs. The service pack CD-ROM contains fixes for all configurations and products available at the time it is built. Each service pack supersedes the previous ones and may be installed on top of the released level or on top of a previous service pack. No individual corrections are delivered in between two service packs. Service packs are made available on a regular basis. Delivery is synchronized for Windows and UNIX platforms.
If you do not commit the service pack during the installation, and certain code components are redelivered with the service pack (for example, shells, executable files), the new version of the component is installed and the previous version of the component is saved using the following naming convention:
Catia Code Level B22
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-killprocess: detects running processes (for example, Orbix) in the installation folder (unload_dir\code\bin) and terminates them before installing the service pack; at the end of the installation, the Orbix process is restarted.
9. Click the Install button to install the service pack, then click the Finish button once the setup phase is complete. Note the following: you are not allowed to choose configurations or products: the service pack CD-ROM contains fixes for all configurations and products available at the time it is built. Fixes are installed for the configurations and products detected in your installation
unlike a normal installation, you are not allowed to start a session directly at the end of the installation procedure.
An installation log is created (or the existing log is updated) in the current temporary directory, located by default in: $HOME/cxinst.log Installing a Service Pack in Batch Mode on UNIX You can also run the installation in batch mode using the following command:start [-b] [-bC] [-s] [-u unloaddir] [-v] [-killprocess][-h] -b: performs batch setup (optional if another batch option other than -s is used) but does not commit the service pack
-bc: installs in batch mode and automatically commits the service pack
-u: specifies the unload directory (by default, /usr/DassaultSystemes/B20)
-v: verbose mode
-killprocess: detects running processes (for example, Orbix) in the installation folder (unload_dir/code/bin) and terminates them before installing the service pack; at the end of the installation, the Orbix process is restarted.
The adenosine A2A receptor (A2AR), dopamine D2 receptor (D2R) and metabotropic glutamate receptor type 5 (mGluR5) form A2AR-D2R-mGluR5 heteroreceptor complexes in living cells and in rat striatal neurons. In the current study, we present experimental data supporting the view that the A2AR protomer plays a major role in the inhibitory modulation of the density and the allosteric receptor-receptor interaction within the D2R-mGluR5 heteromeric component of the A2AR-D2R-mGluR5 complex in vitro and in vivo. The A2AR and mGluR5 protomers interact and modulate D2R protomer recognition and signalling upon forming a trimeric complex from these receptors. Expression of A2AR in HEK293T cells co-expressing D2R and mGluR5 resulted in a significant and marked increase in the formation of the D2R-mGluR5 heteromeric component in both bioluminescence resonance energy transfer and proximity ligation assays. A highly significant increase of the the high-affinity component of D2R (D2RKi High) values was found upon cotreatment with the mGluR5 and A2AR agonists in the cells expressing A2AR, D2R and mGluR5 with a significant effect observed also with the mGluR5 agonist alone compared to cells expressing only D2R and mGluR5. In cells co-expressing A2AR, D2R and mGluR5, stimulation of the cells with an mGluR5 agonist like or D2R antagonist fully counteracted the D2R agonist-induced inhibition of the cAMP levels which was not true in cells only expressing mGluR5 and D2R. In agreement, the mGluR5-negative allosteric modulator raseglurant significantly reduced the haloperidol-induced catalepsy in mice, and in A2AR knockout mice, the haloperidol action had almost disappeared, supporting a functional role for mGluR5 and A2AR in enhancing D2R blockade resulting in catalepsy. The results represent a relevant example of integrative activity within higher-order heteroreceptor complexes.
The parameters for travel time and travel cost are central in travel demand forecasting models. Since valuation of infrastructure investments requires prediction of travel demand for future evaluation years, inter-temporal variation of the travel time and travel cost parameters is a key issue in forecasting. Using two identical stated choice experiments conducted among Swedish drivers with an interval of 13 years, 1994 and 2007, this paper estimates the inter-temporal variation in travel time and cost parameters. It is found that the travel time parameter has remained constant over time but that the travel cost parameter has declined in real terms. The trend decline in the cost parameter can be entirely explained by higher average income level in the 2007 sample compared to the 1994 sample. The results support the recommendation to keep the travel time parameter constant over time in forecast models but to deflate the travel cost parameter according to forecasts of income increases among travellers and the relevant income elasticity of the cost parameter. Evidence from this study further suggests that the inter-temporal and the cross-sectional income elasticity of the cost parameter are equal. The average elasticity is found to be -0.8- -0.9 in the present sample of drivers, and the elasticity is found to increases with real income level, both in the cross-section and over time. 2ff7e9595c
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