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The File Placement category allows the administrator to specify where dependent files, added by Contribute users, are stored in the site. This category is tremendously useful for organizing file clutter by standardized rules. Initially, three document types are predefined, as shown in Figure 31-22; the administrator can modify these settings and declare any others necessary. FIGURE 31-22

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Before Pop at Each Tenure: Count of all customers by the tenure of customers who started before the event date as of the event date. Before Stops at Each Tenure: Count of stopped customers who started and stopped before the event date. After Starts at Each Tenure: Count of all customers who start after the event date by tenure. After Stops at Each Tenure: Count of stopped customers who start and stop after the event date by tenure. Before Enters at Each Tenure: Count of customers who start before the event date by their tenure at the event date. Before Leaves at Each Tenure: Count of customers who start before the event date by their tenure when they stop or are censored. Before/After Stop at Each Tenure: Count of stopped customers who start before the event date and stop after the event date, by tenure.

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public function setStoreData( id:uint, n:String, d:String, t:String, p:String):void {

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of synthesis of acylglycerols and phospholipids, since these synthetic approaches are important in lipid semi-synthesis should a uorescent tag be required etc. Acylglycerols derive from the controlled esteri cation of hydroxyl functional groups in the alkyltriol known as glycerol. One major problem with the synthesis of pure acylglycerols is that mono- and diacylglycerols easily migrate to adjacent free hydroxyl groups, typically catalysed by acid, base or heat. Therefore, a suitable protecting group strategy is absolutely essential for the chemical synthesis of de ned acylglycerols. For instance, glycerol can react with acetone under acidic conditions to give a 1,2-isopropylidene (acetonide), leaving one primary hydroxyl free for subsequent acylation. Alternatively, benzaldehyde can react to give 1,2- or 1,3-O-benzylidenes that can be separated by crystallisation and used for esteri cation. Typically, acylation can then be performed by carbonyl diimidazole (CDI) activation of the selected fatty acids (Figure 2.16). Thereafter, acetal deprotection can be followed by further esteri cation as appropriate. In the case of phospholipid synthesis, this can be reduced to the controlled esteri cation of l- -glycerophosphocholine.CdCl2 (GPC) made possible by CDI activation of the selected fatty acids (Figure 2.17). Other phospholipids can then be prepared from this phosphatidylcholine by headgroup transphosphatidylation mediated by the enzyme known as phospholipaseD. Lipid synthesis may appear trivial, but there is nothing trivial about the puri cation of lipids to homogeneity post synthesis. In this respect reversed phase HPLC becomes a powerful technique, but using a specially developed evaporative light scattering (ELS) detector to allow for the detection of eluting lipid analytes that do not possess any strong chromophore (see later in 2).

As with all nonvisual objects, instances of XML and XMLList must be declared inside an <fx:Declarations> element in Flex 4 applications. n

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