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Another approach to exporting text files with SAS is to use the SAS Enterprise Guide interface. The following example exports the DM data set to a CSV file using SAS Enterprise Guide 3.0. With the DM data set selected in the Process Flow window, click File and then select Export dm from the drop-down list as follows ... [Pg.281]

IMPORT AND EXPORT TEXT FILES, ONE COLUMN AT A TIME... [Pg.236]

Output data can be printed or exported to a spreadsheet. The rendering quality is very good. Structures can be rendered and labeled in several different ways. Molecular structures can be saved in several different formats or as image files. The presentation mode allows molecular structures to be combined with text. [Pg.323]

Figure 3. Mitochondrial fatty acid oxidation. Long-chain fatty acids are converted to their CoA-esters as described in the text, and their fatty-acyl-groups transferred to CoA in the matrix by the concerted action of CPT 1, the acylcarnitine/carnitine exchange carrier and CPT (A) as described in the text. Medium-chain and short-chain fatty acids (Cg or less) diffuse directly into the matrix where they are converted to their acyl-CoA esters by a acyl-CoA synthase. The mechanism of p-oxidation is shown below (B). Each cycle of P-oxidation removes -CH2-CH2- as an acetyl unit until the fatty acids are completely converted to acetyl-CoA. The enzymes catalyzing each stage of P-oxidation have different but overlapping specificities. In muscle mitochondria, most acetyl-CoA is oxidized to CO2 and H2O by the citrate cycle (Figure 4) some is converted to acylcamitine by carnitine acetyltransferase (associated with the inner face of the inner membrane) and exported from the matrix. Some acetyl-CoA (if in excess) is hydrolyzed to acetate and CoASH by acetyl-CoA hydrolase in the matrix. Enzymes ... Figure 3. Mitochondrial fatty acid oxidation. Long-chain fatty acids are converted to their CoA-esters as described in the text, and their fatty-acyl-groups transferred to CoA in the matrix by the concerted action of CPT 1, the acylcarnitine/carnitine exchange carrier and CPT (A) as described in the text. Medium-chain and short-chain fatty acids (Cg or less) diffuse directly into the matrix where they are converted to their acyl-CoA esters by a acyl-CoA synthase. The mechanism of p-oxidation is shown below (B). Each cycle of P-oxidation removes -CH2-CH2- as an acetyl unit until the fatty acids are completely converted to acetyl-CoA. The enzymes catalyzing each stage of P-oxidation have different but overlapping specificities. In muscle mitochondria, most acetyl-CoA is oxidized to CO2 and H2O by the citrate cycle (Figure 4) some is converted to acylcamitine by carnitine acetyltransferase (associated with the inner face of the inner membrane) and exported from the matrix. Some acetyl-CoA (if in excess) is hydrolyzed to acetate and CoASH by acetyl-CoA hydrolase in the matrix. Enzymes ...
The metabolism of amino acids is complex and is described in standard text books. These are usually converted by aminotransferases to the corresponding 2-oxoacids which are partly oxidized in the matrix of muscle mitochondria and partly exported to the liver. Glutamate and aspartate yield 2-oxoglutarate and oxaloacetate, respectively, which enter the citrate cycle directly, and other 2-... [Pg.116]

This equation shows that the contribution of the two components of the PMF differ with different conditions. In state 4, the electrical potential gradient across the inner membrane can be as high as 300,000 Vcm" and the A pH difference one unit. ATP synthesis only occurs when the PMF is sufficiently large. The phosphorylation potential (AG atp) is lower for ATP synthesis in the matnx (AG atp in = 3AP) for ATP exported to the cytosol (AG ajp out = 4AP) because an extra proton is consumed in importing ADP into the matnx (see text). [Pg.149]

As clipboard objects (. bmp format) for export to text and graphics software. [Pg.361]

On occasion you will need to export your SAS data as ASCII text. You may find that the recipient of your data requires that you send some form of delimited ASCII text, because that is all their software can read. In fact, delimited ASCII text is a primitive data exchange format that almost any software can read. [Pg.276]

PROC EXPORT provides a quick way to create ASCII text files from SAS data sets. You can call PROC EXPORT by typing in the SAS code, or you can use the convenient SAS windowing environment Export Wizard that builds the PROC EXPORT code for you. Let s start by looking at using the SAS 9.1 windowing environment Export Wizard... [Pg.276]

You can see how the (pipe) character is entered as the delimiter in the Options dialog box. If you have more complex requirements for the ASCII text file you want to export, you can invoke External File Interface in the Select Export Type window, write customized DATA step code with FILE and PUT statements, or use some of the ODS tagsets supplied by SAS, found at http //support.sas.com/md/base/topics/odsmarkup/, that have the ability to create numerous types of ASCII text formats. [Pg.280]

You may find that you need to export your SAS data as something other than regular ASCII text or Microsoft Office files. In this case, the export wizards in the SAS windowing environment in SAS 9 and SAS Enterprise Guide 3.0 can easily export the following file formats ... [Pg.287]

Imports are shown as a dashed arrow from importer to exporter—strictly with the stereotype marker import . An equivalent is to write an import statement inside the importing package (along with any other contents), as in this diagram. A formal text alternative to the import diagram is... [Pg.317]

Figure 1. Solute transfer across an idealised eukaryote epithelium. The solute must move from the bulk solution (e.g. the external environment, or a body fluid) into an unstirred layer comprising water/mucus secretions, prior to binding to membrane-spanning carrier proteins (and the glycocalyx) which enable solute import. Solutes may then move across the cell by diffusion, or via specific cytosolic carriers, prior to export from the cell. Thus the overall process involves 1. Adsorption 2. Import 3. Solute transfer 4. Export. Some electrolytes may move between the cells (paracellular) by diffusion. The driving force for transport is often an energy-requiring pump (primary transport) located on the basolateral or serosal membrane (blood side), such as an ATPase. Outward electrochemical gradients for other solutes (X+) may drive import of the required solute (M+, metal ion) at the mucosal membrane by an antiporter (AP). Alternatively, the movement of X+ down its electrochemical gradient could enable M+ transport in the same direction across the membrane on a symporter (SP). A, diffusive anion such as chloride. Kl-6 refers to the equilibrium constants for each step in the metal transfer process, Kn indicates that there may be more than one intracellular compartment involved in storage. See the text for details... Figure 1. Solute transfer across an idealised eukaryote epithelium. The solute must move from the bulk solution (e.g. the external environment, or a body fluid) into an unstirred layer comprising water/mucus secretions, prior to binding to membrane-spanning carrier proteins (and the glycocalyx) which enable solute import. Solutes may then move across the cell by diffusion, or via specific cytosolic carriers, prior to export from the cell. Thus the overall process involves 1. Adsorption 2. Import 3. Solute transfer 4. Export. Some electrolytes may move between the cells (paracellular) by diffusion. The driving force for transport is often an energy-requiring pump (primary transport) located on the basolateral or serosal membrane (blood side), such as an ATPase. Outward electrochemical gradients for other solutes (X+) may drive import of the required solute (M+, metal ion) at the mucosal membrane by an antiporter (AP). Alternatively, the movement of X+ down its electrochemical gradient could enable M+ transport in the same direction across the membrane on a symporter (SP). A, diffusive anion such as chloride. Kl-6 refers to the equilibrium constants for each step in the metal transfer process, Kn indicates that there may be more than one intracellular compartment involved in storage. See the text for details...
Station ALOHA (see Figure 23.4 for location information). Three-point running mean observations of N/P molar ratios in (a) total dissolved inorganic plus organic pool, (b) total suspended particulate matter in the upper 0-100 m, (c) in exported particulate matter at 150 m depth, and (d) cycling in nutrient limitation (described in text). Source From Karl, D. M. (2002). Trends in Microbiology 10(9), 410-418. [Pg.689]

Since the schematic we created in previous sections only contains parts in our Digikey database, we can easily create a bill of materials (BOM) that contains information from the database. The information contained in the BOM can be easily configured, and the BOM can be viewed with a text editor or exported to Microsoft Excel. Here, we will show how to create a custom BOM and export the information to Excel, where it can be easily manipulated. We will start with the project created in the earlier sections of this manual. If you have the screen in the previous window, type CTRL-F4 to close the schematic and return to the tree view of the project ... [Pg.595]

According to historical records, around 1500 B.c. the use of opium, as well as its exportation, was beginning to take root. The city of Thebes was so well-known for its poppy fields that it lent its name to the active alkaloid in opium, thebaine. Alkaloids are any of a host of organic compounds, often complex in structure, derived from plants. Many [alkaloids] are useful as medicines and poisons. In medical texts left by the Egyptians, there are more than 700 medicines that contain opium. Under the... [Pg.9]

The capillaries of the brain, the testes, and some other tissues are characterized by the absence of pores that permit aqueous diffusion. They may also contain high concentrations of drug export pumps (MDR pumps see text). These tissues are therefore protected or "sanctuary" sites from many circulating drugs. [Pg.22]

A text editor is also included and is an invaluable tool for viewing the generated output text files of SPICE, as well as investigating syntax errors and other subtleties of the SPICE programming language. The text output of SPICE is in an excellent format for exporting to other useful engineering tools such as Excel or MathCAD. [Pg.9]

If you have installed MAPI (mail application interface) software on your PC, you may exploit the MS-WINDOWS mailslot-function to e-mail NMR data directly to and from your PC. The full version of ID-WIN-NMR allows you to export/irnport FlDs, spectra, tables, text-files, relaxation data and metafiles to/from other users of (the full version of) ID WIN-NMR. Both JCAMP-DX5 and Bruker specific binary format are supported. Compared to the procedure outlined in section 2.6.5 this is an even more convenient way for exporting/importing NMR data via Internet. For further details refer to the ID WIN-NMR manual [2.1] or contact your Bruker/Spectrospin representative. [Pg.32]

Besides the latter approach to storing data, it is possible in IR as in many other analytical techniques to export a spectrum with its annotations stored in memory as a pictorial image to a report via a word processor. It is using this procedure that all spectra shown in this chapter have been integrated into the text. [Pg.181]

Figure 21-3 Major pathways of synthesis of fatty acids and glycerolipids in the green plant Arabidopsis. The major site of fatty acid synthesis is chloroplasts. Most is exported to the cytosol as oleic acid (18 1). After conversion to its coenzyme A derivative it is converted to phosphatidic acid (PA), diacylglycerol (DAG), and the phospholipids phosphatidylcholine (PC), phosphatidylinositol (PI), phosphatidylglycerol (PG), and phosphatidylethanolamine (PE). Desaturation also occurs, and some linoleic and linolenic acids are returned to the chloroplasts. See text also. From Sommerville and Browse.106 See also Figs. 21-4 and 21-5. Other abbreviations monogalactosyldiacylglycerol (MGD), digalactosyldiacylglycerol (DGD), sulfolipid (SL), glycerol 3-phosphate (G3P), lysophosphatidic acid (LPA), acyl carrier protein (ACP), cytidine diphosphate-DAG (CDP-DAG). Figure 21-3 Major pathways of synthesis of fatty acids and glycerolipids in the green plant Arabidopsis. The major site of fatty acid synthesis is chloroplasts. Most is exported to the cytosol as oleic acid (18 1). After conversion to its coenzyme A derivative it is converted to phosphatidic acid (PA), diacylglycerol (DAG), and the phospholipids phosphatidylcholine (PC), phosphatidylinositol (PI), phosphatidylglycerol (PG), and phosphatidylethanolamine (PE). Desaturation also occurs, and some linoleic and linolenic acids are returned to the chloroplasts. See text also. From Sommerville and Browse.106 See also Figs. 21-4 and 21-5. Other abbreviations monogalactosyldiacylglycerol (MGD), digalactosyldiacylglycerol (DGD), sulfolipid (SL), glycerol 3-phosphate (G3P), lysophosphatidic acid (LPA), acyl carrier protein (ACP), cytidine diphosphate-DAG (CDP-DAG).
To make it easier, the obtained concentrations for the test samples can be exported to a text file for this purpose, press Save Queries . Save the data in a text format file in order to use them in a spreadsheet. [Pg.1258]

ChemFolder Database Optiops... Text Export Options... ... [Pg.67]


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See also in sourсe #XX -- [ Pg.236 ]




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ASCII text exporting

Export Text Files, Multiple Columns

Export Text Files, One Column at a Time

Export a Text File

Exported

Exporting

Exporting data ASCII text

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