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Records Omit Multiple Records Modify Last Find Records New Record, or Requests Add New Request This command is mode-specific.
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int n = 0 ; SRSW V[] = n u l l ; / / walue w r i t t e n reader i SFSW = null ; // c o m m u n i c a t i o n b e t w e e n r e a d e r s int seqNo = 0; public MRSW(int r e a d e r s , i n t i n i t V a l ) { n = readers; V = new SRSW[n ] ; for ( i n t i = 0 ; i < n ; i++) V[ i 1 . s e t v a l u e ( i n i t V a l , 0 ) ; Comm = new SRSW[n] [ n ] ; for ( i n t i = 0 ; i < n ; i + + ) for ( i n t j = 0 ; j < n ; j + + ) C r [i ] [ j 1 . s e t V a l l i e ( i n i t V a l , 0 ) ; om
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In order for Dreamweaver to properly process an HTML file using any browser profile, the profile must follow a precise format. Here s an excerpt from the Internet Explorer 6.0 browser profile:
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In direct selection, one needs a method to separate catalytic from non-catalytic RNA. There are three general approaches: (a) differential migration by polyacrylamide gel electrophoresis (b) primer-binding site tagging technique (c) af nity probe tagging technique. In differential migration, the catalytic RNA itself is the product of the reaction, and therefore may be selected. For example, the target may be self-cleavage of RNA or the ligation of RNA that is already covalently linked to the catalytic region elsewhere. Clearly, if a reaction takes place then the result should have a different electrophoretic mobility to the situation where no reaction takes places. Hence PAGE may be used to separate cleanly reacting from nonreacting scenarios. Alternatively, the primer-binding site tagging technique is useful where, for example, a ligation reaction is being analysed. In this case, successful ligation introduces a stretch of RNA sequence onto the catalytic RNA itself that could double as a PCR primer site. Consequently, successful PCR ampli cation will only be possible if the ligation reaction has succeeded in the rst place. Therefore only RNA that is properly catalytic can and will be ampli ed by PCR ampli cation. Finally, af nity probe tagging is useful for the identi cation of catalytic RNA that is able to catalyse other chemical reactions. The chemical reaction of interest should be designed to result in the RNA self-tagging with an af nity probe such as biotin. Hence correctly catalytic RNA may then be simply separated from non-catalytic RNA by streptavidin protein af nity chromatography. A number of attempts have been made to evolve catalytic RNAs or ribozymes from natural ribozymes and also from pools of random sequence RNA. Natural ribozymes have the advantage that a natural active site already exists so can be evolved such approaches have had some success in improving or altering catalytic properties. Otherwise, ribozymes that have been evolved so far include catalytic RNA nucleases, ligases and polynucleotide kinases. Similar approaches have also been employed to evolve ribozymes that catalyse reactions at carbon bonds, such as functional group transfers, including N-alkylation (e.g. using the 2-amino functional group of guanosine to displace iodide from iodoacetamide) and S-alkylation (e.g. using 5 -phosphorothioate to displace bromide from an N-bromacetyl peptide). In general, the structure of catalytic RNAs that catalyse reactions at carbon bonds tends to be more complex than those that catalyse reactions at phosphodiester bonds, re ecting the more complex conformations required to bind non-nucleotide substrates. Overall, natural ribozymes turn out to be much more ef cient catalysts than evolved ribozymes so there is much room for further research in this area.
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The radio link between a base station and a mobile station is best described by a radio link power budget, which numerically de nes the relation between the radio link characteristics and the maximum service distance from the base station, i.e. the cell range. In order to de ne the power budget, the minimum acceptable signal level at the receiver input needs to be speci ed. In interference-free spectrum, the main cause of transmission errors is the system noise that is present in the signal detection. By neglecting the ampli cation in the receiver that also applies to the wanted signal, the noise level can be calculated as the product of Boltzmann s constant k, receiver temperature T , receiver noise bandwidth B and receiver noise factor NF. Then, by assuming certain propagation conditions, the signal-to-noise ratio (SNR) that is required for a particular service to achieve a certain minimum quality of service can be determined. Finally, the required signal level in the receiver input is simply the noise power plus SNR, in decibel scale. Table 11.2 shows a numeric example of these calculations, which apply when the interference level can be assumed to be well below the system noise level. Separate calculations are usually needed for uplink (UL) and downlink (DL) directions. When capacity requirements demand a low frequency reuse, interference typically overrides noise, which must be taken into account by adding an adequate interference degradation margin to the signal
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{ printf( <marker lat= %f lng= %f title= %s ><infowindow> ; <title>%s</title><address>%s</address><city>%s</c\ity> ; <postcode>%s</postcode><phone>%s</phone></infowindow></marker> , $row->{lat}, $row->{lng}, $row->{title}, $row->{title}, $row->{street}, $row->{city}, $row->{postcode}, $row->{phone}, ); } $sth->finish(); print( </marker>\n );
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