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Sample size response with

Peak area responses are linear with sample size. [Pg.352]

The interface should provide quantitative information with a reproducibility better than 10% with low limits of detection and have a linear response over a wide range of sample sizes (low picograms to p,g). [Pg.22]

Often there is a desire to compare responses to multiple treatments rather than simply evaluate active against a placebo control. For instance, it may be useful to evaluate several doses or to assess a product against another marketed product. Increasing the number of treatments will increase the sample size required overall, but will also increase the number of subjects required per treatment arm because the number of statistical comparisons is larger. If all between-group comparisons are to be made, the number of statistical tests increases dramatically as the number of treatment arms increases. With two groups, only one comparison is possible. With three groups, the number... [Pg.242]

The specified amount is, in many instances, just a piece of guesswork since expensive studies of sampling behavior were not incorporated in the certification process. However, the certification process has established that the recommended amount provides sufficient analyte for a reproducible value with many of the analytical techniques operating at an optimal level. Deviation in sample size may change the optimum and reproducible response of some analytical techniques. [Pg.242]

This belief was further supported by the evidence of a correlation between the clinical response and REM sleep suppression as well as a temporal relationship between the onset of clinical response and REM sleep suppression. However, some of the later studies suggested that REM sleep suppression is not necessary for the antidepressant action (Gillin 1983). For example, some studies show evidence of no change or even an increase in REM sleep with the treatment of depression (Gillin et al. 2001). Recently, Landolt Gillin (Landolt and Gillin 2002) have also demonstrated that the antidepressant response to phenelzine treatment does not depend on elimination of REM sleep or inhibition of slow wave activity in non-REM sleep. However, the generalization of some of these studies is limited because of their small sample size. [Pg.437]

Sample sizes required for discovering SNPs associated with drug response depend on a number of factors, among which are the SNP allele frequencies, the number of SNPs being tested and, for LD mapping studies, the strength of LD. A marker... [Pg.50]

Growing experience with complex disease genetics has made clear the need to minimize type I error in genetic studies [41, 109]. Power is especially an issue for SNP-based association studies of susceptibility loci for phenomenon such as response to pharmacological therapy, which are extremely heterogeneous and which are likely to involve genes of small individual effect. Table 10.2 shows some simple estimation of required sample sizes of cases needed to detect a true odds ratio (OR) of 1.5 with 80% power and type I error probability (a) of either 0.05 or 0.005. [Pg.226]

Although TSER 9 appears to be unique to the Ghanaian population, the sample size evaluated in this study cannot deny the presence of this allele in other African populations [83]. Alleles corresponding to 5-8 or >9 tandem repeats were not identified in this study however, considering the low frequencies of TSER 4 and TSER 9 in the populations studied, it is possible that a larger population study may identify novel alleles. In addition, the significance of TSER 4 and TSER 9 is less clear. An increase in TSER repeats is associated with increased TS expression in vitro and TS protein levels in vivo [70, 80, 81]. There is no data in the literature that evaluates the role of ethnicity in response to TS inhibitor chemotherapy. [Pg.505]

Fig. 7.2 Comparison of the proportion of elephants responding with chemosensory behaviors to the general substrate (environment) and to urine/feces for pre- and post-pubescent males and females, (a) Ndarakwai Ranch, Tanzania sample size of different elephants from left to right for environment and to urine/feces 40, 44, 46 and 40. The same animals were observed for response to urine/feces as to the environment, (b) Addo Elephant National Park South Africa sample size from left to right for environment 59, 43, 53 and 48. Many of the same animals were observed for response to urine/feces as to the environment. Sample sizes to urine/feces from left to right 49, 32, 44 and 44... Fig. 7.2 Comparison of the proportion of elephants responding with chemosensory behaviors to the general substrate (environment) and to urine/feces for pre- and post-pubescent males and females, (a) Ndarakwai Ranch, Tanzania sample size of different elephants from left to right for environment and to urine/feces 40, 44, 46 and 40. The same animals were observed for response to urine/feces as to the environment, (b) Addo Elephant National Park South Africa sample size from left to right for environment 59, 43, 53 and 48. Many of the same animals were observed for response to urine/feces as to the environment. Sample sizes to urine/feces from left to right 49, 32, 44 and 44...
Using in vivo techniques, natural and synthetic fibrous materials have been shown to induce fibrosis and carcinogenic responses that were directly related to dose, if the materials were placed on the target tissues. Chrysotile appeared to be more biologically active than the other UICC asbestos samples or fibrous glass, with particle size and shape having some influence on the response. In vitro experiments indicate that fibers can be cytotoxic and possibly mutagenic, increase the secretory activity of fibroblasts, and possibly initiate an immune cascade. [Pg.144]


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Sampling sample size

Sampling size

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