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A number of MD studies have been devoted to different aspects of the fouling process.
There have been a number of MD studies of the dimerization of EphA1 receptor TM domain.
Hence, the feasibility of MD studies for the investigating biochemical alterations in humans are very good with respect to the participating patients and controls.
In the majority of MD studies of chronic trapezius myalgia (and independently of degree of severity of the chronic myalgia) significant increases in [lactate] and [pyruvate] have been reported [ 18– 25, 253]53], but the results with respect to blood flow alterations have not been consistent [ 19, 20, 25].
This is particularly attractive in the case of GR in that a number of MD studies have suggested that Tyr53, although not directly involved in ligand binding and not part of the active site, nevertheless has a dynamic pattern highly associated with distinctive ligand conformers.
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Consider a meta-analysis of M studies.
To determine the value of m, extensive studies and experiments have been performed.
For comparison, our previous meta-analysis of M-CGH studies of 97 strains of C. jejuni showed ~33% of the genes in the genome were divergent in at least one strain [ 21].
Because oligonucleotide-based arrays can lead to erroneous gene absence calls [ 24], the majority of M-CGH studies have used amplicon-based microarrays, which are more sensitive albeit at the expense of specificity [ 25].
For example, in their multivariate analysis, Friedrich and Laurent [10] used sliding windows of 400 ms studying ensemble coding in the zebrafish olfactory system.
For meta-analysis j, j = 1,..., 12, we then simulated 10,000 new meta-analyses of M j study estimates for i = 1,... M j.
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