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The association between depression and dietary patterns has been discussed in a few studies, with controversial results.
The explanation for differences in germination patterns has been discussed by Rojas-Aréchiga et al. (2001) and Otero-Arnaiz et al. (2003) who considered it to be an indirect consequence of selection in favour of larger fruits with larger seeds.
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Finally, selectivity patterns have been discussed in terms of kinetic rates of vitamin B2 release.
The results of [2], [3] and the arguments about periodicity in extinction patterns have been discussed extensively (see [12], [15] [18] and references therein for a detailed review).
These opposite evolutionary effects between different AS patterns have been discussed as a key role of AS in the 'switch-like' regulation of gene expression [ 29].
The reason of the distribution pattern has been discussed based on seismic tomography in the megathrust zone off Tohoku.
The necessity of concentration dependent thresholds in the gap-gene Drosophila patterning has been discussed in [24], and modeled through a Hill type response function with diffusion.
This methylation pattern has been discussed to influence A- versus P-site binding specificity of short CCA/CCPmn substrates.
Hyperactive behavior pattern has been discussed as a possible promoter of LCPD (Wynne-Davies and Gormley 1978, Douglas and Rang 1981).
The powers of the linear risk score tests and Stone's Poisson maximum test to detect a given risk pattern have been discussed by several authors (Bithell, 1995; White-Koning et al, 2004; COMARE, 2005).
The mechanism underlying the pattern formation has been discussed on the light of the Flory–Huggins (FH) lattice theory, grain boundary effects and the Cahn Hilliard equation for mass conservation systems.
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