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The involvement of homologous proteins in vertebrate lens development was subsequently elucidated by the characterization of mutations that cause congenital human or murine ocular disorders and their comparison to mutations in model organisms [1].
Contributing signaling pathways possibly involved were subsequently elucidated by western blot analysis.
Upstream regulators of these genes were subsequently elucidated from IPA and compared.
The molecular basis for this requirement was subsequently elucidated with the discovery of ubiquitin-binding domains (UBDs) in a subset of damage-tolerant DNA polymerases (Kannouche et al. 2004; Watanabe et al. 2004; Bienko et al. 2005; Plosky et al. 2006).
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The relation between the reaction rate coefficient and the initial concentration of Acid Yellow 99, ferrous sulphate concentrations, hydrogen peroxide concentrations and operating temperature will subsequently be elucidated based on the obtained experimental data.
In addition, a number of AM-related genes has been identified by their AM-related expression patterns, and their function has subsequently been elucidated by knock-down or knock-out approaches (reverse genetics).
Facilitated access to such databases is an essential step to better understand how human genetic alterations affect the gene products at the structural level and subsequently to elucidate the relationships between genotypic and phenotypic variations.
Access to such information is essential in order to understand how genetic alterations affect gene products at the molecular level and subsequently to elucidate the relationships between genotypic and phenotypic variations.
Subsequently, other investigators have elucidated the electrophysiologic properties of this pathway leading to the currently accepted concept of slow and decremental anterograde fiber conduction.
Clarifying this relationship may elucidate the impact of explicit chronicity on total medical costs, and subsequently clarify comprehensive care coordination opportunities.
The product ion scan was subsequently used to elucidate the structures for the molecular ions observed from the peaks in the neutral loss scan chromatogram.
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