David E. Matthews

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The vast majority of clinically approved protein kinase inhibitors target the ATP-binding pocket directly. Consequently, many inhibitors have broad selectivity profiles and most have significant off-target effects. Allosteric inhibitors are generally more selective, but are difficult to identify because allosteric binding sites are often unknown or poorly(More)
We propose graphical diagnostic tools to assess the fit of a bivariate accelerated lifetime regression model. Using univariate residuals for each response measurement in a pair, we assess their dependence structure via the bivariate probability integral transformation of univariate residuals, which we call V-residuals. To reduce the computational burden(More)
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