<p>Sorafenib and sorafenib-N-oxide accumulate in human primary keratinocytes (HEKa) via a transporter-mediated process</p>
PDF file, 76K, Identification of sorafenib glucuronide by high resolution mass spectrometry.
<p>Percentage inhibition of kinases by tyrosine kinase inhibitors in a KiNative in situ assay.</p>
PDF file - 345K, Influence of Oatp1b2-deficiency on the liver-to-plasma ratio of sorafenib, sorafenib N-oxide, and sorafenib-glucuronide in vivo.
PDF file, 28K, Error rates and confidence levels for frequency of detection of FLT3 kinase domain mutations by next generation sequencing.
<p>Incidence of hand-foot skin reactions in patients treated with kinase inhibitors.</p>
PDF file, 53K, Patient demographics and steady-state pharmacokinetics of sorafenib and metabolites.
<p>Percentage inhibition of kinases by tyrosine kinase inhibitors in a KiNative in situ assay.</p>
<p>Sorafenib and sorafenib-N-oxide accumulate in human primary keratinocytes (HEKa) via a transporter-mediated process</p>
<p>Identification of OAT-dependent sorafenib transport in human primary keratinocytes</p>
PDF file, 73K, Inhibition of UGT1A9-mediated sorafenib metabolism by azole compounds.