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• Activation of JNK3 alpha 1 requires both MKK4 and MKK7: Kinetic characterization of in vitro phosphorylated JNK3 alpha 1  Academic Article
• Beta-arrestin 2: a receptor-regulated MAPK scaffold for the activation of JNK3  Academic Article
• Design and synthesis of 1-aryl-5-anilinoindazoles as c-Jun N-terminal kinase inhibitors  Academic Article
• Design and synthesis of highly potent and isoform selective JNK3 inhibitors: SAR studies on aminopyrazole derivatives  Academic Article
• Identification of a motif in the carboxyl terminus of β-arrestin2 responsible for activation of JNK3  Academic Article
• Kinetic mechanism and inhibitor characterization for c-jun-N-terminal kinase 3 alpha 1  Academic Article
• Structural basis and biological consequences for JNK2/3 isoform selective aminopyrazoles  Academic Article
• Structural mechanisms of allostery and autoinhibition in JNK family kinases  Academic Article
• Structure-activity relationships and X-ray structures describing the selectivity of aminopyrazole inhibitors for c-jun N-terminal kinase 3 (JNK3) over p38  Academic Article
• Substituting c-jun n-terminal kinase-3 (jnk3) atp-binding site amino acid residues with their p38 counterparts affects binding of jnk- and p38-selective inhibitors  Academic Article
• The structure of jnk3 in complex with small molecule inhibitors: Structural basis for potency and selectivity  Academic Article