G. W. Peet

发表

The discovery of carboline analogs as potent MAPKAP-K2 inhibitors.

Michel Emmanuel, Mohammed A Kashem, Lori Patnaude, 2007, Bioorganic & medicinal chemistry letters.

Landscape and Dynamics of Single Immune Cells in Hepatocellular Carcinoma

Xianwen Ren, Guojie Zhong, Yilei Mao, 2019, Cell.

Catalysis and Function of the p38α·MK2a Signaling Complex

C. Pargellis, B. Werneburg, S. Lukas, 2004 .

The discovery of thienopyridine analogues as potent IkappaB kinase beta inhibitors. Part II.

M. Hao, C. Cywin, E. Hickey, 2009, Bioorganic & medicinal chemistry letters.

The kinetics of binding to p38MAP kinase by analogues of BIRB 796.

C. Pargellis, P. Cirillo, T. Gilmore, 2003, Bioorganic & medicinal chemistry letters.

IκB Kinases α and β Show a Random Sequential Kinetic Mechanism and Are Inhibited by Staurosporine and Quercetin*

G. W. Peet, Jun Li, 1999, The Journal of Biological Chemistry.

The oxidase activity of vascular adhesion protein-1 (VAP-1) is essential for function.

R. Wasti, S. Lukas, G. W. Peet, 2013, American journal of clinical and experimental immunology.

Recombinant IkappaB kinases alpha and beta are direct kinases of Ikappa Balpha.

G. W. Peet, M. Kehry, J. Li, 1998, Journal of Biological Chemistry.

Discovery of 2-phenylamino-imidazo[4,5-h]isoquinolin-9-ones: a new class of inhibitors of lck kinase.

J. Peterson, N. Moss, S. Lukas, 2002, Journal of medicinal chemistry.

Optimization of 2-phenylaminoimidazo[4,5-h]isoquinolin-9-ones: orally active inhibitors of lck kinase.

J. Peterson, S. Pav, N. Moss, 2003, Journal of medicinal chemistry.

Bioluminescent Method for Assaying Multiple Semicarbazide-Sensitive Amine Oxidase (SSAO) Family Members in Both 96- and 384-Well Formats

S. Lukas, Leslie Martin, G. W. Peet, 2011, Journal of biomolecular screening.

IKKα, IKKβ, and NEMO/IKKγ Are Each Required for the NF-κB-mediated Inflammatory Response Program*

G. W. Peet, K. Marcu, P. Massa, 2002, The Journal of Biological Chemistry.

Novel NEMO/IκB Kinase and NF-κB Target Genes at the Pre-B to Immature B Cell Transition*

G. W. Peet, K. Marcu, R. Barton, 2001, The Journal of Biological Chemistry.

Inhibition of pro-inflammatory cytokine production by the dual p38/JNK2 inhibitor BIRB796 correlates with the inhibition of p38 signaling.

J. Woska, C. Pargellis, G. W. Peet, 2009, Biochemical pharmacology.

Novel NEMO/IkappaB kinase and NF-kappa B target genes at the pre-B to immature B cell transition.

G. W. Peet, J. Li, K. Marcu, 2001, The Journal of biological chemistry.

Recombinant IκB Kinases α and β Are Direct Kinases of IκBα*

G. W. Peet, M. Kehry, K. Marcu, 1998, The Journal of Biological Chemistry.

Non-sialate inhibitor of influenza A/WSN/33 neuraminidase.

G. W. Peet, J. Wu, R. Eckner, 1995, Biochemistry.

Thermal denaturation: a method to rank slow binding, high-affinity P38alpha MAP kinase inhibitors.

C. Pargellis, J. Regan, G. W. Peet, 2003, Journal of medicinal chemistry.

Catalysis and function of the p38 alpha.MK2a signaling complex.

C. Pargellis, B. Werneburg, S. Lukas, 2004, Biochemistry.

Discovery and characterization of a substrate selective p38alpha inhibitor.

C. Pargellis, B. Werneburg, S. Lukas, 2004, Biochemistry.

IKKalpha, IKKbeta, and NEMO/IKKgamma are each required for the NF-kappa B-mediated inflammatory response program.

G. W. Peet, K. Marcu, P. Massa, 2002, The Journal of biological chemistry.