M. Morrison

发表

A quantitative analysis of kinase inhibitor selectivity

Mindy I. Davis, L. Wodicka, P. Zarrinkar, 2008, Nature Biotechnology.

Discovery of 2,4-bis-arylamino-1,3-pyrimidines as insulin-like growth factor-1 receptor (IGF-1R) inhibitors.

David P. Carney, P. Gallant, M. Morrison, 2011, Bioorganic & medicinal chemistry letters.

Discovery of a potent, selective, and orally bioavailable pyridinyl-pyrimidine phthalazine aurora kinase inhibitor.

P. Gallant, T. Bush, M. Morrison, 2010, Journal of medicinal chemistry.

Monitoring GAPDH activity and inhibition with cysteine-reactive chemical probes

M. Morrison, E. Larson, E. Weerapana, 2022, RSC chemical biology.

Novel 2,3-dihydro-1,4-benzoxazines as potent and orally bioavailable inhibitors of tumor-driven angiogenesis.

M. Morrison, A. Coxon, D. Whittington, 2008, Journal of medicinal chemistry.

The Renaissance of Bacillosamine and Its Derivatives: Pathway Characterization and Implications in Pathogenicity

B. Imperiali, M. Morrison, 2014, Biochemistry.

Synthesis, structural analysis, and SAR studies of triazine derivatives as potent, selective Tie-2 inhibitors.

P. Gallant, M. Morrison, P. Rose, 2007, Bioorganic & medicinal chemistry letters.

Evolution of a highly selective and potent 2-(pyridin-2-yl)-1,3,5-triazine Tie-2 kinase inhibitor.

Richard Kendall, P. Gallant, M. Morrison, 2007, Journal of medicinal chemistry.

Identification of a peptide inhibitor for the histone methyltransferase WHSC1

K. Swinger, M. Morrison, W. Janzen, 2018, PloS one.

Novel 2-aminopyrimidine carbamates as potent and orally active inhibitors of Lck: synthesis, SAR, and in vivo antiinflammatory activity.

P. Gallant, M. Morrison, D. Elbaum, 2006, Journal of medicinal chemistry.

Alkynylpyrimidine amide derivatives as potent, selective, and orally active inhibitors of Tie-2 kinase.

David Powers, Paul Hughes, Richard Kendall, 2007, Journal of medicinal chemistry.

Targeting Bacillosamine Biosynthesis in Bacterial Pathogens: Development of Inhibitors to a Bacterial Amino-Sugar Acetyltransferase from Campylobacter jejuni.

B. Imperiali, M. Morrison, A. Ciulli, 2017, Journal of medicinal chemistry.

Biochemical Characterization of the O-linked Glycosylation Pathway in Neisseria Gonorrhoeae Responsible for Biosynthesis of Protein Glycans Accessed Terms of Use Detailed Terms Biochemical Characterization of the O-linked Glycosylation Pathway in Neisseria Gonorrhoeae Responsible for Biosynthesis of

B. Imperiali, M. Morrison, M. Koomey, 2022 .

Biosynthesis of UDP-N,N'-diacetylbacillosamine in Acinetobacter baumannii: Biochemical characterization and correlation to existing pathways.

B. Imperiali, M. Morrison, 2013, Archives of biochemistry and biophysics.

Elucidation of the pathways responsible for the biosynthesis of UDP-N,N'-diacetylbacillosamine in bacterial pathogens

M. Morrison, 2013 .

Biochemical Analysis and Structure Determination of Bacterial Acetyltransferases Responsible for the Biosynthesis of UDP-N,N′-Diacetylbacillosamine*

B. Imperiali, M. Morrison, 2013, The Journal of Biological Chemistry.

Biosynthesis of UDP-N,N'-diacetylbacillosamine in Acinetobacter baumannii: Biochemical characterization and correlation to existing pathways.

B. Imperiali, M. Morrison, 2013, Archives of biochemistry and biophysics.

Inverse acyl phosph(on)ates: substrates or inhibitors of beta-lactam-recognizing enzymes?

M. Morrison, R. Pratt, N. Li, 2001, Bioorganic chemistry.