B. Lovejoy

发表

Oxindole-based inhibitors of cyclin-dependent kinase 2 (CDK2): design, synthesis, enzymatic activities, and X-ray crystallographic analysis.

P. A. Harris, L. Kuyper, S. Frye, 2001, Journal of medicinal chemistry.

Crystal Structure of the Catalytic Domain of the Human Cell Cycle Control Phosphatase, Cdc25A

E. Fauman, H. Piwnica-Worms, W. Rocque, 1998, Cell.

Structural Analysis of the Catalytic Domain of Human Fibroblast Collagenase

M. Lambert, A. Hassell, S. Jordan, 1994, Annals of the New York Academy of Sciences.

Design and synthesis of 4-azaindoles as inhibitors of p38 MAP kinase.

Michelle Browner, Stephen D Warren, Eva Papp, 2003, Journal of medicinal chemistry.

Crystal structures of MMP-1 and -13 reveal the structural basis for selectivity of collagenase inhibitors

H. V. Van Wart, C. Broka, C. Luong, 1999, Nature Structural Biology.

Crystal structures of recombinant 19-kDa human fibroblast collagenase complexed to itself.

A. Hassell, S. Jordan, D. Weigl, 1995, Biochemistry.

Crystal structure of a synthetic triple-stranded alpha-helical bundle.

D Eisenberg, D. Eisenberg, W. DeGrado, 1993, Science.

Crystal structure of canine and bovine granulocyte-colony stimulating factor (G-CSF).

D. Eisenberg, D. Cascio, B. Lovejoy, 1993, Journal of molecular biology.

Prevention of chemotherapy-induced alopecia in rats by CDK inhibitors.

B G Benson, A M Hassell, P. A. Harris, 2001, Science.

Structure of the catalytic domain of fibroblast collagenase complexed with an inhibitor.

A M Hassell, M. Lambert, D. Drewry, 1994, Science.