Structure–activity relationships for 2-anilino-6-phenylpyrido[2,3- d]pyrimidin-7(8 H)-ones as inhibitors of the cellular checkpoint kinase Wee1 von Palmer, Brian D., Smaill, Jeff B., Rewcastle, Gordon W., Dobrusin, Ellen M., Kraker, Alan, Moore, Charles W., Steinkampf, Randall W., Denny, William A.

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Resistance to anthrapyrazoles and anthracyclines in multidrug-resistant P388 murine leukemia cells: reversal by calcium blockers and calmodulin antagonists von KLOHS, W. D, STEINKAMPF, R. W, HAVLICK, M. J, JACKSON, R. C

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Possible link between the intrinsic drug resistance of colon tumors and a detoxification mechanism of intestinal cells von KLOHS, W. D, STEINKAMPF, R. W

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2-Substituted Aminopyrido[2,3-d]pyrimidin-7(8H)-ones. Structure−Activity Relationships Against Selected Tyrosine Kinases and in Vitro and in Vivo Anticancer Activity von Klutchko, Sylvester R, Hamby, James M, Boschelli, Diane H, Wu, Zhipei, Kraker, Alan J, Amar, Aneesa M, Hartl, Brian G, Shen, Cynthia, Klohs, Wayne D, Steinkampf, Randall W, Driscoll, Denise L, Nelson, James M, Elliott, William L, Roberts, Billy J, Stoner, Chad L, Vincent, Patrick W, Dykes, Donald J, Panek, Robert L, Lu, Gina H, Major, Terry C, Dahring, Tawny K, Hallak, Hussein, Bradford, Laura A, Showalter, H. D. Hollis, Doherty, Annette M

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3-(3,5-Dimethoxyphenyl)-1,6-naphthyridine-2,7-diamines and Related 2-Urea Derivatives Are Potent and Selective Inhibitors of the FGF Receptor-1 Tyrosine Kinase von Thompson, Andrew M, Connolly, Cleo J. C, Hamby, James M, Boushelle, Stacey, Hartl, Brian G, Amar, Aneesa M, Kraker, Alan J, Driscoll, Denise L, Steinkampf, Randall W, Patmore, Sandra J, Vincent, Patrick W, Roberts, Bill J, Elliott, William L, Klohs, Wayne, Leopold, Wilbur R, Showalter, H. D. Hollis, Denny, William A

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Structure-activity relationships for 2-anilino-6-phenylpyrido[2,3-d]pyrimidin-7(8H)-ones as inhibitors of the cellular checkpoint kinase Weel von PALMER, Brian D, SMAILL, Jeff B, REWCASTLE, Gordon W, DOBRUSIN, Ellen M, KRAKER, Alan, MOORE, Charles W, STEINKAMPF, Randall W, DENNY, William A

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Role of a small molecular weight phosphoprotein in the mechanism of action of CI‐994 (N‐acetyldinaline) von Rummel, Sue A., Kraker, Alan J., Steinkampf, Randall W., Hook, Kenneth E., Klohs, Wayne D.

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Cross resistance of pleiotropically drug resistant P338 leukemia cells to the lipophilic antifolates trimetrexate and BW 301U von Klohs, Wayne D., Steinkampf, Randall W., Besserer, Judith A., Fry, David W.

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Collagen-Production Inhibitors Evaluated as Antitumor Agents von Klohs, Wayne D., Steinkampf, Randall W., Wicha, Max S., Mertus, Amie E., Tunac, Josefino B., Leopold, Wilbur R.

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Structure-Activity Relationships for 2-Anilino-6-phenylpyrido[2,3-d]pyrimidin-7(8H)-ones as Inhibitors of the Cellular Checkpoint Kinase Wee1 von Palmer, Brian D., Smaill, Jeff B., Rewcastle, Gordon W., Dobrusin, Ellen M., Kraker, Alan, Moore, Charles W., Steinkampf, Randall W., Denny, William A.

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Evaluation of galactosyltransferase isoenzyme II in a human colon carcinoma-derived cell line, HCT-8 von Klohs, Wayne D., Chi, Tsu-Tsair, Steinkampf, Randall W., Tunac, Josefino B.

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Anti-angiogenic activity of selected receptor tyrosine kinase inhibitors, PD166285 and PD173074: Implications for combination treatment with photodynamic therapy von DIMITROFF, C. J, KLOHS, W, HENDERSON, B, DOUGHERTY, T. J, BERNACKI, R. J, SHARMA, A, PERA, P, DRISCOLL, D, VEITH, J, STEINKAMPF, R, SCHROEDER, M, KLUTCHKO, S, SUMLIN, A

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The empiric use of gonadotropin therapy and intrauterine insemination von Schlaff, William, Yazigi, Ricardo, Olive, David L., Williams, Daniel B., Steinkampf, Michael, Odem, Randall R.

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