A cyclin D1/cyclin-dependent kinase 4 binding site within the C domain of the retinoblastoma protein von WEIJUN PAN, COX, Sarah, HOESS, Ronald H, GRAFSTRÖM, Robert H

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Identification of Peptide Substrates for Human MMP-11 (Stromelysin-3) Using Phage Display von Pan, Weijun, Arnone, Marc, Kendall, Marvin, Grafstrom, Robert H., Seitz, Steven P., Wasserman, Zelda R., Albright, Charles F.

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Synthesis and Evaluation of Indenopyrazoles as Cyclin-Dependent Kinase Inhibitors. 3. Structure Activity Relationships at C3 von Yue, Eddy W, Higley, C. Anne, DiMeo, Susan V, Carini, David J, Nugiel, David A, Benware, Carrie, Benfield, Pamela A, Burton, Catherine R, Cox, Sarah, Grafstrom, Robert H, Sharp, Diane M, Sisk, Lisa M, Boylan, John F, Muckelbauer, Jodi K, Smallwood, Angela M, Chen, Haiying, Chang, Chong-Hwan, Seitz, Steven P, Trainor, George L

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The Amyloid-β Rise and γ-Secretase Inhibitor Potency Depend on the Level of Substrate Expression von Burton, Catherine R., Meredith, Jere E., Barten, Donna M., Goldstein, Margi E., Krause, Carol M., Kieras, Cathy J., Sisk, Lisa, Iben, Lawrence G., Polson, Craig, Thompson, Mark W., Lin, Xu-Alan, Corsa, Jason, Fiedler, Tracey, Pierdomenico, Maria, Cao, Yang, Roach, Arthur H., Cantone, Joseph L., Ford, Michael J., Drexler, Dieter M., Olson, Richard E., Yang, Michael G., Bergstrom, Carl P., McElhone, Kate E., Bronson, Joanne J., Macor, John E., Blat, Yuval, Grafstrom, Robert H., Stern, Andrew M., Seiffert, Dietmar A., Zaczek, Robert, Albright, Charles F., Toyn, Jeremy H.

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Quinazolines as cyclin dependent kinase inhibitors von Sielecki, Thais M., Johnson, Tricia L., Liu, Jie, Muckelbauer, Jodi K., Grafstrom, Robert H., Cox, Sarah, Boylan, John, Burton, Catherine R., Chen, Haiying, Smallwood, Angela, Chang, Chong-Hwan, Boisclair, Michael, Benfield, Pamela A., Trainor, George L., Seitz, Steven P.

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Defining the substrate specificity of cdk4 kinase-cyclin D1 complex von GRAFSTROM, R. H, WEIJUN PAN, HOESS, R. H

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Synthesis and evaluation of indenopyrazoles as cyclin-dependent kinase inhibitors. Part 4: Heterocycles at C3 von Yue, Eddy W., DiMeo, Susan V., Higley, C.Anne, Markwalder, Jay A., Burton, Catherine R., Benfield, Pamela A., Grafstrom, Robert H., Cox, Sarah, Muckelbauer, Jodi K., Smallwood, Angela M., Chen, Haiying, Chang, Chong-Hwan, Trainor, George L., Seitz, Steven P.

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The DNA binding properties of the MutL protein isolated from Escherichia coli von BENDE, S. M, GRAFSTROÊM, R. H

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Cleavage of pyrimidine dimers in specific DNA sequences by a pyrimidine dimer DNA-glycosylase of M. luteus von Haseltine, William A, Gordon, Lynn K, Lindan, Christina P, Grafstrom, Robert H, Shaper, Nancy L, Grossman, Lawrence

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The Amyloid-β Rise and γ-Secretase Inhibitor Potency Depend on the Level of Substrate Expression von Catherine R. Burton, Jere E. Meredith, Donna M. Barten, Margi E. Goldstein, Carol M. Krause, Cathy J. Kieras, Lisa Sisk, Lawrence G. Iben, Craig Polson, Mark W. Thompson, Xu-Alan Lin, Jason Corsa, Tracey Fiedler, Maria Pierdomenico, Yang Cao, Arthur H. Roach, Joseph L. Cantone, Michael J. Ford, Dieter M. Drexler, Richard E. Olson, Michael G. Yang, Carl P. Bergstrom, Kate E. McElhone, Joanne J. Bronson, John E. Macor, Yuval Blat, Robert H. Grafstrom, Andrew M. Stern, Dietmar A. Seiffert, Robert Zaczek, Charles F. Albright, Jeremy H. Toyn

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The characteristics of DNA methytation in an in vitro DNA synthesizing system from mouse fibroblasts von Grafstrom, Robert H., Yuan, Robert, Hamilton, Daniel L.

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Cloning of mutH and identification of the gene product von Grafstrom, Robert H., Hoess, Ronald H.

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The incorporation of uracil into animal cell DNA in vitro von Grafstrom, Robert H., Tseng, B.Y., Goulian, Mehran

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Tandem duplications resulting from recombination between ribosomal RNA genes in Escherichia coli von Hill, C.W., Grafstrom, Robert H., Harnish, Barbara Wallis, Hillman, Barry S.

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Genetically engineered bacteria to identify and produce medically important agents von GRAFSTROM, ROBERT H, BLOCK, TIMOTHY M

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The terminal repetition of herpes simplex virus DNA von Grafstrom, Robert H., Alwine, James C., Steinhart, William L., Hill, C.W., Hyman, Richard W.

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GENETICALLY ENGINEERED BACTERIA TO IDENTIFY AND PRODUCE MEDICALLY IMPORTANT AGENTS von BLOCK, TIMOTHY, M, GRAFSTROM, ROBERT, H

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Terminal fragments of herpes simplex virus DNA produced by restriction endonuclease von Steinhart, William L., Grafstrom, Robert H., Hill, Charles W.

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Discovery of the CCR1 Antagonist, BMS-817399, for the Treatment of Rheumatoid Arthritis von Santella, Joseph B, Gardner, Daniel S, Duncia, John V, Wu, Hong, Dhar, Murali, Cavallaro, Cullen, Tebben, Andrew J, Carter, Percy H, Barrish, Joel C, Yarde, Melissa, Briceno, Stephanie W, Cvijic, Mary Ellen, Grafstrom, R. Robert, Liu, Richard, Patel, Sima R, Watson, Andrew J, Yang, Guchen, Rose, Anne V, Vickery, Rodney D, Caceres-Cortes, Janet, Caporuscio, Christian, Camac, Daniel M, Khan, Javed A, An, Yongmi, Foster, William R, Davies, Paul, Hynes, John

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The discovery of BMS-457, a potent and selective CCR1 antagonist von Gardner, Daniel S., Santella, Joseph B., Duncia, John V., Carter, Percy H., Dhar, T.G.Murali, Wu, Hong, Guo, Weiwei, Cavallaro, Cullen, Van Kirk, Katy, Yarde, Melissa, Briceno, Stephanie W., Robert Grafstrom, R., Liu, Richard, Patel, Sima R., Tebben, Andrew J., Camac, Dan, Khan, Javed, Watson, Andrew, Yang, Guchen, Rose, Anne, Foster, William R., Cvijic, Mary Ellen, Davies, Paul, Hynes, John

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