The agglutination of erythrocytes by influenza virus is strongly inhibited by liposomes incorporating an analog of sialyl gangliosides by Kingery-Wood, Jill E, Williams, Kevin W, Sigal, George B, Whitesides, George M

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Discovery of heterocyclic ureas as a new class of raf kinase inhibitors: identification of a second generation lead by a combinatorial chemistry approach by Smith, Roger A, Barbosa, James, Blum, Cheri L, Bobko, Mark A, Caringal, Yolanda V, Dally, Robert, Johnson, Jeffrey S, Katz, Michael E, Kennure, Nancy, Kingery-Wood, Jill, Lee, Wendy, Lowinger, Timothy B, Lyons, John, Marsh, Vivienne, Rogers, Daniel H, Swartz, Stephen, Walling, Tracy, Wild, Hanno

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Polyacrylamides Bearing Pendant .alpha.-Sialoside Groups Strongly Inhibit Agglutination of Erythrocytes by Influenza A Virus: Multivalency and Steric Stabilization of Particulate B... by Lees, Watson J, Spaltenstein, Andrew, Kingery-Wood, Jill E, Whitesides, George M

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Secondary Interactions Significantly Removed from the Sulfonamide Binding Pocket of Carbonic Anhydrase II Influence Inhibitor Binding Constants by Boriack, P. Ann, Christianson, David W, Kingery-Wood, Jill, Whitesides, George M

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Omega-carboxypyridyl substituted ureas as Raf kinase inhibitors: SAR of the amide substituent by Khire, Uday R., Bankston, Donald, Barbosa, James, Brittelli, David R., Caringal, Yolanda, Carlson, Robert, Dumas, Jacques, Gane, Todd, Heald, Sarah L., Hibner, Barbara, Johnson, Jeffrey S., Katz, Michael E., Kennure, Nancy, Kingery-Wood, Jill, Lee, Wendy, Liu, Xiao-Gao, Lowinger, Timothy B., McAlexander, Ian, Monahan, Mary-Katherine, Natero, Reina, Renick, Joel, Riedl, Bernd, Rong, Hong, Sibley, Robert N., Smith, Roger A., Wolanin, Donald

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Indole diterpene synthetic studies. 8. The total synthesis of (+)-paspalicine and (+)-paspalinine by Smith, Amos B, Kingery-Wood, Jill, Leenay, Tamara L, Nolen, Ernest G, Sunazuka, Toshiaki

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Discovery of a new class of p38 kinase inhibitors by Dumas, Jacques, Sibley, Robert, Riedl, Bernd, Monahan, Mary Katherine, Lee, Wendy, Lowinger, Timothy B, Redman, Anikó M, Johnson, Jeffrey S, Kingery-Wood, Jill, Scott, William J, Smith, Roger A, Bobko, Mark, Schoenleber, Robert, Ranges, Gerald E, Housley, Timothy J, Bhargava, Ajay, Wilhelm, Scott M, Shrikhande, Alka

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p38 Kinase inhibitors for the treatment of arthritis and osteoporosis: thienyl, furyl, and pyrrolyl ureas by Redman, Anikó M, Johnson, Jeffrey S, Dally, Robert, Swartz, Steve, Wild, Hanno, Paulsen, Holger, Caringal, Yolanda, Gunn, David, Renick, Joel, Osterhout, Martin, Kingery-Wood, Jill, Smith, Roger A, Lee, Wendy, Dumas, Jacques, Wilhelm, Scott M, Housley, Timothy J, Bhargava, Ajay, Ranges, Gerald E, Shrikhande, Alka, Young, Deborah, Bombara, Michael, Scott, William J

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Total syntheses of (+)-paspalicine and (+)-paspalinine by Smith, Amos B, Sunazuka, Toshiaki, Leenay, Tamara L, Kingery-Wood, Jill

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Omega-carboxypyridyl substituted ureas as Raf kinase inhibitors by Khire, Uday R., Bankston, Donald, Barbosa, James, Brittelli, David R., Caringal, Yolanda, Carlson, Robert, Dumas, Jacques, Gane, Todd, Heald, Sarah L., Hibner, Barbara, Johnson, Jeffrey S., Katz, Michael E., Kennure, Nancy, Kingery-Wood, Jill, Lee, Wendy, Liu, Xiao-Gao, Lowinger, Timothy B., McAlexander, Ian, Monahan, Mary-Katherine, Natero, Reina, Renick, Joel, Riedl, Bernd, Rong, Hong, Sibley, Robert N., Smith, Roger A., Wolanin, Donald

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Resolution of anti-3-Oxotricyclo[2.2.1.0]heptane-7-carboxylic acid by Candidia antartica Lipase A by Kingery-Wood, Jill, Johnson, Jeffrey S.

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