X-ray Structure of Citrate Bound to Src SH2 Leads to a High-Affinity, Bone-Targeted Src SH2 Inhibitor von Bohacek, Regine S, Dalgarno, David C, Hatada, Marcos, Jacobsen, Virginia A, Lynch, Berkley A, Macek, Karina J, Merry, Taylor, Metcalf, Chester A, Narula, Surinder S, Sawyer, Tomi K, Shakespeare, William C, Violette, Shelia M, Weigele, Manfred

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Bone-targeted Src SH2 inhibitors block Src cellular activity and osteoclast-mediated resorption von Violette, S.M, Guan, W, Bartlett, C, Smith, J.A, Bardelay, C, Antoine, E, Rickles, R.J, Mandine, E, van Schravendijk, M.R, Adams, S.E, Lynch, B.A, Shakespeare, W.C, Yang, M, Jacobsen, V.A, Takeuchi, C.S, Macek, K.J, Bohacek, R.S, Dalgarno, D.C, Weigele, M, Lesuisse, D, Sawyer, T.K, Baron, R

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Structure-Based Design of an Osteoclast-Selective, Nonpeptide Src Homology 2 Inhibitor with in vivo Antiresorptive Activity von Shakespeare, William, Yang, Michael, Bohacek, Regine, Cerasoli, Franklin, Stebbins, Karin, Sundaramoorthi, Raji, Azimioara, Mihai, Vu, Chi, Pradeepan, Selvi, Metcalf, Chester, Haraldson, Chad, Merry, Taylor, Dalgarno, David, Narula, Surinder, Hatada, Marcos, Lu, Xiaode, van Schravendijk, Marie Rose, Adams, Susan, Violette, Shelia, Smith, Jeremy, Guan, Wei, Bartlett, Catherine, Herson, Jay, Iuliucci, John, Weigele, Manfred, Sawyer, Tomi

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Structural Basis of Src Tyrosine Kinase Inhibition with a New Class of Potent and Selective Trisubstituted Purine-based Compounds von Dalgarno, David, Stehle, Thilo, Narula, Surinder, Schelling, Pierre, Rose van Schravendijk, Marie, Adams, Susan, Andrade, Lawrence, Keats, Jeff, Ram, Mary, Jin, Lei, Grossman, Trudy, MacNeil, Ian, Metcalf III, Chester, Shakespeare, William, Wang, Yihan, Keenan, Terry, Sundaramoorthi, Raji, Bohacek, Regine, Weigele, Manfred, Sawyer, Tomi

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Bone-Targeted 2,6,9-Trisubstituted purines: novel inhibitors of Src tyrosine kinase for the treatment of bone diseases von Wang, Yihan, Metcalf, Chester A., Shakespeare, William C., Sundaramoorthi, Raji, Keenan, Terence P., Bohacek, Regine S., van Schravendijk, Marie Rose, Violette, Shiela M., Narula, Surinder S., Dalgarno, David C., Haraldson, Chad, Keats, Jeffrey, Liou, Shuenn, Mani, Ukti, Pradeepan, Selvi, Ram, Mary, Adams, Susan, Weigele, Manfred, Sawyer, Tomi K.

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LHPP, the light-harvesting NADPH:protochlorophyllide (Pchlide) oxidoreductase:Pchlide complex of etiolated plants, is developmentally expressed across the barley leaf gradient von Reinbothe, Christiane, Pollmann, Stephan, Desvignes, Claire, Weigele, Martina, Beck, Erwin, Reinbothe, Steffen

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Novel reagent for the fluorometric assay of primary amines von Weigele, M, DeBernardo, S. L, Tengi, J. P, Leimgruber, W

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Fluorometric assay of secondary amino acids von Weigele, Manfred, DeBernardo, Silvano, Leimgruber, Willy

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Bone-Targeted Src kinase inhibitors: novel pyrrolo- and pyrazolopyrimidine analogues von Sundaramoorthi, Raji, Shakespeare, William C., Keenan, Terence P., Metcalf, Chester A., Wang, Yihan, Mani, Ukti, Taylor, Merry, Liu, Shuangying, Bohacek, Regine S., Narula, Surinder S., Dalgarno, David C., Van Schravandijk, Marie Rose, Violette, Sheila M., Liou, Shuenn, Adams, Susan, Ram, Mary K., Keats, Jeffrey A., Weigele, Manfred, Sawyer, Tomi K.

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Novel Protein Kinase Inhibitors: SMART Drug Design Technology von Sawyer, Tomi K, Bohacek, Regine S, III, Chester A. Metcalf, Shakespeare, William C, Wang, Yihan, Sundaramoorthi, Raji, Keenan, Terence, Narula, Surinder, Weigele, Manfred, Dalgarno, David C

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Bone-Targeted pyrido[2,3- d]pyrimidin-7-ones: potent inhibitors of Src tyrosine kinase as novel antiresorptive agents von Vu, Chi B., Luke, George P., Kawahata, Noriyuki, Shakespeare, William C., Wang, Yihan, Sundaramoorthi, Raji, Metcalf, Chester A., Keenan, Terence P., Pradeepan, Selvi, Corpuz, Evelyn, Merry, Taylor, Bohacek, Regine S., Dalgarno, David C., Narula, Surinder S., van Schravendijk, Marie Rose, Ram, Mary K., Adams, Susan, Liou, Shuenn, Keats, Jeffrey A., Violette, Shelia M., Guan, Wei, Weigele, Manfred, Sawyer, Tomi K.

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7.0 Tesla MRI von Weigele, John B., MD, PhD

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Virtual reality cylinder head von Weigele, M

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Selective inhibition of Src SH2 by a novel thiol-targeting tricarbonyl-modified inhibitor and mechanistic analysis by (1)H/(13)C NMR spectroscopy von Sundaramoorthi, R, Siedem, C, Vu, C B, Dalgarno, D C, Laird, E C, Botfield, M C, Combs, A B, Adams, S E, Yuan, R W, Weigele, M, Narula, S S

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Synthesis and Anti-HIV Activity of a Novel Series of Isomeric Dideoxynucleosides von HURYN, D. M., SLUBOSKI, B. C., TAM, S. Y., TODARO, L. J., WEIGELE, M., SIM, I. S., FRANK, K. B., RICHMAN, D. D., MITSUYA, H., BRODER, S.

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The absolute configuration of rhizobitoxine von Keith, D.D., De Bernardo, S., Weigele, M.

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Fluorogenic ninhydrin reaction. Structure of the fluorescent principle von Weigele, M, Blount, J. F, Tengi, J. P, Czajkowski, R. C, Leimgruber, W

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The structure of myxin von Weigele, M., Leimgruber, N.

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Synthesis and anti-HIV activity of isonucleosides von Huryn, Donna M, Sluboski, Barbara C, Tam, Steve Y, Weigele, Manfred, Sim, Iain, Anderson, Barry D, Mitsuya, Hiroaki, Broder, Samuel

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A simple method for determining the absolute configuration of α-amino acids von Toome, V., De Bernardo, S., Weigele, M.

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