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Murray, L.A., Chen, Q., Kramer, M.S., Hesson, D.P., Argentieri, R.L., Peng, X., Gulati, M., Homer, R.J., Russell, T., Rooijen, N., Elias, J.A., Hogaboam, C.M., Herzog, E.L., 2010, "TGF-beta driven lung fibrosis is macrophage dependent and blocked by Serum Amyloid P", Int J Biochem Cell Biol. Epub2010 Oct 28.

Moreira, A.P., Cavassani, K.A., Jullinger, R., Rosada,  R.S., Fong, D.J., Murray, L., Hesson, D.P., Hogaboam, C.M., 2010, "Serum amyloid P attenuates M2 macrophage activation and protects against fungal spore-induced allergic airway disease", J Allergy Clin Immunol. Oct;126(4)712-721.e7. Epub2010 Jul 31.

Murray, L.A., Rosada, R., Moreira, A.P., Joshi, A., Kramer, M.S., Hesson, D.P., Argentieri, R.L., Mathai, S., Gulati, M., Herzog, E.L., Hogaboam, C.M., 2010, "Serum amyloid P therapeutically attenuates murine bleomycin-induced pulmonary fibrosis via its effects on macrophages", PLoS One, Mar12;5(3):e9683.

Murray, L.A., Kramer, M.S., Hesson, D.P., Watkins, B.A., Fey, G., Argentieri, R., Shaheen, F., Knight, D.A., Sonis, S.T., 2010, "Serum amyloid P ameliorates radiation-induced oral mucositis and fibrosis", Fibo. Tis. Repair, Jul5;3:11.

Bell, R.D., Powers, B.L., Brock, D., Provemncio, J.J., Flanders, A., Benetiz, R., Rosenwasser, R., Strause, J., Frazer, G., Kramer, M.S., Hesson, D.P., Barnitz, J., and Osterhom, J.L., 2006, "Ventriculo-Lumbar Perfusion in Acute Ischemic Stroke: A Pilot Feasibility and Safety Study", J. Neurocritical Care, 5:21-29.

Hesson, D.P. and Sturgess, M.A., 1997, "Homology Modeling of the AMPA Receptor: A Quantitative Predictive Tool for the Design of Novel Antagonists", Bioorg. & Med. Chem Lett., 7:11, 1437-1442.

Pelletier, J.C., Hesson D.P., Jones, K.A. and Costa, A.M., 1996, "Substituted 1,2-Dihydrophthalazines: Potent, Selective, and Noncompetitive Inhibitors of the AMPA Receptor", J.Med. Chem., Vol. 39: 2, 343-346.

Hesson, D.P., Gu, Z-Q., Pelletier, J., Maccecchini, M-L., Skolnick, P., 1995, "Synthesis, Resolution and Biological Evaluation of the Four Stereoisomers of 4-Methylglutamic Acid: Selective Probes of Kainate Receptors", J. Med. Chem., 38:2518-2520.

Hesson, D.P., Gu, Z-Q., 1995, "A Highly Diastereoselective Synthesis of 4-Alkyl Threo Glutamic Acids", Tetra Asymmetry, Vol 6:9, 2101-2104.

Hesson, D.P., Gu, Z-Q., and Lin, X-F., 1995, "Diastereoselective Synthesis of (2S,4R)-4-Methylglutamic Acid (SYM 2081), A High Affinity Ligeand at the Kainate Subtype of Glutamate Receptor", Bioorg. Med. Chem. Lett, Vol. 5:17, 1973-1976.

Jeffrey C. Pelletier and David P. Hesson, 1995, "A Mild Preparation of Amino Acid N-Acylsufonamides", SynLett, 11, 1141-1142.

Lin. C.M., Kang, J., Roach, M.C., Jiang, J.B., Hesson, D.P., Luduena, R.F., and Hamel, E., 1991, "Investigations of the Mechanism of the Interaction of Tubulin with Derivatives of 2-Styrylquinazolin-4-(3H)-one", Molecular Pharmacology, 40:827-832.

Jiang, J.B., Hesson, D.P., Dusak, B.A., Dexter, D.L., Kang, G.J., and Hamel, E., 1990, "Synthesis and Biological Evaluation of 2-Styrylquinazolin-4(3H)-ones, a New Class of Antimitotic Anticancer Agents Which Inhibit Tubulin Polymerization", J. Med. Chem., 33:1721-1728.

Hesson, D.P., Chen, S-F., Papp, L.M., Ardecky, R.J., Rao, G.V., Forbes, M. and Dexter, D.L., 1990, "Structure-Activity Relationship of Quinolinecarboxylic Acids; A New class of Inhibitors of Dihydroorotate Dehydrogenase", Biochemical Pharmacology, 33(4): 709-7115.

Hesson, D.P., et al, 1985, "Activity of a Novel-4-Quinolinecarboxylic Acid, NSC 368390, 6-Fluoro-2-(2'-fluoro-1,1'-biphenyl-4-yl)-3-methyl-4-Quinolinecarboxylic Acid Sodium Slat, Against Experimental Tumors", Cancer Res., 45:5563-5568.

Bladwin, J.E., Hesson, D.P., Jung, M., 1980, "A Chemical Conversion of Penicillin Sulfoxieds into 6,7-Epi-1-Oxocephams", Tetrahedron, 36: 1627.

Baldwin, J.E., Hesson, D.P., 1976, "Reaction of b-Hydroxy-sulphenyl Chlorides with Phosphenes: A Route to Episulphides, Chem. Commun., 17:667

Baldwin, J.E., Hesson, D.P., Christy, M., Haber, S., Au, A., 1975, "Stereospecific Conversion of Peptides into b-Lactams", J. Am. Chem. Soc., 97-5957.




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