PAPERS, PRESENTATIONS AND PUBLICATIONS FROM 1968-1978

Peer-Reviewed Publications

    1. Dunathan, H. C., Davis, L, Gilmer Kury, P., & Kaplan, M. (1968). "Stereochemistry of enzymatic transamination," Biochemistry 7, 4532-4537.
    2. Bruice, T. C., Gilmer Kury, P., & McMahon, D. M. (1970). "Chromophoric lactones and mechanism of chymotrypsin," J. Am. Chem. Soc. 92, 6674-6676.
    3. Ramwell, P. W., & Kury (Gilmer), P. (1973). Prostaglandines, 43-54, Inserm, Paris.
    4. Gilmer Kury, P., Ramwell, P. W., & McConnell, H. M. (1974). "The effect of prostaglandins E1 and E2 on the human erythrocyte as monitored by spin labels," Biochemical & Biophysical Research Communication, 56, 478-483.
    5. Kury (Gilmer), P., & McConnell H. M. (1975). "Regulation of membrane flexibility in human erythrocytes," Biochemistry 13, 2798-2803.
    6. Gilmer, P. J., McIntire, W. S., & Kirsch, J. F. (1977). "Pyridoxamine-pyruvate transaminase: I. Determination of the active site stoichiometry and the pH dependence of the dissociation constant for 5-deoxypyridoxal," Biochemistry 16, 5241-5246.
    7. Gilmer, P. J., & Kirsch, J. F. (1977). "Pyridoxamine-pyruvate transaminase: II. A temperature-jump and stopped-flow kinetic investigation of the rates and mechanism of the reaction of 5-deoxypyridoxal with the enzyme," Biochemistry 16, 5246-5253.
    8. Gilmer, P. J., McDevitt, H. O., & McConnell, H. M. (1978). "Inhibition of specific effector T cell-target cell conjugates by target cell plasma membranes," J. Immunology 120, 774-776.

Invited Oral Presentations

International:

  • 1974: Invited talk on “Rapid reactions studies of pyridoxamine-pyruvate transaminase,” at the Vitamin B6 Meeting in Leningrad, with H. Winkler, & J. F. Kirsch

State:

  • 1978: Invited speaker at the University of Florida, on biochemistry

Oral or Poster Presentations with Abstracts

National:

  • 1973: Oral presentation on “Stopped-flow and temperature-jump kinetic investigation of the mechanism of binding 5-deoxypyridoxal to pyridoxamine pyruvate transaminase,” at the American Society of Biological Chemists meeting (FASEB), Penny J. Gilmer with J. F. Kirsch

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