M R Deibel

Kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-88204E.

J. Chou, A. Gonzales, D. Romero, 1993, Biochemistry.

Kinetic studies with the non-nucleoside human immunodeficiency virus type-1 reverse transcriptase inhibitor U-90152E.

J. Chou, A. Gonzales, D. Romero, 1994, Biochemical pharmacology.

The quinoline U-78036 is a potent inhibitor of HIV-1 reverse transcriptase.

L. Resnick, J. Chou, A. Gonzales, 1993, The Journal of biological chemistry.

Steady-state kinetic studies with the non-nucleoside HIV-1 reverse transcriptase inhibitor U-87201E.

J. Chou, A. Gonzales, D. Romero, 1993, The Journal of biological chemistry.

Actin, troponin C, Alzheimer amyloid precursor protein and pro-interleukin 1 beta as substrates of the protease from human immunodeficiency virus.

A. Tomasselli, R. Heinrikson, B. Greenberg, 1991, The Journal of biological chemistry.

Biochemical properties of purified human terminal deoxynucleotidyltransferase.

M R Deibel, M S Coleman, M. Deibel, 1980, The Journal of biological chemistry.

The benzylthio-pyrimidine U-31,355, a potent inhibitor of HIV-1 reverse transcriptase.

L. Resnick, D. Romero, I W Althaus, 1996, Biochemical pharmacology.

Crystal structure of the catalytic subunit of Cdc25B required for G2/M phase transition of the cell cycle.

K D Watenpaugh, K. Watenpaugh, M R Deibel, 1999, Journal of molecular biology.