Cynthia F. Bartels

Complete amino acid sequence of human serum cholinesterase.

O. Lockridge, C. Wong, C. Bartels, 1987, The Journal of biological chemistry.

DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sites.

O. Lockridge, C. Bartels, B. La Du, 1992, American journal of human genetics.

An improved cocaine hydrolase: the A328Y mutant of human butyrylcholinesterase is 4-fold more efficient.

J. Cashman, O. Lockridge, C. Bartels, 1999, Molecular pharmacology.

Identification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGT----GGAG).

C. P. Nogueira, O. Lockridge, M. Arpagaus, 1990, American journal of human genetics.

Asp7O in the peripheral anionic site of human butyrylcholinesterase.

M. Froment, P. Masson, O. Lockridge, 1996, European journal of biochemistry.