Comparison of butyrylcholinesterase and acetylcholinesterase.

Por Chatonnet, A, Lockridge, O
Publicado em 1989

Mutation at codon 322 in the human acetylcholinesterase (ACHE) gene accounts for YT blood group polymorphism.

Por Bartels, C F, Zelinski, T, Lockridge, O
Publicado em 1993

Tetramerization domain of human butyrylcholinesterase is at the C-terminus.

Por Blong, R M, Bedows, E, Lockridge, O
Publicado em 1997

Importance of aspartate-70 in organophosphate inhibition, oxime re-activation and aging of human butyrylcholinesterase.

Por Masson, P, Froment, M T, Bartels, C F, Lockridge, O
Publicado em 1997

Aging of di-isopropyl-phosphorylated human butyrylcholinesterase.

Por Masson, P, Fortier, P L, Albaret, C, Froment, M T, Bartels, C F, Lockridge, O
Publicado em 1997

The butyrylcholinesterase gene (BCHE) at 3q26.2 shows two RFLPs

Por McAlpine, P.J., Dixon, M., Allderdice, P.W., Lockridge, O., La Du, B.N.
Publicado em 1991

Reconsideration of the catalytic center and mechanism of mammalian paraoxonase/arylesterase.

Por Sorenson, R C, Primo-Parmo, S L, Kuo, C L, Adkins, S, Lockridge, O, La Du, B N
Publicado em 1995

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

Por Bartels, C F, Jensen, F S, Lockridge, O, van der Spek, A F, Rubinstein, H M, Lubrano, T, La Du, B N
Publicado em 1992

Brain cDNA clone for human cholinesterase.

Por McTiernan, C, Adkins, S, Chatonnet, A, Vaughan, T A, Bartels, C F, Kott, M, Rosenberry, T L, La Du, B N, Lockridge, O
Publicado em 1987

Identification of the structural mutation responsible for the dibucaine-resistant (atypical) variant form of human serum cholinesterase.

Por McGuire, M C, Nogueira, C P, Bartels, C F, Lightstone, H, Hajra, A, Van der Spek, A F, Lockridge, O, La Du, B N
Publicado em 1989

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

Por Nogueira, C P, McGuire, M C, Graeser, C, Bartels, C F, Arpagaus, M, Van der Spek, A F, Lightstone, H, Lockridge, O, La Du, B N
Publicado em 1990

Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesterase.

Por Nogueira, C P, Bartels, C F, McGuire, M C, Adkins, S, Lubrano, T, Rubinstein, H M, Lightstone, H, Van der Spek, A F, Lockridge, O, La Du, B N
Publicado em 1992