Characterization of a soluble mouse liver enzyme capable of hydrolyzing diisopropyl phosphorofluoridate von Billecke, S.S., Primo-Parmo, S.L., Dunlop, C.S., Doorn, J.A., La Du, B.N., Broomfield, C.A.

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Assessment of cassia gum von Hallagan, J.B., La Du, B.N., Pariza, M.W., Putnam, J.M., Borzelleca, J.F.

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The Human Serum Paraoxonase/Arylesterase Gene (PON1) Is One Member of a Multigene Family von Primo-Parmo, Sérgio L., Sorenson, Robert C., Teiber, John, Du, Bert N.La

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Molecular basis for the polymorphic forms of human serum paraoxonase/arylesterase : glutamine or arginine at position 191, for the respective A or B allozymes von ADKINS, S, GAN, K. N, MODY, M, LA DU, B. N

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Structure of the gene for human butyrylcholinesterase. Evidence for a single copy von Arpagaus, Martine, Kott, Matthew, Vatsis, Kostas P, Bartels, Cynthia F, La Du, Bert N, Lockridge, Oksana

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Identification of the Structural Mutation Responsible for the Dibucaine-Resistant (Atypical) Variant Form of Human Serum Cholinesterase von McGuire, Mary C., Nogueira, Christine P., Bartels, Cynthia F., Lightstone, Harold, Hajra, Amitav, Abraham F. L. Van Der Spek, Lockridge, Oksana, La Du, Bert N.

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The genetic mapping and gene structure of mouse paraoxonase/arylesterase von SORENSON, R. C, PRIMO-PARMO, S. L, CAMPER, S. A, LA DU, B. N

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Evidence that several conserved histidine residues are required for hydrolytic activity of human paraoxonase/arylesterase von Doorn, J.A., Sorenson, R.C., Billecke, S.S., Hsu, C., La Du, B.N.

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

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Brain cDNA Clone for Human Cholinesterase von McTiernan, Charles, Adkins, Steve, Chatonnet, Arnaud, Vaughan, Theresa A., Bartels, Cynthia F., Kott, Matthew, Rosenberry, Terrone L., La Du, Bert N., Lockridge, Oksana

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Identification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGt→GGZG) von NOGUEIRA, C. P, MCGUIRE, M. C, GRAESER, C, BARTELS, C. F, ARPAGAUS, M, VAN DER SPEK, A. F. L, LIGHTSTONE, H, LOCKRIDGE, O, LA DU, B. N

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Use of the polymerase chain reaction for homology probing of butyrylcholinesterase from several vertebrates von Arpagaus, M, Chatonnet, A, Masson, P, Newton, M, Vaughan, T A, Bartels, C F, Nogueira, C P, La Du, B N, Lockridge, O

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Proposed nomenclature for human butyrylcholinesterase genetic variants identified by DNA sequencing von LA DU, B. N, BARTELS, C. F, NOGUEIRA, C. P, ARPAGAUS, M, LOCKRIDGE, O

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Phenotypic and molecular biological analysis of human butyrylcholinesterase variants von La Du, B.N., Bartels, C.F., Nogueira, C.P., Hajra, A., Lightstone, H., van der Spek, A., Lockridge, O.

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Evaluation of the safety of sodium pectate as a food ingredient von Borzelleca, J.F., Filer, L.J., Kinoshita, F.K., Gerrish, T.C., Kuo, P.K., La Du, B.N.

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Two polymorphisms in the non-coding regions of the BCHE gene von Bartels, C F, van der Spek, A F, La Du, B N

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Comparison of atypical and usual human serum cholinesterase. Purification, number of active sites, substrate affinity, and turnover number von Lockridge, O, La Du, B N

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Interchain disulfide bonds and subunit organization in human serum cholinesterase von Lockridge, O, Eckerson, H W, La Du, B N

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The butyrylcholinesterase gene (BCHE) at 3q26.2 shows two RFLPs von MCALPINE, P. J, DIXON, M, ALLDERDICE, P. W, LOCKRIDGE, O, LA DU, B. N

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The human serum paraoxonase/arylesterase polymorphism von La Du, B N

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