Showing results (1-10 of 28) with videos related to
Sort By:
Pageof 3
American Journal of Human Genetics|May 1, 1993
Mutation at codon 322 in the human acetylcholinesterase (ACHE) gene accounts for YT blood group polymorphismC F Bartels, T Zelinski, O LockridgeJournal of Neurochemistry|January 26, 2000
The butyrylcholinesterase K-variant shows similar cellular protein turnover and quaternary interaction to the wild-type enzymeC V Altamirano, C F Bartels, O LockridgeAmerican Journal of Human Genetics|May 1, 1992
DNA mutations associated with the human butyrylcholinesterase J-variantC F Bartels, K James, B N La DuPharmacogenetics|October 1, 1992
Structural basis of the butyrylcholinesterase H-variant segregating in two Danish familiesF S Jensen, C F Bartels, B N La DuEuropean Journal of Biochemistry|January 15, 1996
Asp7O in the peripheral anionic site of human butyrylcholinesteraseP Masson, M T Froment, C F Bartels, et al.The Biochemical Journal|July 1, 1997
Importance of aspartate-70 in organophosphate inhibition, oxime re-activation and aging of human butyrylcholinesteraseP Masson, M T Froment, C F Bartels, et al.Toxicon : Official Journal of the International Society on Toxinology|November 1, 1994
Tissue distribution of human acetylcholinesterase and butyrylcholinesterase messenger RNAO Jbilo, C F Bartels, A Chatonnet, et al.Blood|May 15, 1994
Mutation His322Asn in human acetylcholinesterase does not alter electrophoretic and catalytic properties of the erythrocyte enzymeP Masson, M T Froment, R C Sorenson, et al.In Vitro Cellular & Developmental Biology. Animal|October 1, 1994
Endogenous butyrylcholinesterase in SV40 transformed cell lines: COS-1, COS-7, MRC-5 SV40, and WI-38 VA13M Kris, O Jbilo, C F Bartels, et al.Cellular and Molecular Neurobiology|February 1, 1991
Proposed nomenclature for human butyrylcholinesterase genetic variants identified by DNA sequencingB N La Du, C F Bartels, C P Nogueira, et al.Pageof 3