Three point mutations of human butyrylcholinesterase in a Japanese family and the alterations of three-dimensional structure
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference15 articles.
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3. Characterization of 12 silent alleles of the human butyrylcholinesterase (BChE) gene;Primo-Parmo;Am J Hum Genet,1996
4. Conversion of acetylcholinesterase to butyrylcholinesterase: Modeling and mutagenesis;Harel;Proc Natl Acad Sci USA,1992
5. Recombinant human butyrylcholinesterase G390V, Fluorid-2 variant, expressed in Chinese hamster ovary cell, is a low affinity variant;Masson;J Biol Chem,1993
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3. Understanding the non-catalytic behavior of human butyrylcholinesterase silent variants: Comparison of wild-type enzyme, catalytically active Ala328Cys mutant, and silent Ala328Asp variant;Chemico-Biological Interactions;2016-11
4. Review of human butyrylcholinesterase structure, function, genetic variants, history of use in the clinic, and potential therapeutic uses;Pharmacology & Therapeutics;2015-04
5. Esterases;Comprehensive Toxicology;2010
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