Identification of the structural mutation responsible for the dibucaine-resistant (atypical) variant form of human serum cholinesterase
about
Mutation at codon 322 in the human acetylcholinesterase (ACHE) gene accounts for YT blood group polymorphismIdentification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGT----GGAG)New Insights into Butyrylcholinesterase Activity Assay: Serum Dilution Factor as a Crucial ParameterSubstrate inhibition of acetylcholinesterase: residues affecting signal transduction from the surface to the catalytic centerSupporting precision medicine by data mining across multi-disciplines: an integrative approach for generating comprehensive linkages between single nucleotide variants (SNVs) and drug-binding sites.Inactivation of the cholinesterase gene by Alu insertion: possible mechanism for human gene transposition.Inter and intraindividual variations in plasma cholinesterase activity and substance concentration in employees of an organophosphorus insecticide factory.Cholinesterase variants: rapid characterisation by PCR/SSCP and evidence for molecular homogeneity.Natural inhibitors of cholinesterases: implications for adverse drug reactions.Acetylcholinesterase and butyrylcholinesterase genes coamplify in primary ovarian carcinomas.Reversal of succinylcholine induced apnea with an organophosphate scavenging recombinant butyrylcholinesterase.Pharmacogenomics: the future of drug therapy.Butyrylcholinesterase genotype and enzyme activity in relation to Gulf War illness: preliminary evidence of gene-exposure interaction from a case-control study of 1991 Gulf War veterans.Neurobiology of butyrylcholinesterase.Butyrylcholinesterase genetic variants: association with cocaine dependence and related phenotypes.Molecular basis for the polymorphic forms of human serum paraoxonase/arylesterase: glutamine or arginine at position 191, for the respective A or B allozymes.DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sitesDNA mutations associated with the human butyrylcholinesterase J-variant.Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesterase.Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) geneNaturally Occurring Genetic Variants of Human Acetylcholinesterase and Butyrylcholinesterase and Their Potential Impact on the Risk of Toxicity from Cholinesterase Inhibitors.Anionic subsites of the catalytic center of acetylcholinesterase from Torpedo and from cobra venom.Diverse point mutations in the human gene for polymorphic N-acetyltransferase.Overview of pharmacogenetics.Comparison of butyrylcholinesterase and acetylcholinesterase.Butyrylcholinesterase: impact on symptoms and progression of cognitive impairment.Identification of human plasma cholinesterase variants using molecular biological techniques.Prolonged neuromuscular blockade following succinylcholine administration to a patient with a reduced butyrylcholinesterase activity.Investigation of Association between Susceptibility to Leprosy and SNPs inside and near the BCHE Gene of Butyrylcholinesterase.Rapid identification of atypical variant of plasma butyrylcholinesterase by PCR.Interaction of human butyrylcholinesterase variants with bambuterol and terbutaline.Activity of Paraoxonase/Arylesterase and Butyrylcholinesterase in Peripheral Blood of Gulf War Era Veterans With Neurologic Symptom Complexes or Post-Traumatic Stress Disorder.Human Cholinesterases and Anticholinesterases.Synthetic cannabimimetic agents metabolized by carboxylesterases.Genotyping single-nucleotide polymorphisms of human genes involved in organophosphate detoxification by high-resolution melting.Serum cholinesterase polymorphism in France: an epidemiological survey of the deficient alleles detected by an automated micro-method.A novel mutation in the BCHE gene and phenotype identified in a child with low butyrylcholinesterase activity: a case report.Review of the Toxicology of Chlorpyrifos With an Emphasis on Human Exposure and Neurodevelopment
P2860
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P2860
Identification of the structural mutation responsible for the dibucaine-resistant (atypical) variant form of human serum cholinesterase
description
1989 nî lūn-bûn
@nan
1989 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Identification of the structur ...... of human serum cholinesterase
@ast
Identification of the structur ...... of human serum cholinesterase
@en
Identification of the structur ...... of human serum cholinesterase
@nl
type
label
Identification of the structur ...... of human serum cholinesterase
@ast
Identification of the structur ...... of human serum cholinesterase
@en
Identification of the structur ...... of human serum cholinesterase
@nl
prefLabel
Identification of the structur ...... of human serum cholinesterase
@ast
Identification of the structur ...... of human serum cholinesterase
@en
Identification of the structur ...... of human serum cholinesterase
@nl
P2093
P2860
P3181
P356
P1476
Identification of the structur ...... of human serum cholinesterase
@en
P2093
A F Van der Spek
C F Bartels
C P Nogueira
H Lightstone
M C McGuire
O Lockridge
P2860
P3181
P356
10.1073/PNAS.86.3.953
P407
P577
1989-02-01T00:00:00Z