about
Suxamethonium-the development of a modern drug from 1906 to the present dayIdentification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGT----GGAG)Aspects of suxamethonium hydrolysis in man and animalsApnoea following suxamethonium: the genetic study of four generations of a familyE1k, another quantitative variant at cholinesterase locus 1.Evidence for mutation being the source of the abnormal gene for plasma cholinesterase.On the identification and frequency of the J and K cholinesterase phenotypes in a Caucasian population.Identification of the E1fE1k cholinesterase genotype.De novo amplification within a "silent" human cholinesterase gene in a family subjected to prolonged exposure to organophosphorous insecticides.COMPLETE PSEUDOCHOLINESTERASE DEFICIENCY: GENETIC AND IMMUNOLOGIC CHARACTERIZATION.Increased plasma cholinesterase activity and succinylcholine resistance: a genetic variant.Agar diffusion test for serum cholinesterase typing and influence of temperature on dibucaine and fluoride numbers.A second heterozygote for 'silent' and 'fluoride resistant' genes for serum cholinesterase.Cholinesterase Newfoundland: a new succinylcholine-sensitive variant of cholinesterase at locus 1Structural difference at the active site of dibucaine resistant variant of human plasma cholinesteraseFactors influencing cholinesterase activity in a Brazilian populationA pseudocholinesterase variant (E Cynthiana) associated with elevated plasma enzyme activitySilent cholinesterase gene: variations in the properties of serum enzyme in apparent homozygotes.Pharmacogenetics. Cholinesterase variants and suxamethonium apnoea.Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) geneSerum cholinesterase levels in families and twins.GENETIC HETEROGENEITY IN HUMAN ACATALASIA.An original approach to the diagnosis of scoline-induced apnoea.Hydrolysis of suxamethonium by different types of plasma.BLOOD GROUP FREQUENCIES IN MONGOLS.COMPARISONS OF TWO METHODS FOR TYPING OF SERUM CHOLINESTERASE AND PREVALENCE OF ITS VARIANTS IN A BRAZILIAN POPULATIONPurification and properties of human serum cholinesterase.Value of butyrylthiocholine assay for identification of cholinesterase variants.THE "SILENT" GENE FOR SERUM CHOLINESTERASE.ENZYMES AND DRUG SENSITIVITY. THE GENETICS OF SERUM CHOLINESTERASE 'DEFICIENCY' IN RELATION TO SUXAMETHONIUM APNOEA.A novel mutation in the BCHE gene and phenotype identified in a child with low butyrylcholinesterase activity: a case report.A second family demonstrating the homozygote for fluoride-resistant pseudocholinesterase variant.
P2860
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P2860
description
article publié dans la revue scientifique Nature
@fr
scientific article published in Nature
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в Nature в лютому 1962
@uk
name
A 'silent' pseudo-cholinesterase gene
@en
A 'silent' pseudo-cholinesterase gene
@nl
type
label
A 'silent' pseudo-cholinesterase gene
@en
A 'silent' pseudo-cholinesterase gene
@nl
prefLabel
A 'silent' pseudo-cholinesterase gene
@en
A 'silent' pseudo-cholinesterase gene
@nl
P2093
P1433
P1476
A 'silent' pseudo-cholinesterase gene
@en
P2093
P407
P577
1962-02-10T00:00:00Z