Frequency of butyrylcholinesterase gene mutations in individuals with abnormal inhibition numbers: an Italian-population study.
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M. Panteghini | A. Mosca | S. Penco | R. Bonora | A. Marocchi | F. Azzario | M. Patrosso | G. Lando
[1] H. Soreq,et al. Human cholinesterase genes localized by hybridization to chromosomes 3 and 16 , 1987, Human Genetics.
[2] A. Sastre,et al. Naturally occurring mutation, Asp70His, in human butyrylcholinesterase , 2002, Annals of clinical biochemistry.
[3] J. Cashman,et al. An improved cocaine hydrolase: the A328Y mutant of human butyrylcholinesterase is 4-fold more efficient. , 1999, Molecular pharmacology.
[4] A. Mosca,et al. Limits to the Use of the Glucose 6-Phosphate Dehydrogenase/6-Phosphogluconate Dehydrogenase Index for the Detection of Glucose 6-Phosphate Dehydrogenase Deficiency , 1998, Clinical chemistry and laboratory medicine.
[5] M. Maeda,et al. Identification of a point mutation associated with a silent phenotype of human serum butyrylcholinesterase--a case of familial cholinesterasemia. , 1998, Clinica chimica acta; international journal of clinical chemistry.
[6] M. Maekawa,et al. Genetic mutations of butyrylcholine esterase identified from phenotypic abnormalities in Japan. , 1997, Clinical chemistry.
[7] C. Bartels,et al. Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene. , 1996, American journal of human genetics.
[8] M. Maekawa,et al. Genetic basis of the silent phenotype of serum butyrylcholinesterase in three compound heterozygotes. , 1995, Clinica chimica acta; international journal of clinical chemistry.
[9] L. Skovgaard,et al. Identification of human plasma cholinesterase variants in 6,688 individuals using biochemical analysis , 1995, Acta anaesthesiologica Scandinavica.
[10] C. P. Nogueira,et al. Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesterase. , 1992, American journal of human genetics.
[11] C. Bartels,et al. Structural basis of the butyrylcholinesterase H-variant segregating in two Danish families. , 1992, Pharmacogenetics.
[12] O. Lockridge,et al. DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sites. , 1992, American journal of human genetics.
[13] C. Bartels,et al. DNA mutations associated with the human butyrylcholinesterase J-variant. , 1992, American journal of human genetics.
[14] I. Craig,et al. Refinement of the localization of human butyrylcholinesterase to chromosome 3q26.1-q26.2 using a PCR-derived probe. , 1991, Genomics.
[15] O. Lockridge,et al. The cloned butyrylcholinesterase (BCHE) gene maps to a single chromosome site, 3q26. , 1991, Genomics.
[16] M. Panteghini. Methods for serum cholinesterase assay and classification of genetic variants. , 1989, Clinica chimica acta; international journal of clinical chemistry.
[17] C. P. Nogueira,et al. Identification of the structural mutation responsible for the dibucaine-resistant (atypical) variant form of human serum cholinesterase. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[18] M. Whittaker,et al. Comparison of a commercially available assay system with two reference methods for the determination of plasma cholinesterase variants. , 1983, Clinical chemistry.
[19] H. Harris,et al. Differential Inhibition of Human Serum Cholinesterase with Fluoride: Recognition of Two New Phenotypes , 1961, Nature.