Zobrazeno 1 - 10
of 15
pro vyhledávání: '"L. C. Eze"'
Publikováno v:
Biochemical Genetics. 28:1-7
The sulfones are the drug of choice in the treatment of leprosy, with dapsone as the clear favorite. The major route for dapsone metabolism leading to its inactivation and excretion is via acetylation by hepatic N-acetyl transferase (NAT), as is the
Autor:
C. O. Echetebu, L. C. Eze
Publikováno v:
Microbiology. 120:523-527
Summary: Aspartate aminotransferase (EC 2.6.1.1) and alanine aminotransferase (EC 2.6.1.2) were extracted from mycelia of Tricchoderma viride, partially purified and characterized. The pH optima for the enzyme activities were 9.0 and 8.6, respectivel
Autor:
L. Iselius, D. A. P. Evans, L. C. Eze, M. C. K. Tweedie, M. F. Bullen, P. J. J. Wren, D. C. Rao
Publikováno v:
Genetic Epidemiology. 6:619-624
A complex segregation analysis of acid phosphatase activity in 50 British families showed that the essential features of the acid phosphatase polymorphism, i.e., a major gene with three alleles, is retrieved by using the biallelic mixed model. The es
Autor:
L. C. Eze
Publikováno v:
Biochemical Genetics. 25:225-229
Publikováno v:
Journal of Medical Genetics. 7:5-10
Publikováno v:
Journal of Medical Genetics. 9:57-59
Publikováno v:
Biochemical genetics. 16(11-12)
Sulfamethazine (syn. sulfadimidine) is inactivated by conversion to its N-acetyl derivative. Individuals are phenotyped as either “rapid” or “slow” acetylators. We have tested the validity of this theory in a Nigerian population. The frequenc
Autor:
L. C. Eze
Publikováno v:
Biochemical genetics. 27(9-10)
Trehalase is an enzyme which hydrolyzes the disaccharide trehalose, yielding glucose. It is widespread in nature and found in various human tissues as well as in human plasma. The synthesis and degradation of its substrate trehalose have been conside
Publikováno v:
Journal of medical genetics. 13(5)
A method for determining plasma paroxonase activity using an auto-analyser is described. Frequency distributions for British and Indian subjects show bimodality. A study of 40 British families confirms the presence of a genetic polymorphism with rega
Publikováno v:
Indian journal of experimental biology. 17(9)