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Biochemical Pharmacology
|
October 26, 1995
Genetic analysis of microsomal epoxide hydrolase in patients with carbamazepine hypersensitivity
V J Green, M Pirmohamed, N R Kitteringham, et al.
Archives of Biochemistry and Biophysics
|
August 15, 1990
Characterization and primary sequence of a human hepatic microsomal estriol UDPglucuronosyltransferase
B L Coffman, T R Tephly, Y M Irshaid, et al.
Biochemical Pharmacology
|
March 15, 1983
UDP-glucuronosyltransferase activities. Guidelines for consistent interim terminology and assay conditions
K W Bock, B Burchell, G J Dutton, et al.
The Journal of Pediatrics
|
April 6, 1999
Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn
G Monaghan, A McLellan, A McGeehan, et al.
Archives of Disease in Childhood
|
June 23, 2001
Bile bilirubin pigment analysis in disorders of bilirubin metabolism in early infancy
W S Lee, P J McKiernan, S V Beath, et al.
Drug Metabolism Reviews
|
May 21, 1999
Merits and limitations of recombinant models for the study of human P450-mediated drug metabolism and toxicity: an intralaboratory comparison
T Friedberg, M P Pritchard, M Bandera, et al.
European Journal of Biochemistry
|
March 10, 1990
Inhibition of UDP-glucuronosyltransferase activity by possible transition-state analogues in rat-liver microsomes
D Noort, M W Coughtrie, B Burchell, et al.
The Journal of Biological Chemistry
|
July 15, 1993
A novel UDP-Glc-specific glucosyltransferase catalyzing the biosynthesis of 6-O-glucosides of bile acids in human liver microsomes
A Radominska, J Little, J S Pyrek, et al.
DNA and Cell Biology
|
September 1, 1991
The UDP glucuronosyltransferase gene superfamily: suggested nomenclature based on evolutionary divergence
B Burchell, D W Nebert, D R Nelson, et al.
Circulation Research
|
August 1, 1974
The natural (and unnatural) history of hypertrophic obstructive cardiomyopathy
P M Shah, A G Adelman, E D Wigle, et al.
Page
of 27
Search research articles
Search
Showing results (251-260 of 264) with videos related to
Sort By:
Page
of 27
Biochemical Pharmacology
|
October 26, 1995
Genetic analysis of microsomal epoxide hydrolase in patients with carbamazepine hypersensitivity
V J Green, M Pirmohamed, N R Kitteringham, et al.
Archives of Biochemistry and Biophysics
|
August 15, 1990
Characterization and primary sequence of a human hepatic microsomal estriol UDPglucuronosyltransferase
B L Coffman, T R Tephly, Y M Irshaid, et al.
Biochemical Pharmacology
|
March 15, 1983
UDP-glucuronosyltransferase activities. Guidelines for consistent interim terminology and assay conditions
K W Bock, B Burchell, G J Dutton, et al.
The Journal of Pediatrics
|
April 6, 1999
Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn
G Monaghan, A McLellan, A McGeehan, et al.
Archives of Disease in Childhood
|
June 23, 2001
Bile bilirubin pigment analysis in disorders of bilirubin metabolism in early infancy
W S Lee, P J McKiernan, S V Beath, et al.
Drug Metabolism Reviews
|
May 21, 1999
Merits and limitations of recombinant models for the study of human P450-mediated drug metabolism and toxicity: an intralaboratory comparison
T Friedberg, M P Pritchard, M Bandera, et al.
European Journal of Biochemistry
|
March 10, 1990
Inhibition of UDP-glucuronosyltransferase activity by possible transition-state analogues in rat-liver microsomes
D Noort, M W Coughtrie, B Burchell, et al.
The Journal of Biological Chemistry
|
July 15, 1993
A novel UDP-Glc-specific glucosyltransferase catalyzing the biosynthesis of 6-O-glucosides of bile acids in human liver microsomes
A Radominska, J Little, J S Pyrek, et al.
DNA and Cell Biology
|
September 1, 1991
The UDP glucuronosyltransferase gene superfamily: suggested nomenclature based on evolutionary divergence
B Burchell, D W Nebert, D R Nelson, et al.
Circulation Research
|
August 1, 1974
The natural (and unnatural) history of hypertrophic obstructive cardiomyopathy
P M Shah, A G Adelman, E D Wigle, et al.
Page
of 27