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Genomics|December 1, 1993
Structure and organization of the human alpha class glutathione S-transferase genes and related pseudogenesT Suzuki, P N Johnston, P G BoardArchives of Biochemistry and Biophysics|December 1, 1991
Glyoxalase 2 deficiency in the erythrocytes of a horse: 1H NMR studies of enzyme kinetics and transport of S-lactoylglutathioneC Rae, P G Board, P W KuchelBiochimica Et Biophysica Acta|April 14, 1988
Human muscle glutathione S-transferase (GST-4) shows close homology to human liver GST-1P G Board, T Suzuki, D C ShawAnnals of Human Genetics|January 1, 1982
Genetic heterogeneity of prothrombin (FII)P G Board, M Coggan, M E PidcockHuman Genetics|January 1, 1982
Glucose-6-phosphate dehydrogenase deficiency in Papua New Guinea. The description of 13 new variantsK Chockkalingam, P G Board, G T NurseFEBS Letters|November 26, 1990
Do the major human glutathione S-transferases have fatty acid ethyl ester synthase activity?T Suzuki, M S Kovacs, P G BoardGenomics|April 1, 1990
Evolution of human alpha 1-acid glycoprotein genes and surrounding Alu repeatsC M Merritt, S Easteal, P G BoardAnnals of Human Genetics|July 1, 1989
Isolation of a cDNA clone and localization of the human glutathione S-transferase 3 genes to chromosome bands 11q13 and 12q13-14P G Board, G C Webb, M CogganGene|January 1, 1986
Molecular cloning and nucleotide sequence of human alpha 1 acid glycoprotein cDNAP G Board, I M Jones, A K BentleyBlood Reviews|December 1, 1993
Factor XIII: inherited and acquired deficiencyP G Board, M S Losowsky, K J MiloszewskiPageof 67