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Annals 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 MiloszewskiGenomics|October 1, 1993
Chromosomal mapping of the human Mu class glutathione S-transferases to 1p13V L Ross, P G Board, G C WebbThe Journal of Parasitology|August 1, 1988
Glutathione S-transferases in Fasciola hepaticaM J Howell, P G Board, J C BorayThe Biochemical Journal|March 1, 1992
Design of two chimaeric human-rat class alpha glutathione transferases for probing the contribution of C-terminal segments of protein structure to the catalytic propertiesR Björnestedt, M Widersten, P G Board, et al.Pageof 15