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J F Mercer

Showing results (61-70 of 88) with videos related to

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Genomics|August 10, 1995
Molecular structure of the Menkes disease gene (ATP7A)H A Dierick, L Ambrosini, J Spencer, et al.
The Biochemical Journal|November 22, 2000
Defective localization of the Wilson disease protein (ATP7B) in the mammary gland of the toxic milk mouse and the effects of copper supplementationA A Michalczyk, J Rieger, K J Allen, et al.
DNA (Mary Ann Liebert, Inc.)|April 1, 1985
The primary structure of the imported mitochondrial protein, ornithine transcarbamylase from rat liver: mRNA levels during ontogenyP McIntyre, L Graf, J F Mercer, et al.
Journal of Bacteriology|November 1, 1991
Cloning and characterization of cutE, a gene involved in copper transport in Escherichia coliS D Rogers, M R Bhave, J F Mercer, et al.
Plasmid|May 19, 1998
Eukaryotic expression vectors that replicate to low copy number in bacteria: transient expression of the Menkes proteinS L Fontaine, S D Firth, P J Lockhart, et al.
The Biochemical Journal|November 15, 1989
The effect of streptozotocin-induced diabetes on phenylalanine hydroxylase expression in rat liverD S Taylor, H H Dahl, J F Mercer, et al.
Journal of Gastroenterology and Hepatology|December 29, 2000
Conditionally immortalized mouse hepatocytes for use in liver gene therapyK J Allen, R Reyes, K Demmler, et al.
The Journal of Biological Chemistry|September 25, 1984
Two apparent molecular weight forms of human and monkey phenylalanine hydroxylase are due to phosphorylationS C Smith, B E Kemp, W J McAdam, et al.
Biochimica Et Biophysica Acta|October 21, 1991
Developmental variation in copper, zinc and metallothionein mRNA in brindled mutant and nutritionally copper deficient miceJ F Mercer, T Stevenson, S A Wake, et al.
Differentiation; Research in Biological Diversity|June 1, 1988
The development of phenylalanine hydroxylase in rat liver; in vivo, and in vitro studies utilizing fetal hepatocyte culturesG C Yeoh, E Edkins, K Mackenzie, et al.
Pageof 9

Showing results (61-70 of 88) with videos related to

Sort By:
Pageof 9
Genomics|August 10, 1995
Molecular structure of the Menkes disease gene (ATP7A)H A Dierick, L Ambrosini, J Spencer, et al.
The Biochemical Journal|November 22, 2000
Defective localization of the Wilson disease protein (ATP7B) in the mammary gland of the toxic milk mouse and the effects of copper supplementationA A Michalczyk, J Rieger, K J Allen, et al.
DNA (Mary Ann Liebert, Inc.)|April 1, 1985
The primary structure of the imported mitochondrial protein, ornithine transcarbamylase from rat liver: mRNA levels during ontogenyP McIntyre, L Graf, J F Mercer, et al.
Journal of Bacteriology|November 1, 1991
Cloning and characterization of cutE, a gene involved in copper transport in Escherichia coliS D Rogers, M R Bhave, J F Mercer, et al.
Plasmid|May 19, 1998
Eukaryotic expression vectors that replicate to low copy number in bacteria: transient expression of the Menkes proteinS L Fontaine, S D Firth, P J Lockhart, et al.
The Biochemical Journal|November 15, 1989
The effect of streptozotocin-induced diabetes on phenylalanine hydroxylase expression in rat liverD S Taylor, H H Dahl, J F Mercer, et al.
Journal of Gastroenterology and Hepatology|December 29, 2000
Conditionally immortalized mouse hepatocytes for use in liver gene therapyK J Allen, R Reyes, K Demmler, et al.
The Journal of Biological Chemistry|September 25, 1984
Two apparent molecular weight forms of human and monkey phenylalanine hydroxylase are due to phosphorylationS C Smith, B E Kemp, W J McAdam, et al.
Biochimica Et Biophysica Acta|October 21, 1991
Developmental variation in copper, zinc and metallothionein mRNA in brindled mutant and nutritionally copper deficient miceJ F Mercer, T Stevenson, S A Wake, et al.
Differentiation; Research in Biological Diversity|June 1, 1988
The development of phenylalanine hydroxylase in rat liver; in vivo, and in vitro studies utilizing fetal hepatocyte culturesG C Yeoh, E Edkins, K Mackenzie, et al.
Pageof 9