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American Journal of Human Genetics
|
July 31, 1998
Molecular basis for hypertension in the "type II variant" of apparent mineralocorticoid excess
A Li, R Tedde, Z S Krozowski, et al.
The Journal of Clinical Investigation
|
May 1, 1991
Measurement of de novo hepatic lipogenesis in humans using stable isotopes
M K Hellerstein, M Christiansen, S Kaempfer, et al.
Biological Mass Spectrometry
|
February 1, 1993
Collisionally activated dissociation and tandem mass spectrometry of intact hemoglobin beta-chain variant proteins with electrospray ionization
K J Light-Wahl, J A Loo, C G Edmonds, et al.
The American Journal of Physiology
|
January 1, 1997
Measurement of hepatic Ra UDP-glucose in vivo in rats: relation to glycogen deposition and labeling patterns
M K Hellerstein, A Letscher, J M Schwarz, et al.
Endocrinology
|
February 14, 2004
Paralogues of porcine aromatase cytochrome P450: a novel hydroxylase activity is associated with the survival of a duplicated gene
C Jo Corbin, S M Mapes, J Marcos, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1980
Pubertal presentation of congenital delta 5-3 beta-hydroxysteroid dehydrogenase deficiency
R L Rosenfield, B H Rich, J I Wolfsdorf, et al.
Steroids
|
November 1, 1990
Synthesis of 6 beta-hydroxyaldosterone by A6 (toad kidney) cells in culture
D J Morris, S A Latif, T J Conca, et al.
Archives of Biochemistry and Biophysics
|
June 1, 1994
Purification and enzymatic properties of a recombinant fusion protein expressed in Escherichia coli containing the domains of bovine P450 17A and rat NADPH-P450 reductase
M S Shet, C W Fisher, M P Arlotto, et al.
Journal of Hypertension
|
February 12, 1998
Apparent mineralocorticoid excess in a Brazilian kindred: hypertension in the heterozygote state
A Li, K X Li, S Marui, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1995
Several homozygous mutations in the gene for 11 beta-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess
R C Wilson, M D Harbison, Z S Krozowski, et al.
Page
of 18
Search research articles
Search
Showing results (161-170 of 175) with videos related to
Sort By:
Page
of 18
American Journal of Human Genetics
|
July 31, 1998
Molecular basis for hypertension in the "type II variant" of apparent mineralocorticoid excess
A Li, R Tedde, Z S Krozowski, et al.
The Journal of Clinical Investigation
|
May 1, 1991
Measurement of de novo hepatic lipogenesis in humans using stable isotopes
M K Hellerstein, M Christiansen, S Kaempfer, et al.
Biological Mass Spectrometry
|
February 1, 1993
Collisionally activated dissociation and tandem mass spectrometry of intact hemoglobin beta-chain variant proteins with electrospray ionization
K J Light-Wahl, J A Loo, C G Edmonds, et al.
The American Journal of Physiology
|
January 1, 1997
Measurement of hepatic Ra UDP-glucose in vivo in rats: relation to glycogen deposition and labeling patterns
M K Hellerstein, A Letscher, J M Schwarz, et al.
Endocrinology
|
February 14, 2004
Paralogues of porcine aromatase cytochrome P450: a novel hydroxylase activity is associated with the survival of a duplicated gene
C Jo Corbin, S M Mapes, J Marcos, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1980
Pubertal presentation of congenital delta 5-3 beta-hydroxysteroid dehydrogenase deficiency
R L Rosenfield, B H Rich, J I Wolfsdorf, et al.
Steroids
|
November 1, 1990
Synthesis of 6 beta-hydroxyaldosterone by A6 (toad kidney) cells in culture
D J Morris, S A Latif, T J Conca, et al.
Archives of Biochemistry and Biophysics
|
June 1, 1994
Purification and enzymatic properties of a recombinant fusion protein expressed in Escherichia coli containing the domains of bovine P450 17A and rat NADPH-P450 reductase
M S Shet, C W Fisher, M P Arlotto, et al.
Journal of Hypertension
|
February 12, 1998
Apparent mineralocorticoid excess in a Brazilian kindred: hypertension in the heterozygote state
A Li, K X Li, S Marui, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1995
Several homozygous mutations in the gene for 11 beta-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess
R C Wilson, M D Harbison, Z S Krozowski, et al.
Page
of 18