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Steroids|November 1, 1984
11 beta-Hydroxysteroid dehydrogenase: fact or fancy?C Monder, C H ShackletonSteroids|September 1, 1980
Gas chromatographic and mass spectrometric analysis of urinary acidic metabolites of cortisolC H Shackleton, E Roitman, C Monder, et al.The Journal of Clinical Endocrinology and Metabolism|September 1, 1986
The syndrome of apparent mineralocorticoid excess: its association with 11 beta-dehydrogenase and 5 beta-reductase deficiency and some consequences for corticosteroid metabolismC Monder, C H Shackleton, H L Bradlow, et al.The Journal of Steroid Biochemistry and Molecular Biology|January 1, 1991
Heterogeneity of 11 beta-hydroxysteroid dehydrogenase in rat tissuesC MonderFASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 1, 1991
Corticosteroids, receptors, and the organ-specific functions of 11 beta-hydroxysteroid dehydrogenaseC MonderThe Journal of Steroid Biochemistry and Molecular Biology|April 1, 1993
The forms and functions of 11 beta-hydroxysteroid dehydrogenaseC MonderClinical and Experimental Hypertension. Part A, Theory and Practice|January 1, 1982
Evidence against significant 19-nor-deoxycorticosterone production in patients with 17 alpha-hydroxylase deficiencyC H ShackletonSteroids|November 1, 1981
Derivatization of estrogen conjugates for analysis by capillary gas chromatographyC H ShackletonClinical Chemistry|February 1, 1983
Inborn errors of steroid biosynthesis: detection by a new mass-spectrometric methodC H ShackletonClinica Chimica Acta; International Journal of Clinical Chemistry|March 15, 1976
Congenital adrenal hyperplasia caused by defect in steroid 21-hydroxylase. Establishment of definitive urinary steroid excretion pattern during first weeks of lifeC H ShackletonPageof 22