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Deutsche Medizinische Wochenschrift (1946)|January 16, 1987
[Molecular biology of the adrenogenital syndrome. New possibilities of heterozygote screening]B O Böhm, C Rosak, T L Böhm, et al.The Journal of Biological Chemistry|June 8, 1999
Processing, activity, and inhibition of recombinant cyprosin, an aspartic proteinase from cardoon (Cynara cardunculus)P C White, M C Cordeiro, D Arnold, et al.Journal of Molecular Endocrinology|April 5, 2002
Differential regulation of aldosterone synthase and 11beta-hydroxylase transcription by steroidogenic factor-1M H Bassett, Y Zhang, C Clyne, et al.Human Mutation|January 1, 1994
Mutations in steroid 21-hydroxylase (CYP21)P C White, M T Tusie-Luna, M I New, et al.Molecular Endocrinology (Baltimore, Md.)|August 1, 1992
R339H and P453S: CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversionsA Helmberg, M T Tusie-Luna, M Tabarelli, et al.The Journal of Clinical Endocrinology and Metabolism|March 10, 2001
Type 1 aldosterone synthase deficiency presenting in a middle-aged manK M Kayes-Wandover, R E Schindler, H C Taylor, et al.Nature Genetics|August 1, 1995
Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenaseT Mune, F M Rogerson, H Nikkilä, et al.The Journal of Clinical Investigation|July 1, 1988
Nonsense mutation causing steroid 21-hydroxylase deficiencyH Globerman, M Amor, K L Parker, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 1988
Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiencyM Amor, K L Parker, H Globerman, et al.ACS Applied Bio Materials|November 4, 2022
β-Glucosidase Immobilized on Magnetic Nanoparticles: Controlling Biomolecule Footprint and Particle Functional Group Density to Navigate the Activity-Stability TradeoffThaddeus W Vasicek, Sylvester Guillermo, Danny R Swofford, et al.Pageof 29