Bernhardt, Rita

Humans possess two mitochondrial ferredoxins, Fdx1 and Fdx2, with distinct roles in steroidogenesis, heme, and Fe/S cluster biosynthesis

Sheftel, A. D., Stehling, O., Pierik, A. J., Elsässer, H.-P., Mühlenhoff, U., Webert, H., Hobler, A., Hannemann, F., Bernhardt, R., & Lill, R. (2010) · Proceedings of the National Academy of Sciences

Metalloenzymes and iron-sulfur proteinsMitochondrial Function and Pathology

Cited by 406

Prevalence of primary hyperaldosteronism in moderate to severe hypertension in the Central Europe region

Štrauch, B., Zelinka, T., Hampf, M., Bernhardt, R., & Widimsky, J. (2003) · Journal of Human Hypertension

Hormonal Regulation and HypertensionRenin-Angiotensin System Studies

Cited by 237

New aspects of electron transfer revealed by the crystal structure of a truncated bovine adrenodoxin, Adx(4-108)

Müller, A., Müller, J. J., Muller, Y. A., Uhlmann, H., Bernhardt, R., & Heinemann, U. (1998) · Structure

Enzyme Structure and FunctionMetalloenzymes and iron-sulfur proteins

Cited by 142

Differential regulation of 11β-hydroxylase and aldosterone synthase in human adrenocortical H295R cells

Denner, K., Rainey, W. E., Pezzi, V., Bird, I. M., Bernhardt, R., & Mathis, J. M. (1996) · Molecular and Cellular Endocrinology

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

Cited by 85

Conferring aldosterone synthesis to human CYP11B1 by replacing key amino acid residues with CYP11B2-specific ones

Böttner, B., Denner, K., & Bernhardt, R. (1998) · European Journal of Biochemistry

Hormonal Regulation and HypertensionSteroid Chemistry and Biochemistry

Cited by 62

Amino acid substitution R384P in aldosterone synthase causes corticosterone methyloxidase type I deficiency

Geley, S., Jöhrer, K., Peter, M., Denner, K., Bernhardt, R., Sippell, W. G., & Kofler, R. (1995) · The Journal of Clinical Endocrinology & Metabolism

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

Cited by 48

Phenotypic, metabolic, and molecular genetic characterization of six patients with congenital adrenal hyperplasia caused by novel mutations in the CYP11B1 gene

Nguyen, H.-H., Eiden-Plach, A., Hannemann, F., Malunowicz, E. M., Hartmann, M. F., Wudy, S. A., & Bernhardt, R. (2016) · The Journal of Steroid Biochemistry and Molecular Biology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 21