M. Hampf

发表

Unequal crossing-over between aldosterone synthase and 11beta-hydroxylase genes causes congenital adrenal hyperplasia.

R. Bernhardt, M. Hampf, N. T. Dao, 2001, The Journal of clinical endocrinology and metabolism.

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

T. Zelinka, B. Štrauch, R. Bernhardt, 2003, Journal of Human Hypertension.

Amplification, Sequence and Expression of the Harpin Encoding Gene of the Bacterial Canker Pathogen, Pseudomonas syringae pv. syringae Strain NV

J. Hapgood, D. Bellstedt, M. Hampf, 1999 .

New Molecular Genetic Defects Causing 11β-Hydroxylase Deficiency (CAH)

R. Bernhardt, M. Hampf, N. T. Hoan, 2000, Endocrine research.

Aldosterone synthase gene in patients suffering from hyperaldosteronism.

R. Bernhardt, M. Hampf, J. Widimský, 1998, Endocrine research.

Abolished nocturnal blood pressure fall in a boy with glucocorticoid-remediable aldosteronism

T. Seeman, R. Bernhardt, M. Hampf, 1999, Journal of Human Hypertension.

Improved Tet-responsive promoters with minimized background expression

M. Gossen, H. Bujard, R. Loew, 2010, BMC biotechnology.

Promoter crosstalk effects on gene expression.

M. Gossen, Manfred Gossen, Mathias Hampf, 2007, Journal of molecular biology.

A protocol for combined Photinus and Renilla luciferase quantification compatible with protein assays.

M. Gossen, M. Hampf, 2006, Analytical biochemistry.

Sequence of the 11β-hydroxylase gene from the cape baboon (Papio Ursinus)

P. Swart, A. Swart, M. Hampf, 1996 .