C. Büttner

A homozygous HFE gene splice site mutation (IVS5+1 G/A) in a hereditary hemochromatosis patient of Vietnamese origin.

W. Kerner, J. Genschel, H. Lochs, 2002, Gastroenterology.

A sensitive noninvasive method for monitoring successful liver-directed gene transfer of the low-density lipoprotein receptor in Watanabe hyperlipidemic rabbits in vivo

W. Burchert, J. Genschel, H. Lochs, 2004, Gene Therapy.

In vivo kinetics as a sensitive method for testing physiologically intact human recombinant apolipoprotein A-I: comparison of three different expression systems.

M. Manns, C. Strassburg, A. Remaley, 1997, Clinica chimica acta; international journal of clinical chemistry.

Expression and purification of recombinant human apolipoprotein A-I in Chinese hamster ovary cells.

M. Manns, J. Genschel, H. Schmidt, 1997, Protein expression and purification.

Delayed low density lipoprotein (LDL) catabolism despite a functional intact LDL-apolipoprotein B particle and LDL-receptor in a subject with clinical homozygous familial hypercholesterolemia.

H. Brewer, R. Shamburek, H. H. Schmidt, 1998, The Journal of clinical endocrinology and metabolism.

Dyslipemia in familial partial lipodystrophy caused by an R482W mutation in the LMNA gene.

J. Genschel, H. Lochs, J. Ockenga, 2001, The Journal of clinical endocrinology and metabolism.