Zschenker O, Illies T, Ameis D (2006)
Overexpression of lysosomal acid lipase and other proteins in atherosclerosis
J Biochem 140: 23

Zschenker O, Bahr C, Hess UF, Ameis D (2005)
Systematic mutagenesis of potential glycosylation sites of lysosomal acid lipase
J Biochem 137: 387

Du H, Heur M, Witte DP, Ameis D, Grabowski GA (2002)
Lysosomal Acid lipase deficiency: correction of lipid storage by adenovirus-mediated gene transfer in mice
Hum Gene Therapy 13: 1361

Zschenker O, Jung N, Rethmeier J, Trautwein S, Hertel S, Zeigler M, Ameis D (2001)
Characterization of lysosomal acid lipase mutations in the signal peptide and mature polypeptide region causing Wolman disease
J Lipid Res 42: 1033

Ries S, Buchler C, Schindler G, Aslanidis C, Ameis D, Gasche C, Jung N, Schambach A, Fehringer P, Vanier MT, Belli DC, Greten H, Schmitz G (1998)
Different missense mutations in histidine-108 of lysosomal acid lipase cause cholesteryl ester storage disease in unrelated compound heterozygous and hemizygous individuals
Hum Mutat 12: 44

Ameis D, Brockmann G, Knoblich R, Merkel M, Ostlund RE, Jr., Yang JW, Coates PM, Cortner JA, Feinman SV, Greten H (1995)
A 5' splice-region mutation and a dinucleotide deletion in the lysosomal acid lipase gene in two patients with cholesteryl ester storage disease
J Lipid Res 36: 241

Ameis D, Merkel M, Eckerskorn C, Greten H (1994)
Purification, characterization and molecular cloning of human hepatic lysosomal acid lipase
European Journal of Biochemistry 219: 905

Ameis D, Greten H, Schotz MC (1992)
Hepatic and plasma lipases
Semin Liver Dis 12: 397

Kobayashi J, Nishida T, Ameis D, Stahnke G, Schotz MC, Hashimoto H, Fukamachi I, Shirai K, Saito Y, Yoshida S (1992)
A heterozygous mutation (the codon for Ser447----a stop codon) in lipoprotein lipase contributes to a defect in lipid interface recognition in a case with type I hyperlipidemia
Biochemical & Biophysical Research Communications 182: 70

Sprecher DL, Kobayashi J, Rymaszewski M, Goldberg IJ, Harris BV, Bellet PS, Ameis D, Yunker RL, Black DM, Stein EA, Schotz MC, Wiginton DA (1992)
Trp64->nonsense mutation in the lipoprotein lipase gene
J Lipid Res 33: 859

Ameis D, Kobayashi J, Davis RC, Ben-Zeev O, Malloy MJ, Kane JP, Lee G, Wong H, Havel RJ, Schotz MC (1991)
Familial chylomicronemia (type I hyperlipoproteinemia) due to a single missense mutation in the lipoprotein lipase gene
J Clinical Investigation 87: 1165

Reue K, Zambaux J, Wong H, Lee G, Leete TH, Ronk M, Shively JE, Sternby B, Borgstrom B, Ameis D, Schotz MC (1991)
cDNA cloning of carboxyl ester lipase from human pancreas reveals a unique proline-rich repeat unit
J Lipid Res 32: 267

Ameis D, Stahnke G, Kobayashi J, McLean J, Lee G, Buscher M, Schotz MC, Will H (1990)
Isolation and characterization of the human hepatic lipase gene
Journal of Biological Chemistry 265: 6552

Davis RC, Stahnke G, Wong H, Doolittle MH, Ameis D, Will H, Schotz MC (1990)
Hepatic lipase: site-directed mutagenesis of a serine residue important for catalytic activity
Journal of Biological Chemistry 265: 6291

Kirchgessner TG, Chuat JC, Heinzmann C, Etienne J, Guilhot S, Svenson K, Ameis D, Pilon C, d'Auriol L, Andalibi A, et al. (1989)
Organization of the human lipoprotein lipase gene and evolution of the lipase gene family
Proc Natl Acad Sci U S A 86: 9647