S. Busch

发表

Glycosaminoglycans: molecular properties, protein interactions, and role in physiological processes.

R L Jackson, R. Jackson, S. Busch, 1991, Physiological reviews.

Isolation and cDNA sequence of human postheparin plasma hepatic triglyceride lipase.

M. Schafer, S. Mao, S. Busch, 1988, The Journal of biological chemistry.

Concentration-dependent antioxidant activity of probucol in low density lipoproteins in vitro: probucol degradation precedes lipoprotein oxidation.

R. Jackson, S. Busch, R. L. Barnhart, 1989, Journal of lipid research.

Immunoaffinity purification of the lipid transfer protein complex directly from human plasma.

J. Ellsworth, S. Busch, J. Harmony, 1986, Analytical biochemistry.

Human hepatic triglyceride lipase expression reduces high density lipoprotein and aortic cholesterol in cholesterol-fed transgenic mice.

M. Fitzgerald, S. Mao, R. Jackson, 1994, The Journal of biological chemistry.

Kinetics of plasma protein-catalyzed exchange of phosphatidylcholine and cholesteryl ester between plasma lipoproteins.

D. Quinn, S. Busch, Dan, 1982, Journal of lipid research.

Heparin induces the expression of hepatic triglyceride lipase in a human hepatoma (HepG2) cell line.

R. Jackson, S. Busch, G. A. Martin, 1989, The Journal of biological chemistry.

Human hepatoma (HepG2) cells secrete a single 65 K dalton triglyceride lipase immunologically identical to postheparin plasma hepatic lipase.

R. Jackson, S. Busch, T. J. Owen, 1989, Life sciences.

Differential regulation of hepatic triglyceride lipase and 3-hydroxy-3-methylglutaryl-CoA reductase gene expression in a human hepatoma cell line, HepG2.

R. Jackson, S. Busch, G. A. Martin, 1990, The Journal of biological chemistry.

Plasma cholesteryl ester-triglyceride transfer protein. The catalytic domain is a low molecular weight proteolipid.

S. Mao, S. Busch, W. Stuart, 1987, The Journal of biological chemistry.

Regulation of hepatic lipase expression by an intermediate of the cellular cholesterol biosynthetic pathway.

R. Jackson, S. Busch, G. A. Martin, 1991, Advances in experimental medicine and biology.

DNA binding of Jun and Fos bZip domains: homodimers and heterodimers induce a DNA conformational change in solution.

S. Busch, R. Leppik, M. Granger-Schnarr, 1996, Nucleic acids research.

Purification and characterization of apolipoprotein J.

S. Mao, S. Busch, W. Stuart, 1990, The Journal of biological chemistry.

Fos, Jun and CREB basic-domain peptides have intrinsic DNA-binding activity enhanced by a novel stabilizing factor.

P. Sassone-Corsi, S. Busch, 1990, Oncogene.

Cholesteryl ester analogs inhibit cholesteryl ester but not triglyceride transfer catalyzed by the plasma cholesteryl ester-triglyceride transfer protein

S. Busch, J. Harmony, 1990, Lipids.

Trans-repressor activity of nuclear glycosaminoglycans on Fos and Jun/AP-1 oncoprotein-mediated transcription

R. Jackson, S. Busch, A. Cardin, 1992, The Journal of cell biology.

Dimers, leucine zippers and DNA-binding domains.

P. Sassone-Corsi, S. Busch, 1990, Trends in genetics : TIG.

Induction of vascular cell adhesion molecule‐1 expression by IL‐4 in human aortic smooth muscle cells is not associated with increased nuclear NF‐κB levels

P. Wright, S. Busch, K. Kropp, 1999, Journal of cellular physiology.

Nuclear Oncogenes as Transcription Factors

J. Auwerx, P. Sassone-Corsi, N. Foulkes, 1991 .