P. S. Liu

发表

Inclusion of S-sepharose beads in the culture medium significantly improves recovery of secreted rBPI(21) from transfected CHO-K1 cells.

S. Carroll, S F Carroll, R. Williams, 2000, Protein expression and purification.

An amino-terminal fragment of human lipopolysaccharide-binding protein retains lipid A binding but not CD14-stimulatory activity.

S. Carroll, H. Kasler, C. Birr, 1994, Journal of immunology.

Expression and characterization of cysteine-modified variants of an amino-terminal fragment of bactericidal/permeability-increasing protein.

S. Carroll, S. Leigh, R. Williams, 1996, Protein Expression and Purification.

Antitumor properties of 2(1H)-pyrimidinone riboside (zebularine) and its fluorinated analogues.

J. Plowman, V. Marquez, J. Driscoll, 1991, Journal of medicinal chemistry.

Castanospermine-glucosides as selective disaccharidase inhibitors.

C. King, P. S. Liu, K. M. Robinson, 1990, Biochemical pharmacology.

Antiretroviral activity of castanospermine and deoxynojirimycin, specific inhibitors of glycoprotein processing.

A. Sjoerdsma, P. Sunkara, T. Bowlin, 1987, Biochemical and biophysical research communications.

Caffeine‐Sensitive Calcium Stores in Bovine Adrenal Chromaffin Cells

Y. J. Lin, L. Kao, Pei-Shan Liu, 1991, Journal of neurochemistry.

Na(+)-dependent Ca2+ influx in bovine adrenal chromaffin cells.

L. Kao, P. S. Liu, 1990, Cell calcium.

Specificity of cotranslational amino-terminal processing of proteins in yeast.

R A Bradshaw, R. Koduri, R. Bradshaw, 1987, Biochemistry.

Cyclic urea nucleosides. Cytidine deaminase activity as a function of aglycon ring size.

R. Fuller, V. Marquez, J. Driscoll, 1981, Journal of medicinal chemistry.

Castanospermine-glucosides are potent, selective, long-acting sucrase inhibitors.

C. King, P. S. Liu, K. M. Robinson, 1989, Journal of Pharmacology and Experimental Therapeutics.

Castanospermine blocks the hyperglycemic response to carbohydrates in vivo: a result of intestinal disaccharidase inhibition.

P. S. Liu, K. M. Robinson, B. L. Rhinehart, 1987, Life Science.

Inhibition of intestinal disaccharidases and suppression of blood glucose by a new alpha-glucohydrolase inhibitor--MDL 25,637.

P. S. Liu, S. Wagner, K. M. Robinson, 1987, The Journal of pharmacology and experimental therapeutics.

ANTI-HIV ACTIVITY OF CASTANOSPERMINE ANALOGUES

A. Sjoerdsma, P. Sunkara, M. Kang, 1989, The Lancet.

Synthesis of 1,3-diazepin-2-one nucleosides as transition-state inhibitors of cytidine deaminase.

V. Marquez, J. Driscoll, J. Kelley, 1980, Journal of medicinal chemistry.

Inhibition of cytidine deaminase by 2-oxopyrimidine riboside and related compounds.

V. Marquez, J. Driscoll, D. Vistica, 1980, Biochemical pharmacology.

Effects of caffeine on Ca2+ fluxes and secretion in bovine chromaffin cells.

Y. J. Lin, L. Kao, P. S. Liu, 1995, European journal of pharmacology.

Effects of extracellular ATP on Ca2+ mobilization in Madin Darby canine kidney (MDCK) cells.

M. Ho, H. Hsieh, P. S. Liu, 1996, Chinese journal of physiology.

Biphasic effects of chromium compounds on catecholamine secretion from bovine adrenal medullary cells.

P. S. Liu, M. K. Lin, 1997, Toxicology.

6-0-butanoylcastanospermine (MDL 28,574) inhibits glycoprotein processing and the growth of HIVs.

D. Taylor, P. Sunkara, M. Kang, 1991, AIDS.