J. Yates

发表

Synthetic LXR agonists increase LDL in CETP species Published, JLR Papers in Press, July 16, 2005. DOI 10.1194/jlr.M500116-JLR200

M. Jaye, C. Doe, R. Willette, 2005, Journal of Lipid Research.

3.P.183 Bone marrow transplantation in apolipoprotein E deficient mice: Effect of apoE gene-dosage on serum lipid concentrations, βVLDL catabolism, and atherosclerosis

T. J. Berkel, P. Groot, P. Hoogerbrugge, 1997 .

SR-12813 lowers plasma cholesterol in beagle dogs by decreasing cholesterol biosynthesis.

K. Suckling, P. Groot, E. Niesor, 1997, Atherosclerosis.

Bone marrow transplantation in apolipoprotein E-deficient mice. Effect of ApoE gene dosage on serum lipid concentrations, (beta)VLDL catabolism, and atherosclerosis.

T. V. van Berkel, P. Groot, P. Hoogerbrugge, 1997, Arteriosclerosis, thrombosis, and vascular biology.

The role of ATP citrate-lyase in the metabolic regulation of plasma lipids. Hypolipidaemic effects of SB-204990, a lactone prodrug of the potent ATP citrate-lyase inhibitor SB-201076.

D. Tew, H. Boyd, A. Shaw, 1998, The Biochemical journal.

Dietary ethanol stimulates the activity of phosphatidylcholine-specific phospholipase D and the formation of phosphatidylethanol in Drosophila melanogaster larvae.

R. Miller, B. W. Geer, J. Yates, 1993, Insect biochemistry and molecular biology.

Staphylococcal bacteremia in a "Germ-free" unit.

E. Henderson, M. Plaut, J. Yates, 1976, Archives of internal medicine.

Selective small molecule inhibitors of glycogen synthase kinase-3 modulate glycogen metabolism and gene transcription.

J W Yates, A. Reith, J. Holder, 2000, Chemistry & biology.

Dietary ethanol reduces phosphatidylcholine levels and inhibits the uptake of dietary choline in Drosophila melanogaster larvae.

R. Miller, B. W. Geer, J. Yates, 1993, Comparative biochemistry and physiology. Comparative physiology.

Proteomic identification and early validation of complement 1 inhibitor and pigment epithelium‐derived factor: Two novel biomarkers of Alzheimer's disease in human plasma

David R. Willé, A. Roses, P. Cutler, 2008, Proteomics. Clinical applications.

Development of glucose intolerance in male transgenic mice overexpressing human glycogen synthase kinase-3beta on a muscle-specific promoter.

J. Holder, M. Coghlan, J. Clapham, 2004, Metabolism: clinical and experimental.

ATP-Citrate lyase as a target for hypolipidemic intervention. 2. Synthesis and evaluation of (3R,5S)-omega-substituted-3-carboxy-3, 5-dihydroxyalkanoic acids and their gamma-lactone prodrugs as inhibitors of the enzyme in vitro and in vivo.

D. Tew, H. Boyd, A. Shaw, 1998, Journal of medicinal chemistry.

ATP-citrate lyase as a target for hypolipidemic intervention. Design and synthesis of 2-substituted butanedioic acids as novel, potent inhibitors of the enzyme.

D. Tew, A. Shaw, P. Groot, 1996, Journal of medicinal chemistry.

Apolipoprotein E*3-Leiden transgenic mice as a test model for hypolipidaemic drugs.

L. Havekes, M. Hofker, B. Staels, 1998, Arzneimittel-Forschung.