J. Yudkovitz

发表

On the etiology of subcapsular lenticular opacities produced in dogs receiving HMG-CoA reductase inhibitors.

A. Alberts, J. Chen, R. J. Gerson, 1990, Experimental eye research.

Immunolocalization of estrogen receptor beta in the mouse brain: comparison with estrogen receptor alpha.

D. Pfaff, S. Ogawa, B. McEwen, 2003, Endocrinology.

Syntheses and structure-activity relationship studies of piperidine-substituted quinolones as nonpeptide gonadotropin releasing hormone antagonists.

R. DeVita, M. Wyvratt, M. Goulet, 2004, Bioorganic & medicinal chemistry letters.

Estrogen receptor ligands. Part 10: Chromanes: old scaffolds for new SERAMs.

H. Wilkinson, D. Kimmel, L. Freedman, 2005, Bioorganic & medicinal chemistry letters.

Discovery of MK-8153, a Potent and Selective ROMK Inhibitor and Novel Diuretic/Natriuretic.

K. Samuel, Haifeng Tang, B. Pio, 2021, Journal of medicinal chemistry.

Studies on the in vivo synthesis of triacylglycerol in mouse liver.

J. Yudkovitz, M. Greenspan, E. Schroeder, 1982, Biochimica et biophysica acta.

Antagonist-induced, activation function-2-independent estrogen receptor α phosphorylation

G. Rodan, Nan Wei, L. Freedman, 2006 .

Metabolism of lovastatin by rat and human liver microsomes in vitro.

J. L. Smith, A. Alberts, B. Arison, 1988, Drug metabolism and disposition: the biological fate of chemicals.

2-Arylindoles as gonadotropin releasing hormone (GnRH) antagonists: optimization of the tryptamine side chain.

K. Lyons, M. Wyvratt, M. Goulet, 2002, Bioorganic & medicinal chemistry letters.

Selective estrogen receptor-beta (SERM-beta) compounds modulate raphe nuclei tryptophan hydroxylase-1 (TPH-1) mRNA expression and cause antidepressant-like effects in the forced swim test

B. Rocha, H. Wilkinson, J. Schaeffer, 2012, Neuropharmacology.

Orally bioavailable, indole-based nonpeptide GnRH receptor antagonists with high potency and functional activity.

K. Lyons, Y. Yang, M. Goulet, 2001, Bioorganic & medicinal chemistry letters.

Potent nonpeptide GnRH receptor antagonists derived from substituted indole-5-carboxamides and -acetamides bearing a pyridine side-chain terminus.

Y. Yang, P. Gibbons, M. Goulet, 2001, Bioorganic & medicinal chemistry letters.

Substituted indole-5-carboxamides and -acetamides as potent nonpeptide GnRH receptor antagonists.

Y. Yang, M. Goulet, K. Cheng, 2001, Bioorganic & medicinal chemistry letters.

A potent, nonpeptidyl 1H-quinolone antagonist for the gonadotropin-releasing hormone receptor.

R. DeVita, F. Ujjainwalla, D. Macintyre, 2001, Journal of medicinal chemistry.

Potent antagonists of gonadotropin releasing hormone receptors derived from quinolone-6-carboxamides.

R. DeVita, F. Ujjainwalla, M. Fisher, 2000, Bioorganic & medicinal chemistry letters.

Inhibition of hydroxymethylglutaryl-coenzyme A synthase by L-659,699.

A. Alberts, J. Chen, J. C. Chabala, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Immunolocalization of estrogen receptor β in the mouse brain: Comparison with estrogen receptor α

D. Pfaff, S. Ogawa, B. McEwen, 2003 .

Separation and identification of triglycerides, cholesteryl esters, cholesterol, 7-dehydrocholesterol, dolichol, ubiquinone, alpha-tocopherol, and retinol by high performance liquid chromatography with a diode array detector.

J. Yudkovitz, M. Greenspan, C. Lo, 1988, Journal of lipid research.

Mevinolinic acid biosynthesis by Aspergillus terreus and its relationship to fatty acid biosynthesis

J. Yudkovitz, M. Greenspan, 1985, Journal of bacteriology.

Antagonist-induced, activation function-2-independent estrogen receptor alpha phosphorylation.

G. Rodan, Nan Wei, L. Freedman, 2006, Molecular endocrinology.

Quinolones as gonadotropin releasing hormone (GnRH) antagonists: simultaneous optimization of the C(3)-aryl and C(6)-substituents.

R. DeVita, M. Wyvratt, Y. Yang, 2000, Bioorganic & medicinal chemistry letters.

Inhibition of 3-hydroxy-3-methylglutaryl-CoA synthase and cholesterol biosynthesis by beta-lactone inhibitors and binding of these inhibitors to the enzyme.

H. Bull, A. Alberts, J. Yudkovitz, 1993, The Biochemical journal.

Identification of neutral 4-O-alkyl quinolone nonpeptide GnRH receptor antagonists.

R. DeVita, M. Wyvratt, M. Goulet, 2004, Bioorganic & medicinal chemistry letters.

The inhibition of cytoplasmic acetoacetyl-CoA thiolase by a triyne carbonate (L-660, 631).

A. Alberts, J. Chen, J. C. Chabala, 1989, Biochemical and biophysical research communications.

Potent antagonists of gonadotropin releasing hormone receptors derived from quinolone-6-carboxamides.

R. DeVita, F. Ujjainwalla, M. Fisher, 2000, Bioorganic & medicinal chemistry letters.

Modification of the pyridine moiety of non-peptidyl indole GnRH receptor antagonists.

M. Goulet, A. Mao, J. Cui, 2002, Bioorganic & Medicinal Chemistry Letters.

A sensitive assay for phosphatidate phosphohydrolase in mouse liver microsomes.

J. Germershausen, J. Yudkovitz, M. Greenspan, 1980, Biochimica et biophysica acta.

Identification and characterization of a functionally distinct form of human estrogen receptor beta.

H. Liu, H. Wilkinson, S. Nilsson, 2002, Endocrinology.

Identification and Characterization of a Functionally Distinct Form of Human Estrogen Receptor β.

H. Liu, H. Wilkinson, S. Nilsson, 2002, Endocrinology.