B. Conway

发表

Quantification of G-Protein Coupled Receptor Internalization Using G-Protein Coupled Receptor-Green Fluorescent Protein Conjugates with the ArrayScan™ High-Content Screening System

Lubing Zhou, Michael R. D'Andrea, K. Giuliano, 1999 .

Quantitative analysis of agonist‐dependent parathyroid hormone receptor trafficking in whole cells using a functional green fluorescent protein conjugate

M. D'Andrea, R. Ghosh, B. Conway, 2001, Journal of cellular physiology.

Functional Roles for the Pleckstrin and Dbl Homology Regions in the Ras Exchange Factor Son-of-sevenless (*)

U. Banerjee, M. Czech, L. Kozma, 1995, The Journal of Biological Chemistry.

Synthesis and discovery of macrocyclic polyoxygenated bis-7-azaindolylmaleimides as a novel series of potent and highly selective glycogen synthase kinase-3beta inhibitors.

S. Emanuel, P. Connolly, L. Jolliffe, 2003, Journal of medicinal chemistry.

3-(7-Azaindolyl)-4-arylmaleimides as potent, selective inhibitors of glycogen synthase kinase-3.

J. Li, H. Ye, C. Derian, 2004, Bioorganic & medicinal chemistry letters.

3-(7-Azaindolyl)-4-arylmaleimides as potent, selective inhibitors of glycogen synthase kinase-3.

J. Li, H. Ye, C. Derian, 2004, Bioorganic & medicinal chemistry letters.

Heteroaryl-O-glucosides as novel sodium glucose co-transporter 2 inhibitors. Part 1.

B. Conway, K. Demarest, Mona Patel, 2005, Bioorganic & medicinal chemistry letters.

Phosphorylation Validation of a Cell-Based Screen for Insulin Receptor Modulators by Quantification of Insulin Receptor

B. Conway, L. Minor, K. Demarest, 2013 .

Validation of a Cell-Based Screen for Insulin Receptor Modulators by Quantification of Insulin Receptor Phosphorylation

M. Wildey, B. Conway, L. Minor, 2003, Journal of biomolecular screening.

Synthesis and evaluation of 3-anilino-quinoxalinones as glycogen phosphorylase inhibitors.

M. P. Beavers, Yongzhen Zhang, B. Conway, 2005, Bioorganic & medicinal chemistry letters.

Interactions of Cbl with Grb2 and phosphatidylinositol 3'-kinase in activated Jurkat cells

M. Czech, B. Conway, D. Hartley, 1995, Molecular and cellular biology.

Human cardiomyocytes express high level of Na+/glucose cotransporter 1 (SGLT1)

M. D'Andrea, S. Belkowski, B. Conway, 2003, Journal of cellular biochemistry.

Indole-glucosides as novel sodium glucose co-transporter 2 (SGLT2) inhibitors. Part 2.

M. P. Beavers, B. Conway, K. Demarest, 2006, Bioorganic & medicinal chemistry letters.

Glycosylated dihydrochalcones as potent and selective sodium glucose co-transporter 2 (SGLT2) inhibitors.

B. Conway, K. Demarest, P. Rybczynski, 2004, Bioorganic & medicinal chemistry letters.

Heteroaryl‐O‐glucosides as Novel Sodium Glucose Co‐Transporter 2 Inhibitors. Part 1.

M. P. Beavers, B. Conway, K. Demarest, 2006 .

Regulation of phosphatidylinositol 4-kinase activity in rat pancreatic acini.

M. Withiam-Leitch, B. Conway, R. Rubin, 1993, Molecular pharmacology.

Analysis of the regulation of phosphatidylinositol-4,5-bisphosphate synthesis by arachidonic acid in exocrine pancreas.

S. G. Laychock, B. Conway, R. Rubin, 1989, Archives of biochemistry and biophysics.

Indole-glucosides as novel sodium glucose co-transporter 2 (SGLT2) inhibitors. Part 2.

M. P. Beavers, B. Conway, K. Demarest, 2006, Bioorganic & medicinal chemistry letters.

Discovery of (R)-2-amino-6-borono-2-(2-(piperidin-1-yl)ethyl)hexanoic acid and congeners as highly potent inhibitors of human arginases I and II for treatment of myocardial reperfusion injury.

E. Howard, A. Mitschler, M. V. Van Zandt, 2013, Journal of medicinal chemistry.

Design, synthesis, and biological evaluation of novel 7-azaindolyl-heteroaryl-maleimides as potent and selective glycogen synthase kinase-3β (GSK-3β) inhibitors

G. Kuo, B. Maryanoff, W. Murray, 2004 .

Synthesis of quaternary α-amino acid-based arginase inhibitors via the Ugi reaction.

A. Mitschler, M. V. Van Zandt, A. Podjarny, 2013, Bioorganic & medicinal chemistry letters.

Synthesis and biological evaluation of novel macrocyclic bis-7-azaindolylmaleimides as potent and highly selective glycogen synthase kinase-3β (GSK-3β) inhibitors☆

Xin Chen, C. Prouty, M. P. Beavers, 2004 .

Disassembly of Son-of-sevenless Proteins from Grb2 during p21 Desensitization by Insulin (*)

A. Cherniack, M. Czech, J. Klarlund, 1995, The Journal of Biological Chemistry.

Macrocyclic bisindolylmaleimides as inhibitors of protein kinase C and glycogen synthase kinase-3.

S. Emanuel, H. Ye, C. Derian, 2003, Bioorganic & medicinal chemistry letters.

Biochemical lesions in DNA associated with the antiproliferative effects of mitoxantrone in the hepatoma cell.

D. Gewirtz, J. Randolph, B. Conway, 1990, Biochemical pharmacology.

Cell-based, high-content screen for receptor internalization, recycling and intracellular trafficking.

Y. T. Chen, R. Ghosh, B. Conway, 2000, BioTechniques.

Effect of Canagliflozin on Renal Threshold for Glucose, Glycemia, and Body Weight in Normal and Diabetic Animal Models

F. Du, J. Conway, Yi Liu, 2012, PloS one.

Comparative effects of epidermal growth factor and carbachol on phosphoinositide synthesis and breakdown in pancreatic acinar cells.

S. G. Laychock, B. Conway, R. Rubin, 1991, Biochemical and biophysical research communications.

Targeting Acidic Mammalian chitinase Is Effective in Animal Model of Asthma.

J. Gołąb, Firas Fadel, A. Mitschler, 2018, Journal of medicinal chemistry.

The use of biosensors to study GPCR function: applications for high-content screening.

B. Conway, K. Demarest, 2002, Receptors & channels.

Synthesis and biological evaluation of novel macrocyclic bis-7-azaindolylmaleimides as potent and highly selective glycogen synthase kinase-3 beta (GSK-3 beta) inhibitors.

Xin Chen, C. Prouty, M. P. Beavers, 2004, Bioorganic & Medicinal Chemistry.

Substituted pyrrolines useful as kinase inhibitors.

D. McComsey, B. Maryanoff, B. Conway, 2003 .