Quantification of Gi-Mediated Inhibition of Adenylyl Cyclase Activity Reveals That UDP Is a Potent Agonist of the Human P2Y14 Receptor von Carter, Rhonda L, Fricks, Ingrid P, Barrett, Matthew O, Burianek, Lauren E, Zhou, Yixing, Ko, Hyojin, Das, Arijit, Jacobson, Kenneth A, Lazarowski, Eduardo R, Harden, T Kendall

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Gi-Dependent Cell Signaling Responses of the Human P2Y14 Receptor in Model Cell Systems von Fricks, Ingrid P, Carter, Rhonda L, Lazarowski, Eduardo R, Harden, T Kendall

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Polyamidoamine (PAMAM) Dendrimer Conjugates of “Clickable” Agonists of the A3 Adenosine Receptor and Coactivation of the P2Y14 Receptor by a Tethered Nucleotide von Tosh, Dilip K, Yoo, Lena S, Chinn, Moshe, Hong, Kunlun, Kilbey, S. Michael, Barrett, Matthew O, Fricks, Ingrid P, Harden, T. Kendall, Gao, Zhan-Guo, Jacobson, Kenneth A

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Molecular recognition in the P2Y14 receptor: Probing the structurally permissive terminal sugar moiety of uridine-5'-diphosphoglucose von KO, Hyojin, DAS, Rijit, KIRK, Kenneth L, KENDALL HARDEN, T, JACOBSON, Kenneth A, CARTER, Rhonda L, FRICKS, Ingrid P, YIXING ZHOU, IVANOV, Andrei A, MELMAN, Artem, JOSHI, Bhalchandra V, KOVAC, Pavol, HAJDUCH, Jan

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Molecular recognition in the P2Y(14) receptor: Probing the structurally permissive terminal sugar moiety of uridine-5'-diphosphoglucose von Ko, Hyojin, Das, Arijit, Carter, Rhonda L, Fricks, Ingrid P, Zhou, Yixing, Ivanov, Andrei A, Melman, Artem, Joshi, Bhalchandra V, Kovác, Pavol, Hajduch, Jan, Kirk, Kenneth L, Harden, T Kendall, Jacobson, Kenneth A

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G i -Dependent Cell Signaling Responses of the Human P2Y 14 Receptor in Model Cell Systems von Fricks, Ingrid P., Carter, Rhonda L., Lazarowski, Eduardo R., Harden, T. Kendall

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Quantification of G i -Mediated Inhibition of Adenylyl Cyclase Activity Reveals That UDP Is a Potent Agonist of the Human P2Y 14 Receptor von Carter, Rhonda L., Fricks, Ingrid P., Barrett, Matthew O., Burianek, Lauren E., Zhou, Yixing, Ko, Hyojin, Das, Arijit, Jacobson, Kenneth A., Lazarowski, Eduardo R., Harden, T. Kendall

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Polyamidoamine (PAMAM) Dendrimer Conjugates of “Clickable” Agonists of the A 3 Adenosine Receptor and Coactivation of the P2Y 14 Receptor by a Tethered Nucleotide von Tosh, Dilip K., Yoo, Lena S., Chinn, Moshe, Hong, Kunlun, Kilbey, S. Michael, Barrett, Matthew O., Fricks, Ingrid P., Harden, T. Kendall, Gao, Zhan-Guo, Jacobson, Kenneth A.

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Polyamidoamine (PAMAM) Dendrimer Conjugates of "Clickable" Agonists of the A^sub 3^ Adenosine Receptor and Coactivation of the P2Y^sub 14^ Receptor by a Tethered Nucleotide von Tosh, Dilip K, Yoo, Lena S, Chinn, Moshe, Hong, Kunlun, Kilbey, S Michael, Barrett, Matthew O, Fricks, Ingrid P, Hardens, T Kendall, Gao, Zhan-Guo, Jacobson, Kenneth A

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UDP is an antagonist at the hP2Y14 receptor von Fricks, Ingrid P., Maddileti, Savitri, Lazarowski, Eduardo R., Nicholas, Robert A., Jacobson, Kenneth A., Harden, T. Kendall

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Molecular recognition in the P2Y sub(14) receptor: Probing the structurally permissive terminal sugar moiety of uridine-5'-diphosphoglucose von Ko, Hyojin, Das, Arijit, Carter, Rhonda L, Fricks, Ingrid P, Zhou, Yixing, Ivanov, Andrei A, Melman, Artem, Joshi, Bhalchandra V, Kovac, Pavol, Hajduch, Jan, Kirk, Kenneth L, Harden, TKendall, Jacobson, Kenneth A

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Molecular Recognition in the P2Y14 Nucleotide Receptor: Probing the Structurally Permissive Terminal Sugar Moiety of Uridine-5′-diphosphoglucose von Ko, Hyojin, Das, Arijit, Carter, Rhonda L., Fricks, Ingrid P., Zhou, Yixing, Ivanov, Andrei A., Melman, Artem, Joshi, Bhalchandra V., Kováč, Pavol, Hajduch, Jan, Kirk, Kenneth L., Harden, T. Kendall, Jacobson, Kenneth A.

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Molecular recognition in the P2Y 14 receptor: Probing the structurally permissive terminal sugar moiety of uridine-5′-diphosphoglucose von Ko, Hyojin, Das, Arijit, Carter, Rhonda L., Fricks, Ingrid P., Zhou, Yixing, Ivanov, Andrei A., Melman, Artem, Joshi, Bhalchandra V., Kováč, Pavol, Hajduch, Jan, Kirk, Kenneth L., Harden, T. Kendall, Jacobson, Kenneth A.

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Comparison of 2 Transvaginal Surgical Approaches and Perioperative Behavioral Therapy for Apical Vaginal Prolapse: The OPTIMAL Randomized Trial von Barber, Matthew D, Brubaker, Linda, Burgio, Kathryn L, Richter, Holly E, Nygaard, Ingrid, Weidner, Alison C, Menefee, Shawn A, Lukacz, Emily S, Norton, Peggy, Schaffer, Joseph, Nguyen, John N, Borello-France, Diane, Goode, Patricia S, Jakus-Waldman, Sharon, Spino, Cathie, Warren, Lauren Klein, Gantz, Marie G, Meikle, Susan F

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Saxagliptin is non-inferior to glipizide in patients with type 2 diabetes mellitus inadequately controlled on metformin alone: a 52-week randomised controlled trial von Göke, B., Gallwitz, B., Eriksson, J., Hellqvist, Å., Gause-Nilsson, I.

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