Michael Doyle
Novartis
26 Papers
239 Citations
Michael Doyle is an academic researcher from Novartis. The author has contributed to research in topics: Urokinase receptor & Receptor. The author has an hindex of 15, co-authored 26 publications. Previous affiliations of Michael Doyle include Chiron Corporation.
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Papers
Regulation of Integrin Function by the Urokinase Receptor
Ying Wei,Matvey Lukashev,Daniel I. Simon,Sarah C. Bodary,Steven Rosenberg,Michael Doyle,Harold A. Chapman +6 more
TL;DR: The urokinase-type plasminogen activator receptor (uPAR) and integrins formed stable complexes that both inhibited native integrin adhesive function and promoted adhesion to vitronectin via a ligand binding site on uPAR.
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Patent
Human IL-2 as a vaccine adjuvant
Michael Doyle,Arthur D. Newell,Jack H. Nunberg,Thomas James White +3 more
- 24 Feb 1989
TL;DR: In this paper, the authors proposed methods for enhancing the immune response to vaccination in animals, including humans, comprising administering interleukin-2 (IL-2) as part of the vaccination regimen, preferably for 5 to 14 days post-vaccination.
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Inhibitors of Helicobacter pylori ATPase Cagα block CagA transport and cag virulence
Markus Hilleringmann,Werner Pansegrau,Michael Doyle,Susan Kaufman,Mary Lee MacKichan,Claudia Gianfaldoni,Paolo Ruggiero,Antonello Covacci +7 more
TL;DR: Small-molecule Cagalpha inhibitors, the first described inhibitors of a TFSS, are potential candidates for the development of new antibacterial compounds that may lead to alternative medical treatments, since they target virulence functions.
Urokinase receptor antagonists: discovery and application to in vivo models of tumor growth.
Robert J. Tressler,Patrice A. Pitot,Jennifer R. Stratton,Louise D. Forrest,Shaoqiu Zhuo,Robert J. Drummond,Susan Fong,Michael Doyle,Laura V. Doyle,Hye Yeong Min,Steven Rosenberg +10 more
TL;DR: Protein uPA receptor antagonists were tested in an in vivo tumor model using the human breast carcinoma MDAmb231 in immunodeficient mice and showed significant inhibition of primary tumor growth, demonstrating that in vivo, both tumor and stromal cell u PA receptor dependent plasminogen activation can modulate tumor growth.
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Scanning whole cells with phage‐display libraries: Identification of peptide ligands that modulate cell function
TL;DR: It is believed that this strategy, which requires neither purification nor prior knowledge of a particular target receptor, will prove to be generally useful for identifying peptide ligands that influence cellular function.
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