J
Jerrold M. Olefsky
Researcher at University of California, San Diego
Publications - 606
Citations - 83310
Jerrold M. Olefsky is an academic researcher from University of California, San Diego. The author has contributed to research in topics: Insulin & Insulin resistance. The author has an hindex of 143, co-authored 595 publications receiving 77356 citations. Previous affiliations of Jerrold M. Olefsky include University of Colorado Boulder & University of Michigan.
Papers
More filters
Journal ArticleDOI
Amylin Release During Oral Glucose Tolerance Test: AMYLIN RELEASE DURING ORAL GLUCOSE TOLERANCE TEST
Karl Thomaseth,Giovanni Pacini,Martin Clodi,Alexandra Kautzky-Willer,John J. Nolan,R. Prager,Jerrold M. Olefsky,Bernhard Ludvik +7 more
Journal ArticleDOI
Preparation of insulin-like growth factor I and photoaffinity labeling of insulin-like growth factor I receptor
TL;DR: A 120-kDa band, the α subunit of the IGF-I receptor, was specifically labeled in Rat-1 plasma membranes by this photoprobe, indicating the specificity of the photolabeling of the insulin-like growth factor I receptor by this fully active IGF-
Book ChapterDOI
Properties of a Mutant Insulin Species Causing Human Diabetes
Jerrold M. Olefsky,Mark Saekow,Masashi Kobayashi,O. Kolterman,H. Tager,B D Given,D. Baldwin,Mary E. Mako,James J Markese,A.M. Hubenstein,H. Poucher +10 more
Journal ArticleDOI
Photolabeling of the adipocyte hexose carrier with an aryl azide derivative of maltose
TL;DR: These studies show the suitability of using carbon-1-modified sugar photoaffinity labels as probes for the hexose carrier and possibly of its regulation in rat adipocytes.
Patent
Metformin in the treatment of hyperglycemic conditions
Sanford A. Garfield,George A. Bray,Wilfred Y. Fujimoto,Dorothy Gohdes,Edward S. Horton,Steven E. Kahn,William C. Knowler,Boyd E. Metzger,Mark E. Molitch,David M. Nathan,Jerrold M. Olefsky,David Schade,Robert S. Schwartz,Harry Shamoon,Julio V. Santiago +14 more
TL;DR: In this article, the antiglycemic antidiabetic agent is administered to the subject for a period sufficient to alleviate impaired glucose tolerance (IGT) or inhibit the onset of type II diabetes.