J
Jeffrey Alan Dodge
Researcher at Eli Lilly and Company
Publications - 107
Citations - 3407
Jeffrey Alan Dodge is an academic researcher from Eli Lilly and Company. The author has contributed to research in topics: Estrogen receptor & Estrogen. The author has an hindex of 32, co-authored 107 publications receiving 3273 citations. Previous affiliations of Jeffrey Alan Dodge include Indiana University & University of Texas at Austin.
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Efficacious modification of the mitsunobu reaction for inversions of sterically hindered secondary alcohols
TL;DR: In this article, a modification of the Mitsunobu protocol for effecting stereochemical inversions of alcohols has been discovered in which use of p-nitrobenzoic acid as the nucleophilic partner results in significantly improved yields with relatively hindered substrates.
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Molecular determinants of tissue selectivity in estrogen receptor modulators
Timothy Alan Grese,James P. Sluka,Henry Uhlman Bryant,George Joseph Cullinan,Andrew L. Glasebrook,Charles David Jones,Ken Matsumoto,Alan David Palkowitz,Masahiko Sato,John David Termine,Mark A. Winter,Na N. Yang,Jeffrey Alan Dodge +12 more
TL;DR: Structural differences between raloxifene and tamoxifen may influence the conformations of their respective receptor/ligand complexes, thereby affecting which estrogen-responsive genes are modulated in various tissues, indicating that differences in tissue selective actions among benzothiophene and triarylethylene estrogen receptor modulators can be ascribed to discrete ligand conformations.
Journal ArticleDOI
DNA binding alters coactivator interaction surfaces of the intact VDR–RXR complex
Jun Zhang,Michael J. Chalmers,Keith R. Stayrook,Lorri L Burris,Yongjun Wang,Scott A. Busby,Bruce D. Pascal,Ruben D. Garcia-Ordonez,John B. Bruning,Monica A. Istrate,Douglas J. Kojetin,Jeffrey Alan Dodge,Thomas P. Burris,Patrick R. Griffin +13 more
TL;DR: It is shown that binding of intact heterodimer to DNA alters the receptor dynamics in regions remote from the DNA-binding domains (DBDs), including the coactivator binding surfaces of both co-receptors, and that the sequence of the DNA response element can determine these dynamics.
Journal ArticleDOI
Environmental estrogens: effects on cholesterol lowering and bone in the ovariectomized rat.
Jeffrey Alan Dodge,Andrew L. Glasebrook,Magee David Edward,David Lynn Phillips,Masahiko Sato,Lorri L. Short,Henry Uhlman Bryant +6 more
TL;DR: Representative non-steroidal estrogens, from common environmental sources such as plants, pesticides, surfactants, plastics, and animal health products, demonstrated an ability to lower serum cholesterol and prevent bone loss in an estrogen-dependent animal model, the ovariectomized rat.