E
Eric R. Fearon
Researcher at University of Michigan
Publications - 183
Citations - 55140
Eric R. Fearon is an academic researcher from University of Michigan. The author has contributed to research in topics: Wnt signaling pathway & Gene. The author has an hindex of 84, co-authored 179 publications receiving 52910 citations. Previous affiliations of Eric R. Fearon include Johns Hopkins University School of Medicine & Johns Hopkins University.
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Diagnostic method detecting loss of wild-type p53
TL;DR: In this paper, both deletion mutations and point mutations in p53 are observed in the same human tumor cells and these mutations are clonal within the cells of the tumor, and loss of wild-type p53 genes is responsible for neoplastic progression.
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Drosophila split ends homologue SHARP functions as a positive regulator of Wnt/beta-catenin/T-cell factor signaling in neoplastic transformation.
Ying Feng,Guido T. Bommer,Yali Zhai,Aytekin Akyol,Takao Hinoi,Ira Winer,Hua V. Lin,Ken M. Cadigan,Kathleen R. Cho,Eric R. Fearon +9 more
TL;DR: Findings implicate SHARP as an important positive regulator of Wnt signaling in cancers with beta-catenin dysregulation.
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CDX2 Regulates Multidrug Resistance 1 Gene Expression in Malignant Intestinal Epithelium
Yuji Takakura,Takao Hinoi,Naohide Oue,Tatsunari Sasada,Yasuo Kawaguchi,Masazumi Okajima,Aytekin Akyol,Aytekin Akyol,Eric R. Fearon,Wataru Yasui,Hideki Ohdan +10 more
TL;DR: CDX2 is probably important for basal expression of MDR1, regulating drug excretion and absorption in the lower gastrointestinal tract, as well as for multidrug resistance to chemotherapy reagent in CDX2-positive gastrointestinal cancers.
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PARsing the phrase "all in for Axin"- Wnt pathway targets in cancer.
TL;DR: In insights into the role of tankyrase in regulating the Wnt/beta-catenin pathway, it is suggested that compounds targeting tankyr enzyme's poly-ADP-ribosylation (PARsylation) activity may hold promise for cancer therapy.
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CDX2 polymorphisms, RNA expression, and risk of colorectal cancer.
Laura S. Rozek,Steven M. Lipkin,Eric R. Fearon,Samir M. Hanash,Thomas J. Giordano,Joel K. Greenson,Rork Kuick,David E. Misek,Jeremy M. G. Taylor,Julie A. Douglas,Gad Rennert,Gad Rennert,Stephen B. Gruber +12 more
TL;DR: It is unlikely that common CDX2 variants account for a measurable fraction of susceptibility to colorectal cancer in this population, butCDX2 expression levels were strongly associated with microsatellite instability and tumor location in the gastrointestinal tract, consistent with a possible role in the specification of gastrointestinal epithelial cell fate in humans.