B
Benita S. Katzenellenbogen
Researcher at University of Illinois at Urbana–Champaign
Publications - 403
Citations - 41240
Benita S. Katzenellenbogen is an academic researcher from University of Illinois at Urbana–Champaign. The author has contributed to research in topics: Estrogen receptor & Estrogen. The author has an hindex of 113, co-authored 394 publications receiving 39585 citations. Previous affiliations of Benita S. Katzenellenbogen include Dartmouth College & University of Cincinnati.
Papers
More filters
Journal ArticleDOI
Estrogen-Induced CCN1 Is Critical for Establishment of Endometriosis-Like Lesions in Mice
Yuechao Zhao,Quanxi Li,Benita S. Katzenellenbogen,Lester F. Lau,Robert N. Taylor,Indrani C. Bagchi,Milan K. Bagchi +6 more
TL;DR: Results suggest that CCN1, acting downstream of E, critically controls cell proliferation and neovascularization, which support the growth and survival of endometriotic tissue at ectopic sites.
Journal ArticleDOI
Multiple Beneficial Roles of Repressor of Estrogen Receptor Activity (REA) in Suppressing the Progression of Endometriosis.
Yuechao Zhao,Yiru Chen,Ye Kuang,Milan K. Bagchi,Robert N. Taylor,John A. Katzenellenbogen,Benita S. Katzenellenbogen +6 more
TL;DR: REA modulates cross talk among multiple cell types in the uterine tissue and host background, serving as a brake on the estradiol-ER axis and restraining multiple aspects that contribute to the pathologic progression of endometriosis.
Journal ArticleDOI
Nitrosourea and nitrosocarbamate derivatives of the antiestrogen tamoxifen as potential estrogen receptor-mediated cytotoxic agents in human breast cancer cells.
Lisa L. Wei,Lisa L. Wei,Benita S. Katzenellenbogen,Benita S. Katzenellenbogen,David Wayne Robertson,David Wayne Robertson,David M. Simpson,David M. Simpson,John A. Katzenellenbogen,John A. Katzenellenbogen +9 more
TL;DR: It appears likely that the toxic activity displayed by hormone-cytotoxic conjugates is mediated by receptor interactions and whether it operates through the intended toxic mechanism, rather than from a direct receptor-mediated, DNA-directed cytotoxic action of TAM-NU itself.
Anti-estrogen Interaction with Uterine Estrogen Receptors
TL;DR: Radiolabeled anti-estrogen of high specific ac- tivity and radiochemical purity has been prepared by catalytic tritium-iodine exchange and purified by alumina column chromatography and has a lower binding affinity than estradiol.
Journal ArticleDOI
Corrigendum: NFκB selectivity of estrogen receptor ligands revealed by comparative crystallographic analyses (Nature Chemical Biology (2008) 4, (241-247))
Kendall W. Nettles,John B. Bruning,German Gil,Jason Nowak,Sanjay Sharma,Johnnie B. Hahm,Kristen S. Kulp,Richard B. Hochberg,Hai-Bing Zhou,John A. Katzenellenbogen,Benita S. Katzenellenbogen,Younchang Kim,Andrzej Joachimiak,Geoffrey L. Greene +13 more
TL;DR: Corrigendum: NFκB selectivity of estrogen receptor ligands revealed by comparative crystallographic analyses suggests thatNFκB ligand selectivity may be related to ‘cell reprograming’ rather than ‘drug-like’ properties.