J
James N. Ingle
Researcher at Mayo Clinic
Publications - 403
Citations - 52917
James N. Ingle is an academic researcher from Mayo Clinic. The author has contributed to research in topics: Breast cancer & Tamoxifen. The author has an hindex of 82, co-authored 387 publications receiving 47883 citations. Previous affiliations of James N. Ingle include McMaster University & University of Rochester.
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Lipid concentrations in postmenopausal women on letrozole after 5 years of tamoxifen: an NCIC CTG MA.17 sub-study
Kishor M. Wasan,Paul E. Goss,P. Haydn Pritchard,Lois E. Shepherd,Dongsheng Tu,James N. Ingle +5 more
TL;DR: Significant increases in total cholesterol, HDL cholesterol, LDL cholesterol, and, most notably, Lp(a) in postmenopausal women were observed following 5 years of adjuvant letrozole treatment and after 5 years of tamoxifen therapy and such patients should have monitoring of their lipid levels in clinical practice.
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Tamoxifen Metabolism and Breast Cancer Recurrence: A Question Unanswered by CYPTAM.
Matthew P. Goetz,Vera J. Suman,Yusuke Nakamura,Kazuma Kiyotani,V. Craig Jordan,James N. Ingle +5 more
Journal Article
Randomized clinical trial of cyclophosphamide, 5-FU, and prednisone with or without tamoxifen in postmenopausal women with advanced breast cancer
James E. Krook,James N. Ingle,Green Sj,Bowman Wd,L K Everson,H E Windschitl,Marschke Rf,J A Laurie,Stephen A. Cullinan,Pfeifle Dm +9 more
TL;DR: It can be concluded that the addition of tamoxifen to CFP does not substantially improve either the time to disease progression or survival in women with metastatic breast cancer.
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TCL1A Single-Nucleotide Polymorphisms and Estrogen-Mediated Toll-Like Receptor-MYD88-Dependent Nuclear Factor-κB Activation: Single-Nucleotide Polymorphism- and Selective Estrogen Receptor Modulator-Dependent Modification of Inflammation and Immune Response.
Ming Fen Ho,James N. Ingle,Tim Bongartz,Krishna R. Kalari,Paul E. Goss,Lois E. Shepherd,Taisei Mushiroda,Michiaki Kubo,Liewei Wang,Richard M. Weinshilboum +9 more
TL;DR: In this paper, the authors investigated the effect of single nucleotide polymorphisms (SNPs) near the TCL1A gene on NF-κB transcriptional activity and showed that this SNPdependent regulation could be reversed by selective ER modulators.
Journal ArticleDOI
Pharmacogenetics and pharmacogenomics of endocrine agents for breast cancer
TL;DR: The clinician caring for women with early breast cancer is keenly aware of the variability observed when endocrine therapy with tamoxifen or the aromatase inhibitors (AIs) is employed, in which some women develop disabling musculoskeletal events that result in their discontinuing therapy, whereas the majority develops no such adverse events.