Erin A. Kimbrel, Ph.D. - Publications
Affiliations: | 2002 | Duke University, Durham, NC |
Area:
Pharmacology, Molecular BiologyYear | Citation | Score | |||
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2010 | Kobayashi S, Stice JP, Kazmin D, Wittmann BM, Kimbrel EA, Edwards DP, Chang CY, McDonnell DP. Mechanisms of progesterone receptor inhibition of inflammatory responses in cellular models of breast cancer. Molecular Endocrinology (Baltimore, Md.). 24: 2292-302. PMID 20980435 DOI: 10.1210/Me.2010-0289 | 0.568 | |||
2010 | Kobayashi S, Stice JP, Kazmin D, Wittmann BM, Kimbrel EA, Edwards DP, Chang C, McDonnell DP. Mechanisms of Progesterone Receptor Inhibition of Inflammatory Responses in Cellular Models of Breast Cancer Endocrine Reviews. 31: 5457-5457. DOI: 10.1210/Edrv.31.6.9984 | 0.525 | |||
2003 | Kimbrel EA, McDonnell DP. Function and mode of action of nuclear receptors: Estrogen, progesterone, and vitamin D Pure and Applied Chemistry. 75: 1671-1683. DOI: 10.1351/Pac200375111671 | 0.554 | |||
2002 | Li X, Kimbrel EA, Kenan DJ, McDonnell DP. Direct interactions between corepressors and coactivators permit the integration of nuclear receptor-mediated repression and activation. Molecular Endocrinology (Baltimore, Md.). 16: 1482-91. PMID 12089344 DOI: 10.1210/Mend.16.7.0860 | 0.528 | |||
2000 | Giangrande PH, Kimbrel EA, Edwards DP, McDonnell DP. The opposing transcriptional activities of the two isoforms of the human progesterone receptor are due to differential cofactor binding. Molecular and Cellular Biology. 20: 3102-15. PMID 10757795 DOI: 10.1128/Mcb.20.9.3102-3115.2000 | 0.573 | |||
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