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Randal C. Jaffe

Researcher at University of Illinois at Chicago

Publications -  52
Citations -  1803

Randal C. Jaffe is an academic researcher from University of Illinois at Chicago. The author has contributed to research in topics: Oviduct & Receptor. The author has an hindex of 22, co-authored 52 publications receiving 1750 citations. Previous affiliations of Randal C. Jaffe include Schering AG & University of Illinois at Urbana–Champaign.

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Cyclic changes in ciliation, secretion and cell height of the oviductal epithelium in women.

TL;DR: It appears that the serum levels of estradiol were adequate to maintain a mature epithelium at all the reproductive stages included in this study, however, progesterone, when present, blocked the growth-promoting effect of Estradiol in the oviduct.
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Corticosterone concentrations in mice during ethanol drinking and withdrawal.

TL;DR: Ethanol withdrawal symptoms followed the removal of ethanol from the diet and circulating corticosterone concentrations were further increased, and there was no correlation between blood ethanol and glucocorticoid concentrations during the chronic ethanol treatment.
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Complementary Deoxyribonucleic Acid Cloning and Molecular Characterization of an Estrogen-Dependent Human Oviductal Glycoprotein

TL;DR: The presence of significantly greater amounts of the mRNA during the late follicular phase of the menstrual cycle is consistent with the proposed estrogen control and isolated the complete cDNA for a human oviductal glycoprotein.
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The impact of ovulation on fallopian tube epithelial cells: evaluating three hypotheses connecting ovulation and serous ovarian cancer

TL;DR: An immortalized baboon TEC cell line and a three-dimensional organ culture system for mouse oviduct and baboon fallopian tubes were developed to determine which components of ovulation contributed to DNA damage in the fallopian tube.
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Regulation of Insulin-Like Growth Factor Binding Protein-1 Promoter Activity by FKHR and HOXA10 in Primate Endometrial Cells

TL;DR: These studies show that FKHR and HOXA10 interact directly and can function cooperatively to stimulate IGFBP-1 promoter activity in endometrial cells and perhaps in other settings.