Titlebook: Gene Regulation by Steroid Hormones IV; Arun K. Roy,James H. Clark Conference proceedings 1989 Springer-Verlag New York, Inc. 1989 DNA.EGF

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Inhibition of Cell Proliferation by a Nuclear Type II Ligand: Methyl P-Hydroxyphenylactate,tes bind to [.H]estradiol with a relatively low affinity (Markaverich and Clark, 1979) and have a higher affinity for the endogenous ligands (Markaverich .., 1983; 1984), we proposed that these compounds may regulate cell growth by their association with unclear type II binding sites. This hypothesi

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Conference proceedings 1989of a large gene family that includes steroid hormone receptors, transcription factors, protooncogenes and homeobox proteins. Thus a great deal has been learned, but as usual, questions remain. Many of these questions are posed by the findings and observations found in several chapters in this volume

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narcissism

Regulation of Glucocorticoid Receptor Protein and Gene Expression by Glucocorticoids,sed models for the structure of the glucocorticoid receptor (GR) have the common feature that the receptor exists as an oligomeric protein complex that consists of one or more subunits complexed with non-steroid-binding proteins such as the heat shock protein 90 (hsp90). Dissociation of the oligomer

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Differential Regulation of Tyrosine Amino-Transferase by Glucocorticoids: Transcriptional and Post-et al., 1957; Lin et al., 1958; Greengard et al.). By establishing a line of liver-derived hepatoma cells (HTC cells), it was possible to resolve clearly several issues not easy to work out in whole animal or whole-organ systems (Thompson et al., 1966). Among these were the fact that in HTC cells, t

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GHF-1, a Tissue-Specific Transcription Factor, is a Homeobox Protein,ors of lactotropes (GH., PRL.), the last cell type to appear along this lineage (Hoeffler et al., 1985; Behringer et al., 1988). Various data indicate the existence of a subpopulation of GH. cells which can switch to PRL. cells and PRL. cells which can switch to GH. cells, under the influence of cer

知識(shí)分子

Regulation of EGF Receptors and Nuclear Protooncogenes by Estrogen,in organ cultures (McLachlan et al.). Consequently, our laboratories have studied the in vivo induction of the nuclear protooncogene c-fos (Loose-Mitchell et al.) and the EGF receptor (Lingham et al.; Mukku et al., 1985a) by estrogens.

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