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Two pathways for serum regulation of the c-fos serum response element require specific sequence elements and a minimal domain of serum response factor.

Data up to Jan 2025

Published1994
Citations142
References49

Total Citations Per Year

Abstract

References (49)

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1988 • 245 citations

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Displacement of BrdUrd-induced YY1 by serum response factor activates skeletal alpha-actin transcription in embryonic myoblasts.

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Casein kinase II enhances the DNA binding activity of serum response factor.

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1988 • 180 citations

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Casein kinase II phosphorylation increases the rate of serum response factor-binding site exchange.

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The yeast transcription activator PRTF, a homolog of the mammalian serum response factor, is encoded by the MCM1 gene.

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Ternary complex formation over the c-fos serum response element: p62TCF exhibits dual component specificity with contacts to DNA and an extended structure in the DNA-binding domain of p67SRF.

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Casein kinase II induces c-fos expression via the serum response element pathway and p67SRF phosphorylation in living fibroblasts.

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Maximal serum stimulation of the c-fos serum response element requires both the serum response factor and a novel binding factor, SRE-binding protein.

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Two pathways for serum regulation of the c-fos serum response element require specific… (1994) – Molecular and Cellular Biology | Metascience Observatory Explorer