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Journal of Investigative Dermatology
Article
License: Elsevier Non-Commercial
Data sources: UnpayWall
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Journal of Investigative Dermatology
Article . 1997
License: Elsevier Non-Commercial
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Journal of Investigative Dermatology
Article . 1997 . Peer-reviewed
License: Elsevier Non-Commercial
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The Epidermis: Genes On – Genes Off

Authors: Richard L. Eckert; Jean F. Welter; Eric B. Banks; James F. Crish;

The Epidermis: Genes On – Genes Off

Abstract

The epidermal keratinocyte stem cell is distinguished by a relatively undifferentiated phenotype and an ability to proliferate. As part of a carefully orchestrated process, the offspring of these stem cells lose the ability to proliferate and begin a process of morphologic and biochemical transformation that results in their conversion into corneocytes. This process requires the coordinated expression of a host of cellular genes. The mechanisms responsible for regulation of these genes is an area of intense interest. In keratinocytes, as in other cell types, the expression of most genes is regulated at the transcriptional level by a class of proteins called transcription factors. Transcription factors are nuclear proteins that regulate transcription by mediating the final steps in the relay of information from the cell surface to the nucleus and the gene. These factors bind to specific DNA sequence elements located within the target gene. In this brief review we summarize evidence implicating activator protein 1 (AP1), AP2, Sp1, POU domain, CCAAT enhancer binding protein, and several other transcription factors as regulators of expression of keratinocyte genes.

Related Organizations
Keywords

Keratinocytes, Cell Biology, Dermatology, Biochemistry, Suppression, Genetic, Epidermal Cells, Gene Expression Regulation, Animals, Humans, kertinocyte, Epidermis, gene regulation, AP1, Molecular Biology, transcription factor, Transcription Factors

  • BIP!
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    citations
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    184
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
184
Top 10%
Top 10%
Top 1%
hybrid