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    <title>Habets, G.</title>
    <link>http://repub.eur.nl/res/aut/2619/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Nuclear protein factors and erythroid transcription of the human A γ-globin gene. (Article)</title>
      <link>http://repub.eur.nl/res/pub/2436/</link>
      <pubDate>1989-01-01T00:00:00Z</pubDate>
      <description>We have used DNaseI footprinting and gel mobility assays to analyze the upstream region of the human A gamma-globin gene promoter. Four protein factors were found to bind this region. A non-erythroid factor present in the 0.4M KCl fraction of a heparin agarose column binds to the CAC box (-140). A ubiquitous octamer factor present in the 0.2M fraction binds to an ATGCAAT element (-175), but is completed out by the erythroid specific factor NF-E1 (in the 0.4M KCl fraction), which binds a site (-186) immediately flanking the octamer. A novel factor binding to a stretch of 8A around -233, was identified in the 0.2M KCl fraction. This factor is not present in HeLa nuclear extracts. To study the transcriptional importance of these protein binding sites we have used an "A gamma-minilocus", similar to that described for the beta-globin gene (1) in K562 cells. This provides evidence that the NF-E1 and CAC box in the -210 to -122 region of the A gamma-promoter are important for the efficient expression of the gamma-globin gene.</description>
    </item> <item>
      <title>The human β-globin gene contains multiple regulatory regions: identification of one promoter and two downstream enhancers. (Article)</title>
      <link>http://repub.eur.nl/res/pub/2426/</link>
      <pubDate>1988-01-01T00:00:00Z</pubDate>
      <description>We have introduced into murine erythroleukaemia (MEL) cells several series of deletion mutants of hybrid genes between the human beta-globin gene and the murine H-2Kb gene. S1 nuclease and transcriptional run-off analysis showed that the human beta-globin gene contains at least three globin specific transcriptional control elements. One is a promoter element and is located 160 bp upstream from the transcription initiation site; it increases the efficiency of the promoter after MEL cells are induced to differentiate. The other two elements are tissue-specific transcriptional enhancers and are located downstream from the transcription initiation site, the first in the structural beta-globin gene and the second in the 3' flanking sequences.</description>
    </item> <item>
      <title>The Regulation of expression of human β-globin genes. UCLA Symposia (Proceedings) on Molecular and Cellular Biology. "Molecular Approaches to Developmental Biology". (In Book)</title>
      <link>http://repub.eur.nl/res/pub/2410/</link>
      <pubDate>1987-01-01T00:00:00Z</pubDate>
      <description></description>
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