<?xml version="1.0" encoding="UTF-8" standalone="no" ?>
<rss version="2.0">
  <channel>
    <title>Cheah, K.S.E.</title>
    <link>http://repub.eur.nl/res/aut/8847/</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>Isolation and characterization of the human collagen α1(I)-like gene from a cosmid library. (Article)</title>
      <link>http://repub.eur.nl/res/pub/2352/</link>
      <pubDate>1994-01-01T00:00:00Z</pubDate>
      <description>We have isolated a human collagen alpha 1(I)-like gene from a cosmid library. The clone which contains 37kb of human DNA has been shown to contain this gene by DNA sequencing, hybrid arrest and hybrid selection assays and Northern blot hybridizations. The collagen gene sequence extends through most of the cloned DNA and must, therefore, be at least 35kb in length.</description>
    </item> <item>
      <title>Identification and characterization of the human type II collagen gene (COL2A1). (Article)</title>
      <link>http://repub.eur.nl/res/pub/2383/</link>
      <pubDate>1985-01-01T00:00:00Z</pubDate>
      <description>The gene contained in the human cosmid clone CosHcol1, previously designated an alpha 1(I) collagen-like gene, has now been identified. CosHcol1 hybridizes strongly to a single 5.9-kilobase mRNA species present only in tissue in which type II collagen is expressed. DNA sequence analysis shows that this clone is highly homologous to the chicken alpha 1(II) collagen gene. These data together suggest that CosHcol1 contains the human alpha 1(II) collagen gene COL2A1. The clone appears to contain the whole gene (30 kilobases in length) and will be extremely useful in the study of cartilage development and for identifying those inherited chondrodystrophies in which defects occur in this gene.</description>
    </item> <item>
      <title>Lethal osteogenesis imperfecta congenita and a 300 base pair gene deletion for an α1(I)-like collagen. (Article)</title>
      <link>http://repub.eur.nl/res/pub/2373/</link>
      <pubDate>1984-01-01T00:00:00Z</pubDate>
      <description>Broad boned lethal osteogenesis imperfecta is a severely crippling disease of unknown cause. By means of recombinant DNA technology a 300 base pair deletion in an alpha 1(I)-like collagen gene was detected in six patients and four complete parent-child groups including patients with this disease. One from each set of the patients' clinically unaffected parents also carried the deletion, implying that affected patients were genetic compounds. The study suggests that prenatal diagnosis should be possible with 100% accuracy in subjects without the deletion and with 50% accuracy in those who possess it (who would be either heterozygous--normal, or affected with the disease).</description>
    </item>
  </channel>
</rss>