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  <title>DSpace Community:</title>
  <link rel="alternate" href="http://hdl.handle.net/10400.18/5" />
  <subtitle />
  <id>http://hdl.handle.net/10400.18/5</id>
  <updated>2013-05-25T04:08:19Z</updated>
  <dc:date>2013-05-25T04:08:19Z</dc:date>
  <entry>
    <title>Hypercholesterolemia: A disease with expression from childhood</title>
    <link rel="alternate" href="http://hdl.handle.net/10400.18/1584" />
    <author>
      <name>Espinheira, M.C.</name>
    </author>
    <author>
      <name>Vasconcelos, C.</name>
    </author>
    <author>
      <name>Medeiros, A.M.</name>
    </author>
    <author>
      <name>Alves, A.C.</name>
    </author>
    <author>
      <name>Bourbon, M.</name>
    </author>
    <author>
      <name>Guerra, A.</name>
    </author>
    <id>http://hdl.handle.net/10400.18/1584</id>
    <updated>2013-05-24T16:58:59Z</updated>
    <published>2013-05-10T00:00:00Z</published>
    <summary type="text">Title: Hypercholesterolemia: A disease with expression from childhood
Authors: Espinheira, M.C.; Vasconcelos, C.; Medeiros, A.M.; Alves, A.C.; Bourbon, M.; Guerra, A.
Abstract: Hypercholesterolemia results from an alteration, genetic or acquired, in lipoprotein metabolism. Evidence that hypercholesterolemia is associated with the atherosclerotic process from childhood justifies the screening of high-risk children and initiation of therapy at preschool ages.</summary>
    <dc:date>2013-05-10T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Sinapse: à procura de pistas para a etiologia das Perturbações do Espetro do Autismo</title>
    <link rel="alternate" href="http://hdl.handle.net/10400.18/1583" />
    <author>
      <name>Oliveira, Bárbara</name>
    </author>
    <id>http://hdl.handle.net/10400.18/1583</id>
    <updated>2013-05-24T16:55:25Z</updated>
    <published>2013-04-19T00:00:00Z</published>
    <summary type="text">Title: Sinapse: à procura de pistas para a etiologia das Perturbações do Espetro do Autismo
Authors: Oliveira, Bárbara</summary>
    <dc:date>2013-04-19T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Investigação em Promoção da Saúde</title>
    <link rel="alternate" href="http://hdl.handle.net/10400.18/1582" />
    <author>
      <name>Miranda, Natércia</name>
    </author>
    <id>http://hdl.handle.net/10400.18/1582</id>
    <updated>2013-05-24T16:52:42Z</updated>
    <published>2013-04-05T00:00:00Z</published>
    <summary type="text">Title: Investigação em Promoção da Saúde
Authors: Miranda, Natércia</summary>
    <dc:date>2013-04-05T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Carcinogenic Ability of Schistosoma Haematobium Possibly through Oncogenic Mutation of KRAS Gene</title>
    <link rel="alternate" href="http://hdl.handle.net/10400.18/1581" />
    <author>
      <name>Botelho, Mónica C.</name>
    </author>
    <author>
      <name>Veiga, Isabel</name>
    </author>
    <author>
      <name>Oliveira, Paula A.</name>
    </author>
    <author>
      <name>Lopes, Carlos</name>
    </author>
    <author>
      <name>Teixeira, Manuel</name>
    </author>
    <author>
      <name>Costa, José M Correia da</name>
    </author>
    <author>
      <name>Machado, José C.</name>
    </author>
    <id>http://hdl.handle.net/10400.18/1581</id>
    <updated>2013-05-24T16:48:12Z</updated>
    <published>2013-04-28T00:00:00Z</published>
    <summary type="text">Title: Carcinogenic Ability of Schistosoma Haematobium Possibly through Oncogenic Mutation of KRAS Gene
Authors: Botelho, Mónica C.; Veiga, Isabel; Oliveira, Paula A.; Lopes, Carlos; Teixeira, Manuel; Costa, José M Correia da; Machado, José C.
Abstract: Schistosoma haematobium is a parasitic flatworm that infects millions of people, mostly in the developing world, and is associated with high incidence of bladder cancer, although why is not clear. Previously, we have used CD-1 mice to show that Schistosoma haematobium total antigen (Sh) has a carcinogenic ability. Sh intravesically instillation induced the development of several urothelial lesions, namely nodular hyperplasia and dysplasia (LGIUN—Low Grade Intra-Urothelial Neoplasia) after 40 weeks of treatment. These results suggested that Sh induce urothelium malignization. Bladder carcinoma frequently harbours gene mutations that constitutively activate the receptor tyrosine kinase-Ras pathway for this reason we studied activating mutations in KRAS gene. Twenty percent of the bladders with dysplasia presented a KRAS mutation in codon 12 of exon 2. We concluded from these results that the parasite extract of S. haematobium has carcinogenic ability possibly through oncogenic mutation of KRAS gene.</summary>
    <dc:date>2013-04-28T00:00:00Z</dc:date>
  </entry>
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