<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Montagner, Sara</dc:creator>
  <dc:creator>Dehó, Lorenzo</dc:creator>
  <dc:creator>Monticelli, Silvia</dc:creator>
  <dc:date>2014-03-31</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Background: MicroRNAs (miRNAs) are short non-coding RNAs involved in the posttranscriptional  regulation of a wide range of biological processes. By binding to complementary sequences on target  messenger RNAs, they trigger translational repression and degradation of the target, eventually resulting  in reduced protein output. MiRNA-dependent regulation of protein translation is a very widespread and  evolutionarily conserved mechanism of posttranscriptional control of gene expression. Accordingly, a high  proportion of mammalian genes are likely to be regulated by miRNAs. In the hematopoietic system, both  transcriptional and posttranscriptional regulation of gene expression ensure proper differentiation and  function of stem cells, committed progenitors as well as mature cells. Results : In recent years, miRNA  expression profiling of various cell types in the hematopoietic system, as well as gene-targeting  approaches to assess the function of individual miRNAs, revealed the importance of this type of  regulation in the development of both innate and acquired immunity. Conclusions : We discuss the  general role of miRNA biogenesis in the development of hematopoietic cells, as well as specific functions  of individual miRNAs in stem cells as well as in mature immune cells.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://localhost:5000/ark:/12658/srd1318982</dc:identifier>
  <dc:identifier>https://susi.usi.ch/global/documents/318982</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318982/files/Mopntagner_BMCI_2014.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1186/1471-2172-15-14</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318982</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>BMC immunology. - 2014, vol. 15, p. 14</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Adaptive immunity</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Development</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Embryonic stem cells</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Hematopoiesis</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Hematopoietic stem cells</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Innate immunity</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">MiRNAs</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns8="xml" ns8:lang="en">MicroRNAs in hematopoietic development</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
