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    • Home
    • Diagnostics
      • Polycythemia Vera
      • Essential Thrombocythemia
      • Primary Myelofibrosis
      • Congenital Erythrocytosis
      • Hereditary Thrombocytosis
    • Molecular analyses
      • JAK2V617F
      • JAK2 Exon 12 mutations
      • Mpl/TPO_Receptor
      • Calreticulin (CALR)
      • Other genes mutated in MPN
      • EPO-Receptor
      • Oxygen sensing pathway genes
      • THPO
    • Events
    • Useful links
    • Members
    • Registration
    • INTRANET

      Events

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      • Nîmes, France – May 2016

      Nîmes, France – May 2016

      EVENT DESCRIPTION

      Since the discovery of the V617F mutation of tyrosine kinase JAK2 in 2005, other mutations have been described as specific for Myeloproliferative Neoplasms (MPNs) in JAK2 eons 12, 13, 14 (in addition to c1849G>T V617F) and 15, in the exon 10 of MPL, and in the exon 9 of the CALR gene. Moreover, other rare mutations have been described in the JAK2 and MPL genes.

      EVENT CONTENT

      • To acquire competences in the various techniques designed to detect the main MPN mutations. The training school is organized in two sessions:
        • Morning plenary session/lectures: Theory of the techniques.
        • Afternoon practical session: applicants will perform data analysis, assisted by experts.
      • To train in NGS data analysis, moving from raw data to documented diagnostic proposal.
      • To get the latest information on the different mutations leading to MPN or to transformation.
      • To develop cooperation between participants and hopefully, generate new, original studies.

      MORE INFORMATIONS

      Start Time

      8:30 am

      May 17, 2016

      Finish Time

      12:00 pm

      May 20, 2016

      Address

      Place du Pr DEBRE 30 029 Nîmes Cedex 9 - France

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      Former EU-sponsored COST Action BM0902 (2009-2013), a network of experts … “

      by MPN&MPNr-EuroNet.

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