Sökresultat - Myriam Vézain

  • Visas 1 - 3 av 3 resultat
Förfina resultatet
  1. 1
    A large fraction of unclassified variants of the mismatch repair genes<i>MLH1</i>and<i>MSH2</i>is associated with splicing defects

    A large fraction of unclassified variants of the mismatch repair genes<i>MLH1</i>and<i>MSH2</i>is associated with splicing defects av Isabelle Tournier, Myriam Vézain, Alexandra Martins, Françoise Charbonnier, Stéphanie Baert‐Desurmont, Sylviane Olschwang, Qing Wang, Marie Pierre Buisine, Johann Soret, Jamal Tazi, Thierry Frébourg, Mario Tosi

    Publicerad 2008
    Hämta fulltext
    Artigo
    Lägg till i favoriter
    Sparad:
  2. 2
    A rare<i>SMN2</i>variant in a previously unrecognized composite splicing regulatory element induces exon 7 inclusion and reduces the clinical severity of spinal muscular atrophy

    A rare<i>SMN2</i>variant in a previously unrecognized composite splicing regulatory element induces exon 7 inclusion and reduces the clinical severity of spinal muscular atrophy av Myriam Vézain, Pascale Saugier‐Veber, Elisa Goina, Renaud Touraine, V. Manel, Annick Toutain, Séverine Fehrenbach, Thierry Frébourg, Franco Pagani, Mario Tosi, Alexandra Martins

    Publicerad 2009
    Hämta fulltext Hämta fulltext
    Artigo
    Lägg till i favoriter
    Sparad:
  3. 3
    CRISPR-Barcoding for Intratumor Genetic Heterogeneity Modeling and Functional Analysis of Oncogenic Driver Mutations

    CRISPR-Barcoding for Intratumor Genetic Heterogeneity Modeling and Functional Analysis of Oncogenic Driver Mutations av Alexis Guernet, Sathish Kumar Mungamuri, Dorthe Cartier, Ravi Sachidanandam, Anitha D. Jayaprakash, Sahil Adriouch, Myriam Vézain, Françoise Charbonnier, Guy Rohkin, Sophie Coutant, Shen Yao, Hassan Ainani, David Alexandre, Isabelle Tournier, Olivier Boyer, Stuart A. Aaronson, Youssef Anouar, Luca Grumolato

    Publicerad 2016
    Hämta fulltext Hämta fulltext
    Artigo
    Lägg till i favoriter
    Sparad:

Sökverktyg: