Clinical and genetic characteristics of children with acute lymphoblastic leukemia and Li–Fraumeni syndrome

Ítems similars

• Subclonal NT5C2 mutations are associated with poor outcomes after relapse of pediatric acute lymphoblastic leukemia
  per: Barz, Malwine J., et al.
  Publicat: (2020)
• Ras pathway mutations are prevalent in relapsed childhood acute lymphoblastic leukemia and confer sensitivity to MEK inhibition
  per: Irving, Julie, et al.
  Publicat: (2014)
• High VLA-4 expression is associated with adverse outcome and distinct gene expression changes in childhood B-cell precursor acute lymphoblastic leukemia at first relapse
  per: Shalapour, Shabnam, et al.
  Publicat: (2011)
• Cancer surveillance for individuals with Li-Fraumeni syndrome
  per: Kratz, Christian P., et al.
  Publicat: (2020)
• NOTCH1 mutation, TP53 alteration and myeloid antigen expression predict outcome heterogeneity in children with first relapse of T-cell acute lymphoblastic leukemia
  per: Hof, Jana, et al.
  Publicat: (2017)