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

Παρόμοια τεκμήρια

• Subclonal NT5C2 mutations are associated with poor outcomes after relapse of pediatric acute lymphoblastic leukemia
  ανά: Barz, Malwine J., κ.ά.
  Έκδοση: (2020)
• Ras pathway mutations are prevalent in relapsed childhood acute lymphoblastic leukemia and confer sensitivity to MEK inhibition
  ανά: Irving, Julie, κ.ά.
  Έκδοση: (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
  ανά: Shalapour, Shabnam, κ.ά.
  Έκδοση: (2011)
• Cancer surveillance for individuals with Li-Fraumeni syndrome
  ανά: Kratz, Christian P., κ.ά.
  Έκδοση: (2020)
• NOTCH1 mutation, TP53 alteration and myeloid antigen expression predict outcome heterogeneity in children with first relapse of T-cell acute lymphoblastic leukemia
  ανά: Hof, Jana, κ.ά.
  Έκδοση: (2017)