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

Benzer Materyaller

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