Dendritic cell, monocyte, B and NK lymphoid deficiency defines the lost lineages of a new GATA-2 dependent myelodysplastic syndrome

Παρόμοια τεκμήρια

• Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency
  ανά: Dickinson, Rachel Emma, κ.ά.
  Έκδοση: (2011)
• The human syndrome of dendritic cell, monocyte, B and NK lymphoid deficiency
  ανά: Bigley, Venetia, κ.ά.
  Έκδοση: (2011)
• Subsets of CD1c(+) DCs: Dendritic Cell Versus Monocyte Lineage
  ανά: Heger, Lukas, κ.ά.
  Έκδοση: (2020)
• Human dendritic cell subsets: an update
  ανά: Collin, Matthew, κ.ά.
  Έκδοση: (2018)
• Haematopoietic and immune defects associated with GATA2 mutation
  ανά: Collin, Matthew, κ.ά.
  Έκδοση: (2015)