GATA1 erythroid-specific regulation of SEC23B expression and its implication in the pathogenesis of congenital dyserythropoietic anemia type II

مواد مشابهة

• Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein
  بواسطة: Russo, Roberta, وآخرون
  منشور في: (2019)
• Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein
  بواسطة: Russo, Roberta, وآخرون
  منشور في: (2020)
• RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 Pathway
  بواسطة: De Rosa, Gianluca, وآخرون
  منشور في: (2020)
• Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type II
  بواسطة: Russo, Roberta, وآخرون
  منشور في: (2013)
• Mutational spectrum in congenital dyserythropoietic anemia type II: Identification of 19 novel variants in SEC23B gene
  بواسطة: Russo, Roberta, وآخرون
  منشور في: (2010)