Characterization of Wild-Type and ΔF508 Cystic Fibrosis Transmembrane Regulator in Human Respiratory Epithelia

Схожие документы

• Endocytic Trafficking Routes of Wild Type and ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator
  по: Gentzsch, Martina, et al.
  Опубликовано: (2004)
• SERCA Pump Inhibitors Do Not Correct Biosynthetic Arrest of ΔF508 CFTR in Cystic Fibrosis
  по: Grubb, Barbara R., et al.
  Опубликовано: (2006)
• Cystic Fibrosis Transmembrane Regulator Missing the First Four Transmembrane Segments Increases Wild Type and ΔF508 Processing
  по: Cebotaru, Liudmila, et al.
  Опубликовано: (2008)
• The Cystic Fibrosis-causing Mutation ΔF508 Affects Multiple Steps in Cystic Fibrosis Transmembrane Conductance Regulator Biogenesis
  по: Thibodeau, Patrick H., et al.
  Опубликовано: (2010)
• Expression of ΔF508 Cystic Fibrosis Transmembrane Regulator (CFTR) Decreases Membrane Sialylation
  по: Dosanjh, Amrita, et al.
  Опубликовано: (2009)