Analysis of Ankyrin Repeats Reveals How a Single Point Mutation in RFXANK Results in Bare Lymphocyte Syndrome

Gelijkaardige items

• Mutations in the Bare Lymphocyte Syndrome Define Critical Steps in the Assembly of the Regulatory Factor X Complex
  door: Nekrep, Nada, et al.
  Gepubliceerd in: (2000)
• Major Histocompatibility Complex Class II Transcriptional Platform: Assembly of Nuclear Factor Y and Regulatory Factor X (RFX) on DNA Requires RFX5 Dimers
  door: Jabrane-Ferrat, Nabila, et al.
  Gepubliceerd in: (2002)
• Progressive Ataxia and Neurologic Regression in RFXANK-Associated Bare Lymphocyte Syndrome
  door: Alharby, Essa, et al.
  Gepubliceerd in: (2021)
• Phosphorylation of CIITA directs its oligomerization, accumulation and increased activity on MHCII promoters
  door: Tosi, Giovanna, et al.
  Gepubliceerd in: (2002)
• Class II Histone Deacetylases Confer Signal Responsiveness to the Ankyrin-Repeat Proteins ANKRA2 and RFXANK
  door: McKinsey, Timothy A., et al.
  Gepubliceerd in: (2006)