Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain.

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• Identification of mutations in ATRX by RNase mismatch cleavage.
  de réir: Gibbons, R, et al.
  Foilsithe / Cruthaithe: (1997)
• ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.
  de réir: Picketts, D, et al.
  Foilsithe / Cruthaithe: (1996)
• Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains.
  de réir: Picketts, D, et al.
  Foilsithe / Cruthaithe: (1998)
• Disruption of ATRX in mouse by conditional knockout.
  de réir: Gibbons, R, et al.
  Foilsithe / Cruthaithe: (2002)
• ATRX: taming tandem repeats.
  de réir: Gibbons, R, et al.
  Foilsithe / Cruthaithe: (2010)