Identification of mutations in ATRX by RNase mismatch cleavage.

Slični predmeti

• ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.
  od: Picketts, D, i dr.
  Izdano: (1996)
• Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains.
  od: Picketts, D, i dr.
  Izdano: (1998)
• Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain.
  od: Gibbons, R, i dr.
  Izdano: (1997)
• Disruption of ATRX in mouse by conditional knockout.
  od: Gibbons, R, i dr.
  Izdano: (2002)
• Detection of mutations by RNase cleavage.
  od: Watkins, H, i dr.
  Izdano: (2001)