Identification of mutations in ATRX by RNase mismatch cleavage.

Samankaltaisia teoksia

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