Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation.

Ижил төстэй зүйлс

• Mutations in the human ATRX gene, encoding a putative transcription regulator, cause diverse changes in the pattern of DNA methylation.
  -н: Garrick, D, зэрэг
  Хэвлэсэн: (2000)
• A conserved truncated isoform of the ATR-X syndrome protein lacking the SWI/SNF-homology domain.
  -н: Garrick, D, зэрэг
  Хэвлэсэн: (2004)
• Functional significance of mutations in the Snf2 domain of ATRX.
  -н: Mitson, M, зэрэг
  Хэвлэсэн: (2011)
• ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.
  -н: Picketts, D, зэрэг
  Хэвлэсэн: (1996)
• Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS).
  -н: Gibbons, R, зэрэг
  Хэвлэсэн: (2003)