A conserved truncated isoform of the ATR-X syndrome protein lacking the SWI/SNF-homology domain

This publication has 31 references indexed in Scilit:

• Neurodevelopmental defects resulting from ATRX overexpression in transgenic mice.
  Human Molecular Genetics, 2002
• Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association
  Human Molecular Genetics, 2000
• Molecular-clinical spectrum of the ATR-X syndrome
  American Journal of Medical Genetics, 2000
• Specific interaction between the XNP/ATR-X gene product and the SET domain of the human EZH2 protein
  Human Molecular Genetics, 1998
• A male-specific 3′-UTR regulates the steady-state level of theexuperantia mRNA during spermatogenesis in Drosophila
  Molecular Genetics and Genomics, 1995
• Mutations in a putative global transcriptional regulator cause X-linked mental retardation with α-thalassemia (ATR-X syndrome)
  Cell, 1995
• The PHD finger: Implications for chromatin-mediated transcriptional regulation
  Trends in Biochemical Sciences, 1995
• Clinical and hematologic aspects of the X‐linked α‐thalassemia/mental retardation syndrome (ATR‐X)
  American Journal of Medical Genetics, 1995
• Erythroid-specific processing of human beta spectrin I pre-mRNA
  Blood, 1994
• Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 in Xq13.3
  Human Molecular Genetics, 1994