Role of DNA methylation in X inactivation and the fragile X syndrome

This publication has 10 references indexed in Scilit:

• Concerning the role of X‐inactivation and DNA methylation in fragile X syndrome
  American Journal of Medical Genetics, 1992
• Insights into X chromosome inactivation from studies of species variation, DNA methylation and replication, and vice versa
  Genetics Research, 1990
• Sex difference in methylation of single-copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations
  Somatic Cell and Molecular Genetics, 1990
• Frequent derepression of G6PD and HPRT on the Marsupial inactive X chromosome associated with cell proliferation in vitro
  Experimental Cell Research, 1989
• Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNA.
  The EMBO Journal, 1988
• DNA methylation stabilizes X chromosome inactivation in eutherians but not in marsupials: evidence for multistep maintenance of mammalian X dosage compensation.
  Proceedings of the National Academy of Sciences, 1987
• Clusters of CpG dinucleotides implicated by nuclease hypersensitivity as control elements of housekeeping genes
  Nature, 1985
• Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation.
  Proceedings of the National Academy of Sciences, 1984
• Complete concordance between glucose-6-phosphate dehydrogenase activity and hypomethylation of 3′ CpG clusters: implications for X chromosome dosage compensation
  Nucleic Acids Research, 1984