Matsuura T., Sutcliffe J.S., Fang P., Galjaard R.J., Jiang Y.H., Benton C.S., Rommens J.M., and Beaudet A.L., 1997. De novo truncating mutations in E6-AP ubiquitin-protein ligase gene
Mayr B. and Montminy M., 2001. Transcriptional regulation by the phosphoiylation-dependent factor CREB.
Mays- Hoopes L.L., 1989. Age-related changes in DNA methylation: Do they represent continued developmental changes?
McDowell T.L., Gibbons R.J., Sutherland F.L, O’Rourke D.M., Bickmore W.A., Pombo A., Turley H., Gatter K., Picketts D.J., Buckle V.J., et al., 1999. Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes.
Meguro M., Mitsuya K., Nomura N., Kohda M., KashiwagiA., Nishigaki R., Yoshioka H., Nakao M., Oishi M., and Oshimura M., 2001. Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: An imprinted direct repeat cluster resembling small nucleolar RNA genes.
Meins M., Lehmann J., Gerresheim F., Herchenbach J., Hagedom M., Hameister K., and Epplen J.T., 2005. Submicroscopic duplication in Xq28 causes increased expression of the
Meloni I., Bruttini M., Longo I., Mari E., Rizzolio F. D’Adamo P.. Den-vriendt K., Fryns J.P., Toniolo D., and Renieri A., 2000. A mutation in the Rett syndrome gene,
Mullaney B.C., Johnston M.V., and Blue M.E., 2004. Developmental expression of methyl-CpG binding protein 2 is dynamically regulated in the rodent brain.
Murata T., Kurokawa R., Krones A., Tatsumi K., Ishii M., Taki T., Masuno M., Ohashi H, Yanagisawa M., Rosenfeld M.G.. et al., 2001. Defect of histone acetyltransferase activity of the nuclear transcriptional coactivator CBP in Rubinstein-Taybi syndrome
Nan X., Campoy F.J., and Bird A., 1997. MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin.
Neul J.L. and Zoghbi H.Y., 2004. Rett syndrome: A prototypical neurodevelopmental disorder.
Nicholls R.D., Knoll J.H.M., Butler M.G., Karam S., and Lalande M., 1989. Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.
Nuber U.A., Kriaucionis S., RoloffT.C., Guy J., Selfridge J., Stein-hoff G, Schulz R., Lipkowitz B., Ropers H.H., Holmes M.C., and Bird A., 2005. Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome.
Ogryzko V.V., Schiltz R.L., Russanova V., Howard B.H., and Naka-tani Y., 1996. The transcriptional coactivators p300 and CBP are histone acetyltransferases.
Ohta T., Gray T.A., Rogan P.K., Buiting I.C., Gabriel J.M., Saitoh S., Muralidhar B., Bilienska B., Krajewska-Walasek M., Driscoll D.J., et al., 1999. Imprinting-mutation mechanisms in Prader-Willi syndrome.
Okano M., Bell D.W., Haber D.A., and Li E., 1999. DNA meth-yltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development.
Orstavik K.H., Eiklid K., van der Hagen C.B., Spetalen S., Kierulf K., Skjeldal O., and Buiting K., 2003. Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injection.
Petrij E., Giles R.H., Dauwerse H.G., Sans J.J., Hennekam R.C., Masuno M., Tommerup N., van Ommen G J., Goodman R.H., Peters D.J., et al., 1995. Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP.
Petroms A., 2004. The origin of schizophrenia: Genetic thesis, epigenetic antithesis, and resolving synthesis.
Picketts D.J., Higgs D.R., Bachoo S., Blake D.J., Quarrell O.W., and Gibbons R.J., 1996. ATRX encodes a novel member of the SNF2 family of proteins: Mutations point to a common mechanism underlying the ATR-X syndrome.
Pieretti M., Zhang E., Fu Y.-H., Warren S.T., Oostra B.A., Caskey C.T., and Nelson D. L., 1991. Absence of expression of the