Characterization of Six Novel Patients With MECP2 Duplications Due to Unbalanced Rearrangements of the X ChromosomeSANMANN, Jennifer N; BISHAY, Danielle L; STARR, Lois J et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 6, pp 1285-1291, issn 1552-4825, 7 p.Article

Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylationBALMER, Damina; GOLDSTINE, Jared; MANJULA RAO, Y et al.Journal of molecular medicine (Berlin. Print). 2003, Vol 81, Num 1, pp 61-68, issn 0946-2716, 8 p.Article

Les MECP2-Opathies: Mise en place d'une stratégie de diagnostic moléculaire = Rett syndrome: Establishment of molecular diagnosis strategyBIENVENU, T; BELDJORD, C; CHELLY, J et al.L' Eurobiologiste (Paris). 2003, Num 263, issn 0999-5749, 8 p.Article

Intrathecal 5-azacytidine inhibits global DNA methylation and methyl- CpG-binding protein 2 expression and alleviates neuropathic pain in rats following chronic constriction injuryYING WANG; CHANG LIU; GUO, Qu-Lian et al.Brain research. 2011, Vol 1418, pp 64-69, issn 0006-8993, 6 p.Article

Epilepsy in Rett syndrome―The experience of a National Rett CenterNISSENKORN, Andreea; GAK, Eva; VECSLER, Manuela et al.Epilepsia (Copenhagen). 2010, Vol 51, Num 7, pp 1252-1258, issn 0013-9580, 7 p.Article

Methyl CpG-binding protein 2 (a mutation of which causes rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brainsITOH, Masayuki; IDE, Shuhei; TANABE, Yuzo et al.Journal of neuropathology and experimental neurology. 2007, Vol 66, Num 2, pp 117-123, issn 0022-3069, 7 p.Article

A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndromeBUSCHDORF, Jan P; STRÄTLING, Wolf H.Journal of molecular medicine (Berlin. Print). 2004, Vol 82, Num 2, pp 135-143, issn 0946-2716, 9 p.Article

Breathing dysfunction in Rett syndrome : Understanding epigenetic regulation of the respiratory networkOGIER, Michael; KATZ, David M.Respiratory physiology & neurobiology. 2008, Vol 164, Num 1-2, pp 55-63, issn 1569-9048, 9 p.Article

Temporal shift in methyl-CpG binding protein 2 expression in a mouse model of rett syndromeMETCALF, B. M; MULLANEY, B. C; JOHNSTON, M. V et al.Neuroscience. 2006, Vol 139, Num 4, pp 1449-1460, issn 0306-4522, 12 p.Article

Adult Neural Function Requires MeCP2MCGRAW, Christopher M; SAMACO, Rodney C; ZOGHBI, Huda Y et al.Science (Washington, D.C.). 2011, Vol 333, Num 6039, issn 0036-8075, p. 186Article

Rett syndrome : new clinical and molecular insightsWILLIAMSON, Sarah L; CHRISTODOULOU, John.European journal of human genetics. 2006, Vol 14, Num 8, pp 896-903, issn 1018-4813, 8 p.Article

Effects of MECP2 mutation type, location and X-inactivation in modulating Rett syndrome phenotypeWEAVING, Linda S; WILLIAMSON, Sarah L; CHRISTODOULOU, John et al.American journal of medical genetics. 2003, Vol 118A, Num 2, pp 103-114, issn 0148-7299, 12 p.Article

Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of micePELKA, Gregory J; WATSON, Catherine M; RADZIEWIC, Tania et al.Brain. 2006, Vol 129, pp 887-898, issn 0006-8950, 12 p., 4Article

A methyl-CpG-binding protein 2-enhanced green fluorescent protein reporter mouse model provides a new tool for studying the neuronal basis of Rett syndromeSCHMID, Ralf S; TSUJIMOTO, Naomi; QIANG QU et al.Neuroreport (Oxford). 2008, Vol 19, Num 4, pp 393-398, issn 0959-4965, 6 p.Article

MeCP2 controls the expression of RASAL1 in the hepatic fibrosis in ratsHUI TAO; CHENG HUANG; JING JING YANG et al.Toxicology (Amsterdam). 2011, Vol 290, Num 2-3, pp 327-333, issn 0300-483X, 7 p.Article

Neurochemical changes in a mouse model of Rett syndrome : changes over time and in response to perinatal choline nutritional supplementationWARD, Bonnie C; KOLODNY, Nancy H; NAG, Nupur et al.Journal of neurochemistry. 2009, Vol 108, Num 2, pp 361-371, issn 0022-3042, 11 p.Article

A novel transcriptional regulator of myelin gene expression: implications for neurodevelopmental disordersVORA, Parvez; MINA, Raena; NAMAKA, Michael et al.Neuroreport (Oxford). 2010, Vol 21, Num 14, pp 917-921, issn 0959-4965, 5 p.Article

Severe congenital encephalopathy caused by MECP2 null mutations in males : central hypoxia and reduced neuronal dendritic structureSCHÜLE, B; ARMSTRONG, D. D; VOGEL, H et al.Clinical genetics. 2008, Vol 74, Num 2, pp 116-126, issn 0009-9163, 11 p.Article