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Neurology, ISSN 0028-3878, 01/2019, Volume 92, Issue 2, pp. e108 - e114
OBJECTIVEWe characterized the epilepsy features and contribution to cognitive regression in 47 patients with MECP2 duplication syndrome (MDS) and reviewed... 
DEFINITION | XLMR | INCLUDING MECP2 | SEIZURES | RETT-SYNDROME | ILAE COMMISSION | GENE DUPLICATION | PHENOTYPE | FEMALES | CLINICAL NEUROLOGY | FEATURES
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 03/2015, Volume 35, Issue 2, pp. 168 - 181
Journal Article
by Bian, EB and Chen, XR and Xu, YD and Ji, XH and Cheng, M and Wang, HL and Fang, ZY and Zhao, B
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, ISSN 1756-9966, 08/2019, Volume 38, Issue 1, pp. 366 - 15
BackgroundThe epithelial-to-mesenchymal transition (EMT) has been linked to the regulation of glioma progression. However, the underlying signaling mechanisms... 
MeCP2 | CELLS | ACTIVATION | MECHANISM | miR-200c | INITIATION | SUV39H1 | BINDING-PROTEIN MECP2 | CANCER | DNA-METHYLATION | Glioma | ONCOLOGY | GROWTH | GENE-EXPRESSION | MICRORNA | Animal experimentation | Epigenetic inheritance | Development and progression | Gliomas | Analysis | Stem cells
Journal Article
by Miguet, Marguerite and Faivre, Laurence and Amiel, Jeanne and Nizon, Mathilde and Touraine, Renaud and Prieur, Fabienne and Pasquier, Laurent and Lefebvre, Mathilde and Thevenon, Julien and Dubourg, Christèle and Julia, Sophie and Sarret, Catherine and Remerand, Ganaëlle and Francannet, Christine and Laffargue, Fanny and Boespflug-Tanguy, Odile and David, Albert and Isidor, Bertrand and Vigneron, Jacqueline and Leheup, Bruno and Lambert, Laetitia and Philippe, Christophe and Béri-Dexheimer, Mylène and Cuisset, Jean-Marie and Andrieux, Joris and Plessis, Ghislaine and Toutain, Annick and Guibaud, Laurent and Cormier-Daire, Valérie and Rio, Marlene and Bonnefont, Jean-Paul and Echenne, Bernard and Journel, Hubert and Burglen, Lydie and Chantot-Bastaraud, Sandrine and Bienvenu, Thierry and Baumann, Clarisse and Perrin, Laurence and Drunat, Séverine and Jouk, Pierre-Simon and Dieterich, Klaus and Devillard, Françoise and Lacombe, Didier and Philip, Nicole and Sigaudy, Sabine and Moncla, Anne and Missirian, Chantal and Badens, Catherine and Perreton, Nathalie and Thauvin-Robinet, Christel and AChro-Puce, Réseau and Pedespan, Jean-Michel and Rooryck, Caroline and Goizet, Cyril and Vincent-Delorme, Catherine and Duban-Bedu, Bénédicte and Bahi-Buisson, Nadia and Afenjar, Alexandra and Maincent, Kim and Héron, Delphine and Alessandri, Jean-Luc and Martin-Coignard, Dominique and Lesca, Gaëtan and Rossi, Massimiliano and Raynaud, Martine and Callier, Patrick and Mosca-Boidron, Anne-Laure and Marle, Nathalie and Coutton, Charles and Satre, Véronique and Caignec, Cédric Le and Malan, Valérie and Romana, Serge and Keren, Boris and Tabet, Anne-Claude and Kremer, Valérie and Scheidecker, Sophie and Vigouroux, Adeline and Lackmy-Port-Lis, Marilyn and Sanlaville, Damien and Till, Marianne and Carneiro, Maryline and Gilbert-Dussardier, Brigitte and Willems, Marjolaine and Van Esch, Hilde and Portes, Vincent Des and El Chehadeh, Salima
Journal of Medical Genetics, ISSN 0022-2593, 06/2018, Volume 55, Issue 6, pp. 359 - 371
The Xq28 duplication involving the MECP2 gene (MECP2 duplication) has been mainly described in male patients with severe developmental delay (DD) associated... 
X-linked | genetic counselling | MECP2duplication syndrome | Xq28 duplication | MECP2gene | facial dysmorphism | INCLUDING MECP2 | RETT-SYNDROME | SEVERE MENTAL-RETARDATION | RECURRENT INFECTIONS | XQ28 DUPLICATIONS | GENETICS & HEREDITY | FEMALES | HIRSCHSPRUNGS-DISEASE | MUTATIONS | GENE COPY NUMBER | FILAMIN-A | Life Sciences | Genetics | Human genetics
Journal Article
Neoplasia, ISSN 1476-5586, 2013, Volume 15, Issue 5, pp. 511 - IN17
Journal Article
Molecular Cytogenetics, ISSN 1755-8166, 01/2014, Volume 7, Issue 1, pp. 10 - 10
Journal Article
Journal Article
Child Neurology Open, ISSN 2329-048X, 3/2016, Volume 3, p. 2329048X16630673
Xq28 microduplications including the MECP2 gene constitute a 100% penetrant X-linked syndrome in males caused by overexpression of normal MeCP2 protein. A... 
Journal Article
Journal Article
Oncogenesis, ISSN 2157-9024, 04/2019, Volume 8, Issue 4, pp. 26 - 18
HIF-1 alpha has a broad impact on tumors, including enhanced utilization of glucose, tumor cell stemness, migration, metastasis and so on. In pilot study, we... 
METHYLOME | ACTIVATION | METHYLTRANSFERASE | DNA METHYLATION | ONCOLOGY | PATHWAY | DNMT3A | IDENTIFICATION | DE-NOVO METHYLATION | NON-CPG METHYLATION | HYPOXIA-INDUCIBLE FACTOR-1 | Transcription | Invasiveness | Breast cancer | Tumor cell lines | Metastases | Methyl-CpG binding protein | MeCP2 protein | Cell lines | Mastectomy | DNA methylation | Epigenetics | Tumorigenesis | Cell migration | CpG islands
Journal Article
Journal Article