361 related articles for article (PubMed ID: 26733678)
21. Investigation of Rett syndrome using pluripotent stem cells.
Dajani R; Koo SE; Sullivan GJ; Park IH
J Cell Biochem; 2013 Nov; 114(11):2446-53. PubMed ID: 23744605
[TBL] [Abstract][Full Text] [Related]
22. Neuronal non-CG methylation is an essential target for MeCP2 function.
Tillotson R; Cholewa-Waclaw J; Chhatbar K; Connelly JC; Kirschner SA; Webb S; Koerner MV; Selfridge J; Kelly DA; De Sousa D; Brown K; Lyst MJ; Kriaucionis S; Bird A
Mol Cell; 2021 Mar; 81(6):1260-1275.e12. PubMed ID: 33561390
[TBL] [Abstract][Full Text] [Related]
23. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
Samaco RC; Hogart A; LaSalle JM
Hum Mol Genet; 2005 Feb; 14(4):483-92. PubMed ID: 15615769
[TBL] [Abstract][Full Text] [Related]
24. Survey of MeCP2 in the Rett syndrome and the non-Rett syndrome brain.
Armstrong DD; Deguchi K; Antallfy B
J Child Neurol; 2003 Oct; 18(10):683-7. PubMed ID: 14649549
[TBL] [Abstract][Full Text] [Related]
25. MeCP2-regulated miRNAs control early human neurogenesis through differential effects on ERK and AKT signaling.
Mellios N; Feldman DA; Sheridan SD; Ip JPK; Kwok S; Amoah SK; Rosen B; Rodriguez BA; Crawford B; Swaminathan R; Chou S; Li Y; Ziats M; Ernst C; Jaenisch R; Haggarty SJ; Sur M
Mol Psychiatry; 2018 Apr; 23(4):1051-1065. PubMed ID: 28439102
[TBL] [Abstract][Full Text] [Related]
26. KCC2 expression supersedes NKCC1 in mature fiber cells in mouse and rabbit lenses.
Frederikse PH; Kasinathan C
Mol Vis; 2015; 21():1142-50. PubMed ID: 26539026
[TBL] [Abstract][Full Text] [Related]
27. Alterations in the cholinergic system of brain stem neurons in a mouse model of Rett syndrome.
Oginsky MF; Cui N; Zhong W; Johnson CM; Jiang C
Am J Physiol Cell Physiol; 2014 Sep; 307(6):C508-20. PubMed ID: 25009110
[TBL] [Abstract][Full Text] [Related]
28. The role of MeCP2 in CNS development and function.
Na ES; Monteggia LM
Horm Behav; 2011 Mar; 59(3):364-8. PubMed ID: 20515694
[TBL] [Abstract][Full Text] [Related]
29. Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease.
Pejhan S; Rastegar M
Biomolecules; 2021 Jan; 11(1):. PubMed ID: 33429932
[TBL] [Abstract][Full Text] [Related]
30. Rett syndrome induced pluripotent stem cell-derived neurons reveal novel neurophysiological alterations.
Farra N; Zhang WB; Pasceri P; Eubanks JH; Salter MW; Ellis J
Mol Psychiatry; 2012 Dec; 17(12):1261-71. PubMed ID: 22230884
[TBL] [Abstract][Full Text] [Related]
31. Evolving role of MeCP2 in Rett syndrome and autism.
LaSalle JM; Yasui DH
Epigenomics; 2009 Oct; 1(1):119-30. PubMed ID: 20473347
[TBL] [Abstract][Full Text] [Related]
32. GABA and glutamate pathways are spatially and developmentally affected in the brain of Mecp2-deficient mice.
El-Khoury R; Panayotis N; Matagne V; Ghata A; Villard L; Roux JC
PLoS One; 2014; 9(3):e92169. PubMed ID: 24667344
[TBL] [Abstract][Full Text] [Related]
33. Mitochondrial dysfunction in dopaminergic neurons differentiated from exfoliated deciduous tooth-derived pulp stem cells of a child with Rett syndrome.
Hirofuji S; Hirofuji Y; Kato H; Masuda K; Yamaza H; Sato H; Takayama F; Torio M; Sakai Y; Ohga S; Taguchi T; Nonaka K
Biochem Biophys Res Commun; 2018 Apr; 498(4):898-904. PubMed ID: 29534967
[TBL] [Abstract][Full Text] [Related]
34. The protocadherins, PCDHB1 and PCDH7, are regulated by MeCP2 in neuronal cells and brain tissues: implication for pathogenesis of Rett syndrome.
Miyake K; Hirasawa T; Soutome M; Itoh M; Goto Y; Endoh K; Takahashi K; Kudo S; Nakagawa T; Yokoi S; Taira T; Inazawa J; Kubota T
BMC Neurosci; 2011 Aug; 12():81. PubMed ID: 21824415
[TBL] [Abstract][Full Text] [Related]
35. EEA1 restores homeostatic synaptic plasticity in hippocampal neurons from Rett syndrome mice.
Xu X; Pozzo-Miller L
J Physiol; 2017 Aug; 595(16):5699-5712. PubMed ID: 28621434
[TBL] [Abstract][Full Text] [Related]
36. MeCP2 SUMOylation rescues Mecp2-mutant-induced behavioural deficits in a mouse model of Rett syndrome.
Tai DJ; Liu YC; Hsu WL; Ma YL; Cheng SJ; Liu SY; Lee EH
Nat Commun; 2016 Feb; 7():10552. PubMed ID: 26842955
[TBL] [Abstract][Full Text] [Related]
37. Selective preservation of cholinergic MeCP2 rescues specific Rett-syndrome-like phenotypes in MeCP2
Zhou H; Wu W; Zhang Y; He H; Yuan Z; Zhu Z; Zhao Z
Behav Brain Res; 2017 Mar; 322(Pt A):51-59. PubMed ID: 28093257
[TBL] [Abstract][Full Text] [Related]
38. Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.
Hoffbuhr KC; Moses LM; Jerdonek MA; Naidu S; Hoffman EP
Ment Retard Dev Disabil Res Rev; 2002; 8(2):99-105. PubMed ID: 12112735
[TBL] [Abstract][Full Text] [Related]
39. Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples.
Thatcher KN; Peddada S; Yasui DH; Lasalle JM
Hum Mol Genet; 2005 Mar; 14(6):785-97. PubMed ID: 15689352
[TBL] [Abstract][Full Text] [Related]
40. Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation.
Jentarra GM; Olfers SL; Rice SG; Srivastava N; Homanics GE; Blue M; Naidu S; Narayanan V
BMC Neurosci; 2010 Feb; 11():19. PubMed ID: 20163734
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
