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Summary Anatomy Item Literature (12667) Expression Attributions Wiki
XB-ANAT-175

Papers associated with nervous system (and mecp2)

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A cyclin-dependent kinase-mediated phosphorylation switch of disordered protein condensation., Valverde JM., Nat Commun. October 9, 2023; 14 (1): 6316.                                      


A Mixture of Chemicals Found in Human Amniotic Fluid Disrupts Brain Gene Expression and Behavior in Xenopus laevis., Leemans M., Int J Mol Sci. January 30, 2023; 24 (3):               


A convergent molecular network underlying autism and congenital heart disease., Rosenthal SB., Cell Syst. November 17, 2021; 12 (11): 1094-1107.e6.            


5-hydroxymethylcytosine marks postmitotic neural cells in the adult and developing vertebrate central nervous system., Diotel N., J Comp Neurol. February 15, 2017; 525 (3): 478-497.  


An in vivo screen to identify candidate neurogenic genes in the developing Xenopus visual system., Bestman JE., Dev Biol. December 15, 2015; 408 (2): 269-91.                    


Association of modified cytosines and the methylated DNA-binding protein MeCP2 with distinctive structural domains of lampbrush chromatin., Morgan GT., Chromosome Res. December 1, 2012; 20 (8): 925-42.                  


Cell-autonomous alterations in dendritic arbor morphology and connectivity induced by overexpression of MeCP2 in Xenopus central neurons in vivo., Marshak S., PLoS One. January 1, 2012; 7 (3): e33153.                    


Differential expression of the methyl-cytosine binding protein 2 gene in embryonic and adult brain of zebrafish., Coverdale LE., Brain Res Dev Brain Res. November 25, 2004; 153 (2): 281-7.


MeCP2 behaves as an elongated monomer that does not stably associate with the Sin3a chromatin remodeling complex., Klose RJ., J Biol Chem. November 5, 2004; 279 (45): 46490-6.


MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions., Kishi N., Mol Cell Neurosci. November 1, 2004; 27 (3): 306-21.


Methylation gets SMRT. Functional insights into Rett syndrome., Vetter ML., Dev Cell. September 1, 2003; 5 (3): 359-60.


A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos., Stancheva I., Mol Cell. August 1, 2003; 12 (2): 425-35.                          

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