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Results: 1 to 20 of 124

Similar articles for PubMed (Select 19386901)


Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions.

Maezawa I, Swanberg S, Harvey D, LaSalle JM, Jin LW.

J Neurosci. 2009 Apr 22;29(16):5051-61. doi: 10.1523/JNEUROSCI.0324-09.2009.


Rett syndrome microglia damage dendrites and synapses by the elevated release of glutamate.

Maezawa I, Jin LW.

J Neurosci. 2010 Apr 14;30(15):5346-56. doi: 10.1523/JNEUROSCI.5966-09.2010.


MeCP2 deficiency is associated with impaired microtubule stability.

Del├ępine C, Nectoux J, Bahi-Buisson N, Chelly J, Bienvenu T.

FEBS Lett. 2013 Jan 16;587(2):245-53. doi: 10.1016/j.febslet.2012.11.033. Epub 2012 Dec 10.


Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology.

Ballas N, Lioy DT, Grunseich C, Mandel G.

Nat Neurosci. 2009 Mar;12(3):311-7. doi: 10.1038/nn.2275. Epub 2009 Feb 22.


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 17;11:19. doi: 10.1186/1471-2202-11-19.


Alterations of gene expression and glutamate clearance in astrocytes derived from an MeCP2-null mouse model of Rett syndrome.

Okabe Y, Takahashi T, Mitsumasu C, Kosai K, Tanaka E, Matsuishi T.

PLoS One. 2012;7(4):e35354. doi: 10.1371/journal.pone.0035354. Epub 2012 Apr 20.


A role for glia in the progression of Rett's syndrome.

Lioy DT, Garg SK, Monaghan CE, Raber J, Foust KD, Kaspar BK, Hirrlinger PG, Kirchhoff F, Bissonnette JM, Ballas N, Mandel G.

Nature. 2011 Jun 29;475(7357):497-500. doi: 10.1038/nature10214.


Developmental abnormalities of cortical interneurons precede symptoms onset in a mouse model of Rett syndrome.

Tomassy GS, Morello N, Calcagno E, Giustetto M.

J Neurochem. 2014 Oct;131(1):115-27. doi: 10.1111/jnc.12803. Epub 2014 Aug 5.


Neuronal morphology in MeCP2 mouse models is intrinsically variable and depends on age, cell type, and Mecp2 mutation.

Wang IT, Reyes AR, Zhou Z.

Neurobiol Dis. 2013 Oct;58:3-12. doi: 10.1016/j.nbd.2013.04.020. Epub 2013 May 6.


MeCP2+/- mouse model of RTT reproduces auditory phenotypes associated with Rett syndrome and replicate select EEG endophenotypes of autism spectrum disorder.

Liao W, Gandal MJ, Ehrlichman RS, Siegel SJ, Carlson GC.

Neurobiol Dis. 2012 Apr;46(1):88-92. doi: 10.1016/j.nbd.2011.12.048. Epub 2012 Jan 9.


Neural development of methyl-CpG-binding protein 2 null embryonic stem cells: a system for studying Rett syndrome.

Okabe Y, Kusaga A, Takahashi T, Mitsumasu C, Murai Y, Tanaka E, Higashi H, Matsuishi T, Kosai K.

Brain Res. 2010 Nov 11;1360:17-27. doi: 10.1016/j.brainres.2010.08.090. Epub 2010 Sep 25.


Age-dependent expression of MeCP2 in a heterozygous mosaic mouse model.

Smrt RD, Pfeiffer RL, Zhao X.

Hum Mol Genet. 2011 May 1;20(9):1834-43. doi: 10.1093/hmg/ddr066. Epub 2011 Feb 17.


FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice.

Deng V, Matagne V, Banine F, Frerking M, Ohliger P, Budden S, Pevsner J, Dissen GA, Sherman LS, Ojeda SR.

Hum Mol Genet. 2007 Mar 15;16(6):640-50. Epub 2007 Feb 19.


Altered microtubule dynamics in Mecp2-deficient astrocytes.

Nectoux J, Florian C, Delepine C, Bahi-Buisson N, Khelfaoui M, Reibel S, Chelly J, Bienvenu T.

J Neurosci Res. 2012 May;90(5):990-8. doi: 10.1002/jnr.23001. Epub 2012 Jan 18.


Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice.

Chen RZ, Akbarian S, Tudor M, Jaenisch R.

Nat Genet. 2001 Mar;27(3):327-31.


Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome.

Peddada S, Yasui DH, LaSalle JM.

Hum Mol Genet. 2006 Jun 15;15(12):2003-14. Epub 2006 May 8.


MeCP2 is critical for maintaining mature neuronal networks and global brain anatomy during late stages of postnatal brain development and in the mature adult brain.

Nguyen MV, Du F, Felice CA, Shan X, Nigam A, Mandel G, Robinson JK, Ballas N.

J Neurosci. 2012 Jul 18;32(29):10021-34. doi: 10.1523/JNEUROSCI.1316-12.2012.


Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism.

Swanberg SE, Nagarajan RP, Peddada S, Yasui DH, LaSalle JM.

Hum Mol Genet. 2009 Feb 1;18(3):525-34. doi: 10.1093/hmg/ddn380. Epub 2008 Nov 10.


Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations.

Larimore JL, Chapleau CA, Kudo S, Theibert A, Percy AK, Pozzo-Miller L.

Neurobiol Dis. 2009 May;34(2):199-211. doi: 10.1016/j.nbd.2008.12.011. Epub 2009 Jan 3.


Wild-type microglia arrest pathology in a mouse model of Rett syndrome.

Derecki NC, Cronk JC, Lu Z, Xu E, Abbott SB, Guyenet PG, Kipnis J.

Nature. 2012 Mar 18;484(7392):105-9. doi: 10.1038/nature10907.

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