Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 606


Ube3a expression is not altered in Mecp2 mutant mice.

Jordan C, Francke U.

Hum Mol Genet. 2006 Jul 15;15(14):2210-5. Epub 2006 Jun 5.


Disrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndrome.

Urdinguio RG, Fernandez AF, Lopez-Nieva P, Rossi S, Huertas D, Kulis M, Liu CG, Croce CM, Calin GA, Esteller M.

Epigenetics. 2010 Oct 1;5(7):656-63. doi: 10.4161/epi.5.7.13055. Epub 2010 Oct 1.


Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients.

Delgado IJ, Kim DS, Thatcher KN, LaSalle JM, Van den Veyver IB.

BMC Med Genet. 2006 Jul 21;7:61.


Correcting deregulated Fxyd1 expression ameliorates a behavioral impairment in a mouse model of Rett syndrome.

Matagne V, Budden S, Ojeda SR, Raber J.

Brain Res. 2013 Feb 16;1496:104-14. doi: 10.1016/j.brainres.2012.12.009. Epub 2012 Dec 14.


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.


Mecp2-null mice provide new neuronal targets for Rett syndrome.

Urdinguio RG, Lopez-Serra L, Lopez-Nieva P, Alaminos M, Diaz-Uriarte R, Fernandez AF, Esteller M.

PLoS One. 2008;3(11):e3669. doi: 10.1371/journal.pone.0003669. Epub 2008 Nov 7.


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.


MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome.

Wan M, Zhao K, Lee SS, Francke U.

Hum Mol Genet. 2001 May 1;10(10):1085-92.


MeCP2 dysfunction in Rett syndrome and related disorders.

Moretti P, Zoghbi HY.

Curr Opin Genet Dev. 2006 Jun;16(3):276-81. Epub 2006 May 2. Review.


The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis.

Forlani G, Giarda E, Ala U, Di Cunto F, Salani M, Tupler R, Kilstrup-Nielsen C, Landsberger N.

Hum Mol Genet. 2010 Aug 15;19(16):3114-23. doi: 10.1093/hmg/ddq214. Epub 2010 May 26.


DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency.

Schüle B, Li HH, Fisch-Kohl C, Purmann C, Francke U.

Am J Hum Genet. 2007 Sep;81(3):492-506. Epub 2007 Aug 2.


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 brains.

Itoh M, Ide S, Takashima S, Kudo S, Nomura Y, Segawa M, Kubota T, Mori H, Tanaka S, Horie H, Tanabe Y, Goto Y.

J Neuropathol Exp Neurol. 2007 Feb;66(2):117-23.


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. Review.


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.


Rett syndrome: the complex nature of a monogenic disease.

Renieri A, Meloni I, Longo I, Ariani F, Mari F, Pescucci C, Cambi F.

J Mol Med (Berl). 2003 Jun;81(6):346-54. Epub 2003 May 16. Review.


Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus.

Ben-Shachar S, Chahrour M, Thaller C, Shaw CA, Zoghbi HY.

Hum Mol Genet. 2009 Jul 1;18(13):2431-42. doi: 10.1093/hmg/ddp181. Epub 2009 Apr 15.


Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.

Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY.

Nat Genet. 1999 Oct;23(2):185-8.


Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain.

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

Proc Natl Acad Sci U S A. 2002 Nov 26;99(24):15536-41. Epub 2002 Nov 13.


MeCP2 Rett mutations affect large scale chromatin organization.

Agarwal N, Becker A, Jost KL, Haase S, Thakur BK, Brero A, Hardt T, Kudo S, Leonhardt H, Cardoso MC.

Hum Mol Genet. 2011 Nov 1;20(21):4187-95. doi: 10.1093/hmg/ddr346. Epub 2011 Aug 10.

Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk