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X-chromosome inactivation in rett syndrome human induced pluripotent stem cells.

Cheung AY, Horvath LM, Carrel L, Ellis J.

Front Psychiatry. 2012 Mar 23;3:24. doi: 10.3389/fpsyt.2012.00024. eCollection 2012.


A review of Rett syndrome (RTT) with induced pluripotent stem cells.

Balachandar V, Dhivya V, Gomathi M, Mohanadevi S, Venkatesh B, Geetha B.

Stem Cell Investig. 2016 Sep 28;3:52. eCollection 2016. Review.


Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation.

Cheung AY, Horvath LM, Grafodatskaya D, Pasceri P, Weksberg R, Hotta A, Carrel L, Ellis J.

Hum Mol Genet. 2011 Jun 1;20(11):2103-15. doi: 10.1093/hmg/ddr093. Epub 2011 Mar 3.


X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.

Braunschweig D, Simcox T, Samaco RC, LaSalle JM.

Hum Mol Genet. 2004 Jun 15;13(12):1275-86. Epub 2004 Apr 28.


Differentiation of multipotent neural stem cells derived from Rett syndrome patients is biased toward the astrocytic lineage.

Andoh-Noda T, Akamatsu W, Miyake K, Matsumoto T, Yamaguchi R, Sanosaka T, Okada Y, Kobayashi T, Ohyama M, Nakashima K, Kurosawa H, Kubota T, Okano H.

Mol Brain. 2015 May 27;8:31. doi: 10.1186/s13041-015-0121-2.


[Analysis of the parental origin of de novo MECP2 mutations and X chromosome inactivation in fifteen sporadic cases with Rett syndrome].

Zhu XW, Pan H, Li MR, Bao XH, Zhang JJ, Wu XR.

Zhonghua Er Ke Za Zhi. 2009 Aug;47(8):565-9. Chinese.


[X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome].

Jiang SL, Bao XH, Song FY, Pan H, Li MR, Wu XR.

Zhonghua Er Ke Za Zhi. 2006 Sep;44(9):648-52. Chinese.


Transcriptional regulation in pluripotent stem cells by methyl CpG-binding protein 2 (MeCP2).

Tanaka Y, Kim KY, Zhong M, Pan X, Weissman SM, Park IH.

Hum Mol Genet. 2014 Feb 15;23(4):1045-55. doi: 10.1093/hmg/ddt500. Epub 2013 Oct 15.


Neuronal maturation defect in induced pluripotent stem cells from patients with Rett syndrome.

Kim KY, Hysolli E, Park IH.

Proc Natl Acad Sci U S A. 2011 Aug 23;108(34):14169-74. doi: 10.1073/pnas.1018979108. Epub 2011 Aug 1.


Cell cloning-based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes.

Nectoux J, Fichou Y, Rosas-Vargas H, Cagnard N, Bahi-Buisson N, Nusbaum P, Letourneur F, Chelly J, Bienvenu T.

J Cell Mol Med. 2010 Jul;14(7):1962-74. doi: 10.1111/j.1582-4934.2010.01107.x. Epub 2010 Jun 21.


Balanced X chromosome inactivation patterns in the Rett syndrome brain.

Shahbazian MD, Sun Y, Zoghbi HY.

Am J Med Genet. 2002 Aug 1;111(2):164-8.


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.


Two new Rett syndrome families and review of the literature: expanding the knowledge of MECP2 frameshift mutations.

Ravn K, Roende G, Duno M, Fuglsang K, Eiklid KL, Tümer Z, Nielsen JB, Skjeldal OH.

Orphanet J Rare Dis. 2011 Aug 30;6:58. doi: 10.1186/1750-1172-6-58. Review.


Modeling Rett Syndrome Using Human Induced Pluripotent Stem Cells.

Andoh-Noda T, Inouye MO, Miyake K, Kubota T, Okano H, Akamatsu W.

CNS Neurol Disord Drug Targets. 2016;15(5):544-50. Review.


[Genetic features and mechanism of Rett syndrome in Chinese population].

Zhang X, Zhao Y, Bao X, Zhang J, Cao G, Wu X.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Feb;31(1):1-5. doi: 10.3760/cma.j.issn.1003-9406.2014.01.001. Chinese.


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. doi: 10.1038/mp.2011.180. Epub 2012 Jan 10.


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.


Isogenic pairs of wild type and mutant induced pluripotent stem cell (iPSC) lines from Rett syndrome patients as in vitro disease model.

Ananiev G, Williams EC, Li H, Chang Q.

PLoS One. 2011;6(9):e25255. doi: 10.1371/journal.pone.0025255. Epub 2011 Sep 26.


Reduced proportion of Purkinje cells expressing paternally derived mutant Mecp2308 allele in female mouse cerebellum is not due to a skewed primary pattern of X-chromosome inactivation.

Watson CM, Pelka GJ, Radziewic T, Shahbazian MD, Christodoulou J, Williamson SL, Tam PP.

Hum Mol Genet. 2005 Jul 1;14(13):1851-61. Epub 2005 May 11.


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