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Items: 10

1.

A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells.

Marchetto MC, Carromeu C, Acab A, Yu D, Yeo GW, Mu Y, Chen G, Gage FH, Muotri AR.

Cell. 2010 Nov 12;143(4):527-39. doi: 10.1016/j.cell.2010.10.016.

2.

Induced pluripotency: history, mechanisms, and applications.

Stadtfeld M, Hochedlinger K.

Genes Dev. 2010 Oct 15;24(20):2239-63. doi: 10.1101/gad.1963910. Review.

3.

Female human iPSCs retain an inactive X chromosome.

Tchieu J, Kuoy E, Chin MH, Trinh H, Patterson M, Sherman SP, Aimiuwu O, Lindgren A, Hakimian S, Zack JA, Clark AT, Pyle AD, Lowry WE, Plath K.

Cell Stem Cell. 2010 Sep 3;7(3):329-42. doi: 10.1016/j.stem.2010.06.024. Epub 2010 Aug 19.

4.

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice.

Tropea D, Giacometti E, Wilson NR, Beard C, McCurry C, Fu DD, Flannery R, Jaenisch R, Sur M.

Proc Natl Acad Sci U S A. 2009 Feb 10;106(6):2029-34. doi: 10.1073/pnas.0812394106.

5.
6.

Reversal of neurological defects in a mouse model of Rett syndrome.

Guy J, Gan J, Selfridge J, Cobb S, Bird A.

Science. 2007 Feb 23;315(5815):1143-7. Epub 2007 Feb 8.

7.

Rett syndrome: model of neurodevelopmental disorders.

Percy AK, Lane JB.

J Child Neurol. 2005 Sep;20(9):718-21. Review.

PMID:
16225824
8.

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.

PMID:
11242118
9.

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome.

Guy J, Hendrich B, Holmes M, Martin JE, Bird A.

Nat Genet. 2001 Mar;27(3):322-6.

PMID:
11242117
10.

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.

PMID:
10508514

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