Developmental Study of Fragile X Syndrome Using Human Embryonic Stem Cells Derived from Preimplantation Genetically Diagnosed Embryos
Top Cited Papers
- 1 November 2007
- journal article
- research article
- Published by Elsevier in Cell Stem Cell
- Vol. 1 (5) , 568-577
- https://doi.org/10.1016/j.stem.2007.09.001
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutationExperimental Cell Research, 2006
- Overexpression of NANOG in human ES cells enables feeder-free growth while inducing primitive ectoderm featuresDevelopment, 2006
- Temporal gene expression during differentiation of human embryonic stem cells and embryoid bodiesHuman Reproduction, 2004
- Human embryonic stem cells as a model for early human developmentBest Practice & Research Clinical Obstetrics & Gynaecology, 2004
- Histone Modifications Depict an Aberrantly Heterochromatinized FMR1 Gene in Fragile X SyndromeAmerican Journal of Human Genetics, 2002
- FMR1 and the fragile X syndrome: Human genome epidemiology reviewGenetics in Medicine, 2001
- Instability of a (CGG)98 repeat in the Fmr1 promoterHuman Molecular Genetics, 2001
- Fully Expanded FMR1CGG Repeats Exhibit a Length-and Differentiation-Dependent Instability in Cell Hybrids That is Independent of DNA MethylationHuman Molecular Genetics, 1999
- Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cellsNature Genetics, 1999
- FMR1 Premutation Allele (CGG)(81) Is Stable in MicePublished by Wiley ,1997