Developmental Study of Fragile X Syndrome Using Human Embryonic Stem Cells Derived from Preimplantation Genetically Diagnosed Embryos-Reference-Cited by-同舟云学术

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Developmental Study of Fragile X Syndrome Using Human Embryonic Stem Cells Derived from Preimplantation Genetically Diagnosed Embryos

Published:2007-11 Issue:5 Volume:1 Page:568-577
ISSN:1934-5909
Container-title:Cell Stem Cell
language:en
Short-container-title:Cell Stem Cell

Author:

Eiges Rachel,Urbach Achia,Malcov Mira,Frumkin Tsvia,Schwartz Tamar,Amit Ami,Yaron Yuval,Eden Amir,Yanuka Ofra,Benvenisty Nissim,Ben-Yosef Dalit

Publisher

Elsevier BV

Subject

Cell Biology,Genetics,Molecular Medicine

Reference41 articles.

1. FMR1 premutation allele (CGG)81 is stable in mice;Bontekoe;Eur. J. Hum. Genet.,1997

2. Instability of a (CGG)98 repeat in the Fmr1 promoter;Bontekoe;Hum. Mol. Genet.,2001

3. Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation;Brouwer;Exp. Cell Res.,2007

4. Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation;Burman;Hum. Mol. Genet.,1999

5. Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells;Coffee;Nat. Genet.,1999

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1. Epigenetic insights into Fragile X Syndrome;Frontiers in Cell and Developmental Biology;2024-08-16

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