Search filters

List of works by Rachel Eiges

Establishment of Homozygote Mutant Human Embryonic Stem Cells by Parthenogenesis

scientific article published on 16 October 2015

FMR1 epigenetic silencing commonly occurs in undifferentiated fragile X-affected embryonic stem cells

scientific article

Female sex bias in human embryonic stem cell lines.

scientific article published on 24 June 2011

GNE Is Involved in the Early Development of Skeletal and Cardiac Muscle ⬇️

scientific article published on June 24, 2011

Genetic Manipulation of Human Embryonic Stem Cells.

scientific article published in January 2016

Genetic manipulation of human embryonic stem cells.

scientific article

Incomplete methylation of a germ cell tumor (Seminoma) in a Prader-Willi male

scientific article published on 12 July 2018

Marked Differences in C9orf72 Methylation Status and Isoform Expression between C9/ALS Human Embryonic and Induced Pluripotent Stem Cells.

scientific article published on 17 October 2016

Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells

scientific article

Modeling diseases of noncoding unstable repeat expansions using mutant pluripotent stem cells.

scientific article

Monitoring for Epigenetic Modifications at the FMR1 Locus

scientific article published on 01 January 2019

PGD-derived human embryonic stem cell lines as a powerful tool for the study of human genetic disorders.

scientific article

Preventing mucopolysaccharidosis type II (Hunter syndrome): PGD and establishing a Hunter (46, XX) stem cell line.

scientific article published on 27 June 2011

Prevention of lysosomal storage diseases and derivation of mutant stem cell lines by preimplantation genetic diagnosis.

scientific article published on 26 December 2012

Reevaluation of FMR1 Hypermethylation Timing in Fragile X Syndrome.

scientific article published on 6 February 2018

The Contribution of Pluripotent Stem Cell (PSC)-Based Models to the Study of Fragile X Syndrome (FXS)

scientific article published on 15 February 2019

The G-rich Repeats in and Loci Are Hotspots for Local Unpairing of DNA

scientific article published on 05 November 2018

Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem Cells

scientific article

Paulina is supported by:

About Paulina

Help