Silvina Litman-Epsztejn
Jerusalem, JM 91121, Israel
Last Updated: 09/26/2026
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Found 14 publications
SMCHD1 Is Dispensable for Repeat-Induced FMR1 Hypermethylation in Fragile X Pluripotent Stem Cells.
Journal: International journal of molecular sciences
Published: July 16, 2026
Pluripotency-independent induction of human trophoblast stem cells from fibroblasts.
Journal: Nature communications
Published: November 03, 2021
Differentiation shifts from a reversible to an irreversible heterochromatin state at the DM1 locus.
Journal: Nature communications
Published: September 05, 2021
DMPK hypermethylation in sperm cells of myotonic dystrophy type 1 patients.
Journal: European journal of human genetics : EJHG
Published: April 04, 2021
A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decay.
Journal: Neurobiology of aging
Published: November 15, 2020
Monitoring for Epigenetic Modifications at the FMR1 Locus.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: March 23, 2019
The G-rich Repeats in FMR1 and C9orf72 Loci Are Hotspots for Local Unpairing of DNA.
Journal: Genetics
Published: August 25, 2018
Incomplete methylation of a germ cell tumor (Seminoma) in a Prader-Willi male.
Journal: Molecular genetics & genomic medicine
Published: January 31, 2018
Establishment of Homozygote Mutant Human Embryonic Stem Cells by Parthenogenesis.
Journal: PloS one
Published: June 15, 2015
Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem Cells.
Journal: Stem cell reports
Published: May 31, 2015
Marked Differences in C9orf72 Methylation Status and Isoform Expression between C9/ALS Human Embryonic and Induced Pluripotent Stem Cells.
Journal: Stem cell reports
Published: April 02, 2015
Last Updated: 09/26/2026