Sara Selig

Haifa, HA 31096, Israel

Last Updated: 09/26/2026

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Found 18 publications

Missense substitutions in the BTB domain of ZBTB24 can lead to protein instability and cause ICF2 syndrome.

Missense substitutions in the BTB domain of ZBTB24 can lead to protein instability and cause ICF2 syndrome.

Journal: Human molecular genetics

Published: June 25, 2025

ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming.

ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming.

Journal: Biomolecules

Published: August 02, 2023

MBTPS1 regulates proliferation of colorectal cancer primarily through its action on sterol regulatory element-binding proteins.

MBTPS1 regulates proliferation of colorectal cancer primarily through its action on sterol regulatory element-binding proteins.

Journal: Frontiers in oncology

Published: July 26, 2022

The aberrant epigenome of DNMT3B-mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory.

The aberrant epigenome of DNMT3B-mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memory.

Journal: Genome research

Published: June 01, 2022

Comparative Analysis of the APOL1 Variants in the Genetic Landscape of Renal Carcinoma Cells.

Comparative Analysis of the APOL1 Variants in the Genetic Landscape of Renal Carcinoma Cells.

Journal: Cancers

Published: December 13, 2021

Epigenetic Characteristics of Human Subtelomeres Vary in Cells Utilizing the Alternative Lengthening of Telomeres (ALT) Pathway.

Epigenetic Characteristics of Human Subtelomeres Vary in Cells Utilizing the Alternative Lengthening of Telomeres (ALT) Pathway.

Journal: Life (Basel, Switzerland)

Published: March 01, 2021

RBL2 bi-allelic truncating variants cause severe motor and cognitive impairment without evidence for abnormalities in DNA methylation or telomeric function.

RBL2 bi-allelic truncating variants cause severe motor and cognitive impairment without evidence for abnormalities in DNA methylation or telomeric function.

Journal: Journal of human genetics

Published: February 16, 2021

Regulation of telomeric function by DNA methylation differs between humans and mice.

Regulation of telomeric function by DNA methylation differs between humans and mice.

Journal: Human molecular genetics

Published: July 02, 2020

Human subtelomeric DNA methylation: regulation and roles in telomere function.

Human subtelomeric DNA methylation: regulation and roles in telomere function.

Journal: Current opinion in genetics & development

Published: November 27, 2019

Persistent epigenetic memory impedes rescue of the telomeric phenotype in human ICF iPSCs following DNMT3B correction.

Persistent epigenetic memory impedes rescue of the telomeric phenotype in human ICF iPSCs following DNMT3B correction.

Journal: eLife

Published: April 22, 2019

Subtelomeric methylation distinguishes between subtypes of Immunodeficiency, Centromeric instability and Facial anomalies syndrome.

Subtelomeric methylation distinguishes between subtypes of Immunodeficiency, Centromeric instability and Facial anomalies syndrome.

Journal: Human molecular genetics

Published: March 04, 2018

DNA:RNA hybrids at telomeres - when it is better to be out of the (R) loop.

DNA:RNA hybrids at telomeres - when it is better to be out of the (R) loop.

Journal: The FEBS journal

Published: February 15, 2018

Showing 1-12 of 18

Last Updated: 09/26/2026