Publications by authors named "Noa Hourvitz"

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The many faces of the helicase RTEL1 at telomeres and beyond.
Noa Hourvitz, Aya Awad, Yehuda Tzfati

Trends Cell Biol· February 2024

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SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetrance.
Noa Hourvitz, Alina Kurolap, Adi Mory, Karina Krajden Haratz, Dvora Kidron

Prenat Diagn· September 2023

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Accelerated replicative senescence of ataxia-telangiectasia skin fibroblasts is retained at physiologic oxygen levels, with unique and common transcriptional patterns.
Majd Haj, Amit Levon, Yann Frey, Noa Hourvitz, Judith Campisi

Aging Cell· August 2023

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Small STEPs toward a big change.
Noa Hourvitz

Cell· March 2023

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Full length RTEL1 is required for the elongation of the single-stranded telomeric overhang by telomerase.
Aya Awad, Galina Glousker, Noa Lamm, Shadi Tawil, Noa Hourvitz

Nucleic Acids Res· July 2020

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