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SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetrance.
Prenat Diagn. 2023 Sep;43(10):1374-1377. doi: 10.1002/pd.6426. Epub 2023 Aug 28.
Prenat Diagn. 2023.
PMID: 37639281
The many faces of the helicase RTEL1 at telomeres and beyond.
Hourvitz N, Awad A, Tzfati Y.
Hourvitz N, et al.
Trends Cell Biol. 2024 Feb;34(2):109-121. doi: 10.1016/j.tcb.2023.07.002. Epub 2023 Jul 31.
Trends Cell Biol. 2024.
PMID: 37532653
Review.
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Accelerated replicative senescence of ataxia-telangiectasia skin fibroblasts is retained at physiologic oxygen levels, with unique and common transcriptional patterns.
Haj M, Levon A, Frey Y, Hourvitz N, Campisi J, Tzfati Y, Elkon R, Ziv Y, Shiloh Y.
Haj M, et al. Among authors: hourvitz n.
Aging Cell. 2023 Aug;22(8):e13869. doi: 10.1111/acel.13869. Epub 2023 May 30.
Aging Cell. 2023.
PMID: 37254625
Free PMC article.
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Small STEPs toward a big change.
Hourvitz N.
Hourvitz N.
Cell. 2023 Mar 16;186(6):1092-1096. doi: 10.1016/j.cell.2023.02.012.
Cell. 2023.
PMID: 36931238
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Full length RTEL1 is required for the elongation of the single-stranded telomeric overhang by telomerase.
Awad A, Glousker G, Lamm N, Tawil S, Hourvitz N, Smoom R, Revy P, Tzfati Y.
Awad A, et al. Among authors: hourvitz n.
Nucleic Acids Res. 2020 Jul 27;48(13):7239-7251. doi: 10.1093/nar/gkaa503.
Nucleic Acids Res. 2020.
PMID: 32542379
Free PMC article.
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