Associated Papers
Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita.
Sanz-Moreno A et al.
Science Advances, 2025
The landscape of rare genetic variants in familial Waldenström macroglobulinemia.
Pemov A et al.
Blood Neoplasia, 2024
39036705 (PubMed )
Supplement: BNEO_NEO-2023-000111-mmc8.xlsx › Supplementary_Table_7C
Functional Homologous Recombination (HR) Screening Shows the Majority of BRCA1/2-Mutant Breast and Ovarian Cancer Cell Lines Are HR-Proficient.
Meijer TG et al.
Cancers, 2024
38398132 (PubMed )
Supplement: cancers-16-00741-s001.zip › Table_S1-2_WES_results.xlsx › Table_S1
Structural and functional impact of non-synonymous SNPs in the CST complex subunit TEN1: structural genomics approach.
Amir M et al.
Bioscience Reports, 2019
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