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2. The structural mechanism of dimeric DONSON in replicative helicase activation

4. Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly

5. H3K4 methylation by SETD1A/BOD1L facilitates RIF1-dependent NHEJ

6. Histone Methylation by SETD1A Protects Nascent DNA through the Nucleosome Chaperone Activity of FANCD2

8. Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia

9. Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes

10. Histone Methylation by SETD1A Protects Nascent DNA through the Nucleosome Chaperone Activity of FANCD2

12. BOD1L Is Required to Suppress Deleterious Resection of Stressed Replication Forks

13. Mutations in the NHEJ Component XRCC4 Cause Primordial Dwarfism

15. Regulation of DNA-End Resection by hnRNPU-like Proteins Promotes DNA Double-Strand Break Signaling and Repair

16. The hMsh2-hMsh6 Complex Acts in Concert with Monoubiquitinated PCNA and Pol η in Response to Oxidative DNA Damage in Human Cells

20. The RIDDLE Syndrome Protein Mediates a Ubiquitin-Dependent Signaling Cascade at Sites of DNA Damage

21. Variations in ATM Protein Expression During Normal Lymphoid Differentiation and Among B-Cell-Derived Neoplasias

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