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The Bloom’s Syndrome Helicase Unwinds G4 DNA*

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RNA G-quadruplexes are globally unfolded in eukaryotic cells and depleted in bacteria

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Pif1 family helicases suppress genome instability at G-quadruplex motifs

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G-quadruplex structures are stable and detectable in human genomic DNA

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G-quadruplexes and helicases

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FANCJ Helicase Defective in Fanconia Anemia and Breast Cancer Unwinds G-Quadruplex DNA To Defend Genomic Stability

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RTEL1 Maintains Genomic Stability by Suppressing Homologous Recombination

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The Yeast Pif1 Helicase Prevents Genomic Instability Caused by G-Quadruplex-Forming CEB1 Sequences In Vivo

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The RecQ DNA Helicases in DNA Repair

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G-Quadruplex DNA Sequences Are Evolutionarily Conserved and Associated with Distinct Genomic Features in Saccharomyces cerevisiae

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FANCJ Is a Structure-specific DNA Helicase Associated with the Maintenance of Genomic G/C Tracts

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DNA and RNA Quadruplex-Binding Proteins

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FANCJ coordinates two pathways that maintain epigenetic stability at G-quadruplex DNA

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Telomeric repeat-containing RNA TERRA: a noncoding RNA connecting telomere biology to genome integrity

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G4 Resolvase 1 Binds Both DNA and RNA Tetramolecular Quadruplex with High Affinity and Is the Major Source of Tetramolecular Quadruplex G4-DNA and G4-RNA Resolving Activity in HeLa Cell Lysates

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Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability

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Pause Sites Promote Transcriptional Termination of Mammalian RNA Polymerase II

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The BLM helicase contributes to telomere maintenance through processing of late-replicating intermediate structures

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Mammalian DNA2 helicase/nuclease cleaves G‐quadruplex DNA and is required for telomere integrity

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BLM helicase facilitates telomere replication during leading strand synthesis of telomeres

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RecQ Helicases: Conserved Guardians of Genomic Integrity

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The RNA helicase RHAU (DHX36) unwinds a G4-quadruplex in human telomerase RNA and promotes the formation of the P1 helix template boundary

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FANCJ promotes DNA synthesis through G‐quadruplex structures

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Altered gene expression in the Werner and Bloom syndromes is associated with sequences having G-quadruplex forming potential

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G-Quadruplexes in DNA Replication: A Problem or a Necessity?

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The Human RecQ Helicases, BLM and RECQ1, Display Distinct DNA Substrate Specificities

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Telomerase recruitment by the telomere end binding protein-β facilitates G-quadruplex DNA unfolding in ciliates

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Human RECQ1 and RECQ4 Helicases Play Distinct Roles in DNA Replication Initiation

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Specialization among Iron-Sulfur Cluster Helicases to Resolve G-quadruplex DNA Structures That Threaten Genomic Stability

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