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Mechanistic insight into the interaction of BLM helicase with intra-strand G-quadruplex structures
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Werner syndrome protein suppresses the formation of large deletions during the replication of human telomeric sequences
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FANCJ coordinates two pathways that maintain epigenetic stability at G-quadruplex DNA
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Solution Structure of a 2:1 Quindoline-c-MYC G-Quadruplex: Insights into G-Quadruplex-Interactive Small Molecule Drug Design
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c-MYC promoter G-quadruplex formed at the 5′-end of NHE III1 element: insights into biological relevance and parallel-stranded G-quadruplex stability
Raveendra I. Mathad et al.
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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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Structural Basis for DNA Strand Separation by the Unconventional Winged-Helix Domain of RecQ Helicase WRN
Ken Kitano et al.
STRUCTURE (2010)
The RecQ helicase WRN is required for normal replication fork progression after DNA damage or replication fork arrest
Julia M. Sidorova et al.
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FANCJ Is a Structure-specific DNA Helicase Associated with the Maintenance of Genomic G/C Tracts
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A conserved G4 DNA binding domain in RecQ family helicases
Michael D. Huber et al.
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Solution structure of a multifunctional DNA- and protein-binding motif of human Werner syndrome protein
JS Hu et al.
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Helicase-catalysed translocation and strand separation
RL Eoff et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2005)
Modulation of Werner syndrome protein function by a single mutation in the conserved RecQ domain
JW Lee et al.
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Solution structure of the biologically relevant g-quadruplex element in the human c-MYC promoter. implications for g-quadruplex stabilization
A Ambrus et al.
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Defective telomere lagging strand synthesis in cells lacking WRN helicase activity
L Crabbe et al.
SCIENCE (2004)
Gene expression profiling in Werner syndrome closely resembles that of normal aging
KJ Kyng et al.
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Helicase mechanisms and the coupling of helicases within macromolecular machines Part 1: Structures and properties of isolated helicases
E Delagoutte et al.
QUARTERLY REVIEWS OF BIOPHYSICS (2002)
Biochemical characterization of the DNA substrate specificity of Werner syndrome helicase
RM Brosh et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Helicase structure and mechanism
JM Caruthers et al.
CURRENT OPINION IN STRUCTURAL BIOLOGY (2002)
Werner's syndrome protein is required for correct recovery after replication arrest and DNA damage induced in S-phase of cell cycle
P Pichierri et al.
MOLECULAR BIOLOGY OF THE CELL (2001)
The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases
P Mohaghegh et al.
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Interactions between the Werner syndrome helicase and DNA polymerase δ specifically facilitate copying of tetraplex and hairpin structures of the d(CGG)n trinucleotide repeat sequence
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Werner syndrome protein: biochemical properties and functional interactions
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EXPERIMENTAL GERONTOLOGY (2000)
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