Telomeric protein TRF2 protects Holliday junctions with telomeric arms from displacement by the Werner syndrome helicase

The RecQ helicase WRN is required for normal replication fork progression after DNA damage or replication fork arrest

(2010) Julia M. Sidorova et al.   CELL CYCLE

TRF2 promotes, remodels and protects telomeric Holliday junctions

(2009) Anaïs Poulet et al.   EMBO JOURNAL

Human RAP1 inhibits non-homologous end joining at telomeres

(2009) Jay Sarthy et al.   EMBO JOURNAL

Sumoylation of RecQ Helicase Controls the Fate of Dysfunctional Telomeres

(2009) Ofer Rog et al.   MOLECULAR CELL

The Werner Syndrome Helicase/Exonuclease Processes Mobile D-Loops through Branch Migration and Degradation

(2009) Patricia L. Opresko et al.   PLoS One

How Telomeres Solve the End-Protection Problem

(2009) T. de Lange   SCIENCE

Translocation and Unwinding Mechanisms of RNA and DNA Helicases

(2008) Anna Marie Pyle   Annual Review of Biophysics

How Shelterin Protects Mammalian Telomeres

(2008) Wilhelm Palm et al.   Annual Review of Genetics

The Werner Syndrome Protein Binds Replication Fork and Holliday Junction DNAs as an Oligomer

(2008) Sarah A. Compton et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

WRN Controls Formation of Extrachromosomal Telomeric Circles and Is Required for TRF2 B-Mediated Telomere Shortening

(2008) B. Li et al.   MOLECULAR AND CELLULAR BIOLOGY

Mechanism and substrate specificity of telomeric protein POT1 stimulation of the Werner syndrome helicase

(2008) Gregory Sowd et al.   NUCLEIC ACIDS RESEARCH

Telomere ResQue and preservation—Roles for the Werner syndrome protein and other RecQ helicases

(2007) Patricia L. Opresko   MECHANISMS OF AGEING AND DEVELOPMENT

Comparison between TRF2 and TRF1 of their telomeric DNA-bound structures and DNA-binding activities

(2004) Shingo Hanaoka et al.   PROTEIN SCIENCE