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Response to Replication Stress and Maintenance of Genome Stability by WRN, the Werner Syndrome Protein

International journal of molecular sciences, 2024-08, Vol.25 (15), p.8300

2024

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Cigarette Smoke-Induced Epithelial-to-Mesenchymal Transition: Insights into Cellular Mechanisms and Signaling Pathways

Cells (Basel, Switzerland), 2024-08, Vol.13 (17), p.1453

2024

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The Werner and Bloom Syndrome Proteins Help Resolve Replication Blockage by Converting (Regressed) Holliday Junctions to Functional Replication Forks

Biochemistry (Easton), 2011-08, Vol.50 (32), p.6774-6788

2011

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Strand exchange of telomeric DNA catalyzed by the Werner syndrome protein (WRN) is specifically stimulated by TRF2

Nucleic acids research, 2014-07, Vol.42 (12), p.7748-7761

2014

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Intramolecular telomeric G-quadruplexes dramatically inhibit DNA synthesis by replicative and translesion polymerases, revealing their potential to lead to genetic change

PloS one, 2014-01, Vol.9 (1), p.e80664

2014

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The Werner and Bloom Syndrome Proteins Catalyze Regression of a Model Replication Fork

Biochemistry (Easton), 2006-11, Vol.45 (47), p.13939-13946

2006

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The DNA structure and sequence preferences of WRN underlie its function in telomeric recombination events

Nature communications, 2015-09, Vol.6 (1), p.8331, Article 8331

2015

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Molecular Cooperation between the Werner Syndrome Protein and Replication Protein A in Relation to Replication Fork Blockage

The Journal of biological chemistry, 2011-02, Vol.286 (5), p.3497-3508

2011

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RecQ Family Members Combine Strand Pairing and Unwinding Activities to Catalyze Strand Exchange

The Journal of biological chemistry, 2005-06, Vol.280 (24), p.23397-23407

2005

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TRF2 recruits the Werner syndrome (WRN) exonuclease for processing of telomeric DNA

Oncogene, 2004-01, Vol.23 (1), p.149-156

2004

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The Werner syndrome protein promotes CAG/CTG repeat stability by resolving large (CAG)(n)/(CTG)(n) hairpins

The Journal of biological chemistry, 2012-08, Vol.287 (36), p.30151-30156

2012

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Functional and Physical Interaction between WRN Helicase and Human Replication Protein A

The Journal of biological chemistry, 1999-06, Vol.274 (26), p.18341-18350

1999

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Lysine Acetylation of Proteins and Its Characterization in Human Systems

Methods in molecular biology (Clifton, N.J.), 2019, Vol.1983, p.107

2019

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The Werner syndrome protein is involved in RNA polymerase II transcription

Molecular biology of the cell, 1999-08, Vol.10 (8), p.2655-2668

1999

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DNase I Footprinting and Enhanced Exonuclease Function of the Bipartite Werner Syndrome Protein (WRN) Bound to Partially Melted Duplex DNA

The Journal of biological chemistry, 2002-02, Vol.277 (6), p.4492-4504

2002

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Accelerated methylation of ribosomal RNA genes during the cellular senescence of Werner syndrome fibroblasts

The FASEB journal, 2000-09, Vol.14 (12), p.1715-1724

2000

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Role for the Werner syndrome protein (WRN) in replication fork regression

The FASEB journal, 2008-03, Vol.22 (S1)

2008

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The Werner Syndrome Protein Promotes CAG/CTG Repeat Stability by Resolving Large (CAG)n/(CTG)n Hairpins

The Journal of biological chemistry, 2012-08, Vol.287 (36), p.30151-30156

2012

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Replication fork regression in vitro by the Werner syndrome protein (WRN): holliday junction formation, the effect of leading arm structure and a potential role for WRN exonuclease activity

Nucleic acids research, 2007-09, Vol.35 (17), p.5729-5747

2007

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Association and regulation of the BLM helicase by the telomere proteins TRF1 and TRF2

Human molecular genetics, 2004-09, Vol.13 (17), p.1919-1932

2004

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Ku complex interacts with and stimulates the Werner protein

Genes & development, 2000-04, Vol.14 (8), p.907-912

2000

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The Werner Syndrome Helicase/Exonuclease (WRN) Disrupts and Degrades D-Loops in Vitro

Biochemistry (Easton), 2002-11, Vol.41 (46), p.13483-13488

2002

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High constitutive peroxidase activity and constitutive thermotolerance in Neurospora crassa

Mycoscience, 2003-04, Vol.44 (2), p.129-137

2003

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Induction profiles and properties of a novel stress-induced peroxidase in Neurospora crassa

Mycoscience, 2002-04, Vol.43 (2), p.103-111

2002

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Intramolecular Telomeric G-Quadruplexes Dramatically Inhibit DNA Synthesis by Replicative and Translesion Polymerases, Revealing their Potential to Lead to Genetic Change: e80664

PloS one, 2014-01, Vol.9 (1)

2014

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Response to Replication Stress and Maintenance of Genome Stability by WRN, the Werner Syndrome Protein

Cigarette Smoke-Induced Epithelial-to-Mesenchymal Transition: Insights into Cellular Mechanisms and Signaling Pathways

The Werner and Bloom Syndrome Proteins Help Resolve Replication Blockage by Converting (Regressed) Holliday Junctions to Functional Replication Forks

Strand exchange of telomeric DNA catalyzed by the Werner syndrome protein (WRN) is specifically stimulated by TRF2

Intramolecular telomeric G-quadruplexes dramatically inhibit DNA synthesis by replicative and translesion polymerases, revealing their potential to lead to genetic change

The Werner and Bloom Syndrome Proteins Catalyze Regression of a Model Replication Fork

The DNA structure and sequence preferences of WRN underlie its function in telomeric recombination events

Molecular Cooperation between the Werner Syndrome Protein and Replication Protein A in Relation to Replication Fork Blockage

RecQ Family Members Combine Strand Pairing and Unwinding Activities to Catalyze Strand Exchange

TRF2 recruits the Werner syndrome (WRN) exonuclease for processing of telomeric DNA

The Werner syndrome protein promotes CAG/CTG repeat stability by resolving large (CAG)(n)/(CTG)(n) hairpins

Functional and Physical Interaction between WRN Helicase and Human Replication Protein A

Lysine Acetylation of Proteins and Its Characterization in Human Systems

The Werner syndrome protein is involved in RNA polymerase II transcription

DNase I Footprinting and Enhanced Exonuclease Function of the Bipartite Werner Syndrome Protein (WRN) Bound to Partially Melted Duplex DNA

Accelerated methylation of ribosomal RNA genes during the cellular senescence of Werner syndrome fibroblasts

Role for the Werner syndrome protein (WRN) in replication fork regression

The Werner Syndrome Protein Promotes CAG/CTG Repeat Stability by Resolving Large (CAG)n/(CTG)n Hairpins

Replication fork regression in vitro by the Werner syndrome protein (WRN): holliday junction formation, the effect of leading arm structure and a potential role for WRN exonuclease activity

Association and regulation of the BLM helicase by the telomere proteins TRF1 and TRF2

Ku complex interacts with and stimulates the Werner protein

The Werner Syndrome Helicase/Exonuclease (WRN) Disrupts and Degrades D-Loops in Vitro

High constitutive peroxidase activity and constitutive thermotolerance in Neurospora crassa

Induction profiles and properties of a novel stress-induced peroxidase in Neurospora crassa

Intramolecular Telomeric G-Quadruplexes Dramatically Inhibit DNA Synthesis by Replicative and Translesion Polymerases, Revealing their Potential to Lead to Genetic Change: e80664

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