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Welcome the Family of FANCJ-like Helicases to the Block of Genome Stability Maintenance Proteins

Cellular and molecular life sciences : CMLS, 2009-04, Vol.66 (7), p.1209-1222

2009

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The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases

Nucleic acids research, 2001-07, Vol.29 (13), p.2843-2849

2001

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Detection of G-quadruplex DNA in mammalian cells

Nucleic acids research, 2014-01, Vol.42 (2), p.860-869

2014

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Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity

The EMBO journal, 2001-10, Vol.20 (20), p.5791-5801

2001

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Replication Protein A Physically Interacts with the Bloom's Syndrome Protein and Stimulates Its Helicase Activity

The Journal of biological chemistry, 2000-08, Vol.275 (31), p.23500-23508

2000

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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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The Cockayne Syndrome Group B Gene Product Is Involved in General Genome Base Excision Repair of 8-Hydroxyguanine in DNA

The Journal of biological chemistry, 2001-12, Vol.276 (49), p.45772-45779

2001

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Unwinding of a DNA Triple Helix by the Werner and Bloom Syndrome Helicases

The Journal of biological chemistry, 2001-02, Vol.276 (5), p.3024-3030

2001

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Inhibition of the Bloom's and Werner's Syndrome Helicases by G-Quadruplex Interacting Ligands

Biochemistry (Easton), 2001-12, Vol.40 (50), p.15194-15202

2001

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Coordinate action of the helicase and 3' to 5' exonuclease of Werner syndrome protein

The Journal of biological chemistry, 2001-11, Vol.276 (48), p.44677-44687

2001

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Enzymatic and DNA binding properties of purified WRN protein: high affinity binding to single-stranded DNA but not to DNA damage induced by 4NQO

Nucleic acids research, 1999-09, Vol.27 (17), p.3557-3566

1999

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p53 Modulates the Exonuclease Activity of Werner Syndrome Protein

The Journal of biological chemistry, 2001-09, Vol.276 (37), p.35093-35102

2001

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Potent inhibition of werner and bloom helicases by DNA minor groove binding drugs

Nucleic acids research, 2000-06, Vol.28 (12), p.2420-2430

2000

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Role of the ATPase domain of the Cockayne syndrome group B protein in UV induced apoptosis

Oncogene, 2000-01, Vol.19 (4), p.477-489

2000

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Mutations in motif II of Escherichia coli DNA helicase II render the enzyme nonfunctional in both mismatch repair and excision repair with differential effects on the unwinding reaction

Journal of Bacteriology, 1995-10, Vol.177 (19), p.5612-5621

1995

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DNA helicase and helicase-nuclease enzymes with a conserved iron-sulfur cluster

Nucleic acids research, 2012-05, Vol.40 (10), p.4247-4260

2012

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Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest

EMBO reports, 2000-07, Vol.1 (1), p.80-84

2000

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Escherichia coli SecA Helicase Activity Is Not Required in Vivo for Efficient Protein Translocation or Autogenous Regulation

The Journal of biological chemistry, 2001-10, Vol.276 (40), p.37076-37085

2001

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A Dominant Negative Allele of the Escherichia coli uvrD Gene Encoding DNA Helicase II : A Biochemical and Genetic Characterization

Journal of molecular biology, 1994-01, Vol.235 (2), p.424-435

1994

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Molecular characterization of an acidic region deletion mutant of Cockayne syndrome group B protein

Nucleic acids research, 2000-08, Vol.28 (16), p.3151-3159

2000

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Human premature aging, DNA repair and RecQ helicases

Nucleic acids research, 2007-12, Vol.35 (22), p.7527-7544

2007

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A partially functional DNA helicase II mutant defective in forming stable binary complexes with ATP and DNA. A role for helicase motif III

The Journal of biological chemistry, 1996-10, Vol.271 (41), p.25360-25368

1996

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Stimulation of Flap Endonuclease-1 by the Bloom's Syndrome Protein

The Journal of biological chemistry, 2004-03, Vol.279 (11), p.9847-9856

2004

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The ATPase domain but not the acidic region of Cockayne syndrome group B gene product is essential for DNA repair

Molecular biology of the cell, 1999-11, Vol.10 (11), p.3583-3594

1999

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Biochemical Characterization of the DNA Substrate Specificity of Werner Syndrome Helicase

The Journal of biological chemistry, 2002-06, Vol.277 (26), p.23236-23245

2002

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Welcome the Family of FANCJ-like Helicases to the Block of Genome Stability Maintenance Proteins

The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases

Detection of G-quadruplex DNA in mammalian cells

Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity

Replication Protein A Physically Interacts with the Bloom's Syndrome Protein and Stimulates Its Helicase Activity

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

The Cockayne Syndrome Group B Gene Product Is Involved in General Genome Base Excision Repair of 8-Hydroxyguanine in DNA

Unwinding of a DNA Triple Helix by the Werner and Bloom Syndrome Helicases

Inhibition of the Bloom's and Werner's Syndrome Helicases by G-Quadruplex Interacting Ligands

Coordinate action of the helicase and 3' to 5' exonuclease of Werner syndrome protein

Enzymatic and DNA binding properties of purified WRN protein: high affinity binding to single-stranded DNA but not to DNA damage induced by 4NQO

p53 Modulates the Exonuclease Activity of Werner Syndrome Protein

Potent inhibition of werner and bloom helicases by DNA minor groove binding drugs

Role of the ATPase domain of the Cockayne syndrome group B protein in UV induced apoptosis

Mutations in motif II of Escherichia coli DNA helicase II render the enzyme nonfunctional in both mismatch repair and excision repair with differential effects on the unwinding reaction

DNA helicase and helicase-nuclease enzymes with a conserved iron-sulfur cluster

Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest

Escherichia coli SecA Helicase Activity Is Not Required in Vivo for Efficient Protein Translocation or Autogenous Regulation

A Dominant Negative Allele of the Escherichia coli uvrD Gene Encoding DNA Helicase II : A Biochemical and Genetic Characterization

Molecular characterization of an acidic region deletion mutant of Cockayne syndrome group B protein

Human premature aging, DNA repair and RecQ helicases

A partially functional DNA helicase II mutant defective in forming stable binary complexes with ATP and DNA. A role for helicase motif III

Stimulation of Flap Endonuclease-1 by the Bloom's Syndrome Protein

The ATPase domain but not the acidic region of Cockayne syndrome group B gene product is essential for DNA repair

Biochemical Characterization of the DNA Substrate Specificity of Werner Syndrome Helicase

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