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Redundancy of DNA helicases in p53-mediated apoptosis

Oncogene, 2006-03, Vol.25 (14), p.2119-2123

2006

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Vesicular stomatitis virus matrix protein inhibits host cell gene expression by targeting the nucleoporin Nup98

Molecular cell, 2000-11, Vol.6 (5), p.1243-1252

2000

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Poly(ADP-ribose) polymerase 1 regulates both the exonuclease and helicase activities of the Werner syndrome protein

Nucleic acids research, 2004-01, Vol.32 (13), p.4003-4014

2004

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Telomere-binding Protein TRF2 Binds to and Stimulates the Werner and Bloom Syndrome Helicases

The Journal of biological chemistry, 2002-10, Vol.277 (43), p.41110-41119

2002

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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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Cooperation of the Cockayne Syndrome Group B Protein and Poly(ADP-Ribose) Polymerase 1 in the Response to Oxidative Stress

Molecular and Cellular Biology, 2005-09, Vol.25 (17), p.7625-7636

2005

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Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process

Carcinogenesis (New York), 2003-05, Vol.24 (5), p.791-802

2003

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TAP, the human homolog of Mex67p, mediates CTE-dependent RNA export from the nucleus

Molecular cell, 1998-04, Vol.1 (5), p.649-659

1998

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The asymmetric distribution of the constituents of the Ran system is essential for transport into and out of the nucleus

The EMBO journal, 1997-11, Vol.16 (21), p.6535-6547

1997

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Central Role for the Werner Syndrome Protein/Poly(ADP-Ribose) Polymerase 1 Complex in the Poly(ADP-Ribosyl)ation Pathway after DNA Damage

Molecular and Cellular Biology, 2003-12, Vol.23 (23), p.8601-8613

2003

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AMP-Activated Kinase Regulates Cytoplasmic HuR

Molecular and Cellular Biology, 2002-05, Vol.22 (10), p.3425-3436

2002

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Physical and Functional Mapping of the Replication Protein A Interaction Domain of the Werner and Bloom Syndrome Helicases

The Journal of biological chemistry, 2005-08, Vol.280 (33), p.29494-29505

2005

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Werner syndrome cells escape hydrogen peroxide‐induced cell proliferation arrest

The FASEB journal, 2004-12, Vol.18 (15), p.1970-1972

2004

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WRN Interacts Physically and Functionally with the Recombination Mediator Protein RAD52

The Journal of biological chemistry, 2003-09, Vol.278 (38), p.36476-36486

2003

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Werner Syndrome Protein Contains Three Structure-specific DNA Binding Domains

The Journal of biological chemistry, 2003-12, Vol.278 (52), p.52997-53006

2003

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Linkage between Werner Syndrome Protein and the Mre11 Complex via Nbs1

The Journal of biological chemistry, 2004-05, Vol.279 (20), p.21169-21176

2004

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Dbp5, a DEAD-box protein required for mRNA export, is recruited to the cytoplasmic fibrils of nuclear pore complex via a conserved interaction with CAN/Nup159p

The EMBO journal, 1999-08, Vol.18 (15), p.4332-4347

1999

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The C-terminal domain of TAP interacts with the nuclear pore complex and promotes export of specific CTE-bearing RNA substrates

RNA (Cambridge), 2000-01, Vol.6 (1), p.136-158, Article S1355838200991994

2000

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A nucleolar targeting sequence in the Werner syndrome protein resides within residues 949-1092

Journal of cell science, 2002-10, Vol.115 (Pt 20), p.3901-3907

2002

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Colocalization, Physical, and Functional Interaction between Werner and Bloom Syndrome Proteins

The Journal of biological chemistry, 2002-06, Vol.277 (24), p.22035-22044

2002

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The Werner syndrome protein stimulates DNA polymerase beta strand displacement synthesis via its helicase activity

The Journal of biological chemistry, 2003-06, Vol.278 (25), p.22686-22695

2003

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Werner Syndrome Protein Phosphorylation by Abl Tyrosine Kinase Regulates Its Activity and Distribution

Molecular and Cellular Biology, 2003-09, Vol.23 (18), p.6385-6395

2003

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Werner syndrome protein directly binds to the AAA ATPase p97/VCP in an ATP-dependent fashion

Journal of structural biology, 2004-04, Vol.146 (1), p.251-259

2004

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Identification and characterization of a new oncogene derived from the regulatory subunit of phosphoinositide 3-kinase

The EMBO journal, 1998-02, Vol.17 (3), p.743-753

1998

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Modulation of Werner Syndrome Protein Function by a Single Mutation in the Conserved RecQ Domain

The Journal of biological chemistry, 2005-11, Vol.280 (47), p.39627-39636

2005

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Redundancy of DNA helicases in p53-mediated apoptosis

Vesicular stomatitis virus matrix protein inhibits host cell gene expression by targeting the nucleoporin Nup98

Poly(ADP-ribose) polymerase 1 regulates both the exonuclease and helicase activities of the Werner syndrome protein

Telomere-binding Protein TRF2 Binds to and Stimulates the Werner and Bloom Syndrome Helicases

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

Cooperation of the Cockayne Syndrome Group B Protein and Poly(ADP-Ribose) Polymerase 1 in the Response to Oxidative Stress

Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process

TAP, the human homolog of Mex67p, mediates CTE-dependent RNA export from the nucleus

The asymmetric distribution of the constituents of the Ran system is essential for transport into and out of the nucleus

Central Role for the Werner Syndrome Protein/Poly(ADP-Ribose) Polymerase 1 Complex in the Poly(ADP-Ribosyl)ation Pathway after DNA Damage

AMP-Activated Kinase Regulates Cytoplasmic HuR

Physical and Functional Mapping of the Replication Protein A Interaction Domain of the Werner and Bloom Syndrome Helicases

Werner syndrome cells escape hydrogen peroxide‐induced cell proliferation arrest

WRN Interacts Physically and Functionally with the Recombination Mediator Protein RAD52

Werner Syndrome Protein Contains Three Structure-specific DNA Binding Domains

Linkage between Werner Syndrome Protein and the Mre11 Complex via Nbs1

Dbp5, a DEAD-box protein required for mRNA export, is recruited to the cytoplasmic fibrils of nuclear pore complex via a conserved interaction with CAN/Nup159p

The C-terminal domain of TAP interacts with the nuclear pore complex and promotes export of specific CTE-bearing RNA substrates

A nucleolar targeting sequence in the Werner syndrome protein resides within residues 949-1092

Colocalization, Physical, and Functional Interaction between Werner and Bloom Syndrome Proteins

The Werner syndrome protein stimulates DNA polymerase beta strand displacement synthesis via its helicase activity

Werner Syndrome Protein Phosphorylation by Abl Tyrosine Kinase Regulates Its Activity and Distribution

Werner syndrome protein directly binds to the AAA ATPase p97/VCP in an ATP-dependent fashion

Identification and characterization of a new oncogene derived from the regulatory subunit of phosphoinositide 3-kinase

Modulation of Werner Syndrome Protein Function by a Single Mutation in the Conserved RecQ Domain

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