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Correction to: NF-κB mediates radio-sensitization by the PARP-1 inhibitor, AG-014699

Oncogene, 2023-02, Vol.42 (6), p.471-471

2023

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Tumour cell retention of rucaparib, sustained PARP inhibition and efficacy of weekly as well as daily schedules

British journal of cancer, 2014-04, Vol.110 (8), p.1977-1984

2014

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NF-κB mediates radio-sensitization by the PARP-1 inhibitor, AG-014699

Oncogene, 2012-01, Vol.31 (2), p.251-264

2012

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NF-[kappa]B mediates radio-sensitization by the PARP-1 inhibitor, AG-014699

Oncogene, 2012-01, Vol.31 (2), p.251

2012

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Central nervous system penetration and enhancement of temozolomide activity in childhood medulloblastoma models by poly(ADP-ribose) polymerase inhibitor AG-014699

British journal of cancer, 2010-11, Vol.103 (10), p.1588-1596

2010

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Resistance-Modifying Agents. 9. Synthesis and Biological Properties of Benzimidazole Inhibitors of the DNA Repair Enzyme Poly(ADP-ribose) Polymerase

Journal of medicinal chemistry, 2000-11, Vol.43 (22), p.4084-4097

2000

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The NS3 proteinase domain of hepatitis C virus is a zinc-containing enzyme

Journal of Virology, 1997-04, Vol.71 (4), p.2881-2886

1997

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Base Excision Repair Is Impaired in Mammalian Cells Lacking Poly(ADP-ribose) Polymerase-1

Biochemistry (Easton), 2000-06, Vol.39 (25), p.7559-7569

2000

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Novel Poly(ADP-ribose) Polymerase-1 Inhibitor, AG14361, Restores Sensitivity to Temozolomide in Mismatch Repair-Deficient Cells

Clinical cancer research, 2004-02, Vol.10 (3), p.881-889

2004

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Potentiation of Temozolomide and Topotecan Growth Inhibition and Cytotoxicity by Novel Poly(adenosine Diphosphoribose) Polymerase Inhibitors in a Panel of Human Tumor Cell Lines

Clinical cancer research, 2000-07, Vol.6 (7), p.2860-2867

2000

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The Crystal Structure of Hepatitis C Virus NS3 Proteinase Reveals a Trypsin-like Fold and a Structural Zinc Binding Site

Cell, 1996-10, Vol.87 (2), p.331-342

1996

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Reconstitution in vitro of RNase H Activity by Using Purified N-Terminal and C-Terminal Domains of Human Immunodeficiency Virus Type 1 Reverse Transcriptase

Proceedings of the National Academy of Sciences - PNAS, 1991-02, Vol.88 (4), p.1148-1152

1991

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Reverse transcriptase of human immunodeficiency virus type 1: functionality of subunits of the heterodimer in DNA synthesis

Journal of Virology, 1992-05, Vol.66 (5), p.3179-3182

1992

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Subunit composition and domain structure of the Spo0A sporulation transcription factor of Bacillus subtilis

The Journal of biological chemistry, 1994-06, Vol.269 (24), p.16977-16982

1994

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Tricyclic Benzimidazoles as Potent Poly(ADP-ribose) Polymerase-1 Inhibitors

Journal of medicinal chemistry, 2003-01, Vol.46 (2), p.210-213

2003

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Development of a Nonradioactive Ribonuclease H Assay

Analytical biochemistry, 1996-07, Vol.239 (1), p.113-115

1996

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Dicaffeoylquinic and Dicaffeoyltartaric Acids Are Selective Inhibitors of Human Immunodeficiency Virus Type 1 Integrase

Antimicrobial Agents and Chemotherapy, 1998-01, Vol.42 (1), p.140-146

1998

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Identification of potent nontoxic poly(ADP-ribose) polymerase-1 inhibitors: Chemopotentiation and pharmacological studies

Clinical cancer research, 2003-07, Vol.9 (7), p.2711-2718

2003

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Potentiation of cytotoxic drug activity in human tumour cell lines, by amine-substituted 2-arylbenzimidazole-4-carboxamide PARP-1 inhibitors

Bioorganic & medicinal chemistry letters, 2004-05, Vol.14 (10), p.2433-2437

2004

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Redesignation of the RNase D activity associated with retroviral reverse transcriptase as RNase H

Journal of Virology, 1994-03, Vol.68 (3), p.1970-1971

1994

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Proteolytic release and crystallization of the RNase H domain of human immunodeficiency virus type 1 reverse transcriptase

The Journal of biological chemistry, 1991-08, Vol.266 (22), p.14697-14702

1991

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Crystal Structure of the Ribonuclease H Domain of HIV-1 Reverse Transcriptase

Science (American Association for the Advancement of Science), 1991-04, Vol.252 (5002), p.88-95

1991

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High-affinity ssDNA inhibitors of the reverse transcriptase of type 1 human immunodeficiency virus

Biochemistry (Easton), 1995-07, Vol.34 (29), p.9599-9610

1995

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Design, Synthesis, and Evaluation of 3,4-Dihydro-2H-[1,4]diazepino[6,7,1-hi]indol-1-ones as Inhibitors of Poly(ADP-Ribose) Polymerase

Journal of medicinal chemistry, 2004-10, Vol.47 (22), p.5467-5481

2004

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2.3 Å crystal structure of the catalytic domain of DNA polymerase β

Cell, 1994-03, Vol.76 (6), p.1123-1133

1994

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Correction to: NF-κB mediates radio-sensitization by the PARP-1 inhibitor, AG-014699

Tumour cell retention of rucaparib, sustained PARP inhibition and efficacy of weekly as well as daily schedules

NF-κB mediates radio-sensitization by the PARP-1 inhibitor, AG-014699

NF-[kappa]B mediates radio-sensitization by the PARP-1 inhibitor, AG-014699

Central nervous system penetration and enhancement of temozolomide activity in childhood medulloblastoma models by poly(ADP-ribose) polymerase inhibitor AG-014699

Resistance-Modifying Agents. 9. Synthesis and Biological Properties of Benzimidazole Inhibitors of the DNA Repair Enzyme Poly(ADP-ribose) Polymerase

The NS3 proteinase domain of hepatitis C virus is a zinc-containing enzyme

Base Excision Repair Is Impaired in Mammalian Cells Lacking Poly(ADP-ribose) Polymerase-1

Novel Poly(ADP-ribose) Polymerase-1 Inhibitor, AG14361, Restores Sensitivity to Temozolomide in Mismatch Repair-Deficient Cells

Potentiation of Temozolomide and Topotecan Growth Inhibition and Cytotoxicity by Novel Poly(adenosine Diphosphoribose) Polymerase Inhibitors in a Panel of Human Tumor Cell Lines

The Crystal Structure of Hepatitis C Virus NS3 Proteinase Reveals a Trypsin-like Fold and a Structural Zinc Binding Site

Reconstitution in vitro of RNase H Activity by Using Purified N-Terminal and C-Terminal Domains of Human Immunodeficiency Virus Type 1 Reverse Transcriptase

Reverse transcriptase of human immunodeficiency virus type 1: functionality of subunits of the heterodimer in DNA synthesis

Subunit composition and domain structure of the Spo0A sporulation transcription factor of Bacillus subtilis

Tricyclic Benzimidazoles as Potent Poly(ADP-ribose) Polymerase-1 Inhibitors

Development of a Nonradioactive Ribonuclease H Assay

Dicaffeoylquinic and Dicaffeoyltartaric Acids Are Selective Inhibitors of Human Immunodeficiency Virus Type 1 Integrase

Identification of potent nontoxic poly(ADP-ribose) polymerase-1 inhibitors: Chemopotentiation and pharmacological studies

Potentiation of cytotoxic drug activity in human tumour cell lines, by amine-substituted 2-arylbenzimidazole-4-carboxamide PARP-1 inhibitors

Redesignation of the RNase D activity associated with retroviral reverse transcriptase as RNase H

Proteolytic release and crystallization of the RNase H domain of human immunodeficiency virus type 1 reverse transcriptase

Crystal Structure of the Ribonuclease H Domain of HIV-1 Reverse Transcriptase

High-affinity ssDNA inhibitors of the reverse transcriptase of type 1 human immunodeficiency virus

Design, Synthesis, and Evaluation of 3,4-Dihydro-2H-[1,4]diazepino[6,7,1-hi]indol-1-ones as Inhibitors of Poly(ADP-Ribose) Polymerase

2.3 Å crystal structure of the catalytic domain of DNA polymerase β

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