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DNA DSB repair pathway choice: an orchestrated handover mechanism

British journal of radiology, 2014-03, Vol.87 (1035), p.20130685

2014

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DNA Double-strand Break Repair in a Cellular Context

Clinical oncology (Royal College of Radiologists (Great Britain)), 2014-05, Vol.26 (5), p.243-249

2014

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Identification of genes involved in repair of DNA double-strand breaks in mammalian cells

Radiation research, 1998-11, Vol.150 (5 Suppl), p.S80

Jeggo, P A

1998

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CsA can induce DNA double-strand breaks: implications for BMT regimens particularly for individuals with defective DNA repair

Bone marrow transplantation (Basingstoke), 2008-06, Vol.41 (11), p.983-989

2008

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DNA double-strand breaks: their cellular and clinical impact?

Oncogene, 2007-12, Vol.26 (56), p.7717-7719

2007

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Nonhomologous End Joining and V(D)J Recombination Require an Additional Factor

Proceedings of the National Academy of Sciences - PNAS, 2003-03, Vol.100 (5), p.2462-2467

2003

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An overview of three new disorders associated with genetic instability: LIG4 syndrome, RS-SCID and ATR-Seckel syndrome

DNA Repair, 2004-08, Vol.3 (8), p.1227-1235

2004

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Genetic variants of NHEJ DNA ligase IV can affect the risk of developing multiple myeloma, a tumour characterised by aberrant class switch recombination

Journal of medical genetics, 2002-12, Vol.39 (12), p.900-905

2002

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DNA repair: PARP – another guardian angel?

Current biology, 1998-01, Vol.8 (2), p.R49-R51

Jeggo, P.A.

1998

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Endogenously induced DNA double strand breaks arise in heterochromatic DNA regions and require ataxia telangiectasia mutated and Artemis for their repair

Nucleic acids research, 2011-09, Vol.39 (16), p.6986-6997

2011

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Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient

Current biology, 1999-07, Vol.9 (13), p.699,S1-702,S2

1999

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The C Terminus of Ku80 Activates the DNA-Dependent Protein Kinase Catalytic Subunit

Molecular and Cellular Biology, 1999-05, Vol.19 (5), p.3267-3277

1999

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Molecular and biochemical characterization of xrs mutants defective in Ku80

Molecular and Cellular Biology, 1997-03, Vol.17 (3), p.1264-1273

1997

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Ku80: Product of the XRCC5 Gene and Its Role in DNA Repair and V(D)J Recombination

Science (American Association for the Advancement of Science), 1994-09, Vol.265 (5177), p.1442-1445

1994

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Accelerated Telomere Shortening and Telomere Abnormalities in Radiosensitive Cell Lines

Radiation research, 2005-07, Vol.164 (1), p.53-62

2005

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Identification of a Nonsense Mutation in the Carboxyl-Terminal Region of DNA-Dependent Protein Kinase Catalytic Subunit in the scid Mouse

Proceedings of the National Academy of Sciences - PNAS, 1996-09, Vol.93 (19), p.10285-10290

1996

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A Pathway of Double-Strand Break Rejoining Dependent upon ATM, Artemis, and Proteins Locating to γ-H2AX Foci

Molecular cell, 2004-12, Vol.16 (5), p.715-724

2004

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Splitting the ATM: distinct repair and checkpoint defects in ataxia–telangiectasia

Trends in genetics, 1998-08, Vol.14 (8), p.312-316

1998

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The life and death of DNA-PK

Oncogene, 2005-02, Vol.24 (6), p.949-961

2005

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The clinical and biological overlap between Nijmegen Breakage Syndrome and Fanconi anemia

Clinical immunology (Orlando, Fla.), 2004-11, Vol.113 (2), p.214-219

2004

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A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome

Nature genetics, 2003-04, Vol.33 (4), p.497-501

2003

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DNA-Dependent Protein Kinase Activity is Absent in xrs-6 Cells: Implications for Site-Specific Recombination and DNA Double-Strand Break Repair

Proceedings of the National Academy of Sciences - PNAS, 1995-01, Vol.92 (1), p.320-324

1995

Volltextzugriff (PDF)

Impairment of V(D)J Recombination in Double-Strand Break Repair Mutants

Science (American Association for the Advancement of Science), 1993-04, Vol.260 (5105), p.207-210

1993

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Immunodeficiency associated with DNA repair defects

Clinical and experimental immunology, 2000-07, Vol.121 (1), p.1-7

2000

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Chromosomal Double-Strand Break Repair in Ku80-Deficient Cells

Proceedings of the National Academy of Sciences - PNAS, 1996-08, Vol.93 (17), p.8929-8933

1996

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DNA DSB repair pathway choice: an orchestrated handover mechanism

DNA Double-strand Break Repair in a Cellular Context

Identification of genes involved in repair of DNA double-strand breaks in mammalian cells

CsA can induce DNA double-strand breaks: implications for BMT regimens particularly for individuals with defective DNA repair

DNA double-strand breaks: their cellular and clinical impact?

Nonhomologous End Joining and V(D)J Recombination Require an Additional Factor

An overview of three new disorders associated with genetic instability: LIG4 syndrome, RS-SCID and ATR-Seckel syndrome

Genetic variants of NHEJ DNA ligase IV can affect the risk of developing multiple myeloma, a tumour characterised by aberrant class switch recombination

DNA repair: PARP – another guardian angel?

Endogenously induced DNA double strand breaks arise in heterochromatic DNA regions and require ataxia telangiectasia mutated and Artemis for their repair

Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient

The C Terminus of Ku80 Activates the DNA-Dependent Protein Kinase Catalytic Subunit

Molecular and biochemical characterization of xrs mutants defective in Ku80

Ku80: Product of the XRCC5 Gene and Its Role in DNA Repair and V(D)J Recombination

Accelerated Telomere Shortening and Telomere Abnormalities in Radiosensitive Cell Lines

Identification of a Nonsense Mutation in the Carboxyl-Terminal Region of DNA-Dependent Protein Kinase Catalytic Subunit in the scid Mouse

A Pathway of Double-Strand Break Rejoining Dependent upon ATM, Artemis, and Proteins Locating to γ-H2AX Foci

Splitting the ATM: distinct repair and checkpoint defects in ataxia–telangiectasia

The life and death of DNA-PK

The clinical and biological overlap between Nijmegen Breakage Syndrome and Fanconi anemia

A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome

DNA-Dependent Protein Kinase Activity is Absent in xrs-6 Cells: Implications for Site-Specific Recombination and DNA Double-Strand Break Repair

Impairment of V(D)J Recombination in Double-Strand Break Repair Mutants

Immunodeficiency associated with DNA repair defects

Chromosomal Double-Strand Break Repair in Ku80-Deficient Cells

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