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The influence of DNA double-strand break structure on end-joining in human cells

Nucleic acids research, 2001-12, Vol.29 (23), p.4783-4792

2001

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Reactivating Elements: Chemistry, Ecology, Practice

1, 2022

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Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joining

Journal of molecular biology, 1998-06, Vol.279 (2), p.375-385

1998

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Decreased deletion mutation in radioadapted human lymphoblasts

Radiation research, 1993-01, Vol.133 (1), p.94

1993

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Hypomutability in Fanconi Anemia Cells is Associated with Increased Deletion Frequency at the HPRT Locus

Proceedings of the National Academy of Sciences - PNAS, 1990-11, Vol.87 (21), p.8383-8387

1990

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Abnormal rearrangements associated with V(D)J recombination in Fanconi anemia

Journal of molecular biology, 1998-09, Vol.281 (5), p.815-825

1998

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The Transcriptional Histone Acetyltransferase Cofactor TRRAP Associates with the MRN Repair Complex and Plays a Role in DNA Double-Strand Break Repair

Molecular and Cellular Biology, 2006-01, Vol.26 (2), p.402-412

2006

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Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiency

The Journal of clinical investigation, 1993-03, Vol.91 (3), p.1214-1218

1993

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A single mutated BRCA1 allele leads to impaired fidelity of double strand break end-joining

Oncogene, 2002-02, Vol.21 (9), p.1401-1410

2002

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A single mutated BRCA1 allele leads to impaired fidelity of double strand break end-joining

Oncogene, 2002-02, Vol.21 (9), p.1401-1410

2002

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The Molecular Mechanism Underlying Formation of Deletions in Fanconi Anemia Cells May Involve a Site-Specific Recombination

Proceedings of the National Academy of Sciences - PNAS, 1995-01, Vol.92 (3), p.831-835

1995

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The fidelity of double strand breaks processing is impaired in complementation groups B and D of Fanconi anemia, a genetic instability syndrome

Somatic cell and molecular genetics, 1997-11, Vol.23 (6), p.401-411

1997

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Impact of DNA ligase IV on the fidelity of end joining in human cells

Nucleic acids research, 2003-04, Vol.31 (8), p.2157-2167

2003

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Arrest of S-Phase Progression Is Impaired in Fanconi Anemia Cells

Experimental cell research, 2000-11, Vol.260 (2), p.208-215

2000

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A human severe combined immunodeficiency (SCID) condition with increased sensitivity to ionizing radiations and impaired V(D)J rearrangements defines a new DNA recombination/repair deficiency

The Journal of experimental medicine, 1998-08, Vol.188 (4), p.627-634

1998

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Fidelity of DNA double-strand break repair in heterozygous cell lines harbouring BRCA1 missense mutations

Oncogene, 2004-01, Vol.23 (4), p.914-919

2004

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Possible anti-recombinogenic role of Bloom's syndrome helicase in double-strand break processing

Nucleic acids research, 2003-11, Vol.31 (21), p.6272-6282

2003

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Abnormal Response to DNA Crosslinking Agents of Fanconi Anemia Fibroblasts Can Be Corrected by Transfection with Normal Human DNA

Proceedings of the National Academy of Sciences - PNAS, 1986-09, Vol.83 (18), p.7034-7038

1986

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Fanconi anemia: genes and function(s) revisited

M.S. Médecine sciences, 2005-08, Vol.21 (8-9), p.730-736

2005

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Genotoxic potential of psoralen cross-links versus monoadducts in normal human lymphoblasts

Mutation research, 1995-03, Vol.346 (3), p.173-179

1995

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Two complementation groups of Fanconi's anemia differ in their phenotypic response to a DNA-crosslinking treatment

Human genetics, 1987, Vol.75 (1), p.45-47

1987

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Management of atrial fibrillation in Greece: the MANAGE-AF study

Hellenic journal of cardiology, 2014-07, Vol.55 (4), p.281

2014

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HIGH LEVELS OF 4,5′,8-TRIMETHYLPSORALEN PHOTOINDUCED FURAN-SIDE MONOADDUCTS CAN BLOCK CROSS-LINK REMOVAL IN NORMAL HUMAN CELLS

Photochemistry and photobiology, 1988-03, Vol.47 (3), p.321-326

1988

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Mutagenic effects photoinduced in normal human lymphoblasts by a monofunctional pyridopsoralen in comparison to 8-methoxypsoralen

Mutation research, 1990-12, Vol.245 (4), p.259-266

1990

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MUTAGENIC EFFECTS PHOTOINDUCED IN MAMMALIAN CELLS IN VITRO BY TWO MONOFUNCTIONAL PYRIDOPSORALENS

Photochemistry and photobiology, 1986-07, Vol.44 (1), p.31-39

1986

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The influence of DNA double-strand break structure on end-joining in human cells

Reactivating Elements: Chemistry, Ecology, Practice

Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joining

Decreased deletion mutation in radioadapted human lymphoblasts

Hypomutability in Fanconi Anemia Cells is Associated with Increased Deletion Frequency at the HPRT Locus

Abnormal rearrangements associated with V(D)J recombination in Fanconi anemia

The Transcriptional Histone Acetyltransferase Cofactor TRRAP Associates with the MRN Repair Complex and Plays a Role in DNA Double-Strand Break Repair

Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiency

A single mutated BRCA1 allele leads to impaired fidelity of double strand break end-joining

A single mutated BRCA1 allele leads to impaired fidelity of double strand break end-joining

The Molecular Mechanism Underlying Formation of Deletions in Fanconi Anemia Cells May Involve a Site-Specific Recombination

The fidelity of double strand breaks processing is impaired in complementation groups B and D of Fanconi anemia, a genetic instability syndrome

Impact of DNA ligase IV on the fidelity of end joining in human cells

Arrest of S-Phase Progression Is Impaired in Fanconi Anemia Cells

A human severe combined immunodeficiency (SCID) condition with increased sensitivity to ionizing radiations and impaired V(D)J rearrangements defines a new DNA recombination/repair deficiency

Fidelity of DNA double-strand break repair in heterozygous cell lines harbouring BRCA1 missense mutations

Possible anti-recombinogenic role of Bloom's syndrome helicase in double-strand break processing

Abnormal Response to DNA Crosslinking Agents of Fanconi Anemia Fibroblasts Can Be Corrected by Transfection with Normal Human DNA

Fanconi anemia: genes and function(s) revisited

Genotoxic potential of psoralen cross-links versus monoadducts in normal human lymphoblasts

Two complementation groups of Fanconi's anemia differ in their phenotypic response to a DNA-crosslinking treatment

Management of atrial fibrillation in Greece: the MANAGE-AF study

HIGH LEVELS OF 4,5′,8-TRIMETHYLPSORALEN PHOTOINDUCED FURAN-SIDE MONOADDUCTS CAN BLOCK CROSS-LINK REMOVAL IN NORMAL HUMAN CELLS

Mutagenic effects photoinduced in normal human lymphoblasts by a monofunctional pyridopsoralen in comparison to 8-methoxypsoralen

MUTAGENIC EFFECTS PHOTOINDUCED IN MAMMALIAN CELLS IN VITRO BY TWO MONOFUNCTIONAL PYRIDOPSORALENS

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