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DNA Translocase FANCM/MHF Promotes Replication Traverse of DNA Interstrand Crosslinks

Molecular cell, 2013-11, Vol.52 (3), p.434-446

2013

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Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia

American journal of human genetics, 2013-05, Vol.92 (5), p.800-806

2013

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A Ubiquitin-Binding Protein, FAAP20, Links RNF8-Mediated Ubiquitination to the Fanconi Anemia DNA Repair Network

Molecular cell, 2012-07, Vol.47 (1), p.61-75

2012

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The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2

PloS one, 2009-09, Vol.4 (9), p.e6936

2009

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Functional ex vivo assay to select homologous recombination-deficient breast tumors for PARP inhibitor treatment

Clinical cancer research, 2014-09, Vol.20 (18), p.4816-4826

2014

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SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype

Nature genetics, 2011-02, Vol.43 (2), p.138-141

2011

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Biochemical Characterization of Warsaw Breakage Syndrome Helicase

The Journal of biological chemistry, 2012-01, Vol.287 (2), p.1007-1021

2012

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The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

Nature genetics, 2005-09, Vol.37 (9), p.934-935

2005

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A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M

Nature genetics, 2005-09, Vol.37 (9), p.958-963

2005

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Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M

Blood, 2009-07, Vol.114 (1), p.174-180

2009

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Recruitment of Fanconi Anemia and Breast Cancer Proteins to DNA Damage Sites Is Differentially Governed by Replication

Molecular cell, 2009-09, Vol.35 (5), p.716-723

2009

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DNA helicases FANCM and DDX11 are determinants of PARP inhibitor sensitivity

DNA repair, 2015-02, Vol.26, p.54-64

2015

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Learning from a paradox: recent insights into Fanconi anaemia through studying mouse models

Disease models & mechanisms, 2013-01, Vol.6 (1), p.40-47

2013

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Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene

American journal of human genetics, 2000-11, Vol.67 (5), p.1306-1308

2000

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Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis

Anemia, 2012-01, Vol.2012 (2012), p.53-61

2012

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FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway

The EMBO journal, 2007-04, Vol.26 (8), p.2104-2114

2007

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Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes

Blood, 2004-04, Vol.103 (7), p.2498-2503

2004

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Hypomorphic Mutations in the Gene Encoding a Key Fanconi Anemia Protein, FANCD2, Sustain a Significant Group of FA-D2 Patients with Severe Phenotype

American journal of human genetics, 2007-05, Vol.80 (5), p.895-910

2007

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The Fanconi anemia pathway of genomic maintenance

Analytical cellular pathology (Amsterdam), 2006, Vol.28 (1-2), p.3-29

2006

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A protein prioritization approach tailored for the FA/BRCA pathway

PloS one, 2013-04, Vol.8 (4), p.e62017-e62017

2013

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A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51

Nature communications, 2015-12, Vol.6 (1), p.8829, Article 8829

2015

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Correction: A Protein Prioritization Approach Tailored for the FA/BRCA Pathway

PloS one, 2013-10, Vol.8 (10)

2013

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Diagnosis of Fanconi Anemia: Mutation Analysis by Next-Generation Sequencing

Anemia, 2012-01, Vol.2012 (2012), p.13-19

2012

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Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing

Anemia, 2012-01, Vol.2012 (2012), p.206-218

2012

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DNA Translocase FANCM/MHF Promotes Replication Traverse of DNA Interstrand Crosslinks

Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia

A Ubiquitin-Binding Protein, FAAP20, Links RNF8-Mediated Ubiquitination to the Fanconi Anemia DNA Repair Network

The cellular phenotype of Roberts syndrome fibroblasts as revealed by ectopic expression of ESCO2

Functional ex vivo assay to select homologous recombination-deficient breast tumors for PARP inhibitor treatment

SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype

Biochemical Characterization of Warsaw Breakage Syndrome Helicase

A Histone-Fold Complex and FANCM Form a Conserved DNA-Remodeling Complex to Maintain Genome Stability

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M

Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M

Recruitment of Fanconi Anemia and Breast Cancer Proteins to DNA Damage Sites Is Differentially Governed by Replication

DNA helicases FANCM and DDX11 are determinants of PARP inhibitor sensitivity

Learning from a paradox: recent insights into Fanconi anaemia through studying mouse models

Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene

Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis

FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway

Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes

Hypomorphic Mutations in the Gene Encoding a Key Fanconi Anemia Protein, FANCD2, Sustain a Significant Group of FA-D2 Patients with Severe Phenotype

The Fanconi anemia pathway of genomic maintenance

A protein prioritization approach tailored for the FA/BRCA pathway

A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51

Correction: A Protein Prioritization Approach Tailored for the FA/BRCA Pathway

Diagnosis of Fanconi Anemia: Mutation Analysis by Next-Generation Sequencing

Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing

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