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The nuclear DEK interactome supports multi‐functionality

Proteins, structure, function, and bioinformatics, 2018-01, Vol.86 (1), p.88-97

2018

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DEK is required for homologous recombination repair of DNA breaks

Scientific reports, 2017-03, Vol.7 (1), p.44662, Article 44662

2017

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FANCL replaces BRCA1 as the likely ubiquitin ligase responsible for FANCD2 monoubiquitination

Cell cycle (Georgetown, Tex.), 2004-02, Vol.3 (2), p.179-181

2004

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The MHF complex senses branched DNA by binding a pair of crossover DNA duplexes

Nature communications, 2014-01, Vol.5 (1), p.2987-2987, Article 2987

2014

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The nuclear DEK interactome supports multi-functionality “The DEK Interactome”

Proteins, structure, function, and bioinformatics, 2017-11, Vol.86 (1), p.88-97

2017

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Abstract PR21: DEK is critical for homologous recombination and its loss is synthetic lethal with DNA-PK inhibition

Molecular cancer research, 2017-04, Vol.15 (4_Supplement), p.PR21-PR21

2017

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Breast cancer-associated missense mutants of the PALB2 WD40 domain, which directly binds RAD51C, RAD51 and BRCA2, disrupt DNA repair

Oncogene, 2014-10, Vol.33 (40), p.4803-4812

2014

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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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FANCB is essential in the male germline and regulates H3K9 methylation on the sex chromosomes during meiosis

Human molecular genetics, 2015-09, Vol.24 (18), p.5234-5249

2015

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A novel ubiquitin ligase is deficient in Fanconi anemia

Nature genetics, 2003-10, Vol.35 (2), p.165-170

2003

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BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome

Genes & development, 2008-10, Vol.22 (20), p.2856-2868

2008

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A Multiprotein Nuclear Complex Connects Fanconi Anemia and Bloom Syndrome

Molecular and Cellular Biology, 2003-05, Vol.23 (10), p.3417-3426

2003

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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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Loss of Faap20 Causes Hematopoietic Stem and Progenitor Cell Depletion in Mice Under Genotoxic Stress

Stem cells (Dayton, Ohio), 2015-07, Vol.33 (7), p.2320-2330

2015

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BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity

The EMBO journal, 2005-04, Vol.24 (7), p.1465-1476

2005

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A novel interplay between the Fanconi anemia core complex and ATR-ATRIP kinase during DNA cross-link repair

Nucleic acids research, 2013-08, Vol.41 (14), p.6930-6941

2013

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X-linked inheritance of Fanconi anemia complementation group B

Nature genetics, 2004-11, Vol.36 (11), p.1219-1224

2004

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Fancb deficiency impairs hematopoietic stem cell function

Scientific reports, 2015-12, Vol.5 (1), p.18127-18127, Article 18127

2015

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FANCM–FAAP24 and FANCJ: FA proteins that metabolize DNA

Mutation research, 2009-07, Vol.668 (1), p.20-26

2009

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Identification of Two Novel Zinc Finger Modules and Nuclear Localization Signal in Rat Spermatidal Protein TP2 by Site-directed Mutagenesis

The Journal of biological chemistry, 2000-12, Vol.275 (49), p.38500-38507

2000

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Involvement of Protein Kinase A in the Phosphorylation of Spermatidal Protein TP2 and Its Effect on DNA Condensation

Biochemistry (Easton), 2002-01, Vol.41 (1), p.185-195

2002

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Generation of Multiple Site-Specific Mutations in a Single Polymerase Chain Reaction Product

Analytical biochemistry, 1998-11, Vol.264 (2), p.288-291

1998

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Generation of multiple site-specific mutations by polymerase chain reaction

Methods in molecular biology (Clifton, N.J.), 2002, Vol.182, p.95

2002

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Hyperexpression of rat spermatidal protein TP2 in Escherichia coli by codon optimization and engineering the vector-encoded 5' UTR

Protein expression and purification, 1998-07, Vol.13 (2), p.184-190

1998

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Cloning of cDNA encoding rat spermatidal protein TP2 and expression in Escherichia coli

Protein expression and purification, 1996-12, Vol.8 (4), p.409-415

1996

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The nuclear DEK interactome supports multi‐functionality

DEK is required for homologous recombination repair of DNA breaks

FANCL replaces BRCA1 as the likely ubiquitin ligase responsible for FANCD2 monoubiquitination

The MHF complex senses branched DNA by binding a pair of crossover DNA duplexes

The nuclear DEK interactome supports multi-functionality “The DEK Interactome”

Abstract PR21: DEK is critical for homologous recombination and its loss is synthetic lethal with DNA-PK inhibition

Breast cancer-associated missense mutants of the PALB2 WD40 domain, which directly binds RAD51C, RAD51 and BRCA2, disrupt DNA repair

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

FANCB is essential in the male germline and regulates H3K9 methylation on the sex chromosomes during meiosis

A novel ubiquitin ligase is deficient in Fanconi anemia

BLAP18/RMI2, a novel OB-fold-containing protein, is an essential component of the Bloom helicase-double Holliday junction dissolvasome

A Multiprotein Nuclear Complex Connects Fanconi Anemia and Bloom Syndrome

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

Loss of Faap20 Causes Hematopoietic Stem and Progenitor Cell Depletion in Mice Under Genotoxic Stress

BLAP75, an essential component of Bloom's syndrome protein complexes that maintain genome integrity

A novel interplay between the Fanconi anemia core complex and ATR-ATRIP kinase during DNA cross-link repair

X-linked inheritance of Fanconi anemia complementation group B

Fancb deficiency impairs hematopoietic stem cell function

FANCM–FAAP24 and FANCJ: FA proteins that metabolize DNA

Identification of Two Novel Zinc Finger Modules and Nuclear Localization Signal in Rat Spermatidal Protein TP2 by Site-directed Mutagenesis

Involvement of Protein Kinase A in the Phosphorylation of Spermatidal Protein TP2 and Its Effect on DNA Condensation

Generation of Multiple Site-Specific Mutations in a Single Polymerase Chain Reaction Product

Generation of multiple site-specific mutations by polymerase chain reaction

Hyperexpression of rat spermatidal protein TP2 in Escherichia coli by codon optimization and engineering the vector-encoded 5' UTR

Cloning of cDNA encoding rat spermatidal protein TP2 and expression in Escherichia coli

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