H. Odijk

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Molecular cloning of a human DNA repair gene

R. Wood, J. Hoeijmakers, A. Pastink, 1984, Nature.

Molecular cloning of the human DNA excision repair gene ERCC-6

J. Hoeijmakers, L. Thompson, D. Bootsma, 1990, Molecular and cellular biology.

The Structure-Specific Endonuclease Ercc1-Xpf Is Required To Resolve DNA Interstrand Cross-Link-Induced Double-Strand Breaks

J. Hoeijmakers, R. Kanaar, H. Beverloo, 2004, Molecular and Cellular Biology.

Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.

A. Yasui, J. Hoeijmakers, D. Bootsma, 1993, The EMBO journal.

Ionizing radiation-induced foci formation of mammalian Rad51 and Rad54 depends on the Rad51 paralogs, but not on Rad52.

R. Kanaar, J. Essers, L. V. van Veelen, 2005, Mutation research.

HSF2BP Interacts with a Conserved Domain of BRCA2 and Is Required for Mouse Spermatogenesis.

J. Lebbink, R. Kanaar, Koichi Sato, 2019, Cell reports.

Mutational analysis of the human nucleotide excision repair gene ERCC1.

P. J. van der Spek, J. Hoeijmakers, D. Bootsma, 1996, Nucleic acids research.

Augmentation of protein production by a combination of the T7 RNA polymerase system and ubiquitin fusion: overproduction of the human DNA repair protein, ERCC1, as a ubiquitin fusion protein in Escherichia coli.

M. Fornerod, J. Hoeijmakers, H. Odijk, 1993, Biochemical and biophysical research communications.

Differences between rodent and human cell lines in the amount of integrated DNA after transfection.

J. Hoeijmakers, A. Westerveld, H. Odijk, 1987, Experimental cell research.

Partial characterization of the DNA repair protein complex, containing the ERCC1, ERCC4, ERCC11 and XPF correcting activities.

J. Hoeijmakers, J. Egly, A. Eker, 1995, Mutation research.

Molecular cloning and biological characterization of the human excision repair gene ERCC-3

J. Hoeijmakers, R. V. van Ham, A. van der Eb, 1990, Molecular and cellular biology.

The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I.

J. Hoeijmakers, W. Vermeulen, D. Bootsma, 1989, Mutation research.

Molecular Cloning andBiological Characterization oftheHuman Excision Repair GeneERCC-3

D. Bootsma, G. Weeda, A. Westerveld, 1990 .

Ubiquitin ligase Rad18Sc localizes to the XY body and to other chromosomal regions that are unpaired and transcriptionally silenced during male meiotic prophase

J. Hoeijmakers, P. de Boer, J. Grootegoed, 2004, Journal of Cell Science.

Genomic characterization of the human DNA excision repair gene ERCC-1.

J. Hoeijmakers, P. ten Dijke, D. Bootsma, 1987, Nucleic acids research.

Mild hyperthermia inhibits homologous recombination, induces BRCA2 degradation, and sensitizes cancer cells to poly (ADP-ribose) polymerase-1 inhibition

R. Kanaar, J. Aten, L. Stalpers, 2011, Proceedings of the National Academy of Sciences.

Role of BRCA2 DNA-binding and C-terminal domain in its mobility and conformation in DNA repair

R. Kanaar, A. Zelensky, C. Wyman, 2021, eLife.

Role of BRCA2 DNA-binding and C-terminal domain on its mobility and conformation in DNA repair

R. Kanaar, A. Zelensky, C. Wyman, 2021, bioRxiv.

HSF2BP Negatively Regulates Homologous Recombination in DNA Interstrand Crosslink Repair in Human Cells by Direct Interaction With BRCA2

J. Lebbink, R. Kanaar, Koichi Sato, 2018, bioRxiv.

Evolution and mutagenesis of the mammalian excision repair gene ERCC-1.

J. Hoeijmakers, D. Meijer, D. Bootsma, 1988, Nucleic acids research.

Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10

A. Yasui, J. Hoeijmakers, D. Bootsma, 1986, Cell.

Transformation and immortalization of diploid xeroderma pigmentosum fibroblasts.

A. van der Eb, A. Pastink, A. Westerveld, 1990, Experimental cell research.

A Microfluidic Cancer-on-Chip Platform Predicts Drug Response Using Organotypic Tumor Slice Culture

R. Kanaar, J. Jonkers, D. V. van Gent, 2021, Cancer Research.

A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis

J. Hoeijmakers, G. Garinis, W. Vermeulen, 2006, Nature.

Mapping of interaction domains between human repair proteins ERCC1 and XPF.

W. de Laat, J. Hoeijmakers, W. D. Laat, 1998, Nucleic acids research.

On the Mechanism of Hyperthermia-Induced BRCA2 Protein Degradation

Jeroen A. A. Demmers, R. Kanaar, A. Zelensky, 2019, Cancers.

The structure‐specific endonuclease Ercc1—Xpf is required for targeted gene replacement in embryonic stem cells

B. Beverloo, J. Hoeijmakers, R. Kanaar, 2001, The EMBO journal.

Induction of a mutant phenotype in human repair proficient cells after overexpression of a mutated human DNA repair gene.

J. Hoeijmakers, M. V. van Oosterwijk, H. Odijk, 1991, Nucleic acids research.

The effect of thermal dose on hyperthermia-mediated inhibition of DNA repair through homologous recombination

W. V. van Cappellen, G. V. van Rhoon, R. Kanaar, 2017, Oncotarget.

The structure of the human ERCC1/XPF interaction domains reveals a complementary role for the two proteins in nucleotide excision repair.

R. Kaptein, G. Folkers, R. Boelens, 2005, Structure.

A mRad51-GFP antimorphic allele affects homologous recombination and DNA damage sensitivity.

W. V. van Cappellen, J. Hoeijmakers, R. Kanaar, 2015, DNA repair.

Heat-induced BRCA2 degradation in human tumours provides rationale for hyperthermia-PARP-inhibitor combination therapies

A. Jager, G. V. van Rhoon, H. V. van Doorn, 2018, International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group.